DECIPHER	1	Wolf-Hirschhorn Syndrome		HP:0000252	DECIPHER:1	IEA				P	WOLF-HIRSCHHORN SYNDROME	HPO:skoehler	
DECIPHER	1	Wolf-Hirschhorn Syndrome		HP:0001249	DECIPHER:1	IEA				P	WOLF-HIRSCHHORN SYNDROME	HPO:skoehler	
DECIPHER	1	Wolf-Hirschhorn Syndrome		HP:0001250	DECIPHER:1	IEA				P	WOLF-HIRSCHHORN SYNDROME	HPO:skoehler	
DECIPHER	1	Wolf-Hirschhorn Syndrome		HP:0001252	DECIPHER:1	IEA				P	WOLF-HIRSCHHORN SYNDROME	HPO:skoehler	
DECIPHER	1	Wolf-Hirschhorn Syndrome		HP:0001518	DECIPHER:1	IEA				P	WOLF-HIRSCHHORN SYNDROME	HPO:skoehler	
DECIPHER	14	Prader-Willi syndrome (Type 1)		HP:0000135	DECIPHER:14	IEA				P	PRADER-WILLI SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	14	Prader-Willi syndrome (Type 1)		HP:0001249	DECIPHER:14	IEA				P	PRADER-WILLI SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	14	Prader-Willi syndrome (Type 1)		HP:0001252	DECIPHER:14	IEA				P	PRADER-WILLI SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	14	Prader-Willi syndrome (Type 1)		HP:0001956	DECIPHER:14	IEA				P	PRADER-WILLI SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	14	Prader-Willi syndrome (Type 1)		HP:0008872	DECIPHER:14	IEA				P	PRADER-WILLI SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0000280	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0000316	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0000957	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0001067	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0001249	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	15	NF1-microdeletion syndrome		HP:0001627	DECIPHER:15	IEA				P	NF1-MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0000750	DECIPHER:16	IEA				P	22Q11 DELETION SYNDROME (VELOCARDIOFACIAL / DIGEORGE SYNDROME)	HPO:skoehler	
DECIPHER	16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0001611	DECIPHER:16	IEA				P	22Q11 DELETION SYNDROME (VELOCARDIOFACIAL / DIGEORGE SYNDROME)	HPO:skoehler	
DECIPHER	16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0001627	DECIPHER:16	IEA				P	22Q11 DELETION SYNDROME (VELOCARDIOFACIAL / DIGEORGE SYNDROME)	HPO:skoehler	
DECIPHER	16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0002901	DECIPHER:16	IEA				P	22Q11 DELETION SYNDROME (VELOCARDIOFACIAL / DIGEORGE SYNDROME)	HPO:skoehler	
DECIPHER	16	22q11 deletion syndrome (Velocardiofacial / DiGeorge syndrome)		HP:0005403	DECIPHER:16	IEA				P	22Q11 DELETION SYNDROME (VELOCARDIOFACIAL / DIGEORGE SYNDROME)	HPO:skoehler	
DECIPHER	17	Sotos syndrome		HP:0000098	DECIPHER:17	IEA				P	SOTOS SYNDROME	HPO:skoehler	
DECIPHER	17	Sotos syndrome		HP:0000256	DECIPHER:17	IEA				P	SOTOS SYNDROME	HPO:skoehler	
DECIPHER	17	Sotos syndrome		HP:0000303	DECIPHER:17	IEA				P	SOTOS SYNDROME	HPO:skoehler	
DECIPHER	17	Sotos syndrome		HP:0001249	DECIPHER:17	IEA				P	SOTOS SYNDROME	HPO:skoehler	
DECIPHER	17	Sotos syndrome		HP:0005616	DECIPHER:17	IEA				P	SOTOS SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0000270	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0000307	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0000490	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0001249	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0001250	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	18	1p36 microdeletion syndrome		HP:0001252	DECIPHER:18	IEA				P	1P36 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000717	DECIPHER:19	IEA				P	POTOCKI-LUPSKI SYNDROME (17P11.2 DUPLICATION SYNDROME)	HPO:skoehler	
DECIPHER	19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000736	DECIPHER:19	IEA				P	POTOCKI-LUPSKI SYNDROME (17P11.2 DUPLICATION SYNDROME)	HPO:skoehler	
DECIPHER	19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0000752	DECIPHER:19	IEA				P	POTOCKI-LUPSKI SYNDROME (17P11.2 DUPLICATION SYNDROME)	HPO:skoehler	
DECIPHER	19	Potocki-Lupski syndrome (17p11.2 duplication syndrome)		HP:0004322	DECIPHER:19	IEA				P	POTOCKI-LUPSKI SYNDROME (17P11.2 DUPLICATION SYNDROME)	HPO:skoehler	
DECIPHER	2	Cri du Chat Syndrome (5p deletion)		HP:0000252	DECIPHER:2	IEA				P	CRI DU CHAT SYNDROME (5P DELETION)	HPO:skoehler	
DECIPHER	2	Cri du Chat Syndrome (5p deletion)		HP:0001249	DECIPHER:2	IEA				P	CRI DU CHAT SYNDROME (5P DELETION)	HPO:skoehler	
DECIPHER	2	Cri du Chat Syndrome (5p deletion)		HP:0001620	DECIPHER:2	IEA				P	CRI DU CHAT SYNDROME (5P DELETION)	HPO:skoehler	
DECIPHER	20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000717	DECIPHER:20	IEA				P	22Q13 DELETION SYNDROME (PHELAN-MCDERMID SYNDROME)	HPO:skoehler	
DECIPHER	20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000750	DECIPHER:20	IEA				P	22Q13 DELETION SYNDROME (PHELAN-MCDERMID SYNDROME)	HPO:skoehler	
DECIPHER	20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0000752	DECIPHER:20	IEA				P	22Q13 DELETION SYNDROME (PHELAN-MCDERMID SYNDROME)	HPO:skoehler	
DECIPHER	20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0001249	DECIPHER:20	IEA				P	22Q13 DELETION SYNDROME (PHELAN-MCDERMID SYNDROME)	HPO:skoehler	
DECIPHER	20	22q13 deletion syndrome (Phelan-Mcdermid syndrome)		HP:0001252	DECIPHER:20	IEA				P	22Q13 DELETION SYNDROME (PHELAN-MCDERMID SYNDROME)	HPO:skoehler	
DECIPHER	21	Miller-Dieker syndrome (MDS)		HP:0000252	DECIPHER:21	IEA				P	MILLER-DIEKER SYNDROME (MDS)	HPO:skoehler	
DECIPHER	21	Miller-Dieker syndrome (MDS)		HP:0001339	DECIPHER:21	IEA				P	MILLER-DIEKER SYNDROME (MDS)	HPO:skoehler	
DECIPHER	21	Miller-Dieker syndrome (MDS)		HP:0001627	DECIPHER:21	IEA				P	MILLER-DIEKER SYNDROME (MDS)	HPO:skoehler	
DECIPHER	21	Miller-Dieker syndrome (MDS)		HP:0002007	DECIPHER:21	IEA				P	MILLER-DIEKER SYNDROME (MDS)	HPO:skoehler	
DECIPHER	21	Miller-Dieker syndrome (MDS)		HP:0011800	DECIPHER:21	IEA				P	MILLER-DIEKER SYNDROME (MDS)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0001761	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0002450	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0002495	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0003382	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0003431	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0007328	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0010829	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	29	Charcot-Marie-Tooth syndrome type 1A (CMT1A)		HP:0010831	DECIPHER:29	IEA				P	CHARCOT-MARIE-TOOTH SYNDROME TYPE 1A (CMT1A)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0000232	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0000272	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0000691	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0000736	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0001249	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0001650	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	3	Williams-Beuren Syndrome (WBS)		HP:0004322	DECIPHER:3	IEA				P	WILLIAMS-BEUREN SYNDROME (WBS)	HPO:skoehler	
DECIPHER	31	Hereditary Liability to Pressure Palsies (HNPP)		HP:0002450	DECIPHER:31	IEA				P	HEREDITARY LIABILITY TO PRESSURE PALSIES (HNPP)	HPO:skoehler	
DECIPHER	31	Hereditary Liability to Pressure Palsies (HNPP)		HP:0012078	DECIPHER:31	IEA				P	HEREDITARY LIABILITY TO PRESSURE PALSIES (HNPP)	HPO:skoehler	
DECIPHER	32	22q11 duplication syndrome		HP:0000506	DECIPHER:32	IEA				P	22Q11 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	32	22q11 duplication syndrome		HP:0001249	DECIPHER:32	IEA				P	22Q11 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	32	22q11 duplication syndrome		HP:0001611	DECIPHER:32	IEA				P	22Q11 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	34	Potocki-Shaffer syndrome		HP:0000270	DECIPHER:34	IEA				P	POTOCKI-SHAFFER SYNDROME	HPO:skoehler	
DECIPHER	34	Potocki-Shaffer syndrome		HP:0001249	DECIPHER:34	IEA				P	POTOCKI-SHAFFER SYNDROME	HPO:skoehler	
DECIPHER	34	Potocki-Shaffer syndrome		HP:0002697	DECIPHER:34	IEA				P	POTOCKI-SHAFFER SYNDROME	HPO:skoehler	
DECIPHER	34	Potocki-Shaffer syndrome		HP:0002762	DECIPHER:34	IEA				P	POTOCKI-SHAFFER SYNDROME	HPO:skoehler	
DECIPHER	34	Potocki-Shaffer syndrome		HP:0010461	DECIPHER:34	IEA				P	POTOCKI-SHAFFER SYNDROME	HPO:skoehler	
DECIPHER	35	WAGR 11p13 deletion syndrome		HP:0000526	DECIPHER:35	IEA				P	WAGR 11P13 DELETION SYNDROME	HPO:skoehler	
DECIPHER	35	WAGR 11p13 deletion syndrome		HP:0001249	DECIPHER:35	IEA				P	WAGR 11P13 DELETION SYNDROME	HPO:skoehler	
DECIPHER	35	WAGR 11p13 deletion syndrome		HP:0009726	DECIPHER:35	IEA				P	WAGR 11P13 DELETION SYNDROME	HPO:skoehler	
DECIPHER	35	WAGR 11p13 deletion syndrome		HP:0010461	DECIPHER:35	IEA				P	WAGR 11P13 DELETION SYNDROME	HPO:skoehler	
DECIPHER	37	3q29 microdeletion syndrome		HP:0000276	DECIPHER:37	IEA				P	3Q29 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	37	3q29 microdeletion syndrome		HP:0000322	DECIPHER:37	IEA				P	3Q29 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	37	3q29 microdeletion syndrome		HP:0000426	DECIPHER:37	IEA				P	3Q29 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	37	3q29 microdeletion syndrome		HP:0001249	DECIPHER:37	IEA				P	3Q29 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	38	Pelizaeus-Merzbacher disease		HP:0000639	DECIPHER:38	IEA				P	PELIZAEUS-MERZBACHER DISEASE	HPO:skoehler	
DECIPHER	38	Pelizaeus-Merzbacher disease		HP:0001252	DECIPHER:38	IEA				P	PELIZAEUS-MERZBACHER DISEASE	HPO:skoehler	
DECIPHER	38	Pelizaeus-Merzbacher disease		HP:0002415	DECIPHER:38	IEA				P	PELIZAEUS-MERZBACHER DISEASE	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0000028	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0000752	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0000776	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0001249	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0001631	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	39	8p23.1 deletion syndrome		HP:0006695	DECIPHER:39	IEA				P	8P23.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	4	Angelman syndrome (Type 1)		HP:0000252	DECIPHER:4	IEA				P	ANGELMAN SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	4	Angelman syndrome (Type 1)		HP:0001249	DECIPHER:4	IEA				P	ANGELMAN SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	4	Angelman syndrome (Type 1)		HP:0001250	DECIPHER:4	IEA				P	ANGELMAN SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	4	Angelman syndrome (Type 1)		HP:0002078	DECIPHER:4	IEA				P	ANGELMAN SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	4	Angelman syndrome (Type 1)		HP:0002353	DECIPHER:4	IEA				P	ANGELMAN SYNDROME (TYPE 1)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0000347	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0000384	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0000494	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0000612	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0001249	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0001627	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0002023	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0004322	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	42	Cat-Eye Syndrome (Type I)		HP:0004467	DECIPHER:42	IEA				P	CAT-EYE SYNDROME (TYPE I)	HPO:skoehler	
DECIPHER	43	7q11.23 duplication syndrome		HP:0000736	DECIPHER:43	IEA				P	7Q11.23 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	43	7q11.23 duplication syndrome		HP:0000750	DECIPHER:43	IEA				P	7Q11.23 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	43	7q11.23 duplication syndrome		HP:0001249	DECIPHER:43	IEA				P	7Q11.23 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	44	2q37 monosomy		HP:0000219	DECIPHER:44	IEA				P	2Q37 MONOSOMY	HPO:skoehler	
DECIPHER	44	2q37 monosomy		HP:0000311	DECIPHER:44	IEA				P	2Q37 MONOSOMY	HPO:skoehler	
DECIPHER	44	2q37 monosomy		HP:0000490	DECIPHER:44	IEA				P	2Q37 MONOSOMY	HPO:skoehler	
DECIPHER	44	2q37 monosomy		HP:0001156	DECIPHER:44	IEA				P	2Q37 MONOSOMY	HPO:skoehler	
DECIPHER	44	2q37 monosomy		HP:0001249	DECIPHER:44	IEA				P	2Q37 MONOSOMY	HPO:skoehler	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000009	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000160	PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000248	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000252	PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000272	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000400	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000716	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000717	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000733	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0000739	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001319	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001344	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001419	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				I	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0001508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002015	PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002019	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002020	PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002066	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002079	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002191	PMID:17088400	PCS	HP:0003621			P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002205	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002307	PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002540	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0002720	PMID:17088400	PCS	HP:0003621			P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0003819	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				M	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0005280	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0008872	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup	IEA				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	45	Xq28 (MECP2) duplication		HP:0010864	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mecp2-dup;PMID:17088400	PCS				P	XQ28 (MECP2) DUPLICATION	HPO:iea	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0000078	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0000079	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0000161	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0000175	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0000407	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0001171	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0001839	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0004691	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0007925	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	46	Split hand/foot malformation 1 (SHFM1)		HP:0010554	DECIPHER:46	IEA				P	SPLIT HAND/FOOT MALFORMATION 1 (SHFM1)	HPO:skoehler	
DECIPHER	47	RCAD (renal cysts and diabetes)		HP:0000819	DECIPHER:47	IEA				P	RCAD (RENAL CYSTS AND DIABETES)	HPO:skoehler	
DECIPHER	47	RCAD (renal cysts and diabetes)		HP:0001392	DECIPHER:47	IEA				P	RCAD (RENAL CYSTS AND DIABETES)	HPO:skoehler	
DECIPHER	47	RCAD (renal cysts and diabetes)		HP:0005562	DECIPHER:47	IEA				P	RCAD (RENAL CYSTS AND DIABETES)	HPO:skoehler	
DECIPHER	48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0000726	DECIPHER:48	IEA				P	EARLY-ONSET ALZHEIMER DISEASE WITH CEREBRAL AMYLOID ANGIOPATHY	HPO:skoehler	
DECIPHER	48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0002185	DECIPHER:48	IEA				P	EARLY-ONSET ALZHEIMER DISEASE WITH CEREBRAL AMYLOID ANGIOPATHY	HPO:skoehler	
DECIPHER	48	Early-onset Alzheimer disease with cerebral amyloid angiopathy		HP:0100256	DECIPHER:48	IEA				P	EARLY-ONSET ALZHEIMER DISEASE WITH CEREBRAL AMYLOID ANGIOPATHY	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0000023	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0000175	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0000218	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0000708	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0001249	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0001250	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0004322	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	51	2q33.1 deletion syndrome		HP:0008872	DECIPHER:51	IEA				P	2Q33.1 DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0000252	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0000463	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0000664	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0001249	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0001252	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0001627	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0003196	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0010808	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	52	9q subtelomeric deletion syndrome		HP:0011800	DECIPHER:52	IEA				P	9Q SUBTELOMERIC DELETION SYNDROME	HPO:skoehler	
DECIPHER	53	Prader-Willi Syndrome (Type 2)		HP:0000135	DECIPHER:53	IEA				P	PRADER-WILLI SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	53	Prader-Willi Syndrome (Type 2)		HP:0001249	DECIPHER:53	IEA				P	PRADER-WILLI SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	53	Prader-Willi Syndrome (Type 2)		HP:0001252	DECIPHER:53	IEA				P	PRADER-WILLI SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	53	Prader-Willi Syndrome (Type 2)		HP:0001956	DECIPHER:53	IEA				P	PRADER-WILLI SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	53	Prader-Willi Syndrome (Type 2)		HP:0008872	DECIPHER:53	IEA				P	PRADER-WILLI SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	54	Angelman syndrome (Type 2)		HP:0000252	DECIPHER:54	IEA				P	ANGELMAN SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	54	Angelman syndrome (Type 2)		HP:0001249	DECIPHER:54	IEA				P	ANGELMAN SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	54	Angelman syndrome (Type 2)		HP:0001250	DECIPHER:54	IEA				P	ANGELMAN SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	54	Angelman syndrome (Type 2)		HP:0002078	DECIPHER:54	IEA				P	ANGELMAN SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	54	Angelman syndrome (Type 2)		HP:0002353	DECIPHER:54	IEA				P	ANGELMAN SYNDROME (TYPE 2)	HPO:skoehler	
DECIPHER	57	17q21.31 recurrent microdeletion syndrome		HP:0000276	DECIPHER:57	IEA				P	17Q21.31 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	57	17q21.31 recurrent microdeletion syndrome		HP:0001249	DECIPHER:57	IEA				P	17Q21.31 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	57	17q21.31 recurrent microdeletion syndrome		HP:0001252	DECIPHER:57	IEA				P	17Q21.31 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	57	17q21.31 recurrent microdeletion syndrome		HP:0001518	DECIPHER:57	IEA				P	17Q21.31 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	57	17q21.31 recurrent microdeletion syndrome		HP:0008872	DECIPHER:57	IEA				P	17Q21.31 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0002986	DECIPHER:58	IEA				P	LERI-WEILL DYSCHONDROSTOSIS (LWD) - SHOX DELETION	HPO:skoehler	
DECIPHER	58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0003067	DECIPHER:58	IEA				P	LERI-WEILL DYSCHONDROSTOSIS (LWD) - SHOX DELETION	HPO:skoehler	
DECIPHER	58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0006394	DECIPHER:58	IEA				P	LERI-WEILL DYSCHONDROSTOSIS (LWD) - SHOX DELETION	HPO:skoehler	
DECIPHER	58	Leri-Weill dyschondrostosis (LWD) - SHOX deletion		HP:0008873	DECIPHER:58	IEA				P	LERI-WEILL DYSCHONDROSTOSIS (LWD) - SHOX DELETION	HPO:skoehler	
DECIPHER	59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0002415	DECIPHER:59	IEA				P	ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHY (ADLD)	HPO:skoehler	
DECIPHER	59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0007256	DECIPHER:59	IEA				P	ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHY (ADLD)	HPO:skoehler	
DECIPHER	59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0011096	DECIPHER:59	IEA				P	ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHY (ADLD)	HPO:skoehler	
DECIPHER	59	Adult-onset autosomal dominant leukodystrophy (ADLD)		HP:0012332	DECIPHER:59	IEA				P	ADULT-ONSET AUTOSOMAL DOMINANT LEUKODYSTROPHY (ADLD)	HPO:skoehler	
DECIPHER	62	1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)		HP:0000252	DECIPHER:62	IEA				P	1Q21.1 RECURRENT MICRODELETION (SUSCEPTIBILITY LOCUS FOR NEURODEVELOPMENTAL DISORDERS)	HPO:skoehler	
DECIPHER	62	1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)		HP:0001249	DECIPHER:62	IEA				P	1Q21.1 RECURRENT MICRODELETION (SUSCEPTIBILITY LOCUS FOR NEURODEVELOPMENTAL DISORDERS)	HPO:skoehler	
DECIPHER	65	ATR-16 syndrome		HP:0001249	DECIPHER:65	IEA				P	ATR-16 SYNDROME	HPO:skoehler	
DECIPHER	65	ATR-16 syndrome		HP:0001877	DECIPHER:65	IEA				P	ATR-16 SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0000047	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0000252	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0000271	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0001249	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0001388	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0001518	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	66	15q24 recurrent microdeletion syndrome		HP:0004322	DECIPHER:66	IEA				P	15Q24 RECURRENT MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	67	1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)		HP:0000717	DECIPHER:67	IEA				P	1Q21.1 RECURRENT MICRODUPLICATION (POSSIBLE SUSCEPTIBILITY LOCUS FOR NEURODEVELOPMENTAL DISORDERS)	HPO:skoehler	
DECIPHER	67	1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)		HP:0001249	DECIPHER:67	IEA				P	1Q21.1 RECURRENT MICRODUPLICATION (POSSIBLE SUSCEPTIBILITY LOCUS FOR NEURODEVELOPMENTAL DISORDERS)	HPO:skoehler	
DECIPHER	68	16p11.2-p12.2 microdeletion syndrome		HP:0000307	DECIPHER:68	IEA				P	16P11.2-P12.2 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	68	16p11.2-p12.2 microdeletion syndrome		HP:0001249	DECIPHER:68	IEA				P	16P11.2-P12.2 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	68	16p11.2-p12.2 microdeletion syndrome		HP:0008872	DECIPHER:68	IEA				P	16P11.2-P12.2 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0000126	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0000252	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0000494	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0000506	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0000508	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0001249	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0007766	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0008872	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	70	2p15-16.1 microdeletion syndrome		HP:0100490	DECIPHER:70	IEA				P	2P15-16.1 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	72	22q11.2 distal deletion syndrome		HP:0000271	DECIPHER:72	IEA				P	22Q11.2 DISTAL DELETION SYNDROME	HPO:skoehler	
DECIPHER	72	22q11.2 distal deletion syndrome		HP:0001249	DECIPHER:72	IEA				P	22Q11.2 DISTAL DELETION SYNDROME	HPO:skoehler	
DECIPHER	72	22q11.2 distal deletion syndrome		HP:0001518	DECIPHER:72	IEA				P	22Q11.2 DISTAL DELETION SYNDROME	HPO:skoehler	
DECIPHER	72	22q11.2 distal deletion syndrome		HP:0004322	DECIPHER:72	IEA				P	22Q11.2 DISTAL DELETION SYNDROME	HPO:skoehler	
DECIPHER	74	15q13.3 microdeletion syndrome		HP:0000271	DECIPHER:74	IEA				P	15Q13.3 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	74	15q13.3 microdeletion syndrome		HP:0001249	DECIPHER:74	IEA				P	15Q13.3 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	74	15q13.3 microdeletion syndrome		HP:0001250	DECIPHER:74	IEA				P	15Q13.3 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	76	12q14 microdeletion syndrome		HP:0001249	DECIPHER:76	IEA				P	12Q14 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	76	12q14 microdeletion syndrome		HP:0003508	DECIPHER:76	IEA				P	12Q14 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	76	12q14 microdeletion syndrome		HP:0010739	DECIPHER:76	IEA				P	12Q14 MICRODELETION SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0000733	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0000742	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0000752	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0001156	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0001249	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0001252	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0001609	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0002360	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	8	Smith-Magenis Syndrome		HP:0004322	DECIPHER:8	IEA				P	SMITH-MAGENIS SYNDROME	HPO:skoehler	
DECIPHER	81	15q26 overgrowth syndrome		HP:0000076	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	1/16
DECIPHER	81	15q26 overgrowth syndrome		HP:0000085	PMID:19133692;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/22
DECIPHER	81	15q26 overgrowth syndrome		HP:0000104	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	1/16
DECIPHER	81	15q26 overgrowth syndrome		HP:0000113	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	1/16
DECIPHER	81	15q26 overgrowth syndrome		HP:0000126	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/16
DECIPHER	81	15q26 overgrowth syndrome		HP:0000218	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000256	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	8/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0000276	PMID:19133692;PMID:12404101;PMID:20603595	PCS		HP:0040281		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	HP:0040281
DECIPHER	81	15q26 overgrowth syndrome		HP:0000293	PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	8/15
DECIPHER	81	15q26 overgrowth syndrome		HP:0000303	PMID:19133692;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	26/33
DECIPHER	81	15q26 overgrowth syndrome		HP:0000324	PMID:10951463;PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	8/15
DECIPHER	81	15q26 overgrowth syndrome		HP:0000325	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	8/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0000343	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	5/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000347	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000369	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	8/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0000377	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	9/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0000407	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000414	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000431	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	5/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0000448	PMID:19133692;PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	31/36
DECIPHER	81	15q26 overgrowth syndrome		HP:0000470	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0000486	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/28
DECIPHER	81	15q26 overgrowth syndrome		HP:0000494	PMID:10951463;PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	9/15
DECIPHER	81	15q26 overgrowth syndrome		HP:0001156	PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/26
DECIPHER	81	15q26 overgrowth syndrome		HP:0001166	PMID:10951463;PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	9/31
DECIPHER	81	15q26 overgrowth syndrome		HP:0001182	PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/26
DECIPHER	81	15q26 overgrowth syndrome		HP:0001249	PMID:19133692;PMID:12404101	PCS		HP:0040281		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	HP:0040281
DECIPHER	81	15q26 overgrowth syndrome		HP:0001363	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	6/28
DECIPHER	81	15q26 overgrowth syndrome		HP:0001382	PMID:12404101	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	3/10
DECIPHER	81	15q26 overgrowth syndrome		HP:0001548	PMID:19133692;PMID:12404101	PCS		HP:0040282		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	HP:0040282
DECIPHER	81	15q26 overgrowth syndrome		HP:0002167	PMID:20603595	PCS		HP:0040281		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	HP:0040281
DECIPHER	81	15q26 overgrowth syndrome		HP:0002650	PMID:19133692;PMID:12404101;PMID:19262081	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	6/30
DECIPHER	81	15q26 overgrowth syndrome		HP:0005580	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	1/16
DECIPHER	81	15q26 overgrowth syndrome		HP:0009890	PMID:19133692	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	25/26
DECIPHER	81	15q26 overgrowth syndrome		HP:0010511	PMID:10951463	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0030680	PMID:10951463,PMID:19133692;PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	2/5
DECIPHER	81	15q26 overgrowth syndrome		HP:0100490	PMID:12404101;PMID:20603595	PCS		HP:0040284		P	15Q26 OVERGROWTH SYNDROME	HPO:iea	4/26
DECIPHER	85	8p23.1 duplication syndrome		HP:0000750	DECIPHER:85	IEA				P	8P23.1 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	85	8p23.1 duplication syndrome		HP:0001249	DECIPHER:85	IEA				P	8P23.1 DUPLICATION SYNDROME	HPO:skoehler	
DECIPHER	92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0000252	DECIPHER:92	IEA				P	RECURRENT 16P12.1 MICRODELETION (NEURODEVELOPMENTAL SUSCEPTIBILITY LOCUS)	HPO:skoehler	
DECIPHER	92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0000750	DECIPHER:92	IEA				P	RECURRENT 16P12.1 MICRODELETION (NEURODEVELOPMENTAL SUSCEPTIBILITY LOCUS)	HPO:skoehler	
DECIPHER	92	Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)		HP:0001249	DECIPHER:92	IEA				P	RECURRENT 16P12.1 MICRODELETION (NEURODEVELOPMENTAL SUSCEPTIBILITY LOCUS)	HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000028	OMIM:100050	IEA				P		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000049	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000175	OMIM:100050	TAS				P		HPO:probinson	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000202	OMIM:100050	IEA				P		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000204	OMIM:100050	TAS				P		HPO:probinson	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000316	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000327	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000343	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000349	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000394	OMIM:100050	TAS				P		HPO:probinson	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000431	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000463	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000484	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000486	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000494	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000508	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000602	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000765	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000954	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0000974	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001004	OMIM:100050	TAS				P		HPO:probinson	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001156	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001159	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001371	OMIM:100050	IEA				P		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001388	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001394	OMIM:100050	IEA				P		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001417	OMIM:100050	TAS				I		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001470	OMIM:100050	TAS				I		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001763	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0001972	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0002023	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0002055	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0002240	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0002816	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0003318	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0003502	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0004792	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0005190	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0006530	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0009466	OMIM:100050	IEA				P		HPO:iea	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0010886	OMIM:100050	IEA				P		HPO:skoehler	
OMIM	100050	100050 AARSKOG SYNDROME, AUTOSOMAL DOMINANT		HP:0030084	OMIM:100050	TAS				P		HPO:skoehler	
OMIM	100070	AORTIC ANEURYSM, ABDOMINAL		HP:0000006	OMIM:100070	TAS				I		HPO:nvasilevsky	
OMIM	100070	AORTIC ANEURYSM, ABDOMINAL		HP:0000007	OMIM:100070	TAS				I		HPO:nvasilevsky	
OMIM	100070	AORTIC ANEURYSM, ABDOMINAL		HP:0001426	OMIM:100070	TAS				I		HPO:nvasilevsky	
OMIM	100070	AORTIC ANEURYSM, ABDOMINAL		HP:0005112	PMID:7613891	PCS	HP:0003581			P		HPO:probinson	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000007	OMIM:100100	IEA				I		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000028	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000072	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000126	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000217	OMIM:100100	IEA				P		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000767	OMIM:100100	IEA				P		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000768	OMIM:100100	IEA				P		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0000951	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0001374	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0001562	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0001627	OMIM:100100	TAS				P		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0001643	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0001762	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0002023	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0004392	OMIM:100100	IEA				P		HPO:skoehler	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0005199	OMIM:100100	IEA				P		HPO:iea	
OMIM	100100	#100100 PRUNE BELLY SYNDROME; PBS;;ABDOMINAL MUSCLES, ABSENCE OF, WITH URINARY TRACT ABNORMALITY ANDCRYPTORCHIDISM;;EAGLE-BARRETT SYNDROME; EGBRS		HP:0010957	OMIM:100100	IEA				P		HPO:skoehler	
OMIM	100200	ABDUCENS PALSY		HP:0000006	OMIM:100200	IEA				I		HPO:iea	
OMIM	100200	ABDUCENS PALSY		HP:0000486	OMIM:100200	IEA				P		HPO:iea	
OMIM	100200	ABDUCENS PALSY		HP:0011349	OMIM:100200	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000006	PMID:9823488	PCS				I		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000175	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000204	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000252	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000565	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000568	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000822	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0000965	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001156	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001249	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001250	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001252	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001263	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001290	OMIM:100300	TAS				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001302	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001362	OMIM:100300	TAS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001596	OMIM:100300	TAS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001629	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001631	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001636	PMID:9823488	PCS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001642	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001647	PMID:9823488	PCS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001650	PMID:9823488	PCS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001762	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001770	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0001792	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002079	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002084	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002092	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002119	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002126	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002539	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002558	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0002558	OMIM:100300	TAS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0004383	PMID:9823488	PCS				P		HPO:probinson	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0004415	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0006970	OMIM:100300	IEA				P		HPO:skoehler	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0007589	OMIM:100300	IEA				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0007590	PMID:1424238	PCS				P		HPO:iea	
OMIM	100300	ADAMS-OLIVER SYNDROME 1; AOS1		HP:0030011	OMIM:100300	TAS				P		HPO:probinson	
OMIM	100600	ACANTHOSIS NIGRICANS		HP:0000006	OMIM:100600	IEA				I		HPO:iea	
OMIM	100600	ACANTHOSIS NIGRICANS		HP:0000956	OMIM:100600	IEA				P		HPO:iea	
OMIM	100650	ALDEHYDE DEHYDROGENASE 2 FAMILY		HP:0000006	OMIM:100650	TAS				I		HPO:skoehler	
OMIM	100650	ALDEHYDE DEHYDROGENASE 2 FAMILY		HP:0001033	OMIM:100650	TAS				P		HPO:skoehler	
OMIM	100650	ALDEHYDE DEHYDROGENASE 2 FAMILY		HP:0003533	OMIM:100650	TAS				P		HPO:skoehler	
OMIM	100675	ACETAMINOPHEN METABOLISM		HP:0000006	OMIM:100675	TAS				I		HPO:skoehler	
OMIM	100675	ACETAMINOPHEN METABOLISM		HP:0000952	OMIM:100675	TAS				P		HPO:skoehler	
OMIM	100700	ACHARD SYNDROME		HP:0000006	OMIM:100700	IEA				I		HPO:iea	
OMIM	100700	ACHARD SYNDROME		HP:0000248	OMIM:100700	IEA				P		HPO:iea	
OMIM	100700	ACHARD SYNDROME		HP:0000347	OMIM:100700	IEA				P		HPO:iea	
OMIM	100700	ACHARD SYNDROME		HP:0001166	OMIM:100700	IEA				P		HPO:iea	
OMIM	100700	ACHARD SYNDROME		HP:0001388	OMIM:100700	TAS				P		HPO:probinson	
OMIM	100700	ACHARD SYNDROME		HP:0002682	OMIM:100700	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0000006	OMIM:100800	IEA				I		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0000238	OMIM:100800	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0000272	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0000403	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0000405	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0001156	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0001270	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0001355	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0001377	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002007	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002512	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002677	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002761	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002781	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002938	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0002970	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0003015	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0003093	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0004060	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0005280	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0005733	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0008414	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0008905	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0008921	OMIM:100800	TAS				P		HPO:probinson	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0008947	OMIM:100800	IEA				P		HPO:iea	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0011800	OMIM:100800	TAS				P		HPO:skoehler	
OMIM	100800	#100800 ACHONDROPLASIA; ACH		HP:0100864	OMIM:100800	IEA				P		HPO:iea	
OMIM	100820	ACHOO SYNDROME		HP:0000006	OMIM:100820	IEA				I		HPO:iea	
OMIM	100820	ACHOO SYNDROME		HP:0025096	PMID:2275931	PCS				P		HPO:lccarmody	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0000006	OMIM:101000	IEA				I		HPO:iea	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0000360	PMID:1484939	PCS		HP:0040284		P		HPO:probinson	12/120
OMIM	101000	NEUROFIBROMATOSIS, TYPE II	HP:0012833	HP:0000365	PMID:1484939	PCS		HP:0040284		P		HPO:probinson	42/120
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0000957	PMID:1484939	PCS		HP:0040284		P		HPO:iea	43%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0001250	PMID:1484939	PCS		HP:0040284		P		HPO:probinson	10/120
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0001251	PMID:1484939	PCS		HP:0040284		P		HPO:probinson	10/120
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0002315	OMIM:101000	IEA				P		HPO:iea	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0002321	PMID:1484939	PCS		HP:0040284		P		HPO:iea	8%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0002858	PMID:7747758	PCS		HP:0040284		P		HPO:iea	49%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0002888	PMID:19476995	PCS		HP:0040284		P		HPO:iea	18%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0007935	PMID:8318482	PCS		HP:0040284		P		HPO:probinson	36/45
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009589	PMID:19476995	PCS		HP:0040284		P		HPO:iea	90%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009590	PMID:7747758	PCS		HP:0040284		P		HPO:iea	62/63
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009592	OMIM:101000	IEA				P		HPO:iea	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009593	OMIM:101000	IEA				P		HPO:iea	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009594	PMID:7747758	PCS		HP:0040284		P		HPO:iea	13%
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009595	OMIM:101000	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0009830	OMIM:101000	TAS				P		HPO:skoehler	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0100014	OMIM:101000	TAS				P		HPO:skoehler	
OMIM	101000	NEUROFIBROMATOSIS, TYPE II		HP:0100019	PMID:8318482	PCS	HP:0003621	HP:0040284		P		HPO:probinson	17/45
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000006	OMIM:101120	IEA				I		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000263	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000272	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000274	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000303	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000316	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000327	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000369	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000377	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000470	OMIM:101120	TAS				P		HPO:probinson	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000586	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0000678	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0001159	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0001177	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0001363	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0009816	OMIM:101120	IEA				P		HPO:iea	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0010055	OMIM:101120	TAS				P		HPO:probinson	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0011304	OMIM:101120	TAS				P		HPO:probinson	
OMIM	101120	ACROCEPHALOPOLYSYNDACTYLY TYPE III		HP:0012368	OMIM:101120	TAS				P		HPO:skoehler	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000006	OMIM:101200	IEA				I		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000028	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000126	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000148	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000175	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000189	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000193	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000238	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000239	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000244	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000270	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000272	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000303	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000316	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000337	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000348	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000365	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000389	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000452	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000453	OMIM:101200	TAS				P		HPO:skoehler	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000486	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000494	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000586	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000684	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0000689	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001061	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001162	OMIM:101200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001177	OMIM:101200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001249	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001274	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001331	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001355	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001507	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0001629	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0002021	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0002032	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0002119	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0002623	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0003041	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0004397	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0004440	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0004468	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0004487	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0004635	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0005048	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0005280	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0007099	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0007291	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0007343	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0008111	OMIM:101200	IEA				P		HPO:iea	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0009642	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0010554	OMIM:101200	TAS				P		HPO:probinson	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0011800	OMIM:101200	TAS				P		HPO:skoehler	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0012368	OMIM:101200	TAS				P		HPO:skoehler	
OMIM	101200	#101200 APERT SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE I; ACS1;;ACS IAPERT-CROUZON DISEASE, INCLUDED;;ACROCEPHALOSYNDACTYLY, TYPE II, INCLUDED;;ACS II, INCLUDED;;VOGT CEPHALODACTYLY, INCLUDED		HP:0100702	OMIM:101200	IEA				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000006	OMIM:101400	IEA				I		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000175	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000189	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000248	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000263	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000270	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000272	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000294	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000316	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000324	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000327	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000348	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000365	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000369	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000444	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000460	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000486	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000508	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000557	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000586	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0000614	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001156	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001249	OMIM:101400	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001357	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001627	OMIM:101400	TAS				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001770	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0001822	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0002342	OMIM:101400	TAS				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0002644	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0002678	OMIM:101400	TAS				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0002697	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0002974	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0003002	OMIM:101400	TAS				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0003189	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0003828	OMIM:101400	IEA				C		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0004209	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0004322	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0004425	OMIM:101400	IEA				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0004440	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0004443	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0008551	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0009899	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0009951	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0009968	OMIM:101400	TAS				P		HPO:probinson	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0010104	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0011323	OMIM:101400	IEA				P		HPO:iea	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0012368	OMIM:101400	TAS				P		HPO:skoehler	
OMIM	101400	#101400 SAETHRE-CHOTZEN SYNDROME; SCS;;ACROCEPHALOSYNDACTYLY, TYPE III; ACS3;;ACS III;;CHOTZEN SYNDROME;;ACROCEPHALY, SKULL ASYMMETRY, AND MILD SYNDACTYLYSAETHRE-CHOTZEN SYNDROME WITH EYELID ANOMALIES, INCLUDED;;BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS 3, FORMERLY, INCLUDED;BPES3, FORMERLY, INCLUDED		HP:0030680	OMIM:101400	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000006	OMIM:101600	IEA				I		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000218	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000238	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000244	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000303	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000316	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000327	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000452	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000453	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000486	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000494	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000586	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0000678	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0001249	OMIM:101600	IEA				P		HPO:skoehler	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0002308	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0002676	OMIM:101600	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0002780	OMIM:101600	IEA				P		HPO:skoehler	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0003041	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0003070	OMIM:101600	IEA				P		HPO:skoehler	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0003196	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0003795	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0004440	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0005280	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0005347	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0006101	OMIM:101600	TAS				P		HPO:skoehler	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0006110	OMIM:101600	TAS				P		HPO:probinson	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0010055	OMIM:101600	IEA				P		HPO:iea	
OMIM	101600	#101600 PFEIFFER SYNDROME;;ACROCEPHALOSYNDACTYLY, TYPE V; ACS5;;ACS V;;NOACK SYNDROMECRANIOFACIAL-SKELETAL-DERMATOLOGIC DYSPLASIA, INCLUDED		HP:0011304	OMIM:101600	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000006	OMIM:101800	TAS				I		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000028	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000135	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000238	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000248	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000286	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000303	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000316	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000327	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000365	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000455	OMIM:101800	TAS				P		HPO:skoehler	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000486	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000635	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000648	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000668	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000684	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000689	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000858	OMIM:101800	TAS				P		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0000995	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0001169	OMIM:101800	TAS				P		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0001249	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0001530	OMIM:101800	IEA				P		HPO:skoehler	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0001847	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0002650	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0003083	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0003165	OMIM:101800	IEA				P		HPO:skoehler	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0003416	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0004279	OMIM:101800	TAS				P		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0004490	OMIM:101800	TAS				P		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0005280	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0005280	OMIM:101800	TAS				P		HPO:probinson	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0005616	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0005756	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0008450	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0008479	OMIM:101800	IEA				P		HPO:skoehler	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0008873	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0009803	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0010049	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0010230	OMIM:101800	IEA				P		HPO:iea	
OMIM	101800	#101800 ACRODYSOSTOSIS 1, WITH OR WITHOUT HORMONE RESISTANCE; ACRDYS1;;ADOHR		HP:0010743	OMIM:101800	IEA				P		HPO:iea	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000006	OMIM:101805	TAS				I		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000028	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000047	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000252	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000349	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000670	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0000954	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0001511	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0004279	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101805	ACROFACIAL DYSOSTOSIS, CATANIA TYPE		HP:0004467	OMIM:101805	TAS				P		HPO:skoehler	
OMIM	101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT		HP:0000006	OMIM:101840	TAS				I		HPO:probinson	
OMIM	101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT		HP:0002213	OMIM:101840	TAS				P		HPO:probinson	
OMIM	101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT		HP:0012393	OMIM:101840	TAS				P		HPO:probinson	
OMIM	101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT		HP:0200034	OMIM:101840	TAS				P		HPO:probinson	
OMIM	101840	ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT		HP:0200035	OMIM:101840	TAS				P		HPO:probinson	
OMIM	101850	ACROKERATOELASTOIDOSIS		HP:0000006	OMIM:101850	IEA				I		HPO:iea	
OMIM	101850	ACROKERATOELASTOIDOSIS		HP:0000962	OMIM:101850	IEA				P		HPO:iea	
OMIM	101850	ACROKERATOELASTOIDOSIS		HP:0200016	OMIM:101850	IEA				P		HPO:iea	
OMIM	101900	ACROKERATOSIS VERRUCIFORMIS		HP:0000006	OMIM:101900	IEA				I		HPO:iea	
OMIM	101900	ACROKERATOSIS VERRUCIFORMIS		HP:0000962	OMIM:101900	IEA				P		HPO:iea	
OMIM	101900	ACROKERATOSIS VERRUCIFORMIS		HP:0001807	OMIM:101900	IEA				P		HPO:iea	
OMIM	101900	ACROKERATOSIS VERRUCIFORMIS		HP:0025092	OMIM:101900	TAS				P		HPO:skoehler	
OMIM	101900	ACROKERATOSIS VERRUCIFORMIS		HP:0200016	OMIM:101900	IEA				P		HPO:skoehler	
OMIM	102000	ACROLEUKOPATHY, SYMMETRIC		HP:0000006	OMIM:102000	IEA				I		HPO:iea	
OMIM	102000	ACROLEUKOPATHY, SYMMETRIC		HP:0200015	OMIM:102000	IEA				P		HPO:iea	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0000006	OMIM:102100	IEA				I		HPO:iea	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0000098	OMIM:102100	PCS				P		HPO:probinson	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0000303	OMIM:102100	PCS				P		HPO:probinson	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0000478	OMIM:102100	IEA				P		HPO:iea	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0000977	OMIM:102100	IEA				P		HPO:iea	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0001176	OMIM:102100	PCS				P		HPO:probinson	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0001833	OMIM:102100	TAS				P		HPO:skoehler	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0010541	OMIM:102100	PCS				P		HPO:probinson	
OMIM	102100	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA		HP:0030314	OMIM:102100	TAS				P		HPO:skoehler	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0000006	OMIM:102150	IEA				I		HPO:iea	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0000153	OMIM:102150	IEA				P		HPO:iea	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0000414	OMIM:102150	IEA				P		HPO:iea	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0000581	OMIM:102150	IEA				P		HPO:iea	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0001176	OMIM:102150	TAS				P		HPO:probinson	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0001182	OMIM:102150	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0001256	OMIM:102150	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0001328	OMIM:102150	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0001520	OMIM:102150	TAS				P		HPO:probinson	
OMIM	102150	ACROMEGALOID FACIAL APPEARANCE SYNDROME		HP:0002553	OMIM:102150	IEA				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000006	OMIM:102200	TAS				I		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000280	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000822	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000845	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000858	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0000870	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0001428	OMIM:102200	TAS				I		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0001638	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0001712	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0002893	OMIM:102200	IEA				P		HPO:skoehler	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0006767	OMIM:102200	TAS				P		HPO:skoehler	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0011760	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0030269	OMIM:102200	TAS				P		HPO:probinson	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0040278	OMIM:102200	TAS				P		HPO:skoehler	
OMIM	102200	PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 1		HP:0100829	OMIM:102200	TAS				P		HPO:skoehler	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0000006	OMIM:102300	TAS				I		HPO:iea	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0001336	OMIM:102300	TAS				P		HPO:iea	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0001425	OMIM:102300	TAS				I		HPO:skoehler	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0003401	OMIM:102300	TAS				P		HPO:skoehler	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0008991	OMIM:102300	TAS				P		HPO:iea	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0012452	OMIM:102300	TAS				P		HPO:skoehler	
OMIM	102300	RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1		HP:0100785	OMIM:102300	TAS				P		HPO:skoehler	
OMIM	102350	ACROMIAL DIMPLES		HP:0000006	OMIM:102350	IEA				I		HPO:iea	
OMIM	102350	ACROMIAL DIMPLES		HP:0000951	OMIM:102350	IEA				P		HPO:iea	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000006	OMIM:102370	TAS				I		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000160	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000179	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000311	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000343	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000414	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000463	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0000527	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0001072	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0001609	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0001773	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0002002	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0002750	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0003026	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0003300	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0003510	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0004279	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0005900	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0009803	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0010049	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102370	ACROMICRIC DYSPLASIA		HP:0010579	OMIM:102370	TAS				P		HPO:probinson	
OMIM	102400	ACROOSTEOLYSIS		HP:0000006	OMIM:102400	TAS				I		HPO:probinson	
OMIM	102400	ACROOSTEOLYSIS		HP:0003621	OMIM:102400	TAS				C		HPO:probinson	
OMIM	102400	ACROOSTEOLYSIS		HP:0009771	OMIM:102400	TAS				P		HPO:probinson	
OMIM	102400	ACROOSTEOLYSIS		HP:0010177	OMIM:102400	TAS				P		HPO:probinson	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000006	OMIM:102500	IEA				I		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000023	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000028	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000047	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000107	OMIM:102500	IEA				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000218	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000238	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000280	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000286	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000293	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000343	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000347	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000369	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000405	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000445	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000463	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000470	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000494	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000506	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000527	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000574	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000664	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000689	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000938	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0000939	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001007	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001388	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001508	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001537	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001643	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001671	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001799	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0001842	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002566	OMIM:102500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002645	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002688	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002751	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002756	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002857	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0002953	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0003083	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0004322	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0004586	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0005463	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0005758	OMIM:102500	TAS				P		HPO:skoehler	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0006180	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0006480	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0008421	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0008462	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0009748	OMIM:102500	IEA				P		HPO:iea	
OMIM	102500	#102500 HAJDU-CHENEY SYNDROME; HJCYS;;ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE;;CHENEY SYNDROME;;ARTHRODENTOOSTEODYSPLASIA;;SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS		HP:0009771	OMIM:102500	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0000006	OMIM:102510	IEA				I		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0000765	OMIM:102510	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0001241	OMIM:102510	IEA				P		HPO:skoehler	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0001770	OMIM:102510	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0002652	OMIM:102510	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0003468	OMIM:102510	IEA				P		HPO:skoehler	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0004601	OMIM:102510	TAS				P		HPO:probinson	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0004614	OMIM:102510	TAS				P		HPO:probinson	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0005048	OMIM:102510	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0006101	OMIM:102510	IEA				P		HPO:skoehler	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009467	OMIM:102510	TAS				P		HPO:probinson	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009611	OMIM:102510	IEA				P		HPO:iea	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0009778	OMIM:102510	TAS				P		HPO:probinson	
OMIM	102510	ACROPECTOROVERTEBRAL DYSPLASIA, F-FORM OF		HP:0011304	OMIM:102510	TAS				P		HPO:probinson	
OMIM	102520	ACRORENAL SYNDROME		HP:0000006	OMIM:102520	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	102520	ACRORENAL SYNDROME		HP:0001180	OMIM:102520	TAS				P		HPO:skoehler	
OMIM	102520	ACRORENAL SYNDROME		HP:0012210	OMIM:102520	IEA				P		HPO:iea	
OMIM	102530	SPERMATOGENIC FAILURE 6; SPGF6		HP:0000007	OMIM:102530	TAS				I		HPO:skoehler	
OMIM	102530	SPERMATOGENIC FAILURE 6; SPGF6		HP:0000789	OMIM:102530	TAS				P		HPO:probinson	
OMIM	102530	SPERMATOGENIC FAILURE 6; SPGF6		HP:0012205	OMIM:102530	TAS				P		HPO:skoehler	
OMIM	102650	ADACTYLIA, UNILATERAL		HP:0000006	OMIM:102650	IEA				I		HPO:iea	
OMIM	102650	ADACTYLIA, UNILATERAL		HP:0001597	OMIM:102650	IEA				P		HPO:iea	
OMIM	102650	ADACTYLIA, UNILATERAL	HP:0012833	HP:0009776	OMIM:102650	TAS				P		HPO:iea	
OMIM	102650	ADACTYLIA, UNILATERAL	HP:0012825	HP:0009778	OMIM:102650	TAS				P		HPO:probinson	
OMIM	102660	ADAMANTINOMA OF LONG BONES		HP:0000006	OMIM:102660	IEA				I		HPO:iea	
OMIM	102660	ADAMANTINOMA OF LONG BONES		HP:0002664	OMIM:102660	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0000007	OMIM:102700	TAS				I		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0000246	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0000907	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0000926	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001442	OMIM:102700	IEA				I		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001508	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001744	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001880	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001890	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001967	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0001973	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002014	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002090	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002099	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002240	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002644	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002718	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002720	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002841	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0002850	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0003212	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0004429	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0004430	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0005359	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0005365	OMIM:102700	IEA				P		HPO:skoehler	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0005424	OMIM:102700	IEA				P		HPO:iea	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0008348	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY	HP:0012828	HP:0010976	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0012191	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102700	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-NEGATIVE, DUE TO ADENOSINE DEAMINASE DEFICIENCY		HP:0030273	OMIM:102700	TAS				P		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO		HP:0000006	OMIM:102730	TAS				I		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO		HP:0001878	OMIM:102730	TAS				P		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO	HP:0012825	HP:0002149	OMIM:102730	TAS				P		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO		HP:0004446	OMIM:102730	TAS				P		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO		HP:0004823	OMIM:102730	TAS				P		HPO:probinson	
OMIM	102730	ADENOSINE DEAMINASE, ELEVATED, HEMOLYTIC ANEMIA DUE TO		HP:0030270	OMIM:102730	TAS				P		HPO:probinson	
OMIM	102800	ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO		HP:0000006	OMIM:102800	TAS				I		HPO:probinson	
OMIM	102800	ADENOSINE TRIPHOSPHATASE DEFICIENCY, ANEMIA DUE TO		HP:0001930	OMIM:102800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	102900	ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES		HP:0000006	OMIM:102900	TAS				I		HPO:probinson	
OMIM	102900	ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES		HP:0001901	OMIM:102900	TAS				P		HPO:probinson	
OMIM	102900	ADENOSINE TRIPHOSPHATE, ELEVATED, OF ERYTHROCYTES		HP:0030271	OMIM:102900	TAS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000007	OMIM:103050	PCS				I		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000154	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000219	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000219	OMIM:103050	TAS				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000248	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000252	OMIM:103050	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000319	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000343	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000369	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000463	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000486	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000639	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000717	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000718	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000742	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000748	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000750	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000752	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0000817	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001249	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001250	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001263	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001272	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001290	OMIM:103050	TAS				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001336	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001348	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0001510	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0002059	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0002066	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0002179	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0002540	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0003196	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0003202	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0003429	OMIM:103050	IEA				P		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0003593	OMIM:103050	IEA				C		HPO:skoehler	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0005487	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0006808	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0011344	OMIM:103050	PCS				P		HPO:probinson	
OMIM	103050	ADENYLOSUCCINASE DEFICIENCY		HP:0040082	OMIM:103050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	103100	ADIE PUPIL		HP:0000006	OMIM:103100	IEA				I		HPO:iea	
OMIM	103100	ADIE PUPIL		HP:0001265	OMIM:103100	IEA				P		HPO:iea	
OMIM	103100	ADIE PUPIL		HP:0012074	OMIM:103100	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0000006	OMIM:103200	IEA				I		HPO:iea	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0000716	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0000739	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0001513	OMIM:103200	IEA				P		HPO:iea	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0002019	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0002360	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0002829	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0003270	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0003596	OMIM:103200	IEA				C		HPO:iea	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0003828	OMIM:103200	TAS				C		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0007596	OMIM:103200	IEA				P		HPO:iea	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0012378	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103200	ADIPOSIS DOLOROSA		HP:0012532	OMIM:103200	TAS				P		HPO:skoehler	
OMIM	103230	103230 ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL;;ADDISON DISEASE, CONGENITAL		HP:0000006	OMIM:103230	IEA				I		HPO:iea	
OMIM	103230	103230 ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL;;ADDISON DISEASE, CONGENITAL		HP:0000846	OMIM:103230	IEA				P		HPO:iea	
OMIM	103230	103230 ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL;;ADDISON DISEASE, CONGENITAL		HP:0000953	OMIM:103230	IEA				P		HPO:iea	
OMIM	103230	103230 ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL;;ADDISON DISEASE, CONGENITAL		HP:0001939	OMIM:103230	IEA				P		HPO:iea	
OMIM	103230	103230 ADRENOCORTICAL HYPOFUNCTION, CHRONIC PRIMARY CONGENITAL;;ADDISON DISEASE, CONGENITAL		HP:0012605	OMIM:103230	TAS				P		HPO:skoehler	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000006	OMIM:103285	IEA				I		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000202	OMIM:103285	IEA				P		HPO:skoehler	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000509	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000579	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000668	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000677	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000691	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000958	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000963	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000964	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000968	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0000992	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0001171	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0001480	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0001770	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0001803	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0001839	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002209	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002215	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002286	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002293	OMIM:103285	TAS				P		HPO:skoehler	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002557	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0002561	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0003187	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0004334	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0006357	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0006610	OMIM:103285	IEA				P		HPO:iea	
OMIM	103285	#103285 ADULT SYNDROME;;ACRO-DERMATO-UNGUAL-LACRIMAL-TOOTH SYNDROME		HP:0007455	OMIM:103285	IEA				P		HPO:skoehler	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000006	OMIM:103300	IEA				I		HPO:iea	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000160	OMIM:103300	IEA				P		HPO:iea	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000171	OMIM:103300	TAS				P		HPO:skoehler	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000278	OMIM:103300	IEA				P		HPO:iea	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000286	OMIM:103300	IEA				P		HPO:iea	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0000347	OMIM:103300	TAS				P		HPO:skoehler	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0001171	OMIM:103300	IEA				P		HPO:iea	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0003745	OMIM:103300	TAS				I		HPO:skoehler	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0009776	OMIM:103300	TAS				P		HPO:skoehler	
OMIM	103300	HYPOGLOSSIA-HYPODACTYLIA		HP:0012730	OMIM:103300	IEA				P		HPO:skoehler	
OMIM	103400	AINHUM		HP:0000006	OMIM:103400	IEA				I		HPO:iea	
OMIM	103400	AINHUM		HP:0009775	OMIM:103400	IEA				P		HPO:iea	
OMIM	103400	AINHUM		HP:0031009	OMIM:103400	TAS				P		HPO:skoehler	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0000006	OMIM:103420	IEA				I		HPO:iea	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0000522	OMIM:103420	PCS				P		HPO:probinson	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0000584	OMIM:103420	IEA				P		HPO:iea	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0000613	OMIM:103420	IEA				P		HPO:iea	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0007732	OMIM:103420	IEA				P		HPO:iea	
OMIM	103420	ALACRIMA, CONGENITAL		HP:0007820	OMIM:103420	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000006	OMIM:103470	IEA				I		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000407	OMIM:103470	IEA				P		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000486	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000505	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000540	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000613	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0000639	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001003	OMIM:103470	TAS				P		HPO:probinson	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001010	OMIM:103470	TAS				P		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001093	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001107	OMIM:103470	IEA				P		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001417	OMIM:103470	IEA				I		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0001756	OMIM:103470	IEA				P		HPO:iea	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0005592	OMIM:103470	TAS				P		HPO:probinson	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0007663	OMIM:103470	TAS				P		HPO:skoehler	
OMIM	103470	#103470 ALBINISM, OCULAR, WITH SENSORINEURAL DEAFNESS;;WAARDENBURG SYNDROME, TYPE 2, WITH OCULAR ALBINISM, AUTOSOMAL RECESSIVE;WS2-OA		HP:0007750	OMIM:103470	IEA				P		HPO:iea	
OMIM	103500	TIETZ SYNDROME		HP:0000006	OMIM:103500	TAS				I		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0000635	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0002226	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0002227	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0007513	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0007894	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0008527	OMIM:103500	TAS				P		HPO:probinson	
OMIM	103500	TIETZ SYNDROME		HP:0008619	OMIM:103500	TAS				P		HPO:skoehler	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000006	OMIM:103580	IEA				I		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000135	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000293	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000311	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000470	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000518	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000639	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000684	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000821	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000852	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0000939	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0001156	OMIM:103580	TAS				P		HPO:skoehler	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0001249	OMIM:103580	IEA				P		HPO:skoehler	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0001250	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0001513	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0001831	OMIM:103580	TAS				P		HPO:probinson	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0002135	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0002684	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0002905	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0003165	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0003456	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0003472	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0004322	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0005280	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0006297	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0006960	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0009381	OMIM:103580	TAS				P		HPO:probinson	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0010049	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0010743	OMIM:103580	IEA				P		HPO:iea	
OMIM	103580	#103580 PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A;;PHP IA;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITH MULTIPLE HORMONE RESISTANCE		HP:0100543	OMIM:103580	IEA				P		HPO:iea	
OMIM	103780	ALCOHOL DEPENDENCE		HP:0000707	OMIM:103780	IEA				P		HPO:iea	
OMIM	103780	ALCOHOL DEPENDENCE		HP:0030955	OMIM:103780	TAS				P		HPO:skoehler	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0000006	OMIM:103900	IEA				I		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0000079	OMIM:103900	IEA				P		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0000822	OMIM:103900	IEA				P		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0000840	OMIM:103900	IEA				P		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0000859	OMIM:103900	IEA				P		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0003351	OMIM:103900	IEA				P		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0003674	OMIM:103900	IEA				C		HPO:iea	
OMIM	103900	GLUCOCORTICOID-REMEDIABLE ALDOSTERONISM		HP:0008221	OMIM:103900	IEA				P		HPO:skoehler	
OMIM	103920	ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS		HP:0000006	OMIM:103920	IEA				I		HPO:iea	
OMIM	103920	ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS		HP:0002715	OMIM:103920	IEA				P		HPO:iea	
OMIM	104000	ALOPECIA AREATA 1		HP:0001426	OMIM:104000	IEA				I		HPO:iea	
OMIM	104000	ALOPECIA AREATA 1		HP:0001803	OMIM:104000	IEA				P		HPO:iea	
OMIM	104000	ALOPECIA AREATA 1		HP:0002229	OMIM:104000	IEA				P		HPO:skoehler	
OMIM	104000	ALOPECIA AREATA 1		HP:0002289	OMIM:104000	TAS				P		HPO:skoehler	
OMIM	104000	ALOPECIA AREATA 1		HP:0002960	OMIM:104000	IEA				P		HPO:skoehler	
OMIM	104000	ALOPECIA AREATA 1		HP:0007418	OMIM:104000	IEA				P		HPO:iea	
OMIM	104000	ALOPECIA AREATA 1		HP:0030804	OMIM:104000	TAS				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0000006	OMIM:104100	IEA				I		HPO:iea	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0000972	OMIM:104100	IEA				P		HPO:iea	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0000982	OMIM:104100	IEA				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0001000	OMIM:104100	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0001596	OMIM:104100	IEA				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0001820	OMIM:104100	IEA				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1	HP:0012825	HP:0002164	OMIM:104100	IEA				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0002299	OMIM:104100	IEA				P		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0003593	OMIM:104100	IEA				C		HPO:skoehler	
OMIM	104100	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1; PPKCA1		HP:0008391	OMIM:104100	IEA				P		HPO:iea	
OMIM	104110	ALOPECIA, FAMILIAL FOCAL		HP:0000006	OMIM:104110	TAS				I		HPO:iea	
OMIM	104110	ALOPECIA, FAMILIAL FOCAL		HP:0002232	OMIM:104110	TAS				P		HPO:probinson	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0000006	OMIM:104130	IEA				I		HPO:iea	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0000704	OMIM:104130	IEA				P		HPO:iea	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0001250	OMIM:104130	IEA				P		HPO:skoehler	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0001256	OMIM:104130	IEA				P		HPO:iea	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0002289	OMIM:104130	TAS	HP:0003577			P		HPO:skoehler	
OMIM	104130	%104130 ALOPECIA, PSYCHOMOTOR EPILEPSY, PYORRHEA, AND MENTAL SUBNORMALITY;;SHOKEIR SYNDROME		HP:0005597	OMIM:104130	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000006	OMIM:104200	IEA				I		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000083	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000093	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000099	OMIM:104200	IEA				P		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000100	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000121	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000407	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000545	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000790	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0000822	OMIM:104200	IEA				P		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0001134	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0001142	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0002148	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0002157	OMIM:104200	IEA				P		HPO:iea	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0003676	OMIM:104200	IEA				C		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0003774	OMIM:104200	TAS				P		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0004722	OMIM:104200	IEA				P		HPO:skoehler	
OMIM	104200	#104200 ALPORT SYNDROME, AUTOSOMAL DOMINANT		HP:0030034	OMIM:104200	TAS				P		HPO:skoehler	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0000006	OMIM:104290	IEA				I		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0000639	OMIM:104290	IEA				P		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0001249	OMIM:104290	IEA				P		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0001266	OMIM:104290	IEA				P		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0001268	OMIM:104290	IEA				P		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0001332	OMIM:104290	IEA				P		HPO:iea	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0002069	OMIM:104290	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0012194	OMIM:104290	TAS				P		HPO:probinson	
OMIM	104290	#104290 ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1		HP:0200072	OMIM:104290	TAS				P		HPO:skoehler	
OMIM	104300	ALZHEIMER DISEASE		HP:0000006	OMIM:104300	TAS				I		HPO:probinson	
OMIM	104300	ALZHEIMER DISEASE		HP:0000726	OMIM:104300	TAS				P		HPO:skoehler	
OMIM	104300	ALZHEIMER DISEASE		HP:0001300	OMIM:104300	TAS				P		HPO:probinson	
OMIM	104300	ALZHEIMER DISEASE		HP:0001425	OMIM:104300	IEA				I		HPO:skoehler	
OMIM	104300	ALZHEIMER DISEASE		HP:0002185	OMIM:104300	TAS				P		HPO:probinson	
OMIM	104300	ALZHEIMER DISEASE		HP:0002423	OMIM:104300	TAS				P		HPO:probinson	
OMIM	104300	ALZHEIMER DISEASE		HP:0002511	OMIM:104300	TAS				P		HPO:probinson	
OMIM	104300	ALZHEIMER DISEASE		HP:0410054	PMID:17031479	PCS				P		HPO:NicoleVasilevsky	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0000006	OMIM:104310	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0000726	OMIM:104310	IEA				P		HPO:skoehler	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0001300	OMIM:104310	IEA				P		HPO:iea	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0002185	OMIM:104310	TAS				P		HPO:probinson	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0002185	OMIM:104310	IEA				P		HPO:iea	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0002423	OMIM:104310	IEA				P		HPO:iea	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0002511	OMIM:104310	TAS				P		HPO:probinson	
OMIM	104310	ALZHEIMER DISEASE 2		HP:0003584	OMIM:104310	IEA				C		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000006	OMIM:104350	IEA				I		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000126	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000218	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000238	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000286	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000316	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000369	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000431	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000494	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000508	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0000767	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0001159	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0001374	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0001537	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0001634	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0001643	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0002561	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0002650	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0002937	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0002967	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0005280	OMIM:104350	IEA				P		HPO:iea	
OMIM	104350	AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM		HP:0008705	OMIM:104350	IEA				P		HPO:iea	
OMIM	104400	AMELIA AND TERMINAL TRANSVERSE HEMIMELIA		HP:0000006	OMIM:104400	TAS				I		HPO:nvasilevsky	
OMIM	104400	AMELIA AND TERMINAL TRANSVERSE HEMIMELIA		HP:0001426	OMIM:104400	TAS				I		HPO:nvasilevsky	
OMIM	104400	AMELIA AND TERMINAL TRANSVERSE HEMIMELIA		HP:0009827	OMIM:104400	IEA				P		HPO:iea	
OMIM	104500	AMELOGENESIS IMPERFECTA, TYPE IB		HP:0000006	OMIM:104500	IEA				I		HPO:iea	
OMIM	104500	AMELOGENESIS IMPERFECTA, TYPE IB		HP:0000705	OMIM:104500	IEA				P		HPO:iea	
OMIM	104510	AMELOGENESIS IMPERFECTA, TYPE IV		HP:0000006	OMIM:104510	IEA				I		HPO:iea	
OMIM	104510	AMELOGENESIS IMPERFECTA, TYPE IV		HP:0000679	OMIM:104510	IEA				P		HPO:iea	
OMIM	104510	AMELOGENESIS IMPERFECTA, TYPE IV		HP:0000705	OMIM:104510	IEA				P		HPO:iea	
OMIM	104530	#104530 AMELOGENESIS IMPERFECTA, TYPE IA; AI1AAMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IA		HP:0000006	OMIM:104530	IEA				I		HPO:iea	
OMIM	104530	#104530 AMELOGENESIS IMPERFECTA, TYPE IA; AI1AAMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IA		HP:0000679	OMIM:104530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	104530	#104530 AMELOGENESIS IMPERFECTA, TYPE IA; AI1AAMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IA		HP:0000705	OMIM:104530	IEA				P		HPO:iea	
OMIM	104530	#104530 AMELOGENESIS IMPERFECTA, TYPE IA; AI1AAMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IA		HP:0006311	OMIM:104530	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0000006	OMIM:104570	IEA				I		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0000682	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0000958	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0000966	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0001051	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0001595	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0001806	OMIM:104570	IEA				P		HPO:iea	
OMIM	104570	AMELOONYCHOHYPOHIDROTIC SYNDROME		HP:0006291	OMIM:104570	IEA				P		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0000006	OMIM:104600	IEA				I		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0000765	OMIM:104600	IEA				P		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0000869	OMIM:104600	IEA				P		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0002690	OMIM:104600	IEA				P		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0002893	OMIM:104600	IEA				P		HPO:iea	
OMIM	104600	104600 AMENORRHEA-GALACTORRHEA SYNDROME		HP:0100829	OMIM:104600	TAS				P		HPO:skoehler	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0000006	OMIM:105120	IEA				I		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0000083	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0000100	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0000973	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0001149	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0001271	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0001283	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0001438	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0001638	OMIM:105120	IEA				P		HPO:skoehler	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0003216	OMIM:105120	IEA				P		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0003581	OMIM:105120	IEA				C		HPO:iea	
OMIM	105120	AMYLOIDOSIS, FINNISH TYPE		HP:0030843	OMIM:105120	TAS				P		HPO:skoehler	
OMIM	105150	AMYLOIDOSIS VI		HP:0000006	OMIM:105150	IEA				I		HPO:iea	
OMIM	105150	AMYLOIDOSIS VI		HP:0000726	OMIM:105150	IEA				P		HPO:iea	
OMIM	105150	AMYLOIDOSIS VI		HP:0001297	OMIM:105150	IEA				P		HPO:skoehler	
OMIM	105150	AMYLOIDOSIS VI		HP:0001342	OMIM:105150	TAS				P		HPO:skoehler	
OMIM	105150	AMYLOIDOSIS VI		HP:0002170	OMIM:105150	IEA				P		HPO:iea	
OMIM	105150	AMYLOIDOSIS VI		HP:0003216	OMIM:105150	IEA				P		HPO:iea	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000006	OMIM:105200	TAS				I		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000093	PMID:8113408	PCS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000100	OMIM:105200	TAS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000112	OMIM:105200	TAS				P		HPO:skoehler	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000790	OMIM:105200	TAS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000822	PMID:8113408	PCS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000969	PMID:8113408	PCS				P		HPO:skoehler	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0000988	OMIM:105200	TAS				P		HPO:skoehler	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0001396	OMIM:105200	TAS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0001744	OMIM:105200	TAS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0002240	OMIM:105200	TAS				P		HPO:probinson	
OMIM	105200	AMYLOIDOSIS, FAMILIAL VISCERAL		HP:0003216	PMID:22693999	PCS				P		HPO:probinson	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000006	OMIM:105210	IEA				I		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000020	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000365	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000505	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000639	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000726	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0000802	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001250	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001251	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001257	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001260	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001265	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001269	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001271	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001324	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001337	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001638	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0001640	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0002014	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0002019	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0002315	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0002401	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0002922	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0003477	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0003581	OMIM:105210	IEA				C		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0003676	OMIM:105210	IEA				C		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0004926	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0007841	OMIM:105210	IEA				P		HPO:iea	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0010550	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0011034	OMIM:105210	IEA				P		HPO:skoehler	
OMIM	105210	AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED		HP:0012185	OMIM:105210	TAS				P		HPO:skoehler	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0000006	OMIM:105250	TAS				I		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0000958	OMIM:105250	IEA				P		HPO:skoehler	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0000973	OMIM:105250	TAS				P		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0000989	OMIM:105250	TAS				P		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0001149	OMIM:105250	TAS				P		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0001291	OMIM:105250	TAS				P		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0003581	OMIM:105250	TAS				C		HPO:probinson	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0011034	OMIM:105250	TAS				P		HPO:skoehler	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0040189	OMIM:105250	IEA				P		HPO:skoehler	
OMIM	105250	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1; PLCA1		HP:0100725	OMIM:105250	IEA				P		HPO:skoehler	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0000006	OMIM:105300	IEA				I		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0000020	OMIM:105300	TAS				P		HPO:skoehler	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0000639	OMIM:105300	IEA				P		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0001249	OMIM:105300	IEA				P		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0001258	OMIM:105300	IEA				P		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0001332	OMIM:105300	IEA				P		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0002607	OMIM:105300	IEA				P		HPO:iea	
OMIM	105300	AMYOTROPHIC DYSTONIC PARAPLEGIA		HP:0003202	OMIM:105300	IEA				P		HPO:iea	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0000006	PMID:8446170	PCS				I		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0000007	OMIM:105400	IEA				I		HPO:skoehler	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0001257	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0001324	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0001347	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0001425	OMIM:105400	IEA				I		HPO:skoehler	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0002314	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0002380	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0002398	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0003202	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0003394	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0007024	OMIM:105400	TAS				P		HPO:probinson	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0007354	PMID:8446170	PCS				P		HPO:skoehler	
OMIM	105400	AMYOTROPHIC LATERAL SCLEROSIS 1		HP:0010535	OMIM:105400	IEA				P		HPO:skoehler	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0000006	OMIM:105500	TAS				I		HPO:skoehler	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0000726	OMIM:105500	TAS				P		HPO:probinson	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0001283	OMIM:105500	TAS				P		HPO:probinson	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0001300	OMIM:105500	TAS				P		HPO:probinson	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0001324	OMIM:105500	IEA				P		HPO:skoehler	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0002366	OMIM:105500	TAS				P		HPO:probinson	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0003394	OMIM:105500	IEA				P		HPO:probinson	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0003470	OMIM:105500	IEA				P		HPO:skoehler	
OMIM	105500	AMYOTROPHIC LATERAL SCLEROSIS-PARKINSONISM/DEMENTIA COMPLEX 1		HP:0007354	OMIM:105500	IEA				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000006	OMIM:105550	IEA				I		HPO:iea	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000605	OMIM:105550	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000716	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000738	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000741	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0000746	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0001260	OMIM:105550	IEA				P		HPO:skoehler	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0001300	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0001324	OMIM:105550	IEA				P		HPO:skoehler	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002059	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002145	OMIM:105550	IEA				P		HPO:skoehler	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002171	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002186	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002273	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002366	OMIM:105550	IEA				P		HPO:iea	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002385	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002442	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0002529	OMIM:105550	IEA				P		HPO:skoehler	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0003202	OMIM:105550	IEA				P		HPO:skoehler	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0003581	OMIM:105550	TAS				C		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0003678	OMIM:105550	TAS				C		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0007308	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105550	AMYOTROPHIC LATERAL SCLEROSIS AND/OR FRONTOTEMPORAL DEMENTIA 1		HP:0007354	OMIM:105550	TAS				P		HPO:probinson	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0000006	OMIM:105563	IEA				I		HPO:iea	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0002014	OMIM:105563	IEA				P		HPO:skoehler	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0002019	OMIM:105563	IEA				P		HPO:iea	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0002607	OMIM:105563	IEA				P		HPO:iea	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0012450	OMIM:105563	TAS				P		HPO:skoehler	
OMIM	105563	ANAL SPHINCTER DYSPLASIA; ASDP		HP:0040183	OMIM:105563	TAS				P		HPO:skoehler	
OMIM	105565	ANAL SPHINCTER MYOPATHY, INTERNAL		HP:0000006	OMIM:105565	TAS				I		HPO:probinson	
OMIM	105565	ANAL SPHINCTER MYOPATHY, INTERNAL		HP:0002019	OMIM:105565	TAS				P		HPO:probinson	
OMIM	105565	ANAL SPHINCTER MYOPATHY, INTERNAL		HP:0003198	OMIM:105565	IEA				P		HPO:skoehler	
OMIM	105565	ANAL SPHINCTER MYOPATHY, INTERNAL		HP:0004378	OMIM:105565	TAS				P		HPO:probinson	
OMIM	105570	ANDROSTENONE, ABILITY TO SMELL		HP:0000006	OMIM:105570	IEA				I		HPO:iea	
OMIM	105570	ANDROSTENONE, ABILITY TO SMELL		HP:0000707	OMIM:105570	IEA				P		HPO:iea	
OMIM	105580	ANAL CANAL CARCINOMACLOACOGENIC CARCINOMA, INCLUDED		HP:0000006	OMIM:105580	IEA				I		HPO:iea	
OMIM	105580	ANAL CANAL CARCINOMACLOACOGENIC CARCINOMA, INCLUDED		HP:0006763	OMIM:105580	IEA				P		HPO:iea	
OMIM	105600	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III		HP:0000006	OMIM:105600	IEA				I		HPO:iea	
OMIM	105600	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III		HP:0000952	OMIM:105600	IEA				P		HPO:iea	
OMIM	105600	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III		HP:0001972	OMIM:105600	TAS				P		HPO:probinson	
OMIM	105600	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III		HP:0004810	OMIM:105600	IEA				P		HPO:iea	
OMIM	105600	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE III		HP:0012543	OMIM:105600	TAS				P		HPO:probinson	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000006	OMIM:105650	IEA				I		HPO:iea	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000175	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000204	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000218	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000252	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000270	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000278	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000316	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000347	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000457	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000465	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000470	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000486	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000494	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000774	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000878	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000946	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0000980	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001199	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001249	OMIM:105650	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001508	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA	HP:0012825	HP:0001511	OMIM:105650	TAS				P		HPO:probinson	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001622	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001629	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001631	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001635	OMIM:105650	IEA				P		HPO:iea	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001680	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001873	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001875	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001894	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0001896	OMIM:105650	TAS				P		HPO:probinson	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0002669	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0002697	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0002863	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA	HP:0012825	HP:0002984	OMIM:105650	TAS				P		HPO:probinson	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0003003	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0003593	OMIM:105650	IEA				C		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0004322	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0004810	OMIM:105650	TAS				P		HPO:probinson	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0008437	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0008447	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0008475	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0009777	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0009778	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0009944	OMIM:105650	IEA				P		HPO:skoehler	
OMIM	105650	DIAMOND-BLACKFAN ANEMIA		HP:0030270	OMIM:105650	TAS				P		HPO:probinson	
OMIM	105800	ANEURYSM, INTRACRANIAL BERRY, 1		HP:0000006	OMIM:105800	IEA				I		HPO:iea	
OMIM	105800	ANEURYSM, INTRACRANIAL BERRY, 1		HP:0002170	OMIM:105800	IEA				P		HPO:iea	
OMIM	105800	ANEURYSM, INTRACRANIAL BERRY, 1		HP:0004944	OMIM:105800	IEA				P		HPO:iea	
OMIM	105805	ANEURYSM OF INTERVENTRICULAR SEPTUM		HP:0000006	OMIM:105805	IEA				I		HPO:iea	
OMIM	105805	ANEURYSM OF INTERVENTRICULAR SEPTUM		HP:0002617	OMIM:105805	IEA				P		HPO:skoehler	
OMIM	105805	ANEURYSM OF INTERVENTRICULAR SEPTUM		HP:0010438	OMIM:105805	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0000006	OMIM:105830	PCS				I		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000154	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000158	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000248	OMIM:105830	TAS				P		HPO:probinson	
OMIM	105830	ANGELMAN SYNDROME		HP:0000303	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000327	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000486	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000490	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000545	OMIM:105830	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0000577	OMIM:105830	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0000635	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000639	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000687	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000749	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0000752	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001010	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001250	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001252	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001263	OMIM:105830	TAS				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0001270	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001290	OMIM:105830	TAS				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0001344	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001347	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0001513	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0002019	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0002120	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0002136	OMIM:105830	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	105830	ANGELMAN SYNDROME		HP:0002286	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0002307	OMIM:105830	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0002312	OMIM:105830	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	105830	ANGELMAN SYNDROME		HP:0002353	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0002650	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0003745	OMIM:105830	TAS		HP:0040282		I		HPO:iea	HP:0040282
OMIM	105830	ANGELMAN SYNDROME		HP:0005469	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0005484	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0005484	OMIM:105830	TAS				P		HPO:probinson	
OMIM	105830	ANGELMAN SYNDROME		HP:0006887	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0006979	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0007240	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0008872	OMIM:105830	PCS				P		HPO:iea	
OMIM	105830	ANGELMAN SYNDROME		HP:0010808	OMIM:105830	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0010864	OMIM:105830	IEA				P		HPO:skoehler	
OMIM	105830	ANGELMAN SYNDROME		HP:0200085	OMIM:105830	TAS				P		HPO:skoehler	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0001187	OMIM:105835	TAS				P		HPO:probinson	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0001216	OMIM:105835	TAS				P		HPO:probinson	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0003088	OMIM:105835	TAS				P		HPO:probinson	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0004322	OMIM:105835	TAS				P		HPO:probinson	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0008843	OMIM:105835	TAS				P		HPO:probinson	
OMIM	105835	ANGEL-SHAPED PHALANGOEPIPHYSEAL DYSPLASIA		HP:0009193	OMIM:105835	TAS				P		HPO:probinson	
OMIM	106050	ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT		HP:0000006	OMIM:106050	IEA				I		HPO:iea	
OMIM	106050	ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT		HP:0000962	OMIM:106050	IEA				P		HPO:iea	
OMIM	106050	ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT		HP:0003621	OMIM:106050	IEA				C		HPO:iea	
OMIM	106050	ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT		HP:0003677	OMIM:106050	IEA				C		HPO:iea	
OMIM	106050	ANGIOMA SERPIGINOSUM, AUTOSOMAL DOMINANT		HP:0003745	OMIM:106050	IEA				I		HPO:iea	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0000006	OMIM:106070	IEA				I		HPO:iea	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0000790	OMIM:106070	IEA				P		HPO:skoehler	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0001028	OMIM:106070	IEA				P		HPO:skoehler	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0001269	OMIM:106070	IEA				P		HPO:iea	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0002239	OMIM:106070	IEA				P		HPO:iea	
OMIM	106070	ANGIOMA, HEREDITARY NEUROCUTANEOUSSPINAL ARTERIAL VENOUS MALFORMATIONS WITH CUTANEOUS HEMANGIOMAS, INCLUDED		HP:0002277	OMIM:106070	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0000006	OMIM:106100	IEA				I		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0000007	OMIM:106100	IEA				I		HPO:skoehler	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0001600	OMIM:106100	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0002013	OMIM:106100	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0002014	OMIM:106100	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0002027	OMIM:106100	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0002960	OMIM:106100	IEA				P		HPO:skoehler	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0003477	OMIM:106100	IEA				P		HPO:skoehler	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0005225	OMIM:106100	IEA				P		HPO:iea	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0010783	OMIM:106100	IEA				P		HPO:skoehler	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0011855	OMIM:106100	TAS				P		HPO:probinson	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0012027	OMIM:106100	TAS				P		HPO:probinson	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0040078	OMIM:106100	IEA				P		HPO:skoehler	
OMIM	106100	ANGIOEDEMA, HEREDITARY, TYPE I; HAE1		HP:0100665	OMIM:106100	IEA				P		HPO:skoehler	
OMIM	106190	ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS; ANHD		HP:0000007	OMIM:106190	TAS				I		HPO:skoehler	
OMIM	106190	ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS; ANHD		HP:0000970	OMIM:106190	IEA				P		HPO:skoehler	
OMIM	106190	ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS; ANHD		HP:0002046	OMIM:106190	TAS				P		HPO:skoehler	
OMIM	106190	ANHIDROSIS, ISOLATED, WITH NORMAL SWEAT GLANDS; ANHD		HP:0007459	OMIM:106190	TAS				P		HPO:skoehler	
OMIM	106210	ANIRIDIA		HP:0000006	OMIM:106210	IEA				I		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0000501	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0000518	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0000526	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0000609	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0000639	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0001952	PMID:19034419	PCS				P		HPO:lccarmody	
OMIM	106210	ANIRIDIA		HP:0002079	OMIM:106210	TAS				P		HPO:skoehler	
OMIM	106210	ANIRIDIA		HP:0002126	OMIM:106210	TAS				P		HPO:skoehler	
OMIM	106210	ANIRIDIA		HP:0007750	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0007759	OMIM:106210	IEA				P		HPO:iea	
OMIM	106210	ANIRIDIA		HP:0031883	PMID:19034419	PCS				P		HPO:lccarmody	
OMIM	106220	ANIRIDIA AND ABSENT PATELLA		HP:0000006	OMIM:106220	IEA				I		HPO:iea	
OMIM	106220	ANIRIDIA AND ABSENT PATELLA		HP:0000501	OMIM:106220	IEA				P		HPO:iea	
OMIM	106220	ANIRIDIA AND ABSENT PATELLA		HP:0000518	OMIM:106220	IEA				P		HPO:iea	
OMIM	106220	ANIRIDIA AND ABSENT PATELLA		HP:0000526	OMIM:106220	IEA				P		HPO:iea	
OMIM	106220	ANIRIDIA AND ABSENT PATELLA		HP:0006498	OMIM:106220	IEA				P		HPO:iea	
OMIM	106230	ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT		HP:0000006	OMIM:106230	TAS				I		HPO:probinson	
OMIM	106230	ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT		HP:0000482	OMIM:106230	TAS				P		HPO:probinson	
OMIM	106230	ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT		HP:0000518	OMIM:106230	IEA				P		HPO:skoehler	
OMIM	106230	ANIRIDIA, MICROCORNEA, AND SPONTANEOUSLY REABSORBED CATARACT		HP:0000526	OMIM:106230	TAS				P		HPO:probinson	
OMIM	106240	ANISOCORIA		HP:0000006	OMIM:106240	IEA				I		HPO:iea	
OMIM	106240	ANISOCORIA		HP:0009916	OMIM:106240	IEA				P		HPO:skoehler	
OMIM	106240	ANISOCORIA		HP:0012378	OMIM:106240	IEA				P		HPO:skoehler	
OMIM	106250	ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE		HP:0000006	OMIM:106250	TAS				I		HPO:probinson	
OMIM	106250	ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE		HP:0000175	OMIM:106250	TAS				P		HPO:skoehler	
OMIM	106250	ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE		HP:0000204	OMIM:106250	TAS				P		HPO:skoehler	
OMIM	106250	ANKYLOBLEPHARON FILIFORME ADNATUM AND CLEFT PALATE		HP:0009755	OMIM:106250	TAS				P		HPO:probinson	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000006	OMIM:106260	IEA				I		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000047	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000054	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000175	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000204	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000300	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000327	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000405	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000413	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000431	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000498	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000509	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000561	OMIM:106260	IEA				P		HPO:skoehler	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000564	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000653	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000668	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000687	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000698	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000707	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000953	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000970	OMIM:106260	IEA				P		HPO:skoehler	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0000982	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0001592	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0001629	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0001643	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0001795	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0001798	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0002231	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0002232	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0002558	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0004691	OMIM:106260	IEA				P		HPO:iea	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0008404	OMIM:106260	TAS				P		HPO:skoehler	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0009755	OMIM:106260	TAS				P		HPO:probinson	
OMIM	106260	ANKYLOBLEPHARON-ECTODERMAL DEFECTS-CLEFT LIP/PALATE		HP:0031088	OMIM:106260	TAS				P		HPO:skoehler	
OMIM	106280	ANKYLOGLOSSIA		HP:0000006	OMIM:106280	IEA				I		HPO:iea	
OMIM	106280	ANKYLOGLOSSIA		HP:0010296	OMIM:106280	IEA				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0001425	OMIM:106300	TAS				I		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0001426	OMIM:106300	TAS				I		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0001659	OMIM:106300	TAS				P		HPO:probinson	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0002037	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0002808	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0003418	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0003765	OMIM:106300	TAS				P		HPO:probinson	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0008843	OMIM:106300	TAS				P		HPO:iea	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0011675	OMIM:106300	TAS				P		HPO:probinson	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0012122	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0012317	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106300	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1		HP:0100686	OMIM:106300	TAS				P		HPO:skoehler	
OMIM	106400	ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSISDIFFUSE IDIOPATHIC SKELETAL HYPEROSTOSIS, INCLUDED		HP:0000006	OMIM:106400	IEA				I		HPO:iea	
OMIM	106400	ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSISDIFFUSE IDIOPATHIC SKELETAL HYPEROSTOSIS, INCLUDED		HP:0007508	OMIM:106400	IEA				P		HPO:iea	
OMIM	106400	ANKYLOSING VERTEBRAL HYPEROSTOSIS WITH TYLOSISDIFFUSE IDIOPATHIC SKELETAL HYPEROSTOSIS, INCLUDED		HP:0008442	OMIM:106400	IEA				P		HPO:skoehler	
OMIM	106500	ANNULAR ERYTHEMA		HP:0000006	OMIM:106500	IEA				I		HPO:iea	
OMIM	106500	ANNULAR ERYTHEMA		HP:0010783	OMIM:106500	IEA				P		HPO:skoehler	
OMIM	106600	TOOTH AGENESIS, SELECTIVE, 1		HP:0000006	OMIM:106600	TAS				I		HPO:probinson	
OMIM	106600	TOOTH AGENESIS, SELECTIVE, 1		HP:0000668	OMIM:106600	TAS				P		HPO:probinson	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0000006	OMIM:106700	IEA				I		HPO:iea	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0002092	OMIM:106700	IEA				P		HPO:iea	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0002205	OMIM:106700	IEA				P		HPO:iea	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0005160	OMIM:106700	TAS				P		HPO:skoehler	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0008386	OMIM:106700	IEA				P		HPO:skoehler	
OMIM	106700	TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1		HP:0009884	OMIM:106700	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	106750	ANONYCHIA WITH FLEXURAL PIGMENTATION		HP:0000006	OMIM:106750	IEA				I		HPO:iea	
OMIM	106750	ANONYCHIA WITH FLEXURAL PIGMENTATION		HP:0000958	OMIM:106750	TAS				P		HPO:skoehler	
OMIM	106750	ANONYCHIA WITH FLEXURAL PIGMENTATION		HP:0001798	OMIM:106750	IEA				P		HPO:iea	
OMIM	106750	ANONYCHIA WITH FLEXURAL PIGMENTATION		HP:0007471	OMIM:106750	IEA				P		HPO:iea	
OMIM	106900	ANONYCHIA-ECTRODACTYLY		HP:0000006	OMIM:106900	IEA				I		HPO:iea	
OMIM	106900	ANONYCHIA-ECTRODACTYLY		HP:0000968	OMIM:106900	IEA				P		HPO:iea	
OMIM	106900	ANONYCHIA-ECTRODACTYLY		HP:0001171	OMIM:106900	IEA				P		HPO:iea	
OMIM	106900	ANONYCHIA-ECTRODACTYLY		HP:0001798	OMIM:106900	IEA				P		HPO:iea	
OMIM	106900	ANONYCHIA-ECTRODACTYLY		HP:0010048	OMIM:106900	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0000006	OMIM:106990	IEA				I		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0000968	OMIM:106990	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0001171	OMIM:106990	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0001798	OMIM:106990	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0002164	OMIM:106990	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0005831	OMIM:106990	TAS				P		HPO:probinson	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0008404	OMIM:106990	TAS				P		HPO:skoehler	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0009835	OMIM:106990	IEA				P		HPO:iea	
OMIM	106990	106990 ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY		HP:0010743	OMIM:106990	IEA				P		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000006	OMIM:106995	IEA				I		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000218	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000322	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000426	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000430	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000448	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0000494	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0001798	OMIM:106995	IEA				P		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0002164	OMIM:106995	IEA				P		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0005793	OMIM:106995	IEA				P		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0006118	OMIM:106995	TAS				P		HPO:probinson	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0008404	OMIM:106995	TAS				P		HPO:skoehler	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0009237	OMIM:106995	IEA				P		HPO:iea	
OMIM	106995	%106995 ANONYCHIA-ONYCHODYSTROPHY WITH HYPOPLASIA OR ABSENCE OF DISTAL PHALANGES;;COOKS SYNDROME		HP:0009943	OMIM:106995	IEA				P		HPO:iea	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0000006	OMIM:107000	IEA				I		HPO:iea	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0001374	OMIM:107000	IEA				P		HPO:iea	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0001798	OMIM:107000	IEA				P		HPO:iea	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0002164	OMIM:107000	IEA				P		HPO:iea	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0008404	OMIM:107000	TAS				P		HPO:skoehler	
OMIM	107000	%107000 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 6; NDNC6;;ANONYCHIA/HYPONYCHIA AND ONYCHODYSTROPHY;;ANONYCHIA, PARTIAL		HP:0009884	OMIM:107000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	107100	ANORECTAL ANOMALIES		HP:0000006	OMIM:107100	IEA				I		HPO:iea	
OMIM	107100	ANORECTAL ANOMALIES		HP:0000143	OMIM:107100	IEA				P		HPO:iea	
OMIM	107100	ANORECTAL ANOMALIES		HP:0002023	OMIM:107100	IEA				P		HPO:iea	
OMIM	107200	ANOSMIA, CONGENITAL		HP:0000006	OMIM:107200	IEA				I		HPO:iea	
OMIM	107200	ANOSMIA, CONGENITAL		HP:0000458	OMIM:107200	TAS	HP:0003577			P		HPO:skoehler	
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0000006	OMIM:107250	TAS				I		HPO:iea	
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0000482	OMIM:107250	TAS				P		HPO:skoehler	
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0000659	OMIM:107250	TAS				P		HPO:skoehler	
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0001115	PMID:15286169,PMID:16636655,PMID:18989383	PCS		HP:0040284		P		HPO:iea	47/47
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0007700	PMID:15286169,PMID:18989383	PCS		HP:0040284		P		HPO:iea	5/44
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0007759	OMIM:107250	TAS				P		HPO:iea	
OMIM	107250	ANTERIOR SEGMENT DYSGENESIS 1; ASGD1		HP:0007906	OMIM:107250	IEA				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0000006	OMIM:107320	IEA				I		HPO:iea	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0000491	OMIM:107320	IEA				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0000541	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0000572	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0000622	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0001101	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0001973	OMIM:107320	IEA				P		HPO:iea	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0004420	OMIM:107320	IEA				P		HPO:iea	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0004936	OMIM:107320	IEA				P		HPO:iea	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0011531	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0025188	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0025342	OMIM:107320	TAS				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0025343	OMIM:107320	IEA				P		HPO:skoehler	
OMIM	107320	ANTIPHOSPHOLIPID SYNDROME, FAMILIAL		HP:0100532	OMIM:107320	IEA				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000003	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000006	OMIM:107480	IEA				I		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000028	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000047	PMID:9973281	PCS		HP:0040284		P		HPO:iea	3/17
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000048	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000076	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000083	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000089	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000110	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000136	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000143	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000252	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000384	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000400	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000407	PMID:9973281	PCS		HP:0040284		P		HPO:iea	14/17
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000567	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0000821	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001177	OMIM:107480	IEA				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001199	PMID:9973281	IEA		HP:0040284		P		HPO:iea	8/17
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001263	PMID:22308078	PCS		HP:0040284		P		HPO:iea	23/89
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001440	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001537	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001629	PMID:9973281	PCS		HP:0040284		P		HPO:iea	1/17
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001636	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0001864	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0002020	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0002023	PMID:22308078	PCS		HP:0040284		P		HPO:iea	101/154
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0002025	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0002247	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0004453	OMIM:107480	PCS				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0004467	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0004691	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0004792	OMIM:107480	IEA				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0006097	OMIM:107480	IEA				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0006179	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0008551	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0009779	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0009921	OMIM:107480	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0009944	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0010331	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0010481	OMIM:107480	IEA				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0010709	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0010743	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0011304	OMIM:107480	IEA				P		HPO:iea	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0030676	PMID:3180506	PCS				P		HPO:skoehler	
OMIM	107480	TOWNES-BROCKS SYNDROME		HP:0100015	OMIM:107480	IEA				P		HPO:skoehler	
OMIM	107500	AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION		HP:0000006	OMIM:107500	IEA				I		HPO:iea	
OMIM	107500	AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION		HP:0000252	OMIM:107500	IEA				P		HPO:iea	
OMIM	107500	AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION		HP:0001249	OMIM:107500	IEA				P		HPO:iea	
OMIM	107500	AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION		HP:0001999	OMIM:107500	IEA				P		HPO:iea	
OMIM	107500	AORTIC ARCH ANOMALY WITH PECULIAR FACIES AND MENTAL RETARDATION		HP:0002627	OMIM:107500	IEA				P		HPO:iea	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0000006	OMIM:107550	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0001116	OMIM:107550	TAS				P		HPO:probinson	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0001680	OMIM:107550	TAS				P		HPO:probinson	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0010628	OMIM:107550	TAS				P		HPO:skoehler	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0010817	OMIM:107550	TAS				P		HPO:probinson	
OMIM	107550	107550 AORTIC ARCH INTERRUPTION, FACIAL PALSY, AND RETINAL COLOBOMA		HP:0011611	OMIM:107550	TAS				P		HPO:probinson	
OMIM	107600	APLASIA CUTIS CONGENITA, NONSYNDROMIC		HP:0000006	OMIM:107600	TAS				I		HPO:probinson	
OMIM	107600	APLASIA CUTIS CONGENITA, NONSYNDROMIC		HP:0000007	OMIM:107600	TAS				I		HPO:probinson	
OMIM	107600	APLASIA CUTIS CONGENITA, NONSYNDROMIC		HP:0004471	OMIM:107600	TAS				P		HPO:probinson	
OMIM	107640	APNEA, CENTRAL SLEEP		HP:0000006	OMIM:107640	TAS				I		HPO:skoehler	
OMIM	107640	APNEA, CENTRAL SLEEP		HP:0001699	OMIM:107640	TAS				M		HPO:skoehler	
OMIM	107640	APNEA, CENTRAL SLEEP		HP:0010535	OMIM:107640	TAS				P		HPO:skoehler	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0000006	OMIM:107650	TAS				I		HPO:probinson	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0000458	OMIM:107650	TAS				P		HPO:probinson	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0001262	OMIM:107650	TAS				P		HPO:skoehler	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0002384	OMIM:107650	TAS				P		HPO:probinson	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0002870	OMIM:107650	TAS				P		HPO:probinson	
OMIM	107650	APNEA, OBSTRUCTIVE SLEEP		HP:0025267	OMIM:107650	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0000006	OMIM:107680	TAS				I		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0000083	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0001635	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0001677	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0001917	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0004398	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0007957	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107680	APOLIPOPROTEIN A-I		HP:0012280	OMIM:107680	TAS				P		HPO:skoehler	
OMIM	107700	APPENDICITIS, PRONENESS TO		HP:0002250	OMIM:107700	IEA				P		HPO:skoehler	
OMIM	107850	107850 ARM FOLDING PREFERENCE		HP:0010982	OMIM:107850	TAS				I		HPO:skoehler	
OMIM	107900	ARMS, MALFORMATION OF		HP:0000006	OMIM:107900	TAS				I		HPO:probinson	
OMIM	107900	ARMS, MALFORMATION OF		HP:0002974	OMIM:107900	TAS				P		HPO:probinson	
OMIM	107900	ARMS, MALFORMATION OF		HP:0002984	OMIM:107900	TAS				P		HPO:probinson	
OMIM	107900	ARMS, MALFORMATION OF		HP:0003022	OMIM:107900	TAS				P		HPO:probinson	
OMIM	107970	#107970 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1UHL ANOMALY, INCLUDED;;CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED		HP:0000006	OMIM:107970	IEA				I		HPO:iea	
OMIM	107970	#107970 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1UHL ANOMALY, INCLUDED;;CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED		HP:0001425	OMIM:107970	TAS				I		HPO:skoehler	
OMIM	107970	#107970 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1UHL ANOMALY, INCLUDED;;CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED		HP:0001645	OMIM:107970	IEA				P		HPO:iea	
OMIM	107970	#107970 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1UHL ANOMALY, INCLUDED;;CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED		HP:0004308	OMIM:107970	IEA				P		HPO:iea	
OMIM	107970	#107970 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1; ARVC1UHL ANOMALY, INCLUDED;;CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED, INCLUDED		HP:0011663	OMIM:107970	TAS				P		HPO:skoehler	
OMIM	108000	ARTERIES, ANOMALIES OF		HP:0000006	OMIM:108000	IEA				I		HPO:iea	
OMIM	108000	ARTERIES, ANOMALIES OF		HP:0001626	OMIM:108000	IEA				P		HPO:iea	
OMIM	108010	ARTERIOVENOUS MALFORMATIONS OF THE BRAIN		HP:0000006	OMIM:108010	IEA				I		HPO:iea	
OMIM	108010	ARTERIOVENOUS MALFORMATIONS OF THE BRAIN		HP:0002408	OMIM:108010	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0000006	OMIM:108050	IEA				I		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0000822	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0000952	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001085	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001101	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001250	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001370	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001482	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001698	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0001945	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0002202	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0002315	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0002617	OMIM:108050	IEA				P		HPO:skoehler	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0003155	OMIM:108050	IEA				P		HPO:iea	
OMIM	108050	ARTERITIS, FAMILIAL GRANULOMATOUS, WITH JUVENILE POLYARTHRITIS		HP:0006679	OMIM:108050	IEA				P		HPO:iea	
OMIM	108100	ARTHRITIS, SACROILIAC		HP:0000006	OMIM:108100	IEA				I		HPO:iea	
OMIM	108100	ARTHRITIS, SACROILIAC		HP:0000989	OMIM:108100	IEA				P		HPO:skoehler	
OMIM	108100	ARTHRITIS, SACROILIAC		HP:0003401	OMIM:108100	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	108100	ARTHRITIS, SACROILIAC		HP:0012317	OMIM:108100	TAS				P		HPO:probinson	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0000006	OMIM:108120	IEA				I		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0000028	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0000211	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0000954	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001032	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001181	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001188	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001193	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001374	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001425	OMIM:108120	TAS				I		HPO:skoehler	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001762	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001838	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0001848	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0002650	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0002804	OMIM:108120	IEA				P		HPO:skoehler	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0002987	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0003184	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0003273	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0006380	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0009473	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0009742	OMIM:108120	IEA				P		HPO:iea	
OMIM	108120	ARTHROGRYPOSIS, DISTAL, TYPE 1A; DA1A		HP:0012385	OMIM:108120	TAS				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000006	OMIM:108145	IEA				I		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000218	OMIM:108145	TAS				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000286	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000325	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000411	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000483	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000490	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000508	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000512	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000540	OMIM:108145	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000563	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000581	OMIM:108145	TAS				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000602	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0000767	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0001119	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0001166	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0001547	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0001776	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0002091	OMIM:108145	TAS				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0002650	OMIM:108145	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0002804	OMIM:108145	IEA				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0003199	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0003725	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0004322	OMIM:108145	TAS				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0004673	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0005684	OMIM:108145	TAS				P		HPO:probinson	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0005879	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0006109	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0006184	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0006251	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0007703	OMIM:108145	IEA				P		HPO:iea	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0009921	OMIM:108145	IEA				P		HPO:skoehler	
OMIM	108145	#108145 ARTHROGRYPOSIS, DISTAL, TYPE 5; DA5;;ARTHROGRYPOSIS WITH OCULOMOTOR LIMITATION AND ELECTRORETINAL ABNORMALITIES;;OCULOMELIC AMYOPLASIA;;ARTHROGRYPOSIS, DISTAL, TYPE IIB; DAIIB		HP:0030084	OMIM:108145	TAS				P		HPO:skoehler	
OMIM	108200	ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS		HP:0000006	OMIM:108200	IEA				I		HPO:iea	
OMIM	108200	ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS		HP:0000407	OMIM:108200	IEA				P		HPO:iea	
OMIM	108200	ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS		HP:0002804	OMIM:108200	IEA				P		HPO:skoehler	
OMIM	108200	ARTHROGRYPOSIS-LIKE HAND ANOMALY AND SENSORINEURAL DEAFNESS		HP:0005612	OMIM:108200	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000006	OMIM:108300	IEA				I		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000175	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000201	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000272	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000405	OMIM:108300	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000407	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000463	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000501	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000518	OMIM:108300	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000541	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000545	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000618	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000767	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0000926	OMIM:108300	TAS				P		HPO:probinson	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0001166	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0001519	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0001634	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0002650	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0002655	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0002808	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0003040	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0004568	OMIM:108300	TAS				P		HPO:probinson	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0005280	OMIM:108300	IEA				P		HPO:iea	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0006361	OMIM:108300	IEA				P		HPO:skoehler	
OMIM	108300	#108300 STICKLER SYNDROME, TYPE I; STL1;;STICKLER SYNDROME, VITREOUS TYPE 1;;STICKLER SYNDROME, MEMBRANOUS VITREOUS TYPE;;ARTHROOPHTHALMOPATHY, HEREDITARY PROGRESSIVE; AOM		HP:0011800	OMIM:108300	TAS				P		HPO:skoehler	
OMIM	108320	ARTICHOKE, MODIFICATION OF TASTE BY		HP:0000223	OMIM:108320	IEA				P		HPO:skoehler	
OMIM	108390	ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY		HP:0000006	OMIM:108390	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	108390	ASPARAGUS, SPECIFIC SMELL HYPERSENSITIVITY		HP:0000707	OMIM:108390	IEA				P		HPO:iea	
OMIM	108420	SPERMATOGENIC FAILURE 2		HP:0000006	OMIM:108420	TAS				I		HPO:skoehler	
OMIM	108420	SPERMATOGENIC FAILURE 2		HP:0000027	OMIM:108420	TAS				P		HPO:skoehler	
OMIM	108420	SPERMATOGENIC FAILURE 2		HP:0000798	OMIM:108420	TAS				P		HPO:skoehler	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000006	OMIM:108450	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000347	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000444	OMIM:108450	IEA				P		HPO:skoehler	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000540	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000565	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0000678	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0002007	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0002949	OMIM:108450	TAS				P		HPO:probinson	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0004626	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0008929	OMIM:108450	IEA				P		HPO:iea	
OMIM	108450	108450 ASYMMETRIC SHORT STATURE SYNDROME		HP:0200053	OMIM:108450	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0000006	OMIM:108500	IEA				I		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0000360	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0000640	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0000651	OMIM:108500	IEA				P		HPO:skoehler	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0001152	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0001260	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0001324	OMIM:108500	TAS				P		HPO:probinson	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0001332	OMIM:108500	TAS				P		HPO:probinson	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0001751	OMIM:108500	TAS				P		HPO:probinson	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0002073	OMIM:108500	IEA				P		HPO:skoehler	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0002076	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0002131	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0002321	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0002486	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0003401	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0003829	OMIM:108500	IEA				C		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0006855	OMIM:108500	IEA				P		HPO:iea	
OMIM	108500	EPISODIC ATAXIA, TYPE 2		HP:0010545	OMIM:108500	IEA				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0000006	OMIM:108600	IEA				I		HPO:iea	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0000508	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0000514	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0000605	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001258	OMIM:108600	IEA				P		HPO:iea	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001260	OMIM:108600	IEA				P		HPO:iea	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001288	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001332	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001347	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0001761	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0002015	OMIM:108600	TAS				P		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0002354	OMIM:108600	IEA				P		HPO:iea	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0002497	OMIM:108600	IEA				P		HPO:iea	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0003828	OMIM:108600	TAS				C		HPO:skoehler	
OMIM	108600	SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1		HP:0008969	OMIM:108600	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0000006	OMIM:108650	IEA				I		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0000549	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0000639	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0000648	OMIM:108650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0001260	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0001347	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0002075	OMIM:108650	TAS				P		HPO:skoehler	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0002497	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0003487	OMIM:108650	IEA				P		HPO:iea	
OMIM	108650	%108650 SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7;;SPASTIC ATAXIA WITH CONGENITAL MIOSIS;;MIOSIS, CONGENITAL, WITH SPASTIC ATAXIA		HP:0007728	OMIM:108650	IEA				P		HPO:iea	
OMIM	108700	ATAXIA WITH FASCICULATIONS		HP:0000006	OMIM:108700	IEA				I		HPO:iea	
OMIM	108700	ATAXIA WITH FASCICULATIONS		HP:0001251	OMIM:108700	IEA				P		HPO:iea	
OMIM	108700	ATAXIA WITH FASCICULATIONS		HP:0002380	OMIM:108700	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000006	OMIM:108720	TAS				I		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000028	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000175	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000272	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000347	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000470	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000520	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000774	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0000878	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001156	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001217	OMIM:108720	TAS				P		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001561	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001602	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001622	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0001762	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002007	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002084	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002949	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002982	OMIM:108720	IEA				P		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002986	OMIM:108720	IEA				P		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0002990	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003042	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003097	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003196	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003417	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003745	OMIM:108720	IEA				I		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003811	OMIM:108720	TAS				M		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0003826	OMIM:108720	IEA				M		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0004592	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0005280	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0005792	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0006406	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0006408	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0006495	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0008905	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0010049	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0010743	OMIM:108720	IEA				P		HPO:iea	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0011800	OMIM:108720	TAS				P		HPO:skoehler	
OMIM	108720	ATELOSTEOGENESIS, TYPE I; AO1		HP:0030330	OMIM:108720	TAS				P		HPO:probinson	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000006	OMIM:108721	IEA				I		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000175	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000269	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000272	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000327	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000347	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0000470	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0001234	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0001762	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0001852	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0002007	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0002650	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0002947	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0002982	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0002986	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0003042	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0003180	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0003440	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0004632	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0004976	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0005280	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0006060	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0006200	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0008905	OMIM:108721	IEA				P		HPO:iea	
OMIM	108721	#108721 ATELOSTEOGENESIS, TYPE III; AOIII;;AO3		HP:0011800	OMIM:108721	TAS				P		HPO:skoehler	
OMIM	108725	ATHEROSCLEROSIS SUSCEPTIBILITY		HP:0000006	OMIM:108725	IEA				I		HPO:iea	
OMIM	108725	ATHEROSCLEROSIS SUSCEPTIBILITY		HP:0001658	OMIM:108725	TAS				P		HPO:probinson	
OMIM	108725	ATHEROSCLEROSIS SUSCEPTIBILITY		HP:0002155	OMIM:108725	TAS				P		HPO:probinson	
OMIM	108725	ATHEROSCLEROSIS SUSCEPTIBILITY		HP:0003233	OMIM:108725	TAS				P		HPO:probinson	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0000006	OMIM:108760	IEA				I		HPO:iea	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0000402	OMIM:108760	PCS				P		HPO:probinson	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0000405	OMIM:108760	IEA				P		HPO:iea	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0000413	OMIM:108760	PCS				P		HPO:probinson	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0005906	OMIM:108760	IEA				P		HPO:iea	
OMIM	108760	ATRESIA OF EXTERNAL AUDITORY CANAL AND CONDUCTION DEAFNESS		HP:0008773	OMIM:108760	IEA				P		HPO:iea	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0000006	OMIM:108770	PCS				I		HPO:probinson	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0001706	OMIM:108770	PCS				P		HPO:probinson	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0006699	OMIM:108770	PCS				P		HPO:probinson	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0011705	OMIM:108770	PCS				P		HPO:probinson	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0025478	OMIM:108770	TAS				P		HPO:skoehler	
OMIM	108770	ATRIAL STANDSTILL 1		HP:0200127	OMIM:108770	TAS				P		HPO:skoehler	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0000006	OMIM:108800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0001629	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0001647	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0001650	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0001682	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0001684	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0005301	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0011706	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0011995	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108800	ATRIAL SEPTAL DEFECT 1		HP:0012516	PMID:9610535	PCS				P		HPO:lccarmody	
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0000006	OMIM:108900	TAS				I		HPO:probinson	
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0001629	OMIM:108900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0001636	OMIM:108900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0001682	OMIM:108900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0001684	OMIM:108900	TAS				P		HPO:probinson	
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0001712	OMIM:108900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0004935	OMIM:108900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0005110	OMIM:108900	TAS				P		HPO:skoehler	
OMIM	108900	ATRIAL SEPTAL DEFECT WITH ATRIOVENTRICULAR CONDUCTION DEFECTS		HP:0012248	OMIM:108900	TAS				P		HPO:probinson	
OMIM	108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL		HP:0000006	OMIM:108950	PCS				I		HPO:probinson	
OMIM	108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL		HP:0004754	OMIM:108950	PCS				P		HPO:probinson	
OMIM	108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL		HP:0004757	OMIM:108950	PCS				P		HPO:probinson	
OMIM	108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL		HP:0005165	OMIM:108950	PCS				P		HPO:probinson	
OMIM	108950	ATRIAL TACHYARRHYTHMIA WITH SHORT PR INTERVAL		HP:0006671	OMIM:108950	PCS				P		HPO:probinson	
OMIM	108985	SVEINSSON CHORIORETINAL ATROPHY		HP:0000006	OMIM:108985	IEA				I		HPO:iea	
OMIM	108985	SVEINSSON CHORIORETINAL ATROPHY		HP:0000483	OMIM:108985	IEA				P		HPO:skoehler	
OMIM	108985	SVEINSSON CHORIORETINAL ATROPHY		HP:0000545	OMIM:108985	TAS				P		HPO:probinson	
OMIM	108985	SVEINSSON CHORIORETINAL ATROPHY		HP:0003677	OMIM:108985	IEA				C		HPO:iea	
OMIM	108985	SVEINSSON CHORIORETINAL ATROPHY		HP:0007950	OMIM:108985	IEA				P		HPO:iea	
OMIM	109000	AURICULOOSTEODYSPLASIA		HP:0000006	OMIM:109000	IEA				I		HPO:iea	
OMIM	109000	AURICULOOSTEODYSPLASIA		HP:0001385	OMIM:109000	IEA				P		HPO:iea	
OMIM	109000	AURICULOOSTEODYSPLASIA		HP:0003083	OMIM:109000	TAS				P		HPO:skoehler	
OMIM	109000	AURICULOOSTEODYSPLASIA		HP:0004322	OMIM:109000	IEA				P		HPO:iea	
OMIM	109000	AURICULOOSTEODYSPLASIA		HP:0009907	OMIM:109000	TAS				P		HPO:probinson	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0000006	OMIM:109050	IEA				I		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0000365	OMIM:109050	IEA				P		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0001256	OMIM:109050	IEA				P		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0001363	OMIM:109050	IEA				P		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0002000	OMIM:109050	IEA				P		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0004692	OMIM:109050	IEA				P		HPO:iea	
OMIM	109050	AUROCEPHALOSYNDACTYLY		HP:0030680	OMIM:109050	IEA				P		HPO:iea	
OMIM	109100	AUTOIMMUNE DISEASE		HP:0000006	OMIM:109100	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	109100	AUTOIMMUNE DISEASE		HP:0030057	OMIM:109100	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000006	OMIM:109120	IEA				I		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000238	OMIM:109120	IEA				P		HPO:skoehler	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000248	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000256	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000272	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000316	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000327	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000407	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000486	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000506	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000520	OMIM:109120	IEA				P		HPO:skoehler	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000558	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0000925	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0001249	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0001252	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0001274	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0001290	OMIM:109120	TAS				P		HPO:skoehler	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0002119	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0002673	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0002690	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0002827	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0004322	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0006958	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0007873	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0007886	OMIM:109120	IEA				P		HPO:iea	
OMIM	109120	AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVE FACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES		HP:0012368	OMIM:109120	TAS				P		HPO:skoehler	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0000006	OMIM:109130	TAS				I		HPO:probinson	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0000107	OMIM:109130	IEA				P		HPO:skoehler	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0002749	OMIM:109130	TAS				P		HPO:probinson	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0003198	OMIM:109130	TAS				P		HPO:probinson	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0003236	OMIM:109130	TAS				P		HPO:probinson	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0003701	OMIM:109130	TAS				P		HPO:probinson	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0006557	OMIM:109130	IEA				P		HPO:skoehler	
OMIM	109130	AXIAL OSTEOMALACIA		HP:0011001	OMIM:109130	TAS				P		HPO:probinson	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000006	OMIM:109150	TAS				I		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000508	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000520	OMIM:109150	TAS				P		HPO:probinson	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000544	PMID:19659750	PCS		HP:0040284		P		HPO:iea	34/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000623	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000640	PMID:10525976	PCS		HP:0040284		P		HPO:iea	15/20
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000641	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000651	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0000726	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001151	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001251	PMID:19659750	PCS		HP:0040284		P		HPO:iea	57/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001257	PMID:18685131	PCS		HP:0040284		P		HPO:iea	62/139
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001260	PMID:19659750	PCS		HP:0040284		P		HPO:iea	30/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001272	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001300	PMID:19659750	PCS		HP:0040284		P		HPO:iea	3/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0001332	PMID:19659750	PCS		HP:0040284		P		HPO:iea	17/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002015	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002063	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002067	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002070	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002073	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002078	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002171	OMIM:109150	TAS				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002172	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002198	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002380	PMID:19659750	PCS		HP:0040284		P		HPO:iea	12/57
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002495	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002503	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0002839	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003394	OMIM:109150	IEA				P		HPO:skoehler	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003438	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003487	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003676	PMID:19659750	PCS				C		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003693	OMIM:109150	TAS				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0003743	OMIM:109150	IEA				I		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0007089	OMIM:109150	IEA				P		HPO:iea	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0012332	OMIM:109150	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0012532	OMIM:109150	TAS				P		HPO:skoehler	
OMIM	109150	MACHADO-JOSEPH DISEASE; MJD		HP:0030454	OMIM:109150	TAS				P		HPO:skoehler	
OMIM	109160	%109160 AZOTEMIA, FAMILIAL		HP:0000006	OMIM:109160	IEA				I		HPO:iea	
OMIM	109160	%109160 AZOTEMIA, FAMILIAL		HP:0002157	OMIM:109160	IEA				P		HPO:iea	
OMIM	109200	ALOPECIA, ANDROGENETIC, 1		HP:0001470	OMIM:109200	IEA				I		HPO:skoehler	
OMIM	109200	ALOPECIA, ANDROGENETIC, 1		HP:0001596	OMIM:109200	TAS				P		HPO:probinson	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0000006	OMIM:109270	TAS				I		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0000952	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0001744	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0001878	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0001923	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0001927	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0002904	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0004444	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0004445	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0004446	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109270	SOLUTE CARRIER FAMILY 4 (ANION EXCHANGER), MEMBER 1; SLC4A1		HP:0005502	OMIM:109270	TAS				P		HPO:skoehler	
OMIM	109300	109300 BANKI SYNDROME		HP:0000006	OMIM:109300	IEA				I		HPO:iea	
OMIM	109300	109300 BANKI SYNDROME		HP:0009466	OMIM:109300	IEA				P		HPO:iea	
OMIM	109300	109300 BANKI SYNDROME		HP:0030084	OMIM:109300	TAS				P		HPO:skoehler	
OMIM	109350	GASTROESOPHAGEAL REFLUX		HP:0000006	OMIM:109350	TAS				I		HPO:probinson	
OMIM	109350	GASTROESOPHAGEAL REFLUX		HP:0002020	OMIM:109350	TAS				P		HPO:probinson	
OMIM	109350	GASTROESOPHAGEAL REFLUX		HP:0100580	OMIM:109350	TAS				P		HPO:probinson	
OMIM	109350	GASTROESOPHAGEAL REFLUX		HP:0100633	OMIM:109350	TAS				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000006	OMIM:109400	PCS				I		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000175	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000204	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000238	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000242	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000256	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003577			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000280	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000283	OMIM:109400	TAS				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME	HP:0012825	HP:0000303	PMID:12116218	PCS				P		HPO:probinson	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000316	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000431	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000486	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000501	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000568	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000612	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000766	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000773	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000892	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0000912	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001056	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001144	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001156	OMIM:109400	TAS				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001249	OMIM:109400	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001270	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003593			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0001425	OMIM:109400	PCS				I		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002007	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002007	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002414	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002650	OMIM:109400	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002671	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011462			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002751	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002885	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011463			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002937	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0002948	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0003828	OMIM:109400	PCS				C		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0004280	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0004795	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0005449	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0005462	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0011462			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0005815	OMIM:109400	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0008422	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0009650	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0009729	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010044	OMIM:109400	IEA				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010442	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010603	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS	HP:0003621			P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010609	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010610	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010612	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010617	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0010618	PMID:9096761	PCS				P		HPO:iea	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0025318	OMIM:109400	TAS				P		HPO:skoehler	
OMIM	109400	BASAL CELL NEVUS SYNDROME		HP:0200021	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=bcns	PCS				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0000006	OMIM:109500	IEA				I		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0000470	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0002277	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0002691	OMIM:109500	IEA				P		HPO:skoehler	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0002751	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0003396	OMIM:109500	TAS				P		HPO:probinson	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0003690	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0003828	OMIM:109500	TAS				C		HPO:skoehler	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0003829	OMIM:109500	IEA				C		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0004484	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0005758	OMIM:109500	IEA				P		HPO:iea	
OMIM	109500	%109500 BASILAR IMPRESSION, PRIMARY		HP:0005788	OMIM:109500	IEA				P		HPO:iea	
OMIM	109543	B-CELL MALIGNANCY, LOW-GRADE		HP:0000006	OMIM:109543	IEA				I		HPO:iea	
OMIM	109543	B-CELL MALIGNANCY, LOW-GRADE		HP:0005550	OMIM:109543	IEA				P		HPO:iea	
OMIM	109600	BEETURIA		HP:0000006	OMIM:109600	IEA				I		HPO:iea	
OMIM	109600	BEETURIA		HP:0001939	OMIM:109600	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0000007	PMID:12955762	TAS				I		HPO:nvasilevsky	
OMIM	109650	BEHCET SYNDROME		HP:0000031	OMIM:109650	TAS				P		HPO:probinson	
OMIM	109650	BEHCET SYNDROME		HP:0000155	OMIM:109650	TAS				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0000737	OMIM:109650	IEA				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0001094	OMIM:109650	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0001101	OMIM:109650	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0001369	OMIM:109650	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0002229	OMIM:109650	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0002638	OMIM:109650	IEA				P		HPO:iea	
OMIM	109650	BEHCET SYNDROME		HP:0003249	OMIM:109650	TAS				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0010783	OMIM:109650	IEA				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0012219	OMIM:109650	IEA				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0012424	OMIM:109650	TAS				P		HPO:probinson	
OMIM	109650	BEHCET SYNDROME		HP:0030880	OMIM:109650	TAS				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0031615	OMIM:109650	IEA				P		HPO:skoehler	
OMIM	109650	BEHCET SYNDROME		HP:0410060	PMID:29099052	PCS				P		HPO:NicoleVasilevsky	
OMIM	109720	BILIARY CIRRHOSIS, PRIMARY		HP:0000006	OMIM:109720	TAS				I		HPO:skoehler	
OMIM	109720	BILIARY CIRRHOSIS, PRIMARY		HP:0002613	OMIM:109720	TAS				P		HPO:skoehler	
OMIM	109730	#109730 AORTIC VALVE DISEASE 1; AOVD1;;AORTIC VALVE DISEASE;;BICUSPID AORTIC VALVE; BAV;;AORTIC VALVE, BICUSPID;;AORTIC VALVE, CALCIFICATION OF;;AORTIC STENOSIS, CALCIFIC		HP:0000006	OMIM:109730	TAS				I		HPO:skoehler	
OMIM	109730	#109730 AORTIC VALVE DISEASE 1; AOVD1;;AORTIC VALVE DISEASE;;BICUSPID AORTIC VALVE; BAV;;AORTIC VALVE, BICUSPID;;AORTIC VALVE, CALCIFICATION OF;;AORTIC STENOSIS, CALCIFIC		HP:0001647	OMIM:109730	IEA				P		HPO:iea	
OMIM	109730	#109730 AORTIC VALVE DISEASE 1; AOVD1;;AORTIC VALVE DISEASE;;BICUSPID AORTIC VALVE; BAV;;AORTIC VALVE, BICUSPID;;AORTIC VALVE, CALCIFICATION OF;;AORTIC STENOSIS, CALCIFIC		HP:0001650	OMIM:109730	IEA				P		HPO:skoehler	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:109740	TAS				I		HPO:skoehler	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0000028	OMIM:109740	IEA				P		HPO:iea	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0000508	OMIM:109740	IEA				P		HPO:iea	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0000924	OMIM:109740	IEA				P		HPO:iea	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0004122	OMIM:109740	IEA				P		HPO:iea	
OMIM	109740	109740 BIFID NOSE, AUTOSOMAL DOMINANT		HP:0011803	OMIM:109740	TAS				P		HPO:skoehler	
OMIM	109800	BLADDER CANCER		HP:0000006	OMIM:109800	IEA				I		HPO:iea	
OMIM	109800	BLADDER CANCER		HP:0006740	OMIM:109800	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0000006	OMIM:109820	IEA				I		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0000010	OMIM:109820	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0000019	OMIM:109820	TAS				P		HPO:skoehler	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0000790	OMIM:109820	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0008664	OMIM:109820	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0008691	OMIM:109820	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0008742	OMIM:109820	IEA				P		HPO:iea	
OMIM	109820	109820 BLADDER DIVERTICULUM		HP:0100518	OMIM:109820	TAS				P		HPO:skoehler	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0000006	OMIM:109900	IEA				I		HPO:iea	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0000153	OMIM:109900	IEA				P		HPO:iea	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0000478	OMIM:109900	IEA				P		HPO:iea	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0000853	OMIM:109900	IEA				P		HPO:skoehler	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0010749	OMIM:109900	IEA				P		HPO:skoehler	
OMIM	109900	BLEPHAROCHALASIS AND DOUBLE LIP		HP:0040295	OMIM:109900	TAS				P		HPO:skoehler	
OMIM	110000	BLEPHAROCHALASIS, SUPERIOR		HP:0000006	OMIM:110000	TAS				I		HPO:probinson	
OMIM	110000	BLEPHAROCHALASIS, SUPERIOR		HP:0010749	OMIM:110000	TAS				P		HPO:probinson	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0000006	OMIM:110050	IEA				I		HPO:iea	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0000298	OMIM:110050	IEA				P		HPO:iea	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0000506	OMIM:110050	IEA				P		HPO:iea	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0001249	OMIM:110050	IEA				P		HPO:iea	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0001304	OMIM:110050	IEA				P		HPO:iea	
OMIM	110050	BLEPHARONASOFACIAL MALFORMATION SYNDROME		HP:0010628	OMIM:110050	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000006	OMIM:110100	IEA				I		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000013	OMIM:110100	TAS				P		HPO:skoehler	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000141	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000218	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000378	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000431	OMIM:110100	TAS				P		HPO:probinson	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000482	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000486	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000506	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000508	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000537	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000540	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000568	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000581	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000639	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000769	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0000837	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0001595	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0005280	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0005280	OMIM:110100	TAS				P		HPO:probinson	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0008209	OMIM:110100	IEA				P		HPO:iea	
OMIM	110100	BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS		HP:0008222	OMIM:110100	IEA				P		HPO:iea	
OMIM	110150	BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS		HP:0000006	OMIM:110150	IEA				I		HPO:iea	
OMIM	110150	BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS		HP:0000545	OMIM:110150	IEA				P		HPO:iea	
OMIM	110150	BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS		HP:0001083	OMIM:110150	IEA				P		HPO:iea	
OMIM	110150	BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS		HP:0007800	OMIM:110150	TAS				P		HPO:probinson	
OMIM	110150	BLEPHAROPTOSIS, MYOPIA, AND ECTOPIA LENTIS		HP:0007970	OMIM:110150	TAS				P		HPO:skoehler	
OMIM	110700	BLOOD GROUP, DUFFY SYSTEM; FY		HP:0000006	OMIM:110700	IEA				I		HPO:iea	
OMIM	110700	BLOOD GROUP, DUFFY SYSTEM; FY		HP:0000007	OMIM:110700	IEA				I		HPO:skoehler	
OMIM	110700	BLOOD GROUP, DUFFY SYSTEM; FY		HP:0001939	OMIM:110700	IEA				P		HPO:iea	
OMIM	110700	BLOOD GROUP, DUFFY SYSTEM; FY		HP:0002715	OMIM:110700	IEA				P		HPO:iea	
OMIM	110800	BLOOD GROUP, I SYSTEM		HP:0000006	OMIM:110800	TAS				I		HPO:skoehler	
OMIM	110800	BLOOD GROUP, I SYSTEM		HP:0010970	OMIM:110800	IEA				P		HPO:skoehler	
OMIM	111150	BLOOD GROUP--LUTHERAN INHIBITOR; INLU		HP:0000006	OMIM:111150	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	111150	BLOOD GROUP--LUTHERAN INHIBITOR; INLU		HP:0010971	OMIM:111150	IEA				P		HPO:skoehler	
OMIM	111400	#111400 BLOOD GROUP, P1PK SYSTEMP(1) PHENOTYPE, INCLUDED;;P(2) PHENOTYPE, INCLUDED;;P1(k) PHENOTYPE, INCLUDED;;P2(k) PHENOTYPE, INCLUDED;;p PHENOTYPE, INCLUDED;;NOR POLYAGGLUTINATION SYNDROME, INCLUDED		HP:0000006	OMIM:111400	IEA				I	#111400 BLOOD GROUP, P1PK SYSTEMP(1) PHENOTYPE, INCLUDED;;P(2) PHENOTYPE, INCLUDED;;P1(K) PHENOTYPE, INCLUDED;;P2(K) PHENOTYPE, INCLUDED;;P PHENOTYPE, INCLUDED;;NOR POLYAGGLUTINATION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	111400	#111400 BLOOD GROUP, P1PK SYSTEMP(1) PHENOTYPE, INCLUDED;;P(2) PHENOTYPE, INCLUDED;;P1(k) PHENOTYPE, INCLUDED;;P2(k) PHENOTYPE, INCLUDED;;p PHENOTYPE, INCLUDED;;NOR POLYAGGLUTINATION SYNDROME, INCLUDED		HP:0010970	OMIM:111400	IEA				P	#111400 BLOOD GROUP, P1PK SYSTEMP(1) PHENOTYPE, INCLUDED;;P(2) PHENOTYPE, INCLUDED;;P1(K) PHENOTYPE, INCLUDED;;P2(K) PHENOTYPE, INCLUDED;;P PHENOTYPE, INCLUDED;;NOR POLYAGGLUTINATION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	111620	#111620 RADIN BLOOD GROUP ANTIGEN; RD;;BLOOD GROUP--RADIN ANTIGEN		HP:0010701	OMIM:111620	IEA				P		HPO:skoehler	
OMIM	111700	RHESUS BLOOD GROUP, CcEe ANTIGENS; RHCE		HP:0000007	PMID:9657769	PCS				I	RHESUS BLOOD GROUP, CCEE ANTIGENS; RHCE	HPO:probinson	
OMIM	111700	RHESUS BLOOD GROUP, CcEe ANTIGENS; RHCE		HP:0004446	PMID:9657769	PCS				P	RHESUS BLOOD GROUP, CCEE ANTIGENS; RHCE	HPO:probinson	
OMIM	111700	RHESUS BLOOD GROUP, CcEe ANTIGENS; RHCE		HP:0004870	PMID:9657769	PCS				P	RHESUS BLOOD GROUP, CCEE ANTIGENS; RHCE	HPO:probinson	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0000006	OMIM:112200	IEA				I		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0000153	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0001028	OMIM:112200	IEA				P		HPO:skoehler	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0001034	OMIM:112200	IEA				P		HPO:skoehler	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0001392	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0001873	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0001891	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002035	OMIM:112200	TAS				P		HPO:skoehler	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002086	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002576	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002580	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002584	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0002756	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0005520	OMIM:112200	IEA				P		HPO:iea	
OMIM	112200	%112200 BLUE RUBBER BLEB NEVUS;;BEAN SYNDROME		HP:0007129	OMIM:112200	IEA				P		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000006	OMIM:112240	IEA				I		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000238	OMIM:112240	IEA				P		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000347	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000586	OMIM:112240	IEA				P		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000691	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0000938	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1	HP:0003676	HP:0001334	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0001620	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0002007	OMIM:112240	IEA				P		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0002650	OMIM:112240	IEA				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0002757	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0002953	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0004322	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0004440	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0005472	OMIM:112240	IEA				P		HPO:iea	
OMIM	112240	COLE-CARPENTER SYNDROME 1; CLCRP1		HP:0011800	OMIM:112240	TAS				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0000006	OMIM:112250	TAS				I		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0000938	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0000963	OMIM:112250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0000977	OMIM:112250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0000978	OMIM:112250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0002216	OMIM:112250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0002669	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0002756	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0002979	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003084	OMIM:112250	TAS				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003198	OMIM:112250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003202	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003325	OMIM:112250	TAS				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003676	OMIM:112250	TAS				C		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003690	OMIM:112250	TAS	HP:0003584			P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0003701	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0005010	OMIM:112250	TAS				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0005045	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0005686	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0007819	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0012315	OMIM:112250	IEA				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0031367	OMIM:112250	IEA				P		HPO:skoehler	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0100244	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112250	DIAPHYSEAL MEDULLARY STENOSIS WITH MALIGNANT FIBROUS HISTIOCYTOMA; DMSMFH		HP:0100254	OMIM:112250	TAS				P		HPO:probinson	
OMIM	112270	BONE PAIN, PERIODIC		HP:0000006	OMIM:112270	IEA				I		HPO:iea	
OMIM	112270	BONE PAIN, PERIODIC		HP:0002653	OMIM:112270	TAS				P		HPO:probinson	
OMIM	112300	BOOK SYNDROME		HP:0000006	OMIM:112300	TAS				I		HPO:probinson	
OMIM	112300	BOOK SYNDROME		HP:0000668	OMIM:112300	TAS				P		HPO:skoehler	
OMIM	112300	BOOK SYNDROME		HP:0002216	OMIM:112300	TAS				P		HPO:skoehler	
OMIM	112300	BOOK SYNDROME		HP:0007410	OMIM:112300	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0000006	OMIM:112310	IEA				I		HPO:iea	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0000430	OMIM:112310	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0000431	OMIM:112310	IEA				P		HPO:iea	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0002990	OMIM:112310	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0003510	OMIM:112310	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0003811	OMIM:112310	TAS				M		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0003974	OMIM:112310	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0005104	OMIM:112310	TAS				P		HPO:probinson	
OMIM	112310	BOOMERANG DYSPLASIA		HP:0008824	OMIM:112310	IEA				P		HPO:iea	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0000006	OMIM:112350	IEA				I		HPO:iea	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0000696	OMIM:112350	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0001249	OMIM:112350	IEA				P		HPO:iea	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0002650	OMIM:112350	TAS				P		HPO:skoehler	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0002808	OMIM:112350	TAS				P		HPO:skoehler	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0003177	OMIM:112350	IEA				P		HPO:iea	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0003440	OMIM:112350	TAS				P		HPO:skoehler	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0003510	OMIM:112350	IEA				P		HPO:skoehler	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0004490	OMIM:112350	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0006487	OMIM:112350	IEA				P		HPO:iea	
OMIM	112350	%112350 WEISMANN-NETTER SYNDROME; WNS;;BOWING OF LEGS, ANTERIOR, WITH DWARFISM;;TOXOPACHYOSTEOSE DIAPHYSAIRE TIBIO-PERONIERE		HP:0010538	OMIM:112350	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0000006	OMIM:112370	IEA				I		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0000252	OMIM:112370	IEA				P		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0000271	OMIM:112370	IEA				P		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:112370	IEA				P		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0001510	OMIM:112370	IEA				P		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0001840	OMIM:112370	IEA				P		HPO:iea	
OMIM	112370	BRACHMANN-DE LANGE-LIKE FACIAL CHANGES WITH MICROCEPHALY, METATARSUSADDUCTUS, AND DEVELOPMENTAL DELAY		HP:0007560	OMIM:112370	IEA				P		HPO:iea	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0000006	OMIM:112410	IEA				I		HPO:iea	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0000822	OMIM:112410	IEA				P		HPO:iea	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0001156	OMIM:112410	TAS				P		HPO:skoehler	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0004322	OMIM:112410	TAS				P		HPO:skoehler	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0009803	OMIM:112410	IEA				P		HPO:iea	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0010049	OMIM:112410	IEA				P		HPO:iea	
OMIM	112410	#112410 HYPERTENSION AND BRACHYDACTYLY SYNDROME; HTNB;;BRACHYDACTYLY WITH HYPERTENSION;;BRACHYDACTYLY, TYPE E, WITH SHORT STATURE AND HYPERTENSION;;BILGINTURAN SYNDROME		HP:0010579	OMIM:112410	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	112430	LONG-THUMB BRACHYDACTYLY SYNDROME		HP:0000006	OMIM:112430	IEA				I		HPO:iea	
OMIM	112430	LONG-THUMB BRACHYDACTYLY SYNDROME		HP:0001156	OMIM:112430	IEA				P		HPO:skoehler	
OMIM	112430	LONG-THUMB BRACHYDACTYLY SYNDROME		HP:0001367	OMIM:112430	IEA				P		HPO:iea	
OMIM	112430	LONG-THUMB BRACHYDACTYLY SYNDROME		HP:0009381	OMIM:112430	TAS				P		HPO:probinson	
OMIM	112430	LONG-THUMB BRACHYDACTYLY SYNDROME		HP:0011675	OMIM:112430	TAS				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0000006	OMIM:112440	IEA				I		HPO:iea	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0001156	OMIM:112440	IEA				P		HPO:skoehler	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0001598	OMIM:112440	TAS				P		HPO:skoehler	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0004689	OMIM:112440	TAS				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0004689	OMIM:112440	IEA				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0004704	OMIM:112440	IEA				P		HPO:iea	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0009237	OMIM:112440	TAS				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0009280	OMIM:112440	TAS				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0009778	OMIM:112440	TAS				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0009836	OMIM:112440	IEA				P		HPO:iea	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0010044	OMIM:112440	IEA				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0010047	OMIM:112440	IEA				P		HPO:probinson	
OMIM	112440	%112440 BRACHYDACTYLY, COMBINED B AND E TYPES;;PITT-WILLIAMS BRACHYDACTYLY;;BRACHYDACTYLY, BALLARD TYPE		HP:0011304	OMIM:112440	TAS				P		HPO:probinson	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0000006	OMIM:112450	IEA				I		HPO:iea	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0001234	OMIM:112450	TAS				P		HPO:skoehler	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0008080	OMIM:112450	IEA				P		HPO:skoehler	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0009778	OMIM:112450	TAS				P		HPO:skoehler	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0009882	OMIM:112450	IEA				P		HPO:iea	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0010049	OMIM:112450	IEA				P		HPO:iea	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0010109	OMIM:112450	TAS				P		HPO:skoehler	
OMIM	112450	112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION;;CHRISTIAN BRACHYDACTYLY		HP:0010743	OMIM:112450	IEA				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0000006	OMIM:112500	PCS				I		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0001032	OMIM:112500	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0001156	OMIM:112500	IEA				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0001169	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0001204	OMIM:112500	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0001425	OMIM:112500	TAS				I		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0004209	OMIM:112500	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0004279	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0004322	ISBN-13:978-3437214301	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0005194	ISBN-13:978-3437214301	PCS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0006146	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0006165	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0006213	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0006236	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0009279	OMIM:112500	TAS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0009462	OMIM:112500	TAS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0009467	OMIM:112500	TAS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0009638	ISBN-13:978-3437214301	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0009882	OMIM:112500	TAS				P		HPO:skoehler	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0010049	ISBN-13:978-3437214301	PCS				P		HPO:iea	
OMIM	112500	#112500 BRACHYDACTYLY, TYPE A1; BDA1;;FARABEE-TYPE BRACHYDACTYLY		HP:0010107	ISBN-13:978-3437214301	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0000006	PMID:19327734	PCS				I		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0001822	PMID:19327734	PCS				P		HPO:probinson	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0004209	OMIM:112600	TAS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0004220	OMIM:112600	TAS				P		HPO:skoehler	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0004691	OMIM:112600	TAS				P		HPO:skoehler	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0008096	OMIM:112600	TAS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009161	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009182	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009464	OMIM:112600	IEA				P		HPO:skoehler	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009467	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009536	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009568	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0009575	PMID:19327734	PCS				P		HPO:iea	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0010055	OMIM:112600	TAS				P		HPO:probinson	
OMIM	112600	BRACHYDACTYLY, TYPE A2; BDA2		HP:0010109	OMIM:112600	TAS				P		HPO:probinson	
OMIM	112700	BRACHYDACTYLY, TYPE A3		HP:0000006	OMIM:112700	TAS				I		HPO:probinson	
OMIM	112700	BRACHYDACTYLY, TYPE A3		HP:0004209	OMIM:112700	TAS				P		HPO:probinson	
OMIM	112700	BRACHYDACTYLY, TYPE A3		HP:0004220	OMIM:112700	TAS				P		HPO:probinson	
OMIM	112700	BRACHYDACTYLY, TYPE A3		HP:0005910	OMIM:112700	TAS				P		HPO:probinson	
OMIM	112700	BRACHYDACTYLY, TYPE A3		HP:0010579	OMIM:112700	TAS				P		HPO:probinson	
OMIM	112800	BRACHYDACTYLY, TYPE A4		HP:0000006	OMIM:112800	TAS				I		HPO:probinson	
OMIM	112800	BRACHYDACTYLY, TYPE A4		HP:0004220	OMIM:112800	TAS				P		HPO:probinson	
OMIM	112800	BRACHYDACTYLY, TYPE A4		HP:0005850	OMIM:112800	TAS				P		HPO:probinson	
OMIM	112800	BRACHYDACTYLY, TYPE A4		HP:0009577	OMIM:112800	TAS				P		HPO:probinson	
OMIM	112800	BRACHYDACTYLY, TYPE A4		HP:0100387	OMIM:112800	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0000006	OMIM:112910	IEA				I		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0000925	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0001500	OMIM:112910	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0001831	OMIM:112910	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0001837	OMIM:112910	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0002984	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0003022	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0003027	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0003038	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0004322	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0005013	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0005736	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0006135	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0008127	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0008368	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0009370	OMIM:112910	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0009466	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0009702	OMIM:112910	IEA				P		HPO:iea	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0009803	OMIM:112910	TAS				P		HPO:probinson	
OMIM	112910	BRACHYDACTYLY, TYPE A6		HP:0009843	OMIM:112910	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0000006	PMID:10986040	PCS				I		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0000054	PMID:10986040	PCS				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0000260	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0000270	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0000696	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0001159	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0001629	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0001798	OMIM:113000	PCS				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0001804	PMID:9973295	PCS				P		HPO:probinson	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0002937	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0002944	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0002948	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0003026	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0004590	PMID:19461659	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0005819	PMID:9973295	PCS				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0005831	OMIM:113000	TAS				P		HPO:skoehler	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0009473	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0009835	PMID:10986040	PCS		HP:0040281		P		HP:probinson	HP:0040281
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0010185	PMID:9973295	PCS				P		HPO:probinson	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0010554	OMIM:113000	PCS	HP:0003577	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0011304	OMIM:113000	IEA				P		HPO:iea	
OMIM	113000	BRACHYDACTYLY, TYPE B1		HP:0012385	PMID:10986040	PCS				P		HPO:skoehler	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0000006	OMIM:113100	PCS				I		HPO:iea	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0001156	OMIM:113100	TAS				P		HPO:skoehler	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0001762	OMIM:113100	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0001772	OMIM:113100	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0002750	OMIM:113100	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0003067	OMIM:113100	TAS				P		HPO:skoehler	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0004209	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0004322	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0005819	OMIM:113100	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0006206	OMIM:113100	TAS				P		HPO:probinson	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009324	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009331	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009349	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009356	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009417	OMIM:113100	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009436	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009456	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009461	OMIM:113100	IEA		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009463	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009464	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009495	OMIM:113100	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009516	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009523	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009527	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009534	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009536	OMIM:113100	IEA		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009575	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0009587	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0010034	OMIM:113100	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0010259	OMIM:113100	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0010442	OMIM:113100	TAS				P		HPO:skoehler	
OMIM	113100	#113100 BRACHYDACTYLY, TYPE C; BDC;;BRACHYDACTYLY, HAWS TYPE		HP:0011929	OMIM:113100	TAS				P		HPO:probinson	
OMIM	113200	BRACHYDACTYLY, TYPE D		HP:0000006	OMIM:113200	TAS				I		HPO:iea	
OMIM	113200	BRACHYDACTYLY, TYPE D		HP:0005627	OMIM:113200	TAS				P		HPO:iea	
OMIM	113200	BRACHYDACTYLY, TYPE D		HP:0009642	OMIM:113200	TAS				P		HPO:iea	
OMIM	113200	BRACHYDACTYLY, TYPE D		HP:0010077	OMIM:113200	TAS				P		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0000006	OMIM:113300	IEA				I		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0000311	OMIM:113300	IEA				P		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0000894	OMIM:113300	TAS				P		HPO:probinson	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0001156	OMIM:113300	IEA				P		HPO:skoehler	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0001571	OMIM:113300	IEA				P		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0005863	OMIM:113300	TAS				P		HPO:probinson	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0006587	OMIM:113300	TAS				P		HPO:probinson	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0008848	OMIM:113300	IEA				P		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0010049	OMIM:113300	IEA				P		HPO:iea	
OMIM	113300	BRACHYDACTYLY, TYPE E		HP:0010743	OMIM:113300	IEA				P		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0000006	OMIM:113301	IEA				I		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0000311	OMIM:113301	IEA				P		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0001631	OMIM:113301	IEA				P		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0004322	OMIM:113301	IEA				P		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0005863	OMIM:113301	TAS				P		HPO:probinson	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0010044	OMIM:113301	IEA				P		HPO:iea	
OMIM	113301	BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II		HP:0010743	OMIM:113301	IEA				P		HPO:iea	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0000006	OMIM:113310	TAS				I		HPO:skoehler	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0001156	OMIM:113310	IEA				P		HPO:skoehler	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0001839	OMIM:113310	TAS				P		HPO:probinson	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0002990	OMIM:113310	TAS				P		HPO:probinson	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0003828	OMIM:113310	TAS				C		HPO:skoehler	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0003829	OMIM:113310	TAS				C		HPO:skoehler	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0006492	OMIM:113310	IEA				P		HPO:skoehler	
OMIM	113310	BRACHYDACTYLY-ECTRODACTYLY WITH FIBULAR APLASIA OR HYPOPLASIA		HP:0009803	OMIM:113310	IEA				P		HPO:probinson	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0000006	OMIM:113400	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0000486	OMIM:113400	IEA				P		HPO:iea	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0000639	OMIM:113400	IEA				P		HPO:iea	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0001156	OMIM:113400	TAS				P		HPO:skoehler	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0001249	OMIM:113400	IEA				P		HPO:iea	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0001251	OMIM:113400	IEA				P		HPO:iea	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0010049	OMIM:113400	TAS				P		HPO:iea	
OMIM	113400	BRACHYDACTYLY-NYSTAGMUS-CEREBELLAR ATAXIA		HP:0010743	OMIM:113400	TAS				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0000006	OMIM:113450	IEA				I		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME	HP:0012825	HP:0000098	OMIM:113450	PCS				P		HPO:probinson	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0000954	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0001204	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0001761	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0001769	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0002944	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0003180	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0006170	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0007598	OMIM:113450	TAS				P		HPO:skoehler	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0009371	OMIM:113450	TAS				P		HPO:probinson	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0010034	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0010239	OMIM:113450	IEA				P		HPO:iea	
OMIM	113450	113450 BRACHYDACTYLY-DISTAL SYMPHALANGISM SYNDROME		HP:0100490	OMIM:113450	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000083	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000347	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000369	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000581	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000954	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0000965	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0002984	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0003031	OMIM:113470	IEA				P		HPO:skoehler	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0003038	OMIM:113470	TAS				P		HPO:probinson	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0003745	OMIM:113470	IEA				I		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0005011	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0005280	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0007759	OMIM:113470	IEA				P		HPO:iea	
OMIM	113470	113470 BRACHYMESOMELIA-RENAL SYNDROME		HP:0012745	OMIM:113470	TAS				P		HPO:skoehler	
OMIM	113475	113475 BRACHYMETATARSUS IV;;METATARSUS IV, SHORT;;TOE, FOURTH, SHORT		HP:0000006	OMIM:113475	IEA				I		HPO:iea	
OMIM	113475	113475 BRACHYMETATARSUS IV;;METATARSUS IV, SHORT;;TOE, FOURTH, SHORT		HP:0004689	OMIM:113475	IEA				P		HPO:iea	
OMIM	113475	113475 BRACHYMETATARSUS IV;;METATARSUS IV, SHORT;;TOE, FOURTH, SHORT		HP:0008093	OMIM:113475	TAS				P		HPO:skoehler	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0000006	OMIM:113477	IEA				I		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0000154	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0000252	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0000307	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0000445	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0001798	OMIM:113477	PCS				P		HPO:probinson	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0001999	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0002164	OMIM:113477	PCS				P		HPO:probinson	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0004220	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0004227	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0004322	OMIM:113477	IEA				P		HPO:iea	
OMIM	113477	BRACHYMORPHISM-ONYCHODYSPLASIA-DYSPHALANGISM SYNDROME		HP:0010959	OMIM:113477	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000006	OMIM:113480	IEA				I		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000044	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000219	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000219	OMIM:113480	TAS				P		HPO:skoehler	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000319	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000458	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000506	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0000924	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0005280	OMIM:113480	IEA				P		HPO:iea	
OMIM	113480	113480 BRACHYTELEPHALANGY WITH CHARACTERISTIC FACIES AND KALLMANN SYNDROME		HP:0006118	OMIM:113480	TAS				P		HPO:skoehler	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0000006	OMIM:113500	IEA				I		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0000470	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0000540	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0000926	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0001552	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0002176	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0002650	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0002808	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0003411	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0008922	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0009466	OMIM:113500	IEA				P		HPO:iea	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0030084	OMIM:113500	TAS				P		HPO:skoehler	
OMIM	113500	#113500 BRACHYOLMIA TYPE 3;;BRACHYOLMIA, AUTOSOMAL DOMINANT;;BRACHYRACHIA		HP:0100864	OMIM:113500	IEA				P		HPO:iea	
OMIM	113600	BRANCHIAL CLEFT ANOMALIESBRANCHIAL CYSTS, INCLUDED		HP:0000006	OMIM:113600	IEA				I		HPO:iea	
OMIM	113600	BRANCHIAL CLEFT ANOMALIESBRANCHIAL CYSTS, INCLUDED		HP:0000464	OMIM:113600	IEA				P		HPO:iea	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0000006	OMIM:113610	TAS				I		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0000639	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0002078	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA	HP:0012825	HP:0002120	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0002313	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0003581	OMIM:113610	TAS				C		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0006827	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113610	BRANCHIAL MYOCLONUS WITH SPASTIC PARAPARESIS AND CEREBELLAR ATAXIA		HP:0010530	OMIM:113610	TAS				P		HPO:probinson	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000006	OMIM:113620	TAS				I		HPO:probinson	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000028	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000047	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000104	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000107	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000164	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000175	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000196	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000204	OMIM:113620	IEA				P		HPO:skoehler	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000252	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000268	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000272	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000316	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000347	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000350	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000358	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000369	OMIM:113620	TAS				P		HPO:skoehler	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000396	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000405	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000407	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000420	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000455	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000470	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000480	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000486	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000506	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000508	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000518	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000528	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000545	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000568	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000579	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000582	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000612	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000639	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000954	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0000987	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001057	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001177	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001250	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001256	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001511	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001611	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0001804	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002020	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002021	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002162	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002211	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002216	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002335	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002558	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002808	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0002987	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0003307	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0004209	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0004334	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0004464	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0004467	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0004785	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0005217	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0005280	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0005473	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0006610	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0008551	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0008559	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0008606	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0008897	OMIM:113620	TAS		HP:0040284		P		HPO:skoehler	50%
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0009623	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0009778	OMIM:113620	IEA				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0009794	OMIM:113620	TAS				P		HPO:skoehler	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0010517	OMIM:113620	TAS				P		HPO:iea	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0010566	OMIM:113620	IEA				P		HPO:skoehler	
OMIM	113620	BRANCHIOOCULOFACIAL SYNDROME; BOFS		HP:0025247	OMIM:113620	IEA				P		HPO:skoehler	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000006	OMIM:113650	IEA				I		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000076	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000104	OMIM:113650	TAS				P		HPO:probinson	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000110	OMIM:113650	TAS				P		HPO:probinson	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000113	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000175	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000193	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000218	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000275	OMIM:113650	TAS				P		HPO:probinson	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000276	OMIM:113650	TAS				P		HPO:probinson	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000376	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000378	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	45%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000384	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000402	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	30%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000410	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000410	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	50%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000632	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000691	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0000799	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0001374	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0001425	OMIM:113650	TAS				I		HPO:skoehler	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0002060	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0002566	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0003828	OMIM:113650	IEA				C		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0003829	OMIM:113650	IEA				C		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0004458	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0004467	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	75%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0004712	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0004742	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0007678	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0007925	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0008551	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	45%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0008586	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0009795	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0009796	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0009797	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0009798	OMIM:113650	IEA				P		HPO:iea	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0010628	OMIM:113650	TAS		HP:0040284		P		HPO:probinson	10%
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0011094	OMIM:113650	TAS				P		HPO:skoehler	
OMIM	113650	BRANCHIOOTORENAL SYNDROME 1		HP:0100274	OMIM:113650	TAS				P		HPO:skoehler	
OMIM	113670	BREAST, UNILATERAL GIANT		HP:0000765	OMIM:113670	IEA				P		HPO:iea	
OMIM	113670	BREAST, UNILATERAL GIANT		HP:0001470	OMIM:113670	IEA				I		HPO:iea	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0000006	OMIM:113700	TAS				I		HPO:skoehler	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0000453	OMIM:113700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0001417	OMIM:113700	TAS				I		HPO:skoehler	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0002561	OMIM:113700	TAS				P		HPO:skoehler	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0006709	OMIM:113700	IEA				P		HPO:iea	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0010311	OMIM:113700	IEA				P		HPO:iea	
OMIM	113700	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 1; BNAH1		HP:0100853	OMIM:113700	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0000006	OMIM:113750	IEA				I		HPO:iea	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0000007	OMIM:113750	TAS				I		HPO:skoehler	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6	HP:0012825	HP:0000613	OMIM:113750	TAS				P		HPO:skoehler	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6	HP:0012825	HP:0000639	OMIM:113750	TAS				P		HPO:skoehler	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0001595	OMIM:113750	IEA				P		HPO:iea	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0007513	OMIM:113750	IEA				P		HPO:skoehler	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0007663	OMIM:113750	TAS				P		HPO:skoehler	
OMIM	113750	ALBINISM, OCULOCUTANEOUS, TYPE VI; OCA6		HP:0007750	OMIM:113750	IEA				P		HPO:skoehler	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0000006	OMIM:113800	IEA				I		HPO:iea	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0000007	OMIM:113800	TAS				I		HPO:skoehler	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0000972	OMIM:113800	TAS				P		HPO:skoehler	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0001019	OMIM:113800	TAS				P		HPO:probinson	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0007475	OMIM:113800	TAS				P		HPO:skoehler	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0008066	OMIM:113800	TAS				P		HPO:probinson	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0025092	OMIM:113800	TAS				P		HPO:skoehler	
OMIM	113800	EPIDERMOLYTIC HYPERKERATOSIS		HP:0040189	OMIM:113800	TAS				P		HPO:skoehler	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0000006	OMIM:113900	PCS				I		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0001279	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0001425	OMIM:113900	TAS				I		HPO:skoehler	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0001645	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0001699	OMIM:113900	TAS				M		HPO:skoehler	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0002094	OMIM:113900	TAS				P		HPO:skoehler	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0005170	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0005172	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0011711	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113900	#113900 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA; PFHB1A;;PFHBIA;;HEART BLOCK, PROGRESSIVE FAMILIAL, TYPE I; PFHBI;;LENEGRE-LEV DISEASE;;CARDIAC CONDUCTION DEFECT, PROGRESSIVE; PCCD;;BUNDLE BRANCH BLOCK;;HEREDITARY BUNDLE BRANCH SYSTEM DEFECT; HBBDHEART BLOCK, NONPROGRESSIVE, INCLUDED;;CARDIAC CONDUCTION DEFECT, NONPROGRESSIVE, INCLUDED		HP:0011712	OMIM:113900	PCS				P		HPO:probinson	
OMIM	113950	%113950 BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT		HP:0000006	OMIM:113950	IEA				I		HPO:iea	
OMIM	113950	%113950 BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT		HP:0001626	OMIM:113950	IEA				P		HPO:iea	
OMIM	113950	%113950 BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT		HP:0011712	OMIM:113950	TAS				P		HPO:skoehler	
OMIM	113970	BURKITT LYMPHOMA; BL		HP:0002721	OMIM:113970	IEA				P		HPO:skoehler	
OMIM	113970	BURKITT LYMPHOMA; BL		HP:0003745	OMIM:113970	TAS				I		HPO:skoehler	
OMIM	113970	BURKITT LYMPHOMA; BL		HP:0030080	OMIM:113970	TAS				P		HPO:skoehler	
OMIM	114000	CAFFEY DISEASE		HP:0000006	OMIM:114000	TAS				I		HPO:probinson	
OMIM	114000	CAFFEY DISEASE		HP:0001945	OMIM:114000	TAS				P		HPO:probinson	
OMIM	114000	CAFFEY DISEASE		HP:0002982	OMIM:114000	TAS				P		HPO:probinson	
OMIM	114000	CAFFEY DISEASE		HP:0004490	OMIM:114000	TAS	HP:0003593			P		HPO:probinson	
OMIM	114000	CAFFEY DISEASE		HP:0005731	OMIM:114000	TAS				P		HPO:probinson	
OMIM	114000	CAFFEY DISEASE		HP:0006465	OMIM:114000	TAS				P		HPO:probinson	
OMIM	114030	114030 CAFE-AU-LAIT SPOTS, MULTIPLE		HP:0000006	PMID:8825931	PCS				I		HPO:probinson	
OMIM	114030	114030 CAFE-AU-LAIT SPOTS, MULTIPLE		HP:0007565	PMID:8825931	PCS		HP:0040284		P		HPO:probinson	10/10
OMIM	114065	CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL		HP:0000006	OMIM:114065	IEA				I		HPO:iea	
OMIM	114065	CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL		HP:0001650	OMIM:114065	IEA				P		HPO:iea	
OMIM	114065	CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL		HP:0001659	OMIM:114065	TAS				P		HPO:skoehler	
OMIM	114065	CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL		HP:0004380	PMID:8213448	PCS				P		HPO:probinson	
OMIM	114065	CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL		HP:0010702	OMIM:114065	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0000006	OMIM:114100	IEA				I		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0000007	OMIM:114100	IEA				I		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0000252	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0000268	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0001250	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET	HP:0012828	HP:0001257	OMIM:114100	TAS				P		HPO:probinson	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0001260	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0001263	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0002071	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0002135	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0002445	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0002461	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0002504	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET	HP:0012828	HP:0003121	OMIM:114100	TAS				P		HPO:probinson	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0003593	OMIM:114100	IEA				C		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0004322	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0004325	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0006887	OMIM:114100	IEA				P		HPO:iea	
OMIM	114100	%114100 BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET;;IBGC, CHILDHOOD-ONSET;;STRIOPALLIDODENTATE CALCINOSIS, BILATERAL, CHILDHOOD-ONSET;;CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC, IDIOPATHIC, CHILDHOOD-ONSET		HP:0010864	OMIM:114100	TAS				P		HPO:skoehler	
OMIM	114140	CALLOSITIES, HEREDITARY PAINFUL		HP:0000006	OMIM:114140	IEA				I		HPO:iea	
OMIM	114140	CALLOSITIES, HEREDITARY PAINFUL		HP:0000951	OMIM:114140	IEA				P		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0000006	OMIM:114150	IEA				I		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0000020	OMIM:114150	IEA				P		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0001153	OMIM:114150	IEA				P		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0001156	OMIM:114150	TAS				P		HPO:probinson	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0001159	OMIM:114150	IEA				P		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0001161	OMIM:114150	IEA				P		HPO:iea	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0001831	OMIM:114150	TAS				P		HPO:probinson	
OMIM	114150	CAMPTOBRACHYDACTYLY		HP:0005879	OMIM:114150	IEA				P		HPO:iea	
OMIM	114200	CAMPTODACTYLYSTREBLODACTYLY, INCLUDED		HP:0000006	OMIM:114200	IEA				I		HPO:iea	
OMIM	114200	CAMPTODACTYLYSTREBLODACTYLY, INCLUDED		HP:0003166	OMIM:114200	TAS				P		HPO:probinson	
OMIM	114200	CAMPTODACTYLYSTREBLODACTYLY, INCLUDED		HP:0004976	OMIM:114200	IEA				P		HPO:iea	
OMIM	114200	CAMPTODACTYLYSTREBLODACTYLY, INCLUDED		HP:0100490	OMIM:114200	IEA				P		HPO:iea	
OMIM	114200	CAMPTODACTYLYSTREBLODACTYLY, INCLUDED		HP:0100490	OMIM:114200	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000006	OMIM:114290	IEA				I		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000126	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000175	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000238	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000256	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000260	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000274	OMIM:114290	IEA				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000316	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000347	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000348	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000365	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000369	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000457	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000581	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000878	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000882	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0000883	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001252	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001290	OMIM:114290	TAS				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001508	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001561	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001627	OMIM:114290	TAS				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0001762	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002098	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002104	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002751	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002786	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002827	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0002866	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA	HP:0012825	HP:0002980	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0003038	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0005035	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0005257	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0005280	OMIM:114290	TAS				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0006390	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0006628	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0008434	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0008477	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0008873	OMIM:114290	IEA	HP:0003577			P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0008921	OMIM:114290	TAS				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0011910	OMIM:114290	IEA				P		HPO:iea	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0012245	OMIM:114290	TAS				P		HPO:probinson	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0012745	OMIM:114290	TAS				P		HPO:skoehler	
OMIM	114290	CAMPOMELIC DYSPLASIA		HP:0030680	OMIM:114290	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000006	OMIM:114300	IEA				I		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000028	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000176	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000193	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000218	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000286	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3	HP:0012825	HP:0000324	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000347	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000470	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000508	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000602	OMIM:114300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000767	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0000954	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001193	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001256	OMIM:114300	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001263	OMIM:114300	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001374	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001547	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001762	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001836	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0001845	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0002751	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0002804	OMIM:114300	IEA				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0002938	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0002944	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0003184	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0003199	OMIM:114300	TAS				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0004322	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0005684	OMIM:114300	IEA				P		HPO:skoehler	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0006380	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0009803	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0010554	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0100490	OMIM:114300	IEA				P		HPO:iea	
OMIM	114300	ARTHROGRYPOSIS, DISTAL, TYPE 3; DA3		HP:0200021	OMIM:114300	IEA				P		HPO:iea	
OMIM	114450	CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE		HP:0000006	OMIM:114450	IEA				I		HPO:iea	
OMIM	114450	CANCER, FAMILIAL, WITH IN VITRO RADIORESISTANCE		HP:0002664	OMIM:114450	IEA				P		HPO:iea	
OMIM	114480	BREAST CANCER		HP:0000006	OMIM:114480	IEA				I		HPO:iea	
OMIM	114480	BREAST CANCER		HP:0001425	OMIM:114480	TAS				I		HPO:skoehler	
OMIM	114480	BREAST CANCER		HP:0001428	OMIM:114480	IEA				I		HPO:skoehler	
OMIM	114480	BREAST CANCER		HP:0003002	OMIM:114480	IEA				P		HPO:iea	
OMIM	114500	COLORECTAL CANCER		HP:0000006	OMIM:114500	IEA				I		HPO:skoehler	
OMIM	114500	COLORECTAL CANCER		HP:0001428	OMIM:114500	IEA				I		HPO:skoehler	
OMIM	114500	COLORECTAL CANCER		HP:0001428	OMIM:114500	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	114500	COLORECTAL CANCER		HP:0002891	OMIM:114500	TAS				P		HPO:iea	
OMIM	114500	COLORECTAL CANCER		HP:0005584	OMIM:114500	TAS				P		HPO:skoehler	
OMIM	114500	COLORECTAL CANCER		HP:0006716	OMIM:114500	TAS				P		HPO:iea	
OMIM	114500	COLORECTAL CANCER		HP:0006740	OMIM:114500	TAS				P		HPO:iea	
OMIM	114500	COLORECTAL CANCER		HP:0006753	OMIM:114500	TAS				P		HPO:iea	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0000006	OMIM:114550	TAS				I		HPO:probinson	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0001402	OMIM:114550	TAS				P		HPO:probinson	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0001413	OMIM:114550	TAS				P		HPO:probinson	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0001425	OMIM:114550	TAS				I		HPO:skoehler	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0001428	OMIM:114550	TAS				I		HPO:probinson	
OMIM	114550	HEPATOCELLULAR CARCINOMA		HP:0006572	OMIM:114550	TAS				P		HPO:probinson	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:114580	IEA				I		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000818	OMIM:114580	IEA				P		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0001596	OMIM:114580	IEA				P		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002728	OMIM:114580	IEA				P		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002965	OMIM:114580	IEA				P		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0004429	OMIM:114580	IEA				P		HPO:iea	
OMIM	114580	CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0006480	OMIM:114580	TAS				P		HPO:skoehler	
OMIM	114600	CANINE TEETH, ABSENCE OF UPPER PERMANENT		HP:0000006	OMIM:114600	IEA				I		HPO:iea	
OMIM	114600	CANINE TEETH, ABSENCE OF UPPER PERMANENT		HP:0000164	OMIM:114600	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000256	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000280	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000316	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000343	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000369	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000463	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000470	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000520	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000540	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000577	OMIM:114620	IEA				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000666	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000689	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000767	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0000885	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0001256	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0001382	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0001627	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0001640	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0002007	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0002680	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0002750	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0002967	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0003196	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0003745	OMIM:114620	IEA				I		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0004322	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0005280	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0007517	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0008479	OMIM:114620	IEA				P		HPO:iea	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0008839	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0011220	OMIM:114620	TAS				P		HPO:skoehler	
OMIM	114620	CRANIOFACIOFRONTODIGITAL SYNDROME		HP:0031364	OMIM:114620	IEA				P		HPO:skoehler	
OMIM	114650	CAR FACTOR DEFICIENCY		HP:0000006	OMIM:114650	IEA				I		HPO:iea	
OMIM	114650	CAR FACTOR DEFICIENCY		HP:0001892	OMIM:114650	TAS				P		HPO:probinson	
OMIM	114700	CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH		HP:0000164	OMIM:114700	IEA				P		HPO:iea	
OMIM	114700	CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH		HP:0001426	PMID:5079106	TAS				I		HPO:nvasilevsky	
OMIM	114700	CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH		HP:0006358	PMID:5079106	TAS				P		HPO:nvasilevsky	
OMIM	114700	CARABELLI ANOMALY OF MAXILLARY MOLAR TEETH		HP:0011077	PMID:14933364	TAS				P		HPO:nvasilevsky	
OMIM	114835	CARBOXYLESTERASE 1		HP:0000006	OMIM:114835	IEA				I		HPO:iea	
OMIM	114835	CARBOXYLESTERASE 1		HP:0001370	OMIM:114835	IEA				P		HPO:skoehler	
OMIM	114835	CARBOXYLESTERASE 1		HP:0001939	OMIM:114835	IEA				P		HPO:iea	
OMIM	114835	CARBOXYLESTERASE 1		HP:0002665	OMIM:114835	IEA				P		HPO:skoehler	
OMIM	114835	CARBOXYLESTERASE 1		HP:0005550	OMIM:114835	IEA				P		HPO:skoehler	
OMIM	114900	CARCINOID TUMORS, INTESTINAL		HP:0000006	OMIM:114900	IEA				I		HPO:iea	
OMIM	114900	CARCINOID TUMORS, INTESTINAL		HP:0006723	OMIM:114900	IEA				P		HPO:iea	
OMIM	115000	CARDIAC ARRHYTHMIA		HP:0000006	OMIM:115000	IEA				I		HPO:iea	
OMIM	115000	CARDIAC ARRHYTHMIA		HP:0000707	OMIM:115000	IEA				P		HPO:iea	
OMIM	115000	CARDIAC ARRHYTHMIA		HP:0001699	OMIM:115000	IEA				M		HPO:iea	
OMIM	115000	CARDIAC ARRHYTHMIA		HP:0006696	OMIM:115000	IEA				P		HPO:iea	
OMIM	115080	CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED		HP:0000006	OMIM:115080	TAS				I		HPO:probinson	
OMIM	115080	CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED		HP:0001279	OMIM:115080	TAS				P		HPO:probinson	
OMIM	115080	CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED		HP:0001699	OMIM:115080	TAS				M		HPO:probinson	
OMIM	115080	CARDIAC CONDUCTION DEFECTSUDDEN CARDIAC DEATH, INCLUDED		HP:0011675	OMIM:115080	TAS				P		HPO:probinson	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000006	OMIM:115150	TAS				I		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000126	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000164	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000176	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000194	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000218	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000238	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000268	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000280	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000286	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000316	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000341	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000347	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000358	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000365	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000369	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000414	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000463	OMIM:115150	TAS				P		HPO:probinson	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000486	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000494	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000508	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000520	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000529	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000545	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000561	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000639	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000657	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000689	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000767	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000768	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000938	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0000962	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001003	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1	HP:0012828	HP:0001047	OMIM:115150	TAS				P		HPO:probinson	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001048	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001093	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001187	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001249	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001250	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001252	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001276	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001290	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001508	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001561	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001622	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001631	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001639	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001642	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0001744	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002002	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002013	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002019	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002020	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002120	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002212	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002217	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002223	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0002750	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0003196	OMIM:115150	TAS				P		HPO:probinson	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0003477	OMIM:115150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0003577	PMID:16439621	PCS				C		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0004209	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0004322	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0004482	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0005280	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0006114	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0007333	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0007370	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0008064	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0008070	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0008113	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0008872	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0009891	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0009908	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0010807	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0011220	OMIM:115150	IEA				P		HPO:iea	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0032152	OMIM:115150	IEA				P		HPO:skoehler	
OMIM	115150	CARDIOFACIOCUTANEOUS SYNDROME 1; CFC1		HP:0100703	OMIM:115150	TAS				P		HPO:skoehler	
OMIM	115195	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2		HP:0000006	OMIM:115195	IEA				I		HPO:iea	
OMIM	115195	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2		HP:0001639	OMIM:115195	IEA				P		HPO:iea	
OMIM	115196	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3		HP:0000006	OMIM:115196	IEA				I		HPO:iea	
OMIM	115196	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3		HP:0001639	OMIM:115196	IEA				P		HPO:iea	
OMIM	115197	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4		HP:0000006	OMIM:115197	IEA				I		HPO:iea	
OMIM	115197	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4		HP:0001639	OMIM:115197	IEA				P		HPO:iea	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0000006	OMIM:115200	TAS				I		HPO:skoehler	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0001635	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0001644	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0001644	OMIM:115200	TAS				P		HPO:skoehler	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0001698	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0004308	OMIM:115200	IEA				P		HPO:iea	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0004308	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0004749	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115200	#115200 CARDIOMYOPATHY, DILATED, 1A; CMD1A;;CARDIOMYOPATHY, DILATED, WITH CONDUCTION DEFECT 1; CDCD1;;CARDIOMYOPATHY, IDIOPATHIC DILATED;;CARDIOMYOPATHY, FAMILIAL IDIOPATHIC;;CARDIOMYOPATHY, CONGESTIVE		HP:0005110	OMIM:115200	PCS				P		HPO:probinson	
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0000006	PMID:12531876	PCS				I		HPO:iea	
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0001645	PMID:12531876	PCS				P		HP:probinson	
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0001712	PMID:12531876	PCS		HP:0040284		P		HP:probinson	6/9
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0001723	PMID:12531876	PCS				P		HPO:iea	
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0002119	PMID:12531876	PCS				P		HPO:skoehler	
OMIM	115210	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1		HP:0031295	PMID:12531876	PCS		HP:0040284		P		HP:probinson	3/9
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0000006	OMIM:115250	IEA				I		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0000407	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0001089	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0001635	OMIM:115250	IEA				P		HPO:skoehler	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0001638	OMIM:115250	IEA				P		HPO:skoehler	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0002633	OMIM:115250	IEA				P		HPO:skoehler	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0005110	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0005180	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0007534	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0008720	OMIM:115250	IEA				P		HPO:iea	
OMIM	115250	115250 COLLAGENOMA, FAMILIAL CUTANEOUS		HP:0011663	OMIM:115250	TAS				P		HPO:skoehler	
OMIM	115300	CAROTENEMIA, FAMILIAL		HP:0000006	OMIM:115300	TAS				I		HPO:probinson	
OMIM	115300	CAROTENEMIA, FAMILIAL		HP:0000951	OMIM:115300	IEA				P		HPO:iea	
OMIM	115300	CAROTENEMIA, FAMILIAL		HP:0004905	OMIM:115300	TAS				P		HPO:probinson	
OMIM	115310	PARAGANGLIOMAS 4		HP:0000006	OMIM:115310	IEA				I		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0000740	OMIM:115310	IEA				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0000975	OMIM:115310	TAS				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0001649	OMIM:115310	TAS				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0001962	OMIM:115310	TAS				P		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0002331	OMIM:115310	IEA				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0002640	OMIM:115310	IEA				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0002864	OMIM:115310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	115310	PARAGANGLIOMAS 4		HP:0003001	OMIM:115310	IEA				P		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0003006	OMIM:115310	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	115310	PARAGANGLIOMAS 4		HP:0003581	OMIM:115310	IEA				C		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0003829	OMIM:115310	TAS				C		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0005584	OMIM:115310	IEA				P		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0006737	OMIM:115310	IEA				P		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0006748	OMIM:115310	IEA				P		HPO:iea	
OMIM	115310	PARAGANGLIOMAS 4		HP:0006824	OMIM:115310	TAS				P		HPO:probinson	
OMIM	115310	PARAGANGLIOMAS 4		HP:0008629	OMIM:115310	TAS				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0011976	OMIM:115310	TAS				P		HPO:probinson	
OMIM	115310	PARAGANGLIOMAS 4		HP:0030074	OMIM:115310	TAS				P		HPO:skoehler	
OMIM	115310	PARAGANGLIOMAS 4		HP:0100723	OMIM:115310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	115400	CARPAL DISPLACEMENT		HP:0000006	OMIM:115400	IEA				I		HPO:iea	
OMIM	115400	CARPAL DISPLACEMENT		HP:0000924	OMIM:115400	IEA				P		HPO:iea	
OMIM	115430	CARPAL TUNNEL SYNDROME		HP:0000006	OMIM:115430	IEA				I		HPO:iea	
OMIM	115430	CARPAL TUNNEL SYNDROME		HP:0008326	OMIM:115430	IEA				P		HPO:iea	
OMIM	115430	CARPAL TUNNEL SYNDROME		HP:0009830	OMIM:115430	IEA				P		HPO:skoehler	
OMIM	115430	CARPAL TUNNEL SYNDROME		HP:0012185	OMIM:115430	TAS				P		HPO:skoehler	
OMIM	115430	CARPAL TUNNEL SYNDROME		HP:0012276	OMIM:115430	TAS				P		HPO:probinson	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000006	OMIM:115470	IEA				I	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000104	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000175	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000316	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000347	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000369	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000384	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000402	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000494	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000567	OMIM:115470	TAS				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:probinson	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000568	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0000612	OMIM:115470	TAS				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:probinson	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0001256	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:skoehler	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0001507	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0001627	OMIM:115470	TAS				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:skoehler	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0002023	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:skoehler	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0002566	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:skoehler	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0003974	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0004467	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0005160	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115470	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(q11)		HP:0005912	OMIM:115470	IEA				P	#115470 CAT EYE SYNDROME; CES;;SCHMID-FRACCARO SYNDROME;;CHROMOSOME 22 PARTIAL TETRASOMY;;INV DUP(22)(Q11)	HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000006	OMIM:115645	IEA				I		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000191	OMIM:115645	IEA				P		HPO:skoehler	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000286	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000358	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000463	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000508	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000581	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0000582	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0001115	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0002212	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0003196	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0004322	OMIM:115645	IEA				P		HPO:iea	
OMIM	115645	115645 CATARACT, ABERRANT ORAL FRENULA, AND GROWTH RETARDATION		HP:0012745	OMIM:115645	TAS				P		HPO:skoehler	
OMIM	115650	CATARACT, ANTERIOR POLAR, 1		HP:0000006	OMIM:115650	TAS				I		HPO:iea	
OMIM	115650	CATARACT, ANTERIOR POLAR, 1		HP:0001134	OMIM:115650	TAS				P		HPO:iea	
OMIM	115660	CATARACT 7; CTRCT7		HP:0000006	OMIM:115660	IEA				I		HPO:iea	
OMIM	115660	CATARACT 7; CTRCT7		HP:0000519	OMIM:115660	TAS				P		HPO:skoehler	
OMIM	115660	CATARACT 7; CTRCT7		HP:0000572	OMIM:115660	IEA				P		HPO:skoehler	
OMIM	115660	CATARACT 7; CTRCT7		HP:0032037	OMIM:115660	IEA				P		HPO:skoehler	
OMIM	115665	%115665 CATARACT, CONGENITAL, VOLKMANN TYPE; CCV		HP:0000006	OMIM:115665	PCS				I		HPO:iea	
OMIM	115665	%115665 CATARACT, CONGENITAL, VOLKMANN TYPE; CCV		HP:0000519	OMIM:115665	TAS				P		HPO:skoehler	
OMIM	115665	%115665 CATARACT, CONGENITAL, VOLKMANN TYPE; CCV		HP:0000529	PMID:7607651	PCS				P		HPO:iea	
OMIM	115665	%115665 CATARACT, CONGENITAL, VOLKMANN TYPE; CCV		HP:0100018	PMID:7607651	PCS	HP:0003577	HP:0040284		P		HPO:iea	41/41
OMIM	115700	CATARACT, CRYSTALLINE ACULEIFORM		HP:0000006	OMIM:115700	IEA				I		HPO:iea	
OMIM	115700	CATARACT, CRYSTALLINE ACULEIFORM		HP:0000519	OMIM:115700	IEA				P		HPO:iea	
OMIM	115800	CATARACT, CRYSTALLINE CORALLIFORM		HP:0000006	OMIM:115800	IEA				I		HPO:iea	
OMIM	115800	CATARACT, CRYSTALLINE CORALLIFORM		HP:0000518	OMIM:115800	IEA				P		HPO:skoehler	
OMIM	115900	#115900 CATARACT 42; CTRCT42		HP:0000006	OMIM:115900	IEA				I		HPO:iea	
OMIM	115900	#115900 CATARACT 42; CTRCT42		HP:0000501	OMIM:115900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	115900	#115900 CATARACT 42; CTRCT42		HP:0000519	OMIM:115900	IEA				P		HPO:skoehler	
OMIM	115900	#115900 CATARACT 42; CTRCT42		HP:0000545	OMIM:115900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	116100	116100 CATARACT, MEMBRANOUS		HP:0000006	OMIM:116100	IEA				I		HPO:iea	
OMIM	116100	116100 CATARACT, MEMBRANOUS		HP:0000518	OMIM:116100	IEA				P		HPO:skoehler	
OMIM	116100	116100 CATARACT, MEMBRANOUS		HP:0010922	OMIM:116100	TAS				P		HPO:skoehler	
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0000006	OMIM:116200	TAS				I		HPO:probinson	
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0000482	OMIM:116200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0000519	OMIM:116200	TAS				P		HPO:probinson	
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0007787	OMIM:116200	TAS				P		HPO:skoehler	
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0010693	OMIM:116200	TAS				P		HPO:probinson	
OMIM	116200	CATARACT 1, MULTIPLE TYPES		HP:0100018	OMIM:116200	TAS				P		HPO:skoehler	
OMIM	116300	CATARACT 30, MULTIPLE TYPES		HP:0000006	OMIM:116300	IEA				I		HPO:iea	
OMIM	116300	CATARACT 30, MULTIPLE TYPES		HP:0001115	OMIM:116300	TAS				P		HPO:skoehler	
OMIM	116300	CATARACT 30, MULTIPLE TYPES		HP:0003577	OMIM:116300	TAS				C		HPO:skoehler	
OMIM	116300	CATARACT 30, MULTIPLE TYPES		HP:0007657	OMIM:116300	IEA				P		HPO:iea	
OMIM	116300	CATARACT 30, MULTIPLE TYPES		HP:0010693	OMIM:116300	TAS				P		HPO:skoehler	
OMIM	116400	CATARACT, NUCLEAR TOTAL		HP:0000006	OMIM:116400	IEA				I		HPO:iea	
OMIM	116400	CATARACT, NUCLEAR TOTAL		HP:0000519	OMIM:116400	IEA				P		HPO:iea	
OMIM	116400	CATARACT, NUCLEAR TOTAL		HP:0100018	OMIM:116400	IEA				P		HPO:skoehler	
OMIM	116600	CATARACT, POSTERIOR POLAR, 1 CTPA CATARACT, CONGENITAL TOTAL, INCLUDED		HP:0000006	PMID:19005574	PCS				I		HPO:iea	
OMIM	116600	CATARACT, POSTERIOR POLAR, 1 CTPA CATARACT, CONGENITAL TOTAL, INCLUDED		HP:0000519	PMID:19306328	PCS				P		HPO:iea	
OMIM	116600	CATARACT, POSTERIOR POLAR, 1 CTPA CATARACT, CONGENITAL TOTAL, INCLUDED		HP:0000545	OMIM:116600	PCS				P		HPO:iea	
OMIM	116600	CATARACT, POSTERIOR POLAR, 1 CTPA CATARACT, CONGENITAL TOTAL, INCLUDED		HP:0001115	PMID:19005574	PCS		HP:0040284		P		HPO:iea	12/12
OMIM	116600	CATARACT, POSTERIOR POLAR, 1 CTPA CATARACT, CONGENITAL TOTAL, INCLUDED		HP:0001139	OMIM:116600	PCS				P		HPO:iea	
OMIM	116700	CATARACT 13 WITH ADULT I PHENOTYPE		HP:0000006	PMID:21912254	PCS				I		HPO:probinson	
OMIM	116700	CATARACT 13 WITH ADULT I PHENOTYPE		HP:0000007	OMIM:116700	TAS				I		HPO:skoehler	
OMIM	116700	CATARACT 13 WITH ADULT I PHENOTYPE		HP:0000519	PMID:21912254	PCS				P		HPO:skoehler	
OMIM	116790	CATECHOL-O-METHYLTRANSFERASE		HP:0000007	OMIM:116790	IEA				I		HPO:iea	
OMIM	116790	CATECHOL-O-METHYLTRANSFERASE		HP:0001939	OMIM:116790	IEA				P		HPO:iea	
OMIM	116800	#116800 CATARACT, LAMELLAR;;CATARACT, ZONULAR;;PERINUCLEAR CATARACTCATARACT, MARNER TYPE, INCLUDED; CAM, INCLUDED;;CTM, INCLUDED		HP:0000006	PMID:12089525	PCS				I		HPO:iea	
OMIM	116800	#116800 CATARACT, LAMELLAR;;CATARACT, ZONULAR;;PERINUCLEAR CATARACTCATARACT, MARNER TYPE, INCLUDED; CAM, INCLUDED;;CTM, INCLUDED		HP:0001134	OMIM:116800	IEA				P		HPO:iea	
OMIM	116800	#116800 CATARACT, LAMELLAR;;CATARACT, ZONULAR;;PERINUCLEAR CATARACTCATARACT, MARNER TYPE, INCLUDED; CAM, INCLUDED;;CTM, INCLUDED		HP:0007971	PMID:12089525	PCS				P		HPO:skoehler	
OMIM	116800	#116800 CATARACT, LAMELLAR;;CATARACT, ZONULAR;;PERINUCLEAR CATARACTCATARACT, MARNER TYPE, INCLUDED; CAM, INCLUDED;;CTM, INCLUDED		HP:0010693	OMIM:116800	TAS				P		HPO:skoehler	
OMIM	116800	#116800 CATARACT, LAMELLAR;;CATARACT, ZONULAR;;PERINUCLEAR CATARACTCATARACT, MARNER TYPE, INCLUDED; CAM, INCLUDED;;CTM, INCLUDED		HP:0100018	OMIM:116800	IEA				P		HPO:skoehler	
OMIM	116850	CATATRICHY		HP:0000006	OMIM:116850	IEA				I		HPO:iea	
OMIM	116850	CATATRICHY		HP:0001595	OMIM:116850	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0000006	OMIM:116860	IEA				I		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0000951	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0001250	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0001425	OMIM:116860	TAS				I		HPO:skoehler	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0002170	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0002315	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0002514	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0003011	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0003829	OMIM:116860	IEA				C		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0006576	OMIM:116860	IEA				P		HPO:iea	
OMIM	116860	#116860 CEREBRAL CAVERNOUS MALFORMATIONS; CCM;;CAVERNOUS ANGIOMA, FAMILIAL;;CAVERNOUS ANGIOMATOUS MALFORMATIONS; CAM;;CEREBRAL CAPILLARY MALFORMATIONSCEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED;;CAVERNOUS MALFORMATIONS OF CNS AND RETINA, INCLUDED;;HYPERKERATOTIC CUTANEOUS CAPILLARY-VENOUS MALFORMATIONS ASSOCIATEDWITH CEREBRAL CAPILLARY MALFORMATIONS, INCLUDED		HP:0007797	OMIM:116860	IEA				P		HPO:iea	
OMIM	116870	CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENTOF DIAPHRAGM		HP:0000006	OMIM:116870	TAS				I		HPO:iea	
OMIM	116870	CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENTOF DIAPHRAGM		HP:0002027	OMIM:116870	TAS				P		HPO:iea	
OMIM	116870	CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENTOF DIAPHRAGM		HP:0012327	OMIM:116870	TAS				P		HPO:iea	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0000007	PMID:12488604	PCS				I		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0000230	PMID:11703376	PCS				P		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0000704	OMIM:116920	TAS				P		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0001058	PMID:12488604	PCS				P		HP:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0001974	PMID:26639818,PMID:26497373	PCS		HP:0040284		P		HPO:probinson	19/19
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0002718	PMID:1347532	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0002754	PMID:26497373	PCS		HP:0040284		P		HP:probinson	1/12
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0005224	OMIM:116920	TAS				P		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0005420	OMIM:116920	TAS				P		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0007499	OMIM:116920	TAS				P		HPO:probinson	
OMIM	116920	LEUKOCYTE ADHESION DEFICIENCY, TYPE I		HP:0200042	PMID:26639818	PCS	HP:0011463	HP:0040284		P		HP:probinson	5/19
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0000006	OMIM:117000	IEA				I		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0000007	OMIM:117000	IEA				I		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001270	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001319	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001371	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001374	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001763	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0001945	OMIM:117000	TAS				P		HPO:skoehler	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0002047	OMIM:117000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0002751	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003202	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003324	OMIM:117000	IEA				P		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003593	OMIM:117000	IEA				C		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003677	OMIM:117000	TAS				C		HPO:skoehler	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003680	OMIM:117000	IEA				C		HPO:iea	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003798	OMIM:117000	IEA				P		HPO:skoehler	
OMIM	117000	#117000 CENTRAL CORE DISEASE OF MUSCLE;;CCD;;CCOMINICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTICORE MYOPATHY, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;MULTIMINICORE DISEASE, MODERATE, WITH HAND INVOLVEMENT, INCLUDED;;NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER, INCLUDED;CNMDU1, INCLUDED		HP:0003803	OMIM:117000	IEA				P		HPO:iea	
OMIM	117100	CENTRALOPATHIC EPILEPSY		HP:0003745	OMIM:117100	TAS				I		HPO:probinson	
OMIM	117100	CENTRALOPATHIC EPILEPSY		HP:0007334	OMIM:117100	TAS				P		HPO:probinson	
OMIM	117100	CENTRALOPATHIC EPILEPSY		HP:0007359	OMIM:117100	TAS				P		HPO:probinson	
OMIM	117100	CENTRALOPATHIC EPILEPSY		HP:0012557	OMIM:117100	TAS				P		HPO:probinson	
OMIM	117100	CENTRALOPATHIC EPILEPSY		HP:0031951	OMIM:117100	IEA				P		HPO:skoehler	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0000006	OMIM:117210	IEA				I		HPO:iea	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0000407	OMIM:117210	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0001251	OMIM:117210	TAS				P		HPO:probinson	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0001260	OMIM:117210	IEA				P		HPO:iea	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0001272	OMIM:117210	TAS				P		HPO:probinson	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0002066	OMIM:117210	IEA				P		HPO:iea	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0002070	OMIM:117210	IEA				P		HPO:iea	
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0003584	OMIM:117210	TAS		HP:0040282		C		HPO:probinson	HP:0040282
OMIM	117210	SPINOCEREBELLAR ATAXIA 31		HP:0007979	OMIM:117210	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0000006	OMIM:117300	TAS				I		HPO:probinson	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0000365	OMIM:117300	TAS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0000709	OMIM:117300	TAS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0000726	OMIM:117300	TAS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0001115	OMIM:117300	TAS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0001251	PMID:20385796	PCS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0001257	PMID:20385796	PCS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0002080	OMIM:117300	TAS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0002185	PMID:11895040	PCS				P		HPO:iea	
OMIM	117300	DEMENTIA, FAMILIAL DANISH		HP:0011970	PMID:20385796	PCS				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0000006	OMIM:117360	IEA				I		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0000639	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0001260	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0001270	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0001310	OMIM:117360	TAS				P		HPO:skoehler	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002070	OMIM:117360	TAS				P		HPO:skoehler	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002075	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002080	OMIM:117360	TAS				P		HPO:skoehler	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002136	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002335	OMIM:117360	IEA				P		HPO:skoehler	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0002470	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0003577	OMIM:117360	IEA				C		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0006855	OMIM:117360	IEA				P		HPO:iea	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV		HP:0006855	OMIM:117360	TAS				P		HPO:probinson	
OMIM	117360	#117360 SPINOCEREBELLAR ATAXIA 29; SCA29;;CEREBELLAR ATAXIA, CONGENITAL NONPROGRESSIVE, AUTOSOMAL DOMINANT;CNPCA;;CEREBELLAR VERMIS APLASIA;;APLASIA OF CEREBELLAR VERMIS; ACV	HP:0012825	HP:0100543	OMIM:117360	TAS				P		HPO:skoehler	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000006	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				I	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000098	ISBN-13:978-0721606156	TAS	HP:0003577			P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000256	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000268	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000303	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000307	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000316	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000388	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000405	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000486	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000494	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000540	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000639	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0000708	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001176	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001249	OMIM:117550	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:skoehler	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001263	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001319	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001338	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001347	OMIM:117550	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001388	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001629	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001631	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001643	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001763	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001792	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001833	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0001952	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002007	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002280	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002370	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002389	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002474	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002667	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sotos	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002705	OMIM:117550	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:skoehler	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0002857	OMIM:117550	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:skoehler	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0003745	OMIM:117550	TAS				I	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0005616	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0006288	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117550	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5q35 DELETION SYNDROME		HP:0009890	ISBN-13:978-0721606156	TAS				P	#117550 SOTOS SYNDROME 1; SOTOS1;;SOTOS SYNDROME;;CEREBRAL GIGANTISM;;CHROMOSOME 5Q35 DELETION SYNDROME	HPO:iea	
OMIM	117600	117600 CEREBRAL SARCOMA		HP:0000006	OMIM:117600	IEA				I		HPO:iea	
OMIM	117600	117600 CEREBRAL SARCOMA		HP:0002664	OMIM:117600	IEA				P		HPO:iea	
OMIM	117600	117600 CEREBRAL SARCOMA		HP:0100244	OMIM:117600	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000006	OMIM:117650	TAS				I		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000007	OMIM:117650	TAS				I		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000085	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000086	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000107	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000162	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000164	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000185	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000218	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000252	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000272	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000286	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000343	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS	HP:0012828	HP:0000347	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000358	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000369	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000405	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000465	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0000878	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001249	OMIM:117650	TAS		HP:0040284		P		HPO:probinson	50%
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001374	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001545	OMIM:117650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001561	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001591	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001611	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001629	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001631	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0001643	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002020	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002025	OMIM:117650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002132	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002643	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002650	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0002987	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0004209	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0004468	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0004695	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0005257	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0005792	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0006593	OMIM:117650	TAS				P		HPO:probinson	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0008897	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0010290	OMIM:117650	TAS				P		HPO:skoehler	
OMIM	117650	CEREBROCOSTOMANDIBULAR SYNDROME; CCMS		HP:0030280	OMIM:117650	IEA				P		HPO:skoehler	
OMIM	117800	EAR WAX, WET/DRY		HP:0000006	OMIM:117800	IEA				I		HPO:iea	
OMIM	117800	EAR WAX, WET/DRY		HP:0000598	OMIM:117800	IEA				P		HPO:iea	
OMIM	117800	EAR WAX, WET/DRY		HP:0003002	OMIM:117800	IEA				P		HPO:skoehler	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0000006	OMIM:117850	TAS				I		HPO:probinson	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0002751	OMIM:117850	TAS				P		HPO:probinson	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0004532	OMIM:117850	TAS				P		HPO:probinson	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0004535	OMIM:117850	TAS				P		HPO:probinson	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0011913	OMIM:117850	TAS				P		HPO:probinson	
OMIM	117850	CERVICAL HYPERTRICHOSIS WITH UNDERLYING KYPHOSCOLIOSIS		HP:0011914	OMIM:117850	TAS				P		HPO:probinson	
OMIM	117900	CERVICAL RIB		HP:0000006	OMIM:117900	IEA				I		HPO:iea	
OMIM	117900	CERVICAL RIB		HP:0000707	OMIM:117900	IEA				P		HPO:iea	
OMIM	117900	CERVICAL RIB		HP:0000891	OMIM:117900	IEA				P		HPO:iea	
OMIM	118000	CERVICAL VERTEBRAL BRIDGE		HP:0000006	OMIM:118000	IEA				I		HPO:iea	
OMIM	118000	CERVICAL VERTEBRAL BRIDGE		HP:0000925	OMIM:118000	IEA				P		HPO:iea	
OMIM	118005	CERVICAL VERTEBRAL DYSPLASIA		HP:0000006	OMIM:118005	TAS				I		HPO:probinson	
OMIM	118005	CERVICAL VERTEBRAL DYSPLASIA		HP:0005678	OMIM:118005	TAS				P		HPO:probinson	
OMIM	118005	CERVICAL VERTEBRAL DYSPLASIA		HP:0008461	OMIM:118005	TAS				P		HPO:probinson	
OMIM	118005	CERVICAL VERTEBRAL DYSPLASIA		HP:0008469	OMIM:118005	TAS				P		HPO:probinson	
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000006	PMID:18425797	PCS				I		HPO:probinson	
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000122	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	7/45
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000175	PMID:4436358	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000324	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	20%
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000410	PMID:9875048	PCS		HP:0040284		P		HPO:probinson	5/24
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000465	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	20%
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000466	PMID:1739048	PCS		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000470	PMID:1739048	PCS		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000772	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0000912	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	21/50
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0001335	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	9/50
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0001425	OMIM:118100	TAS				I		HPO:skoehler	
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0002162	PMID:1739048;PMID:4436358	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0002650	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	30/50
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0002813	PMID:18425797;PMID:16585825	PCS	HP:0003577	HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0003828	OMIM:118100	TAS				C		HPO:skoehler	
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0004602	PMID:18425797	PCS		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0005640	PMID:18425797	PCS	HP:0003577	HP:0040281		P		HPO:probinson	HP:0040281
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0005988	PMID:4436358	PCS		HP:0040284		P		HPO:probinson	20%
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0007291	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0030325	PMID:11950676	PCS				P		HPO:probinson	
OMIM	118100	KLIPPEL-FEIL SYNDROME 1, AUTOSOMAL DOMINANT; KFS1		HP:0030680	PMID:4436358;PMID:5645110	PCS		HP:0040284		P		HPO:probinson	21/505
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0000006	OMIM:118200	IEA				I		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001171	OMIM:118200	TAS				P		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001178	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001265	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001284	OMIM:118200	TAS				P		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001425	OMIM:118200	TAS				I		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001761	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0001765	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0002460	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0002751	OMIM:118200	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0002936	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003376	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003380	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003382	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003383	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003431	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003449	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003587	OMIM:118200	IEA				C		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003621	OMIM:118200	PCS				C		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003677	OMIM:118200	IEA				C		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003690	OMIM:118200	TAS				P		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003693	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003693	OMIM:118200	PCS				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0003828	OMIM:118200	TAS				C		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0004336	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0009027	OMIM:118200	IEA				P		HPO:probinson	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0009830	OMIM:118200	TAS				P		HPO:skoehler	
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0011096	OMIM:118200	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	118200	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B		HP:0012074	OMIM:118200	TAS				P		HPO:skoehler	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0000006	OMIM:118210	IEA				I		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0001265	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0001284	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0001425	OMIM:118210	TAS				I		HPO:skoehler	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0001761	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0001765	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0002460	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0002936	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003376	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003378	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003380	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003383	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003384	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1	HP:0012825	HP:0003431	OMIM:118210	IEA				P		HPO:probinson	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003674	OMIM:118210	IEA				C		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003677	OMIM:118210	IEA				C		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003690	OMIM:118210	TAS				P		HPO:skoehler	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003693	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0003693	OMIM:118210	TAS				P		HPO:probinson	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0009027	OMIM:118210	IEA				P		HPO:iea	
OMIM	118210	#118210 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CMT2A1;;CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1;;CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 2A1;;HEREDITARY MOTOR AND SENSORY NEUROPATHY IIA1;;HMSN IIA1;;HMSN2A1		HP:0009830	OMIM:118210	TAS				P		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0000006	OMIM:118220	IEA				I		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0000365	OMIM:118220	TAS				P		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001171	OMIM:118220	TAS				P		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001178	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001265	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001284	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001425	OMIM:118220	TAS				I		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001761	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0001765	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0002460	OMIM:118220	TAS				P		HPO:probinson	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0002751	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0002936	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003376	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003380	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003382	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003383	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003431	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003449	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003481	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003587	OMIM:118220	IEA				C		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003621	OMIM:118220	IEA				C		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003677	OMIM:118220	IEA				C		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003690	OMIM:118220	TAS				P		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003693	OMIM:118220	TAS				P		HPO:probinson	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0003828	OMIM:118220	TAS				C		HPO:skoehler	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0004336	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0009027	OMIM:118220	IEA				P		HPO:iea	
OMIM	118220	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A		HP:0009830	OMIM:118220	TAS				P		HPO:skoehler	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0000006	OMIM:118230	IEA				I		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0000470	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0000774	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0000975	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001026	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001270	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001301	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001315	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001417	OMIM:118230	TAS				I		HPO:skoehler	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001600	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001678	OMIM:118230	TAS				P		HPO:skoehler	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001761	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0001999	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0002013	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0002018	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0002028	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003009	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003091	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003447	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003474	OMIM:118230	TAS				P		HPO:probinson	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003593	OMIM:118230	IEA				C		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0003693	OMIM:118230	TAS				P		HPO:probinson	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0004875	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0005853	OMIM:118230	IEA				P		HPO:iea	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0009049	OMIM:118230	TAS				P		HPO:probinson	
OMIM	118230	118230 CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE		HP:0011727	OMIM:118230	TAS				P		HPO:probinson	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0000006	OMIM:118300	IEA				I		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0000407	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001171	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001265	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001284	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001761	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001765	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0001884	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0002460	OMIM:118300	TAS				P		HPO:skoehler	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0002936	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003376	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003431	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003621	OMIM:118300	IEA				C		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003690	OMIM:118300	TAS				P		HPO:skoehler	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003693	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0003693	OMIM:118300	TAS				P		HPO:skoehler	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0009027	OMIM:118300	IEA				P		HPO:iea	
OMIM	118300	#118300 CHARCOT-MARIE-TOOTH DISEASE AND DEAFNESS;;CHARCOT-MARIE-TOOTH NEUROPATHY AND DEAFNESS, AUTOSOMAL DOMINANT;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1E; CMT1E		HP:0011463	OMIM:118300	TAS				C		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000006	OMIM:118301	TAS				I		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000007	OMIM:118301	TAS				I		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000508	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000726	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM	HP:0012825	HP:0000762	OMIM:118301	IEA				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000763	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0000975	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001026	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001278	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001300	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001301	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001315	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001347	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001417	OMIM:118301	TAS				I		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001678	OMIM:118301	TAS				P		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0001761	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0002013	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0002018	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0002028	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0002171	OMIM:118301	TAS				P		HPO:skoehler	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0002398	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0003009	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0003091	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0003447	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0003693	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0005150	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0007110	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0009049	OMIM:118301	IEA				P		HPO:iea	
OMIM	118301	118301 CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM		HP:0011727	OMIM:118301	PCS				P		HPO:probinson	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0000006	OMIM:118330	IEA				I		HPO:iea	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0000232	OMIM:118330	IEA				P		HPO:iea	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0002617	OMIM:118330	IEA				P		HPO:skoehler	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0002860	OMIM:118330	TAS				P		HPO:skoehler	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0030731	OMIM:118330	IEA				P		HPO:skoehler	
OMIM	118330	CHEILITIS GLANDULARIS		HP:0100825	OMIM:118330	IEA				P		HPO:skoehler	
OMIM	118350	CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS		HP:0000006	OMIM:118350	IEA				I		HPO:iea	
OMIM	118350	CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS		HP:0006729	OMIM:118350	IEA				P		HPO:iea	
OMIM	118350	CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS		HP:0006773	OMIM:118350	IEA				P		HPO:iea	
OMIM	118350	CHEMODECTOMA, INTRAABDOMINAL, WITH CUTANEOUS ANGIOLIPOMAS		HP:0030074	OMIM:118350	IEA				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0000006	OMIM:118400	IEA				I		HPO:iea	
OMIM	118400	CHERUBISM		HP:0000311	OMIM:118400	TAS				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0000520	OMIM:118400	IEA				P		HPO:iea	
OMIM	118400	CHERUBISM		HP:0000677	OMIM:118400	IEA				P		HPO:iea	
OMIM	118400	CHERUBISM		HP:0001065	OMIM:118400	IEA				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0001133	OMIM:118400	IEA				P		HPO:iea	
OMIM	118400	CHERUBISM		HP:0001138	OMIM:118400	IEA				P		HPO:iea	
OMIM	118400	CHERUBISM		HP:0007663	OMIM:118400	TAS				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0011463	OMIM:118400	TAS				C		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0030802	OMIM:118400	TAS				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0200056	OMIM:118400	TAS				P		HPO:skoehler	
OMIM	118400	CHERUBISM		HP:0200057	OMIM:118400	TAS				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000006	OMIM:118420	IEA				I		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000020	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000360	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000365	OMIM:118420	TAS				P		HPO:probinson	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000613	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000639	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0000651	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0001260	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002015	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002061	OMIM:118420	TAS				P		HPO:probinson	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002066	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002315	OMIM:118420	TAS				P		HPO:probinson	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002317	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002321	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002395	OMIM:118420	TAS				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0002650	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0003396	OMIM:118420	TAS				P		HPO:probinson	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0003401	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0003487	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0003690	OMIM:118420	IEA				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0005758	OMIM:118420	TAS				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0005759	OMIM:118420	IEA				P		HPO:iea	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0007099	OMIM:118420	TAS				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0010780	OMIM:118420	IEA				P		HPO:skoehler	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0012046	OMIM:118420	TAS				P		HPO:probinson	
OMIM	118420	CHIARI MALFORMATION TYPE I		HP:0030833	OMIM:118420	TAS				P		HPO:skoehler	
OMIM	118430	CHLORPROPAMIDE-ALCOHOL FLUSHING; CPAF		HP:0000006	OMIM:118430	TAS				I		HPO:iea	
OMIM	118430	CHLORPROPAMIDE-ALCOHOL FLUSHING; CPAF		HP:0000488	OMIM:118430	IEA				P		HPO:skoehler	
OMIM	118430	CHLORPROPAMIDE-ALCOHOL FLUSHING; CPAF		HP:0001033	OMIM:118430	TAS				P		HPO:probinson	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000006	OMIM:118450	IEA				I		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000076	PMID:22105858	PCS		HP:0040284		P		HPO:skoehler	6/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000081	PMID:12509572	PCS		HP:0040284		P		HP:probinson	2/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000089	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000097	PMID:12509572	PCS		HP:0040284		P		HP:probinson	2/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000110	PMID:22105858	PCS		HP:0040284		P		HPO:iea	43/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000316	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000325	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000337	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000400	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000482	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000486	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000490	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000518	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000533	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000545	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000580	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000582	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000585	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000593	OMIM:118450	IEA				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000627	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0000772	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001256	OMIM:118450	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001284	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001297	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001328	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001394	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001396	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001399	PMID:12509572	PCS		HP:0040284		P		HP:probinson	38/174
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001402	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001492	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001508	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001629	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001631	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001636	OMIM:118450	IEA				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001680	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001738	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001920	PMID:12509572	PCS		HP:0040284		P		HP:probinson	2/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0001947	PMID:22105858	PCS		HP:0040284		P		HPO:skoehler	7/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0002155	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0002895	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0002910	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0002937	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003022	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003124	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003189	OMIM:118450	TAS				P		HPO:probinson	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003593	OMIM:118450	TAS				C		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003774	PMID:12509572	PCS		HP:0040284		P		HP:probinson	4/187
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0003829	OMIM:118450	TAS				C		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0004617	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0004969	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0005280	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0006571	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0006579	OMIM:118450	TAS				P		HPO:skoehler	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0008659	OMIM:118450	IEA				P		HPO:iea	
OMIM	118450	ALAGILLE SYNDROME 1; ALGS1		HP:0009882	OMIM:118450	IEA				P		HPO:iea	
OMIM	118600	#118600 CHONDROCALCINOSIS 2; CCAL2;;CHONDROCALCINOSIS, FAMILIAL ARTICULAR;;CALCIUM GOUT;;CALCIUM PYROPHOSPHATE ARTHROPATHY;;CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD		HP:0000006	OMIM:118600	IEA				I		HPO:iea	
OMIM	118600	#118600 CHONDROCALCINOSIS 2; CCAL2;;CHONDROCALCINOSIS, FAMILIAL ARTICULAR;;CALCIUM GOUT;;CALCIUM PYROPHOSPHATE ARTHROPATHY;;CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD		HP:0002758	OMIM:118600	IEA				P		HPO:iea	
OMIM	118600	#118600 CHONDROCALCINOSIS 2; CCAL2;;CHONDROCALCINOSIS, FAMILIAL ARTICULAR;;CALCIUM GOUT;;CALCIUM PYROPHOSPHATE ARTHROPATHY;;CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD		HP:0003040	OMIM:118600	IEA				P		HPO:iea	
OMIM	118600	#118600 CHONDROCALCINOSIS 2; CCAL2;;CHONDROCALCINOSIS, FAMILIAL ARTICULAR;;CALCIUM GOUT;;CALCIUM PYROPHOSPHATE ARTHROPATHY;;CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD		HP:0003581	OMIM:118600	TAS				C		HPO:skoehler	
OMIM	118600	#118600 CHONDROCALCINOSIS 2; CCAL2;;CHONDROCALCINOSIS, FAMILIAL ARTICULAR;;CALCIUM GOUT;;CALCIUM PYROPHOSPHATE ARTHROPATHY;;CALCIUM PYROPHOSPHATE DIHYDRATE DEPOSITION DISEASE; CPPDD		HP:0005017	OMIM:118600	IEA				P		HPO:iea	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0000006	OMIM:118610	IEA				I		HPO:iea	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0000934	OMIM:118610	IEA				P		HPO:iea	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0003040	OMIM:118610	IEA				P		HPO:iea	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0004268	OMIM:118610	TAS				P		HPO:skoehler	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0005645	OMIM:118610	IEA				P		HPO:iea	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0006646	OMIM:118610	TAS				P		HPO:probinson	
OMIM	118610	118610 CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION;;FAMILIAL APATITE DISEASE		HP:0006649	OMIM:118610	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0000006	OMIM:118650	IEA				I		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0000518	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0001762	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0002007	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0002208	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0002650	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0003273	OMIM:118650	TAS				P		HPO:probinson	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0004646	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0006380	OMIM:118650	TAS				P		HPO:probinson	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0007390	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0008070	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0008855	OMIM:118650	IEA				P		HPO:iea	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0010655	OMIM:118650	TAS				P		HPO:probinson	
OMIM	118650	CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANTCHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED		HP:0011892	OMIM:118650	TAS				P		HPO:skoehler	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0000006	OMIM:118651	TAS				I		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0000272	OMIM:118651	IEA				P		HPO:iea	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0000457	OMIM:118651	IEA				P		HPO:iea	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0002832	OMIM:118651	TAS				P		HPO:iea	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0002983	OMIM:118651	TAS				P		HPO:skoehler	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0003417	OMIM:118651	TAS				P		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0005736	OMIM:118651	TAS				P		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0010038	OMIM:118651	TAS				P		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0010041	OMIM:118651	TAS				P		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0010044	OMIM:118651	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0010655	PMID:9719382	TAS				P		HPO:probinson	
OMIM	118651	%118651 CHONDRODYSPLASIA PUNCTATA, TIBIA-METACARPAL TYPE;;CHONDRODYSPLASIA PUNCTATA, MT TYPE		HP:0011800	OMIM:118651	TAS				P		HPO:skoehler	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0000006	OMIM:118700	IEA				I		HPO:iea	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0000739	OMIM:118700	IEA				P		HPO:skoehler	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0001260	OMIM:118700	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0001270	OMIM:118700	IEA				P		HPO:iea	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0001288	OMIM:118700	IEA				P		HPO:iea	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0002072	OMIM:118700	IEA				P		HPO:iea	
OMIM	118700	#118700 CHOREA, BENIGN HEREDITARY; BHC;;BCH;;HEREDITARY PROGRESSIVE CHOREA WITHOUT DEMENTIA		HP:0003621	OMIM:118700	IEA				C		HPO:iea	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0000006	OMIM:118750	IEA				I		HPO:iea	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0000726	OMIM:118750	IEA				P		HPO:skoehler	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0001250	OMIM:118750	IEA				P		HPO:skoehler	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0001288	OMIM:118750	IEA				P		HPO:iea	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0002063	OMIM:118750	IEA				P		HPO:skoehler	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0003593	OMIM:118750	IEA				C		HPO:iea	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0007256	OMIM:118750	IEA				P		HPO:iea	
OMIM	118750	CHOREOATHETOSIS, FAMILIAL INVERTED		HP:0007326	OMIM:118750	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0000006	OMIM:118800	IEA				I		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0000273	OMIM:118800	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0000473	OMIM:118800	TAS				P		HPO:probinson	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0001260	OMIM:118800	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0002015	OMIM:118800	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0002268	OMIM:118800	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0002411	OMIM:118800	IEA				P		HPO:iea	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0003593	OMIM:118800	TAS				C		HPO:skoehler	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0007098	OMIM:118800	TAS				P		HPO:probinson	
OMIM	118800	#118800 PAROXYSMAL NONKINESIGENIC DYSKINESIA 1; PNKD1;;PAROXYSMAL DYSTONIC CHOREOATHETOSIS; PDC;;CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1;;MOUNT-REBACK SYNDROME;;CHOREOATHETOSIS, NONKINESIGENIC;;DYSTONIA 8; DYT8		HP:0011463	OMIM:118800	IEA				C		HPO:iea	
OMIM	118830	CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEINLIPASE		HP:0000006	OMIM:118830	TAS				I		HPO:probinson	
OMIM	118830	CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEINLIPASE		HP:0001744	OMIM:118830	TAS				P		HPO:probinson	
OMIM	118830	CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEINLIPASE		HP:0002027	OMIM:118830	TAS				P		HPO:skoehler	
OMIM	118830	CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEINLIPASE		HP:0010980	OMIM:118830	TAS				P		HPO:probinson	
OMIM	118830	CHYLOMICRONEMIA, FAMILIAL, DUE TO CIRCULATING INHIBITOR OF LIPOPROTEINLIPASE		HP:0100027	OMIM:118830	TAS				P		HPO:probinson	
OMIM	118865	CHOROIDAL OSTEOMA, BILATERAL		HP:0000006	OMIM:118865	TAS				I		HPO:skoehler	
OMIM	118865	CHOROIDAL OSTEOMA, BILATERAL		HP:0000610	OMIM:118865	IEA				P		HPO:skoehler	
OMIM	118865	CHOROIDAL OSTEOMA, BILATERAL		HP:0001939	OMIM:118865	IEA				P		HPO:iea	
OMIM	118865	CHOROIDAL OSTEOMA, BILATERAL		HP:0002664	OMIM:118865	IEA				P		HPO:iea	
OMIM	118865	CHOROIDAL OSTEOMA, BILATERAL		HP:0100246	OMIM:118865	TAS				P		HPO:skoehler	
OMIM	118900	118900 CIRRHOSIS, FAMILIAL		HP:0000006	OMIM:118900	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	118900	118900 CIRRHOSIS, FAMILIAL		HP:0001394	OMIM:118900	IEA				P		HPO:iea	
OMIM	118900	118900 CIRRHOSIS, FAMILIAL		HP:0010702	OMIM:118900	IEA				P		HPO:iea	
OMIM	118900	118900 CIRRHOSIS, FAMILIAL		HP:0200120	OMIM:118900	TAS				P		HPO:skoehler	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0000006	OMIM:118980	IEA				I		HPO:iea	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0000164	OMIM:118980	IEA				P		HPO:iea	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0000218	OMIM:118980	IEA				P		HPO:iea	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0002705	OMIM:118980	TAS				P		HPO:skoehler	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0004322	OMIM:118980	IEA				P		HPO:iea	
OMIM	118980	118980 CLAVICLE, PSEUDARTHROSIS OF, CONGENITAL		HP:0006585	OMIM:118980	TAS				P		HPO:probinson	
OMIM	119000	CLEFT CHIN		HP:0000006	OMIM:119000	IEA				I		HPO:iea	
OMIM	119000	CLEFT CHIN		HP:0000271	OMIM:119000	IEA				P		HPO:iea	
OMIM	119000	CLEFT CHIN		HP:0400001	OMIM:119000	TAS				P		HPO:skoehler	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0000006	OMIM:119100	IEA				I		HPO:iea	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0000378	OMIM:119100	IEA				P		HPO:iea	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0001171	OMIM:119100	TAS				P		HPO:probinson	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0001839	OMIM:119100	TAS				P		HPO:probinson	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0004058	OMIM:119100	TAS				P		HPO:probinson	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0005632	OMIM:119100	IEA				P		HPO:iea	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0006443	OMIM:119100	TAS				P		HPO:probinson	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0006495	OMIM:119100	IEA				P		HPO:iea	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0009460	OMIM:119100	TAS				P		HPO:skoehler	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0009556	OMIM:119100	TAS				P		HPO:probinson	
OMIM	119100	SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1		HP:0010109	OMIM:119100	IEA				P		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000006	OMIM:119300	IEA				I		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000175	OMIM:119300	IEA				P		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000193	OMIM:119300	IEA				P		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000196	OMIM:119300	IEA				P		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000204	OMIM:119300	IEA				P		HPO:iea	
OMIM	119300	VAN DER WOUDE SYNDROME		HP:0000668	OMIM:119300	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000006	OMIM:119500	IEA				I		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000013	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000028	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000046	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000048	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000059	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000175	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000196	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000204	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0000726	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0001762	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0003298	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0008726	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0009754	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0009755	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0009756	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0009757	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0009758	OMIM:119500	IEA				P		HPO:iea	
OMIM	119500	POPLITEAL PTERYGIUM SYNDROME		HP:0010554	OMIM:119500	IEA				P		HPO:iea	
OMIM	119530	%119530 OROFACIAL CLEFT 1; OFC1;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 1;;OROFACIAL CLEFT, NONSYNDROMIC; OFC;;CLEFT LIP/PALATE, NONSYNDROMIC		HP:0000006	OMIM:119530	TAS				I		HPO:probinson	
OMIM	119530	%119530 OROFACIAL CLEFT 1; OFC1;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 1;;OROFACIAL CLEFT, NONSYNDROMIC; OFC;;CLEFT LIP/PALATE, NONSYNDROMIC		HP:0000175	OMIM:119530	TAS				P		HPO:skoehler	
OMIM	119530	%119530 OROFACIAL CLEFT 1; OFC1;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 1;;OROFACIAL CLEFT, NONSYNDROMIC; OFC;;CLEFT LIP/PALATE, NONSYNDROMIC		HP:0000204	OMIM:119530	TAS				P		HPO:probinson	
OMIM	119530	%119530 OROFACIAL CLEFT 1; OFC1;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 1;;OROFACIAL CLEFT, NONSYNDROMIC; OFC;;CLEFT LIP/PALATE, NONSYNDROMIC		HP:0001425	OMIM:119530	TAS				I		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0000006	OMIM:119540	IEA				I		HPO:iea	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0000175	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0000212	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0000347	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0001250	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0002187	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0009102	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119540	#119540 CLEFT PALATE, ISOLATED; CPI;;CLEFT PALATE; CPCLEFT PALATE, ISOLATED, AND MENTAL RETARDATION, INCLUDED		HP:0011094	OMIM:119540	TAS				P		HPO:skoehler	
OMIM	119550	CLEFT PALATE-LATERAL SYNECHIA SYNDROME		HP:0000006	OMIM:119550	IEA				I		HPO:iea	
OMIM	119550	CLEFT PALATE-LATERAL SYNECHIA SYNDROME		HP:0000175	OMIM:119550	IEA				P		HPO:iea	
OMIM	119570	CLEFT SOFT PALATE		HP:0000006	OMIM:119570	IEA				I		HPO:iea	
OMIM	119570	CLEFT SOFT PALATE		HP:0000185	OMIM:119570	IEA				P		HPO:iea	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000006	OMIM:119580	IEA				I		HPO:iea	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000204	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000316	OMIM:119580	IEA				P		HPO:iea	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000348	OMIM:119580	IEA				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000668	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0000698	OMIM:119580	IEA				P		HPO:iea	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0001792	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0002023	OMIM:119580	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0007651	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0008070	OMIM:119580	IEA				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0009743	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0009890	OMIM:119580	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0012368	OMIM:119580	IEA				P		HPO:skoehler	
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0012725	OMIM:119580	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	119580	BLEPHAROCHEILODONTIC SYNDROME 1; BCDS1		HP:0030084	OMIM:119580	TAS				P		HPO:skoehler	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000006	OMIM:119600	IEA				I		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000175	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000242	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000272	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000316	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000347	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000365	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000680	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000696	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000773	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000774	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000882	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000891	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0000894	OMIM:119600	TAS				P		HPO:skoehler	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0001156	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002007	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002643	OMIM:119600	TAS				P		HPO:probinson	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002645	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002650	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002659	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002684	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002688	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002689	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002700	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002705	OMIM:119600	TAS				P		HPO:skoehler	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002738	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002808	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002812	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0002866	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0003183	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0003302	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0003304	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0003396	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0004220	OMIM:119600	TAS				P		HPO:probinson	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0004474	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0005259	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0005280	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0006040	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0006297	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0006660	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0008788	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0008848	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0009577	OMIM:119600	TAS				P		HPO:probinson	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0010230	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0011001	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0011069	OMIM:119600	IEA				P		HPO:iea	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0011800	OMIM:119600	TAS				P		HPO:skoehler	
OMIM	119600	#119600 CLEIDOCRANIAL DYSPLASIA; CCD;;CLEIDOCRANIAL DYSOSTOSIS; CLCDCLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, WITH BRACHYDACTYLY, INCLUDED;;CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED		HP:0100864	OMIM:119600	IEA				P		HPO:skoehler	
OMIM	119650	CLEIDORHIZOMELIC SYNDROME		HP:0000006	OMIM:119650	IEA				I		HPO:iea	
OMIM	119650	CLEIDORHIZOMELIC SYNDROME		HP:0000889	OMIM:119650	TAS				P		HPO:probinson	
OMIM	119650	CLEIDORHIZOMELIC SYNDROME		HP:0004209	OMIM:119650	IEA				P		HPO:iea	
OMIM	119650	CLEIDORHIZOMELIC SYNDROME		HP:0004220	OMIM:119650	TAS				P		HPO:probinson	
OMIM	119650	CLEIDORHIZOMELIC SYNDROME		HP:0008905	OMIM:119650	TAS				P		HPO:probinson	
OMIM	119800	#119800 CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/ORMIRROR-IMAGE POLYDACTYLY; CCF		HP:0000006	OMIM:119800	TAS				I		HPO:skoehler	
OMIM	119800	#119800 CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/ORMIRROR-IMAGE POLYDACTYLY; CCF		HP:0001762	OMIM:119800	IEA				P		HPO:iea	
OMIM	119800	#119800 CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/ORMIRROR-IMAGE POLYDACTYLY; CCF		HP:0001829	OMIM:119800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	119800	#119800 CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/ORMIRROR-IMAGE POLYDACTYLY; CCF		HP:0003065	OMIM:119800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	119800	#119800 CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/ORMIRROR-IMAGE POLYDACTYLY; CCF		HP:0003829	OMIM:119800	TAS				C		HPO:skoehler	
OMIM	119900	DIGITAL CLUBBING, ISOLATED CONGENITAL		HP:0000006	OMIM:119900	IEA				I		HPO:iea	
OMIM	119900	DIGITAL CLUBBING, ISOLATED CONGENITAL		HP:0000007	OMIM:119900	TAS				I		HPO:skoehler	
OMIM	119900	DIGITAL CLUBBING, ISOLATED CONGENITAL		HP:0001217	OMIM:119900	IEA				P		HPO:iea	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000006	OMIM:119915	IEA				I		HPO:iea	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000508	OMIM:119915	IEA				P		HPO:skoehler	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000616	OMIM:119915	IEA				P		HPO:skoehler	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000713	OMIM:119915	IEA				P		HPO:iea	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000969	OMIM:119915	IEA				P		HPO:skoehler	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0000975	OMIM:119915	IEA				P		HPO:skoehler	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0012199	OMIM:119915	TAS				P		HPO:probinson	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0012531	OMIM:119915	TAS				P		HPO:skoehler	
OMIM	119915	CLUSTER HEADACHE, FAMILIAL		HP:0031417	OMIM:119915	IEA				P		HPO:skoehler	
OMIM	120000	COARCTATION OF AORTA		HP:0000006	OMIM:120000	TAS				I		HPO:nvasilevsky	
OMIM	120000	COARCTATION OF AORTA		HP:0001426	OMIM:120000	TAS				I		HPO:nvasilevsky	
OMIM	120000	COARCTATION OF AORTA		HP:0001680	OMIM:120000	IEA				P		HPO:iea	
OMIM	120000	COARCTATION OF AORTA		HP:0004383	OMIM:120000	IEA				P		HPO:iea	
OMIM	120040	COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS		HP:0000006	OMIM:120040	IEA				I		HPO:iea	
OMIM	120040	COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS		HP:0000365	OMIM:120040	IEA				P		HPO:iea	
OMIM	120040	COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS		HP:0000707	OMIM:120040	IEA				P		HPO:iea	
OMIM	120040	COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS		HP:0007834	OMIM:120040	IEA				P		HPO:iea	
OMIM	120050	%120050 COXSACKIEVIRUS B3 SUSCEPTIBILITY; CXB3S;;CB3S		HP:0004429	OMIM:120050	IEA				P		HPO:skoehler	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0000006	OMIM:120100	TAS				I		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0000509	OMIM:120100	TAS				P		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0001917	OMIM:120100	TAS	HP:0003584	HP:0040283		P		HPO:probinson	HP:0040283
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0001954	OMIM:120100	TAS				P		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0001974	OMIM:120100	TAS				P		HPO:skoehler	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0002315	OMIM:120100	TAS				P		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0002829	OMIM:120100	TAS				P		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0003326	OMIM:120100	TAS				P		HPO:probinson	
OMIM	120100	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 1		HP:0003593	OMIM:120100	TAS				C		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000006	PMID:12721955	PCS				I		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000076	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000567	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000568	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000588	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000639	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0000659	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0001510	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0002119	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0007663	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0007957	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0007968	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0012521	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120200	COLOBOMA, OCULAR		HP:0025514	PMID:12721955	PCS				P		HPO:probinson	
OMIM	120300	COLOBOMA OF MACULA		HP:0000006	OMIM:120300	TAS				I		HPO:probinson	
OMIM	120300	COLOBOMA OF MACULA		HP:0001116	OMIM:120300	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000003	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000006	OMIM:120330	IEA				I		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000076	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000085	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000089	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000093	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000407	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000480	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000518	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000533	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000541	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000568	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000588	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000608	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000787	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000969	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000974	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0000977	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0001144	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0001249	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0001250	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0001388	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0002171	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0003593	OMIM:120330	TAS				C		HPO:skoehler	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0003774	OMIM:120330	IEA				P		HPO:iea	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0003774	OMIM:120330	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	120330	PAPILLORENAL SYNDROME		HP:0004712	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0007099	OMIM:120330	TAS				P		HPO:probinson	
OMIM	120330	PAPILLORENAL SYNDROME		HP:0011509	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0012019	OMIM:120330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120330	PAPILLORENAL SYNDROME		HP:0025514	OMIM:120330	TAS				P		HPO:skoehler	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0000006	OMIM:120400	IEA				I		HPO:iea	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0000104	OMIM:120400	TAS				P		HPO:probinson	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0000589	OMIM:120400	TAS				P		HPO:probinson	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0005807	OMIM:120400	TAS				P		HPO:probinson	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0005831	OMIM:120400	IEA				P		HPO:iea	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0005848	OMIM:120400	TAS				P		HPO:skoehler	
OMIM	120400	120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY;;APICAL DYSTROPHY;;SORSBY SYNDROME		HP:0009642	OMIM:120400	TAS				P		HPO:probinson	
OMIM	120430	COLOBOMA OF OPTIC NERVEOPTIC NERVE HEAD PITS, BILATERAL CONGENITAL, INCLUDED		HP:0000006	OMIM:120430	IEA				I		HPO:iea	
OMIM	120430	COLOBOMA OF OPTIC NERVEOPTIC NERVE HEAD PITS, BILATERAL CONGENITAL, INCLUDED		HP:0000541	OMIM:120430	IEA				P		HPO:iea	
OMIM	120430	COLOBOMA OF OPTIC NERVEOPTIC NERVE HEAD PITS, BILATERAL CONGENITAL, INCLUDED		HP:0000588	OMIM:120430	IEA				P		HPO:iea	
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000006	OMIM:120433	TAS				I		HPO:skoehler	
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000175	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000204	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000508	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000518	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000568	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000589	OMIM:120433	IEA				P		HPO:skoehler	
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0000790	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120433	COLOBOMA, OCULAR, WITH OR WITHOUT HEARING IMPAIRMENT, CLEFT LIP/PALATE, AND/OR MENTAL RETARDATION; COB1		HP:0001249	OMIM:120433	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	120435	LYNCH SYNDROME I		HP:0000006	OMIM:120435	TAS				I		HPO:skoehler	
OMIM	120435	LYNCH SYNDROME I		HP:0003003	OMIM:120435	TAS				P		HPO:probinson	
OMIM	120440	COLONIC VARICES WITHOUT PORTAL HYPERTENSION		HP:0000006	OMIM:120440	TAS				I		HPO:skoehler	
OMIM	120440	COLONIC VARICES WITHOUT PORTAL HYPERTENSION		HP:0002584	OMIM:120440	TAS				P		HPO:probinson	
OMIM	120440	COLONIC VARICES WITHOUT PORTAL HYPERTENSION		HP:0012550	OMIM:120440	TAS				P		HPO:probinson	
OMIM	120450	COMEDONES, FAMILIAL DYSKERATOTIC		HP:0000006	OMIM:120450	IEA				I		HPO:iea	
OMIM	120450	COMEDONES, FAMILIAL DYSKERATOTIC		HP:0000951	OMIM:120450	IEA				P		HPO:iea	
OMIM	120500	COMMISSURAL LIP PITS		HP:0000006	OMIM:120500	IEA				I		HPO:iea	
OMIM	120500	COMMISSURAL LIP PITS		HP:0002710	OMIM:120500	IEA				P		HPO:iea	
OMIM	120500	COMMISSURAL LIP PITS		HP:0004467	OMIM:120500	IEA				P		HPO:iea	
OMIM	120502	BRANCHIOOTIC SYNDROME 2		HP:0000006	OMIM:120502	TAS				I		HPO:skoehler	
OMIM	120502	BRANCHIOOTIC SYNDROME 2		HP:0000365	OMIM:120502	TAS				P		HPO:skoehler	
OMIM	120502	BRANCHIOOTIC SYNDROME 2		HP:0000377	OMIM:120502	TAS				P		HPO:skoehler	
OMIM	120502	BRANCHIOOTIC SYNDROME 2		HP:0002710	OMIM:120502	TAS				P		HPO:skoehler	
OMIM	120502	BRANCHIOOTIC SYNDROME 2		HP:0004467	OMIM:120502	TAS				P		HPO:skoehler	
OMIM	120790	COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF		HP:0000006	OMIM:120790	IEA				I		HPO:iea	
OMIM	120790	COMPLEMENT COMPONENT 4, PARTIAL DEFICIENCY OF		HP:0002725	OMIM:120790	IEA				P		HPO:iea	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000006	PMID:9610810	PCS				I		HPO:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000512	PMID:24136862	PCS				P		HP:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000533	OMIM:120970	TAS				P		HPO:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000548	PMID:9610810	PCS				P		HPO:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000551	PMID:9610810	PCS	HP:0003621	HP:0040284		P		HPO:skoehler	7/7
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000603	PMID:7864751	PCS				P		HP:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000618	OMIM:120970	TAS				P		HPO:skoehler	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0000662	PMID:7864751	PCS	HP:0011462			P		HPO:probinson	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0001133	PMID:9610810	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0007663	PMID:9610810	PCS	HP:0003621	HP:0040284		P		HPO:probinson	7/7
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0007722	PMID:15531334	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0007737	PMID:15531334	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0007994	OMIM:120970	TAS				P		HPO:skoehler	
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0011509	PMID:24136862	PCS		HP:0040284		P		HP:probinson	7/7
OMIM	120970	CONE-ROD DYSTROPHY 2		HP:0012508	PMID:15531334	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000006	OMIM:121050	IEA				I		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000218	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000248	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000268	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000347	OMIM:121050	TAS		HP:0040284		P		HPO:probinson	27%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000470	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000545	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000768	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0000938	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001083	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001166	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001181	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001270	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001519	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001629	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001631	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001634	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001643	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001647	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001653	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001762	OMIM:121050	IEA		HP:0040284		P		HPO:probinson	32%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0001840	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0002007	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0002616	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0002751	OMIM:121050	TAS	HP:0003577	HP:0040284		P		HPO:probinson	45%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0002987	OMIM:121050	TAS		HP:0040284		P		HPO:probinson	86%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0002999	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0003273	OMIM:121050	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0005684	OMIM:121050	IEA				P		HPO:skoehler	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0006380	OMIM:121050	TAS		HP:0040284		P		HPO:probinson	81%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0008453	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0008962	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0009465	OMIM:121050	IEA				P		HPO:iea	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0009901	OMIM:121050	TAS		HP:0040284		P		HPO:probinson	78%
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0010499	OMIM:121050	IEA				P		HPO:skoehler	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0030799	OMIM:121050	TAS				P		HPO:skoehler	
OMIM	121050	ARTHROGRYPOSIS, DISTAL, TYPE 9		HP:0100490	OMIM:121050	IEA				P		HPO:iea	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0000006	OMIM:121070	IEA				I		HPO:iea	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0000160	OMIM:121070	IEA				P		HPO:iea	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0000211	OMIM:121070	TAS				P		HPO:skoehler	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E	HP:0012825	HP:0000252	OMIM:121070	TAS				P		HPO:probinson	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0000347	OMIM:121070	IEA				P		HPO:iea	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0001762	OMIM:121070	IEA				P		HPO:iea	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0002804	OMIM:121070	IEA				P		HPO:skoehler	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0005684	OMIM:121070	TAS				P		HPO:probinson	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E	HP:0012828	HP:0009473	OMIM:121070	TAS				P		HPO:probinson	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0011234	OMIM:121070	TAS				P		HPO:probinson	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E		HP:0040196	OMIM:121070	TAS				P		HPO:skoehler	
OMIM	121070	ARTHROGRYPOSIS, DISTAL, TYPE 2E	HP:0012828	HP:0100492	OMIM:121070	TAS				P		HPO:probinson	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0000006	OMIM:121200	TAS				I		HPO:probinson	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0000007	OMIM:121200	TAS		HP:0040283		I		HPO:skoehler	HP:0040283
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0001263	OMIM:121200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0001270	OMIM:121200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0001425	OMIM:121200	TAS				I		HPO:skoehler	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0002069	OMIM:121200	TAS				P		HPO:probinson	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0002266	OMIM:121200	TAS				P		HPO:probinson	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0002373	OMIM:121200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0002411	OMIM:121200	TAS				P		HPO:skoehler	
OMIM	121200	#121200 SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1EPILEPSY, BENIGN NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED;;SEIZURES, BENIGN FAMILIAL NEONATAL, 1, AND/OR MYOKYMIA, INCLUDED		HP:0003623	OMIM:121200	TAS				C		HPO:skoehler	
OMIM	121201	EPILEPSY, BENIGN NEONATAL, 2		HP:0000006	OMIM:121201	TAS				I		HPO:probinson	
OMIM	121201	EPILEPSY, BENIGN NEONATAL, 2		HP:0002069	OMIM:121201	TAS	HP:0003623			P		HPO:probinson	
OMIM	121201	EPILEPSY, BENIGN NEONATAL, 2		HP:0002266	OMIM:121201	TAS				P		HPO:probinson	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0000006	OMIM:121210	IEA				I		HPO:iea	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0001425	OMIM:121210	TAS				I		HPO:skoehler	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0002069	OMIM:121210	IEA				P		HPO:iea	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0002373	OMIM:121210	IEA				P		HPO:iea	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0010818	OMIM:121210	IEA				P		HPO:iea	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0010819	OMIM:121210	IEA				P		HPO:iea	
OMIM	121210	%121210 FEBRILE SEIZURES, FAMILIAL, 1; FEB1;;CONVULSIONS, FAMILIAL FEBRILE;  1		HP:0011463	OMIM:121210	IEA				C		HPO:iea	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0000006	OMIM:121270	TAS				I		HPO:nvasilevsky	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0000924	OMIM:121270	IEA				P		HPO:iea	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0001051	OMIM:121270	IEA				P		HPO:iea	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0001250	OMIM:121270	IEA				P		HPO:iea	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0001417	OMIM:121270	TAS				I		HPO:nvasilevsky	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0001508	OMIM:121270	IEA				P		HPO:iea	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN	HP:0012825	HP:0001903	OMIM:121270	TAS				P		HPO:nvasilevsky	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0002212	OMIM:121270	TAS				P		HPO:probinson	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0002234	OMIM:121270	TAS				P		HPO:probinson	
OMIM	121270	COPPER DEFICIENCY, FAMILIAL BENIGN		HP:0011967	OMIM:121270	TAS				P		HPO:probinson	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000006	OMIM:121300	IEA				I		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000716	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000738	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000739	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000822	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000952	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0000992	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0001289	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0001649	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0001744	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0001939	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002013	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002014	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002019	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002027	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002203	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0002240	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0003489	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0003829	OMIM:121300	TAS				C		HPO:skoehler	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0004804	OMIM:121300	IEA				P		HPO:iea	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0009830	OMIM:121300	TAS				P		HPO:probinson	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0011999	OMIM:121300	TAS				P		HPO:skoehler	
OMIM	121300	#121300 COPROPORPHYRIA, HEREDITARY; HCP;;COPROPORPHYRINOGEN OXIDASE DEFICIENCY;;CPOX DEFICIENCY;;CPO DEFICIENCY;;CPX DEFICIENCYHARDEROPORPHYRIA, INCLUDED		HP:0100785	OMIM:121300	TAS				P		HPO:skoehler	
OMIM	121350	CORACOCLAVICULAR JOINT, ANOMALOUS		HP:0000006	OMIM:121350	IEA				I		HPO:iea	
OMIM	121350	CORACOCLAVICULAR JOINT, ANOMALOUS		HP:0001367	OMIM:121350	IEA				P		HPO:iea	
OMIM	121390	CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS		HP:0000006	OMIM:121390	IEA				I		HPO:iea	
OMIM	121390	CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS		HP:0000505	OMIM:121390	IEA				P		HPO:iea	
OMIM	121390	CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS		HP:0001134	OMIM:121390	IEA				P		HPO:iea	
OMIM	121400	%121400 CORNEA PLANA 1; CNA1		HP:0000006	OMIM:121400	TAS				I		HPO:skoehler	
OMIM	121400	%121400 CORNEA PLANA 1; CNA1		HP:0000007	OMIM:121400	TAS				I		HPO:skoehler	
OMIM	121400	%121400 CORNEA PLANA 1; CNA1		HP:0007720	OMIM:121400	IEA				P		HPO:iea	
OMIM	121450	121450 CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS;;BAND KERATOPATHY WITH DEAFNESS		HP:0000006	OMIM:121450	IEA				I		HPO:iea	
OMIM	121450	121450 CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS;;BAND KERATOPATHY WITH DEAFNESS		HP:0000365	OMIM:121450	IEA				P		HPO:iea	
OMIM	121450	121450 CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS;;BAND KERATOPATHY WITH DEAFNESS		HP:0000585	OMIM:121450	IEA				P		HPO:iea	
OMIM	121450	121450 CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS;;BAND KERATOPATHY WITH DEAFNESS		HP:0200066	OMIM:121450	TAS				P		HPO:skoehler	
OMIM	121800	CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER		HP:0000006	OMIM:121800	IEA				I		HPO:iea	
OMIM	121800	CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER		HP:0001131	OMIM:121800	IEA				P		HPO:skoehler	
OMIM	121800	CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER		HP:0007760	OMIM:121800	IEA				P		HPO:iea	
OMIM	121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE		HP:0000006	OMIM:121820	IEA				I		HPO:iea	
OMIM	121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE		HP:0000495	OMIM:121820	IEA				P		HPO:skoehler	
OMIM	121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE		HP:0001131	OMIM:121820	IEA				P		HPO:skoehler	
OMIM	121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE		HP:0007690	OMIM:121820	IEA				P		HPO:iea	
OMIM	121850	CORNEAL FLECK DYSTROPHY		HP:0000006	OMIM:121850	IEA				I		HPO:iea	
OMIM	121850	CORNEAL FLECK DYSTROPHY		HP:0000613	OMIM:121850	IEA				P		HPO:skoehler	
OMIM	121850	CORNEAL FLECK DYSTROPHY		HP:0007962	OMIM:121850	IEA				P		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0000006	OMIM:121900	IEA				I		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0000486	OMIM:121900	IEA				P		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0000518	OMIM:121900	IEA				P		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0007802	OMIM:121900	IEA				P		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0007809	OMIM:121900	IEA				P		HPO:iea	
OMIM	121900	GROENOUW TYPE I CORNEAL DYSTROPHY		HP:0007827	OMIM:121900	IEA				P		HPO:iea	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0000006	PMID:26749309	PCS				I		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0000501	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0000585	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0000613	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0001089	OMIM:122000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0007915	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0009918	OMIM:122000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0009926	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0011483	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0025358	PMID:26749309	PCS				P		HPO:probinson	
OMIM	122000	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1		HP:0031159	PMID:26749309	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0000006	OMIM:122100	TAS				I		HPO:probinson	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0000613	OMIM:122100	TAS				P		HPO:skoehler	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0001131	OMIM:122100	TAS				P		HPO:probinson	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0003680	OMIM:122100	TAS				C		HPO:probinson	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0007663	OMIM:122100	TAS				P		HPO:skoehler	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0007856	OMIM:122100	TAS				P		HPO:probinson	
OMIM	122100	CORNEAL DYSTROPHY, MEESMANN		HP:0009926	OMIM:122100	TAS				P		HPO:skoehler	
OMIM	122200	CORNEAL DYSTROPHY, LATTICE TYPE I		HP:0000006	OMIM:122200	IEA				I		HPO:iea	
OMIM	122200	CORNEAL DYSTROPHY, LATTICE TYPE I		HP:0000495	OMIM:122200	IEA				P		HPO:iea	
OMIM	122200	CORNEAL DYSTROPHY, LATTICE TYPE I		HP:0000529	OMIM:122200	IEA				P		HPO:iea	
OMIM	122200	CORNEAL DYSTROPHY, LATTICE TYPE I		HP:0001149	OMIM:122200	TAS				P		HPO:probinson	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0000006	OMIM:122400	IEA				I		HPO:iea	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0000505	OMIM:122400	TAS				P		HPO:skoehler	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0000613	OMIM:122400	TAS				P		HPO:skoehler	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0009926	OMIM:122400	TAS				P		HPO:skoehler	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0012531	OMIM:122400	TAS				P		HPO:skoehler	
OMIM	122400	EPITHELIAL RECURRENT EROSION DYSTROPHY		HP:0200020	OMIM:122400	IEA				P		HPO:skoehler	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000006	OMIM:122430	IEA				I		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000272	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000316	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000369	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000407	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000463	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000491	OMIM:122430	IEA				P		HPO:skoehler	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000505	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0000582	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0001249	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0001508	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0001595	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0001643	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0002007	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0004322	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0005280	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0007663	OMIM:122430	TAS				P		HPO:skoehler	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0007980	OMIM:122430	IEA				P		HPO:iea	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0011229	OMIM:122430	TAS				P		HPO:skoehler	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0011800	OMIM:122430	TAS				P		HPO:skoehler	
OMIM	122430	122430 CORNEAL HYPESTHESIA WITH RETINAL ABNORMALITIES, SENSORINEURAL DEAFNESS,UNUSUAL FACIES, PERSISTENT DUCTUS ARTERIOSUS, AND MENTAL RETARDATION;;RAMOS-ARROYO SYNDROME		HP:0012155	OMIM:122430	IEA				P		HPO:skoehler	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0000006	OMIM:122440	IEA				I		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0000164	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0000613	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0000972	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0001019	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0001131	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0001156	OMIM:122440	TAS				P		HPO:skoehler	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0001622	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0001806	OMIM:122440	IEA				P		HPO:skoehler	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0004322	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0009882	OMIM:122440	IEA				P		HPO:iea	
OMIM	122440	CORNEODERMATOOSSEOUS SYNDROME		HP:0011085	OMIM:122440	TAS				P		HPO:skoehler	
OMIM	122450	%122450 CORNEAL HYPESTHESIA, FAMILIAL;;TRIGEMINAL ANESTHESIA, FAMILIAL		HP:0000006	OMIM:122450	IEA				I		HPO:iea	
OMIM	122450	%122450 CORNEAL HYPESTHESIA, FAMILIAL;;TRIGEMINAL ANESTHESIA, FAMILIAL		HP:0000495	OMIM:122450	IEA				P		HPO:iea	
OMIM	122450	%122450 CORNEAL HYPESTHESIA, FAMILIAL;;TRIGEMINAL ANESTHESIA, FAMILIAL		HP:0000924	OMIM:122450	IEA				P		HPO:iea	
OMIM	122450	%122450 CORNEAL HYPESTHESIA, FAMILIAL;;TRIGEMINAL ANESTHESIA, FAMILIAL		HP:0012155	OMIM:122450	TAS				P		HPO:skoehler	
OMIM	122455	CORONARY ARTERY DISSECTION, SPONTANEOUS		HP:0000006	OMIM:122455	IEA				I		HPO:iea	
OMIM	122455	CORONARY ARTERY DISSECTION, SPONTANEOUS		HP:0001939	OMIM:122455	IEA				P		HPO:iea	
OMIM	122455	CORONARY ARTERY DISSECTION, SPONTANEOUS		HP:0006702	OMIM:122455	IEA				P		HPO:iea	
OMIM	122460	CORONAVIRUS 229E SUSCEPTIBILITY		HP:0000006	OMIM:122460	IEA				I		HPO:iea	
OMIM	122460	CORONAVIRUS 229E SUSCEPTIBILITY		HP:0005396	OMIM:122460	IEA				P		HPO:iea	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000006	OMIM:122470	IEA				I		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000023	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000028	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000047	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000050	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000059	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000076	OMIM:122470	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000086	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000089	OMIM:122470	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000093	OMIM:122470	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000107	OMIM:122470	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000175	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000204	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000218	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000219	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000219	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000248	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000252	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000343	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000347	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000369	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000388	OMIM:122470	IEA				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000405	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000407	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000453	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000463	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000470	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000482	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000483	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000486	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000508	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000520	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000527	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000545	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000588	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000639	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000648	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000664	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000684	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000687	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000708	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000750	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000776	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000879	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000954	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0000965	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001007	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001180	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001249	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001250	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001276	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001377	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001511	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001551	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001612	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001629	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0001873	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002020	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002021	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002036	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002090	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002162	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002553	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002557	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002705	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002714	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002750	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002983	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002984	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0002987	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0003083	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0003083	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0003745	OMIM:122470	IEA				I		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0003997	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0004209	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0004322	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0004691	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0004785	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0005217	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0005280	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0005565	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0005815	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0007665	OMIM:122470	TAS				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0009623	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0009829	OMIM:122470	IEA				P		HPO:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0031228	PMID:19764039	IEA				P		HP:probinson	
OMIM	122470	CORNELIA DE LANGE SYNDROME 1		HP:0100716	OMIM:122470	TAS				P		HPO:skoehler	
OMIM	122580	COSTOCORACOID LIGAMENT, CONGENITALLY SHORT		HP:0000006	OMIM:122580	IEA				I		HPO:iea	
OMIM	122580	COSTOCORACOID LIGAMENT, CONGENITALLY SHORT		HP:0000782	OMIM:122580	IEA				P		HPO:skoehler	
OMIM	122580	COSTOCORACOID LIGAMENT, CONGENITALLY SHORT		HP:0001435	OMIM:122580	IEA				P		HPO:skoehler	
OMIM	122580	COSTOCORACOID LIGAMENT, CONGENITALLY SHORT		HP:0200021	OMIM:122580	IEA				P		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000006	PMID:23335591	PCS				I		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000007	OMIM:122600	TAS				I		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000470	OMIM:122600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000768	OMIM:122600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000913	OMIM:122600	TAS				P		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0000921	OMIM:122600	TAS				P		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0002650	PMID:23335591	PCS				P		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0002937	PMID:23335591	PCS				P		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0002948	PMID:23335591	PCS				P		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0003316	OMIM:122600	TAS				P		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0003396	OMIM:122600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0003419	OMIM:122600	TAS				P		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0003510	OMIM:122600	TAS				P		HPO:skoehler	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0003521	PMID:23335591	PCS				P		HPO:probinson	
OMIM	122600	SPONDYLOCOSTAL DYSOSTOSIS 5		HP:0005815	OMIM:122600	TAS				P		HPO:skoehler	
OMIM	122700	COUMARIN RESISTANCE		HP:0000006	OMIM:122700	IEA				I		HPO:iea	
OMIM	122700	COUMARIN RESISTANCE		HP:0001871	OMIM:122700	IEA				P		HPO:iea	
OMIM	122700	COUMARIN RESISTANCE		HP:0001939	OMIM:122700	IEA				P		HPO:iea	
OMIM	122750	COXA VARA		HP:0000006	OMIM:122750	IEA				I		HPO:iea	
OMIM	122750	COXA VARA		HP:0002812	OMIM:122750	IEA				P		HPO:iea	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0000006	OMIM:122780	TAS				I		HPO:nvasilevsky	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0000365	OMIM:122780	IEA				P		HPO:iea	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0001423	OMIM:122780	TAS				I		HPO:nvasilevsky	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0002827	OMIM:122780	IEA				P		HPO:iea	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0004322	OMIM:122780	IEA				P		HPO:iea	
OMIM	122780	COXOAURICULAR SYNDROME		HP:0008551	OMIM:122780	IEA				P		HPO:iea	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0000006	OMIM:122850	IEA				I		HPO:iea	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0000275	OMIM:122850	TAS				P		HPO:probinson	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0001629	OMIM:122850	IEA				P		HPO:iea	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0001642	OMIM:122850	IEA				P		HPO:iea	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0005679	OMIM:122850	IEA				P		HPO:iea	
OMIM	122850	CRANIOACROFACIAL SYNDROME		HP:0005922	OMIM:122850	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000006	OMIM:122860	TAS				I		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000256	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000303	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000316	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000365	OMIM:122860	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000431	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000452	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000529	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000648	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0000900	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0001085	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0001349	OMIM:122860	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0002315	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0002516	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0003034	OMIM:122860	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0003155	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0003165	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0003593	OMIM:122860	TAS				C		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0003676	OMIM:122860	TAS				C		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0004322	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0004493	OMIM:122860	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0005280	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0005464	OMIM:122860	TAS				P		HPO:probinson	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0005652	OMIM:122860	IEA				P		HPO:skoehler	
OMIM	122860	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CDD		HP:0011120	OMIM:122860	TAS				P		HPO:skoehler	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0000006	OMIM:122880	IEA				I		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0000272	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0000316	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0000327	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0000407	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0001193	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0003196	OMIM:122880	IEA				P		HPO:iea	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0009487	OMIM:122880	TAS				P		HPO:skoehler	
OMIM	122880	CRANIOFACIAL-DEAFNESS-HAND SYNDROME; CDHS		HP:0012368	OMIM:122880	TAS				P		HPO:skoehler	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0000006	OMIM:122900	IEA				I		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0000248	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0000252	OMIM:122900	TAS				P		HPO:skoehler	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0000520	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0000767	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0001156	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0002751	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0002983	OMIM:122900	TAS				P		HPO:skoehler	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0004322	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0004439	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0005665	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0009826	OMIM:122900	IEA				P		HPO:iea	
OMIM	122900	CRANIOFACIAL DYSOSTOSIS WITH DIAPHYSEAL HYPERPLASIA		HP:0010539	OMIM:122900	TAS				P		HPO:skoehler	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:123000	IEA				I		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000256	OMIM:123000	TAS				P		HPO:skoehler	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000303	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000316	OMIM:123000	TAS				P		HPO:skoehler	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000410	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000692	OMIM:123000	TAS				P		HPO:probinson	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0000925	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0001739	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0001742	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0002644	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0002694	OMIM:123000	TAS				P		HPO:probinson	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0003016	OMIM:123000	TAS				P		HPO:probinson	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0004407	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0004975	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0005450	OMIM:123000	TAS				P		HPO:probinson	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0006384	OMIM:123000	IEA				P		HPO:iea	
OMIM	123000	CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT		HP:0010628	OMIM:123000	IEA				P		HPO:iea	
OMIM	123050	CRANIORHINY		HP:0000006	OMIM:123050	IEA				I		HPO:iea	
OMIM	123050	CRANIORHINY		HP:0000262	OMIM:123050	IEA				P		HPO:iea	
OMIM	123050	CRANIORHINY		HP:0000263	OMIM:123050	TAS				P		HPO:skoehler	
OMIM	123050	CRANIORHINY		HP:0000445	OMIM:123050	TAS				P		HPO:skoehler	
OMIM	123050	CRANIORHINY		HP:0000463	OMIM:123050	TAS				P		HPO:skoehler	
OMIM	123050	CRANIORHINY		HP:0001007	OMIM:123050	IEA				P		HPO:skoehler	
OMIM	123050	CRANIORHINY		HP:0001363	OMIM:123050	IEA				P		HPO:iea	
OMIM	123100	CRANIOSYNOSTOSIS 1		HP:0000006	OMIM:123100	IEA				I		HPO:probinson	
OMIM	123100	CRANIOSYNOSTOSIS 1		HP:0000262	OMIM:123100	IEA				P		HPO:probinson	
OMIM	123100	CRANIOSYNOSTOSIS 1		HP:0000263	OMIM:123100	TAS				P		HPO:skoehler	
OMIM	123100	CRANIOSYNOSTOSIS 1		HP:0001363	OMIM:123100	TAS				P		HPO:probinson	
OMIM	123100	CRANIOSYNOSTOSIS 1		HP:0030799	OMIM:123100	TAS				P		HPO:skoehler	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0000006	OMIM:123150	IEA				I		HPO:iea	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0000272	OMIM:123150	IEA				P		HPO:iea	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0001363	OMIM:123150	IEA				P		HPO:iea	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0001783	OMIM:123150	TAS				P		HPO:probinson	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0004691	OMIM:123150	IEA				P		HPO:iea	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0008080	OMIM:123150	TAS				P		HPO:probinson	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0008122	OMIM:123150	IEA				P		HPO:iea	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0010055	OMIM:123150	TAS				P		HPO:probinson	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0010743	OMIM:123150	TAS				P		HPO:probinson	
OMIM	123150	#123150 JACKSON-WEISS SYNDROME; JWS;;CRANIOSYNOSTOSIS, MIDFACIAL HYPOPLASIA, AND FOOT ABNORMALITIES		HP:0011800	OMIM:123150	TAS				P		HPO:skoehler	
OMIM	123155	CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS		HP:0000006	OMIM:123155	TAS				I		HPO:skoehler	
OMIM	123155	CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS		HP:0000238	OMIM:123155	TAS				P		HPO:skoehler	
OMIM	123155	CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS		HP:0001305	OMIM:123155	TAS				P		HPO:skoehler	
OMIM	123155	CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS		HP:0004442	OMIM:123155	TAS				P		HPO:skoehler	
OMIM	123155	CRANIOSYNOSTOSIS, SAGITTAL, WITH DANDY-WALKER MALFORMATION AND HYDROCEPHALUS		HP:0007291	OMIM:123155	TAS				P		HPO:skoehler	
OMIM	123270	123270 CREATINE KINASE, BRAIN TYPE, ECTOPIC EXPRESSION OF; CKBE		HP:0012113	OMIM:123270	IEA				P		HPO:skoehler	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0000006	OMIM:123320	IEA				I		HPO:iea	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003236	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003326	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003394	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003458	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003560	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003710	OMIM:123320	IEA				P		HPO:iea	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003737	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0003750	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0004303	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0009071	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123320	CREATINE PHOSPHOKINASE, ELEVATED SERUM		HP:0012378	PMID:9660505	PCS				P		HPO:lccarmody	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000006	OMIM:123400	TAS				I		HPO:probinson	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000505	OMIM:123400	TAS				P		HPO:probinson	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000605	OMIM:123400	TAS				P		HPO:probinson	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000716	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000726	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000737	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000738	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000739	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000741	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000746	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0000751	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0001269	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0001289	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0001317	OMIM:123400	IEA				P		HPO:skoehler	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0001336	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0002066	OMIM:123400	TAS				P		HPO:probinson	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0002354	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0002381	OMIM:123400	TAS				P		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD	HP:0012825	HP:0002922	OMIM:123400	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0003678	OMIM:123400	TAS				C		HPO:iea	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0005327	OMIM:123400	TAS				P		HPO:probinson	
OMIM	123400	CREUTZFELDT-JAKOB DISEASE; CJD		HP:0007076	OMIM:123400	TAS				P		HPO:probinson	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000023	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000028	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000047	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000077	PMID:16953888;PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000179	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000193	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000202	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000218	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000252	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000273	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000275	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000276	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000286	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000308	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000311	PMID:16953888;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000316	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000322	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000324	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000336	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000365	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000369	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000377	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000384	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000402	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000431	PMID:1695388	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000470	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000486	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000494	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000518	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000545	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000648	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000717	PMID:18564888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000718	PMID:11869383	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000733	PMID:11869383	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000736	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000739	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000742	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000750	PMID:10355811	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000752	PMID:16953888;PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0000954	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001042	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001159	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001249	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001276	PMID:20038906	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001319	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001510	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001518	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001540	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001763	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0001840	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002020	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002216	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002355	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002650	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002714	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0002795	PMID:20038906	PCS	HP:0003623			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0003745	ISBN-13:978-0721606156	PCS				I		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0005437	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0008872	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0009102	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0010049	PMID:16953888	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0010529	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0010743	PMID:16953888	PCS	HP:0003621			P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0010780	PMID:20038906	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0010865	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0030680	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0100024	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0100025	PMID:8957962	PCS				P		HPO:iea	
OMIM	123450	CRI-DU-CHAT SYNDROME		HP:0200046	PMID:1695388	PCS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000006	OMIM:123500	IEA				I		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000248	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000303	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000316	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000327	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000405	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000413	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000486	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000491	OMIM:123500	IEA				P		HPO:skoehler	
OMIM	123500	CROUZON SYNDROME		HP:0000505	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000509	OMIM:123500	TAS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000586	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000648	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0000678	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0001249	OMIM:123500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	123500	CROUZON SYNDROME		HP:0001250	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0001739	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0002007	OMIM:123500	PCS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0003319	OMIM:123500	IEA				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0004439	OMIM:123500	IEA				P		HPO:skoehler	
OMIM	123500	CROUZON SYNDROME		HP:0004440	OMIM:123500	PCS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0004442	OMIM:123500	PCS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0004443	OMIM:123500	PCS				P		HPO:iea	
OMIM	123500	CROUZON SYNDROME		HP:0010535	OMIM:123500	TAS				P		HPO:skoehler	
OMIM	123500	CROUZON SYNDROME		HP:0100621	OMIM:123500	TAS				P		HPO:skoehler	
OMIM	123540	CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY		HP:0000006	OMIM:123540	IEA				I		HPO:iea	
OMIM	123540	CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY		HP:0000790	OMIM:123540	IEA				P		HPO:iea	
OMIM	123540	CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY		HP:0001063	OMIM:123540	TAS				P		HPO:probinson	
OMIM	123540	CRYOFIBRINOGENEMIA, FAMILIAL PRIMARY		HP:0008695	OMIM:123540	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0000006	OMIM:123550	IEA				I		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0000093	OMIM:123550	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0000790	OMIM:123550	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0000822	OMIM:123550	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0001871	OMIM:123550	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0003259	OMIM:123550	IEA				P		HPO:iea	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0012050	OMIM:123550	TAS				P		HPO:skoehler	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0012622	OMIM:123550	TAS				P		HPO:skoehler	
OMIM	123550	%123550 CRYOGLOBULINEMIA, FAMILIAL MIXED;;MELTZER SYNDROME		HP:0100778	OMIM:123550	TAS				P		HPO:skoehler	
OMIM	123557	CRYPTOTIA, FAMILIAL		HP:0000006	OMIM:123557	IEA				I		HPO:iea	
OMIM	123557	CRYPTOTIA, FAMILIAL		HP:0011252	OMIM:123557	IEA				P		HPO:skoehler	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0000006	OMIM:123560	TAS				I		HPO:probinson	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0000041	OMIM:123560	TAS				P		HPO:probinson	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0000048	OMIM:123560	TAS				P		HPO:probinson	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0001800	OMIM:123560	TAS				P		HPO:probinson	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0005872	OMIM:123560	TAS				P		HPO:probinson	
OMIM	123560	123560 CRYPTOMICROTIA-BRACHYDACTYLY SYNDROME		HP:0008551	OMIM:123560	TAS				P		HPO:probinson	
OMIM	123570	CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED		HP:0000006	OMIM:123570	IEA				I		HPO:iea	
OMIM	123570	CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED		HP:0000501	OMIM:123570	IEA				P		HPO:iea	
OMIM	123570	CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED		HP:0000568	OMIM:123570	IEA				P		HPO:iea	
OMIM	123570	CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED		HP:0001126	OMIM:123570	IEA				P		HPO:iea	
OMIM	123570	CRYPTOPHTHALMOS, UNILATERAL OR BILATERAL, ISOLATED		HP:0009755	OMIM:123570	IEA				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0000006	OMIM:123700	TAS				I		HPO:probinson	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0000023	OMIM:123700	IEA				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0000271	OMIM:123700	IEA				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0001425	OMIM:123700	TAS				I		HPO:skoehler	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0001582	OMIM:123700	IEA				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0001653	OMIM:123700	TAS				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0001659	OMIM:123700	TAS				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0002097	OMIM:123700	TAS				P		HPO:iea	
OMIM	123700	#123700 CUTIS LAXA, AUTOSOMAL DOMINANT 1; ADCL1		HP:0007495	OMIM:123700	TAS				P		HPO:probinson	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000006	OMIM:123790	IEA				I		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000048	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000189	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000238	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000272	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000316	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000368	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000452	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000453	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000494	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000520	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0000956	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001263	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001274	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001363	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001377	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001545	OMIM:123790	TAS				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0001792	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0002098	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0002676	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0003246	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0004450	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0007517	OMIM:123790	IEA				P		HPO:iea	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0010609	OMIM:123790	IEA				P		HPO:skoehler	
OMIM	123790	BEARE-STEVENSON CUTIS GYRATA SYNDROME; BSTVS		HP:0011800	OMIM:123790	TAS				P		HPO:skoehler	
OMIM	123880	CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE		HP:0000006	OMIM:123880	IEA				I		HPO:iea	
OMIM	123880	CYSTIC ANGIOMATOSIS OF BONE, DIFFUSE		HP:0002833	OMIM:123880	IEA				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000007	OMIM:124000	IEA				I		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000365	OMIM:124000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000510	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000518	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000712	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000716	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0000738	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001249	OMIM:124000	IEA				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001250	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001251	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001252	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001257	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001263	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001272	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001290	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001324	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001347	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001396	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001410	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001414	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001427	OMIM:124000	IEA				I		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001508	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001639	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001942	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001943	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0001970	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0002059	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0002151	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0002299	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0002353	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0002910	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003128	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003200	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003201	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003256	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003355	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003546	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0003593	OMIM:124000	TAS				C		HPO:skoehler	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0004298	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0006558	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0006789	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0008872	OMIM:124000	IEA				P		HPO:iea	
OMIM	124000	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1		HP:0030151	OMIM:124000	TAS				P		HPO:skoehler	
OMIM	124060	CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2		HP:0000006	OMIM:124060	IEA				I		HPO:iea	
OMIM	124060	CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2		HP:0001939	OMIM:124060	IEA				P		HPO:iea	
OMIM	124100	DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY		HP:0000112	OMIM:124100	IEA				P		HPO:skoehler	
OMIM	124200	DARIER-WHITE DISEASE		HP:0000006	OMIM:124200	IEA				I		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0000989	OMIM:124200	TAS				P		HPO:probinson	
OMIM	124200	DARIER-WHITE DISEASE		HP:0001034	OMIM:124200	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	124200	DARIER-WHITE DISEASE		HP:0001250	OMIM:124200	IEA				P		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0001256	OMIM:124200	IEA				P		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0001807	OMIM:124200	IEA				P		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0007302	OMIM:124200	IEA				P		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0008410	OMIM:124200	IEA				P		HPO:iea	
OMIM	124200	DARIER-WHITE DISEASE		HP:0010610	OMIM:124200	IEA				P		HPO:skoehler	
OMIM	124200	DARIER-WHITE DISEASE		HP:0010612	OMIM:124200	IEA				P		HPO:skoehler	
OMIM	124200	DARIER-WHITE DISEASE		HP:0011801	OMIM:124200	TAS				P		HPO:probinson	
OMIM	124200	DARIER-WHITE DISEASE		HP:0100753	OMIM:124200	TAS				P		HPO:skoehler	
OMIM	124200	DARIER-WHITE DISEASE		HP:0200016	OMIM:124200	IEA				P		HPO:skoehler	
OMIM	124300	DARWINIAN POINT OF PINNA		HP:0000006	OMIM:124300	IEA				I		HPO:iea	
OMIM	124300	DARWINIAN POINT OF PINNA		HP:0000598	OMIM:124300	IEA				P		HPO:iea	
OMIM	124400	DARWINIAN TUBERCLE OF PINNA		HP:0000006	OMIM:124400	IEA				I		HPO:iea	
OMIM	124400	DARWINIAN TUBERCLE OF PINNA		HP:0000598	OMIM:124400	IEA				P		HPO:iea	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:124480	TAS				I		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0000407	OMIM:124480	TAS				P		HPO:probinson	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0000698	OMIM:124480	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001156	OMIM:124480	TAS				P		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001199	OMIM:124480	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001592	OMIM:124480	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001770	OMIM:124480	TAS				P		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001792	OMIM:124480	TAS				P		HPO:probinson	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0001798	OMIM:124480	TAS				P		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0003577	OMIM:124480	TAS				C		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0007529	OMIM:124480	IEA				P		HPO:skoehler	
OMIM	124480	DEAFNESS, CONGENITAL, AND ONYCHODYSTROPHY, AUTOSOMAL DOMINANT		HP:0008404	OMIM:124480	TAS				P		HPO:skoehler	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0000006	OMIM:124490	IEA				I		HPO:iea	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0000405	OMIM:124490	IEA				P		HPO:skoehler	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0007209	OMIM:124490	TAS				P		HPO:skoehler	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0008572	OMIM:124490	IEA				P		HPO:iea	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0008628	OMIM:124490	IEA				P		HPO:iea	
OMIM	124490	124490 DEAFNESS, CONDUCTIVE STAPEDIAL, WITH EAR MALFORMATION AND FACIAL PALSY		HP:0010628	OMIM:124490	IEA				P		HPO:iea	
OMIM	124500	DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OFFINGERS AND TOES		HP:0000006	OMIM:124500	TAS				I		HPO:probinson	
OMIM	124500	DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OFFINGERS AND TOES		HP:0000365	OMIM:124500	TAS				P		HPO:probinson	
OMIM	124500	DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OFFINGERS AND TOES		HP:0007460	OMIM:124500	IEA				P		HPO:iea	
OMIM	124500	DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OFFINGERS AND TOES		HP:0007465	OMIM:124500	TAS				P		HPO:probinson	
OMIM	124500	DEAFNESS, CONGENITAL, WITH KERATOPACHYDERMIA AND CONSTRICTIONS OFFINGERS AND TOES		HP:0009775	OMIM:124500	TAS				P		HPO:probinson	
OMIM	124700	DEAFNESS, MID-TONE NEURAL		HP:0000006	OMIM:124700	IEA				I		HPO:iea	
OMIM	124700	DEAFNESS, MID-TONE NEURAL		HP:0000407	OMIM:124700	IEA				P		HPO:skoehler	
OMIM	124700	DEAFNESS, MID-TONE NEURAL		HP:0001730	OMIM:124700	IEA				P		HPO:iea	
OMIM	124700	DEAFNESS, MID-TONE NEURAL		HP:0011463	OMIM:124700	IEA				C		HPO:iea	
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0000006	OMIM:124900	TAS				I		HPO:skoehler	
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0000407	OMIM:124900	TAS				P		HPO:skoehler	
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0001730	OMIM:124900	TAS				P		HPO:skoehler	
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0001873	OMIM:124900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0008542	OMIM:124900	TAS				P		HPO:skoehler	
OMIM	124900	DEAFNESS, AUTOSOMAL DOMINANT 1		HP:0011463	OMIM:124900	TAS				C		HPO:skoehler	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0000006	OMIM:124950	IEA				I		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0000988	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0001085	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0001271	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0001730	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0002315	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0002922	OMIM:124950	TAS				P		HPO:probinson	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0004950	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0008043	OMIM:124950	IEA				P		HPO:iea	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE		HP:0008619	OMIM:124950	IEA				P		HPO:skoehler	
OMIM	124950	DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE	HP:0012825	HP:0011120	OMIM:124950	TAS				P		HPO:probinson	
OMIM	125000	DEAFNESS, UNILATERAL		HP:0000006	OMIM:125000	TAS				I		HPO:probinson	
OMIM	125000	DEAFNESS, UNILATERAL		HP:0009900	OMIM:125000	TAS				P		HPO:probinson	
OMIM	125050	DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA		HP:0000006	OMIM:125050	TAS				I		HPO:probinson	
OMIM	125050	DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA		HP:0001730	OMIM:125050	TAS				P		HPO:probinson	
OMIM	125050	DEAFNESS WITH ANHIDROTIC ECTODERMAL DYSPLASIA		HP:0007476	OMIM:125050	TAS				P		HPO:probinson	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000006	OMIM:125230	IEA				I		HPO:iea	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000200	OMIM:125230	IEA				P		HPO:iea	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000324	OMIM:125230	IEA				P		HPO:iea	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000365	OMIM:125230	IEA				P		HPO:iea	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000430	OMIM:125230	TAS				P		HPO:skoehler	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0000431	OMIM:125230	IEA				P		HPO:iea	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0001596	OMIM:125230	IEA				P		HPO:skoehler	
OMIM	125230	DEAFNESS-CRANIOFACIAL SYNDROME		HP:0002007	OMIM:125230	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000006	OMIM:125250	IEA				I		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000408	OMIM:125250	PCS				P		HPO:probinson	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000486	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000508	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000552	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000576	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000602	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000603	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000642	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000648	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000650	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0000666	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0001251	OMIM:125250	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0001257	OMIM:125250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0001288	OMIM:125250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0003198	OMIM:125250	TAS				P		HPO:skoehler	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0003557	OMIM:125250	TAS				P		HPO:skoehler	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0003676	OMIM:125250	TAS				C		HPO:skoehler	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0006958	OMIM:125250	IEA				P		HPO:iea	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0007663	OMIM:125250	TAS				P		HPO:skoehler	
OMIM	125250	OPTIC ATROPHY WITH OR WITHOUT DEAFNESS, OPHTHALMOPLEGIA, MYOPATHY, ATAXIA, AND NEUROPATHY		HP:0009830	OMIM:125250	TAS				P		HPO:skoehler	
OMIM	125260	DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF		HP:0000006	OMIM:125260	IEA				I		HPO:iea	
OMIM	125260	DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF		HP:0002715	OMIM:125260	IEA				P		HPO:iea	
OMIM	125280	DENS EVAGINATUS		HP:0000006	OMIM:125280	IEA				I		HPO:iea	
OMIM	125280	DENS EVAGINATUS		HP:0000164	OMIM:125280	IEA				P		HPO:iea	
OMIM	125280	DENS EVAGINATUS		HP:0011087	OMIM:125280	TAS				P		HPO:skoehler	
OMIM	125300	125300 DENS IN DENTE AND PALATAL INVAGINATIONS		HP:0000006	OMIM:125300	IEA				I		HPO:iea	
OMIM	125300	125300 DENS IN DENTE AND PALATAL INVAGINATIONS		HP:0000164	OMIM:125300	IEA				P		HPO:iea	
OMIM	125300	125300 DENS IN DENTE AND PALATAL INVAGINATIONS		HP:0011088	OMIM:125300	TAS				P		HPO:skoehler	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000006	OMIM:125310	IEA				I		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000020	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000512	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000572	OMIM:125310	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000649	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000708	OMIM:125310	TAS		HP:0040284		P		HPO:skoehler	9%
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0000951	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0001250	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0001288	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0001297	OMIM:125310	IEA				P		HPO:skoehler	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0002076	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0002352	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0002619	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0003581	OMIM:125310	IEA				C		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0007024	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0007123	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0007236	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0007634	OMIM:125310	IEA				P		HPO:iea	
OMIM	125310	#125310 CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTSAND LEUKOENCEPHALOPATHY; CADASIL;;DEMENTIA, HEREDITARY MULTI-INFARCT TYPE;;CASIL		HP:0009830	OMIM:125310	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125320	DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES		HP:0000006	OMIM:125320	TAS				I		HPO:probinson	
OMIM	125320	DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES	HP:0012828	HP:0000726	OMIM:125320	TAS				P		HPO:skoehler	
OMIM	125320	DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES		HP:0001300	OMIM:125320	TAS				P		HPO:skoehler	
OMIM	125320	DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES		HP:0011960	OMIM:125320	TAS				P		HPO:probinson	
OMIM	125350	DENTAL NONERUPTION		HP:0000006	OMIM:125350	IEA				I		HPO:iea	
OMIM	125350	DENTAL NONERUPTION		HP:0000668	OMIM:125350	IEA				P		HPO:skoehler	
OMIM	125350	DENTAL NONERUPTION		HP:0006335	OMIM:125350	IEA				P		HPO:iea	
OMIM	125350	DENTAL NONERUPTION		HP:0006352	OMIM:125350	IEA				P		HPO:iea	
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0000006	OMIM:125370	TAS				I		HPO:iea	
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0000639	PMID:19659750	PCS		HP:0040284		P		HPO:iea	9/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0000726	PMID:19659750	PCS		HP:0040284		P		HPO:iea	14/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0001250	PMID:19659750	PCS		HP:0040284		P		HPO:iea	12/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0001251	PMID:19659750	PCS		HP:0040284		P		HPO:iea	25/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0001266	OMIM:125370	TAS				P		HPO:iea	
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0001336	PMID:19659750	PCS		HP:0040284		P		HPO:iea	6/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0002072	PMID:19659750	PCS		HP:0040284		P		HPO:iea	7/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0003743	OMIM:125370	TAS				I		HPO:iea	
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0007047	PMID:20500452	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0007256	PMID:19659750	PCS		HP:0040284		P		HPO:iea	5/25
OMIM	125370	DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY NAITO-OYANAGI DISEASE HAW RIVER SYNDROME ATAXIA, CHOREA, SEIZURES, AND DEMENTIA		HP:0010878	PMID:20500452	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0000006	OMIM:125400	IEA				I		HPO:iea	
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0000007	OMIM:125400	TAS				I		HPO:skoehler	
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0000679	OMIM:125400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0000691	OMIM:125400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0000700	OMIM:125400	IEA				P		HPO:iea	
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0006350	OMIM:125400	IEA				P		HPO:iea	
OMIM	125400	#125400 DENTIN DYSPLASIA, TYPE I; DTDP1;;DENTIN DYSPLASIA, SHIELDS TYPE I;;ROOTLESS TEETH;;RADICULAR DENTIN DYSPLASIADENTIN DYSPLASIA, TYPE I, WITH EXTREME MICRODONTIA AND MISSHAPEN TEETH,INCLUDED		HP:0011060	OMIM:125400	IEA				P		HPO:skoehler	
OMIM	125420	DENTIN DYSPLASIA, TYPE II		HP:0000006	OMIM:125420	TAS				I		HPO:probinson	
OMIM	125420	DENTIN DYSPLASIA, TYPE II		HP:0003771	OMIM:125420	TAS				P		HPO:skoehler	
OMIM	125420	DENTIN DYSPLASIA, TYPE II		HP:0011060	OMIM:125420	TAS				P		HPO:skoehler	
OMIM	125440	DENTIN DYSPLASIA WITH SCLEROTIC BONES		HP:0000006	OMIM:125440	IEA				I		HPO:iea	
OMIM	125440	DENTIN DYSPLASIA WITH SCLEROTIC BONES		HP:0005652	OMIM:125440	IEA				P		HPO:iea	
OMIM	125440	DENTIN DYSPLASIA WITH SCLEROTIC BONES		HP:0011060	OMIM:125440	IEA				P		HPO:skoehler	
OMIM	125460	DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY		HP:0000007	OMIM:125460	TAS				I		HPO:nvasilevsky	
OMIM	125460	DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY		HP:0001419	OMIM:125460	TAS				I		HPO:nvasilevsky	
OMIM	125460	DEOXYRIBOSE-5-PHOSPHATE ALDOLASE DEFICIENCY		HP:0012379	OMIM:125460	IEA				P		HPO:iea	
OMIM	125480	MAJOR AFFECTIVE DISORDER 1		HP:0000006	OMIM:125480	TAS				I		HPO:iea	
OMIM	125480	MAJOR AFFECTIVE DISORDER 1		HP:0000716	OMIM:125480	TAS				P		HPO:probinson	
OMIM	125480	MAJOR AFFECTIVE DISORDER 1		HP:0100754	OMIM:125480	TAS				P		HPO:probinson	
OMIM	125490	DENTINOGENESIS IMPERFECTA 1		HP:0000006	OMIM:125490	IEA				I		HPO:iea	
OMIM	125490	DENTINOGENESIS IMPERFECTA 1		HP:0000703	OMIM:125490	IEA				P		HPO:iea	
OMIM	125500	DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III		HP:0000006	OMIM:125500	IEA				I		HPO:iea	
OMIM	125500	DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III		HP:0000694	OMIM:125500	IEA				P		HPO:iea	
OMIM	125500	DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III		HP:0000700	OMIM:125500	IEA				P		HPO:iea	
OMIM	125500	DENTINOGENESIS IMPERFECTA, SHIELDS TYPE III		HP:0000703	OMIM:125500	TAS				P		HPO:skoehler	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0000006	OMIM:125520	TAS				I		HPO:probinson	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0001629	OMIM:125520	TAS				P		HPO:probinson	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0001636	OMIM:125520	TAS				P		HPO:probinson	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0001643	OMIM:125520	TAS				P		HPO:probinson	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0003577	OMIM:125520	TAS				C		HPO:probinson	
OMIM	125520	CAYLER CARDIOFACIAL SYNDROME		HP:0011333	OMIM:125520	TAS				P		HPO:probinson	
OMIM	125530	DERMAL RIDGES, NELSON SYNDROME		HP:0000006	OMIM:125530	TAS				I		HPO:probinson	
OMIM	125530	DERMAL RIDGES, NELSON SYNDROME		HP:0007477	OMIM:125530	TAS				P		HPO:probinson	
OMIM	125540	DERMAL RIDGES, PATTERNLESS		HP:0000006	OMIM:125540	IEA				I		HPO:iea	
OMIM	125540	DERMAL RIDGES, PATTERNLESS		HP:0000951	OMIM:125540	IEA				P		HPO:iea	
OMIM	125550	DERMAL RIDGES-OFF-THE-END		HP:0000006	OMIM:125550	TAS				I		HPO:iea	
OMIM	125550	DERMAL RIDGES-OFF-THE-END		HP:0007608	OMIM:125550	TAS				P		HPO:skoehler	
OMIM	125570	DERMATOGLYPHICS--ARCH ON ANY DIGIT		HP:0000006	OMIM:125570	TAS				I		HPO:iea	
OMIM	125570	DERMATOGLYPHICS--ARCH ON ANY DIGIT		HP:0007608	OMIM:125570	TAS				P		HPO:iea	
OMIM	125590	DERMATOGLYPHICS--FINGERPRINT PATTERN		HP:0000006	OMIM:125590	TAS				I		HPO:iea	
OMIM	125590	DERMATOGLYPHICS--FINGERPRINT PATTERN		HP:0007477	OMIM:125590	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0000006	OMIM:125595	TAS				I		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0000502	OMIM:125595	IEA				P		HPO:iea	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0000966	OMIM:125595	IEA				P		HPO:skoehler	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0000972	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0002293	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0007455	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0007550	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0007588	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0008404	OMIM:125595	TAS				P		HPO:skoehler	
OMIM	125595	DERMATOPATHIA PIGMENTOSA RETICULARIS; DPR		HP:0012788	OMIM:125595	TAS				P		HPO:probinson	
OMIM	125600	DERMATOSIS PAPULOSA NIGRA		HP:0000006	OMIM:125600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	125600	DERMATOSIS PAPULOSA NIGRA		HP:0000951	OMIM:125600	IEA				P		HPO:iea	
OMIM	125630	DERMODISTORTIVE URTICARIA		HP:0000006	OMIM:125630	TAS				I		HPO:iea	
OMIM	125630	DERMODISTORTIVE URTICARIA		HP:0001025	OMIM:125630	TAS				P		HPO:skoehler	
OMIM	125630	DERMODISTORTIVE URTICARIA		HP:0001041	OMIM:125630	IEA				P		HPO:skoehler	
OMIM	125630	DERMODISTORTIVE URTICARIA		HP:0031284	PMID:26841242	PCS				P		HPO:probinson	
OMIM	125635	DERMOGRAPHISM, FAMILIAL		HP:0000006	OMIM:125635	TAS				I		HPO:probinson	
OMIM	125635	DERMOGRAPHISM, FAMILIAL		HP:0001297	OMIM:125635	IEA				P		HPO:skoehler	
OMIM	125635	DERMOGRAPHISM, FAMILIAL		HP:0011971	OMIM:125635	TAS				P		HPO:probinson	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000006	OMIM:125640	IEA				I		HPO:iea	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000668	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000958	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000963	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000968	OMIM:125640	IEA				P		HPO:iea	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0000968	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0002164	OMIM:125640	IEA				P		HPO:iea	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0002164	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0002552	OMIM:125640	IEA				P		HPO:iea	
OMIM	125640	DERMOODONTODYSPLASIA		HP:0002552	PMID:6616948	PCS				P		HPO:lccarmody	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000006	OMIM:125700	TAS				I		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000316	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000343	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000445	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000863	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000938	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0001939	OMIM:125700	IEA				P		HPO:probinson	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0002171	OMIM:125700	TAS				P		HPO:skoehler	
OMIM	125700	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0003196	OMIM:125700	TAS				P		HPO:probinson	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0000006	OMIM:125800	IEA				I		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0000007	OMIM:125800	IEA				I		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0000021	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0000103	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0000737	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001249	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001250	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001425	OMIM:125800	TAS				I		HPO:skoehler	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001508	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001955	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001959	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0001986	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0002013	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0002019	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0003228	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0003623	OMIM:125800	IEA				C		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0004322	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0008872	OMIM:125800	IEA				P		HPO:iea	
OMIM	125800	DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL		HP:0009806	OMIM:125800	TAS				P		HPO:probinson	
OMIM	125850	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1; MODY1		HP:0000006	OMIM:125850	IEA				I		HPO:iea	
OMIM	125850	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1; MODY1		HP:0004904	OMIM:125850	TAS				P		HPO:iea	
OMIM	125850	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 1; MODY1		HP:0031284	OMIM:125850	IEA				P		HPO:skoehler	
OMIM	125851	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE II		HP:0000006	OMIM:125851	TAS				I		HPO:skoehler	
OMIM	125851	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE II		HP:0004904	OMIM:125851	TAS				P		HPO:skoehler	
OMIM	125852	DIABETES MELLITUS, INSULIN-DEPENDENT, 2		HP:0000006	OMIM:125852	TAS				I		HPO:skoehler	
OMIM	125852	DIABETES MELLITUS, INSULIN-DEPENDENT, 2		HP:0000819	OMIM:125852	IEA				P		HPO:iea	
OMIM	125852	DIABETES MELLITUS, INSULIN-DEPENDENT, 2		HP:0100651	OMIM:125852	TAS				P		HPO:skoehler	
OMIM	125853	DIABETES MELLITUS, NONINSULIN-DEPENDENT		HP:0000006	OMIM:125853	TAS				I		HPO:probinson	
OMIM	125853	DIABETES MELLITUS, NONINSULIN-DEPENDENT		HP:0000855	OMIM:125853	TAS				P		HPO:probinson	
OMIM	125853	DIABETES MELLITUS, NONINSULIN-DEPENDENT		HP:0003584	OMIM:125853	TAS				C		HPO:probinson	
OMIM	125853	DIABETES MELLITUS, NONINSULIN-DEPENDENT		HP:0005978	OMIM:125853	TAS				P		HPO:probinson	
OMIM	125853	DIABETES MELLITUS, NONINSULIN-DEPENDENT		HP:0031820	OMIM:125853	TAS				P		HPO:lccarmody	
OMIM	125900	DIASTEMA, DENTAL MEDIAL		HP:0000006	OMIM:125900	IEA				I		HPO:iea	
OMIM	125900	DIASTEMA, DENTAL MEDIAL		HP:0000699	OMIM:125900	TAS				P		HPO:probinson	
OMIM	125900	DIASTEMA, DENTAL MEDIAL		HP:0001566	OMIM:125900	IEA				P		HPO:iea	
OMIM	126050	DIGITOTALAR DYSMORPHISM		HP:0000006	OMIM:126050	TAS				I		HPO:probinson	
OMIM	126050	DIGITOTALAR DYSMORPHISM		HP:0001838	OMIM:126050	TAS				P		HPO:probinson	
OMIM	126050	DIGITOTALAR DYSMORPHISM		HP:0003502	OMIM:126050	TAS				P		HPO:probinson	
OMIM	126050	DIGITOTALAR DYSMORPHISM		HP:0009465	OMIM:126050	TAS				P		HPO:probinson	
OMIM	126050	DIGITOTALAR DYSMORPHISM		HP:0100490	OMIM:126050	TAS				P		HPO:probinson	
OMIM	126070	DILUTION, PIGMENTARY		HP:0000006	OMIM:126070	IEA				I		HPO:iea	
OMIM	126070	DILUTION, PIGMENTARY		HP:0001010	OMIM:126070	TAS				P		HPO:skoehler	
OMIM	126070	DILUTION, PIGMENTARY		HP:0005599	OMIM:126070	TAS				P		HPO:probinson	
OMIM	126070	DILUTION, PIGMENTARY		HP:0007730	OMIM:126070	TAS				P		HPO:probinson	
OMIM	126070	DILUTION, PIGMENTARY		HP:0007894	OMIM:126070	TAS				P		HPO:probinson	
OMIM	126100	DIMPLES, FACIAL		HP:0000006	OMIM:126100	IEA				I		HPO:iea	
OMIM	126100	DIMPLES, FACIAL		HP:0000271	OMIM:126100	IEA				P		HPO:iea	
OMIM	126180	DISCRIMINATION, TWO-POINT, REDUCTION IN		HP:0000006	OMIM:126180	IEA				I		HPO:iea	
OMIM	126180	DISCRIMINATION, TWO-POINT, REDUCTION IN		HP:0000707	OMIM:126180	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0000006	OMIM:126190	IEA				I		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0000164	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0000218	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0000508	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0001642	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0001654	OMIM:126190	IEA				P		HPO:skoehler	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0003498	OMIM:126190	TAS				P		HPO:probinson	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0004279	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0004322	OMIM:126190	IEA				P		HPO:skoehler	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0006385	OMIM:126190	TAS				P		HPO:probinson	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0009466	OMIM:126190	IEA				P		HPO:iea	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0030084	OMIM:126190	TAS				P		HPO:skoehler	
OMIM	126190	DISPROPORTIONATE SHORT STATURE WITH PTOSIS AND VALVULAR HEART LESIONS		HP:0200055	OMIM:126190	TAS				P		HPO:skoehler	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0000019	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0000020	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0000651	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0000712	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0000716	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0001257	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0001324	OMIM:126200	TAS				P		HPO:probinson	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0001426	OMIM:126200	IEA				I		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0002311	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0003401	OMIM:126200	IEA				P		HPO:iea	
OMIM	126200	MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO		HP:0007305	OMIM:126200	TAS				P		HPO:probinson	
OMIM	126250	DISTAL OSTEOSCLEROSIS		HP:0000006	OMIM:126250	IEA				I		HPO:iea	
OMIM	126250	DISTAL OSTEOSCLEROSIS		HP:0003034	OMIM:126250	TAS				P		HPO:iea	
OMIM	126250	DISTAL OSTEOSCLEROSIS		HP:0005464	OMIM:126250	TAS				P		HPO:iea	
OMIM	126250	DISTAL OSTEOSCLEROSIS		HP:0100774	OMIM:126250	IEA				P		HPO:skoehler	
OMIM	126300	DISTICHIASIS		HP:0000006	OMIM:126300	IEA				I		HPO:iea	
OMIM	126300	DISTICHIASIS		HP:0009743	OMIM:126300	IEA				P		HPO:iea	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0000006	OMIM:126320	PCS				I		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0001629	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0001643	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0001688	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0002619	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0004950	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0009743	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126320	DISTICHIASIS WITH CONGENITAL ANOMALIES OF THE HEART AND PERIPHERAL		HP:0010741	OMIM:126320	PCS				P		HPO:probinson	
OMIM	126500	DOUBLE NAIL FOR FIFTH TOE		HP:0000006	OMIM:126500	IEA				I		HPO:iea	
OMIM	126500	DOUBLE NAIL FOR FIFTH TOE		HP:0000924	OMIM:126500	IEA				P		HPO:iea	
OMIM	126550	DOUGHNUT LESIONS OF SKULL, FAMILIAL		HP:0000006	PMID:11241496	PCS				I		HPO:iea	
OMIM	126550	DOUGHNUT LESIONS OF SKULL, FAMILIAL		HP:0000670	PMID:11241496	PCS				P		HPO:iea	
OMIM	126550	DOUGHNUT LESIONS OF SKULL, FAMILIAL		HP:0002757	PMID:11241496	PCS				P		HPO:iea	
OMIM	126550	DOUGHNUT LESIONS OF SKULL, FAMILIAL		HP:0003155	PMID:11241496	PCS				P		HPO:iea	
OMIM	126600	DOYNE HONEYCOMB RETINAL DYSTROPHY		HP:0000006	OMIM:126600	TAS				I		HPO:probinson	
OMIM	126600	DOYNE HONEYCOMB RETINAL DYSTROPHY		HP:0000505	OMIM:126600	TAS				P		HPO:probinson	
OMIM	126600	DOYNE HONEYCOMB RETINAL DYSTROPHY		HP:0000556	OMIM:126600	TAS				P		HPO:skoehler	
OMIM	126600	DOYNE HONEYCOMB RETINAL DYSTROPHY		HP:0007937	OMIM:126600	TAS				P		HPO:probinson	
OMIM	126700	BASAL LAMINAR DRUSEN		HP:0000006	OMIM:126700	IEA				I		HPO:iea	
OMIM	126700	BASAL LAMINAR DRUSEN		HP:0000529	OMIM:126700	IEA				P		HPO:iea	
OMIM	126700	BASAL LAMINAR DRUSEN		HP:0011510	OMIM:126700	IEA				P		HPO:skoehler	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000006	PMID:9781021	PCS				I		HPO:iea	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000542	PMID:12395297	PCS				P		HPO:iea	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000565	PMID:29133973	PCS				P		HP:probinson	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000619	OMIM:126800	TAS				P		HPO:iea	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000634	PMID:12395297	PCS				P		HPO:iea	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0000661	PMID:29133973	PCS				P		HPO:iea	
OMIM	126800	DUANE RETRACTION SYNDROME 1		HP:0009921	PMID:29133973	PCS	HP:0003577			P		HPO:iea	
OMIM	126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0000006	OMIM:126840	IEA				I		HPO:iea	
OMIM	126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0002588	OMIM:126840	IEA				P		HPO:iea	
OMIM	126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0003238	OMIM:126840	IEA				P		HPO:iea	
OMIM	126840	DUODENAL ULCER DUE TO ANTRAL G-CELL HYPERFUNCTION		HP:0500167	OMIM:126840	TAS				P		HPO:lccarmody	
OMIM	126850	DUODENAL ULCER, HYPERPEPSINOGENEMIC I		HP:0000006	OMIM:126850	IEA				I		HPO:iea	
OMIM	126850	DUODENAL ULCER, HYPERPEPSINOGENEMIC I		HP:0002588	OMIM:126850	IEA				P		HPO:iea	
OMIM	126850	DUODENAL ULCER, HYPERPEPSINOGENEMIC I		HP:0003238	OMIM:126850	IEA				P		HPO:iea	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0000006	OMIM:126900	TAS				I		HPO:iea	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0003581	OMIM:126900	TAS				C		HPO:probinson	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0003676	OMIM:126900	TAS				C		HPO:skoehler	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0003829	OMIM:126900	TAS				C		HPO:iea	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0005679	OMIM:126900	TAS				P		HPO:skoehler	
OMIM	126900	DUPUYTREN CONTRACTUREDUPUYTREN CONTRACTURE 1, INCLUDED		HP:0009473	OMIM:126900	IEA				P		HPO:iea	
OMIM	126950	DWARFISM WITH TALL VERTEBRAE		HP:0000006	OMIM:126950	IEA				I		HPO:iea	
OMIM	126950	DWARFISM WITH TALL VERTEBRAE		HP:0002812	OMIM:126950	IEA				P		HPO:iea	
OMIM	126950	DWARFISM WITH TALL VERTEBRAE		HP:0003510	OMIM:126950	IEA				P		HPO:iea	
OMIM	126950	DWARFISM WITH TALL VERTEBRAE		HP:0004570	OMIM:126950	IEA				P		HPO:iea	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000006	OMIM:127000	TAS				I		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000256	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000519	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000540	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000568	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000829	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0000935	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001085	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001250	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001476	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001518	OMIM:127000	TAS				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001620	OMIM:127000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0001903	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0002135	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0002901	OMIM:127000	TAS				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0002905	OMIM:127000	IEA				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0003510	OMIM:127000	TAS				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0007862	OMIM:127000	TAS				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0008285	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0011001	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0011220	OMIM:127000	TAS				P		HPO:skoehler	
OMIM	127000	KENNY-CAFFEY SYNDROME, TYPE 2; KCS2		HP:0100253	OMIM:127000	TAS				P		HPO:probinson	
OMIM	127100	DWARFISM, LEVI TYPE		HP:0000006	OMIM:127100	IEA				I		HPO:iea	
OMIM	127100	DWARFISM, LEVI TYPE		HP:0000007	OMIM:127100	IEA				I		HPO:iea	
OMIM	127100	DWARFISM, LEVI TYPE		HP:0000271	OMIM:127100	IEA				P		HPO:iea	
OMIM	127100	DWARFISM, LEVI TYPE		HP:0001518	OMIM:127100	IEA				P		HPO:iea	
OMIM	127100	DWARFISM, LEVI TYPE		HP:0003510	OMIM:127100	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0000006	OMIM:127200	IEA				I		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0000501	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0000518	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0000540	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0000541	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0001072	OMIM:127200	TAS				P		HPO:probinson	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0001216	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0001387	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0003510	OMIM:127200	IEA				P		HPO:skoehler	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0006385	OMIM:127200	TAS				P		HPO:skoehler	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0008873	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0009803	OMIM:127200	IEA				P		HPO:iea	
OMIM	127200	127200 DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES;;MOORE-FEDERMAN SYNDROME		HP:0009816	OMIM:127200	IEA				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0000006	OMIM:127300	PCS				I		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0000218	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0001191	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0001831	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0001832	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002650	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002673	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002762	PMID:11739418;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002982	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002984	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002986	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0002996	OMIM:127300	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003022	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003027	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003038	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003063	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003067	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003102	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0003712	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0005736	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0006248	OMIM:127300	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0006459	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0008873	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127300	LERI-WEILL DYSCHONDROSTEOSIS		HP:0010044	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=lwd	PCS				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0000006	OMIM:127350	TAS				I		HPO:nvasilevsky	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0000123	OMIM:127350	IEA				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0002986	OMIM:127350	IEA				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0003031	OMIM:127350	IEA				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0003067	OMIM:127350	TAS				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0005736	OMIM:127350	IEA				P		HPO:iea	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0005773	OMIM:127350	TAS				P		HPO:skoehler	
OMIM	127350	DYSCHONDROSTEOSIS AND NEPHRITIS		HP:0008845	OMIM:127350	TAS				P		HPO:iea	
OMIM	127400	DYSCHROMATOSIS SYMMETRICA HEREDITARIA 1		HP:0000006	OMIM:127400	IEA				I		HPO:iea	
OMIM	127400	DYSCHROMATOSIS SYMMETRICA HEREDITARIA 1		HP:0003593	OMIM:127400	TAS				C		HPO:skoehler	
OMIM	127400	DYSCHROMATOSIS SYMMETRICA HEREDITARIA 1		HP:0007441	OMIM:127400	IEA				P		HPO:iea	
OMIM	127500	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA		HP:0000006	OMIM:127500	IEA				I		HPO:iea	
OMIM	127500	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA		HP:0003593	OMIM:127500	TAS				C		HPO:skoehler	
OMIM	127500	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA		HP:0007441	OMIM:127500	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0000006	OMIM:127550	IEA				I		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0000670	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0000939	OMIM:127550	IEA				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001251	OMIM:127550	IEA				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001321	OMIM:127550	IEA				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001328	OMIM:127550	IEA				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001394	OMIM:127550	TAS				P		HPO:probinson	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001596	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001803	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001807	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001873	OMIM:127550	TAS				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001888	OMIM:127550	TAS				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001903	OMIM:127550	TAS				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0001915	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0002206	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0002216	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0002745	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0002863	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0004334	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0005528	OMIM:127550	TAS				P		HPO:skoehler	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0006480	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0006515	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0006739	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0007588	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0008070	OMIM:127550	IEA				P		HPO:iea	
OMIM	127550	#127550 DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; DKCA1;;DYSKERATOSIS CONGENITA, SCOGGINS TYPE		HP:0008404	OMIM:127550	TAS				P		HPO:skoehler	
OMIM	127600	DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID		HP:0000006	OMIM:127600	IEA				I		HPO:iea	
OMIM	127600	DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID		HP:0000505	OMIM:127600	IEA				P		HPO:iea	
OMIM	127600	DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID		HP:0000613	OMIM:127600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	127600	DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID		HP:0002745	OMIM:127600	IEA				P		HPO:iea	
OMIM	127600	DYSKERATOSIS, HEREDITARY BENIGN INTRAEPITHELIAL; HBID		HP:0025337	OMIM:127600	IEA				P		HPO:skoehler	
OMIM	127700	DYSLEXIA, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:127700	TAS				I		HPO:skoehler	
OMIM	127700	DYSLEXIA, SUSCEPTIBILITY TO, 1		HP:0002167	OMIM:127700	TAS				P		HPO:skoehler	
OMIM	127700	DYSLEXIA, SUSCEPTIBILITY TO, 1		HP:0010522	OMIM:127700	TAS				P		HPO:skoehler	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0000006	OMIM:127750	IEA				I		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0000726	OMIM:127750	IEA				P		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0000746	OMIM:127750	IEA				P		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0001300	OMIM:127750	IEA				P		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0002367	OMIM:127750	IEA				P		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0007159	OMIM:127750	IEA				P		HPO:iea	
OMIM	127750	DEMENTIA, LEWY BODY; DLB		HP:0100315	OMIM:127750	IEA				P		HPO:skoehler	
OMIM	127800	DYSPLASIA EPIPHYSEALIS HEMIMELICA		HP:0000924	OMIM:127800	IEA				P		HPO:iea	
OMIM	127800	DYSPLASIA EPIPHYSEALIS HEMIMELICA		HP:0001548	OMIM:127800	IEA				P		HPO:skoehler	
OMIM	127820	127820 DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS;;OSTEOCHONDROMATOSIS, DOMINANT CARPOTARSAL		HP:0000006	OMIM:127820	IEA				I		HPO:iea	
OMIM	127820	127820 DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS;;OSTEOCHONDROMATOSIS, DOMINANT CARPOTARSAL		HP:0001386	OMIM:127820	IEA				P		HPO:iea	
OMIM	127820	127820 DYSPLASIA EPIPHYSEALIS HEMIMELICA WITH CHONDROMAS AND OSTEOCHONDROMAS;;OSTEOCHONDROMATOSIS, DOMINANT CARPOTARSAL		HP:0030431	OMIM:127820	TAS				P		HPO:skoehler	
OMIM	128000	DYSTELEPHALANGY		HP:0000006	OMIM:128000	IEA				I		HPO:iea	
OMIM	128000	DYSTELEPHALANGY		HP:0004226	OMIM:128000	TAS				P		HPO:probinson	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0000006	OMIM:128100	IEA				I		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0000473	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0000643	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0000716	OMIM:128100	TAS				P		HPO:skoehler	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001252	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001260	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001276	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001290	OMIM:128100	TAS				P		HPO:skoehler	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001304	OMIM:128100	TAS				P		HPO:probinson	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0001337	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0002356	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0002533	OMIM:128100	IEA				P		HPO:skoehler	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0002650	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0002808	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0003307	OMIM:128100	IEA				P		HPO:iea	
OMIM	128100	DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT		HP:0003829	OMIM:128100	TAS		HP:0040284		C		HPO:skoehler	30%
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0000006	OMIM:128101	TAS				I		HPO:probinson	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0000275	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0000473	OMIM:128101	TAS				P		HPO:probinson	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0001304	OMIM:128101	TAS				P		HPO:probinson	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0001618	OMIM:128101	TAS				P		HPO:probinson	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0002015	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0002066	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0002451	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0007325	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128101	#128101 DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4;;WHISPERING DYSPHONIA, HEREDITARY;;DYSTONIA MUSCULORUM DEFORMANS 4		HP:0009938	OMIM:128101	TAS				P		HPO:skoehler	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0000006	OMIM:128200	IEA				I		HPO:iea	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0000271	OMIM:128200	IEA				P		HPO:iea	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0001250	OMIM:128200	IEA		HP:0040284		P		HPO:skoehler	40%
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0002268	OMIM:128200	IEA				P		HPO:iea	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0002310	OMIM:128200	IEA				P		HPO:iea	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0003829	OMIM:128200	TAS				C		HPO:skoehler	
OMIM	128200	#128200 EPISODIC KINESIGENIC DYSKINESIA 1; EKD1;;PAROXYSMAL KINESIGENIC CHOREOATHETOSIS; PKC;;PAROXYSMAL KINESIGENIC DYSKINESIA; PKD;;DYSTONIA, FAMILIAL PAROXYSMAL;;DYSTONIA 10; DYT10		HP:0007098	OMIM:128200	TAS				P		HPO:probinson	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0000006	OMIM:128230	IEA				I		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0000007	OMIM:128230	TAS		HP:0040283		I		HPO:skoehler	HP:0040283
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0000473	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0001300	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0001347	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0001425	OMIM:128230	TAS				I		HPO:skoehler	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0001761	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0001762	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0002066	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0002174	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0002356	OMIM:128230	IEA				P		HPO:skoehler	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0002548	OMIM:128230	TAS				P		HPO:probinson	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0002650	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0003487	OMIM:128230	IEA				P		HPO:iea	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0008297	OMIM:128230	IEA				P		HPO:skoehler	
OMIM	128230	DYSTONIA, DOPA-RESPONSIVE; DRD		HP:0011463	OMIM:128230	TAS				C		HPO:probinson	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000006	OMIM:128235	IEA				I		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000338	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000473	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000712	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000716	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0000739	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0001260	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0001300	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0001945	OMIM:128235	IEA				P		HPO:skoehler	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002015	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002067	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002172	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002300	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002307	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0002317	OMIM:128235	IEA				P		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0003829	OMIM:128235	IEA				C		HPO:iea	
OMIM	128235	DYSTONIA 12; DYT12		HP:0011462	OMIM:128235	TAS		HP:0040282		C		HPO:probinson	HP:0040282
OMIM	128290	EAR ANTITRAGUS, TAG AT BASE OF		HP:0000006	OMIM:128290	IEA				I		HPO:iea	
OMIM	128290	EAR ANTITRAGUS, TAG AT BASE OF		HP:0000598	OMIM:128290	IEA				P		HPO:iea	
OMIM	128300	EAR EXOSTOSES		HP:0000006	OMIM:128300	IEA				I		HPO:iea	
OMIM	128300	EAR EXOSTOSES		HP:0000365	PMID:25459316	PCS				P		HPO:lccarmody	
OMIM	128300	EAR EXOSTOSES		HP:0004459	OMIM:128300	IEA				P		HPO:iea	
OMIM	128300	EAR EXOSTOSES		HP:0030788	PMID:25459316	PCS				P		HPO:lccarmody	
OMIM	128300	EAR EXOSTOSES		HP:0100777	PMID:25459316	PCS				P		HPO:lccarmody	
OMIM	128300	EAR EXOSTOSES		HP:0410017	PMID:25459316	PCS				P		HPO:lccarmody	
OMIM	128500	EAR FOLDING		HP:0000006	OMIM:128500	IEA				I		HPO:iea	
OMIM	128500	EAR FOLDING		HP:0000598	OMIM:128500	IEA				P		HPO:iea	
OMIM	128600	EAR MALFORMATION		HP:0000006	OMIM:128600	IEA				I		HPO:iea	
OMIM	128600	EAR MALFORMATION		HP:0000598	OMIM:128600	IEA				P		HPO:iea	
OMIM	128700	PREAURICULAR FISTULAE, CONGENITAL		HP:0000006	OMIM:128700	IEA				I		HPO:iea	
OMIM	128700	PREAURICULAR FISTULAE, CONGENITAL		HP:0004467	OMIM:128700	TAS				P		HPO:probinson	
OMIM	128710	EAR PITS, POSTERIOR HELICAL		HP:0000006	OMIM:128710	TAS				I		HPO:probinson	
OMIM	128710	EAR PITS, POSTERIOR HELICAL		HP:0008523	OMIM:128710	TAS				P		HPO:probinson	
OMIM	128800	EAR WITHOUT HELIX		HP:0000006	OMIM:128800	IEA				I		HPO:iea	
OMIM	128800	EAR WITHOUT HELIX		HP:0000598	OMIM:128800	IEA				P		HPO:iea	
OMIM	128950	EARLOBE CREASE		HP:0000006	OMIM:128950	TAS				I		HPO:skoehler	
OMIM	128950	EARLOBE CREASE		HP:0009908	OMIM:128950	TAS				P		HPO:skoehler	
OMIM	128950	EARLOBE CREASE		HP:0031511	OMIM:128950	IEA				P		HPO:skoehler	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0000006	PMID:6476090	PCS				I		HPO:iea	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0000347	PMID:6476090	PCS				P		HPO:lccarmody	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0000377	PMID:6476090	PCS				P		HPO:lccarmody	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0008513	PMID:6476090	PCS				P		HPO:lccarmody	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0008591	PMID:6476090	PCS				P		HPO:iea	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0008628	PMID:6476090	PCS				P		HPO:lccarmody	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0011454	PMID:6476090	PCS				P		HPO:lccarmody	
OMIM	128980	EARLOBES, THICKENED, WITH CONDUCTIVE DEAFNESS FROM INCUDOSTAPEDIALABNORMALITIES		HP:0200111	OMIM:128980	TAS				P		HPO:skoehler	
OMIM	129000	EARRING HOLES, NATURAL		HP:0000006	OMIM:129000	IEA				I		HPO:iea	
OMIM	129000	EARRING HOLES, NATURAL		HP:0004461	OMIM:129000	IEA				P		HPO:iea	
OMIM	129100	EARS, ABILITY TO MOVE		HP:0000006	OMIM:129100	TAS				I		HPO:skoehler	
OMIM	129150	ECHO VIRUS 11 SENSITIVITY		HP:0000006	OMIM:129150	IEA				I		HPO:iea	
OMIM	129150	ECHO VIRUS 11 SENSITIVITY		HP:0002715	OMIM:129150	IEA				P		HPO:iea	
OMIM	129200	BASAN SYNDROME		HP:0000006	OMIM:129200	IEA				I		HPO:iea	
OMIM	129200	BASAN SYNDROME		HP:0000954	OMIM:129200	IEA				P		HPO:iea	
OMIM	129200	BASAN SYNDROME		HP:0000962	OMIM:129200	IEA				P		HPO:skoehler	
OMIM	129200	BASAN SYNDROME		HP:0000968	OMIM:129200	IEA				P		HPO:skoehler	
OMIM	129200	BASAN SYNDROME		HP:0001056	OMIM:129200	IEA				P		HPO:skoehler	
OMIM	129200	BASAN SYNDROME		HP:0001182	OMIM:129200	IEA				P		HPO:iea	
OMIM	129200	BASAN SYNDROME		HP:0001371	OMIM:129200	TAS				P		HPO:skoehler	
OMIM	129200	BASAN SYNDROME		HP:0007455	OMIM:129200	IEA				P		HPO:skoehler	
OMIM	129200	BASAN SYNDROME		HP:0010621	OMIM:129200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	129200	BASAN SYNDROME		HP:0025092	OMIM:129200	TAS				P		HPO:skoehler	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000006	OMIM:129400	IEA				I		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000047	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000059	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000160	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000175	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000193	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000204	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000220	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000327	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000348	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000365	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000403	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000430	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000460	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000508	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000668	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000963	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0000966	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0001092	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0001159	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0001792	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0001805	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0002213	OMIM:129400	PCS				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0002235	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0002287	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0004322	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0005280	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0007476	OMIM:129400	IEA				P		HPO:skoehler	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0007500	OMIM:129400	IEA				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0008070	OMIM:129400	PCS				P		HPO:iea	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0008070	OMIM:129400	TAS				P		HPO:skoehler	
OMIM	129400	#129400 RAPP-HODGKIN SYNDROME; RHS;;ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH CLEFT LIP/PALATEOROFACIAL CLEFT 8, INCLUDED; OFC8, INCLUDED;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 8, INCLUDED		HP:0200141	OMIM:129400	TAS				P		HPO:skoehler	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000006	OMIM:129490	IEA				I		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000535	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000653	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000668	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000674	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000691	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000958	OMIM:129490	TAS				P		HPO:skoehler	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000966	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0000968	OMIM:129490	IEA				P		HPO:skoehler	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0001006	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0001425	OMIM:129490	TAS				I		HPO:skoehler	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0002046	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0002164	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0002213	OMIM:129490	IEA				P		HPO:iea	
OMIM	129490	#129490 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT;ECTD10A;;ECTODERMAL DYSPLASIA, HYPOHIDROTIC, AUTOSOMAL DOMINANT; HED		HP:0002217	OMIM:129490	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000006	OMIM:129500	IEA				I		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000164	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000486	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000498	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000509	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000518	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000535	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000613	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000653	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000953	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000968	OMIM:129500	IEA				P		HPO:skoehler	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0000972	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0001792	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0001806	OMIM:129500	IEA				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002164	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002213	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002217	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002221	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002299	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0002555	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0003828	OMIM:129500	TAS				C		HPO:skoehler	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0004322	OMIM:129500	PCS				P		HPO:iea	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY		HP:0007418	OMIM:129500	TAS				P		HPO:skoehler	
OMIM	129500	#129500 CLOUSTON SYNDROME;;ECTODERMAL DYSPLASIA 2, CLOUSTON TYPE; ECTD2;;ECTODERMAL DYSPLASIA, HIDROTIC, AUTOSOMAL DOMINANT;;CLOUSTON HIDROTIC ECTODERMAL DYSPLASIA;;ECTODERMAL DYSPLASIA, HIDROTIC, 2, FORMERLY; HED2, FORMERLY	HP:0012828	HP:0008404	OMIM:129500	TAS				P		HPO:skoehler	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0000006	OMIM:129510	IEA				I		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0000668	OMIM:129510	IEA				P		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0000765	OMIM:129510	IEA				P		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0000968	OMIM:129510	IEA				P		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0001006	OMIM:129510	IEA				P		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0002561	OMIM:129510	TAS				P		HPO:skoehler	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0007521	OMIM:129510	IEA				P		HPO:iea	
OMIM	129510	ECTODERMAL DYSPLASIA, TRICHOODONTOONYCHIAL TYPE		HP:0008587	OMIM:129510	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000219	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000219	OMIM:129540	TAS				P		HPO:skoehler	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000272	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000319	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000347	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000506	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000535	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000653	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000670	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000750	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0000968	OMIM:129540	IEA				P		HPO:skoehler	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0001596	OMIM:129540	IEA				P		HPO:skoehler	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0001597	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0003745	OMIM:129540	IEA				I		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0004209	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0005280	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0006297	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0009084	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0010098	OMIM:129540	IEA				P		HPO:iea	
OMIM	129540	129540 ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET		HP:0100258	OMIM:129540	TAS				P		HPO:skoehler	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0000006	OMIM:129550	IEA				I		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0000684	OMIM:129550	IEA				P		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0000818	OMIM:129550	IEA				P		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0000966	OMIM:129550	IEA				P		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0000968	OMIM:129550	IEA				P		HPO:skoehler	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0002164	OMIM:129550	IEA				P		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0002557	OMIM:129550	IEA				P		HPO:iea	
OMIM	129550	ECTODERMAL DYSPLASIA WITH ADRENAL CYST		HP:0003187	OMIM:129550	IEA				P		HPO:iea	
OMIM	129600	ECTOPIA LENTIS, ISOLATED		HP:0000006	OMIM:129600	IEA				I		HPO:iea	
OMIM	129600	ECTOPIA LENTIS, ISOLATED		HP:0001083	OMIM:129600	IEA				P		HPO:iea	
OMIM	129750	ECTOPIA PUPILLAE		HP:0000006	OMIM:129750	IEA				I		HPO:iea	
OMIM	129750	ECTOPIA PUPILLAE		HP:0009918	OMIM:129750	IEA				P		HPO:skoehler	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0000006	OMIM:129810	IEA				I		HPO:iea	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0000164	OMIM:129810	IEA				P		HPO:iea	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0000968	OMIM:129810	IEA				P		HPO:iea	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0001006	OMIM:129810	IEA				P		HPO:iea	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0001171	OMIM:129810	IEA				P		HPO:skoehler	
OMIM	129810	ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE		HP:0001839	OMIM:129810	IEA				P		HPO:skoehler	
OMIM	129830	129830 ECTRODACTYLY-CLEFT PALATE SYNDROME;;ECP SYNDROME		HP:0000006	OMIM:129830	IEA				I		HPO:iea	
OMIM	129830	129830 ECTRODACTYLY-CLEFT PALATE SYNDROME;;ECP SYNDROME		HP:0000175	OMIM:129830	IEA				P		HPO:iea	
OMIM	129830	129830 ECTRODACTYLY-CLEFT PALATE SYNDROME;;ECP SYNDROME		HP:0000951	OMIM:129830	IEA				P		HPO:iea	
OMIM	129830	129830 ECTRODACTYLY-CLEFT PALATE SYNDROME;;ECP SYNDROME		HP:0001171	OMIM:129830	IEA				P		HPO:iea	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0000006	OMIM:129840	IEA				I		HPO:iea	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0000119	OMIM:129840	IEA				P		HPO:iea	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0000737	OMIM:129840	IEA				P		HPO:iea	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0000819	OMIM:129840	IEA				P		HPO:iea	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0000969	OMIM:129840	IEA				P		HPO:skoehler	
OMIM	129840	EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL		HP:0002013	OMIM:129840	IEA				P		HPO:skoehler	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0000006	OMIM:129850	IEA				I		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0000238	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0000271	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0000952	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0001249	OMIM:129850	IEA				P		HPO:skoehler	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0001270	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0001508	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0001522	OMIM:129850	IEA				M		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0003265	OMIM:129850	IEA				P		HPO:iea	
OMIM	129850	EDINBURGH MALFORMATION SYNDROME		HP:0005616	OMIM:129850	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000006	OMIM:129900	IEA				I		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000015	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000023	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000028	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000044	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000054	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000070	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000072	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000076	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000081	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000104	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000110	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000126	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000143	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000145	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000175	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000198	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000204	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000217	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000252	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1	HP:0012825	HP:0000272	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000316	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000327	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000405	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000437	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000453	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000455	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000498	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000506	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000535	OMIM:129900	PCS				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000581	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000613	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000620	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000635	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000653	OMIM:129900	PCS				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000670	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000677	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000691	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000824	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000863	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1	HP:0012825	HP:0000962	OMIM:129900	PCS				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000963	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0000968	OMIM:129900	IEA				P		HPO:skoehler	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001161	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001171	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001249	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001425	OMIM:129900	TAS				I		HPO:skoehler	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001592	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001739	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001770	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001803	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0001839	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002023	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002205	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002209	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002215	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002225	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002286	OMIM:129900	TAS				P		HPO:skoehler	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002507	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0002557	OMIM:129900	IEA				P		HPO:iea	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0007513	OMIM:129900	TAS				P		HPO:skoehler	
OMIM	129900	%129900 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1; EEC1;;EEC;;EEC SYNDROME 1		HP:0008551	OMIM:129900	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000006	PMID:9557891	PCS				I		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000023	PMID:9557891	PCS				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000286	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000394	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000545	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000592	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000974	PMID:9557891	PCS				P		HPO:probinson	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000977	PMID:9557891	PCS				P		HPO:skoehler	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000978	PMID:9557891	PCS				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0000993	PMID:9557891;PMID:9557891	PCS				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001030	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001058	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001073	OMIM:130000,PMID:9557891	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001083	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001187	PMID:9557891	PCS				P		HPO:probinson	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001373	OMIM:130000	IEA				P		HPO:skoehler	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001537	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001634	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0001763	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0002010	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0002616	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0002758	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0004322	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0005100	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0005222	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0006316	OMIM:130000	IEA				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0008947	PMID:9557891	PCS				P		HPO:iea	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0010485	PMID:9557891	PCS				P		HPO:probinson	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0010500	PMID:9557891	PCS				P		HPO:probinson	
OMIM	130000	EHLERS-DANLOS SYNDROME, TYPE I		HP:0025014	PMID:9557891	PCS				P		HPO:probinson	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0000006	OMIM:130020	IEA				I		HPO:iea	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0000974	OMIM:130020	IEA				P		HPO:iea	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0000977	OMIM:130020	IEA				P		HPO:iea	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0001065	OMIM:130020	IEA				P		HPO:skoehler	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0001373	OMIM:130020	IEA				P		HPO:iea	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0001382	OMIM:130020	TAS				P		HPO:skoehler	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0001388	OMIM:130020	IEA				P		HPO:skoehler	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0001634	OMIM:130020	IEA				P		HPO:iea	
OMIM	130020	EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE		HP:0002758	OMIM:130020	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000006	OMIM:130050	IEA				I		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000023	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000139	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000233	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000387	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000563	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000704	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000978	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0000993	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0001030	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0001073	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0001634	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0001762	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0001842	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0002105	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0002108	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0002293	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0004322	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0004944	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0005267	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0006201	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0006480	OMIM:130050	IEA				P		HPO:skoehler	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0009771	OMIM:130050	IEA				P		HPO:iea	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0030009	OMIM:130050	IEA				P		HPO:skoehler	
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0031157	PMID:24922459	PCS		HP:0040284		P		HP:probinson	27/638
OMIM	130050	EHLERS-DANLOS SYNDROME, VASCULAR TYPE; EDSVASC		HP:0100718	OMIM:130050	IEA				P		HPO:skoehler	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000006	OMIM:130060	IEA				I		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000272	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000938	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000974	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000977	OMIM:130060	IEA				P		HPO:skoehler	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0000978	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001058	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001075	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001252	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001290	OMIM:130060	TAS				P		HPO:skoehler	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001388	OMIM:130060	IEA				P		HPO:skoehler	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0001623	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0002194	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0002650	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0002659	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0002808	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0003088	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0003502	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0008780	OMIM:130060	IEA				P		HPO:iea	
OMIM	130060	EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL DOMINANT		HP:0011800	OMIM:130060	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000007	OMIM:130070	IEA				I		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000160	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000175	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000193	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000256	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000274	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000316	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000369	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000387	OMIM:130070	TAS				P		HPO:probinson	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000431	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000520	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000592	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000768	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000774	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000894	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000938	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0000954	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001075	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001166	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001252	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001263	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001290	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001388	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001508	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001762	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001763	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0001772	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0002209	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0002650	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0002673	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0002816	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0002974	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0004322	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0004425	OMIM:130070	IEA				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0005616	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0006243	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0006487	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0007469	OMIM:130070	IEA				P		HPO:iea	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0010511	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0011308	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0011342	OMIM:130070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130070	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1; EDSSPD1		HP:0011800	OMIM:130070	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000006	OMIM:130080	IEA				I		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000023	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000098	OMIM:130080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000225	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000592	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000704	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000963	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000974	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000977	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0000978	OMIM:130080	IEA				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0001058	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0001075	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0001166	OMIM:130080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0001388	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0001609	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0002650	OMIM:130080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0002719	OMIM:130080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0002761	OMIM:130080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0002960	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0006480	OMIM:130080	IEA				P		HPO:iea	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0007517	OMIM:130080	IEA				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0030816	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0031368	OMIM:130080	IEA				P		HPO:skoehler	
OMIM	130080	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1; EDSPD1		HP:0410027	OMIM:130080	TAS				P		HPO:skoehler	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000006	OMIM:130090	TAS				I		HPO:skoehler	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000324	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000347	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000426	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000974	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0000976	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0001073	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0001388	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0001425	OMIM:130090	IEA				I		HPO:skoehler	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0002099	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0002647	OMIM:130090	TAS				P		HPO:probinson	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0003423	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0004764	OMIM:130090	TAS				P		HPO:probinson	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0004942	OMIM:130090	TAS				P		HPO:probinson	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0005656	OMIM:130090	IEA				P		HPO:iea	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0100790	OMIM:130090	TAS				P		HPO:skoehler	
OMIM	130090	EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED		HP:0200146	OMIM:130090	TAS				P		HPO:skoehler	
OMIM	130100	ELASTOSIS PERFORANS SERPIGINOSA		HP:0000006	OMIM:130100	IEA				I		HPO:iea	
OMIM	130100	ELASTOSIS PERFORANS SERPIGINOSA		HP:0003764	OMIM:130100	IEA				P		HPO:skoehler	
OMIM	130180	ELECTROENCEPHALOGRAM, LOW-VOLTAGE		HP:0000006	OMIM:130180	TAS				I		HPO:iea	
OMIM	130180	ELECTROENCEPHALOGRAM, LOW-VOLTAGE		HP:0011181	OMIM:130180	TAS				P		HPO:probinson	
OMIM	130190	ELECTROENCEPHALOGRAPHIC PATTERNS		HP:0000006	OMIM:130190	IEA				I		HPO:iea	
OMIM	130190	ELECTROENCEPHALOGRAPHIC PATTERNS		HP:0002353	OMIM:130190	IEA				P		HPO:skoehler	
OMIM	130200	ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKEPHENOMENON		HP:0000006	OMIM:130200	IEA				I		HPO:iea	
OMIM	130200	ELECTROENCEPHALOGRAPHIC PECULIARITY: 14 AND 6 PER SEC. POSITIVE SPIKEPHENOMENON		HP:0002353	OMIM:130200	IEA				P		HPO:skoehler	
OMIM	130300	ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS		HP:0000006	OMIM:130300	IEA				I		HPO:iea	
OMIM	130300	ELECTROENCEPHALOGRAPHIC PECULIARITY: FRONTO-PRECENTRAL BETA WAVE GROUPS		HP:0002353	OMIM:130300	IEA				P		HPO:skoehler	
OMIM	130400	ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES		HP:0000006	OMIM:130400	IEA				I		HPO:iea	
OMIM	130400	ELECTROENCEPHALOGRAPHIC PECULIARITY: OCCIPITAL SLOW BETA WAVES		HP:0002353	OMIM:130400	IEA				P		HPO:skoehler	
OMIM	130600	#130600 ELLIPTOCYTOSIS 2; EL2;;ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE		HP:0000006	OMIM:130600	TAS				I		HPO:probinson	
OMIM	130600	#130600 ELLIPTOCYTOSIS 2; EL2;;ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE		HP:0001425	OMIM:130600	TAS				I		HPO:skoehler	
OMIM	130600	#130600 ELLIPTOCYTOSIS 2; EL2;;ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE		HP:0004445	OMIM:130600	TAS				P		HPO:probinson	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000006	OMIM:130650	TAS				I		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000028	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000076	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000105	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000121	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000150	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000158	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000239	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000269	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000280	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000520	PMID:23511928	PCS				P		HPO:probinson	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000787	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0000803	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001052	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001305	OMIM:130650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001528	OMIM:130650	TAS				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001539	OMIM:130650	TAS				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001540	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001548	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001638	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001640	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0001998	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0002240	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0002667	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0002884	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0003247	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0005487	OMIM:130650	TAS				P		HPO:probinson	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0005616	OMIM:130650	IEA				P		HPO:skoehler	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0006277	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0006744	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0008186	OMIM:130650	IEA				P		HPO:iea	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0008523	PMID:17223397	PCS				P		HPO:probinson	
OMIM	130650	BECKWITH-WIEDEMANN SYNDROME		HP:0011800	OMIM:130650	TAS				P		HPO:skoehler	
OMIM	130700	EMPHYSEMA, HEREDITARY PULMONARY		HP:0002097	OMIM:130700	IEA				P		HPO:iea	
OMIM	130700	EMPHYSEMA, HEREDITARY PULMONARY		HP:0004469	OMIM:130700	IEA				P		HPO:iea	
OMIM	130700	EMPHYSEMA, HEREDITARY PULMONARY		HP:0006510	OMIM:130700	IEA				P		HPO:iea	
OMIM	130710	EMPHYSEMA, CONGENITAL LOBAR		HP:0000006	OMIM:130710	IEA				I		HPO:iea	
OMIM	130710	EMPHYSEMA, CONGENITAL LOBAR		HP:0002098	OMIM:130710	IEA				P		HPO:skoehler	
OMIM	130710	EMPHYSEMA, CONGENITAL LOBAR		HP:0006539	OMIM:130710	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000006	OMIM:130720	IEA				I		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000023	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000028	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000218	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000268	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000272	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000316	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000319	OMIM:130720	TAS				P		HPO:probinson	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000343	OMIM:130720	TAS				P		HPO:probinson	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000347	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000358	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000369	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000405	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000470	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000494	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000508	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000678	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000767	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0000951	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001270	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001290	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001382	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001537	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001547	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001643	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0001647	OMIM:130720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002208	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002435	OMIM:130720	IEA				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002645	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002650	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002691	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002694	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002808	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0002948	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0003194	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0003396	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0004322	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0004452	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0004586	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0007099	OMIM:130720	IEA				P		HPO:iea	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0100702	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130720	LATERAL MENINGOCELE SYNDROME		HP:0100775	OMIM:130720	TAS				P		HPO:skoehler	
OMIM	130900	#130900 AMELOGENESIS IMPERFECTA, TYPE III; AI3;;AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT;ADHCAI;;AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE		HP:0000006	OMIM:130900	IEA				I		HPO:iea	
OMIM	130900	#130900 AMELOGENESIS IMPERFECTA, TYPE III; AI3;;AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT;ADHCAI;;AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE		HP:0000689	OMIM:130900	IEA				P		HPO:skoehler	
OMIM	130900	#130900 AMELOGENESIS IMPERFECTA, TYPE III; AI3;;AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT;ADHCAI;;AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE		HP:0000705	OMIM:130900	IEA				P		HPO:skoehler	
OMIM	130900	#130900 AMELOGENESIS IMPERFECTA, TYPE III; AI3;;AMELOGENESIS IMPERFECTA, HYPOCALCIFICATION TYPE, AUTOSOMAL DOMINANT;ADHCAI;;AMELOGENESIS IMPERFECTA, HYPOMINERALIZATION TYPE		HP:0200095	OMIM:130900	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0000006	OMIM:130950	IEA				I		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0001254	OMIM:130950	IEA				P		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0001260	OMIM:130950	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0001266	OMIM:130950	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0001284	OMIM:130950	IEA				P		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0001290	OMIM:130950	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0002072	OMIM:130950	IEA				P		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0002078	OMIM:130950	IEA				P		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0002080	OMIM:130950	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0002305	OMIM:130950	IEA				P		HPO:iea	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0002311	OMIM:130950	TAS				P		HPO:skoehler	
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0003487	OMIM:130950	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	130950	ENCEPHALOPATHY, RECURRENT, OF CHILDHOOD		HP:0007335	OMIM:130950	TAS				P		HPO:probinson	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0000006	OMIM:131100	IEA				I		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0000820	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0000845	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0000957	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0001031	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0001943	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0002014	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0002044	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0002893	OMIM:131100	IEA				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0002897	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0003072	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0003118	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0004398	OMIM:131100	IEA				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0006767	OMIM:131100	TAS				P		HPO:probinson	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0007449	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0008256	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0008261	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0009720	OMIM:131100	IEA				P		HPO:iea	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0012197	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0030404	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0040278	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0100570	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131100	MULTIPLE ENDOCRINE NEOPLASIA, TYPE I		HP:0100633	OMIM:131100	TAS				P		HPO:skoehler	
OMIM	131200	%131200 ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1;;ENDO1		HP:0000007	OMIM:131200	IEA				I		HPO:iea	
OMIM	131200	%131200 ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1;;ENDO1		HP:0000144	OMIM:131200	IEA				P		HPO:iea	
OMIM	131200	%131200 ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1;;ENDO1		HP:0001426	OMIM:131200	IEA				I		HPO:iea	
OMIM	131200	%131200 ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1;;ENDO1		HP:0030127	OMIM:131200	TAS				P		HPO:skoehler	
OMIM	131200	%131200 ENDOMETRIOSIS, SUSCEPTIBILITY TO, 1;;ENDO1	HP:0012828	HP:0100607	OMIM:131200	TAS				P		HPO:skoehler	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000006	PMID:15894597	IEA				I		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000303	PMID:20301335	PCS	HP:0003581			P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000365	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000520	PMID:15894597	IEA	HP:0003581			P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000520	PMID:29620655	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000651	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000670	PMID:20301335	PCS				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0000823	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0001324	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0001324	PMID:29620655	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0001533	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0001903	PMID:20301335	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002315	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002515	PMID:20301335	PCS				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002650	PMID:20301335	PCS				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002650	PMID:29620655	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002694	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0002857	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003034	ISBN-13:978-3437214301	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003202	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003388	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003388	PMID:29620655	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003621	PMID:15894597	IEA				C		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0003758	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0004396	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0005528	OMIM:131300	TAS				P		HPO:skoehler	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0005791	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0007807	PMID:20301335	PCS				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0009763	PMID:15894597	IEA				P		HPO:iea	
OMIM	131300	CAMURATI-ENGELMANN DISEASE		HP:0012514	PMID:29620655	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0000006	OMIM:131400	IEA				I		HPO:iea	
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0001873	PMID:6033105	PCS		HP:0040283		P		HPO:lccarmody	HP:0040283
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0001880	OMIM:131400	IEA				P		HPO:iea	
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0001880	PMID:9758611	PCS				P		HPO:lccarmody	
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0001903	PMID:9758611	PCS				P		HPO:lccarmody	
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0002113	PMID:6033105	PCS		HP:0040282		P		HPO:lccarmody	HP:0040282
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0002837	PMID:6033105	PCS				P		HPO:lccarmody	
OMIM	131400	EOSINOPHILIA, FAMILIAL		HP:0031323	PMID:9758611	PCS				P		HPO:lccarmody	
OMIM	131430	EOSINOPHILOPENIA		HP:0001025	PMID:6465701	PCS				P		HPO:lccarmody	
OMIM	131430	EOSINOPHILOPENIA		HP:0001871	OMIM:131430	IEA				P		HPO:iea	
OMIM	131430	EOSINOPHILOPENIA		HP:0002960	PMID:6465701	PCS				P		HPO:lccarmody	
OMIM	131430	EOSINOPHILOPENIA		HP:0003193	PMID:6465701	PCS				P		HPO:lccarmody	
OMIM	131430	EOSINOPHILOPENIA		HP:0031891	PMID:6465701	PCS				P		HPO:lccarmody	
OMIM	131440	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA		HP:0000006	OMIM:131440	TAS				I		HPO:skoehler	
OMIM	131440	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA		HP:0001880	OMIM:131440	IEA				P		HPO:skoehler	
OMIM	131440	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA		HP:0005547	OMIM:131440	TAS				P		HPO:skoehler	
OMIM	131440	MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA		HP:0006782	OMIM:131440	TAS				P		HPO:skoehler	
OMIM	131450	EPIBLEPHARON OF LOWER LID		HP:0000006	OMIM:131450	TAS				I		HPO:iea	
OMIM	131450	EPIBLEPHARON OF LOWER LID		HP:0040151	OMIM:131450	TAS				P		HPO:skoehler	
OMIM	131460	EPIBLEPHARON OF UPPER LID		HP:0000006	OMIM:131460	TAS				I		HPO:iea	
OMIM	131460	EPIBLEPHARON OF UPPER LID		HP:0040150	OMIM:131460	TAS				P		HPO:skoehler	
OMIM	131500	EPICANTHUS		HP:0000006	OMIM:131500	TAS				I		HPO:probinson	
OMIM	131500	EPICANTHUS		HP:0000286	OMIM:131500	TAS				P		HPO:probinson	
OMIM	131600	131600 EPIDERMOID CYSTS		HP:0000006	OMIM:131600	IEA				I		HPO:iea	
OMIM	131600	131600 EPIDERMOID CYSTS		HP:0000951	OMIM:131600	IEA				P		HPO:iea	
OMIM	131600	131600 EPIDERMOID CYSTS		HP:0200040	OMIM:131600	TAS				P		HPO:skoehler	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0000006	OMIM:131705	TAS				I		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0000007	OMIM:131705	TAS				I		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0001030	OMIM:131705	TAS				P		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0001056	OMIM:131705	TAS				P		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN	HP:0012825	HP:0001075	OMIM:131705	TAS				P		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0001939	OMIM:131705	IEA				P		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0003577	OMIM:131705	TAS				C		HPO:probinson	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0008066	OMIM:131705	TAS				P		HPO:skoehler	
OMIM	131705	TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN		HP:0008404	OMIM:131705	TAS				P		HPO:skoehler	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0000006	OMIM:131750	TAS				I		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0001056	OMIM:131750	TAS				P		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0001075	OMIM:131750	TAS				P		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0002164	OMIM:131750	TAS				P		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0003577	OMIM:131750	TAS				C		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0008066	OMIM:131750	TAS				P		HPO:probinson	
OMIM	131750	#131750 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT; DDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL DOMINANT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, COCKAYNE-TOURAINE TYPE; EBDCT;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, PASINI TYPE;;ALBOPAPULOID DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA; EBDDEPIDERMOLYSIS BULLOSA DYSTROPHICA WITH SUBCORNEAL CLEAVAGE, INCLUDED;EBDSC, INCLUDED		HP:0008404	OMIM:131750	TAS				P		HPO:skoehler	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0000006	OMIM:131760	TAS				I		HPO:probinson	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0000972	OMIM:131760	TAS				P		HPO:probinson	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0001056	OMIM:131760	TAS				P		HPO:probinson	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0001075	OMIM:131760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0001510	OMIM:131760	TAS				P		HPO:skoehler	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0002164	OMIM:131760	TAS				P		HPO:skoehler	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0003623	OMIM:131760	TAS				C		HPO:probinson	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0008066	OMIM:131760	TAS				P		HPO:skoehler	
OMIM	131760	EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE		HP:0008404	OMIM:131760	TAS				P		HPO:skoehler	
OMIM	131800	EPIDERMOLYSIS BULLOSA SIMPLEX, WEBER-COCKAYNE TYPE		HP:0000006	OMIM:131800	IEA				I		HPO:iea	
OMIM	131800	EPIDERMOLYSIS BULLOSA SIMPLEX, WEBER-COCKAYNE TYPE		HP:0000962	OMIM:131800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131800	EPIDERMOLYSIS BULLOSA SIMPLEX, WEBER-COCKAYNE TYPE		HP:0001056	OMIM:131800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131800	EPIDERMOLYSIS BULLOSA SIMPLEX, WEBER-COCKAYNE TYPE		HP:0007446	OMIM:131800	IEA				P		HPO:iea	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0000006	OMIM:131850	IEA				I		HPO:iea	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0000007	OMIM:131850	TAS				I		HPO:skoehler	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0000951	OMIM:131850	IEA				P		HPO:iea	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0000962	OMIM:131850	TAS				P		HPO:skoehler	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0000989	OMIM:131850	TAS				P		HPO:skoehler	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0008404	OMIM:131850	TAS				P		HPO:skoehler	
OMIM	131850	EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL		HP:0012221	OMIM:131850	TAS				P		HPO:skoehler	
OMIM	131880	EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE		HP:0000006	OMIM:131880	TAS				I		HPO:probinson	
OMIM	131880	EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE		HP:0003593	OMIM:131880	TAS				C		HPO:probinson	
OMIM	131880	EPIDERMOLYSIS BULLOSA WITH DEFICIENCY OF GALACTOSYLHYDROXYLYSYL GLUCOSYLTRANSFERASE		HP:0008066	OMIM:131880	TAS				P		HPO:probinson	
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0000006	PMID:7682883	PCS				I		HPO:iea	
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0000972	PMID:11407989	PCS				P		HPO:skoehler	
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0001056	OMIM:131900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0002164	OMIM:131900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0008066	OMIM:131900	IEA				P		HPO:skoehler	
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0008404	OMIM:131900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	131900	EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE		HP:0200097	PMID:3372762	PCS				P		HP:probinson	
OMIM	131950	EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE		HP:0000006	OMIM:131950	IEA				I		HPO:iea	
OMIM	131950	EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE		HP:0000978	OMIM:131950	IEA				P		HPO:iea	
OMIM	131950	EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE		HP:0007585	OMIM:131950	IEA				P		HPO:iea	
OMIM	131950	EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE		HP:0008401	OMIM:131950	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0000006	OMIM:131960	IEA				I		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0001805	OMIM:131960	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0002164	OMIM:131960	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0007438	OMIM:131960	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0007494	OMIM:131960	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0007530	OMIM:131960	IEA				P		HPO:iea	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0008066	OMIM:131960	TAS				P		HPO:probinson	
OMIM	131960	#131960 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MOTTLED PIGMENTATION; EBS-MP;;SPECKLED HYPERPIGMENTATION WITH PUNCTATE PALMOPLANTAR KERATOSES ANDCHILDHOOD BLISTERING		HP:0008404	OMIM:131960	TAS				P		HPO:skoehler	
OMIM	132000	#132000 EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE		HP:0000006	OMIM:132000	IEA				I		HPO:iea	
OMIM	132000	#132000 EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE		HP:0001030	OMIM:132000	IEA				P		HPO:iea	
OMIM	132000	#132000 EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE		HP:0002164	OMIM:132000	IEA				P		HPO:iea	
OMIM	132000	#132000 EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE		HP:0007383	OMIM:132000	IEA				P		HPO:iea	
OMIM	132000	#132000 EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, BART TYPE		HP:0008404	OMIM:132000	TAS				P		HPO:skoehler	
OMIM	132090	EPILEPSY, BENIGN OCCIPITAL		HP:0000006	OMIM:132090	TAS				I		HPO:skoehler	
OMIM	132090	EPILEPSY, BENIGN OCCIPITAL		HP:0001250	OMIM:132090	TAS				P		HPO:skoehler	
OMIM	132090	EPILEPSY, BENIGN OCCIPITAL		HP:0002353	OMIM:132090	TAS				P		HPO:skoehler	
OMIM	132100	PHOTOPAROXYSMAL RESPONSE 1; PPR1		HP:0000006	OMIM:132100	TAS				I		HPO:probinson	
OMIM	132100	PHOTOPAROXYSMAL RESPONSE 1; PPR1		HP:0001425	OMIM:132100	TAS				I		HPO:skoehler	
OMIM	132100	PHOTOPAROXYSMAL RESPONSE 1; PPR1		HP:0003831	OMIM:132100	TAS				C		HPO:skoehler	
OMIM	132100	PHOTOPAROXYSMAL RESPONSE 1; PPR1		HP:0010852	OMIM:132100	TAS				P		HPO:probinson	
OMIM	132300	EPILEPSY, READING		HP:0000006	OMIM:132300	TAS				I		HPO:iea	
OMIM	132300	EPILEPSY, READING		HP:0001250	OMIM:132300	TAS				P		HPO:probinson	
OMIM	132300	EPILEPSY, READING		HP:0002353	OMIM:132300	TAS				P		HPO:probinson	
OMIM	132300	EPILEPSY, READING		HP:0003621	OMIM:132300	TAS				C		HPO:iea	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0000006	OMIM:132400	TAS				I		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0001387	OMIM:132400	TAS				P		HPO:skoehler	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0001425	OMIM:132400	TAS				I		HPO:skoehler	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0002515	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0002656	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0002663	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0002761	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0002857	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0003300	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1	HP:0012825	HP:0003301	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0003502	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0003510	OMIM:132400	TAS				P		HPO:skoehler	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0005743	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0006429	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0008800	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0008843	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1	HP:0012825	HP:0008873	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0009803	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0010049	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0010582	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0010585	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132400	EPIPHYSEAL DYSPLASIA, MULTIPLE, 1		HP:0100864	OMIM:132400	TAS				P		HPO:probinson	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000006	OMIM:132450	IEA				I		HPO:iea	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000160	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000311	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000405	OMIM:132450	IEA				P		HPO:iea	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000518	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0000545	OMIM:132450	IEA				P		HPO:iea	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0001156	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0002656	OMIM:132450	IEA				P		HPO:iea	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0002673	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0002857	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0004322	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0009803	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0012368	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0030329	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132450	#132450 EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS;EDMMD		HP:0030672	OMIM:132450	TAS				P		HPO:skoehler	
OMIM	132500	EPISTAXIS, HEREDITARY		HP:0000006	OMIM:132500	IEA				I		HPO:iea	
OMIM	132500	EPISTAXIS, HEREDITARY		HP:0000421	OMIM:132500	IEA				P		HPO:iea	
OMIM	132600	#132600 PILOMATRIXOMA;;PILOMATRICOMA; PTR;;EPITHELIOMA CALCIFICANS OF MALHERBE		HP:0000006	OMIM:132600	IEA				I		HPO:iea	
OMIM	132600	#132600 PILOMATRIXOMA;;PILOMATRICOMA; PTR;;EPITHELIOMA CALCIFICANS OF MALHERBE		HP:0001428	OMIM:132600	IEA				I		HPO:iea	
OMIM	132600	#132600 PILOMATRIXOMA;;PILOMATRICOMA; PTR;;EPITHELIOMA CALCIFICANS OF MALHERBE		HP:0008069	OMIM:132600	IEA				P		HPO:skoehler	
OMIM	132600	#132600 PILOMATRIXOMA;;PILOMATRICOMA; PTR;;EPITHELIOMA CALCIFICANS OF MALHERBE		HP:0030434	OMIM:132600	TAS				P		HPO:skoehler	
OMIM	132700	CYLINDROMATOSIS, FAMILIAL		HP:0000006	OMIM:132700	IEA				I		HPO:iea	
OMIM	132700	CYLINDROMATOSIS, FAMILIAL		HP:0003581	OMIM:132700	IEA				C		HPO:iea	
OMIM	132700	CYLINDROMATOSIS, FAMILIAL		HP:0008069	OMIM:132700	IEA				P		HPO:skoehler	
OMIM	132800	MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA		HP:0000006	OMIM:132800	IEA				I		HPO:iea	
OMIM	132800	MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA		HP:0000951	OMIM:132800	IEA				P		HPO:iea	
OMIM	132800	MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA		HP:0002664	OMIM:132800	IEA				P		HPO:iea	
OMIM	132800	MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA		HP:0003674	OMIM:132800	IEA				C		HPO:iea	
OMIM	132810	EPOXIDE HYDROLASE 1, MICROSOMAL		HP:0000006	OMIM:132810	IEA				I		HPO:iea	
OMIM	132810	EPOXIDE HYDROLASE 1, MICROSOMAL		HP:0001939	OMIM:132810	IEA				P		HPO:iea	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0000006	OMIM:132900	TAS				I		HPO:probinson	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0001297	OMIM:132900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0001643	PMID:17666408	PCS				P		HPO:skoehler	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0001647	OMIM:132900	TAS				P		HPO:skoehler	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0001659	OMIM:132900	TAS				P		HPO:skoehler	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0001677	PMID:17666408	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0004933	PMID:17666408	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0004942	OMIM:132900	TAS				P		HPO:probinson	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0005162	OMIM:132900	TAS				P		HPO:skoehler	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0008034	OMIM:132900	TAS				P		HPO:probinson	
OMIM	132900	AORTIC ANEURYSM, FAMILIAL THORACIC 4		HP:0012180	OMIM:132900	TAS				P		HPO:probinson	
OMIM	132990	ERYTHEMA NODOSUM, FAMILIAL		HP:0000006	OMIM:132990	IEA				I		HPO:iea	
OMIM	132990	ERYTHEMA NODOSUM, FAMILIAL		HP:0010783	OMIM:132990	IEA				P		HPO:skoehler	
OMIM	132990	ERYTHEMA NODOSUM, FAMILIAL		HP:0012219	OMIM:132990	IEA				P		HPO:skoehler	
OMIM	133000	ERYTHEMA PALMARE HEREDITARIUM		HP:0000006	OMIM:133000	IEA				I		HPO:iea	
OMIM	133000	ERYTHEMA PALMARE HEREDITARIUM		HP:0010783	OMIM:133000	IEA				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000006	OMIM:133020	IEA				I		HPO:iea	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000217	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000622	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000707	OMIM:133020	IEA				P		HPO:iea	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000975	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0000989	OMIM:133020	IEA				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0001097	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0001962	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0002014	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0002019	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0003011	OMIM:133020	IEA				P		HPO:iea	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0003326	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0003621	OMIM:133020	IEA				C		HPO:iea	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0012332	OMIM:133020	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0032147	PMID:14985375	PCS				P		HPO:lccarmody	
OMIM	133020	ERYTHERMALGIA, PRIMARY		HP:0040264	OMIM:133020	TAS				P		HPO:skoehler	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0000006	OMIM:133100	IEA				I		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0000822	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001050	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001342	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001658	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001744	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001898	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001899	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0001900	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0002315	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0002321	OMIM:133100	TAS				P		HPO:skoehler	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0002641	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0002875	OMIM:133100	IEA				P		HPO:iea	
OMIM	133100	#133100 ERYTHROCYTOSIS, FAMILIAL, 1; ECYT1;;POLYCYTHEMIA, PRIMARY FAMILIAL AND CONGENITAL; PFCP;;ERYTHROCYTOSIS, AUTOSOMAL DOMINANT BENIGN		HP:0012378	OMIM:133100	TAS				P		HPO:skoehler	
OMIM	133180	ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO; FERLK		HP:0000006	OMIM:133180	IEA				I		HPO:iea	
OMIM	133180	ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO; FERLK		HP:0003829	OMIM:133180	IEA				C		HPO:skoehler	
OMIM	133180	ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO; FERLK		HP:0004808	OMIM:133180	IEA				P		HPO:skoehler	
OMIM	133180	ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO; FERLK		HP:0004828	OMIM:133180	IEA				P		HPO:iea	
OMIM	133180	ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO; FERLK		HP:0004828	OMIM:133180	TAS				P		HPO:probinson	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0000006	OMIM:133190	IEA				I		HPO:iea	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0000605	OMIM:133190	IEA				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0000639	OMIM:133190	IEA				P		HPO:iea	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0000951	OMIM:133190	IEA				P		HPO:iea	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0000962	OMIM:133190	TAS				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0001257	OMIM:133190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0001260	OMIM:133190	IEA				P		HPO:iea	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0001265	OMIM:133190	IEA				P		HPO:iea	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0001272	OMIM:133190	TAS				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0001347	OMIM:133190	IEA				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0002066	OMIM:133190	TAS				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0002070	OMIM:133190	IEA				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0002075	OMIM:133190	TAS				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0002080	OMIM:133190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0002380	OMIM:133190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0003477	OMIM:133190	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0003829	OMIM:133190	TAS				C		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0007256	OMIM:133190	IEA				P		HPO:skoehler	
OMIM	133190	SPINOCEREBELLAR ATAXIA 34; SCA34		HP:0007772	OMIM:133190	IEA				P		HPO:skoehler	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0000006	OMIM:133200	TAS				I		HPO:iea	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0000007	OMIM:133200	TAS				I		HPO:skoehler	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0003593	OMIM:133200	TAS				C		HPO:iea	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0005588	OMIM:133200	TAS				P		HPO:iea	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0005595	OMIM:133200	TAS				P		HPO:iea	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0010783	OMIM:133200	TAS				P		HPO:skoehler	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0025092	OMIM:133200	TAS				P		HPO:skoehler	
OMIM	133200	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1		HP:0025114	OMIM:133200	TAS				P		HPO:skoehler	
OMIM	133239	ESOPHAGEAL CANCER		HP:0000006	OMIM:133239	IEA				I		HPO:iea	
OMIM	133239	ESOPHAGEAL CANCER		HP:0001428	OMIM:133239	IEA				I		HPO:skoehler	
OMIM	133239	ESOPHAGEAL CANCER		HP:0002860	OMIM:133239	IEA				P		HPO:skoehler	
OMIM	133240	ESOPHAGEAL RING, LOWER		HP:0000006	OMIM:133240	IEA				I		HPO:iea	
OMIM	133240	ESOPHAGEAL RING, LOWER		HP:0002015	OMIM:133240	IEA				P		HPO:iea	
OMIM	133240	ESOPHAGEAL RING, LOWER		HP:0002036	OMIM:133240	IEA				P		HPO:iea	
OMIM	133500	EXCHONDROSIS OF PINNA, POSTERIOR		HP:0000006	OMIM:133500	IEA				I		HPO:iea	
OMIM	133500	EXCHONDROSIS OF PINNA, POSTERIOR		HP:0000598	OMIM:133500	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000007	OMIM:133540	IEA				I		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000028	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000054	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000083	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000093	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000252	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000292	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000303	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000377	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000407	OMIM:133540	TAS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000417	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000482	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000486	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000518	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000540	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000568	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000580	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000633	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000639	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000648	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000649	OMIM:133540	IEA				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000670	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000680	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000685	OMIM:133540	PCS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000689	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000762	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000822	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000939	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000958	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000970	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000987	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0000992	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001000	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001249	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001250	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001251	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001271	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001324	OMIM:133540	TAS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001337	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001376	OMIM:133540	PCS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001511	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001518	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001525	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001595	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0001744	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002059	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002135	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002240	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002343	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002545	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002684	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002808	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0002866	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003130	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003224	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003278	OMIM:133540	TAS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003469	OMIM:133540	PCS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003510	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0003758	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0004334	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0005328	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0006958	OMIM:133540	IEA				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0007346	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0007352	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0007676	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0007759	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0008070	OMIM:133540	TAS				P		HPO:skoehler	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0008839	OMIM:133540	TAS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0008897	OMIM:133540	PCS				P		HPO:probinson	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0010234	OMIM:133540	IEA				P		HPO:iea	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0011359	OMIM:133540	TAS				P		HPO:skoehler	
OMIM	133540	#133540 COCKAYNE SYNDROME, TYPE B; CSB;;CKN2		HP:0011675	OMIM:133540	IEA				P		HPO:iea	
OMIM	133600	EXOSTOSES OF HEEL		HP:0000006	OMIM:133600	IEA				I		HPO:iea	
OMIM	133600	EXOSTOSES OF HEEL		HP:0100777	OMIM:133600	IEA				P		HPO:skoehler	
OMIM	133690	EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E		HP:0000006	OMIM:133690	IEA				I		HPO:iea	
OMIM	133690	EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E		HP:0002762	OMIM:133690	IEA				P		HPO:iea	
OMIM	133690	EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E		HP:0004334	OMIM:133690	IEA				P		HPO:skoehler	
OMIM	133690	EXOSTOSES WITH ANETODERMIA AND BRACHYDACTYLY, TYPE E		HP:0005863	OMIM:133690	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0000006	OMIM:133700	IEA				I		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0000896	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0000918	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0001760	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0002318	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0002812	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0002857	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0003068	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0003105	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0003276	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0003406	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0003621	OMIM:133700	IEA				C		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0004322	OMIM:133700	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0006765	OMIM:133700	IEA				P		HPO:iea	
OMIM	133700	EXOSTOSES, MULTIPLE, TYPE I		HP:0010049	OMIM:133700	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0000006	OMIM:133701	IEA				I		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0000896	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0000918	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0002318	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0002812	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0002857	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0003068	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0003105	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0003276	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0003406	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0003621	OMIM:133701	IEA				C		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0004322	OMIM:133701	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0006765	OMIM:133701	IEA				P		HPO:iea	
OMIM	133701	EXOSTOSES, MULTIPLE, TYPE II		HP:0010049	OMIM:133701	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000006	OMIM:133705	IEA				I		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000286	OMIM:133705	TAS				P		HPO:skoehler	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000405	OMIM:133705	TAS				P		HPO:skoehler	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000413	OMIM:133705	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000577	OMIM:133705	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0000954	OMIM:133705	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0001374	OMIM:133705	TAS				P		HPO:skoehler	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0001838	OMIM:133705	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0002021	OMIM:133705	IEA				P		HPO:iea	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0007598	OMIM:133705	TAS				P		HPO:skoehler	
OMIM	133705	133705 EXTERNAL AUDITORY CANAL, BILATERAL ATRESIA OF, WITH CONGENITAL VERTICALTALUS;;RASMUSSEN SYNDROME		HP:0009237	OMIM:133705	IEA				P		HPO:iea	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0000006	OMIM:133750	IEA				I		HPO:iea	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0000252	OMIM:133750	IEA				P		HPO:iea	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0000953	OMIM:133750	PCS				P		HPO:probinson	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0004322	OMIM:133750	PCS				P		HPO:probinson	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0006682	OMIM:133750	TAS				P		HPO:skoehler	
OMIM	133750	133750 EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY		HP:0006889	OMIM:133750	PCS				P		HPO:probinson	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0000006	OMIM:133780	IEA				I		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0000523	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0000541	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0000618	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0001147	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0001489	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0001493	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0002757	OMIM:133780	TAS				P		HPO:skoehler	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0003593	OMIM:133780	IEA				C		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0003677	OMIM:133780	IEA				C		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0007663	OMIM:133780	TAS				P		HPO:skoehler	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0007685	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0007902	OMIM:133780	IEA				P		HPO:iea	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0030490	OMIM:133780	IEA				P		HPO:skoehler	
OMIM	133780	#133780 EXUDATIVE VITREORETINOPATHY 1; EVR1;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT;;FEVR, AUTOSOMAL DOMINANT;;CRISWICK-SCHEPENS SYNDROMERETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED		HP:0030666	OMIM:133780	TAS				P		HPO:skoehler	
OMIM	133800	EYEBROW, WHORL IN		HP:0000006	OMIM:133800	TAS				I		HPO:skoehler	
OMIM	133900	HEMIFACIAL HYPERPLASIA		HP:0000006	OMIM:133900	IEA				I		HPO:iea	
OMIM	133900	HEMIFACIAL HYPERPLASIA		HP:0000324	OMIM:133900	IEA				P		HPO:iea	
OMIM	133900	HEMIFACIAL HYPERPLASIA		HP:0000327	OMIM:133900	IEA				P		HPO:iea	
OMIM	133900	HEMIFACIAL HYPERPLASIA		HP:0000689	OMIM:133900	IEA				P		HPO:iea	
OMIM	134000	FACIAL HYPERTRICHOSIS		HP:0000006	OMIM:134000	IEA				I		HPO:iea	
OMIM	134000	FACIAL HYPERTRICHOSIS		HP:0002219	OMIM:134000	IEA				P		HPO:iea	
OMIM	134200	FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL		HP:0000006	OMIM:134200	IEA				I		HPO:iea	
OMIM	134200	FACIAL PALSY, FAMILIAL RECURRENT PERIPHERAL		HP:0010628	OMIM:134200	IEA				P		HPO:iea	
OMIM	134300	FACIAL SPASM		HP:0000006	OMIM:134300	IEA				I		HPO:iea	
OMIM	134300	FACIAL SPASM		HP:0001265	OMIM:134300	IEA				P		HPO:iea	
OMIM	134300	FACIAL SPASM		HP:0009916	OMIM:134300	IEA				P		HPO:skoehler	
OMIM	134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS		HP:0000006	OMIM:134400	TAS				I		HPO:iea	
OMIM	134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS		HP:0002204	OMIM:134400	TAS				P		HPO:iea	
OMIM	134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS		HP:0004419	OMIM:134400	TAS				P		HPO:iea	
OMIM	134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS		HP:0004950	OMIM:134400	TAS				P		HPO:iea	
OMIM	134400	FACTOR V EXCESS WITH SPONTANEOUS THROMBOSIS		HP:0011996	OMIM:134400	TAS				P		HPO:iea	
OMIM	134430	FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0000006	OMIM:134430	TAS				I		HPO:probinson	
OMIM	134430	FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0002584	OMIM:134430	TAS				P		HPO:skoehler	
OMIM	134430	FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0003125	OMIM:134430	TAS				P		HPO:probinson	
OMIM	134430	FACTOR VII AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0008169	OMIM:134430	TAS				P		HPO:probinson	
OMIM	134500	FACTOR VIII DEFICIENCY		HP:0000006	OMIM:134500	IEA				I		HPO:iea	
OMIM	134500	FACTOR VIII DEFICIENCY		HP:0001892	OMIM:134500	IEA				P		HPO:iea	
OMIM	134500	FACTOR VIII DEFICIENCY		HP:0003125	OMIM:134500	IEA				P		HPO:iea	
OMIM	134510	FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF		HP:0000006	OMIM:134510	TAS				I		HPO:probinson	
OMIM	134510	FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF		HP:0003125	OMIM:134510	TAS				P		HPO:probinson	
OMIM	134510	FACTOR VIII AND FACTOR IX, COMBINED DEFICIENCY OF		HP:0011858	OMIM:134510	TAS				P		HPO:probinson	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0000006	OMIM:134520	IEA				I		HPO:iea	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0000978	OMIM:134520	IEA				P		HPO:iea	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0001373	OMIM:134520	IEA				P		HPO:iea	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0003645	OMIM:134520	IEA				P		HPO:iea	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0005261	OMIM:134520	IEA				P		HPO:iea	
OMIM	134520	FACTORS VIII, IX AND XI, COMBINED DEFICIENCY OF		HP:0031364	OMIM:134520	IEA				P		HPO:skoehler	
OMIM	134540	FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF		HP:0000006	OMIM:134540	IEA				I		HPO:probinson	
OMIM	134540	FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF		HP:0001929	OMIM:134540	IEA				P		HPO:probinson	
OMIM	134540	FACTOR IX AND FACTOR XI, COMBINED DEFICIENCY OF		HP:0011858	OMIM:134540	IEA				P		HPO:probinson	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0000006	OMIM:134600	IEA				I		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0000083	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0000093	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0000124	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0001324	OMIM:134600	TAS	HP:0003581			P		HPO:skoehler	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0002148	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0002748	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0002749	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0002900	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0003076	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0003648	OMIM:134600	IEA				P		HPO:iea	
OMIM	134600	FANCONI RENOTUBULAR SYNDROME		HP:0004322	OMIM:134600	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0000006	OMIM:134610	IEA				I		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0000083	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0000093	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0001369	OMIM:134610	IEA				P		HPO:skoehler	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0001917	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0001954	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0002027	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0002102	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0002586	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0002829	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0003621	OMIM:134610	IEA				C		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0005764	OMIM:134610	IEA				P		HPO:iea	
OMIM	134610	#134610 FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT;;FMF, AUTOSOMAL DOMINANT		HP:0100749	OMIM:134610	TAS				P		HPO:skoehler	
OMIM	134750	FELTY SYNDROME		HP:0000006	OMIM:134750	IEA				I		HPO:iea	
OMIM	134750	FELTY SYNDROME		HP:0001370	OMIM:134750	IEA				P		HPO:iea	
OMIM	134750	FELTY SYNDROME		HP:0001744	OMIM:134750	IEA				P		HPO:iea	
OMIM	134750	FELTY SYNDROME		HP:0001875	OMIM:134750	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000023	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000028	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000054	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000059	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000104	OMIM:134780	TAS				P		HPO:probinson	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000113	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000175	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000219	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000219	OMIM:134780	TAS				P		HPO:skoehler	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000319	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000343	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000347	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000369	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000377	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000430	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000565	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000582	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000902	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000912	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0000921	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001177	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001629	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001642	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001660	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001762	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001770	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001841	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0001999	OMIM:134780	IEA				P		HPO:skoehler	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0002020	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0002650	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0002937	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0002974	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0002996	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0003041	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0003196	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0003274	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0003745	OMIM:134780	IEA				I		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0004322	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0004686	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0004689	OMIM:134780	TAS				P		HPO:probinson	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0004704	OMIM:134780	TAS				P		HPO:probinson	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0004742	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0005613	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0005792	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0006467	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0008455	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0008465	OMIM:134780	IEA				P		HPO:iea	
OMIM	134780	134780 FEMORAL-FACIAL SYNDROME; FFS;;FEMORAL HYPOPLASIA-UNUSUAL FACIES SYNDROME; FHUFS		HP:0009800	OMIM:134780	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	134900	FIBRINOLYTIC DEFECT		HP:0000006	OMIM:134900	IEA				I		HPO:iea	
OMIM	134900	FIBRINOLYTIC DEFECT		HP:0000974	OMIM:134900	IEA				P		HPO:iea	
OMIM	134900	FIBRINOLYTIC DEFECT		HP:0007420	OMIM:134900	IEA				P		HPO:iea	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0000006	OMIM:135100	TAS				I		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0000405	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0000407	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0000687	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0001249	OMIM:135100	TAS		HP:0040284		P		HPO:probinson	6%
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0001256	OMIM:135100	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0001596	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0001822	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0002135	OMIM:135100	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0002650	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0002878	OMIM:135100	TAS				P		HPO:skoehler	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0003016	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0004209	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0004629	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0006429	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0008449	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0010034	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0010054	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0010109	OMIM:135100	TAS				P		HPO:skoehler	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0010566	OMIM:135100	IEA				P		HPO:skoehler	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0011987	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0011988	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135100	FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP		HP:0011989	OMIM:135100	TAS				P		HPO:probinson	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0000006	PMID:18234728	PCS				I		HPO:iea	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0000107	OMIM:135150	TAS				P		HPO:skoehler	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0001012	PMID:8734663	PCS				P		HPO:skoehler	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0002108	PMID:18234728	IEA		HP:0040284		P		HPO:iea	27/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0003003	PMID:18234728	PCS		HP:0040284		P		HP:probinson	2/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0005584	PMID:18234728	PCS		HP:0040284		P		HPO:skoehler	30/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0006755	PMID:18234728	PCS		HP:0040284		P		HP:probinson	1/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0007620	PMID:18234728	PCS		HP:0040284		P		HP:probinson	1/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0009726	OMIM:135150	IEA				P		HPO:iea	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0030255	PMID:9835964	PCS				P		HP:probinson	
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0030436	PMID:18234728	PCS		HP:0040284		P		HPO:skoehler	75/89
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0032227	PMID:18234728	PCS		HP:0040284		P		HP:probinson	4/51
OMIM	135150	BIRT-HOGG-DUBE SYNDROME		HP:0032228	PMID:18234728	PCS		HP:0040284		P		HP:probinson	9/51
OMIM	135290	DESMOID DISEASE, HEREDITARY		HP:0000006	OMIM:135290	PCS				I		HPO:iea	
OMIM	135290	DESMOID DISEASE, HEREDITARY		HP:0003003	PMID:1078292	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	135290	DESMOID DISEASE, HEREDITARY		HP:0100245	OMIM:135290	PCS	HP:0003593	HP:0040281		P		HPO:iea	HP:0040281
OMIM	135290	DESMOID DISEASE, HEREDITARY		HP:0200040	PMID:1078292;PMID:8940264	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	135300	FIBROMATOSIS, GINGIVAL, 1		HP:0000006	OMIM:135300	TAS				I		HPO:probinson	
OMIM	135300	FIBROMATOSIS, GINGIVAL, 1		HP:0000169	OMIM:135300	TAS				P		HPO:probinson	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000006	OMIM:135400	IEA				I		HPO:iea	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000007	OMIM:135400	TAS				I		HPO:skoehler	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000169	OMIM:135400	IEA				P		HPO:iea	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000286	OMIM:135400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000414	OMIM:135400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000494	OMIM:135400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0000998	OMIM:135400	TAS				P		HPO:skoehler	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0001007	OMIM:135400	IEA				P		HPO:iea	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0004540	OMIM:135400	IEA				P		HPO:skoehler	
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0009928	OMIM:135400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135400	HYPERTRICHOSIS, CONGENITAL GENERALIZED, WITH OR WITHOUT GINGIVAL HYPERPLASIA		HP:0012810	OMIM:135400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000006	OMIM:135500	IEA				I		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000040	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000169	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000179	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000212	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000218	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000280	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000303	OMIM:135500	TAS				P		HPO:skoehler	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000358	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000365	OMIM:135500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000431	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000518	OMIM:135500	TAS				P		HPO:skoehler	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000545	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000574	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000664	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000684	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0000787	OMIM:135500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001007	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001187	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001250	OMIM:135500	TAS				P		HPO:skoehler	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001252	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001290	OMIM:135500	TAS				P		HPO:skoehler	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001507	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001537	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001638	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001643	OMIM:135500	TAS				P		HPO:skoehler	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001744	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001792	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0001857	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0002240	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0002616	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0002650	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0003298	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0005113	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0006887	OMIM:135500	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0009882	OMIM:135500	IEA				P		HPO:iea	
OMIM	135500	ZIMMERMANN-LABAND SYNDROME 1		HP:0010864	OMIM:135500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	135550	FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS		HP:0000006	OMIM:135550	IEA				I		HPO:iea	
OMIM	135550	FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS		HP:0000169	OMIM:135550	IEA				P		HPO:iea	
OMIM	135550	FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS		HP:0000408	OMIM:135550	IEA				P		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0000006	OMIM:135580	TAS				I		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0001297	OMIM:135580	TAS				P		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0001658	OMIM:135580	TAS				P		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0002647	OMIM:135580	TAS				P		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0004417	OMIM:135580	TAS				P		HPO:probinson	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0005313	OMIM:135580	TAS				P		HPO:iea	
OMIM	135580	FIBROMUSCULAR DYSPLASIA OF ARTERIES		HP:0100817	OMIM:135580	TAS				P		HPO:iea	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0000006	OMIM:135700	TAS				I		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0000565	OMIM:135700	TAS				P		HPO:skoehler	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0000577	OMIM:135700	TAS				P		HPO:skoehler	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0001477	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0001488	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0001491	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0007936	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0012241	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0012242	OMIM:135700	TAS				P		HPO:probinson	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0031721	OMIM:135700	IEA				P		HPO:skoehler	
OMIM	135700	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1		HP:0031723	OMIM:135700	IEA				P		HPO:skoehler	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0000006	OMIM:135750	IEA				I		HPO:iea	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0000271	OMIM:135750	IEA				P		HPO:iea	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0000430	OMIM:135750	TAS				P		HPO:skoehler	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0001159	OMIM:135750	IEA				P		HPO:iea	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0001161	OMIM:135750	IEA				P		HPO:iea	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0001199	OMIM:135750	TAS				P		HPO:skoehler	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0001769	OMIM:135750	TAS				P		HPO:probinson	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0001773	OMIM:135750	TAS				P		HPO:probinson	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0003974	OMIM:135750	IEA				P		HPO:iea	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0006443	OMIM:135750	TAS				P		HPO:skoehler	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0009556	OMIM:135750	TAS				P		HPO:skoehler	
OMIM	135750	%135750 LAURIN-SANDROW SYNDROME;;LSS;;SANDROW SYNDROME;;MIRROR HANDS AND FEET WITH NASAL DEFECTS;;TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP;;MIRROR-IMAGE POLYDACTYLY; MIP;;FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUSLAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED		HP:0010503	OMIM:135750	IEA				P		HPO:skoehler	
OMIM	135800	135800 FIBULA, RECURRENT DISLOCATION OF HEAD OF		HP:0000006	OMIM:135800	IEA				I		HPO:iea	
OMIM	135800	135800 FIBULA, RECURRENT DISLOCATION OF HEAD OF		HP:0002991	OMIM:135800	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000006	OMIM:135900	TAS				I		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000007	OMIM:135900	IEA				I		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000023	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000028	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000047	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000086	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000089	OMIM:135900	TAS				P		HPO:probinson	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000126	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000151	OMIM:135900	TAS				P		HPO:probinson	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000154	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000175	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000179	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000218	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000219	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000252	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000280	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000358	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000365	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000369	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000384	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000453	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000455	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000483	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000486	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000494	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000505	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000508	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000527	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000545	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000574	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000601	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000639	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000684	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000718	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000729	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000776	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000879	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000954	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000960	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0000965	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001028	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001249	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001250	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001252	OMIM:135900	IEA				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001263	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001305	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001338	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001388	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001511	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001537	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001629	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001631	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001636	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0001643	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002079	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002205	OMIM:135900	TAS				P		HPO:probinson	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002209	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002219	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002566	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002576	OMIM:135900	IEA				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002588	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002592	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002650	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002673	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002750	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0002808	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0003083	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0003298	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0004227	OMIM:135900	TAS				P		HPO:probinson	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0004322	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0005280	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0006237	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0006498	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0006863	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0008398	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0008398	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0008872	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0008897	OMIM:135900	TAS				P		HPO:skoehler	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0009747	OMIM:135900	IEA				P		HPO:iea	
OMIM	135900	COFFIN-SIRIS SYNDROME 1		HP:0100391	OMIM:135900	TAS				P		HPO:probinson	
OMIM	135950	FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION ANDPROPORTIONATE SHORT STATURE		HP:0000006	OMIM:135950	IEA				I		HPO:iea	
OMIM	135950	FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION ANDPROPORTIONATE SHORT STATURE		HP:0001511	OMIM:135950	TAS				P		HPO:probinson	
OMIM	135950	FINGER LOCKING, RECURRENT, WITH INTRAUTERINE GROWTH RETARDATION ANDPROPORTIONATE SHORT STATURE		HP:0004322	OMIM:135950	IEA				P		HPO:iea	
OMIM	136000	FINGERPRINTS, ABSENCE OF		HP:0000006	OMIM:136000	TAS				I		HPO:probinson	
OMIM	136000	FINGERPRINTS, ABSENCE OF		HP:0001217	OMIM:136000	TAS				P		HPO:probinson	
OMIM	136000	FINGERPRINTS, ABSENCE OF		HP:0007455	OMIM:136000	TAS				P		HPO:probinson	
OMIM	136000	FINGERPRINTS, ABSENCE OF	HP:0012825	HP:0010765	OMIM:136000	TAS				P		HPO:probinson	
OMIM	136100	FINGERS, RELATIVE LENGTH OF		HP:0000006	OMIM:136100	IEA				I		HPO:iea	
OMIM	136100	FINGERS, RELATIVE LENGTH OF		HP:0009536	OMIM:136100	IEA				P		HPO:iea	
OMIM	136120	FISH-EYE DISEASE		HP:0000007	OMIM:136120	TAS				I		HPO:skoehler	
OMIM	136120	FISH-EYE DISEASE		HP:0002155	OMIM:136120	TAS				P		HPO:skoehler	
OMIM	136120	FISH-EYE DISEASE		HP:0003141	OMIM:136120	TAS				P		HPO:probinson	
OMIM	136120	FISH-EYE DISEASE		HP:0003233	OMIM:136120	TAS				P		HPO:skoehler	
OMIM	136120	FISH-EYE DISEASE		HP:0003362	OMIM:136120	TAS				P		HPO:probinson	
OMIM	136120	FISH-EYE DISEASE		HP:0007759	OMIM:136120	TAS				P		HPO:skoehler	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000006	OMIM:136140	IEA				I		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000023	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000028	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000047	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000121	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000126	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000154	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000233	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000319	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000325	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000358	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000403	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000405	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000448	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000470	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000486	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000490	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000527	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0000540	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0001007	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0001388	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0001537	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0001631	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0001680	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0002162	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0002474	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0002608	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0002714	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0002750	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0004209	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0004322	OMIM:136140	TAS				P		HPO:probinson	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0005301	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0010230	OMIM:136140	IEA				P		HPO:iea	
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0010957	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0011599	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0012871	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0030424	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136140	FLOATING-HARBOR SYNDROME		HP:0100543	OMIM:136140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136150	FLOOD FACTOR DEFICIENCY		HP:0000006	OMIM:136150	IEA				I		HPO:iea	
OMIM	136150	FLOOD FACTOR DEFICIENCY		HP:0001871	OMIM:136150	IEA				P		HPO:iea	
OMIM	136150	FLOOD FACTOR DEFICIENCY		HP:0001939	OMIM:136150	IEA				P		HPO:iea	
OMIM	136200	FLUSHING OF EARS AND SOMNOLENCE		HP:0000006	OMIM:136200	IEA				I		HPO:iea	
OMIM	136200	FLUSHING OF EARS AND SOMNOLENCE		HP:0001262	OMIM:136200	IEA				P		HPO:iea	
OMIM	136200	FLUSHING OF EARS AND SOMNOLENCE		HP:0031284	OMIM:136200	IEA				P		HPO:skoehler	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000006	OMIM:136300	IEA				I		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000408	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000510	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000518	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000545	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000670	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000726	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000939	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0000962	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0001250	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0001251	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0001387	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0002293	OMIM:136300	TAS				P		HPO:skoehler	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0002381	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0002751	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0002922	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0004334	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0005700	OMIM:136300	IEA				P		HPO:iea	
OMIM	136300	FLYNN-AIRD SYNDROME		HP:0009830	OMIM:136300	TAS				P		HPO:skoehler	
OMIM	136400	FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA		HP:0000006	OMIM:136400	TAS				I		HPO:nvasilevsky	
OMIM	136400	FOCAL EPITHELIAL HYPERPLASIA OF THE ORAL MUCOSA		HP:0000153	OMIM:136400	IEA				P		HPO:iea	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0000006	OMIM:136480	IEA				I		HPO:iea	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0000542	PMID:3985833	PCS				P		HPO:lccarmody	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0007011	OMIM:136480	IEA				P		HPO:iea	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0011514	PMID:3985833	PCS				P		HPO:lccarmody	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0025404	PMID:3985833	PCS				P		HPO:lccarmody	
OMIM	136480	FOURTH CRANIAL NERVE PALSY, FAMILIAL CONGENITAL		HP:0025592	OMIM:136480	IEA				P		HPO:skoehler	
OMIM	136500	FOCAL FACIAL DERMAL DYSPLASIA		HP:0000006	OMIM:136500	IEA				I		HPO:iea	
OMIM	136500	FOCAL FACIAL DERMAL DYSPLASIA		HP:0003758	OMIM:136500	TAS				P		HPO:skoehler	
OMIM	136520	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROMEFOVEAL HYPOPLASIA, ISOLATED, INCLUDED		HP:0000006	OMIM:136520	IEA				I		HPO:iea	
OMIM	136520	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROMEFOVEAL HYPOPLASIA, ISOLATED, INCLUDED		HP:0000505	OMIM:136520	IEA				P		HPO:iea	
OMIM	136520	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROMEFOVEAL HYPOPLASIA, ISOLATED, INCLUDED		HP:0006934	OMIM:136520	IEA				P		HPO:iea	
OMIM	136520	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROMEFOVEAL HYPOPLASIA, ISOLATED, INCLUDED		HP:0007750	OMIM:136520	IEA				P		HPO:iea	
OMIM	136520	FOVEAL HYPOPLASIA AND PRESENILE CATARACT SYNDROMEFOVEAL HYPOPLASIA, ISOLATED, INCLUDED		HP:0007819	OMIM:136520	IEA				P		HPO:iea	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0000006	OMIM:136550	TAS				I		HPO:probinson	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0000603	OMIM:136550	TAS				P		HPO:skoehler	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0002909	OMIM:136550	TAS				P		HPO:probinson	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0007663	OMIM:136550	TAS				P		HPO:skoehler	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0007754	OMIM:136550	TAS				P		HPO:probinson	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0008002	OMIM:136550	TAS				P		HPO:skoehler	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0011510	OMIM:136550	TAS				P		HPO:probinson	
OMIM	136550	MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE		HP:0200070	OMIM:136550	TAS				P		HPO:skoehler	
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0000708	OMIM:136570	IEA		HP:0040284		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	9/16
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0000750	OMIM:136570	IEA		HP:0040281		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	HP:0040281
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0001250	OMIM:136570	IEA		HP:0040284		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	8/22
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0001263	OMIM:136570	IEA		HP:0040281		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	HP:0040281
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0001290	OMIM:136570	IEA		HP:0040284		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	10/21
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0001999	OMIM:136570	IEA		HP:0040281		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	HP:0040281
OMIM	136570	#136570 CHROMOSOME 16p12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16p12, INCLUDED		HP:0030680	OMIM:136570	IEA		HP:0040281		P	#136570 CHROMOSOME 16P12.1 DELETION SYNDROME, 520-KBFRAGILE SITE 16P12, INCLUDED	HPO:skoehler	HP:0040281
OMIM	136580	#136580 FRAGILE SITE 16q22; FRA16A		HP:0000789	OMIM:136580	IEA				P	#136580 FRAGILE SITE 16Q22; FRA16A	HPO:skoehler	
OMIM	136580	#136580 FRAGILE SITE 16q22; FRA16A		HP:0002733	OMIM:136580	IEA				P	#136580 FRAGILE SITE 16Q22; FRA16A	HPO:skoehler	
OMIM	136580	#136580 FRAGILE SITE 16q22; FRA16A		HP:0002916	OMIM:136580	IEA				P	#136580 FRAGILE SITE 16Q22; FRA16A	HPO:skoehler	
OMIM	136580	#136580 FRAGILE SITE 16q22; FRA16A		HP:0005268	OMIM:136580	IEA				P	#136580 FRAGILE SITE 16Q22; FRA16A	HPO:skoehler	
OMIM	136600	FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS		HP:0000006	OMIM:136600	IEA				I		HPO:iea	
OMIM	136600	FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS		HP:0000407	OMIM:136600	IEA				P		HPO:iea	
OMIM	136600	FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS		HP:0000648	OMIM:136600	IEA				P		HPO:iea	
OMIM	136600	FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS		HP:0001251	OMIM:136600	IEA				P		HPO:iea	
OMIM	136600	FRIEDREICH ATAXIA, SO-CALLED, WITH OPTIC ATROPHY AND SENSORINEURALDEAFNESS		HP:0001265	OMIM:136600	IEA				P		HPO:iea	
OMIM	136630	MENTAL RETARDATION, FRA12A TYPE		HP:0000006	OMIM:136630	TAS				I		HPO:skoehler	
OMIM	136630	MENTAL RETARDATION, FRA12A TYPE		HP:0000962	OMIM:136630	TAS				P		HPO:skoehler	
OMIM	136630	MENTAL RETARDATION, FRA12A TYPE		HP:0001249	OMIM:136630	IEA				P		HPO:skoehler	
OMIM	136630	MENTAL RETARDATION, FRA12A TYPE		HP:0001250	OMIM:136630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	136680	FRASIER SYNDROME		HP:0000006	OMIM:136680	IEA				I		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000037	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000097	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000100	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000133	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000149	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0000786	OMIM:136680	IEA				P		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0001428	OMIM:136680	IEA				I		HPO:iea	
OMIM	136680	FRASIER SYNDROME		HP:0003774	OMIM:136680	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000007	OMIM:136760	TAS				I		HPO:skoehler	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000161	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000286	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000316	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000327	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000349	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000369	OMIM:136760	TAS				P		HPO:skoehler	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000384	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000405	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000431	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000431	OMIM:136760	TAS				P		HPO:skoehler	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000455	OMIM:136760	TAS				P		HPO:probinson	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000456	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000508	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000518	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000568	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0000589	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001156	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001162	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001249	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001274	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001566	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0001636	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0002000	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0002738	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0003745	OMIM:136760	IEA				I		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0004423	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0005258	OMIM:136760	TAS				P		HPO:probinson	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0006931	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0006992	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0007541	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0009099	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0009466	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0009473	OMIM:136760	IEA				P		HPO:iea	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0011803	OMIM:136760	IEA				P		HPO:skoehler	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0012385	OMIM:136760	TAS				P		HPO:skoehler	
OMIM	136760	FRONTONASAL DYSPLASIA 1; FND1		HP:0030084	OMIM:136760	TAS				P		HPO:skoehler	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0000006	OMIM:136800	TAS				I		HPO:probinson	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0001131	OMIM:136800	TAS				P		HPO:probinson	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0007705	OMIM:136800	TAS				P		HPO:probinson	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0012038	OMIM:136800	TAS				P		HPO:probinson	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0012039	OMIM:136800	TAS				P		HPO:probinson	
OMIM	136800	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1		HP:0012040	OMIM:136800	TAS				P		HPO:probinson	
OMIM	136880	FUNDUS ALBIPUNCTATUS		HP:0000006	OMIM:136880	TAS				I		HPO:probinson	
OMIM	136880	FUNDUS ALBIPUNCTATUS		HP:0000007	OMIM:136880	TAS				I		HPO:skoehler	
OMIM	136880	FUNDUS ALBIPUNCTATUS		HP:0030642	OMIM:136880	TAS				P		HPO:skoehler	
OMIM	136900	SORSBY FUNDUS DYSTROPHY; SFD		HP:0000006	OMIM:136900	IEA				I		HPO:iea	
OMIM	136900	SORSBY FUNDUS DYSTROPHY; SFD		HP:0000501	OMIM:136900	IEA				P		HPO:skoehler	
OMIM	136900	SORSBY FUNDUS DYSTROPHY; SFD		HP:0000512	OMIM:136900	IEA				P		HPO:skoehler	
OMIM	136900	SORSBY FUNDUS DYSTROPHY; SFD		HP:0000618	OMIM:136900	IEA				P		HPO:skoehler	
OMIM	136900	SORSBY FUNDUS DYSTROPHY; SFD		HP:0007754	OMIM:136900	IEA				P		HPO:iea	
OMIM	137000	FUTCHER LINE		HP:0000006	OMIM:137000	IEA				I		HPO:iea	
OMIM	137000	FUTCHER LINE		HP:0000951	OMIM:137000	IEA				P		HPO:iea	
OMIM	137040	GALLBLADDER, AGENESIS OF		HP:0000006	OMIM:137040	IEA				I		HPO:iea	
OMIM	137040	GALLBLADDER, AGENESIS OF		HP:0001438	OMIM:137040	IEA				P		HPO:iea	
OMIM	137050	GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF		HP:0000006	OMIM:137050	TAS				I		HPO:probinson	
OMIM	137050	GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF		HP:0002205	OMIM:137050	TAS				P		HPO:probinson	
OMIM	137050	GAMMA-A-GLOBULIN, DEFECT IN ASSEMBLY OF		HP:0002720	OMIM:137050	TAS				P		HPO:probinson	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0000006	OMIM:137100	TAS				I		HPO:skoehler	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0000007	OMIM:137100	TAS				I		HPO:skoehler	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0001425	OMIM:137100	IEA				I		HPO:iea	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0002024	OMIM:137100	IEA				P		HPO:iea	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0002205	OMIM:137100	TAS				P		HPO:skoehler	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0002719	OMIM:137100	IEA				P		HPO:iea	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0002720	OMIM:137100	IEA				P		HPO:iea	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0002960	OMIM:137100	IEA				P		HPO:iea	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0003745	OMIM:137100	TAS				I		HPO:skoehler	
OMIM	137100	IMMUNOGLOBULIN A DEFICIENCY 1; IGAD1		HP:0004798	OMIM:137100	TAS				P		HPO:skoehler	
OMIM	137130	GASTRIC SNEEZING		HP:0000006	OMIM:137130	IEA				I		HPO:iea	
OMIM	137130	GASTRIC SNEEZING		HP:0001438	OMIM:137130	IEA				P		HPO:iea	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:137200	TAS				I		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0000975	OMIM:137200	IEA				P		HPO:iea	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0001760	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0002380	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0002411	OMIM:137200	IEA				P		HPO:iea	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0002486	OMIM:137200	IEA				P		HPO:iea	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0002936	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003202	OMIM:137200	IEA				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003236	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003390	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003394	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003552	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:137200	TAS				C		HPO:skoehler	
OMIM	137200	NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE		HP:0009027	OMIM:137200	TAS				P		HPO:skoehler	
OMIM	137210	137210 GASTRIC VOLVULUS, INTRATHORACIC		HP:0000006	OMIM:137210	TAS				I		HPO:skoehler	
OMIM	137210	137210 GASTRIC VOLVULUS, INTRATHORACIC		HP:0002036	OMIM:137210	IEA				P		HPO:iea	
OMIM	137210	137210 GASTRIC VOLVULUS, INTRATHORACIC		HP:0002580	OMIM:137210	IEA				P		HPO:skoehler	
OMIM	137215	#137215 GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC;;GASTRIC CANCER, FAMILIAL DIFFUSEGASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFTPALATE, INCLUDED		HP:0000006	OMIM:137215	TAS				I		HPO:skoehler	
OMIM	137215	#137215 GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC;;GASTRIC CANCER, FAMILIAL DIFFUSEGASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFTPALATE, INCLUDED		HP:0000175	OMIM:137215	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	137215	#137215 GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC;;GASTRIC CANCER, FAMILIAL DIFFUSEGASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFTPALATE, INCLUDED		HP:0000204	OMIM:137215	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	137215	#137215 GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC;;GASTRIC CANCER, FAMILIAL DIFFUSEGASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFTPALATE, INCLUDED		HP:0002582	OMIM:137215	IEA				P		HPO:iea	
OMIM	137215	#137215 GASTRIC CANCER, HEREDITARY DIFFUSE; HDGC;;GASTRIC CANCER, FAMILIAL DIFFUSEGASTRIC CANCER, FAMILIAL DIFFUSE, AND CLEFT LIP WITH OR WITHOUT CLEFTPALATE, INCLUDED		HP:0012126	OMIM:137215	IEA				P		HPO:skoehler	
OMIM	137245	137245 GASTRIC LYMPHOMA, PRIMARY		HP:0045038	OMIM:137245	IEA				P		HPO:skoehler	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0000006	OMIM:137270	IEA				I		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0000316	OMIM:137270	IEA				P		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0000545	OMIM:137270	IEA				P		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0000957	OMIM:137270	IEA				P		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0001003	OMIM:137270	IEA				P		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0002036	OMIM:137270	IEA				P		HPO:iea	
OMIM	137270	GASTROCUTANEOUS SYNDROME		HP:0004398	OMIM:137270	IEA				P		HPO:iea	
OMIM	137280	GASTRITIS, FAMILIAL GIANT HYPERTROPHIC		HP:0000007	OMIM:137280	TAS				I		HPO:skoehler	
OMIM	137280	GASTRITIS, FAMILIAL GIANT HYPERTROPHIC		HP:0002617	OMIM:137280	IEA				P		HPO:skoehler	
OMIM	137280	GASTRITIS, FAMILIAL GIANT HYPERTROPHIC		HP:0003075	OMIM:137280	IEA				P		HPO:iea	
OMIM	137280	GASTRITIS, FAMILIAL GIANT HYPERTROPHIC		HP:0005246	OMIM:137280	IEA				P		HPO:iea	
OMIM	137360	GENOCHONDROMATOSIS		HP:0000006	PMID:17632779	PCS				I		HPO:iea	
OMIM	137360	GENOCHONDROMATOSIS		HP:0030295	PMID:17632779	PCS				P		HPO:lccarmody	
OMIM	137360	GENOCHONDROMATOSIS		HP:0030298	PMID:17632779	PCS				P		HPO:lccarmody	
OMIM	137370	137370 GENU VALGUM, ST. HELENA FAMILIAL;;GENU VALGUM, HEREDITARY PUBERTAL		HP:0000006	OMIM:137370	TAS				I		HPO:skoehler	
OMIM	137370	137370 GENU VALGUM, ST. HELENA FAMILIAL;;GENU VALGUM, HEREDITARY PUBERTAL		HP:0002857	OMIM:137370	IEA				P		HPO:iea	
OMIM	137400	GEOGRAPHIC TONGUE AND FISSURED TONGUE		HP:0000006	OMIM:137400	IEA				I		HPO:iea	
OMIM	137400	GEOGRAPHIC TONGUE AND FISSURED TONGUE		HP:0000221	OMIM:137400	IEA				P		HPO:iea	
OMIM	137400	GEOGRAPHIC TONGUE AND FISSURED TONGUE		HP:0025252	OMIM:137400	TAS				P		HPO:skoehler	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000006	OMIM:137440	TAS				I		HPO:probinson	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000709	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000712	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000716	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000718	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000726	OMIM:137440	TAS	HP:0003584			P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0000751	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001257	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001260	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001272	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001284	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001300	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001336	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001337	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001347	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0001824	OMIM:137440	TAS				P		HPO:skoehler	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002063	OMIM:137440	TAS				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002066	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002067	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002070	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002078	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002185	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002186	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0002354	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0003581	OMIM:137440	TAS				C		HPO:skoehler	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0003678	OMIM:137440	TAS				C		HPO:skoehler	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0007340	OMIM:137440	IEA				P		HPO:iea	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0007772	OMIM:137440	IEA				P		HPO:skoehler	
OMIM	137440	#137440 GERSTMANN-STRAUSSLER DISEASE; GSD;;ENCEPHALOPATHY, SUBACUTE SPONGIFORM, GERSTMANN-STRAUSSLER TYPE;;GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; GSS;;CEREBELLAR ATAXIA, PROGRESSIVE DEMENTIA, AND AMYLOID DEPOSITS IN CNS;;AMYLOIDOSIS, CEREBRAL, WITH SPONGIFORM ENCEPHALOPATHY;;PRION DEMENTIACEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED, INCLUDED		HP:0030223	OMIM:137440	TAS				P		HPO:skoehler	
OMIM	137500	GIANT NEUTROPHIL LEUKOCYTES		HP:0000006	OMIM:137500	IEA				I		HPO:iea	
OMIM	137500	GIANT NEUTROPHIL LEUKOCYTES		HP:0001871	OMIM:137500	IEA				P		HPO:iea	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000006	OMIM:137550	IEA				I		HPO:iea	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000194	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000232	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000293	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000311	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000316	OMIM:137550	IEA				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000337	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000343	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000418	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000455	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0000629	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0002002	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0003196	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0003577	OMIM:137550	TAS				C		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0005600	OMIM:137550	TAS				P		HPO:probinson	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0010759	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0011220	OMIM:137550	TAS				P		HPO:skoehler	
OMIM	137550	MELANOCYTIC NEVUS SYNDROME, CONGENITAL; CMNS		HP:0012056	OMIM:137550	TAS				P		HPO:probinson	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0000006	OMIM:137560	IEA				I		HPO:iea	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0000978	OMIM:137560	IEA				P		HPO:iea	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0001873	OMIM:137560	IEA				P		HPO:iea	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0001902	OMIM:137560	IEA				P		HPO:iea	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0002239	OMIM:137560	IEA				P		HPO:iea	
OMIM	137560	GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA		HP:0006298	OMIM:137560	TAS				P		HPO:probinson	
OMIM	137575	GIGANTIFORM CEMENTOMA, FAMILIAL		HP:0000006	OMIM:137575	TAS				I		HPO:probinson	
OMIM	137575	GIGANTIFORM CEMENTOMA, FAMILIAL		HP:0000692	OMIM:137575	TAS				P		HPO:probinson	
OMIM	137575	GIGANTIFORM CEMENTOMA, FAMILIAL		HP:0001571	OMIM:137575	TAS				P		HPO:probinson	
OMIM	137575	GIGANTIFORM CEMENTOMA, FAMILIAL		HP:0012328	OMIM:137575	TAS				P		HPO:probinson	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0000006	OMIM:137580	IEA				I		HPO:iea	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0000718	OMIM:137580	TAS				P		HPO:skoehler	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0000722	OMIM:137580	IEA				P		HPO:iea	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0000742	OMIM:137580	IEA				P		HPO:iea	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0002360	OMIM:137580	IEA				P		HPO:iea	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0007018	OMIM:137580	IEA				P		HPO:iea	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0010529	OMIM:137580	IEA				P		HPO:skoehler	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0100034	OMIM:137580	TAS				P		HPO:skoehler	
OMIM	137580	#137580 GILLES DE LA TOURETTE SYNDROME; GTS;;TOURETTE SYNDROME; TS;;TOURETTE DISORDERCHRONIC MOTOR TICS, INCLUDED		HP:0100035	OMIM:137580	IEA				P		HPO:skoehler	
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0000006	PMID:9618168;PMID:5804028	PCS				I		HPO:curators	
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0000164	PMID:9618168	PCS		HP:0040281		P		HPO:curators	HP:0040281
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0000501	PMID:9618168;PMID:6881141	PCS		HP:0040281		P		HPO:curators	HP:0040281
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0001999	PMID:9618168;PMID:8942889	PCS				P		HPO:curators	
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0007730	PMID:9618168;PMID:5804028	PCS		HP:0040281		P		HPO:curators	HP:0040281
OMIM	137600	IRIDOGONIODYSGENESIS, TYPE 2		HP:0007990	PMID:9618168;PMID:5804028	PCS		HP:0040281		P		HPO:curators	HP:0040281
OMIM	137700	GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE		HP:0000006	OMIM:137700	TAS				I		HPO:probinson	
OMIM	137700	GLAUCOMA WITH ELEVATED EPISCLERAL VENOUS PRESSURE		HP:0012108	OMIM:137700	TAS				P		HPO:skoehler	
OMIM	137750	GLAUCOMA 1, OPEN ANGLE, A		HP:0000006	OMIM:137750	IEA				I		HPO:iea	
OMIM	137750	GLAUCOMA 1, OPEN ANGLE, A		HP:0000501	OMIM:137750	IEA				P		HPO:iea	
OMIM	137750	GLAUCOMA 1, OPEN ANGLE, A		HP:0000545	OMIM:137750	IEA				P		HPO:iea	
OMIM	137750	GLAUCOMA 1, OPEN ANGLE, A		HP:0007905	OMIM:137750	IEA				P		HPO:iea	
OMIM	137760	GLAUCOMA, PRIMARY OPEN ANGLE		HP:0000006	OMIM:137760	IEA				I		HPO:iea	
OMIM	137760	GLAUCOMA, PRIMARY OPEN ANGLE		HP:0000545	OMIM:137760	IEA				P		HPO:iea	
OMIM	137760	GLAUCOMA, PRIMARY OPEN ANGLE		HP:0012108	OMIM:137760	TAS				P		HPO:skoehler	
OMIM	137763	GLAUCOMA - SLEEP APNEA		HP:0010535	OMIM:137763	IEA				P		HPO:skoehler	
OMIM	137800	#137800 GLIOMA SUSCEPTIBILITY 1; GLM1GLIOMA OF BRAIN, FAMILIAL, INCLUDED; GLM, INCLUDED;;GLIOBLASTOMA MULTIFORME, INCLUDED; GBM, INCLUDED;;ASTROCYTOMA, INCLUDED;;OLIGODENDROGLIOMA, INCLUDED;;EPENDYMOMA, INCLUDED;;SUBEPENDYMOMA, INCLUDED		HP:0000006	OMIM:137800	TAS				I		HPO:skoehler	
OMIM	137800	#137800 GLIOMA SUSCEPTIBILITY 1; GLM1GLIOMA OF BRAIN, FAMILIAL, INCLUDED; GLM, INCLUDED;;GLIOBLASTOMA MULTIFORME, INCLUDED; GBM, INCLUDED;;ASTROCYTOMA, INCLUDED;;OLIGODENDROGLIOMA, INCLUDED;;EPENDYMOMA, INCLUDED;;SUBEPENDYMOMA, INCLUDED		HP:0001428	OMIM:137800	TAS				I		HPO:skoehler	
OMIM	137800	#137800 GLIOMA SUSCEPTIBILITY 1; GLM1GLIOMA OF BRAIN, FAMILIAL, INCLUDED; GLM, INCLUDED;;GLIOBLASTOMA MULTIFORME, INCLUDED; GBM, INCLUDED;;ASTROCYTOMA, INCLUDED;;OLIGODENDROGLIOMA, INCLUDED;;EPENDYMOMA, INCLUDED;;SUBEPENDYMOMA, INCLUDED		HP:0002888	OMIM:137800	TAS				P		HPO:skoehler	
OMIM	137800	#137800 GLIOMA SUSCEPTIBILITY 1; GLM1GLIOMA OF BRAIN, FAMILIAL, INCLUDED; GLM, INCLUDED;;GLIOBLASTOMA MULTIFORME, INCLUDED; GBM, INCLUDED;;ASTROCYTOMA, INCLUDED;;OLIGODENDROGLIOMA, INCLUDED;;EPENDYMOMA, INCLUDED;;SUBEPENDYMOMA, INCLUDED		HP:0009592	OMIM:137800	TAS				P		HPO:skoehler	
OMIM	137800	#137800 GLIOMA SUSCEPTIBILITY 1; GLM1GLIOMA OF BRAIN, FAMILIAL, INCLUDED; GLM, INCLUDED;;GLIOBLASTOMA MULTIFORME, INCLUDED; GBM, INCLUDED;;ASTROCYTOMA, INCLUDED;;OLIGODENDROGLIOMA, INCLUDED;;EPENDYMOMA, INCLUDED;;SUBEPENDYMOMA, INCLUDED		HP:0012174	OMIM:137800	TAS				P		HPO:probinson	
OMIM	137900	GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN		HP:0000006	OMIM:137900	IEA				I		HPO:iea	
OMIM	137900	GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN		HP:0002715	OMIM:137900	IEA				P		HPO:iea	
OMIM	137900	GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN		HP:0003256	OMIM:137900	TAS				P		HPO:probinson	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000006	OMIM:137920	PCS				I		HPO:iea	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000013	PMID:15930087	PCS		HP:0040284		P		HPO:iea	1/23
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000047	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000074	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000089	PMID:15930087	PCS		HP:0040284		P		HPO:iea	1/23
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000093	PMID:15930087	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000107	PMID:15930087	PCS		HP:0040284		P		HPO:iea	19/23
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000122	PMID:15930087	PCS		HP:0040284		P		HPO:iea	1/23
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000787	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0000813	PMID:15930087	PCS		HP:0040284		P		HPO:iea	1/23
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0001080	PMID:15930087	PCS				P		HPO:iea	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0001738	PMID:15068978	PCS		HP:0040284		P		HPO:iea	6/7
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0001997	PMID:15930087	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0002120	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0002149	PMID:15930087	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0002594	PMID:15068978	PCS		HP:0040284		P		HPO:iea	5/6
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0002910	PMID:15930087	PCS				P		HPO:iea	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0003076	OMIM:137920	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0003259	PMID:15068978	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0003774	OMIM:137920	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0004379	PMID:15930087	PCS		HP:0040284		P		HPO:iea	4/7
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0004904	PMID:15068978	PCS	HP:0003581	HP:0040284		P		HPO:iea	10/13
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0005563	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0012207	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0030424	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0030997	OMIM:137920	TAS				P		HPO:skoehler	
OMIM	137920	RENAL CYSTS AND DIABETES SYNDROME		HP:0100611	PMID:15930087	PCS		HP:0040284		P		HPO:iea	4/23
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000006	OMIM:137940	TAS				I		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000034	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000286	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000300	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000303	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000426	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000431	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000535	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000561	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000653	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0000793	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0001004	OMIM:137940	IEA				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0001006	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0001263	OMIM:137940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0001480	OMIM:137940	IEA				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0001596	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0002223	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0003189	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0003577	OMIM:137940	TAS				C		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0003676	OMIM:137940	TAS				C		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0003758	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0005598	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0006521	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0007543	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0007621	OMIM:137940	TAS				P		HPO:probinson	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0012471	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0012622	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137940	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME; HLTRS		HP:0100540	OMIM:137940	TAS				P		HPO:skoehler	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0000006	OMIM:137950	IEA				I		HPO:iea	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0000093	OMIM:137950	IEA				P		HPO:iea	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0000100	OMIM:137950	IEA				P		HPO:iea	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0000112	OMIM:137950	IEA				P		HPO:iea	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0000822	OMIM:137950	IEA				P		HPO:iea	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0001941	OMIM:137950	IEA				P		HPO:skoehler	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0002907	OMIM:137950	TAS				P		HPO:probinson	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0003677	OMIM:137950	TAS				C		HPO:skoehler	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0003774	OMIM:137950	TAS				P		HPO:skoehler	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0008636	OMIM:137950	IEA				P		HPO:skoehler	
OMIM	137950	GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1; GFND1		HP:0100820	OMIM:137950	IEA				P		HPO:skoehler	
OMIM	138000	GLOMUVENOUS MALFORMATIONS		HP:0000006	OMIM:138000	IEA				I		HPO:iea	
OMIM	138000	GLOMUVENOUS MALFORMATIONS		HP:0000951	OMIM:138000	IEA				P		HPO:iea	
OMIM	138000	GLOMUVENOUS MALFORMATIONS		HP:0001939	OMIM:138000	IEA				P		HPO:iea	
OMIM	138070	GLUCOGLYCINURIA		HP:0000006	OMIM:138070	IEA				I		HPO:iea	
OMIM	138070	GLUCOGLYCINURIA		HP:0003076	OMIM:138070	IEA				P		HPO:skoehler	
OMIM	138070	GLUCOGLYCINURIA		HP:0003108	OMIM:138070	IEA				P		HPO:iea	
OMIM	138300	GLUTATHIONE REDUCTASE		HP:0000007	OMIM:138300	IEA				I		HPO:iea	
OMIM	138300	GLUTATHIONE REDUCTASE		HP:0001878	OMIM:138300	IEA				P		HPO:iea	
OMIM	138300	GLUTATHIONE REDUCTASE		HP:0001939	OMIM:138300	IEA				P		HPO:iea	
OMIM	138500	GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS		HP:0000006	OMIM:138500	TAS				I		HPO:probinson	
OMIM	138500	GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS		HP:0003108	OMIM:138500	TAS				P		HPO:probinson	
OMIM	138500	GLYCINURIA WITH OR WITHOUT OXALATE UROLITHIASIS		HP:0008672	OMIM:138500	TAS				P		HPO:probinson	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000006	OMIM:138770	IEA				I		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000252	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000286	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000322	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000369	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000494	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0000558	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0001249	OMIM:138770	IEA				P		HPO:skoehler	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0003196	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0003508	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0004279	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0004467	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0005180	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0005280	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0008551	OMIM:138770	IEA				P		HPO:iea	
OMIM	138770	138770 GMS SYNDROME;;GONIODYSGENESIS--MENTAL RETARDATION--SHORT STATURE SYNDROME		HP:0200055	OMIM:138770	TAS				P		HPO:skoehler	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0000006	OMIM:138790	IEA				I		HPO:iea	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0000107	OMIM:138790	TAS				P		HPO:skoehler	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0000119	OMIM:138790	IEA				P		HPO:iea	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0001162	OMIM:138790	IEA				P		HPO:iea	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0001841	OMIM:138790	IEA				P		HPO:iea	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0005707	OMIM:138790	IEA				P		HPO:iea	
OMIM	138790	138790 GOITER, MULTINODULAR, CYSTIC RENAL DISEASE, AND DIGITAL ANOMALIES;;MULTINODULAR GOITER/CYSTIC RENAL DISEASE/DIGITAL ANOMALIES;;MNG/CRD/DA		HP:0005987	OMIM:138790	IEA				P		HPO:iea	
OMIM	138800	GOITER, MULTINODULAR 1		HP:0000006	OMIM:138800	IEA				I		HPO:iea	
OMIM	138800	GOITER, MULTINODULAR 1		HP:0000866	OMIM:138800	IEA				P		HPO:iea	
OMIM	138800	GOITER, MULTINODULAR 1		HP:0002895	OMIM:138800	IEA				P		HPO:iea	
OMIM	138900	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1		HP:0000006	OMIM:138900	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	138900	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1		HP:0000951	OMIM:138900	IEA				P		HPO:iea	
OMIM	138900	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1		HP:0001369	OMIM:138900	IEA				P		HPO:iea	
OMIM	138900	URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1		HP:0002149	OMIM:138900	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000006	OMIM:138920	IEA				I		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000233	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000325	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000411	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000430	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0000490	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0001511	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0001595	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0002007	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0003758	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0005322	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0005328	OMIM:138920	IEA				P		HPO:iea	
OMIM	138920	138920 GRANDDAD SYNDROME;;GROWTH RETARDATION, AGED FACIES, NORMAL DEVELOPMENT, DECREASED SUBCUTANEOUSFAT, AUTOSOMAL DOMINANT INHERITANCE		HP:0011220	OMIM:138920	TAS				P		HPO:skoehler	
OMIM	138930	GRANT SYNDROME		HP:0000006	OMIM:138930	IEA				I		HPO:iea	
OMIM	138930	GRANT SYNDROME		HP:0000347	OMIM:138930	IEA				P		HPO:iea	
OMIM	138930	GRANT SYNDROME		HP:0000592	OMIM:138930	IEA				P		HPO:iea	
OMIM	138930	GRANT SYNDROME		HP:0002645	OMIM:138930	IEA				P		HPO:skoehler	
OMIM	138930	GRANT SYNDROME		HP:0002982	OMIM:138930	IEA				P		HPO:skoehler	
OMIM	138930	GRANT SYNDROME		HP:0200021	OMIM:138930	IEA				P		HPO:iea	
OMIM	138990	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL DOMINANT TYPE		HP:0000006	OMIM:138990	TAS				I		HPO:skoehler	
OMIM	138990	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL DOMINANT TYPE		HP:0002955	OMIM:138990	TAS				P		HPO:probinson	
OMIM	139000	GRANULOSIS RUBRA NASI		HP:0000006	OMIM:139000	TAS				I		HPO:probinson	
OMIM	139000	GRANULOSIS RUBRA NASI		HP:0000975	OMIM:139000	TAS				P		HPO:probinson	
OMIM	139000	GRANULOSIS RUBRA NASI		HP:0011463	OMIM:139000	TAS				C		HPO:probinson	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0000006	OMIM:139090	IEA				I		HPO:iea	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0000007	OMIM:139090	TAS				I		HPO:skoehler	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0000132	OMIM:139090	IEA				P		HPO:skoehler	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0000421	OMIM:139090	TAS				P		HPO:probinson	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0000978	OMIM:139090	TAS				P		HPO:skoehler	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0001744	OMIM:139090	IEA				P		HPO:iea	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0001873	OMIM:139090	IEA				P		HPO:iea	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0003010	OMIM:139090	IEA				P		HPO:iea	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0003676	OMIM:139090	TAS				C		HPO:skoehler	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0008320	OMIM:139090	TAS				P		HPO:probinson	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0008330	OMIM:139090	IEA				P		HPO:iea	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0011872	OMIM:139090	TAS				P		HPO:probinson	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0011974	OMIM:139090	TAS				P		HPO:skoehler	
OMIM	139090	#139090 GRAY PLATELET SYNDROME; GPS;;BLEEDING DISORDER, PLATELET-TYPE, 4; BDPLT4;;PLATELET ALPHA-GRANULE DEFICIENCY		HP:0012147	OMIM:139090	TAS				P		HPO:skoehler	
OMIM	139100	%139100 GRAYING OF HAIR, PRECOCIOUS;;WHITE HAIR, PREMATURE		HP:0000006	OMIM:139100	TAS				I		HPO:skoehler	
OMIM	139100	%139100 GRAYING OF HAIR, PRECOCIOUS;;WHITE HAIR, PREMATURE		HP:0002216	OMIM:139100	IEA				P		HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000006	PMID:22243968	PCS				I	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000028	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	2/5
OMIM	139210	Myhre syndrome		HP:0000160	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	7/8
OMIM	139210	Myhre syndrome		HP:0000175	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	1/8
OMIM	139210	Myhre syndrome		HP:0000219	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000219	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000219	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	7/8
OMIM	139210	Myhre syndrome		HP:0000252	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000256	enuItem	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	2/8
OMIM	139210	Myhre syndrome		HP:0000272	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000303	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	8/8
OMIM	139210	Myhre syndrome		HP:0000316	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000322	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	8/8
OMIM	139210	Myhre syndrome		HP:0000327	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000365	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	8/8
OMIM	139210	Myhre syndrome		HP:0000369	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000426	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000470	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000486	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000490	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000518	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	1/7
OMIM	139210	Myhre syndrome		HP:0000540	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000568	OMIM:139210	TAS		HP:0040283		P	MYHRE SYNDROME	HPO:skoehler	HP:0040283
OMIM	139210	Myhre syndrome		HP:0000574	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0000581	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0000717	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	2/8
OMIM	139210	Myhre syndrome		HP:0000822	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	2/8
OMIM	139210	Myhre syndrome		HP:0000885	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	4/8
OMIM	139210	Myhre syndrome		HP:0000926	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:probinson	6/8
OMIM	139210	Myhre syndrome		HP:0001072	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0001156	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001249	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001250	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0001251	OMIM:139210	TAS		HP:0040283		P	MYHRE SYNDROME	HPO:skoehler	HP:0040283
OMIM	139210	Myhre syndrome		HP:0001376	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0001387	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	8/8
OMIM	139210	Myhre syndrome		HP:0001511	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0001513	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	5/8
OMIM	139210	Myhre syndrome		HP:0001518	PMID:22243968	PCS	HP:0003577	HP:0040284		P	MYHRE SYNDROME	HP:probinson	5/7
OMIM	139210	Myhre syndrome		HP:0001608	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001629	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	1/8
OMIM	139210	Myhre syndrome		HP:0001631	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	1/8
OMIM	139210	Myhre syndrome		HP:0001643	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001650	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001680	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001698	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0001831	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:probinson	
OMIM	139210	Myhre syndrome		HP:0001845	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0002213	OMIM:139210	TAS	HP:0003577			P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0002684	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	8/8
OMIM	139210	Myhre syndrome		HP:0002866	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:iea	8/8
OMIM	139210	Myhre syndrome		HP:0002878	OMIM:139210	TAS		HP:0040283		P	MYHRE SYNDROME	HPO:skoehler	HP:0040283
OMIM	139210	Myhre syndrome		HP:0002948	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0003026	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0003561	PMID:22243968	PCS	HP:0003577	HP:0040284		P	MYHRE SYNDROME	HP:probinson	3/5
OMIM	139210	Myhre syndrome		HP:0003712	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HP:probinson	8/8
OMIM	139210	Myhre syndrome		HP:0003720	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0004322	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0004621	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:probinson	
OMIM	139210	Myhre syndrome		HP:0004691	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0004894	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0008070	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0008551	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0009381	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:probinson	
OMIM	139210	Myhre syndrome		HP:0009466	OMIM:139210	IEA				P	MYHRE SYNDROME	HPO:iea	
OMIM	139210	Myhre syndrome		HP:0010579	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0011800	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	8/8
OMIM	139210	Myhre syndrome		HP:0012385	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0030053	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	6/8
OMIM	139210	Myhre syndrome		HP:0030084	OMIM:139210	TAS				P	MYHRE SYNDROME	HPO:skoehler	
OMIM	139210	Myhre syndrome		HP:0045025	PMID:22243968	PCS		HP:0040284		P	MYHRE SYNDROME	HPO:skoehler	8/8
OMIM	139210	Myhre syndrome		HP:0410030	PMID:22243968	PCS	HP:0003577	HP:0040284		P	MYHRE SYNDROME	HP:probinson	1/8
OMIM	139300	AROMATASE EXCESS SYNDROME		HP:0000006	OMIM:139300	TAS				I		HPO:probinson	
OMIM	139300	AROMATASE EXCESS SYNDROME		HP:0000771	OMIM:139300	TAS				P		HPO:probinson	
OMIM	139300	AROMATASE EXCESS SYNDROME		HP:0004322	OMIM:139300	TAS				P		HPO:probinson	
OMIM	139300	AROMATASE EXCESS SYNDROME		HP:0005616	OMIM:139300	TAS				P		HPO:probinson	
OMIM	139393	GUILLAIN-BARRE SYNDROME, FAMILIAL		HP:0000006	OMIM:139393	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	139393	GUILLAIN-BARRE SYNDROME, FAMILIAL		HP:0007131	OMIM:139393	IEA				P		HPO:iea	
OMIM	139400	HAIR WHORL		HP:0000006	OMIM:139400	IEA				I		HPO:iea	
OMIM	139400	HAIR WHORL		HP:0001595	OMIM:139400	IEA				P		HPO:iea	
OMIM	139450	HAIR, CURLY		HP:0000006	OMIM:139450	IEA				I		HPO:iea	
OMIM	139450	HAIR, CURLY		HP:0002212	OMIM:139450	IEA				P		HPO:iea	
OMIM	139500	HAIRY EARS		HP:0000006	OMIM:139500	TAS				I		HPO:nvasilevsky	
OMIM	139500	HAIRY EARS		HP:0001450	OMIM:139500	TAS				I		HPO:nvasilevsky	
OMIM	139500	HAIRY EARS		HP:0008528	PMID:2364572	PCS	HP:0003581	HP:0040284		P		HPO:iea	83/500
OMIM	139600	HAIRY ELBOWS		HP:0000006	OMIM:139600	IEA				I		HPO:skoehler	
OMIM	139600	HAIRY ELBOWS		HP:0000006	OMIM:139600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	139600	HAIRY ELBOWS		HP:0001999	PMID:14791960	PCS		HP:0040284		P		HPO:lccarmody	25%
OMIM	139600	HAIRY ELBOWS		HP:0004322	PMID:139600	PCS		HP:0040284		P		HPO:iea	75%
OMIM	139600	HAIRY ELBOWS		HP:0004780	PMID:139600	IEA				P		HPO:iea	
OMIM	139630	HAIRY NOSE TIP		HP:0001595	OMIM:139630	IEA				P		HPO:iea	
OMIM	139650	HAIRY PALMS AND SOLES		HP:0000006	OMIM:139650	IEA				I		HPO:iea	
OMIM	139650	HAIRY PALMS AND SOLES		HP:0001034	OMIM:139650	IEA				P		HPO:skoehler	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0000006	OMIM:139750	IEA				I		HPO:iea	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0000272	OMIM:139750	IEA				P		HPO:iea	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0001249	OMIM:139750	IEA				P		HPO:iea	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0001319	OMIM:139750	IEA				P		HPO:iea	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0001760	OMIM:139750	IEA				P		HPO:skoehler	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0004322	OMIM:139750	IEA				P		HPO:iea	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0006070	OMIM:139750	TAS				P		HPO:probinson	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0009626	OMIM:139750	TAS				P		HPO:probinson	
OMIM	139750	139750 HAND AND FOOT DEFORMITY WITH FLAT FACIES		HP:0012368	OMIM:139750	TAS				P		HPO:skoehler	
OMIM	139900	%139900 HAND SKILL, RELATIVE; HSR;;HANDEDNESS		HP:0000006	OMIM:139900	TAS				I		HPO:skoehler	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000006	OMIM:140000	IEA				I		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000041	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000047	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000048	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000054	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000074	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000076	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0000083	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0001156	OMIM:140000	TAS				P		HPO:skoehler	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0001216	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0001245	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0001885	OMIM:140000	TAS				P		HPO:probinson	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0003762	OMIM:140000	TAS				P		HPO:skoehler	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0004209	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0006110	OMIM:140000	TAS				P		HPO:probinson	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0008080	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0008103	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0008740	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0009237	OMIM:140000	TAS				P		HPO:probinson	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0009237	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0009464	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0009623	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0010034	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0010105	OMIM:140000	IEA				P		HPO:iea	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0010109	OMIM:140000	TAS				P		HPO:skoehler	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0010584	OMIM:140000	IEA				P		HPO:skoehler	
OMIM	140000	HAND-FOOT-GENITAL SYNDROME; HFG		HP:0012330	OMIM:140000	IEA				P		HPO:skoehler	
OMIM	140300	HASHIMOTO THYROIDITIS		HP:0000006	OMIM:140300	TAS				I		HPO:probinson	
OMIM	140300	HASHIMOTO THYROIDITIS		HP:0000872	OMIM:140300	TAS				P		HPO:probinson	
OMIM	140300	HASHIMOTO THYROIDITIS		HP:0030057	OMIM:140300	TAS				P		HPO:probinson	
OMIM	140350	HAWKINSINURIA		HP:0000006	OMIM:140350	IEA				I		HPO:iea	
OMIM	140350	HAWKINSINURIA		HP:0001508	OMIM:140350	IEA				P		HPO:iea	
OMIM	140350	HAWKINSINURIA		HP:0001942	OMIM:140350	IEA				P		HPO:iea	
OMIM	140350	HAWKINSINURIA		HP:0003161	OMIM:140350	IEA				P		HPO:iea	
OMIM	140350	HAWKINSINURIA		HP:0003231	OMIM:140350	IEA				P		HPO:iea	
OMIM	140350	HAWKINSINURIA		HP:0003607	OMIM:140350	IEA				P		HPO:iea	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0000006	OMIM:140400	PCS				I		HPO:probinson	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0001279	OMIM:140400	PCS				P		HPO:probinson	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0001645	OMIM:140400	PCS				P		HPO:probinson	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0001688	OMIM:140400	PCS				P		HPO:probinson	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0001699	OMIM:140400	TAS				M		HPO:skoehler	
OMIM	140400	%140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE II; PFHB2;;PFHBII		HP:0005178	OMIM:140400	PCS				P		HPO:probinson	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0000006	OMIM:140450	IEA				I		HPO:iea	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0001156	OMIM:140450	IEA				P		HPO:iea	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0001626	OMIM:140450	IEA				P		HPO:iea	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0005819	OMIM:140450	TAS				P		HPO:skoehler	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0009464	OMIM:140450	IEA				P		HPO:iea	
OMIM	140450	140450 HEART-HAND SYNDROME, SPANISH TYPE		HP:0011704	OMIM:140450	TAS				P		HPO:skoehler	
OMIM	140500	HEART, MALFORMATION OF		HP:0000006	OMIM:140500	TAS				I		HPO:nvasilevsky	
OMIM	140500	HEART, MALFORMATION OF		HP:0001426	OMIM:140500	TAS				I		HPO:nvasilevsky	
OMIM	140500	HEART, MALFORMATION OF		HP:0004383	OMIM:140500	IEA				P		HPO:skoehler	
OMIM	140600	OSTEOARTHRITIS OF DISTAL INTERPHALANGEAL JOINTS		HP:0000006	OMIM:140600	TAS				I		HPO:probinson	
OMIM	140600	OSTEOARTHRITIS OF DISTAL INTERPHALANGEAL JOINTS		HP:0002758	OMIM:140600	TAS				P		HPO:probinson	
OMIM	140600	OSTEOARTHRITIS OF DISTAL INTERPHALANGEAL JOINTS		HP:0012313	OMIM:140600	TAS				P		HPO:probinson	
OMIM	140700	HEINZ BODY ANEMIAS		HP:0000006	OMIM:140700	IEA				I		HPO:iea	
OMIM	140700	HEINZ BODY ANEMIAS		HP:0001930	OMIM:140700	IEA				P		HPO:iea	
OMIM	140700	HEINZ BODY ANEMIAS		HP:0001939	OMIM:140700	IEA				P		HPO:iea	
OMIM	140700	HEINZ BODY ANEMIAS		HP:0005511	OMIM:140700	IEA				P		HPO:skoehler	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0000006	OMIM:140850	IEA				I		HPO:iea	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0001680	PMID:10826620	PCS				P		HPO:nvasilevsky	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0007486	OMIM:140850	IEA				P		HPO:iea	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0010309	PMID:10826620	PCS				P		HPO:nvasilevsky	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0012020	PMID:10826620	PCS				P		HPO:nvasilevsky	
OMIM	140850	HEMANGIOMAS, CAVERNOUS, OF FACE AND SUPRAUMBILICAL MIDLINE RAPHE		HP:0410276	PMID:10826620	PCS				P		HPO:nvasilevsky	
OMIM	140900	HEMANGIOMAS OF SMALL INTESTINE		HP:0000006	OMIM:140900	IEA				I		HPO:iea	
OMIM	140900	HEMANGIOMAS OF SMALL INTESTINE		HP:0001048	OMIM:140900	TAS				P		HPO:iea	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0000006	OMIM:141000	IEA				I		HPO:iea	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0001028	OMIM:141000	IEA				P		HPO:skoehler	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0001873	OMIM:141000	IEA				P		HPO:iea	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0001937	OMIM:141000	IEA				P		HPO:iea	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0002153	OMIM:141000	IEA				P		HPO:iea	
OMIM	141000	HEMANGIOMA-THROMBOCYTOPENIA SYNDROME		HP:0004308	OMIM:141000	IEA				P		HPO:skoehler	
OMIM	141200	#141200 HEMATURIA, BENIGN FAMILIAL; BFH;;THIN-BASEMENT-MEMBRANE NEPHROPATHY;;THIN MEMBRANE NEPHROPATHY; TMN		HP:0000006	OMIM:141200	IEA				I		HPO:iea	
OMIM	141200	#141200 HEMATURIA, BENIGN FAMILIAL; BFH;;THIN-BASEMENT-MEMBRANE NEPHROPATHY;;THIN MEMBRANE NEPHROPATHY; TMN		HP:0000790	OMIM:141200	IEA				P		HPO:iea	
OMIM	141200	#141200 HEMATURIA, BENIGN FAMILIAL; BFH;;THIN-BASEMENT-MEMBRANE NEPHROPATHY;;THIN MEMBRANE NEPHROPATHY; TMN		HP:0003680	OMIM:141200	TAS				C		HPO:skoehler	
OMIM	141200	#141200 HEMATURIA, BENIGN FAMILIAL; BFH;;THIN-BASEMENT-MEMBRANE NEPHROPATHY;;THIN MEMBRANE NEPHROPATHY; TMN		HP:0012577	OMIM:141200	TAS				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0000490	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0000581	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0000684	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0000689	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0001250	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0001251	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0002076	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0002229	OMIM:141300	TAS				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0002277	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0002290	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0002808	OMIM:141300	IEA				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0003674	OMIM:141300	IEA				C		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0003745	OMIM:141300	IEA				I		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0003778	OMIM:141300	IEA				P		HPO:iea	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0008551	OMIM:141300	TAS				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0011331	OMIM:141300	TAS				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0012473	OMIM:141300	TAS				P		HPO:skoehler	
OMIM	141300	HEMIFACIAL ATROPHY, PROGRESSIVE; HFA		HP:0100661	OMIM:141300	TAS				P		HPO:skoehler	
OMIM	141350	HEMIFACIAL HYPERPLASIA WITH STRABISMUS		HP:0000006	OMIM:141350	IEA				I		HPO:iea	
OMIM	141350	HEMIFACIAL HYPERPLASIA WITH STRABISMUS		HP:0000176	OMIM:141350	IEA				P		HPO:iea	
OMIM	141350	HEMIFACIAL HYPERPLASIA WITH STRABISMUS		HP:0000486	OMIM:141350	IEA				P		HPO:iea	
OMIM	141350	HEMIFACIAL HYPERPLASIA WITH STRABISMUS		HP:0000646	OMIM:141350	IEA				P		HPO:iea	
OMIM	141350	HEMIFACIAL HYPERPLASIA WITH STRABISMUS		HP:0005323	OMIM:141350	IEA				P		HPO:iea	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0000006	OMIM:141400	TAS				I		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0000175	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0000384	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0000405	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0000413	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0001199	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0003778	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0004467	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0008551	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0009943	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0011332	OMIM:141400	TAS				P		HPO:skoehler	
OMIM	141400	HEMIFACIAL MICROSOMIA WITH RADIAL DEFECTS		HP:0100335	OMIM:141400	TAS				P		HPO:probinson	
OMIM	141405	141405 HEMIFACIAL SPASM, FAMILIAL		HP:0000006	OMIM:141405	IEA				I		HPO:iea	
OMIM	141405	141405 HEMIFACIAL SPASM, FAMILIAL		HP:0000707	OMIM:141405	IEA				P		HPO:iea	
OMIM	141405	141405 HEMIFACIAL SPASM, FAMILIAL		HP:0010828	OMIM:141405	TAS				P		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0000006	OMIM:141500	IEA				I		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0000639	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0000709	OMIM:141500	TAS				P		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0000713	OMIM:141500	TAS				P		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0000739	OMIM:141500	TAS				P		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001125	OMIM:141500	PCS				P		HPO:probinson	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001250	OMIM:141500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001251	OMIM:141500	PCS				P		HPO:probinson	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001259	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001269	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001272	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001289	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001337	OMIM:141500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001425	OMIM:141500	TAS				I		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0001945	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002076	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002077	OMIM:141500	TAS				P		HPO:skoehler	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002301	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002329	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002357	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002367	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0002442	OMIM:141500	IEA				P		HPO:iea	
OMIM	141500	#141500 MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1;;FHM;;MHP1MIGRAINE, FAMILIAL HEMIPLEGIC 1, WITH PROGRESSIVE CEREBELLAR ATAXIA,INCLUDED;;MIGRAINE, SPORADIC HEMIPLEGIC, INCLUDED		HP:0008765	OMIM:141500	IEA				P		HPO:iea	
OMIM	141700	141700 HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES		HP:0000006	OMIM:141700	TAS				I		HPO:iea	
OMIM	141700	141700 HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES		HP:0001930	OMIM:141700	TAS				P		HPO:iea	
OMIM	141700	141700 HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES		HP:0004445	OMIM:141700	TAS				P		HPO:skoehler	
OMIM	141700	141700 HEMOLYTIC POIKILOCYTIC ANEMIA DUE TO REDUCED ANKYRIN BINDING SITES		HP:0005511	OMIM:141700	TAS				P		HPO:iea	
OMIM	141749	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1		HP:0000006	OMIM:141749	TAS				I		HPO:probinson	
OMIM	141749	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 1		HP:0011904	OMIM:141749	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000006	OMIM:141750	TAS				I		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000028	OMIM:141750	TAS				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000047	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000054	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000158	OMIM:141750	IEA				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000218	OMIM:141750	TAS				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000252	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED	HP:0012825	HP:0000278	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000286	OMIM:141750	TAS				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000316	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000337	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000343	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000431	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000451	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000463	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000465	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000470	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000494	OMIM:141750	TAS				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000508	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0000678	OMIM:141750	TAS				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001249	OMIM:141750	IEA				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001250	OMIM:141750	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001466	OMIM:141750	IEA				I		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001513	OMIM:141750	TAS				P		HPO:skoehler	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001555	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001643	OMIM:141750	IEA				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0001762	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0002558	OMIM:141750	IEA				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0004322	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0004425	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0004840	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0005280	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0008551	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0009466	OMIM:141750	IEA				P		HPO:iea	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0010808	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0011903	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141750	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, CHROMOSOME 16-RELATED		HP:0011907	OMIM:141750	TAS				P		HPO:probinson	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0000006	OMIM:141800	IEA				I		HPO:iea	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0000952	OMIM:141800	TAS				P		HPO:skoehler	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0000961	OMIM:141800	TAS				P		HPO:skoehler	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0001789	OMIM:141800	IEA				P		HPO:skoehler	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0001901	OMIM:141800	TAS				P		HPO:skoehler	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0004840	OMIM:141800	TAS				P		HPO:probinson	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0005511	OMIM:141800	TAS				P		HPO:skoehler	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0011907	OMIM:141800	TAS				P		HPO:probinson	
OMIM	141800	HEMOGLOBIN--ALPHA LOCUS 1; HBA1		HP:0012119	OMIM:141800	TAS				P		HPO:skoehler	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0000006	OMIM:141900	TAS				I		HPO:nvasilevsky	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0000007	OMIM:141900	TAS				I		HPO:nvasilevsky	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0000790	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0000952	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0000961	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0001081	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0001744	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS	HP:0012825	HP:0001878	OMIM:141900	TAS				P		HPO:probinson	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0001901	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0001935	OMIM:141900	TAS				P		HPO:probinson	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0002754	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0004727	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0004810	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0005511	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0005524	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0008346	OMIM:141900	IEA				P		HPO:iea	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0010885	OMIM:141900	TAS				P		HPO:skoehler	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0011904	OMIM:141900	TAS				P		HPO:probinson	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0025066	OMIM:141900	TAS				P		HPO:skoehler	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0032231	OMIM:141900	IEA				P		HPO:skoehler	
OMIM	141900	HEMOGLOBIN--BETA LOCUS		HP:0200023	OMIM:141900	IEA				P		HPO:skoehler	
OMIM	142000	HEMOGLOBIN--DELTA LOCUS		HP:0000006	OMIM:142000	IEA				I		HPO:iea	
OMIM	142000	HEMOGLOBIN--DELTA LOCUS		HP:0001903	OMIM:142000	TAS				P		HPO:iea	
OMIM	142000	HEMOGLOBIN--DELTA LOCUS		HP:0005560	OMIM:142000	TAS				P		HPO:iea	
OMIM	142309	HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION ISUNKNOWN OR UNCERTAIN		HP:0000006	OMIM:142309	IEA				I		HPO:iea	
OMIM	142309	HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION ISUNKNOWN OR UNCERTAIN		HP:0004825	OMIM:142309	IEA				P		HPO:iea	
OMIM	142309	HEMOGLOBIN--VARIANTS FOR WHICH THE CHAIN CARRYING THE MUTATION ISUNKNOWN OR UNCERTAIN		HP:0004863	OMIM:142309	TAS				P		HPO:probinson	
OMIM	142330	HEPATIC ADENOMAS, FAMILIAL		HP:0000006	OMIM:142330	IEA				I		HPO:iea	
OMIM	142330	HEPATIC ADENOMAS, FAMILIAL		HP:0000147	OMIM:142330	IEA				P		HPO:iea	
OMIM	142330	HEPATIC ADENOMAS, FAMILIAL		HP:0004904	OMIM:142330	IEA				P		HPO:iea	
OMIM	142330	HEPATIC ADENOMAS, FAMILIAL		HP:0012028	OMIM:142330	TAS				P		HPO:probinson	
OMIM	142335	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5		HP:0000006	OMIM:142335	TAS				I		HPO:iea	
OMIM	142335	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5		HP:0011904	PMID:17767159	PCS				P		HP:probinson	
OMIM	142340	DIAPHRAGMATIC HERNIA, CONGENITAL		HP:0000776	OMIM:142340	IEA				P		HPO:iea	
OMIM	142340	DIAPHRAGMATIC HERNIA, CONGENITAL		HP:0001426	OMIM:142340	IEA				I		HPO:iea	
OMIM	142350	HERNIA, DOUBLE INGUINAL		HP:0000006	OMIM:142350	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	142350	HERNIA, DOUBLE INGUINAL		HP:0000023	OMIM:142350	IEA				P		HPO:skoehler	
OMIM	142395	HEPATITIS B VACCINE, RESPONSE TO		HP:0000006	OMIM:142395	IEA				I		HPO:iea	
OMIM	142395	HEPATITIS B VACCINE, RESPONSE TO		HP:0012115	OMIM:142395	IEA				P		HPO:skoehler	
OMIM	142400	HERNIA, HIATUS		HP:0000006	OMIM:142400	IEA				I		HPO:iea	
OMIM	142400	HERNIA, HIATUS		HP:0000765	OMIM:142400	IEA				P		HPO:iea	
OMIM	142400	HERNIA, HIATUS		HP:0002036	OMIM:142400	IEA				P		HPO:iea	
OMIM	142470	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2		HP:0000006	OMIM:142470	IEA				I		HPO:iea	
OMIM	142470	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 2		HP:0001871	OMIM:142470	IEA				P		HPO:iea	
OMIM	142500	142500 HETEROCHROMIA IRIDIS		HP:0000006	OMIM:142500	IEA				I		HPO:iea	
OMIM	142500	142500 HETEROCHROMIA IRIDIS		HP:0001100	OMIM:142500	IEA				P		HPO:iea	
OMIM	142500	142500 HETEROCHROMIA IRIDIS		HP:0200064	OMIM:142500	TAS				P		HPO:skoehler	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0000006	OMIM:142623	IEA				I		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0002013	OMIM:142623	IEA				P		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0002019	OMIM:142623	IEA				P		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0002251	OMIM:142623	IEA				P		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0003270	OMIM:142623	IEA				P		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0004362	OMIM:142623	TAS				P		HPO:iea	
OMIM	142623	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1; HSCR1		HP:0004387	OMIM:142623	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000006	OMIM:142625	IEA				I		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000232	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000248	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000431	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000472	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0000494	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0001007	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0001761	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0002149	OMIM:142625	TAS				P		HPO:probinson	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0002652	OMIM:142625	IEA				P		HPO:skoehler	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0002673	OMIM:142625	IEA				P		HPO:iea	
OMIM	142625	HIRSUTISM--SKELETAL DYSPLASIA--MENTAL RETARDATION SYNDROME		HP:0200021	OMIM:142625	TAS				P		HPO:probinson	
OMIM	142630	HISTIOCYTOSIS, PROGRESSIVE MUCINOUS		HP:0000006	OMIM:142630	IEA				I		HPO:iea	
OMIM	142630	HISTIOCYTOSIS, PROGRESSIVE MUCINOUS		HP:0008069	OMIM:142630	IEA				P		HPO:skoehler	
OMIM	142630	HISTIOCYTOSIS, PROGRESSIVE MUCINOUS		HP:0040138	OMIM:142630	IEA				P		HPO:skoehler	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0000006	OMIM:142669	TAS				I		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0001385	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0002758	OMIM:142669	TAS				P		HPO:skoehler	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0003182	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0003370	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0005041	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0005743	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0006429	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0008783	OMIM:142669	TAS				P		HPO:probinson	
OMIM	142669	HIP DYSPLASIA, BEUKES TYPE		HP:0011463	OMIM:142669	TAS				C		HPO:probinson	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0000006	OMIM:142680	IEA				I		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0000969	OMIM:142680	IEA				P		HPO:skoehler	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0000988	OMIM:142680	TAS				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0001954	OMIM:142680	TAS				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0002027	OMIM:142680	IEA				P		HPO:skoehler	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0002829	OMIM:142680	IEA				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0003326	OMIM:142680	TAS				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0003552	OMIM:142680	IEA				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0003565	OMIM:142680	IEA				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0011034	OMIM:142680	IEA				P		HPO:iea	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0012280	OMIM:142680	TAS				P		HPO:probinson	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0030953	OMIM:142680	TAS				P		HPO:skoehler	
OMIM	142680	PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT		HP:0100539	OMIM:142680	TAS				P		HPO:skoehler	
OMIM	142690	ACNE INVERSA, FAMILIAL		HP:0000006	OMIM:142690	IEA				I		HPO:iea	
OMIM	142690	ACNE INVERSA, FAMILIAL		HP:0000987	OMIM:142690	IEA				P		HPO:iea	
OMIM	142690	ACNE INVERSA, FAMILIAL		HP:0040154	OMIM:142690	IEA				P		HPO:skoehler	
OMIM	142700	ACETABULAR DYSPLASIAHIP, DISLOCATION OF, CONGENITAL, INCLUDED		HP:0001374	OMIM:142700	IEA				P		HPO:iea	
OMIM	142700	ACETABULAR DYSPLASIAHIP, DISLOCATION OF, CONGENITAL, INCLUDED		HP:0001426	OMIM:142700	IEA				I		HPO:iea	
OMIM	142700	ACETABULAR DYSPLASIAHIP, DISLOCATION OF, CONGENITAL, INCLUDED		HP:0008807	OMIM:142700	IEA				P		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0000006	PMID:8730285	PCS				I		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0000767	PMID:8730285	PCS		HP:0040284		P		HPO:iea	19/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0000894	PMID:8730285	PCS		HP:0040284		P		HPO:iea	40/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001159	PMID:8730285	PCS		HP:0040284		P		HPO:iea	7/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001191	OMIM:142900	IEA				P		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001199	PMID:8730285	PCS		HP:0040284		P		HPO:iea	10/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001245	OMIM:142900	PCS		HP:0040284		P		HPO:iea	42/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001377	PMID:8730285	PCS		HP:0040284		P		HPO:iea	29/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001629	PMID:8730285	PCS		HP:0040284		P		HPO:iea	15/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001643	PMID:8730285	IEA		HP:0040284		P		HPO:iea	1/11
OMIM	142900	HOLT-ORAM SYNDROME		HP:0001684	PMID:8730285	PCS		HP:0040284		P		HPO:iea	20/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0002943	OMIM:142900	IEA				P		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0002984	OMIM:142900	PCS		HP:0040284		P		HPO:iea	24/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0003022	PMID:8730285	PCS		HP:0040284		P		HPO:iea	20/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0003468	OMIM:142900	TAS				P		HPO:skoehler	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0003974	PMID:8730285	PCS		HP:0040284		P		HPO:iea	13/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0003982	PMID:8730285	PCS		HP:0040284		P		HPO:iea	4/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0004383	OMIM:142900	IEA				P		HPO:skoehler	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0005792	PMID:8730285	PCS		HP:0040284		P		HPO:iea	28/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0009751	PMID:8730285	PCS		HP:0040284		P		HPO:iea	34/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0009777	PMID:8730285	PCS		HP:0040284		P		HPO:iea	27/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0009829	OMIM:142900	IEA				P		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0009944	OMIM:142900	IEA				P		HPO:iea	
OMIM	142900	HOLT-ORAM SYNDROME		HP:0011927	PMID:8730285	PCS		HP:0040284		P		HPO:iea	28/55
OMIM	142900	HOLT-ORAM SYNDROME		HP:0040019	OMIM:142900	PCS		HP:0040284		P		HPO:iea	33/55
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0000006	OMIM:142945	IEA				I		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0000126	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0000272	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0000366	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0000601	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0001360	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0003829	OMIM:142945	IEA				C		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0009914	OMIM:142945	IEA				P		HPO:iea	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0011800	OMIM:142945	TAS				P		HPO:skoehler	
OMIM	142945	#142945 HOLOPROSENCEPHALY 3; HPE3;;HLP3		HP:0012806	OMIM:142945	TAS				P		HPO:skoehler	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0000006	OMIM:142946	IEA				I		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0000161	OMIM:142946	TAS				P		HPO:skoehler	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0000437	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0000508	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0000601	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0002507	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0005273	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0005280	OMIM:142946	IEA				P		HPO:iea	
OMIM	142946	HOLOPROSENCEPHALY 4		HP:0008501	OMIM:142946	IEA				P		HPO:iea	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0000006	OMIM:143000	IEA				I		HPO:iea	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0000490	OMIM:143000	IEA				P		HPO:iea	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0001100	OMIM:143000	IEA				P		HPO:iea	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0003470	OMIM:143000	IEA				P		HPO:skoehler	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0006837	OMIM:143000	IEA				P		HPO:iea	
OMIM	143000	HORNER SYNDROME, CONGENITAL		HP:0007451	OMIM:143000	IEA				P		HPO:iea	
OMIM	143050	HUMERORADIAL SYNOSTOSIS		HP:0000006	OMIM:143050	IEA				I		HPO:iea	
OMIM	143050	HUMERORADIAL SYNOSTOSIS		HP:0003041	OMIM:143050	IEA				P		HPO:iea	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000006	OMIM:143095	TAS				I		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000007	OMIM:143095	TAS				I		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000218	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000316	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000337	OMIM:143095	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000343	OMIM:143095	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000365	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000470	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000535	OMIM:143095	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000684	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000687	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000691	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0000914	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001156	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001552	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001629	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012825	HP:0001642	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012825	HP:0001650	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001653	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012826	HP:0001659	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001714	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012828	HP:0001718	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001762	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0001763	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002092	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002194	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002515	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002553	OMIM:143095	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002655	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002750	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012828	HP:0002751	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002829	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002857	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002938	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002945	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002967	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0002982	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003022	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012840	HP:0003031	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003040	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003042	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003071	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003090	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003093	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003184	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003301	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003417	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0003834	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0004976	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS	HP:0012826	HP:0005180	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0006067	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0006462	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0006471	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0006610	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0007598	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0008450	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0008551	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0008905	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0009179	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0009882	OMIM:143095	TAS				P		HPO:skoehler	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0010049	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0010446	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0010585	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0100490	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143095	SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS		HP:0100864	OMIM:143095	TAS				P		HPO:probinson	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0000006	OMIM:143100	IEA				I		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0000496	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0000716	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0000726	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0000751	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0001250	OMIM:143100	TAS				P		HPO:skoehler	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0001272	OMIM:143100	TAS				P		HPO:skoehler	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0001347	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002063	OMIM:143100	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002066	OMIM:143100	TAS				P		HPO:skoehler	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002067	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002072	OMIM:143100	IEA				P		HPO:iea	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002171	OMIM:143100	TAS				P		HPO:probinson	
OMIM	143100	HUNTINGTON DISEASE; HD		HP:0002529	OMIM:143100	TAS				P		HPO:probinson	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000006	OMIM:143200	IEA				I		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000501	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000518	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000533	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000545	OMIM:143200	IEA				P		HPO:skoehler	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000572	OMIM:143200	IEA				P		HPO:skoehler	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0000648	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0001123	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0007643	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0007722	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0007773	OMIM:143200	IEA				P		HPO:iea	
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0030490	OMIM:143200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	143200	#143200 WAGNER VITREORETINOPATHY; WGVRP;;EROSIVE VITREORETINOPATHY; ERVR;;WAGNER VITREORETINAL DEGENERATION;;HYALOIDEORETINAL DEGENERATION OF WAGNER;;WAGNER SYNDROME 1; WGN1		HP:0030663	PMID:18309337	TAS				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000003	OMIM:143400	TAS				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000006	OMIM:143400	IEA				I		HPO:iea	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000072	OMIM:143400	TAS				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000074	OMIM:143400	IEA				P		HPO:iea	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000083	OMIM:143400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000089	OMIM:143400	TAS				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000100	OMIM:143400	IEA				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000110	OMIM:143400	TAS				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000126	OMIM:143400	IEA				P		HPO:iea	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0000800	OMIM:143400	IEA				P		HPO:skoehler	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0008663	OMIM:143400	IEA				P		HPO:iea	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0008676	OMIM:143400	IEA				P		HPO:iea	
OMIM	143400	#143400 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 2;;URETEROPELVIC JUNCTION OBSTRUCTION; UPJO;;PELVIURETERIC JUNCTION OBSTRUCTION; PUJO;;HYDRONEPHROSIS DUE TO PUJO;;MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MCRD		HP:0030157	OMIM:143400	TAS				P		HPO:skoehler	
OMIM	143465	ATTENTION DEFICIT-HYPERACTIVITY DISORDER		HP:0000006	OMIM:143465	IEA				I		HPO:iea	
OMIM	143465	ATTENTION DEFICIT-HYPERACTIVITY DISORDER		HP:0000752	OMIM:143465	IEA				P		HPO:iea	
OMIM	143465	ATTENTION DEFICIT-HYPERACTIVITY DISORDER		HP:0007018	OMIM:143465	TAS				P		HPO:skoehler	
OMIM	143470	HYPERALPHALIPOPROTEINEMIA		HP:0000006	OMIM:143470	TAS				I		HPO:skoehler	
OMIM	143470	HYPERALPHALIPOPROTEINEMIA		HP:0012184	OMIM:143470	TAS				P		HPO:probinson	
OMIM	143500	GILBERT SYNDROME		HP:0000007	OMIM:143500	IEA				I		HPO:iea	
OMIM	143500	GILBERT SYNDROME		HP:0000952	OMIM:143500	IEA				P		HPO:skoehler	
OMIM	143500	GILBERT SYNDROME		HP:0001944	OMIM:143500	IEA				P		HPO:skoehler	
OMIM	143500	GILBERT SYNDROME		HP:0008282	OMIM:143500	IEA				P		HPO:skoehler	
OMIM	143850	ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE		HP:0000006	OMIM:143850	TAS				I		HPO:probinson	
OMIM	143850	ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE		HP:0000978	OMIM:143850	TAS				P		HPO:skoehler	
OMIM	143850	ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE		HP:0001041	OMIM:143850	TAS				P		HPO:probinson	
OMIM	143850	ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE		HP:0001278	OMIM:143850	TAS				P		HPO:probinson	
OMIM	143850	ORTHOSTATIC HYPOTENSIVE DISORDER, STREETEN TYPE		HP:0001279	OMIM:143850	TAS				P		HPO:probinson	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0000006	OMIM:143860	IEA				I		HPO:iea	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0000007	OMIM:143860	TAS				I		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0001508	OMIM:143860	TAS				P		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0001939	OMIM:143860	IEA				P		HPO:iea	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0001944	OMIM:143860	TAS				P		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0002153	OMIM:143860	TAS				P		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0002902	OMIM:143860	TAS				P		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0003593	OMIM:143860	TAS				C		HPO:skoehler	
OMIM	143860	#143860 HYPERCHLORHIDROSIS, ISOLATED		HP:0011968	OMIM:143860	TAS				P		HPO:skoehler	
OMIM	143870	#143870 HYPERCALCIURIA, ABSORPTIVE, 2; HCA2;;HYPERCALCIURIA, FAMILIAL IDIOPATHIC		HP:0000006	OMIM:143870	TAS				I		HPO:skoehler	
OMIM	143870	#143870 HYPERCALCIURIA, ABSORPTIVE, 2; HCA2;;HYPERCALCIURIA, FAMILIAL IDIOPATHIC		HP:0001425	OMIM:143870	TAS				I		HPO:skoehler	
OMIM	143870	#143870 HYPERCALCIURIA, ABSORPTIVE, 2; HCA2;;HYPERCALCIURIA, FAMILIAL IDIOPATHIC		HP:0002150	OMIM:143870	TAS				P		HPO:skoehler	
OMIM	143870	#143870 HYPERCALCIURIA, ABSORPTIVE, 2; HCA2;;HYPERCALCIURIA, FAMILIAL IDIOPATHIC		HP:0008672	OMIM:143870	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000006	OMIM:143880	IEA				I		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000007	OMIM:143880	TAS				I		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000103	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000121	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000179	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000478	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0000787	OMIM:143880	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001249	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001254	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001290	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001508	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001642	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001650	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001824	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0001944	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0002013	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0002150	OMIM:143880	TAS				P		HPO:skoehler	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0004428	OMIM:143880	IEA				P		HPO:iea	
OMIM	143880	HYPERCALCEMIA, INFANTILE, 1		HP:0008250	OMIM:143880	IEA				P		HPO:iea	
OMIM	143890	HYPERCHOLESTEROLEMIA, FAMILIAL		HP:0000006	OMIM:143890	TAS				I		HPO:skoehler	
OMIM	143890	HYPERCHOLESTEROLEMIA, FAMILIAL		HP:0001084	OMIM:143890	TAS				P		HPO:skoehler	
OMIM	143890	HYPERCHOLESTEROLEMIA, FAMILIAL		HP:0001114	OMIM:143890	TAS				P		HPO:skoehler	
OMIM	143890	HYPERCHOLESTEROLEMIA, FAMILIAL		HP:0003124	OMIM:143890	IEA				P		HPO:skoehler	
OMIM	144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B		HP:0000006	OMIM:144010	IEA				I		HPO:iea	
OMIM	144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B		HP:0001084	OMIM:144010	IEA				P		HPO:iea	
OMIM	144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B		HP:0001114	OMIM:144010	IEA				P		HPO:iea	
OMIM	144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B		HP:0001677	OMIM:144010	IEA				P		HPO:iea	
OMIM	144010	HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B		HP:0003124	OMIM:144010	IEA				P		HPO:iea	
OMIM	144020	HYPERCHOLESTEROLEMIA SUPPRESSOR		HP:0000006	OMIM:144020	IEA				I		HPO:iea	
OMIM	144050	HYPERHEPARINEMIA		HP:0000006	OMIM:144050	IEA				I		HPO:iea	
OMIM	144050	HYPERHEPARINEMIA		HP:0001892	OMIM:144050	IEA	HP:0003577			P		HPO:iea	
OMIM	144100	HYPERHIDROSIS, GUSTATORY		HP:0000006	OMIM:144100	IEA				I		HPO:iea	
OMIM	144100	HYPERHIDROSIS, GUSTATORY		HP:0000975	OMIM:144100	TAS				P		HPO:probinson	
OMIM	144110	HYPERHIDROSIS PALMARIS ET PLANTARIS		HP:0000006	OMIM:144110	IEA				I		HPO:iea	
OMIM	144110	HYPERHIDROSIS PALMARIS ET PLANTARIS		HP:0007410	OMIM:144110	IEA				P		HPO:iea	
OMIM	144120	144120 HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED; IGHR		HP:0000006	OMIM:144120	IEA				I		HPO:iea	
OMIM	144120	144120 HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED; IGHR		HP:0003237	OMIM:144120	TAS				P		HPO:probinson	
OMIM	144120	144120 HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED; IGHR		HP:0003261	OMIM:144120	TAS				P		HPO:probinson	
OMIM	144120	144120 HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED; IGHR		HP:0003565	OMIM:144120	IEA				P		HPO:iea	
OMIM	144120	144120 HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED; IGHR		HP:0012432	OMIM:144120	TAS				P		HPO:skoehler	
OMIM	144150	HYPERKERATOSIS LENTICULARIS PERSTANS		HP:0000006	OMIM:144150	IEA				I		HPO:iea	
OMIM	144150	HYPERKERATOSIS LENTICULARIS PERSTANS		HP:0003581	OMIM:144150	IEA				C		HPO:iea	
OMIM	144150	HYPERKERATOSIS LENTICULARIS PERSTANS		HP:0007570	OMIM:144150	IEA				P		HPO:iea	
OMIM	144200	PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC		HP:0000006	PMID:12192490	PCS				I		HPO:skoehler	
OMIM	144200	PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC		HP:0000972	OMIM:144200	TAS				P		HPO:skoehler	
OMIM	144200	PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC		HP:0003212	OMIM:144200	TAS				P		HPO:skoehler	
OMIM	144200	PALMOPLANTAR KERATODERMA, EPIDERMOLYTIC		HP:0007559	PMID:12192490	PCS				P		HPO:skoehler	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0000006	OMIM:144250	TAS				I		HPO:iea	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0001114	OMIM:144250	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0001658	PMID:4718953	PCS				P		HPO:iea	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0003141	PMID:4718953	PCS				P		HPO:probinson	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0003362	PMID:4718953	PCS				P		HPO:probinson	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0031798	PMID:9373757	PCS				P		HPO:probinson	
OMIM	144250	HYPERLIPIDEMIA, FAMILIAL COMBINED		HP:0031800	PMID:12738753	PCS				P		HPO:probinson	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0000006	OMIM:144300	IEA				I		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0000365	OMIM:144300	IEA				P		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0000951	OMIM:144300	IEA				P		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0001084	OMIM:144300	IEA				P		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0002155	OMIM:144300	IEA				P		HPO:skoehler	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0002635	OMIM:144300	IEA				P		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0003124	OMIM:144300	IEA				P		HPO:iea	
OMIM	144300	HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS		HP:0003141	OMIM:144300	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0000006	OMIM:144600	IEA				I		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0001039	OMIM:144600	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0001425	OMIM:144600	IEA				I		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0001952	OMIM:144600	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0002155	OMIM:144600	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0003362	OMIM:144600	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0004416	OMIM:144600	IEA				P		HPO:iea	
OMIM	144600	HYPERLIPOPROTEINEMIA, TYPE IV		HP:0040075	OMIM:144600	IEA				P		HPO:skoehler	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0000006	OMIM:144650	TAS				I		HPO:probinson	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0000819	OMIM:144650	IEA				P		HPO:skoehler	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0003233	OMIM:144650	TAS				P		HPO:probinson	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0003362	OMIM:144650	TAS				P		HPO:probinson	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0003563	OMIM:144650	TAS				P		HPO:probinson	
OMIM	144650	HYPERLIPOPROTEINEMIA, TYPE V		HP:0012238	OMIM:144650	TAS				P		HPO:probinson	
OMIM	144700	RENAL CELL CARCINOMA, NONPAPILLARY		HP:0003745	OMIM:144700	TAS				I		HPO:iea	
OMIM	144700	RENAL CELL CARCINOMA, NONPAPILLARY		HP:0005584	OMIM:144700	TAS				P		HPO:probinson	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:144750	TAS				I		HPO:probinson	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0000407	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0000689	OMIM:144750	TAS				P		HPO:probinson	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0000935	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0001507	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0002644	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0004425	OMIM:144750	TAS				P		HPO:probinson	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0006174	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0008114	OMIM:144750	IEA				P		HPO:iea	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0100774	OMIM:144750	IEA				P		HPO:skoehler	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT		HP:0100789	OMIM:144750	TAS				P		HPO:skoehler	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT	HP:0012825	HP:0100861	OMIM:144750	TAS				P		HPO:probinson	
OMIM	144750	ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT	HP:0012825	HP:0100923	OMIM:144750	TAS				P		HPO:probinson	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000006	OMIM:144755	IEA				I		HPO:iea	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000265	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000360	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000407	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000520	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0000648	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0001751	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0004490	OMIM:144755	TAS				P		HPO:probinson	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0005746	OMIM:144755	TAS				P		HPO:probinson	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0005890	OMIM:144755	IEA				P		HPO:iea	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0007099	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0007663	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0007906	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0009926	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0010628	OMIM:144755	IEA				P		HPO:skoehler	
OMIM	144755	HYPEROSTOSIS CRANIALIS INTERNA; HCIN		HP:0200026	OMIM:144755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0000006	OMIM:144800	IEA				I		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0000819	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0000858	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0000870	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0000998	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0001513	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0003155	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0004438	OMIM:144800	IEA				P		HPO:iea	
OMIM	144800	144800 HYPEROSTOSIS FRONTALIS INTERNA;;MORGAGNI-STEWART-MOREL SYNDROME		HP:0100829	OMIM:144800	TAS				P		HPO:skoehler	
OMIM	145000	HYPERPARATHYROIDISM 1		HP:0000006	OMIM:145000	IEA				I		HPO:iea	
OMIM	145000	HYPERPARATHYROIDISM 1		HP:0003072	OMIM:145000	IEA				P		HPO:iea	
OMIM	145000	HYPERPARATHYROIDISM 1		HP:0008200	OMIM:145000	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0000006	OMIM:145001	IEA				I		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0000113	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0000234	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0000787	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0000843	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0002667	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0002897	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0003072	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0006725	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0006735	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0006766	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0006780	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0006781	OMIM:145001	IEA				P		HPO:iea	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0010566	OMIM:145001	IEA				P		HPO:skoehler	
OMIM	145001	HYPERPARATHYROIDISM 2		HP:0100027	OMIM:145001	IEA				P		HPO:iea	
OMIM	145100	HYPERPIGMENTATION OF EYELIDS		HP:0000006	OMIM:145100	IEA				I		HPO:iea	
OMIM	145100	HYPERPIGMENTATION OF EYELIDS		HP:0007406	OMIM:145100	IEA				P		HPO:iea	
OMIM	145200	HYPERPIGMENTATION OF FULDAUER AND KUIJPERS		HP:0000006	OMIM:145200	IEA				I		HPO:iea	
OMIM	145200	HYPERPIGMENTATION OF FULDAUER AND KUIJPERS		HP:0000953	OMIM:145200	TAS				P		HPO:probinson	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0000006	PMID:21368769	PCS				I		HPO:probinson	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0000957	PMID:21368769	PCS				P		HPO:skoehler	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0000962	OMIM:145250	TAS				P		HPO:skoehler	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0001003	PMID:21368769	PCS				P		HPO:probinson	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0001045	OMIM:145250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0001053	PMID:21368769	PCS				P		HPO:skoehler	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0003593	PMID:19375057	PCS				C		HPO:probinson	
OMIM	145250	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE		HP:0007505	PMID:21368769	PCS				P		HPO:probinson	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0000006	OMIM:145260	IEA				I		HPO:iea	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0000822	OMIM:145260	IEA				P		HPO:iea	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0001995	OMIM:145260	IEA				P		HPO:iea	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0002153	OMIM:145260	IEA				P		HPO:iea	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0007215	OMIM:145260	IEA				P		HPO:iea	
OMIM	145260	PSEUDOHYPOALDOSTERONISM, TYPE II		HP:0008242	OMIM:145260	TAS				P		HPO:probinson	
OMIM	145270	HYPERPROGLUCAGONEMIA		HP:0000006	OMIM:145270	IEA				I		HPO:iea	
OMIM	145270	HYPERPROGLUCAGONEMIA		HP:0001939	OMIM:145270	IEA				P		HPO:iea	
OMIM	145290	HYPERREFLEXIA		HP:0000006	OMIM:145290	TAS				I		HPO:probinson	
OMIM	145290	HYPERREFLEXIA		HP:0000252	OMIM:145290	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	145290	HYPERREFLEXIA		HP:0007703	OMIM:145290	TAS				P		HPO:probinson	
OMIM	145290	HYPERREFLEXIA		HP:0011448	OMIM:145290	TAS				P		HPO:probinson	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0000006	OMIM:145295	IEA				I		HPO:iea	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0000141	OMIM:145295	IEA				P		HPO:iea	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0001007	OMIM:145295	IEA				P		HPO:iea	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0002717	OMIM:145295	TAS				P		HPO:probinson	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0012411	OMIM:145295	TAS				P		HPO:skoehler	
OMIM	145295	HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL		HP:0030348	OMIM:145295	TAS				P		HPO:probinson	
OMIM	145300	HYPERSENSITIVITY PNEUMONITIS, FAMILIAL		HP:0000006	OMIM:145300	IEA				I		HPO:iea	
OMIM	145300	HYPERSENSITIVITY PNEUMONITIS, FAMILIAL		HP:0006516	OMIM:145300	IEA				P		HPO:iea	
OMIM	145350	HYPERTAURINURIC CARDIOMYOPATHY		HP:0000006	OMIM:145350	TAS				I		HPO:skoehler	
OMIM	145350	HYPERTAURINURIC CARDIOMYOPATHY		HP:0001634	OMIM:145350	TAS				P		HPO:skoehler	
OMIM	145350	HYPERTAURINURIC CARDIOMYOPATHY		HP:0001644	OMIM:145350	TAS				P		HPO:skoehler	
OMIM	145350	HYPERTAURINURIC CARDIOMYOPATHY		HP:0003166	OMIM:145350	TAS				P		HPO:probinson	
OMIM	145400	HYPERTELORISM		HP:0000006	OMIM:145400	IEA				I		HPO:iea	
OMIM	145400	HYPERTELORISM		HP:0000316	OMIM:145400	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000006	OMIM:145410	TAS				I		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000023	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000028	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000047	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000048	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000069	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000077	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000175	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000193	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000200	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000204	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000218	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000219	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000267	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000286	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000316	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000319	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000347	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000349	OMIM:145410	TAS				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000358	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000405	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000431	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000486	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000494	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0000506	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001249	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001252	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001263	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001274	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001290	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001320	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001363	OMIM:145410	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001537	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001540	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001612	OMIM:145410	TAS				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001629	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001631	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001643	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0001680	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002007	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002015	OMIM:145410	TAS				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002023	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002025	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002036	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002089	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002092	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002119	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002120	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002389	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002575	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0002835	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0003593	OMIM:145410	TAS				C		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0005280	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0006817	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0008751	OMIM:145410	IEA				P		HPO:iea	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0011220	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145410	OPITZ GBBB SYNDROME, TYPE II		HP:0011467	OMIM:145410	TAS				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000006	OMIM:145420	IEA				I		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000049	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000316	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000343	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000349	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000431	OMIM:145420	TAS				P		HPO:probinson	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000494	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000508	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000582	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000678	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000695	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0000739	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0001169	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0001539	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0001629	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0001631	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0002007	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0002553	OMIM:145420	IEA				P		HPO:skoehler	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0003196	OMIM:145420	IEA				P		HPO:iea	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0005280	OMIM:145420	TAS				P		HPO:probinson	
OMIM	145420	HYPERTELORISM, TEEBI TYPE; TBHS		HP:0011220	OMIM:145420	TAS				P		HPO:skoehler	
OMIM	145500	HYPERTENSION, ESSENTIAL		HP:0001426	OMIM:145500	IEA				I		HPO:iea	
OMIM	145500	HYPERTENSION, ESSENTIAL		HP:0004421	OMIM:145500	IEA				P		HPO:iea	
OMIM	145500	HYPERTENSION, ESSENTIAL		HP:0004972	OMIM:145500	IEA				P		HPO:iea	
OMIM	145500	HYPERTENSION, ESSENTIAL		HP:0005117	OMIM:145500	IEA				P		HPO:iea	
OMIM	145590	HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA		HP:0000006	OMIM:145590	IEA				I		HPO:iea	
OMIM	145590	HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA		HP:0001945	OMIM:145590	TAS				P		HPO:probinson	
OMIM	145590	HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA		HP:0002013	OMIM:145590	IEA				P		HPO:iea	
OMIM	145590	HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA		HP:0002018	OMIM:145590	IEA				P		HPO:iea	
OMIM	145590	HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA		HP:0002315	OMIM:145590	TAS				P		HPO:probinson	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0000006	OMIM:145600	IEA				I		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0001649	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0001945	OMIM:145600	TAS				P		HPO:skoehler	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002047	OMIM:145600	TAS				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002063	OMIM:145600	TAS				P		HPO:skoehler	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002153	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002615	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002905	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0002913	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0003201	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0003236	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0003256	OMIM:145600	IEA				P		HPO:iea	
OMIM	145600	#145600 MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 1; MHS1;;MHS;;HYPERTHERMIA OF ANESTHESIA;;HYPERPYREXIA, MALIGNANT; MHKING SYNDROME, INCLUDED;;KING-DENBOROUGH SYNDROME, INCLUDED		HP:0005967	OMIM:145600	IEA				P		HPO:iea	
OMIM	145650	THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY		HP:0000006	OMIM:145650	TAS				I		HPO:probinson	
OMIM	145650	THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY		HP:0000836	OMIM:145650	TAS				P		HPO:probinson	
OMIM	145650	THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY		HP:0002925	OMIM:145650	TAS				P		HPO:probinson	
OMIM	145650	THYROID HORMONE RESISTANCE, SELECTIVE PITUITARY		HP:0002930	OMIM:145650	TAS				P		HPO:skoehler	
OMIM	145680	DYSTRANSTHYRETINEMIC EUTHYROIDAL HYPERTHYROXINEMIA		HP:0000006	OMIM:145680	IEA				I		HPO:probinson	
OMIM	145680	DYSTRANSTHYRETINEMIC EUTHYROIDAL HYPERTHYROXINEMIA		HP:0008247	OMIM:145680	IEA				P		HPO:probinson	
OMIM	145700	HYPERTRICHOSIS UNIVERSALIS		HP:0000006	OMIM:145700	IEA				I		HPO:iea	
OMIM	145700	HYPERTRICHOSIS UNIVERSALIS		HP:0004540	OMIM:145700	IEA				P		HPO:iea	
OMIM	145700	HYPERTRICHOSIS UNIVERSALIS		HP:0010730	OMIM:145700	IEA				P		HPO:skoehler	
OMIM	145701	HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE		HP:0000006	OMIM:145701	IEA				I		HPO:iea	
OMIM	145701	HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE		HP:0004540	OMIM:145701	TAS				P		HPO:skoehler	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0000006	OMIM:145750	IEA				I		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0001039	OMIM:145750	IEA				P		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0001952	OMIM:145750	IEA				P		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0002155	OMIM:145750	IEA				P		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0003362	OMIM:145750	IEA				P		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0004416	OMIM:145750	IEA				P		HPO:iea	
OMIM	145750	HYPERTRIGLYCERIDEMIA, FAMILIAL		HP:0040075	OMIM:145750	IEA				P		HPO:skoehler	
OMIM	145800	HYPERTROPHIA MUSCULORUM VERA		HP:0000006	OMIM:145800	IEA				I		HPO:iea	
OMIM	145800	HYPERTROPHIA MUSCULORUM VERA		HP:0008981	OMIM:145800	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0000006	OMIM:145900	IEA				I		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0000007	OMIM:145900	IEA				I		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0000639	OMIM:145900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001171	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001178	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001252	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001265	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001270	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001284	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001290	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001425	OMIM:145900	IEA				I		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001761	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0001765	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0002460	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0002460	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0002751	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0002922	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0002936	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003376	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003380	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003382	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003383	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003431	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003481	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003593	OMIM:145900	IEA				C		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003693	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0003828	OMIM:145900	IEA				C		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0009027	OMIM:145900	IEA				P		HPO:iea	
OMIM	145900	HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS		HP:0010871	OMIM:145900	TAS				P		HPO:skoehler	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0000006	OMIM:145980	IEA				I		HPO:iea	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0000787	OMIM:145980	IEA				P		HPO:iea	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0000843	OMIM:145980	IEA				P		HPO:skoehler	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0001733	OMIM:145980	IEA				P		HPO:iea	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0002150	OMIM:145980	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0002918	OMIM:145980	IEA				P		HPO:iea	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0003072	OMIM:145980	IEA				P		HPO:iea	
OMIM	145980	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE I; HHC1		HP:0003127	OMIM:145980	IEA				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0000006	PMID:23802516	PCS				I		HP:probinson	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0000006	OMIM:145981	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0000787	OMIM:145981	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0000934	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0001012	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0001733	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0002918	PMID:23802516	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0003072	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0003127	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0003529	OMIM:145981	TAS				P		HPO:iea	
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0004398	OMIM:145981	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	145981	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II		HP:0008200	OMIM:145981	IEA				P		HPO:skoehler	
OMIM	146000	HYPOCHONDROPLASIA		HP:0000006	OMIM:146000	IEA				I		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0000256	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0000272	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0000956	OMIM:146000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146000	HYPOCHONDROPLASIA		HP:0001156	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0001249	OMIM:146000	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146000	HYPOCHONDROPLASIA		HP:0001377	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0002007	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0002644	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0002938	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA		HP:0002970	OMIM:146000	IEA				P		HPO:iea	
OMIM	146000	HYPOCHONDROPLASIA	HP:0012825	HP:0003015	OMIM:146000	TAS				P		HPO:probinson	
OMIM	146000	HYPOCHONDROPLASIA	HP:0012825	HP:0003026	OMIM:146000	TAS				P		HPO:probinson	
OMIM	146000	HYPOCHONDROPLASIA		HP:0009815	OMIM:146000	TAS				P		HPO:skoehler	
OMIM	146000	HYPOCHONDROPLASIA		HP:0011405	OMIM:146000	IEA				P		HPO:iea	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000006	OMIM:146110	IEA				I		HPO:iea	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000007	OMIM:146110	TAS				I		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000028	OMIM:146110	TAS				P		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000044	OMIM:146110	IEA				P		HPO:iea	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000054	OMIM:146110	TAS				P		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000771	OMIM:146110	TAS				P		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000786	OMIM:146110	IEA				P		HPO:iea	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0000789	OMIM:146110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0002215	OMIM:146110	TAS				P		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0002225	OMIM:146110	TAS				P		HPO:skoehler	
OMIM	146110	HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA; HH7		HP:0008734	OMIM:146110	IEA				P		HPO:iea	
OMIM	146160	HYPOMELIA WITH MULLERIAN DUCT ANOMALIES		HP:0000006	OMIM:146160	IEA				I		HPO:iea	
OMIM	146160	HYPOMELIA WITH MULLERIAN DUCT ANOMALIES		HP:0001162	OMIM:146160	IEA				P		HPO:iea	
OMIM	146160	HYPOMELIA WITH MULLERIAN DUCT ANOMALIES		HP:0001171	OMIM:146160	IEA				P		HPO:iea	
OMIM	146160	HYPOMELIA WITH MULLERIAN DUCT ANOMALIES		HP:0003762	OMIM:146160	IEA				P		HPO:iea	
OMIM	146160	HYPOMELIA WITH MULLERIAN DUCT ANOMALIES		HP:0008740	OMIM:146160	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0000006	OMIM:146200	IEA				I		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0000518	OMIM:146200	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0000829	PMID:28740581	PCS				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0001250	OMIM:146200	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0001281	OMIM:146200	IEA				P		HPO:skoehler	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0002514	OMIM:146200	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0002901	OMIM:146200	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0002905	OMIM:146200	IEA				P		HPO:iea	
OMIM	146200	HYPOPARATHYROIDISM, FAMILIAL ISOLATED		HP:0031817	PMID:28740581	PCS				P		HPO:lccarmody	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000006	PMID:29663634	PCS				I		HPO:iea	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000093	PMID:29663634	PCS				P		HPO:nvasilevsky	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000100	PMID:29663634	PCS				P		HPO:iea	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000110	OMIM:146255	IEA				P		HPO:iea	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000121	PMID:29663634	PCS				P		HPO:nvasilevsky	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000407	PMID:29663634	PCS		HP:0040284		P		HPO:nvasilevsky	174/180
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000790	PMID:29663634	PCS				P		HPO:nvasilevsky	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0000829	PMID:29663634	PCS		HP:0040284		P		HPO:iea	168/180
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0001153	PMID:17309062	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0002049	PMID:29663634	PCS				P		HPO:nvasilevsky	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0003762	PMID:17309062	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0004722	OMIM:146255	TAS				P		HPO:probinson	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0008341	PMID:29663634	PCS				P		HPO:nvasilevsky	
OMIM	146255	HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE		HP:0012622	PMID:29663634	PCS				P		HPO:probinson	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0000006	OMIM:146300	IEA				I		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0000007	OMIM:146300	IEA				I		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0000670	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0000934	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0001760	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0002748	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0002749	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0002756	OMIM:146300	TAS				P		HPO:skoehler	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0002757	OMIM:146300	TAS				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0003040	OMIM:146300	IEA				P		HPO:skoehler	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0003282	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0006323	OMIM:146300	IEA				P		HPO:iea	
OMIM	146300	HYPOPHOSPHATASIA, ADULT		HP:0006357	OMIM:146300	IEA				P		HPO:iea	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0000006	OMIM:146350	IEA				I		HPO:iea	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0002148	OMIM:146350	IEA				P		HPO:iea	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0002652	OMIM:146350	IEA				P		HPO:iea	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0002748	OMIM:146350	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0002749	OMIM:146350	IEA				P		HPO:skoehler	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0002979	OMIM:146350	IEA				P		HPO:iea	
OMIM	146350	HYPOPHOSPHATEMIC BONE DISEASE		HP:0004322	OMIM:146350	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000006	OMIM:146390	IEA				I		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000028	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000054	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000133	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000218	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000311	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000316	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000347	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000400	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000431	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000463	OMIM:146390	TAS				P		HPO:skoehler	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0000692	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0001249	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0001263	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0001332	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0001518	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0003745	OMIM:146390	IEA				I		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0004322	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0005989	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0008734	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0009466	OMIM:146390	IEA				P		HPO:iea	
OMIM	146390	CHROMOSOME 18P DELETION SYNDROME		HP:0030084	OMIM:146390	TAS				P		HPO:skoehler	
OMIM	146450	%146450 HYPOSPADIAS 3, AUTOSOMAL; HYSP3		HP:0000006	OMIM:146450	TAS				I		HPO:skoehler	
OMIM	146450	%146450 HYPOSPADIAS 3, AUTOSOMAL; HYSP3		HP:0000047	OMIM:146450	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000006	OMIM:146500	IEA				I		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000007	OMIM:146500	TAS				I		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000012	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000020	OMIM:146500	TAS				P		HPO:probinson	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000508	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000640	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000802	OMIM:146500	TAS				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000966	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0000970	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001089	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001251	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001260	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001278	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001300	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001337	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0001347	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0002063	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0002067	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0002172	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0002180	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0002542	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0003202	OMIM:146500	IEA				P		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0003487	OMIM:146500	IEA				P		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0003581	OMIM:146500	IEA				C		HPO:iea	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0003676	OMIM:146500	IEA				C		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0003745	OMIM:146500	IEA				I		HPO:skoehler	
OMIM	146500	MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO; MSA1		HP:0100543	OMIM:146500	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000006	OMIM:146510	TAS				I		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000028	OMIM:146510	TAS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000054	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000072	PMID:26604140	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000086	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000086	OMIM:146510	TAS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000089	PMID:26604140	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000107	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000110	PMID:26604140	PCS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000126	PMID:26604140	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000171	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000204	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000358	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000413	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000463	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000568	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000695	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000824	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000826	PMID:20301638	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000835	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000871	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0000902	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001162	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001250	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001263	PMID:24736735	PCS		HP:0040284		P		HPO:probinson	3/14
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001360	OMIM:146510	TAS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001511	OMIM:146510	TAS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001629	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001643	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001770	PMID:24736735	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0001830	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002023	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002101	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002164	PMID:24736735	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002444	PMID:24736735	PCS		HP:0040284		P		HPO:probinson	12/12
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002827	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0002937	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0003027	PMID:24736735	PCS		HP:0040284		P		HPO:probinson	4/21
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0003048	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0003196	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0003811	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				M		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0003828	OMIM:146510	TAS				C		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0004322	OMIM:146510	TAS				P		HPO:skoehler	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0005151	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0005280	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0005349	PMID:15782417	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0006042	PMID:24736735	PCS		HP:0040284		P		HPO:probinson	15/18
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0006159	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0006402	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0007601	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008163	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008188	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008551	OMIM:146510	TAS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008706	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008734	OMIM:146510	TAS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0008751	OMIM:146510	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0010044	OMIM:146510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0010112	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=phs	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0010564	PMID:15782417	PCS				P		HPO:probinson	
OMIM	146510	PALLISTER-HALL SYNDROME		HP:0012165	PMID:24736735	PCS		HP:0040284		P		HPO:skoehler	3/21
OMIM	146520	HYPOTRICHOSIS 2; HYPT2		HP:0000006	OMIM:146520	IEA				I		HPO:iea	
OMIM	146520	HYPOTRICHOSIS 2; HYPT2		HP:0002209	OMIM:146520	IEA				P		HPO:skoehler	
OMIM	146520	HYPOTRICHOSIS 2; HYPT2		HP:0004782	OMIM:146520	IEA				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0000006	OMIM:146550	IEA				I		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0000535	OMIM:146550	PCS				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0000653	OMIM:146550	PCS				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0001006	OMIM:146550	IEA				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0001596	OMIM:146550	IEA				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0002231	OMIM:146550	PCS				P		HPO:iea	
OMIM	146550	MARIE UNNA HEREDITARY HYPOTRICHOSIS 1		HP:0003777	OMIM:146550	PCS				P		HPO:iea	
OMIM	146590	ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE		HP:0000006	OMIM:146590	IEA				I		HPO:iea	
OMIM	146590	ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE		HP:0001939	OMIM:146590	IEA				P		HPO:iea	
OMIM	146590	ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE		HP:0008064	OMIM:146590	IEA				P		HPO:skoehler	
OMIM	146600	ICHTHYOSIS HYSTRIX GRAVIOR		HP:0000006	OMIM:146600	IEA				I		HPO:iea	
OMIM	146600	ICHTHYOSIS HYSTRIX GRAVIOR		HP:0008064	OMIM:146600	IEA				P		HPO:skoehler	
OMIM	146700	ICHTHYOSIS VULGARIS		HP:0000006	OMIM:146700	TAS				I		HPO:skoehler	
OMIM	146700	ICHTHYOSIS VULGARIS		HP:0000976	OMIM:146700	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	146700	ICHTHYOSIS VULGARIS		HP:0002099	OMIM:146700	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	146700	ICHTHYOSIS VULGARIS		HP:0008064	OMIM:146700	TAS				P		HPO:skoehler	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0000006	OMIM:146720	IEA				I		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0000218	OMIM:146720	IEA				P		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0000293	OMIM:146720	IEA				P		HPO:skoehler	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0000765	OMIM:146720	IEA				P		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0001763	OMIM:146720	IEA				P		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0002751	OMIM:146720	IEA				P		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0005338	OMIM:146720	IEA				P		HPO:iea	
OMIM	146720	ICHTHYOSIS--CHEEK--EYEBROW SYNDROME		HP:0008064	OMIM:146720	IEA				P		HPO:skoehler	
OMIM	146750	ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT		HP:0000006	OMIM:146750	IEA				I		HPO:iea	
OMIM	146750	ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT		HP:0000962	OMIM:146750	IEA				P		HPO:skoehler	
OMIM	146750	ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT		HP:0000989	OMIM:146750	IEA				P		HPO:iea	
OMIM	146750	ICHTHYOSIS, LAMELLAR, AUTOSOMAL DOMINANT		HP:0007479	OMIM:146750	TAS				P		HPO:skoehler	
OMIM	146800	ICHTHYOSIS, BULLOUS TYPE		HP:0000006	OMIM:146800	IEA				I		HPO:probinson	
OMIM	146800	ICHTHYOSIS, BULLOUS TYPE		HP:0007475	OMIM:146800	TAS				P		HPO:probinson	
OMIM	146830	IMMUNE DEFICIENCY, FAMILIAL VARIABLE		HP:0000006	OMIM:146830	IEA				I		HPO:iea	
OMIM	146830	IMMUNE DEFICIENCY, FAMILIAL VARIABLE		HP:0002719	OMIM:146830	TAS				P		HPO:skoehler	
OMIM	146830	IMMUNE DEFICIENCY, FAMILIAL VARIABLE		HP:0002720	OMIM:146830	IEA				P		HPO:iea	
OMIM	146830	IMMUNE DEFICIENCY, FAMILIAL VARIABLE		HP:0002721	OMIM:146830	IEA				P		HPO:iea	
OMIM	146830	IMMUNE DEFICIENCY, FAMILIAL VARIABLE		HP:0004315	OMIM:146830	IEA				P		HPO:iea	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0000006	OMIM:146840	TAS				I		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0000495	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0000559	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0000999	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0001047	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0002721	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0003347	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0005512	OMIM:146840	TAS				P		HPO:probinson	
OMIM	146840	IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTION AND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST		HP:0025084	OMIM:146840	TAS				P		HPO:skoehler	
OMIM	146850	IMMUNE SUPPRESSION		HP:0000006	OMIM:146850	IEA				I		HPO:iea	
OMIM	146850	IMMUNE SUPPRESSION		HP:0002715	OMIM:146850	IEA				P		HPO:iea	
OMIM	147050	IGE RESPONSIVENESS, ATOPIC		HP:0000006	OMIM:147050	IEA				I		HPO:iea	
OMIM	147050	IGE RESPONSIVENESS, ATOPIC		HP:0000964	OMIM:147050	IEA				P		HPO:iea	
OMIM	147050	IGE RESPONSIVENESS, ATOPIC		HP:0002099	OMIM:147050	IEA				P		HPO:iea	
OMIM	147050	IGE RESPONSIVENESS, ATOPIC		HP:0003193	OMIM:147050	TAS				P		HPO:skoehler	
OMIM	147050	IGE RESPONSIVENESS, ATOPIC		HP:0003212	OMIM:147050	TAS				P		HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000006	PMID:17881745	PCS				I	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000218	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000280	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000316	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000445	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000938	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HP:0012828	HP:0000976	PMID:18978467	TAS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0000988	PMID:22441639	PCS	HP:0003623			P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HP:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0001363	PMID:18978467	PCS		HP:0040283		P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	HP:0040283
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0001382	PMID:18978467	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0001880	PMID:18978467	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002007	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002650	PMID:18978467	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002726	PMID:17881745	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:skoehler	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002728	PMID:18978467	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HP:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002757	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0002841	OMIM:147060	TAS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0003212	PMID:17881745	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0003593	OMIM:147060	IEA				C	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:iea	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0005425	OMIM:147060	TAS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0006335	PMID:17881745	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0006532	PMID:18978467	PCS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HP:probinson	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0007099	PMID:18978467	PCS		HP:0040284		P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HP:probinson	18%
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0010783	OMIM:147060	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:skoehler	
OMIM	147060	HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT		HP:0011220	OMIM:147060	TAS				P	HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT	HPO:skoehler	
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000006	OMIM:147250	PCS				I		HPO:iea	
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000204	PMID:11471164	PCS		HP:0040284		P		HPO:iea	1/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000252	OMIM:147250	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000252	PMID:11471164	PCS		HP:0040284		P		HPO:iea	6/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000453	PMID:11471164	PCS		HP:0040284		P		HPO:iea	8/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000458	OMIM:147250	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000528	PMID:12503095	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000568	PMID:12503095	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000589	PMID:12503095	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000601	PMID:11471164	PCS		HP:0040284		P		HPO:iea	8/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0000824	PMID:925821	PCS		HP:0040284		P		HPO:iea	5/7
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0001256	PMID:11471164	PCS		HP:0040284		P		HPO:iea	3/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0001328	PMID:11471164	PCS		HP:0040284		P		HPO:iea	5/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0001360	OMIM:147250	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0001739	PMID:11471164	PCS		HP:0040284		P		HPO:iea	1/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0002708	PMID:11471164	PCS		HP:0040284		P		HPO:iea	14/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0002916	PMID:11471164	PCS		HP:0040284		P		HPO:iea	2/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0003828	OMIM:147250	PCS				C		HPO:iea	
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0004322	PMID:11471164	PCS		HP:0040284		P		HPO:iea	7/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0006315	OMIM:147250	PCS		HP:0040284		P		HPO:iea	100%
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0009914	PMID:12503095	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0010644	PMID:11471164	PCS		HP:0040284		P		HPO:iea	9/14
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0025011	OMIM:147250	IEA				P		HPO:skoehler	
OMIM	147250	SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR; SMMCI		HP:0100789	OMIM:147250	TAS				P		HPO:skoehler	
OMIM	147251	INCISORS, FUSED MANDIBULAR		HP:0000006	OMIM:147251	IEA				I		HPO:iea	
OMIM	147251	INCISORS, FUSED MANDIBULAR		HP:0000164	OMIM:147251	IEA				P		HPO:iea	
OMIM	147300	INCISORS, LONG UPPER CENTRAL		HP:0000006	OMIM:147300	IEA				I		HPO:iea	
OMIM	147300	INCISORS, LONG UPPER CENTRAL		HP:0000675	OMIM:147300	IEA				P		HPO:iea	
OMIM	147320	INSULIN RECEPTORS, FAMILIAL INCREASE IN		HP:0000006	OMIM:147320	TAS				I		HPO:skoehler	
OMIM	147330	INCISORS, LOWER CENTRAL, ABSENCE OF		HP:0000006	OMIM:147330	IEA				I		HPO:iea	
OMIM	147330	INCISORS, LOWER CENTRAL, ABSENCE OF		HP:0006355	OMIM:147330	IEA				P		HPO:iea	
OMIM	147350	INCISORS, ROTATION OF UPPER CENTRAL		HP:0000006	OMIM:147350	IEA				I		HPO:iea	
OMIM	147350	INCISORS, ROTATION OF UPPER CENTRAL		HP:0006330	OMIM:147350	IEA				P		HPO:iea	
OMIM	147400	INCISORS, SHOVEL-SHAPED		HP:0000006	OMIM:147400	TAS				I		HPO:nvasilevsky	
OMIM	147400	INCISORS, SHOVEL-SHAPED		HP:0006358	OMIM:147400	IEA				P		HPO:iea	
OMIM	147400	INCISORS, SHOVEL-SHAPED		HP:0010982	OMIM:147400	TAS				I		HPO:nvasilevsky	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0000006	OMIM:147421	IEA				I		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0001265	OMIM:147421	IEA				P		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0002015	OMIM:147421	TAS				P		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0002460	OMIM:147421	TAS				P		HPO:skoehler	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0003677	OMIM:147421	TAS				C		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0003701	OMIM:147421	TAS				P		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0003745	OMIM:147421	TAS				I		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0003805	OMIM:147421	TAS				P		HPO:iea	
OMIM	147421	INCLUSION BODY MYOSITIS		HP:0009071	OMIM:147421	TAS				P		HPO:iea	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0000006	OMIM:147430	TAS				I		HPO:skoehler	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0000966	PMID:8983665	PCS				P		HPO:lccarmody	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0001954	PMID:8983665	PCS				P		HPO:lccarmody	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0001954	OMIM:147430	IEA				P		HPO:skoehler	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0002315	PMID:8983665	PCS				P		HPO:lccarmody	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0002661	PMID:8983665	PCS				P		HPO:lccarmody	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0006901	PMID:18983665	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0007021	PMID:18983665	PCS	HP:0003593			P		HPO:skoehler	
OMIM	147430	MARSILI SYNDROME; MARSIS		HP:0008000	PMID:18983665	PCS				P		HPO:lccarmody	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0000006	OMIM:147480	IEA				I		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0000952	OMIM:147480	IEA				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0000989	OMIM:147480	IEA				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0001406	OMIM:147480	IEA				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0001622	OMIM:147480	IEA				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0002910	OMIM:147480	IEA				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0025116	OMIM:147480	TAS				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0200148	OMIM:147480	TAS				P		HPO:skoehler	
OMIM	147480	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY, 1; ICP1		HP:0200150	OMIM:147480	TAS				P		HPO:skoehler	
OMIM	147530	INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY		HP:0000006	OMIM:147530	TAS				I		HPO:probinson	
OMIM	147530	INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY		HP:0003130	OMIM:147530	TAS				P		HPO:probinson	
OMIM	147530	INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY		HP:0007021	OMIM:147530	TAS				P		HPO:skoehler	
OMIM	147530	INSENSITIVITY TO PAIN WITH HYPERPLASTIC MYELINOPATHY		HP:0010830	OMIM:147530	TAS				P		HPO:probinson	
OMIM	147540	INSECT STINGS, HYPERSENSITIVITY TO		HP:0000006	OMIM:147540	IEA				I		HPO:iea	
OMIM	147540	INSECT STINGS, HYPERSENSITIVITY TO		HP:0000951	OMIM:147540	IEA				P		HPO:iea	
OMIM	147610	IRIS PIGMENT LAYER, CLEAVAGE OF		HP:0000006	OMIM:147610	IEA				I		HPO:iea	
OMIM	147610	IRIS PIGMENT LAYER, CLEAVAGE OF		HP:0000501	OMIM:147610	IEA				P		HPO:iea	
OMIM	147610	IRIS PIGMENT LAYER, CLEAVAGE OF		HP:0000518	OMIM:147610	IEA				P		HPO:iea	
OMIM	147610	IRIS PIGMENT LAYER, CLEAVAGE OF		HP:0007929	OMIM:147610	IEA				P		HPO:iea	
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0000006	OMIM:147630	IEA				I		HPO:iea	
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0000519	OMIM:147630	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0000819	OMIM:147630	IEA				P		HPO:iea	
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0000825	OMIM:147630	IEA				P		HPO:skoehler	
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0001087	OMIM:147630	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	147630	INSULINOMATOSIS AND DIABETES MELLITUS; INSDM		HP:0008194	OMIM:147630	IEA				P		HPO:iea	
OMIM	147710	INTUSSUSCEPTION		HP:0000006	OMIM:147710	IEA				I		HPO:iea	
OMIM	147710	INTUSSUSCEPTION		HP:0002576	OMIM:147710	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0000006	OMIM:147750	IEA				I		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0000143	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0000365	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0000486	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0000544	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0001199	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0001245	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0001498	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0001873	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0001974	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0002023	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0002566	OMIM:147750	IEA				P		HPO:skoehler	
OMIM	147750	IVIC SYNDROME		HP:0002650	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0002974	OMIM:147750	TAS				P		HPO:probinson	
OMIM	147750	IVIC SYNDROME		HP:0002984	OMIM:147750	TAS				P		HPO:probinson	
OMIM	147750	IVIC SYNDROME		HP:0002996	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0006064	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0006248	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0008953	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0009702	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0009777	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0010034	OMIM:147750	IEA				P		HPO:iea	
OMIM	147750	IVIC SYNDROME		HP:0030241	OMIM:147750	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000006	OMIM:147770	IEA				I		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000044	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000054	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000175	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000252	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000278	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000324	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000405	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000411	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000413	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000452	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000458	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000561	OMIM:147770	TAS				P		HPO:skoehler	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000670	OMIM:147770	IEA				P		HPO:skoehler	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0000966	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0001249	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0001510	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0001596	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0001629	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0001643	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0002223	OMIM:147770	TAS				P		HPO:skoehler	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0004322	OMIM:147770	TAS				P		HPO:skoehler	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0007565	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0008070	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0008551	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0008734	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0010628	OMIM:147770	IEA				P		HPO:iea	
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0012020	OMIM:147770	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147770	%147770 JOHNSON NEUROECTODERMAL SYNDROME;;JOHNSON-MCMILLIN SYNDROME; JMS;;ALOPECIA-ANOSMIA-DEAFNESS-HYPOGONADISM SYNDROME;;AADH SYNDROME		HP:0030680	OMIM:147770	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000028	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000047	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000060	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000066	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000238	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000243	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000252	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000256	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000286	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000316	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000347	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000369	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000463	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000470	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000482	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000486	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000499	OMIM:147791	TAS				P		HPO:skoehler	
OMIM	147791	JACOBSEN SYNDROME		HP:0000506	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000508	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000567	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000568	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000579	OMIM:147791	IEA				P		HPO:skoehler	
OMIM	147791	JACOBSEN SYNDROME		HP:0000612	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000625	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000646	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000648	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000767	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0000921	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001104	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001156	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001249	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001257	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001290	OMIM:147791	TAS				P		HPO:skoehler	
OMIM	147791	JACOBSEN SYNDROME		HP:0001360	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001371	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001508	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001511	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001629	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001631	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001734	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0001873	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0002021	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0002205	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0003196	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0003745	OMIM:147791	IEA				I		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0004209	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0005280	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0005469	OMIM:147791	IEA				P		HPO:iea	
OMIM	147791	JACOBSEN SYNDROME		HP:0008947	OMIM:147791	IEA				P		HPO:skoehler	
OMIM	147791	JACOBSEN SYNDROME		HP:0010806	OMIM:147791	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000006	OMIM:147800	IEA				I		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000175	OMIM:147800	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000194	OMIM:147800	IEA				P		HPO:skoehler	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000238	OMIM:147800	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000377	OMIM:147800	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0000508	OMIM:147800	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001238	OMIM:147800	IEA				P		HPO:skoehler	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001305	OMIM:147800	IEA				P		HPO:skoehler	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001371	OMIM:147800	IEA				P		HPO:skoehler	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001522	OMIM:147800	IEA				M		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001629	OMIM:147800	IEA				P		HPO:skoehler	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0001762	OMIM:147800	IEA				P		HPO:iea	
OMIM	147800	AASE-SMITH SYNDROME I		HP:0006742	OMIM:147800	IEA				P		HPO:iea	
OMIM	147820	INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF		HP:0000006	OMIM:147820	IEA				I		HPO:iea	
OMIM	147820	INTERNAL CAROTID ARTERY, SPONTANEOUS DISSECTION OF		HP:0004945	OMIM:147820	IEA				P		HPO:iea	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0000006	OMIM:147891	TAS				I		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0000175	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0000218	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0000347	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0001763	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0001852	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0002812	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0002999	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0003065	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME	HP:0012826	HP:0003097	OMIM:147891	TAS				P		HPO:skoehler	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0003370	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0004322	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0005682	OMIM:147891	TAS				P		HPO:skoehler	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0006443	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0008784	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147891	ISCHIOCOXOPODOPATELLAR SYNDROME		HP:0008801	OMIM:147891	TAS				P		HPO:probinson	
OMIM	147892	DEIODINASE, IODOTHYRONINE, TYPE I; DIO1		HP:0000006	OMIM:147892	TAS				I		HPO:probinson	
OMIM	147892	DEIODINASE, IODOTHYRONINE, TYPE I; DIO1		HP:0000853	OMIM:147892	TAS				P		HPO:skoehler	
OMIM	147892	DEIODINASE, IODOTHYRONINE, TYPE I; DIO1		HP:0008247	OMIM:147892	TAS				P		HPO:probinson	
OMIM	147900	JOINT LAXITY, FAMILIAL		HP:0000006	OMIM:147900	IEA				I		HPO:iea	
OMIM	147900	JOINT LAXITY, FAMILIAL		HP:0001374	OMIM:147900	IEA				P		HPO:iea	
OMIM	147900	JOINT LAXITY, FAMILIAL		HP:0001388	OMIM:147900	IEA				P		HPO:iea	
OMIM	147900	JOINT LAXITY, FAMILIAL		HP:0031869	OMIM:147900	IEA				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0000006	OMIM:147920	IEA				I		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000028	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000054	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000074	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000164	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000175	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000218	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000252	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000358	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000365	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000400	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000403	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000431	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000437	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000486	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000508	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000535	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000592	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000637	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000851	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0000957	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001007	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001212	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001249	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001250	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001252	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001263	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001290	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0001374	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001382	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001629	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001631	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001680	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001878	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0001973	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002023	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002024	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002025	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002100	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002553	OMIM:147920	PCS				P		HPO:probinson	
OMIM	147920	KABUKI SYNDROME 1		HP:0002566	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0002650	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0003468	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0004322	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0004467	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0004736	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0005218	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0007655	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0008872	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0008897	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0009237	OMIM:147920	IEA				P		HPO:iea	
OMIM	147920	KABUKI SYNDROME 1		HP:0010314	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147920	KABUKI SYNDROME 1		HP:0011231	OMIM:147920	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000006	OMIM:147950	IEA				I		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000028	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000044	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000054	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000175	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000204	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000407	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000453	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000458	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000612	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000771	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000786	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0000938	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0001249	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0001274	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0001335	OMIM:147950	TAS				P		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0001425	OMIM:147950	IEA				I		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0003829	OMIM:147950	TAS				C		HPO:skoehler	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0004322	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0009804	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0030084	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0030680	OMIM:147950	IEA				P		HPO:iea	
OMIM	147950	HYPOGONADOTROPIC HYPOGONADISM 2 WITH OR WITHOUT ANOSMIA		HP:0100257	OMIM:147950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	148000	KAPOSI SARCOMA, SUSCEPTIBILITY TO		HP:0000006	OMIM:148000	IEA				I		HPO:iea	
OMIM	148000	KAPOSI SARCOMA, SUSCEPTIBILITY TO		HP:0000969	OMIM:148000	IEA				P		HPO:skoehler	
OMIM	148000	KAPOSI SARCOMA, SUSCEPTIBILITY TO		HP:0001034	OMIM:148000	IEA				P		HPO:skoehler	
OMIM	148000	KAPOSI SARCOMA, SUSCEPTIBILITY TO		HP:0100242	OMIM:148000	IEA				P		HPO:skoehler	
OMIM	148050	KBG SYNDROME		HP:0000006	OMIM:148050	IEA				I		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000028	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000252	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000294	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000311	OMIM:148050	IEA				P		HPO:skoehler	
OMIM	148050	KBG SYNDROME		HP:0000316	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000325	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000343	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000400	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000430	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000463	OMIM:148050	IEA				P		HPO:skoehler	
OMIM	148050	KBG SYNDROME		HP:0000506	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000574	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000637	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000677	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0000891	OMIM:148050	IEA				P		HPO:skoehler	
OMIM	148050	KBG SYNDROME		HP:0000902	OMIM:148050	IEA				P		HPO:skoehler	
OMIM	148050	KBG SYNDROME		HP:0000954	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0001159	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0001249	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0001250	OMIM:148050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	148050	KBG SYNDROME		HP:0001263	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0001566	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0001572	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0002162	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0002750	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0002942	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0002948	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0004322	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0008438	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0009466	OMIM:148050	IEA				P		HPO:iea	
OMIM	148050	KBG SYNDROME		HP:0030084	OMIM:148050	TAS				P		HPO:skoehler	
OMIM	148100	KELOIDS		HP:0000006	OMIM:148100	IEA				I		HPO:iea	
OMIM	148100	KELOIDS		HP:0010562	OMIM:148100	IEA				P		HPO:skoehler	
OMIM	148190	KERATITIS, HEREDITARY		HP:0000006	OMIM:148190	IEA				I		HPO:iea	
OMIM	148190	KERATITIS, HEREDITARY		HP:0000491	OMIM:148190	IEA				P		HPO:skoehler	
OMIM	148190	KERATITIS, HEREDITARY		HP:0007759	OMIM:148190	IEA				P		HPO:iea	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0000006	OMIM:148200	IEA				I		HPO:iea	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0000491	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0000613	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0000622	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0000969	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0003621	OMIM:148200	IEA				C		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0007759	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0009926	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148200	KERATOENDOTHELIITIS FUGAX HEREDITARIA; KEFH		HP:0030953	OMIM:148200	IEA				P		HPO:skoehler	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000006	OMIM:148210	IEA				I		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000221	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000407	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000495	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000535	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000559	OMIM:148210	TAS				P		HPO:skoehler	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000613	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000618	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000653	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000962	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0000966	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0001097	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0001128	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0001761	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0002164	OMIM:148210	TAS				P		HPO:skoehler	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0002745	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0002860	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0002987	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0005406	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0006380	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0008064	OMIM:148210	TAS				P		HPO:skoehler	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0008404	OMIM:148210	IEA				P		HPO:iea	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0011492	OMIM:148210	TAS				P		HPO:skoehler	
OMIM	148210	#148210 KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT;;KID SYNDROME, AUTOSOMAL DOMINANT		HP:0012804	OMIM:148210	TAS				P		HPO:skoehler	
OMIM	148300	#148300 KERATOCONUS 1; KTCN1		HP:0000006	OMIM:148300	TAS				I		HPO:skoehler	
OMIM	148300	#148300 KERATOCONUS 1; KTCN1		HP:0000483	OMIM:148300	IEA				P		HPO:iea	
OMIM	148300	#148300 KERATOCONUS 1; KTCN1		HP:0000563	OMIM:148300	IEA				P		HPO:iea	
OMIM	148300	#148300 KERATOCONUS 1; KTCN1		HP:0001425	OMIM:148300	IEA				I		HPO:iea	
OMIM	148300	#148300 KERATOCONUS 1; KTCN1		HP:0011462	OMIM:148300	TAS				C		HPO:skoehler	
OMIM	148350	KERATODERMA, PALMOPLANTAR, WITH DEAFNESS		HP:0000006	OMIM:148350	IEA				I		HPO:iea	
OMIM	148350	KERATODERMA, PALMOPLANTAR, WITH DEAFNESS		HP:0000365	OMIM:148350	IEA	HP:0011463			P		HPO:skoehler	
OMIM	148350	KERATODERMA, PALMOPLANTAR, WITH DEAFNESS		HP:0000972	OMIM:148350	IEA				P		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0000006	OMIM:148360	IEA				I		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0000982	OMIM:148360	IEA				P		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0001425	OMIM:148360	IEA				I		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0001761	OMIM:148360	IEA				P		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0002164	OMIM:148360	IEA				P		HPO:iea	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0003390	OMIM:148360	PCS				P		HPO:probinson	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0007002	OMIM:148360	PCS				P		HPO:probinson	
OMIM	148360	148360 KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORYNEUROPATHY;;AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA;;CHARCOT-MARIE-TOOTH DISEASE WITH PALMOPLANTAR KERATODERMA AND NAILDYSTROPHY		HP:0008404	OMIM:148360	TAS				P		HPO:skoehler	
OMIM	148370	KERATOLYTIC WINTER ERYTHEMA; KWE		HP:0000006	OMIM:148370	IEA				I		HPO:iea	
OMIM	148370	KERATOLYTIC WINTER ERYTHEMA; KWE		HP:0007410	OMIM:148370	IEA				P		HPO:skoehler	
OMIM	148370	KERATOLYTIC WINTER ERYTHEMA; KWE		HP:0010783	OMIM:148370	IEA				P		HPO:skoehler	
OMIM	148390	KERATOSIS, FAMILIAL ACTINIC		HP:0000006	OMIM:148390	TAS				I		HPO:iea	
OMIM	148390	KERATOSIS, FAMILIAL ACTINIC		HP:0000951	OMIM:148390	IEA				P		HPO:iea	
OMIM	148390	KERATOSIS, FAMILIAL ACTINIC		HP:0001939	OMIM:148390	IEA				P		HPO:iea	
OMIM	148390	KERATOSIS, FAMILIAL ACTINIC		HP:0010784	OMIM:148390	TAS				P		HPO:probinson	
OMIM	148390	KERATOSIS, FAMILIAL ACTINIC		HP:0030731	OMIM:148390	IEA				P		HPO:skoehler	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0000006	OMIM:148500	IEA				I		HPO:iea	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0000153	OMIM:148500	IEA				P		HPO:iea	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0001036	OMIM:148500	IEA				P		HPO:skoehler	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0002664	OMIM:148500	IEA				P		HPO:iea	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0007447	OMIM:148500	IEA				P		HPO:iea	
OMIM	148500	#148500 TYLOSIS WITH ESOPHAGEAL CANCER; TOC;;KERATOSIS PALMARIS ET PLANTARIS WITH ESOPHAGEAL CANCER		HP:0011459	OMIM:148500	TAS				P		HPO:skoehler	
OMIM	148520	KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY		HP:0000006	OMIM:148520	IEA				I		HPO:iea	
OMIM	148520	KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY		HP:0000951	OMIM:148520	IEA				P		HPO:iea	
OMIM	148520	KERATOSIS PALMARIS ET PLANTARIS WITH CLINODACTYLY		HP:0004209	OMIM:148520	IEA				P		HPO:iea	
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0000006	PMID:23064416	PCS				I		HPO:iea	
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0007530	PMID:14684683	TAS		HP:0040280		P		HP:probinson	HP:0040280
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0007530	PMID:23064416	PCS	HP:0003621	HP:0040280		P		HP:probinson	HP:0040280
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0025092	PMID:23064416	PCS				P		HP:probinson	
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0025114	PMID:23064416	PCS				P		HP:probinson	
OMIM	148600	KERATOSIS PALMOPLANTARIS PAPULOSA		HP:0040162	PMID:23064416	PCS				P		HP:probinson	
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0000006	OMIM:148700	IEA				I		HPO:iea	
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0000975	OMIM:148700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0000982	OMIM:148700	IEA				P		HPO:skoehler	
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0001806	OMIM:148700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0007501	OMIM:148700	IEA				P		HPO:iea	
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0008404	OMIM:148700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0025092	OMIM:148700	TAS				P		HPO:skoehler	
OMIM	148700	PALMOPLANTAR KERATODERMA I, STRIATE, FOCAL, OR DIFFUSE; PPKS1		HP:0025114	OMIM:148700	IEA				P		HPO:skoehler	
OMIM	148730	KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL		HP:0000006	OMIM:148730	IEA				I		HPO:iea	
OMIM	148730	KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL		HP:0000222	OMIM:148730	IEA				P		HPO:iea	
OMIM	148730	KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL		HP:0007497	OMIM:148730	IEA				P		HPO:iea	
OMIM	148730	KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL		HP:0008392	OMIM:148730	IEA				P		HPO:iea	
OMIM	148730	KERATOSIS, FOCAL PALMOPLANTAR AND GINGIVAL		HP:0008399	OMIM:148730	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0000006	OMIM:148800	IEA				I		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0000238	OMIM:148800	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0000495	OMIM:148800	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0000520	OMIM:148800	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0001363	OMIM:148800	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0002676	OMIM:148800	IEA				P		HPO:skoehler	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0003070	OMIM:148800	IEA				P		HPO:iea	
OMIM	148800	KLEEBLATTSCHAEDEL SYNDROME		HP:0003745	OMIM:148800	IEA				I		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000007	OMIM:148820	IEA				I		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000252	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000303	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000407	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000426	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000431	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000506	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000581	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000635	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0000664	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001053	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001100	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001156	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001249	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001258	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0001452	OMIM:148820	IEA				I		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0002211	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0002216	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0002251	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0003691	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0003828	OMIM:148820	IEA				C		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0007443	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0009473	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0009702	OMIM:148820	IEA				P		HPO:iea	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0010554	OMIM:148820	IEA				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0030084	OMIM:148820	TAS				P		HPO:skoehler	
OMIM	148820	#148820 WAARDENBURG SYNDROME, TYPE 3; WS3;;WAARDENBURG SYNDROME WITH UPPER LIMB ANOMALIES;;WAARDENBURG SYNDROME, TYPE III;;KLEIN-WAARDENBURG SYNDROME		HP:0100490	OMIM:148820	TAS				P		HPO:skoehler	
OMIM	148840	KLEINE-LEVIN HIBERNATION SYNDROME		HP:0000006	OMIM:148840	IEA				I		HPO:iea	
OMIM	148840	KLEINE-LEVIN HIBERNATION SYNDROME		HP:0001289	OMIM:148840	IEA				P		HPO:iea	
OMIM	148840	KLEINE-LEVIN HIBERNATION SYNDROME		HP:0002591	OMIM:148840	IEA				P		HPO:skoehler	
OMIM	148840	KLEINE-LEVIN HIBERNATION SYNDROME		HP:0006803	OMIM:148840	IEA				P		HPO:iea	
OMIM	148840	KLEINE-LEVIN HIBERNATION SYNDROME		HP:0007200	OMIM:148840	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0000501	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001004	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001028	OMIM:149000	IEA				P		HPO:skoehler	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001159	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001161	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001180	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001249	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001250	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001528	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0001871	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0003745	OMIM:149000	IEA				I		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0004099	OMIM:149000	IEA				P		HPO:skoehler	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0004947	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0005606	OMIM:149000	IEA				P		HPO:iea	
OMIM	149000	%149000 KLIPPEL-TRENAUNAY-WEBER SYNDROME;;KTW SYNDROME;;KLIPPEL-TRENAUNAY SYNDROME; KTS;;ANGIOOSTEOHYPERTROPHY SYNDROME		HP:0100764	OMIM:149000	TAS				P		HPO:skoehler	
OMIM	149100	KNUCKLE PADS		HP:0000006	OMIM:149100	IEA				I		HPO:iea	
OMIM	149100	KNUCKLE PADS		HP:0000924	OMIM:149100	IEA				P		HPO:iea	
OMIM	149100	KNUCKLE PADS		HP:0001482	OMIM:149100	IEA				P		HPO:skoehler	
OMIM	149200	KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS		HP:0000006	OMIM:149200	IEA				I		HPO:iea	
OMIM	149200	KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS		HP:0000365	OMIM:149200	IEA				P		HPO:skoehler	
OMIM	149200	KNUCKLE PADS, LEUKONYCHIA, AND SENSORINEURAL DEAFNESS		HP:0001820	OMIM:149200	IEA				P		HPO:iea	
OMIM	149300	KOILONYCHIA, HEREDITARY		HP:0000006	OMIM:149300	IEA				I		HPO:iea	
OMIM	149300	KOILONYCHIA, HEREDITARY		HP:0001598	OMIM:149300	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0000006	OMIM:149400	IEA				I		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0000007	OMIM:149400	IEA				I		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0000023	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0001276	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0001336	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0001537	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002104	OMIM:149400	IEA				P		HPO:skoehler	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002267	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002359	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002375	OMIM:149400	IEA				P		HPO:skoehler	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002827	OMIM:149400	IEA				P		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0002835	OMIM:149400	IEA				P		HPO:skoehler	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0003593	OMIM:149400	IEA				C		HPO:iea	
OMIM	149400	HYPEREKPLEXIA 1; HKPX1		HP:0031951	OMIM:149400	IEA				P		HPO:skoehler	
OMIM	149500	KYRLE DISEASE		HP:0000006	OMIM:149500	IEA				I		HPO:iea	
OMIM	149500	KYRLE DISEASE		HP:0000951	OMIM:149500	IEA				P		HPO:iea	
OMIM	149500	KYRLE DISEASE		HP:0007787	OMIM:149500	IEA				P		HPO:iea	
OMIM	149600	LABIA MINORA, INCOMPLETE ADHESION OF		HP:0000006	OMIM:149600	IEA				I		HPO:iea	
OMIM	149600	LABIA MINORA, INCOMPLETE ADHESION OF		HP:0000119	OMIM:149600	IEA				P		HPO:iea	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000006	OMIM:149700	IEA				I		HPO:iea	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000007	OMIM:149700	TAS				I		HPO:skoehler	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000246	OMIM:149700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000509	OMIM:149700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000564	OMIM:149700	IEA				P		HPO:iea	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0000620	OMIM:149700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0009926	OMIM:149700	TAS				P		HPO:skoehler	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0030752	OMIM:149700	TAS				P		HPO:skoehler	
OMIM	149700	LACRIMAL DUCT DEFECT		HP:0100539	OMIM:149700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000006	OMIM:149730	TAS				I		HPO:skoehler	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000104	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000198	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000217	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000316	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000337	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000378	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000410	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000494	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000495	OMIM:149730	TAS				P		HPO:skoehler	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000506	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000522	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000579	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000620	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000629	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000668	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD	HP:0012828	HP:0000670	OMIM:149730	TAS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000680	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0000974	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0001092	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0001233	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0001245	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0002984	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0003022	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0003974	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0004209	OMIM:149730	TAS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0005707	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0006297	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0007656	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0007732	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0007892	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0007900	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0008743	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0009462	OMIM:149730	TAS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0009637	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0009740	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0009741	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0009944	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0010055	OMIM:149730	IEA				P		HPO:iea	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0011065	OMIM:149730	PCS				P		HPO:probinson	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0032107	OMIM:149730	IEA				P		HPO:skoehler	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0100258	OMIM:149730	TAS				P		HPO:skoehler	
OMIM	149730	LACRIMOAURICULODENTODIGITAL SYNDROME; LADD		HP:0100583	OMIM:149730	PCS				P		HPO:probinson	
OMIM	150170	LACTIC ACIDOSIS, CHRONIC ADULT FORM		HP:0000006	OMIM:150170	IEA				I		HPO:iea	
OMIM	150170	LACTIC ACIDOSIS, CHRONIC ADULT FORM		HP:0002149	OMIM:150170	IEA				P		HPO:iea	
OMIM	150170	LACTIC ACIDOSIS, CHRONIC ADULT FORM		HP:0004925	OMIM:150170	TAS				P		HPO:skoehler	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000006	OMIM:150230	IEA				I		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000076	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000252	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000365	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000400	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000414	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000431	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000490	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000577	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000750	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000896	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0000918	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001159	OMIM:150230	IEA				P		HPO:skoehler	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001249	OMIM:150230	TAS				P		HPO:skoehler	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001252	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001290	OMIM:150230	TAS				P		HPO:skoehler	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001382	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001530	OMIM:150230	TAS				P		HPO:probinson	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0001808	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0002002	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0002209	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0002650	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0002788	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0003691	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0003764	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0005039	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0005743	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0007595	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0010230	OMIM:150230	IEA				P		HPO:iea	
OMIM	150230	TRICHORHINOPHALANGEAL SYNDROME, TYPE II		HP:0030010	OMIM:150230	TAS				P		HPO:skoehler	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000006	OMIM:150250	IEA				I		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000028	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000175	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000204	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000272	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000316	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000405	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000586	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000668	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000767	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0000768	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001222	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001249	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001388	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001511	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001629	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001631	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001762	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001772	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0001799	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002007	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002176	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002650	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002777	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002779	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002780	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002827	OMIM:150250	TAS				P		HPO:skoehler	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0002947	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0003042	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0003298	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0003304	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0003994	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0004232	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0004322	OMIM:150250	IEA				P		HPO:skoehler	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0004568	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0004942	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0004976	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0005280	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0006067	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0007957	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0008127	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0008434	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0010049	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0010743	OMIM:150250	IEA				P		HPO:iea	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0011220	OMIM:150250	TAS				P		HPO:skoehler	
OMIM	150250	#150250 LARSEN SYNDROME; LRS		HP:0012368	OMIM:150250	TAS				P		HPO:skoehler	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0000006	OMIM:150260	IEA				I		HPO:iea	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0000252	OMIM:150260	IEA				P		HPO:iea	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001249	OMIM:150260	IEA				P		HPO:iea	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001605	OMIM:150260	IEA				P		HPO:iea	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001609	OMIM:150260	IEA				P		HPO:skoehler	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001621	OMIM:150260	IEA				P		HPO:skoehler	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0002015	OMIM:150260	IEA				P		HPO:skoehler	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0003593	OMIM:150260	IEA				C		HPO:skoehler	
OMIM	150260	LARYNGEAL ABDUCTOR PARALYSIS		HP:0010307	OMIM:150260	IEA				P		HPO:skoehler	
OMIM	150270	LARYNGEAL ADDUCTOR PARALYSIS; LAP		HP:0000006	PMID:709905	PCS				I		HPO:iea	
OMIM	150270	LARYNGEAL ADDUCTOR PARALYSIS; LAP		HP:0001609	OMIM:150270	TAS	HP:0003577			P		HPO:iea	
OMIM	150270	LARYNGEAL ADDUCTOR PARALYSIS; LAP		HP:0003470	OMIM:150270	IEA				P		HPO:skoehler	
OMIM	150280	LARYNGOMALACIA		HP:0000006	OMIM:150280	TAS				I		HPO:probinson	
OMIM	150280	LARYNGOMALACIA		HP:0001601	OMIM:150280	TAS				P		HPO:probinson	
OMIM	150280	LARYNGOMALACIA		HP:0002098	OMIM:150280	TAS				P		HPO:probinson	
OMIM	150280	LARYNGOMALACIA		HP:0002778	OMIM:150280	TAS				P		HPO:probinson	
OMIM	150280	LARYNGOMALACIA		HP:0004886	OMIM:150280	TAS				P		HPO:skoehler	
OMIM	150300	LARYNX, CONGENITAL PARTIAL ATRESIA OF		HP:0000006	OMIM:150300	IEA				I		HPO:iea	
OMIM	150300	LARYNX, CONGENITAL PARTIAL ATRESIA OF		HP:0005945	OMIM:150300	IEA				P		HPO:iea	
OMIM	150300	LARYNX, CONGENITAL PARTIAL ATRESIA OF		HP:0005950	OMIM:150300	IEA				P		HPO:iea	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0000006	OMIM:150360	TAS				I		HPO:probinson	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0001609	OMIM:150360	TAS				P		HPO:probinson	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0001621	OMIM:150360	IEA				P		HPO:skoehler	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0002098	OMIM:150360	TAS				P		HPO:probinson	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0002788	OMIM:150360	TAS				P		HPO:probinson	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0005950	OMIM:150360	TAS				P		HPO:skoehler	
OMIM	150360	LARYNGEAL WEB, FAMILIAL		HP:0010307	OMIM:150360	TAS				P		HPO:probinson	
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0000006	OMIM:150400	IEA				I		HPO:iea	
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0000007	OMIM:150400	TAS				I		HPO:skoehler	
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0000958	OMIM:150400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0006342	OMIM:150400	IEA				P		HPO:iea	
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0008070	OMIM:150400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0009804	OMIM:150400	IEA				P		HPO:skoehler	
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0010764	OMIM:150400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	150400	TOOTH AGENESIS, SELECTIVE, 4		HP:0045075	OMIM:150400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	150500	150500 LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT		HP:0000006	OMIM:150500	IEA				I		HPO:iea	
OMIM	150500	150500 LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT		HP:0000541	OMIM:150500	IEA				P		HPO:iea	
OMIM	150500	150500 LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT		HP:0007992	OMIM:150500	IEA				P		HPO:iea	
OMIM	150550	LAZY LEUKOCYTE SYNDROME		HP:0001875	OMIM:150550	TAS				P		HPO:skoehler	
OMIM	150550	LAZY LEUKOCYTE SYNDROME		HP:0002719	OMIM:150550	TAS				P		HPO:skoehler	
OMIM	150550	LAZY LEUKOCYTE SYNDROME		HP:0003745	OMIM:150550	TAS				I		HPO:skoehler	
OMIM	150590	150590 LEG ULCERS, FAMILIAL, OF JUVENILE ONSET		HP:0000951	OMIM:150590	IEA				P		HPO:iea	
OMIM	150590	150590 LEG ULCERS, FAMILIAL, OF JUVENILE ONSET		HP:0001475	OMIM:150590	IEA				I		HPO:iea	
OMIM	150590	150590 LEG ULCERS, FAMILIAL, OF JUVENILE ONSET		HP:0001626	OMIM:150590	IEA				P		HPO:iea	
OMIM	150590	150590 LEG ULCERS, FAMILIAL, OF JUVENILE ONSET		HP:0003621	OMIM:150590	IEA				C		HPO:iea	
OMIM	150600	LEGG-CALVE-PERTHES DISEASE		HP:0000006	OMIM:150600	TAS				I		HPO:nvasilevsky	
OMIM	150600	LEGG-CALVE-PERTHES DISEASE		HP:0001426	OMIM:150600	TAS				I		HPO:nvasilevsky	
OMIM	150600	LEGG-CALVE-PERTHES DISEASE		HP:0002750	OMIM:150600	TAS				P		HPO:skoehler	
OMIM	150600	LEGG-CALVE-PERTHES DISEASE		HP:0004322	OMIM:150600	TAS				P		HPO:skoehler	
OMIM	150600	LEGG-CALVE-PERTHES DISEASE		HP:0005743	OMIM:150600	TAS				P		HPO:skoehler	
OMIM	150699	#150699 LEIOMYOMA, UTERINE; UL		HP:0000006	OMIM:150699	IEA				I		HPO:iea	
OMIM	150699	#150699 LEIOMYOMA, UTERINE; UL		HP:0000131	OMIM:150699	IEA				P		HPO:iea	
OMIM	150699	#150699 LEIOMYOMA, UTERINE; UL		HP:0001428	OMIM:150699	TAS				I		HPO:skoehler	
OMIM	150700	LEIOMYOMA OF VULVA AND ESOPHAGUS		HP:0000006	OMIM:150700	IEA				I		HPO:iea	
OMIM	150700	LEIOMYOMA OF VULVA AND ESOPHAGUS		HP:0005240	OMIM:150700	IEA				P		HPO:iea	
OMIM	150700	LEIOMYOMA OF VULVA AND ESOPHAGUS		HP:0008665	OMIM:150700	IEA				P		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0000006	OMIM:150800	IEA				I		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0000131	OMIM:150800	IEA				P		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0002891	OMIM:150800	IEA				P		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0003536	OMIM:150800	IEA				P		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0003829	OMIM:150800	TAS				C		HPO:skoehler	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0005584	OMIM:150800	TAS				P		HPO:skoehler	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0006755	OMIM:150800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0007437	OMIM:150800	IEA				P		HPO:iea	
OMIM	150800	#150800 HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER; HLRCC;;MULTIPLE CUTANEOUS AND UTERINE LEIOMYOMATA 1, WITH OR WITHOUT RENALCELL CARCINOMA; MCUL1;;LEIOMYOMATOSIS AND RENAL CELL CANCER, HEREDITARY; LRCC;;LEIOMYOMA, MULTIPLE CUTANEOUS; MCL		HP:0007620	OMIM:150800	IEA				P		HPO:skoehler	
OMIM	150900	LENTIGINES		HP:0000006	OMIM:150900	IEA				I		HPO:iea	
OMIM	150900	LENTIGINES		HP:0000639	OMIM:150900	IEA				P		HPO:iea	
OMIM	150900	LENTIGINES		HP:0000951	OMIM:150900	IEA				P		HPO:iea	
OMIM	151000	LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC		HP:0000006	OMIM:151000	IEA				I		HPO:iea	
OMIM	151000	LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC		HP:0000951	OMIM:151000	IEA				P		HPO:iea	
OMIM	151000	LENTIGINOSIS, CENTROFACIAL NEURODYSRAPHIC		HP:0001249	OMIM:151000	IEA				P		HPO:iea	
OMIM	151001	LENTIGINOSIS, INHERITED PATTERNED		HP:0000006	OMIM:151001	IEA				I		HPO:iea	
OMIM	151001	LENTIGINOSIS, INHERITED PATTERNED		HP:0001034	OMIM:151001	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000006	OMIM:151050	IEA				I		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000023	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000028	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000041	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000047	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000164	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000171	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000239	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000252	OMIM:151050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000270	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000316	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000337	OMIM:151050	TAS				P		HPO:skoehler	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000347	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000400	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000400	OMIM:151050	TAS				P		HPO:probinson	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000407	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000452	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000453	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000885	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000916	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000963	OMIM:151050	TAS				P		HPO:probinson	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000965	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0000973	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001043	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001159	OMIM:151050	IEA				P		HPO:skoehler	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001187	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001249	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001252	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001274	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001290	OMIM:151050	TAS				P		HPO:skoehler	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001508	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001511	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0001545	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0002007	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0002342	OMIM:151050	TAS				P		HPO:probinson	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0002750	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0002987	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0003015	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0003041	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0003745	OMIM:151050	IEA				I		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0004322	OMIM:151050	IEA	HP:0003593			P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0004482	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0005019	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0005477	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0006152	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0006380	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0007678	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0008070	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0009843	OMIM:151050	IEA				P		HPO:iea	
OMIM	151050	LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM		HP:0011220	OMIM:151050	TAS				P		HPO:skoehler	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000006	OMIM:151100	IEA				I		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000028	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000047	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000054	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000122	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000175	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000242	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000286	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000303	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000316	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000325	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000358	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000369	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000407	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000411	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000457	OMIM:151100	IEA				P		HPO:skoehler	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000465	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000470	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000486	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000508	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000767	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000768	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000823	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000921	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0000957	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001003	OMIM:151100	IEA				P		HPO:skoehler	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001256	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001639	OMIM:151100	TAS		HP:0040284		P		HPO:probinson	20%
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001642	OMIM:151100	TAS		HP:0040284		P		HPO:probinson	40%
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001682	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0001709	OMIM:151100	TAS				P		HPO:probinson	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0002751	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0002967	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0002996	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0003298	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0003691	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0004322	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0004409	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0008724	OMIM:151100	IEA				P		HPO:iea	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0010463	OMIM:151100	TAS				P		HPO:skoehler	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0011710	OMIM:151100	TAS				P		HPO:probinson	
OMIM	151100	#151100 LEOPARD SYNDROME 1;;LENTIGINOSIS, CARDIOMYOPATHIC;;MULTIPLE LENTIGINES SYNDROME		HP:0012569	OMIM:151100	TAS				P		HPO:probinson	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0000006	OMIM:151200	IEA				I	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0000482	OMIM:151200	TAS		HP:0040283		P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0000581	OMIM:151200	TAS		HP:0040283		P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0000582	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0000925	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001156	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001191	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001230	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001376	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001387	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001602	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001761	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0001822	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:probinson	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0002816	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0002967	OMIM:151200	TAS		HP:0040283		P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0003676	OMIM:151200	TAS				C	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0004279	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0004322	OMIM:151200	IEA				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:iea	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0006247	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0007311	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0009778	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0009803	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0010049	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0010743	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151200	CHROMOSOME 8q22.1 DUPLICATION SYNDROME		HP:0011304	OMIM:151200	TAS				P	CHROMOSOME 8Q22.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000006	OMIM:151210	IEA				I		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000256	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000280	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000470	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000773	OMIM:151210	TAS				P		HPO:probinson	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000774	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000883	OMIM:151210	TAS				P		HPO:probinson	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0000946	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0001538	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0003021	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0003026	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0003173	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0003175	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0003180	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0004298	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0004565	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0004591	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0005451	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0005716	OMIM:151210	TAS				P		HPO:probinson	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0008921	OMIM:151210	IEA				P		HPO:iea	
OMIM	151210	#151210 PLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, TORRANCE TYPE; PLSDT;;LETHAL SHORT-LIMBED PLATYSPONDYLIC DWARFISM, TORRANCE TYPE;;THANATOPHORIC DYSPLASIA, TORRANCE VARIANTPLATYSPONDYLIC LETHAL SKELETAL DYSPLASIA, LUTON TYPE, INCLUDED; PLSDL,INCLUDED;;THANATOPHORIC DYSPLASIA, LUTON VARIANT, INCLUDED		HP:0200083	OMIM:151210	TAS				P		HPO:skoehler	
OMIM	151380	LEUKEMIA, ACUTE MONOCYTIC		HP:0001444	OMIM:151380	IEA				I		HPO:iea	
OMIM	151380	LEUKEMIA, ACUTE MONOCYTIC		HP:0004845	OMIM:151380	IEA				P		HPO:iea	
OMIM	151400	LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL		HP:0001428	OMIM:151400	TAS				I		HPO:skoehler	
OMIM	151400	LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL		HP:0001444	OMIM:151400	IEA				I		HPO:iea	
OMIM	151400	LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL		HP:0005374	OMIM:151400	IEA				P		HPO:iea	
OMIM	151400	LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL		HP:0005550	OMIM:151400	IEA				P		HPO:iea	
OMIM	151430	B-CELL CLL/LYMPHOMA 2		HP:0001428	OMIM:151430	TAS				I		HPO:probinson	
OMIM	151430	B-CELL CLL/LYMPHOMA 2		HP:0012191	OMIM:151430	TAS				P		HPO:probinson	
OMIM	151500	LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF		HP:0000006	OMIM:151500	IEA				I		HPO:iea	
OMIM	151500	LEUKOCYTE NUCLEAR APPENDAGES, HEREDITARY PREVALENCE OF		HP:0001871	OMIM:151500	IEA				P		HPO:iea	
OMIM	151590	LICHEN SCLEROSUS ET ATROPHICUS; LSA		HP:0000006	OMIM:151590	IEA				I		HPO:iea	
OMIM	151590	LICHEN SCLEROSUS ET ATROPHICUS; LSA		HP:0002860	OMIM:151590	IEA				P		HPO:skoehler	
OMIM	151590	LICHEN SCLEROSUS ET ATROPHICUS; LSA		HP:0030731	OMIM:151590	IEA				P		HPO:skoehler	
OMIM	151600	#151600 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3; NDNC3;;LEUKONYCHIA TOTALIS AND/OR PARTIALIS;;PORCELAIN NAILSLEUKONYCHIA STRIATUS, INCLUDED;;LEUKONYCHIA PUNCTATA, INCLUDED		HP:0000006	OMIM:151600	IEA				I		HPO:iea	
OMIM	151600	#151600 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3; NDNC3;;LEUKONYCHIA TOTALIS AND/OR PARTIALIS;;PORCELAIN NAILSLEUKONYCHIA STRIATUS, INCLUDED;;LEUKONYCHIA PUNCTATA, INCLUDED		HP:0000007	OMIM:151600	TAS				I		HPO:skoehler	
OMIM	151600	#151600 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3; NDNC3;;LEUKONYCHIA TOTALIS AND/OR PARTIALIS;;PORCELAIN NAILSLEUKONYCHIA STRIATUS, INCLUDED;;LEUKONYCHIA PUNCTATA, INCLUDED		HP:0000787	OMIM:151600	IEA				P		HPO:iea	
OMIM	151600	#151600 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3; NDNC3;;LEUKONYCHIA TOTALIS AND/OR PARTIALIS;;PORCELAIN NAILSLEUKONYCHIA STRIATUS, INCLUDED;;LEUKONYCHIA PUNCTATA, INCLUDED		HP:0001598	OMIM:151600	IEA				P		HPO:iea	
OMIM	151600	#151600 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 3; NDNC3;;LEUKONYCHIA TOTALIS AND/OR PARTIALIS;;PORCELAIN NAILSLEUKONYCHIA STRIATUS, INCLUDED;;LEUKONYCHIA PUNCTATA, INCLUDED		HP:0001820	OMIM:151600	IEA				P		HPO:skoehler	
OMIM	151610	LEVATOR-MEDIAL RECTUS SYNKINESIS		HP:0000006	OMIM:151610	IEA				I		HPO:iea	
OMIM	151610	LEVATOR-MEDIAL RECTUS SYNKINESIS		HP:0000478	OMIM:151610	IEA				P		HPO:iea	
OMIM	151610	LEVATOR-MEDIAL RECTUS SYNKINESIS		HP:0000508	PMID:3767680	PCS				P		HPO:lccarmody	
OMIM	151610	LEVATOR-MEDIAL RECTUS SYNKINESIS		HP:0500043	PMID:3767680,OMIM:151610	IEA				P		HPO:lccarmody	
OMIM	151620	LICHEN PLANUS, FAMILIAL		HP:0000006	OMIM:151620	IEA				I		HPO:iea	
OMIM	151620	LICHEN PLANUS, FAMILIAL		HP:0000951	OMIM:151620	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0000006	OMIM:151623	IEA				I		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0002488	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0002667	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0002669	OMIM:151623	TAS				P		HPO:probinson	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0002894	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0003002	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0003003	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0006744	OMIM:151623	IEA				P		HPO:iea	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0012125	OMIM:151623	TAS				P		HPO:skoehler	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0030078	OMIM:151623	TAS				P		HPO:skoehler	
OMIM	151623	#151623 LI-FRAUMENI SYNDROME 1; LFS1;;SARCOMA FAMILY SYNDROME OF LI AND FRAUMENI;;SBLA SYNDROMELI-FRAUMENI-LIKE SYNDROME, INCLUDED; LFL, INCLUDED		HP:0030448	OMIM:151623	TAS				P		HPO:skoehler	
OMIM	151630	LIP, MEDIAN NODULE OF UPPER		HP:0000006	OMIM:151630	IEA				I		HPO:iea	
OMIM	151630	LIP, MEDIAN NODULE OF UPPER		HP:0000153	OMIM:151630	IEA				P		HPO:iea	
OMIM	151640	LIP, HAMARTOMATOUS		HP:0000006	OMIM:151640	IEA				I		HPO:iea	
OMIM	151640	LIP, HAMARTOMATOUS		HP:0000153	OMIM:151640	IEA				P		HPO:iea	
OMIM	151640	LIP, HAMARTOMATOUS		HP:0010566	OMIM:151640	IEA				P		HPO:skoehler	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000006	OMIM:151660	IEA				I		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000147	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000287	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000311	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000468	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000822	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000831	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000842	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000956	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0000991	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0001007	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0001015	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0001397	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0001735	OMIM:151660	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0002155	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0002240	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0002621	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003074	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003124	PMID:28450900	TAS				P		HPO:nvasilevsky	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003233	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003326	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003635	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003712	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0003758	OMIM:151660	TAS				P		HPO:probinson	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0008739	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0008887	OMIM:151660	TAS				P		HPO:probinson	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0008985	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0008993	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0009002	OMIM:151660	IEA				P		HPO:iea	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0009125	OMIM:151660	TAS				P		HPO:probinson	
OMIM	151660	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2		HP:0012645	OMIM:151660	TAS				P		HPO:skoehler	
OMIM	151700	LIPOMA OF THE CONJUNCTIVA		HP:0000006	OMIM:151700	TAS				I		HPO:probinson	
OMIM	151700	LIPOMA OF THE CONJUNCTIVA		HP:0012032	OMIM:151700	IEA				P		HPO:skoehler	
OMIM	151700	LIPOMA OF THE CONJUNCTIVA		HP:0012549	OMIM:151700	TAS				P		HPO:probinson	
OMIM	151800	LIPOMATOSIS, FAMILIAL BENIGN CERVICAL		HP:0000006	OMIM:151800	IEA				I		HPO:iea	
OMIM	151800	LIPOMATOSIS, FAMILIAL BENIGN CERVICAL		HP:0000951	OMIM:151800	IEA				P		HPO:iea	
OMIM	151800	LIPOMATOSIS, FAMILIAL BENIGN CERVICAL		HP:0009830	OMIM:151800	IEA				P		HPO:skoehler	
OMIM	151800	LIPOMATOSIS, FAMILIAL BENIGN CERVICAL		HP:0012032	OMIM:151800	TAS				P		HPO:skoehler	
OMIM	151900	LIPOMATOSIS, MULTIPLE		HP:0000006	OMIM:151900	TAS				I		HPO:iea	
OMIM	151900	LIPOMATOSIS, MULTIPLE		HP:0001012	OMIM:151900	TAS				P		HPO:skoehler	
OMIM	152200	APOLIPOPROTEIN(A)		HP:0000006	OMIM:152200	IEA				I		HPO:iea	
OMIM	152200	APOLIPOPROTEIN(A)		HP:0001939	OMIM:152200	IEA				P		HPO:iea	
OMIM	152200	APOLIPOPROTEIN(A)		HP:0002621	OMIM:152200	IEA				P		HPO:skoehler	
OMIM	152420	LITHIUM TRANSPORT		HP:0000006	OMIM:152420	IEA				I		HPO:iea	
OMIM	152420	LITHIUM TRANSPORT		HP:0007302	OMIM:152420	TAS				P		HPO:probinson	
OMIM	152550	LUMBAR STENOSIS, FAMILIAL		HP:0000006	OMIM:152550	IEA				I		HPO:iea	
OMIM	152550	LUMBAR STENOSIS, FAMILIAL		HP:0004610	OMIM:152550	IEA				P		HPO:iea	
OMIM	152600	LUNULAE OF FINGERNAILS		HP:0000006	OMIM:152600	IEA				I		HPO:iea	
OMIM	152600	LUNULAE OF FINGERNAILS		HP:0001597	OMIM:152600	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0000006	OMIM:152700	IEA				I		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0000123	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0000709	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0000992	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001250	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001369	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001701	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001873	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001878	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0001882	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0002102	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0002725	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0003493	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0003613	OMIM:152700	IEA				P		HPO:iea	
OMIM	152700	SYSTEMIC LUPUS ERYTHEMATOSUS; SLE		HP:0025300	OMIM:152700	IEA				P		HPO:skoehler	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0000006	OMIM:152800	IEA				I		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0000969	OMIM:152800	IEA				P		HPO:skoehler	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0001595	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0001888	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0002024	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0002593	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0003826	OMIM:152800	IEA				M		HPO:skoehler	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0004315	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0006641	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0008360	OMIM:152800	IEA				P		HPO:iea	
OMIM	152800	%152800 LYMPHANGIECTASIA, INTESTINAL		HP:0010741	OMIM:152800	TAS				P		HPO:skoehler	
OMIM	152900	LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY		HP:0000006	OMIM:152900	TAS				I		HPO:probinson	
OMIM	152900	LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY		HP:0001004	OMIM:152900	TAS				P		HPO:skoehler	
OMIM	152900	LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY		HP:0002092	OMIM:152900	TAS				P		HPO:skoehler	
OMIM	152900	LYMPHEDEMA AND CEREBRAL ARTERIOVENOUS ANOMALY		HP:0100659	OMIM:152900	TAS				P		HPO:probinson	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000006	OMIM:152950	IEA				I		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000179	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000219	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000252	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000286	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000303	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000340	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000343	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000411	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000455	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000463	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000482	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000494	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000518	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000540	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000541	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000545	OMIM:152950	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000568	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000582	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000639	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000648	OMIM:152950	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000713	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0000718	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0001004	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0001250	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0001256	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0002002	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0002360	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0003828	OMIM:152950	IEA				C		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0003829	OMIM:152950	IEA				C		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0005280	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0005469	OMIM:152950	IEA				P		HPO:iea	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0007018	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0007663	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0007731	OMIM:152950	TAS				P		HPO:probinson	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0007858	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0007957	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0008052	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0009879	OMIM:152950	TAS				P		HPO:skoehler	
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0011220	OMIM:152950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	152950	MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR		HP:0500041	OMIM:152950	IEA				P		HPO:skoehler	
OMIM	153100	Lymphatic malformation 1		HP:0000006	PMID:15689446	PCS				I	LYMPHATIC MALFORMATION 1	HPO:iea	
OMIM	153100	Lymphatic malformation 1		HP:0000034	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HPO:iea	13/35
OMIM	153100	Lymphatic malformation 1		HP:0001015	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HP:probinson	16/71
OMIM	153100	Lymphatic malformation 1		HP:0001028	OMIM:153100	TAS				P	LYMPHATIC MALFORMATION 1	HPO:iea	
OMIM	153100	Lymphatic malformation 1		HP:0001790	PMID:16965327	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HPO:iea	HP:0040284
OMIM	153100	Lymphatic malformation 1		HP:0003550	PMID:15689446	PCS	HP:0003577	HP:0040284		P	LYMPHATIC MALFORMATION 1	HPO:probinson	64/71
OMIM	153100	Lymphatic malformation 1		HP:0003577	PMID:15689446	PCS				C	LYMPHATIC MALFORMATION 1	HPO:iea	
OMIM	153100	Lymphatic malformation 1		HP:0003759	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HPO:iea	4/4
OMIM	153100	Lymphatic malformation 1		HP:0007448	OMIM:153100	TAS				P	LYMPHATIC MALFORMATION 1	HPO:iea	
OMIM	153100	Lymphatic malformation 1		HP:0008388	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HP:probinson	10/71
OMIM	153100	Lymphatic malformation 1		HP:0012227	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HP:probinson	2/35
OMIM	153100	Lymphatic malformation 1		HP:0012740	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HP:probinson	7/71
OMIM	153100	Lymphatic malformation 1		HP:0100658	PMID:15689446	PCS		HP:0040284		P	LYMPHATIC MALFORMATION 1	HP:probinson	14/71
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0000006	OMIM:153200	TAS				I		HPO:probinson	
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0000175	OMIM:153200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0000282	OMIM:153200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0003550	OMIM:153200	TAS				P		HPO:probinson	
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0003759	OMIM:153200	TAS				P		HPO:probinson	
OMIM	153200	LYMPHEDEMA, HEREDITARY, II		HP:0011367	OMIM:153200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0000006	OMIM:153300	IEA				I		HPO:iea	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0001004	OMIM:153300	TAS				P		HPO:probinson	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0003011	OMIM:153300	IEA				P		HPO:iea	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0003550	OMIM:153300	IEA				P		HPO:iea	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0003759	OMIM:153300	TAS				P		HPO:probinson	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0008383	OMIM:153300	IEA				P		HPO:iea	
OMIM	153300	%153300 YELLOW NAIL SYNDROME;;YNS;;LYMPHEDEMA AND YELLOW NAILS		HP:0011367	OMIM:153300	TAS				P		HPO:skoehler	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000006	OMIM:153400	IEA				I		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000175	OMIM:153400	TAS		HP:0040284		P		HPO:probinson	4%
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000204	OMIM:153400	IEA		HP:0040284		P		HPO:probinson	4%
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000495	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000508	OMIM:153400	TAS				P		HPO:skoehler	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000509	OMIM:153400	TAS				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0000613	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0001004	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0001629	OMIM:153400	TAS				P		HPO:probinson	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0001636	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0001643	OMIM:153400	TAS				P		HPO:skoehler	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0002619	OMIM:153400	TAS				P		HPO:probinson	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0003011	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0003550	OMIM:153400	TAS				P		HPO:probinson	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0009743	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0011675	OMIM:153400	IEA				P		HPO:iea	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0012804	OMIM:153400	TAS				P		HPO:skoehler	
OMIM	153400	LYMPHEDEMA-DISTICHIASIS SYNDROME		HP:0100658	OMIM:153400	IEA				P		HPO:skoehler	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0000256	OMIM:153470	IEA				P		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0000268	OMIM:153470	IEA				P		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0000343	OMIM:153470	IEA				P		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0001475	OMIM:153470	IEA				I		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0002007	OMIM:153470	IEA				P		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0002119	OMIM:153470	IEA				P		HPO:iea	
OMIM	153470	MACROCEPHALY, BENIGN FAMILIAL		HP:0004422	OMIM:153470	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000006	OMIM:153480	IEA				I		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000040	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000218	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000256	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000486	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000494	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000538	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000646	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000750	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000767	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000872	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000956	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0000957	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001012	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001014	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001028	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001249	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001250	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001252	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001290	OMIM:153480	TAS				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001382	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0001943	OMIM:153480	IEA				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002007	OMIM:153480	IEA				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002194	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002558	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002573	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002576	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002650	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0002858	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0003198	OMIM:153480	IEA				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0003517	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0003621	OMIM:153480	IEA				C		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0004099	OMIM:153480	IEA				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0004390	OMIM:153480	IEA				P		HPO:skoehler	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0007074	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0007873	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0008897	OMIM:153480	IEA				P		HPO:iea	
OMIM	153480	BANNAYAN-RILEY-RUVALCABA SYNDROME		HP:0012032	OMIM:153480	TAS				P		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0001428	OMIM:153550	IEA				I		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0001452	OMIM:153550	IEA				I		HPO:iea	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0002863	OMIM:153550	TAS				P		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0003745	OMIM:153550	IEA				I		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0004861	OMIM:153550	TAS				P		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0012133	OMIM:153550	TAS				P		HPO:skoehler	
OMIM	153550	CHROMOSOME 5Q DELETION SYNDROME		HP:0012143	OMIM:153550	TAS				P		HPO:probinson	
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:153600	IEA				I		HPO:iea	
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0001271	OMIM:153600	TAS				P		HPO:iea	
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0001909	OMIM:153600	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0002665	OMIM:153600	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0003347	OMIM:153600	IEA				P		HPO:iea	
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0003459	OMIM:153600	IEA				P		HPO:iea	
OMIM	153600	MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1		HP:0005508	OMIM:153600	IEA				P		HPO:iea	
OMIM	153630	MACROGLOSSIA		HP:0000006	OMIM:153630	IEA				I		HPO:iea	
OMIM	153630	MACROGLOSSIA		HP:0000158	OMIM:153630	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000006	OMIM:153640	IEA				I		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000093	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000123	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000132	OMIM:153640	TAS				P		HPO:probinson	
OMIM	153640	FECHTNER SYNDROME		HP:0000519	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000790	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0000978	OMIM:153640	TAS				P		HPO:probinson	
OMIM	153640	FECHTNER SYNDROME		HP:0001757	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0001757	OMIM:153640	TAS		HP:0040284		P		HPO:iea	67%
OMIM	153640	FECHTNER SYNDROME		HP:0001873	OMIM:153640	TAS				P		HPO:probinson	
OMIM	153640	FECHTNER SYNDROME		HP:0001902	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0003010	OMIM:153640	IEA				P		HPO:skoehler	
OMIM	153640	FECHTNER SYNDROME		HP:0003774	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0008264	OMIM:153640	IEA				P		HPO:iea	
OMIM	153640	FECHTNER SYNDROME		HP:0040235	OMIM:153640	TAS				P		HPO:skoehler	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000006	OMIM:153670	IEA				I		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000132	OMIM:153670	TAS				P		HPO:probinson	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000225	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000421	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000967	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0000978	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2	HP:0012825	HP:0001744	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0001878	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0004446	OMIM:153670	IEA				P		HPO:iea	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0006298	OMIM:153670	TAS				P		HPO:probinson	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0011877	OMIM:153670	TAS				P		HPO:skoehler	
OMIM	153670	BERNARD-SOULIER SYNDROME, TYPE A2, AUTOSOMAL DOMINANT; BSSA2		HP:0031364	OMIM:153670	IEA				P		HPO:skoehler	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0000006	OMIM:153700	IEA				I		HPO:iea	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0000505	OMIM:153700	IEA				P		HPO:iea	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0000512	OMIM:153700	IEA				P		HPO:iea	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0007663	OMIM:153700	TAS				P		HPO:skoehler	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0007754	OMIM:153700	IEA				P		HPO:skoehler	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0008028	OMIM:153700	IEA				P		HPO:iea	
OMIM	153700	MACULAR DYSTROPHY, VITELLIFORM, 2; VMD2		HP:0031526	OMIM:153700	IEA				P		HPO:skoehler	
OMIM	153800	MACULAR DEGENERATION, AGE-RELATED, 2		HP:0000006	OMIM:153800	TAS				I		HPO:iea	
OMIM	153800	MACULAR DEGENERATION, AGE-RELATED, 2		HP:0000608	PMID:9295268	PCS	HP:0003584			P		HP:probinson	
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0000006	OMIM:153840	TAS				I		HPO:skoehler	
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0001123	OMIM:153840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0003584	OMIM:153840	TAS				C		HPO:skoehler	
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0007663	OMIM:153840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0007677	OMIM:153840	TAS				P		HPO:skoehler	
OMIM	153840	%153840 MACULAR DYSTROPHY, VITELLIFORM, 1; VMD1;;MACULAR DYSTROPHY, ATYPICAL VITELLIFORM		HP:0007754	OMIM:153840	IEA				P		HPO:skoehler	
OMIM	153870	%153870 MACULAR DYSTROPHY, CONCENTRIC ANNULAR;;MCDCA;;MACULAR DYSTROPHY, BENIGN CONCENTRIC ANNULAR; BCAMD		HP:0000006	OMIM:153870	TAS				I		HPO:skoehler	
OMIM	153870	%153870 MACULAR DYSTROPHY, CONCENTRIC ANNULAR;;MCDCA;;MACULAR DYSTROPHY, BENIGN CONCENTRIC ANNULAR; BCAMD		HP:0007641	OMIM:153870	TAS				P		HPO:skoehler	
OMIM	153870	%153870 MACULAR DYSTROPHY, CONCENTRIC ANNULAR;;MCDCA;;MACULAR DYSTROPHY, BENIGN CONCENTRIC ANNULAR; BCAMD		HP:0007754	OMIM:153870	TAS				P		HPO:skoehler	
OMIM	153870	%153870 MACULAR DYSTROPHY, CONCENTRIC ANNULAR;;MCDCA;;MACULAR DYSTROPHY, BENIGN CONCENTRIC ANNULAR; BCAMD		HP:0008001	OMIM:153870	TAS				P		HPO:skoehler	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0000006	OMIM:153880	IEA				I		HPO:iea	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0000486	OMIM:153880	IEA				P		HPO:iea	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0000540	OMIM:153880	IEA				P		HPO:skoehler	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0000969	OMIM:153880	IEA				P		HPO:skoehler	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0007754	OMIM:153880	TAS				P		HPO:skoehler	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0007947	OMIM:153880	IEA				P		HPO:iea	
OMIM	153880	%153880 MACULAR EDEMA, CYSTOID;;CYSTOID MACULAR DYSTROPHY; CYMD;;MACULAR DYSTROPHY, DOMINANT CYSTOID; MDDC;;DCMD		HP:0011505	OMIM:153880	TAS				P		HPO:skoehler	
OMIM	153890	MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE		HP:0000006	OMIM:153890	IEA				I		HPO:iea	
OMIM	153890	MACULAR DYSTROPHY, FENESTRATED SHEEN TYPE		HP:0007754	OMIM:153890	IEA				P		HPO:iea	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0000006	OMIM:154020	TAS				I		HPO:skoehler	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0000083	OMIM:154020	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0000934	OMIM:154020	TAS				P		HPO:skoehler	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0001250	OMIM:154020	IEA				P		HPO:iea	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0002900	OMIM:154020	TAS				P		HPO:skoehler	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0002917	OMIM:154020	IEA				P		HPO:iea	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0003127	OMIM:154020	TAS				P		HPO:skoehler	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0003324	OMIM:154020	TAS				P		HPO:skoehler	
OMIM	154020	HYPOMAGNESEMIA 2, RENAL		HP:0005567	OMIM:154020	IEA				P		HPO:iea	
OMIM	154230	46,XY SEX REVERSAL 4; SRXY4		HP:0000006	OMIM:154230	TAS				I		HPO:probinson	
OMIM	154230	46,XY SEX REVERSAL 4; SRXY4		HP:0000133	OMIM:154230	TAS				P		HPO:probinson	
OMIM	154230	46,XY SEX REVERSAL 4; SRXY4		HP:0012245	OMIM:154230	TAS				P		HPO:skoehler	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:154275	TAS				I		HPO:skoehler	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0001425	OMIM:154275	TAS				I		HPO:skoehler	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0001945	OMIM:154275	TAS				P		HPO:skoehler	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0002047	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0002153	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0002905	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0003128	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0003198	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0003236	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0003558	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0009045	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0011439	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154275	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 2		HP:0011440	OMIM:145600	TAS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0000006	OMIM:154276	TAS				I		HPO:skoehler	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0001276	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0001425	OMIM:154276	IEA				I		HPO:iea	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0001945	OMIM:154276	TAS				P		HPO:skoehler	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0002047	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0002153	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0002905	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0003128	OMIM:154276	TAS				P		HPO:skoehler	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0003198	OMIM:154276	IEA				P		HPO:iea	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0003236	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0003558	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0009045	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0011439	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154276	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 3		HP:0011440	OMIM:154276	PCS				P		HPO:probinson	
OMIM	154300	MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH		HP:0000006	OMIM:154300	IEA				I		HPO:iea	
OMIM	154300	MALOCCLUSION DUE TO PROTUBERANT UPPER FRONT TEETH		HP:0000689	OMIM:154300	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000006	OMIM:154400	IEA				I		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000122	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000154	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000175	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000204	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000211	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000220	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000238	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000252	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000272	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000278	OMIM:154400	TAS				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000347	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000358	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000369	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000384	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000405	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000413	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000426	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000494	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000652	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000750	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0000813	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001025	OMIM:154400	IEA				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001199	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001377	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001543	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001622	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001629	OMIM:154400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001636	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001643	OMIM:154400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001762	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001770	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001822	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001831	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001845	OMIM:154400	TAS				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0001849	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002126	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002251	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002410	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002650	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002827	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002974	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0002984	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0003319	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0003828	OMIM:154400	TAS				C		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0003974	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0004322	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0005349	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0006657	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0007776	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0008749	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0009466	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0009601	OMIM:154400	IEA				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0009777	OMIM:154400	TAS				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0010055	OMIM:154400	IEA				P		HPO:iea	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0011800	OMIM:154400	TAS				P		HPO:skoehler	
OMIM	154400	ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1		HP:0030084	OMIM:154400	TAS				P		HPO:skoehler	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000006	PMID:25790162	PCS				I		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000028	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000154	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000160	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000175	PMID:25790162	PCS		HP:0040284		P		HPO:skoehler	14/64
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000185	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000197	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000272	PMID:25790162	PCS		HP:0040284		P		HPO:iea	70/71
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000347	PMID:25790162	PCS	HP:0003577	HP:0040284		P		HPO:iea	62/71
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000384	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000405	PMID:25790162	PCS		HP:0040284		P		HPO:iea	64/70
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000413	PMID:25790162	PCS		HP:0040284		P		HPO:iea	44/61
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000453	PMID:25790162	PCS		HP:0040284		P		HPO:iea	8/56
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000486	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000494	PMID:12939661	PCS		HP:0040284		P		HPO:iea	89%
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000508	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000572	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000636	PMID:25790162	PCS		HP:0040284		P		HPO:iea	43/66
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0000652	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0001249	PMID:25790162	PCS		HP:0040284		P		HPO:iea	1/53
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0001627	PMID:19050407	PCS				P		HPO:lccarmody	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0007633	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0007678	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0007776	OMIM:154500	IEA				P		HPO:iea	
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0008551	PMID:25790162	PCS		HP:0040284		P		HPO:iea	51/72
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0009554	PMID:25790162	PCS		HP:0040284		P		HPO:iea	22/46
OMIM	154500	TREACHER COLLINS-FRANCESCHETTI SYNDROME		HP:0009555	OMIM:154500	IEA				P		HPO:iea	
OMIM	154570	MANNOSE 6-PHOSPHATE RECEPTOR RECOGNITION DEFECT, LEBANESE TYPE		HP:0000006	OMIM:154570	IEA				I		HPO:iea	
OMIM	154570	MANNOSE 6-PHOSPHATE RECEPTOR RECOGNITION DEFECT, LEBANESE TYPE		HP:0004356	OMIM:154570	IEA				P		HPO:iea	
OMIM	154600	MARCUS GUNN PHENOMENON		HP:0000006	OMIM:154600	TAS				I		HPO:probinson	
OMIM	154600	MARCUS GUNN PHENOMENON		HP:0007687	OMIM:154600	TAS				P		HPO:probinson	
OMIM	154600	MARCUS GUNN PHENOMENON	HP:0012833	HP:0007970	OMIM:154600	TAS				P		HPO:skoehler	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000006	PMID:17502658	PCS				I		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000098	OMIM:154700	TAS				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000189	OMIM:154700	TAS				P		HPO:skoehler	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000218	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000268	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000272	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000275	OMIM:154700	TAS				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000276	OMIM:154700	TAS				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000278	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000347	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000490	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000494	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000501	PMID:26903188	PCS				P		HPO:skoehler	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000518	PMID:26903188	PCS		HP:0040284		P		HPO:probinson	113/146
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000541	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000545	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000565	OMIM:154700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000577	OMIM:154700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000678	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000767	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0000768	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001065	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001083	PMID:26903188	PCS				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001166	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001371	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001382	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001634	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001635	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001653	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001659	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001704	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001761	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001763	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0001765	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002097	OMIM:154700	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002107	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002616	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002647	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002751	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0002816	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0003088	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0003179	PMID:26339165	PCS		HP:0040284		P		HPO:probinson	113/146
OMIM	154700	MARFAN SYNDROME; MFS		HP:0003199	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0003302	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0003758	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0004872	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0004927	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0004970	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0005136	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0007676	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0007800	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0008132	OMIM:154700	IEA				P		HPO:probinson	
OMIM	154700	MARFAN SYNDROME; MFS		HP:0025586	OMIM:154700	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	154700	MARFAN SYNDROME; MFS		HP:0100775	OMIM:154700	TAS				P		HPO:skoehler	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0000006	OMIM:154750	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0000218	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0000767	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0000768	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0000951	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001083	OMIM:154750	IEA				P		HPO:skoehler	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001166	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001382	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001507	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001653	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0001659	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0002650	OMIM:154750	IEA				P		HPO:iea	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0002705	OMIM:154750	TAS				P		HPO:skoehler	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0004942	OMIM:154750	TAS				P		HPO:probinson	
OMIM	154750	MARFANOID HYPERMOBILITY SYNDROME		HP:0007700	OMIM:154750	IEA				P		HPO:iea	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000006	OMIM:154780	TAS				I		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000175	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000179	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000201	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000215	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000272	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000286	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000316	OMIM:154780	TAS				P		HPO:skoehler	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000343	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000347	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000369	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000407	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000463	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000501	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000519	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000541	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000545	OMIM:154780	TAS				P		HPO:skoehler	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000565	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000675	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS	HP:0012825	HP:0000926	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0000946	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0002673	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0002684	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0002688	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0002986	OMIM:154780	TAS				P		HPO:skoehler	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0003031	OMIM:154780	TAS				P		HPO:skoehler	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0003196	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0004322	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0005280	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0005462	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0006095	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0006407	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0006456	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0007773	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0011800	OMIM:154780	TAS				P		HPO:skoehler	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0012019	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0012283	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0012284	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154780	#154780 MARSHALL SYNDROME; MRSHS		HP:0100250	OMIM:154780	TAS				P		HPO:probinson	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0000006	OMIM:154800	IEA				I		HPO:iea	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0000969	OMIM:154800	IEA				P		HPO:skoehler	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0001025	OMIM:154800	IEA				P		HPO:skoehler	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0001034	OMIM:154800	TAS				P		HPO:probinson	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0007583	OMIM:154800	IEA				P		HPO:iea	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0010783	OMIM:154800	IEA				P		HPO:skoehler	
OMIM	154800	MASTOCYTOSIS, CUTANEOUS; MASTC		HP:0200151	OMIM:154800	TAS				P		HPO:skoehler	
OMIM	154850	MASTICATORY MUSCLES, HYPERTROPHY OF		HP:0000006	OMIM:154850	IEA				I		HPO:iea	
OMIM	154850	MASTICATORY MUSCLES, HYPERTROPHY OF		HP:0003674	OMIM:154850	IEA				C		HPO:iea	
OMIM	154850	MASTICATORY MUSCLES, HYPERTROPHY OF		HP:0003712	OMIM:154850	IEA				P		HPO:skoehler	
OMIM	155000	MAXILLOFACIAL DYSOSTOSIS		HP:0000006	OMIM:155000	IEA				I		HPO:iea	
OMIM	155000	MAXILLOFACIAL DYSOSTOSIS		HP:0000303	OMIM:155000	IEA				P		HPO:iea	
OMIM	155000	MAXILLOFACIAL DYSOSTOSIS		HP:0000377	OMIM:155000	IEA				P		HPO:iea	
OMIM	155000	MAXILLOFACIAL DYSOSTOSIS		HP:0000494	OMIM:155000	IEA				P		HPO:iea	
OMIM	155000	MAXILLOFACIAL DYSOSTOSIS		HP:0000750	OMIM:155000	IEA				P		HPO:skoehler	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0000689	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0001425	OMIM:155050	IEA				I		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0002000	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0003196	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0004609	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0005280	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0008428	OMIM:155050	TAS				P		HPO:skoehler	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0009748	OMIM:155050	IEA				P		HPO:iea	
OMIM	155050	%155050 MAXILLONASAL DYSPLASIA, BINDER TYPE;;BINDER SYNDROME		HP:0009882	OMIM:155050	TAS				P		HPO:probinson	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0000006	OMIM:155100	IEA				I		HPO:iea	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0000132	OMIM:155100	IEA				P		HPO:skoehler	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0000421	OMIM:155100	TAS				P		HPO:probinson	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0000978	OMIM:155100	TAS				P		HPO:probinson	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0001658	OMIM:155100	IEA				P		HPO:iea	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0001873	OMIM:155100	IEA				P		HPO:iea	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0001902	OMIM:155100	IEA				P		HPO:iea	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0001977	OMIM:155100	IEA				P		HPO:skoehler	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0003010	OMIM:155100	IEA				P		HPO:iea	
OMIM	155100	MACROTHROMBOCYTOPENIA AND GRANULOCYTE INCLUSIONS WITH OR WITHOUT NEPHRITIS OR SENSORINEURAL HEARING LOSS; MATINS		HP:0040235	OMIM:155100	IEA				P		HPO:skoehler	
OMIM	155140	MECKEL DIVERTICULUM		HP:0000006	OMIM:155140	IEA				I		HPO:iea	
OMIM	155140	MECKEL DIVERTICULUM		HP:0002245	OMIM:155140	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000006	OMIM:155145	IEA				I		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000161	OMIM:155145	TAS				P		HPO:skoehler	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000193	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000218	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000316	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000337	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000494	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0000612	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0006866	OMIM:155145	IEA				P		HPO:iea	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0010609	OMIM:155145	IEA				P		HPO:skoehler	
OMIM	155145	CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA		HP:0100582	OMIM:155145	TAS				P		HPO:skoehler	
OMIM	155150	MEDIAN-ULNAR NERVE COMMUNICATIONS		HP:0000006	OMIM:155150	IEA				I		HPO:iea	
OMIM	155150	MEDIAN-ULNAR NERVE COMMUNICATIONS		HP:0000707	OMIM:155150	IEA				P		HPO:iea	
OMIM	155200	MEDIOSTERNAL DEPIGMENTATION LINE		HP:0000006	OMIM:155200	IEA				I		HPO:iea	
OMIM	155200	MEDIOSTERNAL DEPIGMENTATION LINE		HP:0007581	OMIM:155200	IEA				P		HPO:iea	
OMIM	155240	THYROID CARCINOMA, FAMILIAL MEDULLARY		HP:0000006	OMIM:155240	IEA				I		HPO:iea	
OMIM	155240	THYROID CARCINOMA, FAMILIAL MEDULLARY		HP:0002865	OMIM:155240	IEA				P		HPO:iea	
OMIM	155255	MEDULLOBLASTOMA		HP:0000006	OMIM:155255	TAS				I		HPO:probinson	
OMIM	155255	MEDULLOBLASTOMA		HP:0000007	OMIM:155255	TAS				I		HPO:skoehler	
OMIM	155255	MEDULLOBLASTOMA		HP:0002885	OMIM:155255	TAS				P		HPO:probinson	
OMIM	155255	MEDULLOBLASTOMA		HP:0003829	OMIM:155255	TAS				C		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0000006	OMIM:155310	TAS				I		HPO:iea	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0000016	OMIM:155310	IEA				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0000021	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0000076	OMIM:155310	IEA				P		HPO:iea	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0000126	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0001561	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0001733	OMIM:155310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002013	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002014	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002015	OMIM:155310	IEA				P		HPO:iea	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002019	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002027	OMIM:155310	IEA				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0002251	OMIM:155310	IEA				P		HPO:iea	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0003270	OMIM:155310	IEA				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0004388	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0004389	OMIM:155310	TAS				P		HPO:probinson	
OMIM	155310	VISCERAL MYOPATHY; VSCM		HP:0004395	OMIM:155310	TAS				P		HPO:skoehler	
OMIM	155350	MEGALENCEPHALY		HP:0000006	PMID:7274594	PCS				I		HPO:iea	
OMIM	155350	MEGALENCEPHALY		HP:0000238	PMID:4855950	PCS		HP:0040284		P		HPO:lccarmody	2/10
OMIM	155350	MEGALENCEPHALY		HP:0000256	PMID:7274594	PCS				P		HPO:lccarmody	
OMIM	155350	MEGALENCEPHALY		HP:0001249	PMID:7274594	PCS		HP:0040284		P		HPO:iea	7/109
OMIM	155350	MEGALENCEPHALY		HP:0001355	PMID:7274594	PCS		HP:0040280		P		HPO:iea	HP:0040280
OMIM	155500	MEGALODACTYLY		HP:0004099	OMIM:155500	IEA				P		HPO:skoehler	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0000006	OMIM:155600	IEA				I		HPO:iea	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0000478	OMIM:155600	IEA				P		HPO:iea	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0001054	OMIM:155600	IEA				P		HPO:iea	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0001062	OMIM:155600	IEA				P		HPO:iea	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0001074	OMIM:155600	IEA				P		HPO:skoehler	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0007716	OMIM:155600	TAS				P		HPO:skoehler	
OMIM	155600	MELANOMA, CUTANEOUS MALIGNANT		HP:0012056	OMIM:155600	TAS				P		HPO:skoehler	
OMIM	155601	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:155601	TAS				I		HPO:probinson	
OMIM	155601	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2		HP:0012056	OMIM:155601	TAS				P		HPO:probinson	
OMIM	155700	MELANOMA, MALIGNANT FAMILIAL INTRAOCULAR		HP:0000006	OMIM:155700	TAS				I		HPO:probinson	
OMIM	155700	MELANOMA, MALIGNANT FAMILIAL INTRAOCULAR		HP:0007716	OMIM:155700	TAS				P		HPO:probinson	
OMIM	155720	MELANOMA, UVEAL		HP:0000006	OMIM:155720	TAS				I		HPO:probinson	
OMIM	155720	MELANOMA, UVEAL		HP:0007716	OMIM:155720	TAS				P		HPO:probinson	
OMIM	155755	MELANOMA-ASTROCYTOMA SYNDROME		HP:0000006	OMIM:155755	TAS				I		HPO:probinson	
OMIM	155755	MELANOMA-ASTROCYTOMA SYNDROME		HP:0009592	OMIM:155755	TAS				P		HPO:skoehler	
OMIM	155755	MELANOMA-ASTROCYTOMA SYNDROME		HP:0012056	OMIM:155755	TAS				P		HPO:probinson	
OMIM	155900	MELKERSSON-ROSENTHAL SYNDROME		HP:0000006	OMIM:155900	IEA				I		HPO:iea	
OMIM	155900	MELKERSSON-ROSENTHAL SYNDROME		HP:0000221	OMIM:155900	IEA				P		HPO:iea	
OMIM	155900	MELKERSSON-ROSENTHAL SYNDROME		HP:0000282	OMIM:155900	IEA				P		HPO:iea	
OMIM	155900	MELKERSSON-ROSENTHAL SYNDROME		HP:0000478	OMIM:155900	IEA				P		HPO:iea	
OMIM	155900	MELKERSSON-ROSENTHAL SYNDROME		HP:0010628	OMIM:155900	IEA				P		HPO:skoehler	
OMIM	155950	MELORHEOSTOSIS, ISOLATED		HP:0003676	OMIM:155950	TAS				C		HPO:skoehler	
OMIM	155950	MELORHEOSTOSIS, ISOLATED		HP:0003745	OMIM:155950	TAS				I		HPO:skoehler	
OMIM	155950	MELORHEOSTOSIS, ISOLATED		HP:0011001	OMIM:155950	IEA				P		HPO:iea	
OMIM	155950	MELORHEOSTOSIS, ISOLATED		HP:0100774	OMIM:155950	IEA				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0000006	OMIM:155980	TAS				I		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0000316	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0000348	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0000369	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0000494	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0002007	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	155980	MEMBRANOUS CRANIAL OSSIFICATION, DELAYED		HP:0005280	OMIM:155980	TAS				P		HPO:skoehler	
OMIM	156000	MENIERE DISEASE		HP:0000006	OMIM:156000	IEA				I		HPO:iea	
OMIM	156000	MENIERE DISEASE		HP:0000360	OMIM:156000	TAS				P		HPO:skoehler	
OMIM	156000	MENIERE DISEASE		HP:0000365	OMIM:156000	IEA				P		HPO:iea	
OMIM	156000	MENIERE DISEASE		HP:0002321	OMIM:156000	IEA				P		HPO:skoehler	
OMIM	156000	MENIERE DISEASE		HP:0003829	OMIM:156000	TAS				C		HPO:skoehler	
OMIM	156190	MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA		HP:0000006	OMIM:156190	TAS				I		HPO:probinson	
OMIM	156190	MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA		HP:0000646	OMIM:156190	TAS				P		HPO:probinson	
OMIM	156190	MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA		HP:0001249	OMIM:156190	TAS				P		HPO:probinson	
OMIM	156190	MENTAL AND GROWTH RETARDATION WITH AMBLYOPIA		HP:0001510	OMIM:156190	TAS				P		HPO:probinson	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000006	OMIM:156200	IEA				I	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:iea	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000154	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000178	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000194	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000219	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000252	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000278	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000331	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000337	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000347	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000369	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000378	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000411	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000414	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000448	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000483	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000505	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000540	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000545	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000565	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000574	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000687	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000718	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0000736	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0001249	OMIM:156200	IEA				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0001251	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0001270	OMIM:156200	IEA				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:iea	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0001773	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0001852	OMIM:156200	IEA				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002007	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002373	OMIM:156200	TAS	HP:0003593			P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:iea	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002463	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002553	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002591	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0002714	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0003196	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0004322	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0008551	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0008872	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0008897	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0100716	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156200	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2q23.1 DELETION SYNDROME, INCLUDED		HP:0200055	OMIM:156200	TAS				P	#156200 MENTAL RETARDATION, AUTOSOMAL DOMINANT 1; MRD1CHROMOSOME 2Q23.1 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	156220	MERALGIA PARAESTHETICA, FAMILIAL		HP:0000006	OMIM:156220	IEA				I		HPO:iea	
OMIM	156220	MERALGIA PARAESTHETICA, FAMILIAL		HP:0000707	OMIM:156220	IEA				P		HPO:iea	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0000006	OMIM:156230	IEA				I		HPO:iea	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0002984	OMIM:156230	IEA				P		HPO:iea	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0005736	OMIM:156230	IEA				P		HPO:iea	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0005864	OMIM:156230	IEA				P		HPO:iea	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0008845	OMIM:156230	TAS				P		HPO:probinson	
OMIM	156230	%156230 MESOMELIC DWARFISM OF HYPOPLASTIC TIBIA AND RADIUS TYPE		HP:0008921	OMIM:156230	TAS				P		HPO:skoehler	
OMIM	156232	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE		HP:0000006	OMIM:156232	IEA				I		HPO:iea	
OMIM	156232	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE		HP:0002986	OMIM:156232	IEA				P		HPO:iea	
OMIM	156232	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE		HP:0003027	OMIM:156232	IEA				P		HPO:iea	
OMIM	156232	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE		HP:0008368	OMIM:156232	TAS				P		HPO:probinson	
OMIM	156232	MESOMELIC DYSPLASIA, KANTAPUTRA TYPE		HP:0009702	OMIM:156232	TAS				P		HPO:probinson	
OMIM	156240	MESOTHELIOMA, MALIGNANT		HP:0001428	OMIM:156240	TAS				I		HPO:skoehler	
OMIM	156240	MESOTHELIOMA, MALIGNANT		HP:0100001	OMIM:156240	IEA				P		HPO:skoehler	
OMIM	156250	METACHONDROMATOSIS		HP:0000006	OMIM:156250	IEA				I		HPO:iea	
OMIM	156250	METACHONDROMATOSIS		HP:0001367	OMIM:156250	IEA				P		HPO:iea	
OMIM	156250	METACHONDROMATOSIS		HP:0005655	OMIM:156250	IEA				P		HPO:iea	
OMIM	156250	METACHONDROMATOSIS		HP:0005701	OMIM:156250	IEA				P		HPO:iea	
OMIM	156250	METACHONDROMATOSIS		HP:0006487	OMIM:156250	IEA				P		HPO:skoehler	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0000006	OMIM:156310	TAS				I		HPO:iea	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0000012	OMIM:156310	TAS				P		HPO:iea	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0000020	OMIM:156310	TAS				P		HPO:iea	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0002270	OMIM:156310	TAS				P		HPO:skoehler	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0002615	OMIM:156310	TAS				P		HPO:skoehler	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0003581	OMIM:156310	TAS				C		HPO:skoehler	
OMIM	156310	METACHROMATIC LEUKODYSTROPHY, ADULT-ONSET, WITH NORMAL ARYLSULFATASEA		HP:0006926	OMIM:156310	TAS	HP:0003581			P		HPO:iea	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000006	OMIM:156400	TAS				I		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000121	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000248	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000316	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000347	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000365	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000452	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000453	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000520	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000692	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000773	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000829	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0000938	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0002148	OMIM:156400	IEA				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0002150	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0002515	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0002737	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0002756	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003021	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003026	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003072	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003109	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003155	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003273	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0003510	OMIM:156400	TAS	HP:0003593			P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0004209	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0004676	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0005871	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0006380	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0006487	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156400	METAPHYSEAL CHONDRODYSPLASIA, JANSEN TYPE		HP:0100759	OMIM:156400	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0000006	OMIM:156500	TAS				I		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE	HP:0012825	HP:0000926	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0002515	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0002812	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0002970	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0002980	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0003301	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0003371	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0003502	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0005819	OMIM:156500	TAS				P		HPO:skoehler	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0005871	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0006028	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0006208	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0006414	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0006431	OMIM:156500	IEA				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0008833	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0009844	OMIM:156500	TAS				P		HPO:skoehler	
OMIM	156500	#156500 METAPHYSEAL CHONDRODYSPLASIA, SCHMID TYPE; MCDS;;SPONDYLOMETAPHYSEAL DYSPLASIA, JAPANESE TYPE		HP:0009882	OMIM:156500	TAS				P		HPO:probinson	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000006	OMIM:156510	IEA				I		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000233	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000322	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000327	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000444	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0000926	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0003015	OMIM:156510	TAS				P		HPO:probinson	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0004220	OMIM:156510	TAS				P		HPO:probinson	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0004322	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0005625	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0005877	OMIM:156510	TAS				P		HPO:probinson	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0006480	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0009577	OMIM:156510	TAS				P		HPO:probinson	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0010047	OMIM:156510	IEA				P		HPO:iea	
OMIM	156510	METAPHYSEAL DYSPLASIA WITH MAXILLARY HYPOPLASIA AND BRACHYDACTYLY		HP:0100255	OMIM:156510	IEA				P		HPO:iea	
OMIM	156520	%156520 METATARSUS VARUS, TYPE I		HP:0000006	OMIM:156520	TAS				I		HPO:skoehler	
OMIM	156520	%156520 METATARSUS VARUS, TYPE I		HP:0001840	OMIM:156520	IEA				P		HPO:iea	
OMIM	156530	METATROPIC DYSPLASIA		HP:0000006	OMIM:156530	TAS				I		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0000774	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0000926	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0001156	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0001371	OMIM:156530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156530	METATROPIC DYSPLASIA		HP:0001989	OMIM:156530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156530	METATROPIC DYSPLASIA	HP:0012828	HP:0002650	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002656	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002766	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002804	OMIM:156530	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	156530	METATROPIC DYSPLASIA	HP:0012828	HP:0002808	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002810	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002822	OMIM:156530	IEA				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002825	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002826	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002831	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002834	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002878	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0002879	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003037	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003332	OMIM:156530	IEA				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003336	OMIM:156530	IEA				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003336	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003477	OMIM:156530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156530	METATROPIC DYSPLASIA		HP:0003510	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003562	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0003911	OMIM:156530	TAS				P		HPO:probinson	
OMIM	156530	METATROPIC DYSPLASIA		HP:0009381	OMIM:156530	TAS				P		HPO:skoehler	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000006	OMIM:156550	IEA				I		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000023	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000175	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000272	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000311	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000403	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000405	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000470	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000518	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000520	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000541	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000545	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000926	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0000947	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0001270	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0001288	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0001537	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0002098	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0002663	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0002779	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0002812	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0002827	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0003015	OMIM:156550	TAS				P		HPO:probinson	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0003037	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0003273	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0003417	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0003521	OMIM:156550	IEA				P		HPO:skoehler	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0004619	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0005280	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0006172	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0008271	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0008839	OMIM:156550	IEA				P		HPO:iea	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0011800	OMIM:156550	TAS				P		HPO:skoehler	
OMIM	156550	#156550 KNIEST DYSPLASIA		HP:0200003	OMIM:156550	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:156580	TAS				I		HPO:skoehler	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000252	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000340	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000350	OMIM:156580	IEA				P		HPO:skoehler	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000411	OMIM:156580	IEA				P		HPO:iea	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000582	OMIM:156580	IEA				P		HPO:iea	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000601	OMIM:156580	IEA				P		HPO:iea	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0000666	OMIM:156580	IEA				P		HPO:iea	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0001137	OMIM:156580	IEA				P		HPO:iea	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0004322	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0010055	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0011094	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156580	MICROCEPHALY, AUTOSOMAL DOMINANT		HP:0011304	OMIM:156580	TAS				P		HPO:probinson	
OMIM	156600	MICROCORIA, CONGENITAL		HP:0000006	OMIM:156600	IEA				I		HPO:iea	
OMIM	156600	MICROCORIA, CONGENITAL		HP:0000501	OMIM:156600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156600	MICROCORIA, CONGENITAL		HP:0000545	OMIM:156600	IEA				P		HPO:iea	
OMIM	156600	MICROCORIA, CONGENITAL		HP:0000616	OMIM:156600	TAS				P		HPO:probinson	
OMIM	156600	MICROCORIA, CONGENITAL		HP:0007906	OMIM:156600	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	156600	MICROCORIA, CONGENITAL		HP:0008345	OMIM:156600	IEA				P		HPO:iea	
OMIM	156600	MICROCORIA, CONGENITAL		HP:0025492	OMIM:156600	TAS	HP:0003577			P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000006	OMIM:156610	IEA				I		HPO:iea	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000160	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000175	OMIM:156610	IEA				P		HPO:iea	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000218	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000248	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000252	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000286	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000316	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000347	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000358	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000369	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000470	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000482	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000568	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000581	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000582	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000629	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1	HP:0012825	HP:0000750	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000767	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0000951	OMIM:156610	IEA				P		HPO:iea	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0001249	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0001270	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0001290	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0001305	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0002079	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0002557	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0006610	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0006768	OMIM:156610	IEA				P		HPO:iea	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0006855	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0012368	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0012745	OMIM:156610	TAS				P		HPO:skoehler	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0030680	OMIM:156610	IEA				P		HPO:iea	
OMIM	156610	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 1		HP:0100807	OMIM:156610	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000006	OMIM:156620	TAS				I		HPO:skoehler	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000232	OMIM:156620	TAS				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000252	OMIM:156620	IEA				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000324	OMIM:156620	IEA				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000347	OMIM:156620	TAS				P		HPO:skoehler	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000365	OMIM:156620	IEA				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000369	OMIM:156620	TAS				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0000378	OMIM:156620	TAS				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0001249	OMIM:156620	IEA				P		HPO:probinson	
OMIM	156620	156620 MICROCEPHALY-DEAFNESS SYNDROME		HP:0002057	OMIM:156620	IEA				P		HPO:probinson	
OMIM	156700	MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES		HP:0000006	OMIM:156700	IEA				I		HPO:iea	
OMIM	156700	MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES		HP:0000482	OMIM:156700	IEA				P		HPO:iea	
OMIM	156700	MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES		HP:0000501	OMIM:156700	IEA				P		HPO:iea	
OMIM	156700	MICROCORNEA, GLAUCOMA, AND ABSENT FRONTAL SINUSES		HP:0002688	OMIM:156700	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000028	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000085	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000122	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000125	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000528	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000800	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0000813	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001080	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001180	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001274	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001508	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001684	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0001746	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002020	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002101	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002126	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002132	OMIM:156810	IEA				P		HPO:skoehler	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002139	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002251	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002566	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0002984	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0003022	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0003745	OMIM:156810	IEA				I		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0004384	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0009777	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0009829	OMIM:156810	IEA				P		HPO:iea	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0010664	OMIM:156810	IEA				P		HPO:skoehler	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0011467	OMIM:156810	TAS				P		HPO:skoehler	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0025410	OMIM:156810	TAS				P		HPO:skoehler	
OMIM	156810	MICROGASTRIA-LIMB REDUCTION DEFECTS ASSOCIATION; MLRD		HP:0100841	OMIM:156810	TAS				P		HPO:skoehler	
OMIM	156830	MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL		HP:0000006	OMIM:156830	TAS				I		HPO:nvasilevsky	
OMIM	156830	MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL		HP:0000007	PMID:4073120	TAS				I		HPO:nvasilevsky	
OMIM	156830	MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL		HP:0002676	OMIM:156830	TAS				P		HPO:skoehler	
OMIM	156830	MICROMELIC BONE DYSPLASIA WITH CLOVERLEAF SKULL		HP:0002983	OMIM:156830	TAS				P		HPO:skoehler	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000006	OMIM:156850	IEA				I		HPO:iea	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000486	OMIM:156850	IEA				P		HPO:iea	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000518	OMIM:156850	IEA				P		HPO:iea	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000568	OMIM:156850	IEA				P		HPO:iea	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000616	OMIM:156850	IEA				P		HPO:iea	
OMIM	156850	MICROPHTHALMIA, ISOLATED, WITH CATARACT 1		HP:0000639	OMIM:156850	IEA				P		HPO:iea	
OMIM	156900	MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA		HP:0000006	OMIM:156900	IEA				I		HPO:iea	
OMIM	156900	MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA		HP:0000545	OMIM:156900	IEA				P		HPO:iea	
OMIM	156900	MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA		HP:0000568	OMIM:156900	IEA				P		HPO:iea	
OMIM	156900	MICROPHTHALMIA, ISOLATED, WITH CORECTOPIA		HP:0009918	OMIM:156900	IEA				P		HPO:skoehler	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0000006	OMIM:157150	IEA				I		HPO:iea	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0000023	OMIM:157150	IEA				P		HPO:iea	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0000541	OMIM:157150	IEA				P		HPO:iea	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0000545	OMIM:157150	IEA				P		HPO:iea	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0008019	OMIM:157150	IEA				P		HPO:iea	
OMIM	157150	MICROSPHEROPHAKIA WITH HERNIA		HP:0030961	OMIM:157150	TAS				P		HPO:skoehler	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0000006	OMIM:157151	IEA				I		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0000541	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0000545	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0001132	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0001510	OMIM:157151	TAS				P		HPO:probinson	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0002652	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0004322	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0005733	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0005752	OMIM:157151	IEA				P		HPO:iea	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0010582	OMIM:157151	TAS				P		HPO:probinson	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0030961	OMIM:157151	TAS				P		HPO:skoehler	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0100255	OMIM:157151	TAS				P		HPO:skoehler	
OMIM	157151	MICROSPHEROPHAKIA-METAPHYSEAL DYSPLASIA		HP:0100719	OMIM:157151	TAS				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000006	OMIM:157170	IEA				I		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000176	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000193	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000252	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000272	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000568	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000601	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000835	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0000873	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001249	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001250	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001252	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001263	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001274	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001290	OMIM:157170	TAS				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001321	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001360	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001425	OMIM:157170	IEA				I		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0001750	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0002019	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0002650	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0003745	OMIM:157170	IEA				I		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0003828	OMIM:157170	TAS				C		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0003829	OMIM:157170	IEA				C		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0005273	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0006315	OMIM:157170	IEA				P		HPO:iea	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0008501	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0009914	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0009927	OMIM:157170	TAS				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0010626	OMIM:157170	TAS				P		HPO:probinson	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0011800	OMIM:157170	TAS				P		HPO:skoehler	
OMIM	157170	HOLOPROSENCEPHALY 2; HPE2		HP:0012806	OMIM:157170	IEA				P		HPO:skoehler	
OMIM	157200	MIDPHALANGEAL HAIR		HP:0000006	OMIM:157200	IEA				I		HPO:iea	
OMIM	157200	MIDPHALANGEAL HAIR		HP:0001595	OMIM:157200	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:157300	IEA				I		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0000613	OMIM:157300	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0002013	OMIM:157300	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0002018	OMIM:157300	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0002077	OMIM:157300	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0002083	OMIM:157300	IEA				P		HPO:iea	
OMIM	157300	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1		HP:0002183	OMIM:157300	IEA				P		HPO:iea	
OMIM	157400	MILIA, MULTIPLE ERUPTIVE		HP:0000006	OMIM:157400	IEA				I		HPO:iea	
OMIM	157400	MILIA, MULTIPLE ERUPTIVE		HP:0001056	OMIM:157400	TAS				P		HPO:probinson	
OMIM	157600	MIRROR MOVEMENTS 1; MRMV1		HP:0000006	OMIM:157600	IEA				I		HPO:iea	
OMIM	157600	MIRROR MOVEMENTS 1; MRMV1		HP:0001256	OMIM:157600	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	157600	MIRROR MOVEMENTS 1; MRMV1		HP:0001274	OMIM:157600	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	157600	MIRROR MOVEMENTS 1; MRMV1		HP:0001335	OMIM:157600	IEA				P		HPO:iea	
OMIM	157600	MIRROR MOVEMENTS 1; MRMV1		HP:0003829	OMIM:157600	TAS				C		HPO:skoehler	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000006	OMIM:157640	IEA				I		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000029	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000407	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000508	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000518	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000590	OMIM:157640	IEA				P		HPO:skoehler	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000716	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000786	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000815	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0000869	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0001260	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0001265	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0001425	OMIM:157640	TAS				I		HPO:skoehler	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0001761	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002015	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002063	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002066	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002067	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002151	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002322	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002548	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0002578	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003200	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003201	OMIM:157640	IEA				P		HPO:skoehler	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003202	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003323	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003390	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003458	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003546	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003548	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003557	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003581	OMIM:157640	IEA				C		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003676	OMIM:157640	IEA				C		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003688	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003689	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003690	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0003713	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0006858	OMIM:157640	TAS				P		HPO:probinson	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0006886	OMIM:157640	TAS				P		HPO:probinson	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0008209	OMIM:157640	IEA				P		HPO:iea	
OMIM	157640	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 1; PEOA1		HP:0010628	OMIM:157640	IEA				P		HPO:iea	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0000006	OMIM:157700	IEA				I		HPO:iea	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0000218	OMIM:157700	IEA				P		HPO:iea	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME	HP:0012825	HP:0000767	OMIM:157700	TAS				P		HPO:probinson	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0001065	OMIM:157700	TAS				P		HPO:probinson	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0001519	OMIM:157700	IEA				P		HPO:skoehler	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0001634	OMIM:157700	IEA				P		HPO:iea	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0001653	OMIM:157700	IEA				P		HPO:skoehler	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0002705	OMIM:157700	TAS				P		HPO:skoehler	
OMIM	157700	%157700 MITRAL VALVE PROLAPSE 1; MVP1;;MITRAL VALVE PROLAPSE, MYXOMATOUS 1; MMVP1;;MYXOMATOUS MITRAL VALVE PROLAPSE 1;;MITRAL VALVE PROLAPSE, FAMILIAL; MVP PROLAPSED MITRAL VALVE; PMV;;MITRAL REGURGITATION, FAMILIAL;;FLOPPY MITRAL VALVE;;BARLOW SYNDROME;;MYXOMATOUS VALVULAR DISEASE, FAMILIAL;;CLICK-MURMUR SYNDROME		HP:0008433	OMIM:157700	IEA				P		HPO:iea	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000006	OMIM:157800	IEA				I		HPO:iea	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000076	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000085	OMIM:157800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000164	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000293	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000316	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000343	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000358	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000403	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000405	OMIM:157800	TAS				P		HPO:probinson	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000431	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000463	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000478	OMIM:157800	IEA				P		HPO:iea	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000486	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000506	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000582	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0000902	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001156	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001388	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001480	OMIM:157800	IEA				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001508	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001653	OMIM:157800	TAS				P		HPO:probinson	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0001773	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0002020	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0002650	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0002750	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0002949	OMIM:157800	IEA				P		HPO:iea	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0004322	OMIM:157800	IEA				P		HPO:iea	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0008368	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0008527	OMIM:157800	TAS				P		HPO:probinson	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0008734	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0009702	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0010579	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0010584	OMIM:157800	TAS				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0011968	OMIM:157800	IEA				P		HPO:skoehler	
OMIM	157800	CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF		HP:0100266	OMIM:157800	IEA				P		HPO:iea	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000006	OMIM:157900	IEA				I		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000044	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000054	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000164	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	37%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000193	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	11%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000218	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000286	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000298	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000316	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000347	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	64%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000377	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000470	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000565	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000568	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000577	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000750	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	55%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0000932	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001156	OMIM:157900	TAS				P		HPO:skoehler	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001159	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001171	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001188	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001188	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001256	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001260	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001270	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001288	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001349	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001491	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001597	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001608	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001739	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001762	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0001763	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002015	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002075	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002098	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002312	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002365	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002370	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002644	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0002804	OMIM:157900	TAS		HP:0040284		P		HPO:probinson	6%
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0003745	OMIM:157900	IEA				I		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0005280	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0005914	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0006897	OMIM:157900	IEA				P		HPO:skoehler	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0008734	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0008872	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0008947	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0009466	OMIM:157900	TAS				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0009803	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0009816	OMIM:157900	IEA				P		HPO:probinson	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0009830	OMIM:157900	IEA				P		HPO:skoehler	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0012385	OMIM:157900	TAS				P		HPO:skoehler	
OMIM	157900	MOEBIUS SYNDROME; MBS		HP:0030084	OMIM:157900	TAS				P		HPO:skoehler	
OMIM	157950	MOLAR I REINCLUSION		HP:0000006	OMIM:157950	IEA				I		HPO:iea	
OMIM	157950	MOLAR I REINCLUSION		HP:0000164	OMIM:157950	IEA				P		HPO:iea	
OMIM	157950	MOLAR I REINCLUSION		HP:0000303	OMIM:157950	IEA				P		HPO:iea	
OMIM	157950	MOLAR I REINCLUSION		HP:0004209	OMIM:157950	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000006	OMIM:157980	IEA				I		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000179	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000218	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000248	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000256	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000286	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000316	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000319	OMIM:157980	TAS				P		HPO:probinson	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000337	OMIM:157980	TAS				P		HPO:probinson	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000343	OMIM:157980	TAS				P		HPO:probinson	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000348	OMIM:157980	TAS				P		HPO:probinson	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000431	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000470	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000480	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000486	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000494	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000501	OMIM:157980	TAS				P		HPO:skoehler	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000618	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000625	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000639	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000679	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000684	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000689	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000879	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0000965	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001176	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001249	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001513	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001548	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001795	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0001833	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0002007	OMIM:157980	TAS				P		HPO:skoehler	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0002750	OMIM:157980	IEA				P		HPO:iea	
OMIM	157980	157980 MOMO SYNDROME;;MACROSOMIA, OBESITY, MACROCEPHALY, AND OCULAR ABNORMALITIES		HP:0008577	OMIM:157980	TAS				P		HPO:probinson	
OMIM	158000	MONILETHRIX; MNLIX		HP:0000006	OMIM:158000	TAS				I		HPO:iea	
OMIM	158000	MONILETHRIX; MNLIX		HP:0001006	OMIM:158000	TAS				P		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0001425	OMIM:158000	TAS				I		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0001596	OMIM:158000	IEA				P		HPO:iea	
OMIM	158000	MONILETHRIX; MNLIX		HP:0002164	OMIM:158000	IEA				P		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0002299	OMIM:158000	TAS				P		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0003593	OMIM:158000	IEA				C		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0003828	OMIM:158000	IEA				C		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0007468	OMIM:158000	IEA				P		HPO:iea	
OMIM	158000	MONILETHRIX; MNLIX		HP:0008404	OMIM:158000	TAS				P		HPO:skoehler	
OMIM	158000	MONILETHRIX; MNLIX		HP:0032152	OMIM:158000	IEA				P		HPO:skoehler	
OMIM	158100	MONOPHALANGY OF GREAT TOE		HP:0000006	OMIM:158100	IEA				I		HPO:iea	
OMIM	158100	MONOPHALANGY OF GREAT TOE		HP:0000924	OMIM:158100	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000006	OMIM:158170	IEA				I		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000023	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000047	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000054	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000160	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000219	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000219	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000243	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000272	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000286	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000316	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000343	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000347	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000358	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000369	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000377	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000431	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000453	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000463	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000470	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000545	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000582	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0000750	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001182	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001249	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001252	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001263	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001290	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001539	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001629	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001631	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001643	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001763	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0001795	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0002286	OMIM:158170	IEA				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0002553	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0002650	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0002705	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0003745	OMIM:158170	IEA				I		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0005280	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0005882	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0006610	OMIM:158170	IEA				P		HPO:iea	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0011800	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0030148	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158170	CHROMOSOME 9P DELETION SYNDROME		HP:0045025	OMIM:158170	TAS				P		HPO:skoehler	
OMIM	158250	NONDISJUNCTION		HP:0000006	OMIM:158250	IEA				I		HPO:iea	
OMIM	158250	NONDISJUNCTION		HP:0000007	OMIM:158250	IEA				I		HPO:iea	
OMIM	158250	NONDISJUNCTION		HP:0000144	OMIM:158250	IEA				P		HPO:iea	
OMIM	158250	NONDISJUNCTION		HP:0002916	OMIM:158250	IEA				P		HPO:iea	
OMIM	158280	MOTION SICKNESS		HP:0000707	OMIM:158280	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000006	OMIM:158300	IEA				I		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000211	OMIM:158300	IEA				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000256	OMIM:158300	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000324	OMIM:158300	IEA				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000347	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0000508	OMIM:158300	IEA				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0001762	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0001765	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0001840	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0002002	OMIM:158300	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0002015	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0002804	OMIM:158300	IEA				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0002827	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0004322	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0005684	OMIM:158300	IEA				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0010621	OMIM:158300	IEA				P		HPO:iea	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0011968	OMIM:158300	TAS				P		HPO:skoehler	
OMIM	158300	ARTHROGRYPOSIS, DISTAL, TYPE 7		HP:0400000	OMIM:158300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000006	OMIM:158310	IEA				I		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000518	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000565	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000613	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000618	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000639	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0000790	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0001096	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0001596	OMIM:158310	TAS				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0001648	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY	HP:0012825	HP:0001880	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002028	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002090	OMIM:158310	IEA				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002164	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002208	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002249	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0002728	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0003577	OMIM:158310	TAS				C		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0006532	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0006552	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0007759	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0008396	OMIM:158310	IEA				P		HPO:iea	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0008404	OMIM:158310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0009926	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158310	MUCOEPITHELIAL DYSPLASIA, HEREDITARY		HP:0011496	OMIM:158310	TAS				P		HPO:skoehler	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0000006	OMIM:158320	IEA				I		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0002253	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0002671	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0003002	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0003003	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0006719	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0006758	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0006771	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0006778	OMIM:158320	IEA				P		HPO:iea	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0009720	OMIM:158320	TAS				P		HPO:skoehler	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0012118	OMIM:158320	TAS				P		HPO:skoehler	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0030410	OMIM:158320	TAS				P		HPO:skoehler	
OMIM	158320	MUIR-TORRE SYNDROME; MRTES		HP:0030731	OMIM:158320	IEA				P		HPO:skoehler	
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0000006	OMIM:158330	PCS				I		HPO:iea	
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0000122	OMIM:158330	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0000141	OMIM:158330	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0000151	OMIM:158330	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0001007	OMIM:158330	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0001061	OMIM:158330	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0003250	OMIM:158330	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	158330	#158330 MULLERIAN APLASIA AND HYPERANDROGENISM;;MULLERIAN DUCT FAILURE AND HYPERANDROGENISM		HP:0008655	OMIM:158330	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	158345	MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS		HP:0000006	OMIM:158345	IEA				I		HPO:iea	
OMIM	158345	MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS		HP:0001285	OMIM:158345	IEA				P		HPO:iea	
OMIM	158345	MULTIPLE EXOSTOSES WITH SPASTIC TETRAPARESIS		HP:0002762	OMIM:158345	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000006	OMIM:158350	IEA				I		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000034	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000138	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000160	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000218	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000221	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000327	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000347	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000365	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000518	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000545	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000767	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000771	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000821	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000836	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000853	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000854	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0000972	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001031	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001102	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001250	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001256	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001263	OMIM:158350	IEA				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0001888	OMIM:158350	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002080	OMIM:158350	IEA				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002253	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002597	OMIM:158350	TAS				P		HPO:probinson	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002650	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002719	OMIM:158350	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002808	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0002858	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0003002	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0003581	OMIM:158350	TAS				C		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0004313	OMIM:158350	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0004390	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0004481	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0006740	OMIM:158350	TAS				P		HPO:iea	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0010609	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0010619	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0012871	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0025318	OMIM:158350	IEA				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0030731	OMIM:158350	IEA				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0100646	OMIM:158350	TAS				P		HPO:skoehler	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0200016	OMIM:158350	TAS				P		HPO:probinson	
OMIM	158350	#158350 COWDEN SYNDROME 1; CWS1;;CS; CD;;MULTIPLE HAMARTOMA SYNDROME; MHAMDYSPLASTIC GANGLIOCYTOMA OF THE CEREBELLUM, INCLUDED;;CEREBELLOPARENCHYMAL DISORDER VI, INCLUDED; CPD6, INCLUDED;;CEREBELLAR GRANULE CELL HYPERTROPHY AND MEGALENCEPHALY, INCLUDED;;LHERMITTE-DUCLOS DISEASE, INCLUDED; LDD, INCLUDED;;PROTEUS-LIKE SYNDROME, INCLUDED		HP:0500009	OMIM:158350	IEA				P		HPO:skoehler	
OMIM	158400	MUSCLE CRAMPS, FAMILIAL		HP:0000006	OMIM:158400	TAS				I		HPO:probinson	
OMIM	158400	MUSCLE CRAMPS, FAMILIAL		HP:0003236	OMIM:158400	TAS				P		HPO:probinson	
OMIM	158400	MUSCLE CRAMPS, FAMILIAL		HP:0003394	OMIM:158400	TAS				P		HPO:probinson	
OMIM	158400	MUSCLE CRAMPS, FAMILIAL		HP:0003445	OMIM:158400	TAS				P		HPO:probinson	
OMIM	158500	MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS		HP:0000006	OMIM:158500	IEA				I		HPO:iea	
OMIM	158500	MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS		HP:0000510	OMIM:158500	IEA				P		HPO:iea	
OMIM	158500	MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS		HP:0000819	OMIM:158500	IEA				P		HPO:iea	
OMIM	158500	MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS		HP:0001251	OMIM:158500	IEA				P		HPO:iea	
OMIM	158500	MUSCULAR ATROPHY, ATAXIA, RETINITIS PIGMENTOSA, AND DIABETES MELLITUS		HP:0003202	OMIM:158500	IEA				P		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0000006	OMIM:158580	IEA				I		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0001265	OMIM:158580	IEA				P		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0001337	OMIM:158580	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0001604	OMIM:158580	IEA				P		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0001605	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0001761	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0002355	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0002460	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0003674	OMIM:158580	IEA				C		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0003677	OMIM:158580	IEA				C		HPO:iea	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0003693	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158580	#158580 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA; HMN7A;;HMN VIIA;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA;;DHMN7A;;DHMNVP;;SPINAL MUSCULAR ATROPHY, DISTAL, WITH VOCAL CORD PARALYSIS;;HARPER-YOUNG MYOPATHY		HP:0009830	OMIM:158580	TAS				P		HPO:skoehler	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0000006	OMIM:158590	IEA				I		HPO:iea	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0002522	OMIM:158590	IEA				P		HPO:iea	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0002600	OMIM:158590	TAS				P		HPO:skoehler	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0002601	OMIM:158590	IEA				P		HPO:iea	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0003445	OMIM:158590	IEA				P		HPO:iea	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0003470	OMIM:158590	IEA				P		HPO:skoehler	
OMIM	158590	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A		HP:0009053	OMIM:158590	TAS				P		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0000006	OMIM:158600	TAS				I		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0001263	OMIM:158600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0001760	OMIM:158600	TAS				P		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0002515	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0003445	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0003474	OMIM:158600	TAS				P		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0003677	OMIM:158600	TAS				C		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0007269	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0008956	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0008994	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0009046	OMIM:158600	TAS				P		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0010602	OMIM:158600	TAS				P		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0011463	OMIM:158600	TAS				C		HPO:probinson	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0011808	OMIM:158600	TAS				P		HPO:skoehler	
OMIM	158600	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 1, AUTOSOMAL DOMINANT; SMALED1		HP:0031936	OMIM:158600	IEA				P		HPO:skoehler	
OMIM	158650	MUSCULAR ATROPHY, MALIGNANT NEUROGENIC		HP:0000006	OMIM:158650	TAS				I		HPO:probinson	
OMIM	158650	MUSCULAR ATROPHY, MALIGNANT NEUROGENIC		HP:0002203	OMIM:158650	TAS				P		HPO:probinson	
OMIM	158650	MUSCULAR ATROPHY, MALIGNANT NEUROGENIC		HP:0003202	OMIM:158650	TAS				P		HPO:probinson	
OMIM	158650	MUSCULAR ATROPHY, MALIGNANT NEUROGENIC		HP:0003581	OMIM:158650	TAS				C		HPO:probinson	
OMIM	158800	MUSCULAR DYSTROPHY, BARNES TYPE		HP:0000006	OMIM:158800	TAS				I		HPO:probinson	
OMIM	158800	MUSCULAR DYSTROPHY, BARNES TYPE		HP:0002486	OMIM:158800	TAS				P		HPO:probinson	
OMIM	158800	MUSCULAR DYSTROPHY, BARNES TYPE		HP:0003198	OMIM:158800	TAS				P		HPO:skoehler	
OMIM	158800	MUSCULAR DYSTROPHY, BARNES TYPE		HP:0003560	OMIM:158800	TAS				P		HPO:probinson	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0000006	OMIM:158810	IEA				I		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0000007	OMIM:158810	TAS				I		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0000473	OMIM:158810	TAS	HP:0003577			P		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0001270	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0001319	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0001558	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0001626	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0002460	OMIM:158810	IEA				P		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0002747	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0002987	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003198	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003202	OMIM:158810	TAS				P		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1	HP:0012825	HP:0003236	OMIM:158810	TAS				P		HPO:probinson	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003325	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003677	OMIM:158810	IEA				C		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003701	OMIM:158810	IEA				P		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0003828	OMIM:158810	TAS				C		HPO:skoehler	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0005988	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0006466	OMIM:158810	IEA				P		HPO:iea	
OMIM	158810	BETHLEM MYOPATHY 1		HP:0100490	OMIM:158810	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0000006	OMIM:158900	IEA				I		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0000407	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0000544	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0001249	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0001250	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0002015	OMIM:158900	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0002111	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0003236	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0003547	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0003677	OMIM:158900	IEA				C		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0003691	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0003724	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0007763	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0008970	OMIM:158900	IEA				P		HPO:skoehler	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0008981	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0009023	OMIM:158900	IEA				P		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0010628	OMIM:158900	TAS				P		HPO:probinson	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0011463	OMIM:158900	IEA				C		HPO:iea	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0012231	OMIM:158900	TAS				P		HPO:skoehler	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0012473	OMIM:158900	TAS				P		HPO:skoehler	
OMIM	158900	#158900 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FSHD; FMD;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1A; FSHD1A;;LANDOUZY-DEJERINE MUSCULAR DYSTROPHYFACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY, INFANTILE, INCLUDED;;FACIOSCAPULOHUMERAL DYSTROPHY WITH SENSORINEURAL HEARING LOSS ANDTORTUOSITY OF RETINAL ARTERIOLES, INCLUDED		HP:0030664	OMIM:158900	TAS				P		HPO:skoehler	
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0000365	PMID:20975055	PCS		HP:0040284		P		HPO:probinson	6/33
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0003581	PMID:20975055	PCS				C		HPO:probinson	
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0003691	PMID:8328457	PCS		HP:0040284		P		HPO:probinson	33/33
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0003691	OMIM:158901	PCS				P		HPO:probinson	
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0003749	PMID:20975055	PCS		HP:0040284		P		HPO:probinson	3/33
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0008970	PMID:20975055	PCS				P		HPO:skoehler	
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0009027	PMID:20975055	PCS		HP:0040284		P		HPO:probinson	26/33
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0010628	PMID:20975055	PCS		HP:0040284		P		HPO:probinson	3/33
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0010984	OMIM:158901	TAS				I		HPO:probinson	
OMIM	158901	#158901 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2; FSHD2;;FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 2, DIGENIC;;FSHD2, DIGENIC;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 2;;MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL, TYPE 1B; FSHD1B		HP:0030664	PMID:20975055	PCS		HP:0040284		P		HPO:skoehler	12/18
OMIM	159050	MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES		HP:0000006	OMIM:159050	IEA				I		HPO:iea	
OMIM	159050	MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES		HP:0001324	OMIM:159050	IEA				P		HPO:iea	
OMIM	159050	MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES		HP:0003560	OMIM:159050	TAS				P		HPO:skoehler	
OMIM	159050	MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC, WITH INTERNALIZED CAPILLARIES		HP:0030230	OMIM:159050	TAS				P		HPO:probinson	
OMIM	159100	159100 MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE		HP:0000006	OMIM:159100	TAS				I		HPO:skoehler	
OMIM	159100	159100 MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE		HP:0001324	OMIM:159100	TAS				P		HPO:skoehler	
OMIM	159100	159100 MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE		HP:0001425	OMIM:159100	TAS				I		HPO:skoehler	
OMIM	159100	159100 MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE		HP:0004303	OMIM:159100	TAS				P		HPO:skoehler	
OMIM	159100	159100 MUSCULAR HYPOPLASIA, CONGENITAL UNIVERSAL, OF KRABBE		HP:0009004	OMIM:159100	TAS	HP:0003577			P		HPO:skoehler	
OMIM	159300	MUSICAL PERFECT PITCH		HP:0000006	OMIM:159300	IEA				I		HPO:iea	
OMIM	159300	MUSICAL PERFECT PITCH		HP:0000598	OMIM:159300	IEA				P		HPO:iea	
OMIM	159300	MUSICAL PERFECT PITCH		HP:0001328	OMIM:159300	IEA				P		HPO:skoehler	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0000508	OMIM:159400	IEA				P		HPO:skoehler	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0000597	OMIM:159400	IEA				P		HPO:skoehler	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0000872	OMIM:159400	IEA				P		HPO:skoehler	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0002664	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0002725	OMIM:159400	IEA				P		HPO:skoehler	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0003403	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0003473	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0003554	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0003581	OMIM:159400	IEA				C		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0003745	OMIM:159400	IEA				I		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0007126	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0008180	OMIM:159400	IEA				P		HPO:iea	
OMIM	159400	MYASTHENIA, LIMB-GIRDLE, AUTOIMMUNE		HP:0100522	OMIM:159400	TAS				P		HPO:skoehler	
OMIM	159410	MYDRIATIC RESPONSE TO PHARMACOLOGIC AGENTS		HP:0000006	OMIM:159410	IEA				I		HPO:iea	
OMIM	159410	MYDRIATIC RESPONSE TO PHARMACOLOGIC AGENTS		HP:0000478	OMIM:159410	IEA				P		HPO:iea	
OMIM	159420	MYDRIASIS, CONGENITAL		HP:0000006	OMIM:159420	IEA				I		HPO:iea	
OMIM	159420	MYDRIASIS, CONGENITAL		HP:0007932	OMIM:159420	IEA				P		HPO:iea	
OMIM	159500	MYELINATED OPTIC NERVE FIBERS		HP:0000006	OMIM:159500	IEA				I		HPO:iea	
OMIM	159500	MYELINATED OPTIC NERVE FIBERS		HP:0000478	OMIM:159500	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0000006	PMID:27259050	PCS				I		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0000639	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0000762	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001251	PMID:27259050	PCS				P		HPO:probinson	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001260	OMIM:159550	TAS				P		HPO:skoehler	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001272	PMID:27259050	PCS				P		HPO:probinson	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001310	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001876	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0001908	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0002166	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0002317	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0002500	OMIM:159550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0002936	OMIM:159550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0003487	OMIM:159550	TAS				P		HPO:skoehler	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0003828	OMIM:159550	TAS				C		HPO:skoehler	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0004820	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0006801	OMIM:159550	IEA				P		HPO:iea	
OMIM	159550	ATAXIA-PANCYTOPENIA SYNDROME		HP:0011448	OMIM:159550	TAS				P		HPO:skoehler	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0000006	OMIM:159555	IEA				I		HPO:iea	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0004808	OMIM:159555	IEA				P		HPO:iea	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0004820	OMIM:159555	IEA				P		HPO:iea	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0004845	OMIM:159555	IEA				P		HPO:iea	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0005531	OMIM:159555	IEA				P		HPO:iea	
OMIM	159555	LYSINE-SPECIFIC METHYLTRANSFERASE 2A; KMT2A		HP:0006721	OMIM:159555	IEA				P		HPO:iea	
OMIM	159580	MYELOPATHY, HTLV-1-ASSOCIATED		HP:0002196	OMIM:159580	TAS				P		HPO:probinson	
OMIM	159580	MYELOPATHY, HTLV-1-ASSOCIATED		HP:0002313	OMIM:159580	TAS				P		HPO:probinson	
OMIM	159580	MYELOPATHY, HTLV-1-ASSOCIATED		HP:0007256	OMIM:159580	TAS				P		HPO:probinson	
OMIM	159595	MYELOPROLIFERATIVE SYNDROME, TRANSIENT		HP:0001974	OMIM:159595	IEA				P		HPO:iea	
OMIM	159595	MYELOPROLIFERATIVE SYNDROME, TRANSIENT		HP:0005534	OMIM:159595	IEA				P		HPO:iea	
OMIM	159600	MYOCLONIC EPILEPSY, HARTUNG TYPE		HP:0000006	OMIM:159600	TAS				I		HPO:skoehler	
OMIM	159600	MYOCLONIC EPILEPSY, HARTUNG TYPE		HP:0002123	OMIM:159600	TAS				P		HPO:skoehler	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0000006	OMIM:159700	TAS				I		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0001251	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0001336	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0001425	OMIM:159700	TAS				I		HPO:skoehler	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0002080	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0002197	OMIM:159700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0003200	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0007132	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0012103	OMIM:159700	TAS				P		HPO:skoehler	
OMIM	159700	MYOCLONUS AND ATAXIA		HP:0100321	OMIM:159700	TAS				P		HPO:probinson	
OMIM	159800	MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS		HP:0000006	OMIM:159800	IEA				I		HPO:iea	
OMIM	159800	MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS		HP:0000365	OMIM:159800	IEA				P		HPO:iea	
OMIM	159800	MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS		HP:0001251	OMIM:159800	IEA				P		HPO:iea	
OMIM	159800	MYOCLONUS, CEREBELLAR ATAXIA, AND DEAFNESS		HP:0001336	OMIM:159800	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000006	OMIM:159900	IEA				I		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000473	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000716	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000722	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000739	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0000756	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0001290	OMIM:159900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0001336	OMIM:159900	TAS				P		HPO:skoehler	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0001337	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0002356	OMIM:159900	IEA				P		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0003621	OMIM:159900	IEA				C		HPO:iea	
OMIM	159900	DYSTONIA 11, MYOCLONIC		HP:0003829	OMIM:159900	TAS				C		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0000006	OMIM:159950	IEA				I		HPO:iea	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0000007	OMIM:159950	TAS				I		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0000726	OMIM:159950	IEA				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0001284	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0001308	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0001336	OMIM:159950	IEA				P		HPO:iea	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0001337	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002123	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002205	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002355	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002359	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002398	OMIM:159950	IEA				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002650	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0002747	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0003391	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0003621	OMIM:159950	TAS				C		HPO:probinson	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0003676	OMIM:159950	TAS				C		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0007269	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0008955	OMIM:159950	IEA				P		HPO:iea	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0010628	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	159950	SPINAL MUSCULAR ATROPHY WITH PROGRESSIVE MYOCLONIC EPILEPSY		HP:0200136	OMIM:159950	TAS				P		HPO:skoehler	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:160010	TAS				I		HPO:skoehler	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0001324	OMIM:160010	IEA				P		HPO:skoehler	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0001919	OMIM:160010	IEA				P		HPO:iea	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0002913	OMIM:160010	IEA				P		HPO:iea	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0003236	OMIM:160010	TAS				P		HPO:skoehler	
OMIM	160010	%160010 MYOGLOBINURIA, AUTOSOMAL DOMINANT		HP:0003326	OMIM:160010	IEA				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0000006	OMIM:160120	IEA				I		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0000622	OMIM:160120	TAS				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0001155	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0001260	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0001337	OMIM:160120	IEA				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0001347	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0001350	OMIM:160120	TAS				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002064	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002131	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002311	OMIM:160120	IEA				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002315	OMIM:160120	TAS				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002321	OMIM:160120	TAS				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0002411	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0003236	OMIM:160120	TAS				P		HPO:skoehler	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0003487	OMIM:160120	IEA				P		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0003621	OMIM:160120	IEA				C		HPO:iea	
OMIM	160120	EPISODIC ATAXIA, TYPE 1; EA1		HP:0003828	OMIM:160120	TAS				C		HPO:skoehler	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0000006	PMID:22396310	PCS				I		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0000508	PMID:22396310	PCS				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0000544	PMID:22396310	PCS				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0001270	OMIM:160150	IEA				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0001284	PMID:22396310	PCS				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0001371	PMID:22396310	PCS				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003307	PMID:22396310	PCS				P		HP:probinson	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003388	OMIM:160150	IEA				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003458	PMID:22396310	PCS				P		HP:probinson	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003677	OMIM:160150	IEA				C		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003687	PMID:22396310	PCS				P		HPO:skoehler	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003701	OMIM:160150	TAS				P		HPO:skoehler	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003712	PMID:22396310	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0003803	PMID:22396310	PCS				P		HP:probinson	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0005335	OMIM:160150	IEA				P		HPO:iea	
OMIM	160150	MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT		HP:0010628	PMID:22396310	PCS				P		HPO:iea	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0000006	OMIM:160300	TAS				I		HPO:probinson	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0002460	OMIM:160300	TAS				P		HPO:probinson	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0003236	OMIM:160300	TAS				P		HPO:skoehler	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0003376	OMIM:160300	TAS				P		HPO:skoehler	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0003593	OMIM:160300	TAS				C		HPO:probinson	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0008981	OMIM:160300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0009025	OMIM:160300	IEA				P		HPO:skoehler	
OMIM	160300	MYOPATHY, DISTAL, INFANTILE-ONSET		HP:0009027	OMIM:160300	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0000006	OMIM:160500	TAS				I		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0000218	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0000467	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0001288	OMIM:160500	IEA				P		HPO:iea	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0001644	OMIM:160500	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0001761	OMIM:160500	TAS				P		HPO:skoehler	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0002460	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0002650	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003200	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003326	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003445	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003593	OMIM:160500	IEA				C		HPO:iea	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003677	OMIM:160500	IEA				C		HPO:iea	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003701	OMIM:160500	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003803	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0003805	OMIM:160500	IEA				P		HPO:skoehler	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0008180	OMIM:160500	TAS				P		HPO:skoehler	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0009031	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0009077	OMIM:160500	IEA				P		HPO:iea	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1	HP:0012825	HP:0010628	OMIM:160500	TAS				P		HPO:skoehler	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0011463	OMIM:160500	IEA				C		HPO:iea	
OMIM	160500	MYOPATHY, DISTAL, 1; MPD1		HP:0011916	OMIM:160500	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0000006	OMIM:160565	TAS				I		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0000544	OMIM:160565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0000615	OMIM:160565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0000662	OMIM:160565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0001371	OMIM:160565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0002093	OMIM:160565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0002359	OMIM:160565	TAS				P		HPO:skoehler	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0002522	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0002600	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003198	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003236	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003388	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003394	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003552	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003554	OMIM:160565	TAS				P		HPO:skoehler	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003557	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003581	OMIM:160565	TAS				C		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003677	OMIM:160565	TAS				C		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003701	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0003738	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0007126	OMIM:160565	TAS				P		HPO:skoehler	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0009005	OMIM:160565	TAS				P		HPO:probinson	
OMIM	160565	#160565 MYOPATHY, TUBULAR AGGREGATE, 1; TAM1;;MYOPATHY, TUBULAR AGGREGATE; TAM;;TUBULAR AGGREGATE MYOPATHY		HP:0009046	OMIM:160565	TAS				P		HPO:skoehler	
OMIM	160570	MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS		HP:0000006	OMIM:160570	IEA				I		HPO:iea	
OMIM	160570	MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS		HP:0003198	OMIM:160570	TAS				P		HPO:skoehler	
OMIM	160570	MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS		HP:0003236	OMIM:160570	TAS				P		HPO:iea	
OMIM	160570	MYOPATHY WITH STORAGE OF GLYCOPROTEINS AND GLYCOSAMINOGLYCANS		HP:0008970	OMIM:160570	IEA				P		HPO:skoehler	
OMIM	160700	%160700 MYOPIA 2, AUTOSOMAL DOMINANT; MYP2		HP:0000006	OMIM:160700	TAS				I		HPO:skoehler	
OMIM	160700	%160700 MYOPIA 2, AUTOSOMAL DOMINANT; MYP2		HP:0000541	OMIM:160700	IEA				P		HPO:iea	
OMIM	160700	%160700 MYOPIA 2, AUTOSOMAL DOMINANT; MYP2		HP:0000707	OMIM:160700	IEA				P		HPO:iea	
OMIM	160700	%160700 MYOPIA 2, AUTOSOMAL DOMINANT; MYP2		HP:0011003	OMIM:160700	IEA				P		HPO:iea	
OMIM	160750	MYOSITIS		HP:0000006	OMIM:160750	TAS				I		HPO:probinson	
OMIM	160750	MYOSITIS		HP:0003701	OMIM:160750	TAS				P		HPO:probinson	
OMIM	160750	MYOSITIS		HP:0100614	OMIM:160750	TAS				P		HPO:probinson	
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:160800	TAS				I		HPO:probinson	
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0003326	OMIM:160800	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0003552	PMID:18337100	PCS		HP:0040284		P		HPO:probinson	7/9
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0003712	OMIM:160800	PCS		HP:0040284		P		HPO:probinson	7/9
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0003730	OMIM:160800	PCS				P		HPO:probinson	
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0003740	PMID:18337100	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0010548	PMID:18337100	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0012899	OMIM:160800	TAS				P		HPO:skoehler	
OMIM	160800	MYOTONIA CONGENITA, AUTOSOMAL DOMINANT		HP:0025605	OMIM:160800	IEA				P		HPO:skoehler	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0000006	OMIM:160900	IEA				I		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0000029	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0000135	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0000518	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001081	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001252	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001290	OMIM:160900	TAS				P		HPO:skoehler	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001324	OMIM:160900	TAS				P		HPO:probinson	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001349	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001558	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0001561	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002015	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002059	OMIM:160900	TAS				P		HPO:skoehler	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002098	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002189	OMIM:160900	TAS				P		HPO:skoehler	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002292	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0002486	OMIM:160900	TAS				P		HPO:probinson	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0004749	PMID:15557517	PCS		HP:0040284		P		HPO:probinson	4/11
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0005110	PMID:15557517	PCS		HP:0040284		P		HPO:probinson	1/11
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0006887	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0008770	OMIM:160900	IEA				P		HPO:iea	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0008872	OMIM:160900	PCS				P		HPO:probinson	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0010864	OMIM:160900	TAS	HP:0003577			P		HPO:skoehler	
OMIM	160900	MYOTONIC DYSTROPHY 1		HP:0011705	OMIM:160900	PCS				P		HPO:probinson	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0000006	OMIM:160980	IEA				I		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0000478	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0000845	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0001007	OMIM:160980	TAS				P		HPO:skoehler	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0001425	OMIM:160980	TAS				I		HPO:skoehler	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0001480	OMIM:160980	TAS				P		HPO:skoehler	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0001635	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0002297	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0002666	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0002890	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0002893	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0003764	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0005587	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0006769	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0008225	OMIM:160980	IEA				P		HPO:iea	
OMIM	160980	CARNEY COMPLEX, TYPE 1; CNC1		HP:0100008	OMIM:160980	TAS				P		HPO:skoehler	
OMIM	160990	MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS		HP:0000006	OMIM:160990	IEA				I		HPO:iea	
OMIM	160990	MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS		HP:0001939	OMIM:160990	IEA				P		HPO:iea	
OMIM	160990	MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS		HP:0003394	OMIM:160990	IEA				P		HPO:iea	
OMIM	160990	MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS		HP:0003552	OMIM:160990	IEA				P		HPO:iea	
OMIM	160990	MYOTONIC MYOPATHY WITH CYLINDRICAL SPIRALS		HP:0010548	OMIM:160990	IEA				P		HPO:skoehler	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0000006	OMIM:161000	IEA				I		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0000670	OMIM:161000	IEA				P		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0000966	OMIM:161000	IEA				P		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0000982	OMIM:161000	IEA				P		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0001808	OMIM:161000	IEA				P		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0002046	OMIM:161000	TAS				P		HPO:skoehler	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0006480	OMIM:161000	IEA				P		HPO:iea	
OMIM	161000	#161000 NAEGELI SYNDROME;;NAEGELI-FRANCESCHETTI-JADASSOHN SYNDROME;;NFJ SYNDROME; NFJS		HP:0007588	OMIM:161000	IEA				P		HPO:iea	
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0000006	OMIM:161050	IEA				I		HPO:iea	
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0001805	OMIM:161050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0001806	OMIM:161050	IEA				P		HPO:skoehler	
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0001816	OMIM:161050	TAS				P		HPO:skoehler	
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0003677	OMIM:161050	TAS				C		HPO:skoehler	
OMIM	161050	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 1; NDNC1		HP:0030804	OMIM:161050	IEA				P		HPO:skoehler	
OMIM	161070	NAIL HIGH-SULFUR PROTEIN		HP:0000006	OMIM:161070	IEA				I		HPO:iea	
OMIM	161070	NAIL HIGH-SULFUR PROTEIN		HP:0001597	OMIM:161070	IEA				P		HPO:iea	
OMIM	161080	NAIL LOW-SULFUR PROTEIN		HP:0000006	OMIM:161080	IEA				I		HPO:iea	
OMIM	161080	NAIL LOW-SULFUR PROTEIN		HP:0001597	OMIM:161080	IEA				P		HPO:iea	
OMIM	161100	NAILBEDS, PIGMENTATION OF		HP:0000006	OMIM:161100	IEA				I		HPO:iea	
OMIM	161100	NAILBEDS, PIGMENTATION OF		HP:0001597	OMIM:161100	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000006	OMIM:161200	IEA				I		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000083	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000093	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000099	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000100	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000175	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000204	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000407	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000482	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000501	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000508	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000518	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000563	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000767	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0000790	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001032	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001377	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001598	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001762	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001763	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001798	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0001807	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0002414	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0002650	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0002938	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0002999	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0003997	OMIM:161200	TAS				P		HPO:probinson	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0004209	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0004322	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0005255	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006424	OMIM:161200	TAS				P		HPO:probinson	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006437	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006443	OMIM:161200	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006633	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006650	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0006657	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009760	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009780	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009781	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009783	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009785	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0009788	OMIM:161200	IEA				P		HPO:iea	
OMIM	161200	#161200 NAIL-PATELLA SYNDROME; NPS;;NPS1;;ONYCHOOSTEODYSPLASIA;;TURNER-KIESER SYNDROME;;FONG DISEASE		HP:0012376	OMIM:161200	TAS				P		HPO:skoehler	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0000006	OMIM:161400	IEA				I		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0001425	OMIM:161400	TAS				I		HPO:skoehler	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0002189	OMIM:161400	IEA				P		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0002330	OMIM:161400	IEA				P		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0002494	OMIM:161400	IEA				P		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0002519	OMIM:161400	IEA				P		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0002524	OMIM:161400	TAS				P		HPO:probinson	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0006896	OMIM:161400	IEA				P		HPO:iea	
OMIM	161400	NARCOLEPSY 1; NRCLP1		HP:0030050	OMIM:161400	TAS				P		HPO:skoehler	
OMIM	161470	NASAL ALAR COLLAPSE, BILATERAL		HP:0000006	OMIM:161470	IEA				I		HPO:iea	
OMIM	161470	NASAL ALAR COLLAPSE, BILATERAL		HP:0000271	OMIM:161470	IEA				P		HPO:iea	
OMIM	161480	NASAL BONES, ABSENCE OF		HP:0000006	OMIM:161480	IEA				I		HPO:iea	
OMIM	161480	NASAL BONES, ABSENCE OF		HP:0000271	OMIM:161480	IEA				P		HPO:iea	
OMIM	161480	NASAL BONES, ABSENCE OF		HP:0002000	OMIM:161480	TAS				P		HPO:skoehler	
OMIM	161480	NASAL BONES, ABSENCE OF		HP:0009933	OMIM:161480	TAS				P		HPO:skoehler	
OMIM	161500	NASAL GROOVE, FAMILIAL TRANSVERSE		HP:0000006	OMIM:161500	IEA				I		HPO:iea	
OMIM	161500	NASAL GROOVE, FAMILIAL TRANSVERSE		HP:0000271	OMIM:161500	IEA				P		HPO:iea	
OMIM	161530	NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE		HP:0000006	OMIM:161530	IEA				I		HPO:iea	
OMIM	161530	NASAL HYPERPIGMENTATION, FAMILIAL TRANSVERSE		HP:0000953	OMIM:161530	TAS				P		HPO:probinson	
OMIM	161550	NASOPHARYNGEAL CARCINOMA		HP:0002664	OMIM:161550	IEA				P		HPO:iea	
OMIM	161600	NAVICULAR BONE, ACCESSORY		HP:0000006	OMIM:161600	IEA				I		HPO:iea	
OMIM	161600	NAVICULAR BONE, ACCESSORY		HP:0001763	PMID:10668560	PCS				P		HPO:lccarmody	
OMIM	161600	NAVICULAR BONE, ACCESSORY		HP:0100339	PMID:13437469	PCS				P		HPO:lccarmody	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0000006	OMIM:161700	IEA				I		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0000280	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0000508	OMIM:161700	IEA				P		HPO:skoehler	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0000975	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0001217	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0001369	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0001626	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0001805	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0001842	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0002592	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0002653	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0002829	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0005207	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0006051	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0006175	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0006465	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0008074	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0009771	OMIM:161700	IEA				P		HPO:iea	
OMIM	161700	NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT		HP:0010541	OMIM:161700	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0000006	OMIM:161800	IEA				I		HPO:iea	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0000007	OMIM:161800	TAS				I		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0000218	OMIM:161800	TAS				P		HPO:iea	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0000278	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0000298	OMIM:161800	TAS				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001265	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001270	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001276	OMIM:161800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001283	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001284	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001319	OMIM:161800	IEA				P		HPO:iea	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001347	OMIM:161800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001425	OMIM:161800	IEA				I		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001533	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001558	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001561	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001644	OMIM:161800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0001761	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002015	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002058	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002063	OMIM:161800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002359	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002515	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002650	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002747	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0002804	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003306	OMIM:161800	TAS				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003307	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003324	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003445	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003458	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003690	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003701	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003722	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003798	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003803	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0003810	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0008180	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0008872	OMIM:161800	IEA				P		HPO:skoehler	
OMIM	161800	NEMALINE MYOPATHY 3; NEM3		HP:0010628	OMIM:161800	TAS				P		HPO:skoehler	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0000006	OMIM:161900	IEA				I		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0000083	OMIM:161900	IEA				P		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0000093	OMIM:161900	IEA				P		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0000123	OMIM:161900	IEA				P		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0000822	OMIM:161900	IEA				P		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0002907	OMIM:161900	IEA				P		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0003259	OMIM:161900	TAS				P		HPO:skoehler	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0003581	OMIM:161900	IEA				C		HPO:iea	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0003676	OMIM:161900	TAS				C		HPO:skoehler	
OMIM	161900	%161900 RENAL FAILURE, PROGRESSIVE, WITH HYPERTENSION; RFH1;;NEPHROPATHY, FAMILIAL;;NEPHRITIS, FAMILIAL, WITHOUT DEAFNESS OR OCULAR DEFECT;;RENAL FAILURE, ADULT-ONSET; AORF		HP:0003774	OMIM:161900	TAS				P		HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000006	OMIM:161950	TAS				I	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000093	OMIM:161950	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000123	OMIM:161950	IEA				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000790	OMIM:161950	IEA				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000794	OMIM:161950	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000822	OMIM:161950	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0000979	OMIM:161950	IEA				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0001425	OMIM:161950	IEA				I	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:iea	
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0002829	OMIM:161950	TAS		HP:0040283		P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	HP:0040283
OMIM	161950	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1		HP:0003774	OMIM:161950	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 1; IGAN1	HPO:skoehler	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0000006	OMIM:162000	IEA				I		HPO:iea	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0000083	OMIM:162000	IEA				P		HPO:iea	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0000092	OMIM:162000	TAS				P		HPO:skoehler	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0000112	OMIM:162000	IEA				P		HPO:iea	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0000123	OMIM:162000	IEA				P		HPO:skoehler	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0001997	OMIM:162000	IEA				P		HPO:iea	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0003621	OMIM:162000	IEA				C		HPO:iea	
OMIM	162000	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1; HNFJ1		HP:0003676	OMIM:162000	TAS				C		HPO:skoehler	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0000006	OMIM:162091	IEA				I		HPO:iea	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0000925	OMIM:162091	IEA				P		HPO:iea	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0000951	OMIM:162091	IEA				P		HPO:iea	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0001428	OMIM:162091	TAS				I		HPO:skoehler	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0002858	OMIM:162091	TAS				P		HPO:skoehler	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0003828	OMIM:162091	IEA				C		HPO:iea	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0003829	OMIM:162091	IEA				C		HPO:iea	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0010302	OMIM:162091	IEA				P		HPO:skoehler	
OMIM	162091	#162091 SCHWANNOMATOSIS;;NEURILEMMOMATOSIS, CONGENITAL CUTANEOUS		HP:0100008	OMIM:162091	TAS				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000006	OMIM:162100	IEA				I		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000160	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000175	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000286	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000324	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000369	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000490	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000508	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000581	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000582	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000601	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0000764	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0001265	OMIM:162100	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0001324	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0003202	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0004322	OMIM:162100	IEA				P		HPO:iea	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0005280	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0009830	OMIM:162100	IEA				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0040078	OMIM:162100	TAS				P		HPO:skoehler	
OMIM	162100	#162100 AMYOTROPHY, HEREDITARY NEURALGIC; HNA;;NEURITIS WITH BRACHIAL PREDILECTION; NAPB;;BRACHIAL PLEXUS NEUROPATHY, HEREDITARY;;AMYOTROPHY, HEREDITARY NEURALGIC, WITH PREDILECTION FOR BRACHIAL PLEXUS		HP:0045054	OMIM:162100	TAS				P		HPO:skoehler	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000006	PMID:10204844	PCS				I		HPO:probinson	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000238	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000256	PMID:12151887	PCS		HP:0040284		P		HPO:iea	25%
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000316	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000501	PMID:22138687	PCS				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000767	PMID:29618358	PCS		HP:0040284		P		HPO:probinson	2/112
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000822	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0000997	PMID:10204844	PCS		HP:0040284		P		HPO:iea	310/370
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0001250	PMID:29566708	PCS		HP:0040284		P		HPO:probinson	19/437
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0001256	OMIM:162200	IEA				P		HPO:skoehler	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0001328	PMID:10204844	PCS		HP:0040284		P		HPO:iea	186/300
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0001548	OMIM:162200	IEA				P		HPO:skoehler	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0001920	PMID:10204844	PCS		HP:0040284		P		HPO:iea	3/523
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002410	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002414	OMIM:162200	IEA		HP:0040284		P		HPO:iea	151/357
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002521	PMID:18802710	PCS				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002650	PMID:12151887	PCS		HP:0040284		P		HPO:iea	20%
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002666	PMID:25130111	PCS		HP:0040284		P		HPO:iea	1%
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002857	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002858	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002859	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0002897	OMIM:162200	IEA				P		HPO:iea	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0004322	PMID:12151887	PCS		HP:0040284		P		HPO:iea	30%
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0007565	PMID:10204844	PCS		HP:0040284		P		HPO:iea	383/442
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009592	OMIM:162200	IEA				P		HPO:skoehler	
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009732	PMID:23035791	PCS		HP:0040284		P		HPO:iea	71/171
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009734	PMID:10204844	PCS		HP:0040284		P		HPO:iea	25/300
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009735	PMID:10204844	PCS		HP:0040284		P		HPO:iea	11/300
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009736	PMID:10204844	PCS		HP:0040284		P		HPO:iea	10/300
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0009737	PMID:10204844	PCS		HP:0040284		P		HPO:iea	157/249
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0030052	PMID:10204844	PCS	HP:0011463	HP:0040284		P		HPO:skoehler	151/357
OMIM	162200	NEUROFIBROMATOSIS, TYPE I		HP:0100697	OMIM:162200	PCS				P		HPO:skoehler	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0000006	OMIM:162210	IEA				I		HPO:iea	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0000957	OMIM:162210	IEA				P		HPO:iea	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0001480	OMIM:162210	IEA				P		HPO:skoehler	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0002385	OMIM:162210	TAS				P		HPO:probinson	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0006851	OMIM:162210	IEA				P		HPO:iea	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0007340	OMIM:162210	TAS				P		HPO:skoehler	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0009737	OMIM:162210	IEA				P		HPO:skoehler	
OMIM	162210	#162210 NEUROFIBROMATOSIS, FAMILIAL SPINAL;;FSNF		HP:0010302	OMIM:162210	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	162240	NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME		HP:0000006	OMIM:162240	IEA				I		HPO:iea	
OMIM	162240	NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME		HP:0000952	OMIM:162240	IEA				P		HPO:skoehler	
OMIM	162240	NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME		HP:0001067	OMIM:162240	IEA				P		HPO:iea	
OMIM	162240	NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME		HP:0002666	OMIM:162240	IEA				P		HPO:iea	
OMIM	162240	NEUROFIBROMATOSIS-PHEOCHROMOCYTOMA-DUODENAL CARCINOID SYNDROME		HP:0100570	OMIM:162240	IEA				P		HPO:skoehler	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0000006	OMIM:162260	IEA				I		HPO:iea	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0002858	OMIM:162260	IEA				P		HPO:iea	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0006751	OMIM:162260	IEA				P		HPO:iea	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0007429	OMIM:162260	IEA				P		HPO:iea	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0007576	OMIM:162260	IEA				P		HPO:iea	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0009589	OMIM:162260	IEA				P		HPO:skoehler	
OMIM	162260	NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL		HP:0009737	OMIM:162260	IEA				P		HPO:skoehler	
OMIM	162270	NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI		HP:0000006	OMIM:162270	IEA				I		HPO:iea	
OMIM	162270	NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI		HP:0001425	OMIM:162270	IEA				I		HPO:iea	
OMIM	162270	NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI		HP:0007524	OMIM:162270	IEA				P		HPO:iea	
OMIM	162270	NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI		HP:0009737	OMIM:162270	IEA				P		HPO:skoehler	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000006	OMIM:162300	IEA				I		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000179	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000218	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000574	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000767	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0000951	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001252	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001263	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001290	OMIM:162300	TAS				P		HPO:skoehler	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001388	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001519	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001531	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0001761	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002014	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002019	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002251	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002253	OMIM:162300	TAS				P		HPO:skoehler	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002650	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002666	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002705	OMIM:162300	TAS				P		HPO:skoehler	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002808	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0002865	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0003005	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0003198	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0003307	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0003528	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0003639	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0005994	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0006461	OMIM:162300	IEA				P		HPO:iea	
OMIM	162300	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB		HP:0008208	OMIM:162300	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0000006	OMIM:162350	IEA				I		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0000716	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0000726	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0001250	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0001251	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0001300	OMIM:162350	IEA				P		HPO:skoehler	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0001317	OMIM:162350	IEA				P		HPO:skoehler	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0001336	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0002074	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0002367	OMIM:162350	TAS				P		HPO:probinson	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003205	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003208	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003226	OMIM:162350	IEA				P		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003581	OMIM:162350	IEA				C		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003657	OMIM:162350	IEA				P		HPO:skoehler	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0003678	OMIM:162350	IEA				C		HPO:iea	
OMIM	162350	CEROID LIPOFUSCINOSIS, NEURONAL, 4B, AUTOSOMAL DOMINANT; CLN4B		HP:0008765	OMIM:162350	TAS				P		HPO:probinson	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0000006	OMIM:162370	IEA				I		HPO:iea	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0001257	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0001848	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0002136	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0002460	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0002522	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0002600	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0002804	OMIM:162370	IEA				P		HPO:iea	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003307	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003487	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003577	OMIM:162370	TAS				C		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003680	OMIM:162370	TAS				C		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003693	OMIM:162370	TAS				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0003701	OMIM:162370	IEA				P		HPO:skoehler	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0006903	OMIM:162370	IEA				P		HPO:iea	
OMIM	162370	NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX		HP:0031936	OMIM:162370	IEA				P		HPO:skoehler	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0001284	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0002127	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0002270	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0002460	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0003487	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0003693	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0007141	OMIM:162380	TAS				P		HPO:probinson	
OMIM	162380	NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE		HP:0009063	OMIM:162380	IEA				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0000006	OMIM:162400	IEA				I		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0000407	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0000951	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0001265	OMIM:162400	IEA				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0001284	OMIM:162400	IEA				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0001761	OMIM:162400	TAS				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0001868	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0001886	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0002460	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0002936	OMIM:162400	IEA				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0003202	OMIM:162400	IEA				P		HPO:skoehler	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0003387	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0003448	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0006984	OMIM:162400	IEA				P		HPO:iea	
OMIM	162400	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A		HP:0007267	OMIM:162400	IEA				P		HPO:iea	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0000006	OMIM:162500	IEA				I		HPO:iea	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0001265	OMIM:162500	IEA				P		HPO:iea	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0001324	OMIM:162500	IEA				P		HPO:skoehler	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0001605	OMIM:162500	IEA				P		HPO:skoehler	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0003431	OMIM:162500	IEA				P		HPO:skoehler	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0003481	OMIM:162500	IEA				P		HPO:iea	
OMIM	162500	NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP		HP:0009830	OMIM:162500	IEA				P		HPO:skoehler	
OMIM	162600	NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE		HP:0000006	OMIM:16200	PCS				I		HPO:probinson	
OMIM	162600	NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE		HP:0000762	OMIM:16200	PCS				P		HPO:probinson	
OMIM	162600	NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE		HP:0009830	OMIM:162600	IEA				P		HPO:skoehler	
OMIM	162600	NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE		HP:0011096	OMIM:16200	PCS				P		HPO:probinson	
OMIM	162600	NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE		HP:0031003	OMIM:162600	IEA				P		HPO:skoehler	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0000006	OMIM:162700	TAS				I		HPO:skoehler	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0000230	OMIM:162700	IEA				P		HPO:skoehler	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0000704	OMIM:162700	IEA				P		HPO:iea	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0001217	OMIM:162700	IEA				P		HPO:iea	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0001875	OMIM:162700	IEA				P		HPO:iea	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0006480	OMIM:162700	IEA				P		HPO:iea	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0010702	OMIM:162700	IEA				P		HPO:iea	
OMIM	162700	%162700 NEUTROPENIA, CHRONIC FAMILIAL;;LEUKOPENIA, BENIGN FAMILIAL		HP:0100759	OMIM:162700	TAS				P		HPO:skoehler	
OMIM	162800	CYCLIC NEUTROPENIA		HP:0000006	OMIM:162800	IEA				I		HPO:iea	
OMIM	162800	CYCLIC NEUTROPENIA		HP:0000153	OMIM:162800	IEA				P		HPO:iea	
OMIM	162800	CYCLIC NEUTROPENIA		HP:0001875	OMIM:162800	IEA				P		HPO:skoehler	
OMIM	162800	CYCLIC NEUTROPENIA		HP:0001945	OMIM:162800	IEA				P		HPO:skoehler	
OMIM	162800	CYCLIC NEUTROPENIA		HP:0040289	OMIM:162800	TAS				P		HPO:skoehler	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0000006	OMIM:162820	IEA				I		HPO:iea	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0000964	PMID:865918	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0001581	PMID:865918	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0001881	PMID:4718002	PCS				P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0002099	PMID:865918	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0002718	PMID:865918	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0002721	OMIM:162820	IEA				P		HPO:iea	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0002841	PMID:4718002	PCS				P		HPO:lccarmody	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0007431	OMIM:162820	IEA				P		HPO:iea	
OMIM	162820	NEUTROPHIL CHEMOTACTIC RESPONSE		HP:0007431	PMID:4718002	PCS				P		HPO:lccarmody	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0000006	OMIM:162830	IEA				I		HPO:iea	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0001433	OMIM:162830	IEA				P		HPO:iea	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0002684	OMIM:162830	IEA				P		HPO:iea	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0002863	OMIM:162830	IEA				P		HPO:skoehler	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0008318	OMIM:162830	IEA				P		HPO:iea	
OMIM	162830	NEUTROPHILIA, HEREDITARY		HP:0011897	OMIM:162830	TAS				P		HPO:skoehler	
OMIM	162900	NEVUS, KERATINOCYTIC, NONEPIDERMOLYTIC		HP:0000006	OMIM:162900	IEA				I		HPO:iea	
OMIM	162900	NEVUS, KERATINOCYTIC, NONEPIDERMOLYTIC		HP:0000995	OMIM:162900	IEA				P		HPO:skoehler	
OMIM	162900	NEVUS, KERATINOCYTIC, NONEPIDERMOLYTIC		HP:0001054	OMIM:162900	IEA				P		HPO:skoehler	
OMIM	163000	NEVI FLAMMEI, FAMILIAL MULTIPLE		HP:0000006	OMIM:163000	IEA				I		HPO:iea	
OMIM	163000	NEVI FLAMMEI, FAMILIAL MULTIPLE		HP:0001052	OMIM:163000	IEA				P		HPO:skoehler	
OMIM	163050	NEVUS ANEMICUS		HP:0000006	OMIM:163050	IEA				I		HPO:iea	
OMIM	163050	NEVUS ANEMICUS		HP:0003764	OMIM:163050	IEA				P		HPO:skoehler	
OMIM	163050	NEVUS ANEMICUS		HP:0025105	OMIM:163050	TAS				P		HPO:skoehler	
OMIM	163100	NEVUS FLAMMEUS OF NAPE OF NECK		HP:0000006	OMIM:163100	IEA				I		HPO:iea	
OMIM	163100	NEVUS FLAMMEUS OF NAPE OF NECK		HP:0007616	OMIM:163100	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000085	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000267	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000589	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000602	OMIM:163200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000826	OMIM:163200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0000938	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001010	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001028	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001167	OMIM:163200	TAS				P		HPO:probinson	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001249	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001250	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001442	OMIM:163200	TAS				I		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001528	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001548	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001596	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001680	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0001780	OMIM:163200	TAS				P		HPO:probinson	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0002671	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0002751	OMIM:163200	IEA				P		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0002757	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0003109	OMIM:163200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0003745	OMIM:163200	IEA				I		HPO:iea	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0004322	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0004912	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0006482	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0007206	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0007957	OMIM:163200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0008064	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0010815	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0010817	OMIM:163200	IEA				P		HPO:skoehler	
OMIM	163200	SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM		HP:0011073	OMIM:163200	TAS				P		HPO:skoehler	
OMIM	163400	NIEVERGELT SYNDROME		HP:0000006	OMIM:163400	IEA				I		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0001440	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0001548	OMIM:163400	IEA				P		HPO:skoehler	
OMIM	163400	NIEVERGELT SYNDROME		HP:0001762	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0002857	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0002974	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0003027	OMIM:163400	IEA				P		HPO:skoehler	
OMIM	163400	NIEVERGELT SYNDROME		HP:0003048	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0008368	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0008845	OMIM:163400	IEA				P		HPO:iea	
OMIM	163400	NIEVERGELT SYNDROME		HP:0010781	OMIM:163400	IEA				P		HPO:skoehler	
OMIM	163500	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2		HP:0000006	OMIM:163500	TAS				I		HPO:probinson	
OMIM	163500	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2		HP:0007642	OMIM:163500	TAS				P		HPO:probinson	
OMIM	163600	NIPPLES INVERTED		HP:0000006	OMIM:163600	IEA				I		HPO:iea	
OMIM	163600	NIPPLES INVERTED		HP:0003186	OMIM:163600	IEA				P		HPO:iea	
OMIM	163700	NIPPLES, SUPERNUMERARY		HP:0000006	OMIM:163700	IEA				I		HPO:iea	
OMIM	163700	NIPPLES, SUPERNUMERARY		HP:0000077	OMIM:163700	IEA				P		HPO:iea	
OMIM	163700	NIPPLES, SUPERNUMERARY		HP:0000765	OMIM:163700	IEA				P		HPO:iea	
OMIM	163700	NIPPLES, SUPERNUMERARY		HP:0002558	OMIM:163700	IEA				P		HPO:iea	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0000006	OMIM:163800	IEA				I		HPO:iea	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001634	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001659	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001663	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001688	OMIM:163800	IEA				P		HPO:iea	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001695	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163800	SICK SINUS SYNDROME 2		HP:0001712	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163800	SICK SINUS SYNDROME 2		HP:0003577	OMIM:163800	IEA				C		HPO:iea	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0005110	OMIM:163800	IEA				P		HPO:iea	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0011704	OMIM:163800	IEA				P		HPO:skoehler	
OMIM	163800	SICK SINUS SYNDROME 2		HP:0030682	OMIM:163800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163850	NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES		HP:0000006	OMIM:163850	IEA				I		HPO:iea	
OMIM	163850	NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES		HP:0000081	OMIM:163850	IEA				P		HPO:iea	
OMIM	163850	NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES		HP:0000126	OMIM:163850	IEA				P		HPO:iea	
OMIM	163850	NODULI CUTANEI, MULTIPLE, WITH URINARY TRACT ABNORMALITIES		HP:0000951	OMIM:163850	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000006	OMIM:163950	IEA				I		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000028	OMIM:163950	TAS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000135	OMIM:163950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000218	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000286	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000316	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000325	OMIM:163950	PCS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000347	OMIM:163950	PCS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000368	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000407	OMIM:163950	PCS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000465	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000470	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000476	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000494	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000508	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000545	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000689	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000914	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000915	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000917	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0000925	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001004	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001156	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001249	OMIM:163950	PCS		HP:0040284		P		HPO:probinson	25%
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001425	OMIM:163950	TAS				I		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001531	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001629	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001631	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001639	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001642	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001643	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001680	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0001892	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0002162	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0002664	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0002705	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0002751	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0002967	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0003251	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0004322	OMIM:163950	TAS	HP:0003593			P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0004841	OMIM:163950	IEA				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0004859	OMIM:163950	IEA				P		HPO:iea	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0008357	OMIM:163950	TAS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0008897	OMIM:163950	PCS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0009466	OMIM:163950	PCS				P		HPO:probinson	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0030084	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0100697	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	163950	#163950 NOONAN SYNDROME 1; NS1;;NOONAN SYNDROME;;MALE TURNER SYNDROME;;FEMALE PSEUDO-TURNER SYNDROME;;TURNER PHENOTYPE WITH NORMAL KARYOTYPEPTERYGIUM COLLI SYNDROME, INCLUDED		HP:0100769	OMIM:163950	TAS				P		HPO:skoehler	
OMIM	164000	NOSE, ANOMALOUS SHAPE OF		HP:0000006	OMIM:164000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	164000	NOSE, ANOMALOUS SHAPE OF		HP:0000414	OMIM:164000	TAS				P		HPO:skoehler	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0000006	OMIM:164100	IEA				I		HPO:iea	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0000486	OMIM:164100	PCS				P		HPO:probinson	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2	HP:0012825	HP:0000505	OMIM:164100	PCS				P		HPO:probinson	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2	HP:0012825	HP:0000666	OMIM:164100	PCS				P		HPO:probinson	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0001425	OMIM:164100	TAS				I		HPO:skoehler	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0003593	OMIM:164100	TAS				C		HPO:skoehler	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0007663	OMIM:164100	TAS				P		HPO:skoehler	
OMIM	164100	NYSTAGMUS 2, CONGENITAL, AUTOSOMAL DOMINANT; NYS2		HP:0032037	OMIM:164100	IEA				P		HPO:skoehler	
OMIM	164150	NYSTAGMUS, HEREDITARY VERTICAL		HP:0000006	OMIM:164150	TAS				I		HPO:probinson	
OMIM	164150	NYSTAGMUS, HEREDITARY VERTICAL	HP:0012825	HP:0001251	OMIM:164150	TAS				P		HPO:skoehler	
OMIM	164150	NYSTAGMUS, HEREDITARY VERTICAL		HP:0007670	OMIM:164150	TAS				P		HPO:probinson	
OMIM	164150	NYSTAGMUS, HEREDITARY VERTICAL		HP:0010544	OMIM:164150	TAS				P		HPO:skoehler	
OMIM	164170	NYSTAGMUS, VOLUNTARY		HP:0000006	OMIM:164170	IEA				I		HPO:iea	
OMIM	164170	NYSTAGMUS, VOLUNTARY		HP:0000639	OMIM:164170	TAS				P		HPO:probinson	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000028	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000175	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000324	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000528	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000568	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000625	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000639	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0000765	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001144	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001249	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001250	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001274	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001305	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001374	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0001596	OMIM:164180	IEA				P		HPO:skoehler	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0002079	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0002282	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0003191	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0003745	OMIM:164180	IEA				I		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0007115	OMIM:164180	IEA				P		HPO:iea	
OMIM	164180	OCULOCEREBROCUTANEOUS SYNDROME		HP:0007510	OMIM:164180	IEA				P		HPO:iea	
OMIM	164185	OCULAR CICATRICIAL PEMPHIGOID		HP:0000006	OMIM:164185	IEA				I		HPO:iea	
OMIM	164185	OCULAR CICATRICIAL PEMPHIGOID		HP:0000478	OMIM:164185	IEA				P		HPO:iea	
OMIM	164190	OCULAR DOMINANCE		HP:0000006	OMIM:164190	IEA				I		HPO:iea	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000006	OMIM:164200	IEA				I		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000011	OMIM:164200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000011	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000175	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000187	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000204	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000252	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000286	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000377	OMIM:164200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000405	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000430	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000446	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000482	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000501	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000518	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000568	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000581	OMIM:164200	TAS				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000670	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000679	OMIM:164200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0000691	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001249	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001250	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001251	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001257	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001260	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001592	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001631	OMIM:164200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0001808	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002135	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002213	OMIM:164200	IEA				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002217	OMIM:164200	TAS				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002273	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002385	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002500	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002827	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0002967	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0004220	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0004495	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0006297	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0006480	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0006801	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0008070	OMIM:164200	PCS				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0008442	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0009183	OMIM:164200	IEA				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0009765	OMIM:164200	IEA				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0009779	OMIM:164200	TAS				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0010705	OMIM:164200	TAS				P		HPO:probinson	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0011359	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0011675	OMIM:164200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0012745	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164200	OCULODENTODIGITAL DYSPLASIA; ODDD		HP:0030084	OMIM:164200	TAS				P		HPO:skoehler	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000003	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000006	OMIM:164210	IEA				I		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000074	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000076	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000086	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000104	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000154	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000175	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000204	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000238	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000272	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000324	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000327	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000347	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000384	OMIM:164210	TAS				P		HPO:probinson	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000405	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000407	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000413	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000486	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000528	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000568	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000581	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0000636	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001140	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001249	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001274	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001629	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001636	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001643	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0001680	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0002085	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0002089	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0002308	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0002937	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0003305	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0004660	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0008417	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0008551	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0008605	OMIM:164210	IEA				P		HPO:iea	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0009794	OMIM:164210	TAS				P		HPO:probinson	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0009892	OMIM:164210	IEA				P		HPO:skoehler	
OMIM	164210	HEMIFACIAL MICROSOMIA		HP:0011332	OMIM:164210	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000006	OMIM:164220	IEA				I		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000047	OMIM:164220	IEA				P		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000160	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000176	OMIM:164220	IEA				P		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000193	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000252	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000286	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000347	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000358	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000448	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000581	OMIM:164220	IEA				P		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000582	OMIM:164220	IEA				P		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0000601	OMIM:164220	IEA				P		HPO:iea	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0001256	OMIM:164220	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0003189	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0004322	OMIM:164220	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0005709	OMIM:164220	TAS				P		HPO:probinson	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0007018	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0008551	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0011939	OMIM:164220	TAS				P		HPO:probinson	
OMIM	164220	%164220 SCHILBACH-ROTT SYNDROME;;OCULAR HYPOTELORISM, SUBMUCOSAL CLEFT PALATE, AND HYPOSPADIAS;;CLEFT PALATE, HYPOTELORISM, AND HYPOSPADIAS;;BLEPHAROFACIOSKELETAL SYNDROME; BRSS		HP:0030084	OMIM:164220	TAS				P		HPO:skoehler	
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0000006	OMIM:164230	TAS				I		HPO:skoehler	
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0000716	PMID:15820710	PCS				P		HPO:lccarmody	
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0000722	OMIM:164230	IEA		HP:0040284		P		HPO:iea	HP:0040284
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0000739	PMID:15820710	PCS				P		HPO:lccarmody	
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0012166	PMID:15820710	PCS				P		HPO:lccarmody	
OMIM	164230	OBSESSIVE-COMPULSIVE DISORDER 1		HP:0030212	PMID:15820710	PCS				P		HPO:lccarmody	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000006	OMIM:164280	IEA				I		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000218	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000232	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000237	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000252	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000269	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000286	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000324	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000325	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000347	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000358	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000365	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000369	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000431	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000437	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000463	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000581	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0000582	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001249	OMIM:164280	TAS				P		HPO:skoehler	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001328	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001558	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001561	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001605	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001643	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001734	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001746	OMIM:164280	TAS	HP:0003577			P		HPO:skoehler	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001747	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001748	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0001831	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0002032	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0002247	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0002575	OMIM:164280	IEA				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0004691	OMIM:164280	TAS		HP:0040284		P		HPO:probinson	56%
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0004692	OMIM:164280	TAS		HP:0040284		P		HPO:probinson	86%
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0009161	OMIM:164280	TAS				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0009568	OMIM:164280	TAS				P		HPO:iea	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0012471	OMIM:164280	TAS				P		HPO:skoehler	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0012745	OMIM:164280	TAS				P		HPO:skoehler	
OMIM	164280	FEINGOLD SYNDROME 1; FGLDS1		HP:0045025	OMIM:164280	IEA				P		HPO:skoehler	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0000006	OMIM:164300	IEA				I		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0000298	OMIM:164300	TAS				P		HPO:skoehler	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0000467	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0001260	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0001288	OMIM:164300	TAS	HP:0003584			P		HPO:probinson	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0002015	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0002460	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0003581	OMIM:164300	TAS				C		HPO:probinson	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0003676	OMIM:164300	IEA				C		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0003690	OMIM:164300	IEA				P		HPO:skoehler	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0003701	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0007838	OMIM:164300	IEA				P		HPO:iea	
OMIM	164300	#164300 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD;;MUSCULAR DYSTROPHY, OCULOPHARYNGEAL		HP:0010628	OMIM:164300	IEA				P		HPO:iea	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000006	OMIM:164310	TAS				I		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000007	OMIM:164310	TAS				I		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000218	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000407	OMIM:164310	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000508	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0000544	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0001260	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0001284	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0001611	OMIM:164310	TAS				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002015	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002058	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002091	OMIM:164310	TAS				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002355	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002460	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002747	OMIM:164310	TAS				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0002835	OMIM:164310	IEA				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003236	OMIM:164310	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003458	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003557	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003677	OMIM:164310	TAS				C		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003693	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003701	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003736	OMIM:164310	IEA				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0003805	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0008756	OMIM:164310	TAS				P		HPO:skoehler	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0009027	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164310	OCULOPHARYNGODISTAL MYOPATHY; OPDM		HP:0010628	OMIM:164310	TAS				P		HPO:probinson	
OMIM	164330	ODONTOMA-DYSPHAGIA SYNDROME		HP:0000006	OMIM:164330	TAS				I		HPO:probinson	
OMIM	164330	ODONTOMA-DYSPHAGIA SYNDROME		HP:0002015	OMIM:164330	TAS				P		HPO:probinson	
OMIM	164330	ODONTOMA-DYSPHAGIA SYNDROME		HP:0002031	OMIM:164330	TAS				P		HPO:probinson	
OMIM	164330	ODONTOMA-DYSPHAGIA SYNDROME		HP:0011068	OMIM:164330	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000006	OMIM:164400	IEA				I		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000514	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000543	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000623	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000639	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000640	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000641	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0000648	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001151	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001252	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001257	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001260	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001283	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001284	OMIM:164400	PCS				P		HPO:probinson	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001290	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001310	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0001347	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002015	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002070	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002071	OMIM:164400	PCS				P		HPO:probinson	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002072	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002073	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002075	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002078	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002168	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002198	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002495	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002503	OMIM:164400	PCS				P		HPO:probinson	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002542	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0002839	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003202	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003431	PMID:9448569	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003448	PMID:9448569	PCS		HP:0040284		P		HPO:probinson	1/9
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003487	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003581	OMIM:164400	PCS				C		HPO:probinson	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003693	OMIM:164400	TAS				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0003744	OMIM:164400	IEA				I		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0007006	OMIM:164400	IEA				P		HPO:iea	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0007078	PMID:9448569	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	164400	SPINOCEREBELLAR ATAXIA 1		HP:0007263	OMIM:164400	IEA				P		HPO:skoehler	
OMIM	164400	SPINOCEREBELLAR ATAXIA 1	HP:0012825	HP:0100543	OMIM:164400	PCS				P		HPO:probinson	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000006	OMIM:164500	TAS				I		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000514	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000529	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000580	OMIM:164500	TAS				P		HPO:probinson	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000608	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000623	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000639	PMID:19659750	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0000648	PMID:19659750	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001257	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001260	PMID:19659750	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001268	PMID:9781533	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001310	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001337	PMID:19659750	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0001347	OMIM:164500	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002015	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002071	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002072	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002073	PMID:19659750	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002310	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0002542	OMIM:164500	TAS				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0003487	OMIM:164500	IEA				P		HPO:iea	
OMIM	164500	SPINOCEREBELLAR ATAXIA 7 OPCA III OPCA WITH RETINAL DEGENERATION OPCA WITH MACULAR DEGENERATION AND EXTERNAL OPHTHALMOPLEGIA AUTOSOMAL DOMINANT CEREBELLAR ATAXIA, TYPE II ADCA, TYPE II		HP:0003744	OMIM:164500	TAS				I		HPO:iea	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0000006	OMIM:164680	IEA				I		HPO:iea	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0002208	OMIM:164680	IEA				P		HPO:skoehler	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0007556	OMIM:164680	IEA				P		HPO:iea	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0008070	OMIM:164680	IEA				P		HPO:skoehler	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0008401	OMIM:164680	IEA				P		HPO:iea	
OMIM	164680	164680 ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR		HP:0011359	OMIM:164680	TAS				P		HPO:skoehler	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0000006	OMIM:164700	IEA				I		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0000726	OMIM:164700	IEA				P		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0001251	OMIM:164700	IEA				P		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0001272	OMIM:164700	TAS				P		HPO:probinson	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0002063	OMIM:164700	IEA				P		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0002071	OMIM:164700	IEA				P		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0002072	OMIM:164700	IEA				P		HPO:iea	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0002542	OMIM:164700	TAS				P		HPO:skoehler	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0008303	OMIM:164700	TAS				P		HPO:probinson	
OMIM	164700	164700 OLIVOPONTOCEREBELLAR ATROPHY V; OPCA V;;OPCA WITH DEMENTIA AND EXTRAPYRAMIDAL SIGNS		HP:0200147	OMIM:164700	TAS				P		HPO:skoehler	
OMIM	164745	OMODYSPLASIA		HP:0000006	OMIM:164745	IEA				I		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0000028	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0000047	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0000054	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0000343	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0000456	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0002007	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0003083	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0004991	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0005025	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0005060	OMIM:164745	TAS				P		HPO:skoehler	
OMIM	164745	OMODYSPLASIA		HP:0005280	OMIM:164745	IEA				P		HPO:iea	
OMIM	164745	OMODYSPLASIA		HP:0005792	OMIM:164745	TAS				P		HPO:probinson	
OMIM	164745	OMODYSPLASIA		HP:0010034	OMIM:164745	IEA				P		HPO:iea	
OMIM	164750	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1p31 DUPLICATION SYNDROME		HP:0000006	OMIM:164750	TAS				I	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1P31 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	164750	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1p31 DUPLICATION SYNDROME		HP:0000023	OMIM:164750	IEA				P	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1P31 DUPLICATION SYNDROME	HPO:iea	
OMIM	164750	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1p31 DUPLICATION SYNDROME		HP:0001539	OMIM:164750	IEA				P	#164750 OMPHALOCELE, AUTOSOMAL;;CHROMOSOME 1P31 DUPLICATION SYNDROME	HPO:iea	
OMIM	164800	%164800 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 5; NDNC5;;ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA;;ONYCHOLYSIS, HEREDITARY DISTAL		HP:0000006	OMIM:164800	IEA				I		HPO:iea	
OMIM	164800	%164800 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 5; NDNC5;;ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA;;ONYCHOLYSIS, HEREDITARY DISTAL		HP:0007410	OMIM:164800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	164800	%164800 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 5; NDNC5;;ONYCHOLYSIS, PARTIAL, WITH SCLERONYCHIA;;ONYCHOLYSIS, HEREDITARY DISTAL		HP:0008400	OMIM:164800	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0000006	OMIM:164900	IEA				I		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0000485	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0000618	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0000765	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0002673	OMIM:164900	TAS				P		HPO:probinson	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0002986	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0003027	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0003038	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0003042	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0006055	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0006169	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0006439	OMIM:164900	IEA				P		HPO:skoehler	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0006441	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0007759	OMIM:164900	IEA				P		HPO:iea	
OMIM	164900	%164900 OPHTHALMOMANDIBULOMELIC DYSPLASIA;;OMM SYNDROME		HP:0012478	OMIM:164900	TAS				P		HPO:skoehler	
OMIM	165000	OPHTHALMOPLEGIA, FAMILIAL STATIC		HP:0000006	OMIM:165000	IEA				I		HPO:iea	
OMIM	165000	OPHTHALMOPLEGIA, FAMILIAL STATIC		HP:0000508	OMIM:165000	IEA				P		HPO:iea	
OMIM	165000	OPHTHALMOPLEGIA, FAMILIAL STATIC		HP:0000602	OMIM:165000	IEA				P		HPO:iea	
OMIM	165000	OPHTHALMOPLEGIA, FAMILIAL STATIC		HP:0000639	OMIM:165000	TAS				P		HPO:probinson	
OMIM	165000	OPHTHALMOPLEGIA, FAMILIAL STATIC		HP:0009916	OMIM:165000	IEA				P		HPO:skoehler	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0000006	OMIM:165098	IEA				I		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0000271	OMIM:165098	IEA				P		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0000508	OMIM:165098	IEA				P		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0000544	OMIM:165098	IEA				P		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0000577	OMIM:165098	IEA				P		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0007824	OMIM:165098	IEA				P		HPO:iea	
OMIM	165098	OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION		HP:0007942	OMIM:165098	IEA				P		HPO:iea	
OMIM	165150	OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY		HP:0000006	OMIM:165150	IEA				I		HPO:iea	
OMIM	165150	OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY		HP:0000221	OMIM:165150	IEA				P		HPO:iea	
OMIM	165150	OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY		HP:0001249	OMIM:165150	IEA				P		HPO:iea	
OMIM	165150	OPHTHALMOPLEGIA, PROGRESSIVE, WITH SCROTAL TONGUE AND MENTAL DEFICIENCY		HP:0007650	OMIM:165150	IEA				P		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0000006	OMIM:165199	IEA				I		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0000408	OMIM:165199	IEA	HP:0003621			P		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0000505	OMIM:165199	IEA	HP:0003621			P		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0000648	OMIM:165199	IEA				P		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0002166	OMIM:165199	IEA				P		HPO:iea	
OMIM	165199	OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALDOMINANT		HP:0002522	OMIM:165199	IEA				P		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0000006	OMIM:165200	IEA				I		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0000648	OMIM:165200	IEA				P		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0001251	OMIM:165200	IEA				P		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0001260	OMIM:165200	IEA				P		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0001269	OMIM:165200	IEA				P		HPO:iea	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0007305	OMIM:165200	PCS				P		HPO:probinson	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0011096	OMIM:165200	TAS				P		HPO:skoehler	
OMIM	165200	165200 OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS		HP:0100653	OMIM:165200	TAS				P		HPO:skoehler	
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000006	PMID:15342707	PCS				I		HPO:iea	
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000365	PMID:24136862	PCS		HP:0040284		P		HP:probinson	5/14
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000518	PMID:25159689,PMID:24136862	PCS		HP:0040284		P		HPO:iea	27/31
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000543	PMID:24136862	PCS		HP:0040284		P		HP:probinson	11/14
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000575	PMID:24136862	PCS		HP:0040284		P		HP:probinson	9/9
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000648	PMID:15342707	PCS				P		HPO:iea	
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0000648	PMID:24136862	PCS		HP:0040284		P		HP:probinson	14/14
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT	HP:0012825	HP:0001337	PMID:15342707	PCS				P		HPO:skoehler	
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT	HP:0012825	HP:0002071	PMID:15342707	PCS				P		HPO:skoehler	
OMIM	165300	OPTIC ATROPHY 3, AUTOSOMAL DOMINANT		HP:0007663	PMID:15342707	PCS				P		HPO:skoehler	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000006	OMIM:165500	IEA				I		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000486	OMIM:165500	PCS		HP:0040284		P		HPO:probinson	10%
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000552	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000576	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000590	PMID:20157015	PCS		HP:0040284		P		HPO:probinson	48/104
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000603	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000642	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000648	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000650	OMIM:165500	IEA				P		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000666	OMIM:165500	PCS		HP:0040284		P		HPO:probinson	5%
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0000980	OMIM:165500	IEA				P		HPO:skoehler	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0001251	PMID:20157015	PCS		HP:0040284		P		HPO:probinson	31/104
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0003587	OMIM:165500	IEA				C		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0003701	PMID:20157015	PCS		HP:0040284		P		HPO:probinson	37/104
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0003829	OMIM:165500	IEA				C		HPO:iea	
OMIM	165500	OPTIC ATROPHY 1; OPA1		HP:0007663	OMIM:165500	TAS				P		HPO:skoehler	
OMIM	165510	OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS		HP:0000006	OMIM:165510	TAS				I		HPO:skoehler	
OMIM	165510	OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS		HP:0000512	OMIM:165510	IEA				P		HPO:iea	
OMIM	165510	OPTIC ATROPHY WITH NEGATIVE ELECTRORETINOGRAMS		HP:0000648	OMIM:165510	IEA				P		HPO:iea	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0000006	OMIM:165550	IEA				I		HPO:iea	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0000505	OMIM:165550	IEA				P		HPO:iea	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0000609	OMIM:165550	IEA				P		HPO:iea	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0007663	OMIM:165550	TAS				P		HPO:skoehler	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0012521	OMIM:165550	IEA				P		HPO:skoehler	
OMIM	165550	#165550 OPTIC NERVE HYPOPLASIA, BILATERALOPTIC NERVE APLASIA, BILATERAL, INCLUDED		HP:0012795	OMIM:165550	TAS				P		HPO:skoehler	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0000006	OMIM:165590	IEA				I		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0000175	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0000278	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0000506	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0001177	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0001180	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0002990	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0005280	OMIM:165590	IEA				P		HPO:iea	
OMIM	165590	OROFACIODIGITAL SYNDROME X		HP:0005802	OMIM:165590	IEA				P		HPO:iea	
OMIM	165600	ORBITAL MARGIN, HYPOPLASIA OF		HP:0000006	OMIM:165600	IEA				I		HPO:iea	
OMIM	165600	ORBITAL MARGIN, HYPOPLASIA OF		HP:0000564	OMIM:165600	IEA				P		HPO:iea	
OMIM	165600	ORBITAL MARGIN, HYPOPLASIA OF		HP:0000652	OMIM:165600	IEA				P		HPO:iea	
OMIM	165600	ORBITAL MARGIN, HYPOPLASIA OF		HP:0007647	OMIM:165600	IEA				P		HPO:iea	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0000006	OMIM:165660	IEA				I		HPO:iea	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0001903	OMIM:165660	IEA				P		HPO:skoehler	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0002664	OMIM:165660	IEA				P		HPO:skoehler	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0002669	OMIM:165660	TAS				P		HPO:skoehler	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0002974	OMIM:165660	IEA				P		HPO:iea	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0009466	OMIM:165660	IEA				P		HPO:iea	
OMIM	165660	%165660 OSLAM SYNDROME;;OSTEOSARCOMA, LIMB ANOMALIES, AND MACROCYTOSIS;;OSTEOSARCOMA, LIMB ANOMALIES, AND ERYTHROID MACROCYTOSIS WITH MEGALOBLASTICMARROW		HP:0030084	OMIM:165660	TAS				P		HPO:skoehler	
OMIM	165670	OSSIFIED EAR CARTILAGES		HP:0000006	OMIM:165670	IEA				I		HPO:iea	
OMIM	165670	OSSIFIED EAR CARTILAGES		HP:0000598	OMIM:165670	IEA				P		HPO:iea	
OMIM	165680	OSSICULAR MALFORMATIONS, FAMILIAL		HP:0000006	OMIM:165680	IEA				I		HPO:iea	
OMIM	165680	OSSICULAR MALFORMATIONS, FAMILIAL		HP:0004452	OMIM:165680	IEA				P		HPO:iea	
OMIM	165680	OSSICULAR MALFORMATIONS, FAMILIAL		HP:0008591	OMIM:165680	IEA				P		HPO:iea	
OMIM	165700	OSTEOARTHROPATHY OF FINGERS, FAMILIAL		HP:0000006	OMIM:165700	IEA				I		HPO:iea	
OMIM	165700	OSTEOARTHROPATHY OF FINGERS, FAMILIAL		HP:0006009	OMIM:165700	TAS				P		HPO:iea	
OMIM	165700	OSTEOARTHROPATHY OF FINGERS, FAMILIAL		HP:0009803	OMIM:165700	TAS				P		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0000006	OMIM:165720	IEA				I		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0000007	OMIM:165720	IEA				I		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0001425	OMIM:165720	IEA				I		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0001426	OMIM:165720	IEA				I		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0002644	OMIM:165720	IEA				P		HPO:iea	
OMIM	165720	OSTEOARTHRITIS		HP:0008843	OMIM:165720	IEA				P		HPO:iea	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0000006	OMIM:165800	IEA				I		HPO:iea	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0001156	OMIM:165800	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0001507	OMIM:165800	IEA				P		HPO:iea	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0002007	OMIM:165800	IEA				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0002515	OMIM:165800	TAS				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0002758	OMIM:165800	TAS				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0002938	OMIM:165800	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0004322	OMIM:165800	TAS				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0005616	OMIM:165800	IEA				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0009778	OMIM:165800	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0010886	OMIM:165800	TAS				P		HPO:skoehler	
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0011800	OMIM:165800	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	165800	SHORT STATURE AND ADVANCED BONE AGE, WITH OR WITHOUT EARLY-ONSET OSTEOARTHRITIS AND/OR OSTEOCHONDRITIS DISSECANS; SSOAOD		HP:0100777	OMIM:165800	TAS				P		HPO:skoehler	
OMIM	166000	ENCHONDROMATOSIS, MULTIPLE		HP:0000006	OMIM:166000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	166000	ENCHONDROMATOSIS, MULTIPLE		HP:0001028	OMIM:166000	TAS				P		HPO:skoehler	
OMIM	166000	ENCHONDROMATOSIS, MULTIPLE		HP:0005701	OMIM:166000	TAS				P		HPO:skoehler	
OMIM	166000	ENCHONDROMATOSIS, MULTIPLE		HP:0006765	OMIM:166000	TAS				P		HPO:skoehler	
OMIM	166000	ENCHONDROMATOSIS, MULTIPLE		HP:0011314	OMIM:166000	TAS				P		HPO:skoehler	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000006	OMIM:166200	IEA				I		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000362	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000365	OMIM:166200	TAS	HP:0003581			P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000592	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000703	OMIM:166200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I	HP:0012825	HP:0000938	OMIM:166200	TAS				P		HPO:probinson	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000963	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0000978	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0001382	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0001507	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0001634	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0002645	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0002659	OMIM:166200	TAS				P		HPO:probinson	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0002757	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0002980	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0003321	OMIM:166200	IEA				P		HPO:iea	
OMIM	166200	OSTEOGENESIS IMPERFECTA, TYPE I		HP:0004942	OMIM:166200	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000006	OMIM:166210	IEA				I		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000239	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000444	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000592	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000923	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000926	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0000963	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0001518	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0001622	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0001635	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0001790	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0002093	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0002644	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0002645	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0002757	OMIM:166210	TAS				P		HPO:probinson	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0002982	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0005622	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0005623	OMIM:166210	TAS				P		HPO:probinson	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0005855	OMIM:166210	TAS				P		HPO:probinson	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0006367	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0008873	OMIM:166210	IEA				P		HPO:iea	
OMIM	166210	OSTEOGENESIS IMPERFECTA, TYPE IIA		HP:0010444	OMIM:166210	IEA				P		HPO:skoehler	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0000006	OMIM:166220	TAS				I		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0000362	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0000365	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0000592	OMIM:166220	TAS		HP:0040284		P		HPO:skoehler	10%
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0000703	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0002645	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0002650	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0002757	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0002808	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0003023	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0003321	OMIM:166220	TAS				P		HPO:iea	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0004322	OMIM:166220	TAS	HP:0003593			P		HPO:probinson	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0004349	PMID:19533842	PCS				P		HPO:probinson	
OMIM	166220	OSTEOGENESIS IMPERFECTA, TYPE IV		HP:0005005	OMIM:166220	TAS				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0000006	OMIM:166230	IEA				I		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0000164	OMIM:166230	IEA				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0000592	OMIM:166230	IEA				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0001367	OMIM:166230	IEA				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0002645	OMIM:166230	IEA				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0002691	OMIM:166230	IEA				P		HPO:skoehler	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0003321	OMIM:166230	IEA				P		HPO:iea	
OMIM	166230	OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES		HP:0005653	OMIM:166230	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000006	OMIM:166250	IEA				I		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000023	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000028	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000041	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000047	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000218	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000272	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000303	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000316	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000343	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000369	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000463	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000470	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000494	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000586	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000706	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000750	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000882	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0000926	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001169	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001230	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001363	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001508	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001739	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001742	OMIM:166250	TAS				P		HPO:skoehler	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001769	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001773	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001783	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0001800	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0002007	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0002098	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0002659	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0002676	OMIM:166250	IEA				P		HPO:skoehler	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0003196	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0004279	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0005280	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0005864	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0006009	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0006487	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0008905	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0009803	OMIM:166250	IEA				P		HPO:iea	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0009826	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0010049	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0010743	OMIM:166250	TAS				P		HPO:probinson	
OMIM	166250	#166250 OSTEOGLOPHONIC DYSPLASIA; OGD;;OSTEOGLOPHONIC DWARFISM		HP:0011800	OMIM:166250	TAS				P		HPO:skoehler	
OMIM	166260	GNATHODIAPHYSEAL DYSPLASIA		HP:0000006	OMIM:166260	IEA				I		HPO:iea	
OMIM	166260	GNATHODIAPHYSEAL DYSPLASIA		HP:0000938	OMIM:166260	IEA				P		HPO:iea	
OMIM	166260	GNATHODIAPHYSEAL DYSPLASIA		HP:0002659	OMIM:166260	IEA				P		HPO:iea	
OMIM	166260	GNATHODIAPHYSEAL DYSPLASIA		HP:0005045	OMIM:166260	IEA				P		HPO:iea	
OMIM	166260	GNATHODIAPHYSEAL DYSPLASIA		HP:0006487	OMIM:166260	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000006	OMIM:166300	IEA				I		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000083	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000093	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000112	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000327	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000347	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000520	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000822	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0000938	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001193	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001225	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001473	OMIM:166300	TAS				P		HPO:probinson	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001495	OMIM:166300	TAS				P		HPO:probinson	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001504	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001761	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0001785	OMIM:166300	IEA				P		HPO:iea	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0002829	OMIM:166300	IEA				P		HPO:skoehler	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0006234	OMIM:166300	TAS				P		HPO:probinson	
OMIM	166300	MULTICENTRIC CARPOTARSAL OSTEOLYSIS SYNDROME; MCTO		HP:0009487	OMIM:166300	TAS				P		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0000006	OMIM:166350	IEA				I		HPO:iea	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0001510	OMIM:166350	TAS				P		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0003011	OMIM:166350	IEA				P		HPO:iea	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0003593	OMIM:166350	TAS				C		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0003621	OMIM:166350	IEA				C		HPO:iea	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0003676	OMIM:166350	IEA				C		HPO:iea	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0003828	OMIM:166350	TAS				C		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0025027	OMIM:166350	IEA				P		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0031013	OMIM:166350	IEA				P		HPO:skoehler	
OMIM	166350	OSSEOUS HETEROPLASIA, PROGRESSIVE; POH		HP:0100246	OMIM:166350	TAS				P		HPO:skoehler	
OMIM	166400	OSTEOMAS OF MANDIBLE		HP:0000006	OMIM:166400	IEA				I		HPO:iea	
OMIM	166400	OSTEOMAS OF MANDIBLE		HP:0000277	OMIM:166400	IEA				P		HPO:iea	
OMIM	166400	OSTEOMAS OF MANDIBLE		HP:0100246	OMIM:166400	IEA				P		HPO:skoehler	
OMIM	166450	OSTEOMESOPYKNOSIS		HP:0000006	OMIM:166450	IEA				I		HPO:iea	
OMIM	166450	OSTEOMESOPYKNOSIS		HP:0000789	OMIM:166450	IEA				P		HPO:iea	
OMIM	166450	OSTEOMESOPYKNOSIS		HP:0003419	OMIM:166450	IEA				P		HPO:iea	
OMIM	166450	OSTEOMESOPYKNOSIS		HP:0011001	OMIM:166450	TAS				P		HPO:probinson	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0000006	OMIM:166600	IEA				I		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0000572	OMIM:166600	TAS				P		HPO:skoehler	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0001425	OMIM:166600	TAS				I		HPO:skoehler	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0002644	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0002757	OMIM:166600	TAS				P		HPO:skoehler	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0003084	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0003148	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0003621	OMIM:166600	IEA				C		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0005106	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0005528	OMIM:166600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0005789	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0007209	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0007626	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0008843	OMIM:166600	IEA				P		HPO:iea	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0010628	OMIM:166600	TAS				P		HPO:skoehler	
OMIM	166600	OSTEOPETROSIS, AUTOSOMAL DOMINANT 2		HP:0011002	OMIM:166600	TAS				P		HPO:skoehler	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0000006	OMIM:166700	IEA				I		HPO:iea	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0001371	OMIM:166700	IEA				P		HPO:skoehler	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0001387	OMIM:166700	IEA				P		HPO:iea	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0001609	OMIM:166700	IEA				P		HPO:iea	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0010739	OMIM:166700	IEA				P		HPO:skoehler	
OMIM	166700	BUSCHKE-OLLENDORFF SYNDROME; BOS		HP:0100898	OMIM:166700	IEA				P		HPO:skoehler	
OMIM	166705	OSTEOPOIKILOSIS AND DACRYOCYSTITIS		HP:0000006	OMIM:166705	IEA				I		HPO:iea	
OMIM	166705	OSTEOPOIKILOSIS AND DACRYOCYSTITIS		HP:0000620	OMIM:166705	IEA				P		HPO:iea	
OMIM	166705	OSTEOPOIKILOSIS AND DACRYOCYSTITIS		HP:0010739	OMIM:166705	IEA				P		HPO:skoehler	
OMIM	166710	OSTEOPOROSIS		HP:0000006	OMIM:166710	IEA				I		HPO:iea	
OMIM	166710	OSTEOPOROSIS		HP:0000939	OMIM:166710	IEA				P		HPO:iea	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0000006	OMIM:166740	IEA				I		HPO:iea	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0002757	OMIM:166740	IEA				P		HPO:iea	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0002980	OMIM:166740	TAS				P		HPO:probinson	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0002982	OMIM:166740	TAS				P		HPO:probinson	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0005791	OMIM:166740	IEA				P		HPO:iea	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0008064	OMIM:166740	IEA				P		HPO:iea	
OMIM	166740	OSTEOSCLEROSIS WITH ICHTHYOSIS AND FRACTURES		HP:0011001	OMIM:166740	IEA				P		HPO:iea	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000006	OMIM:166750	IEA				I		HPO:iea	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000276	OMIM:166750	IEA				P		HPO:skoehler	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000343	OMIM:166750	IEA				P		HPO:skoehler	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000407	OMIM:166750	IEA				P		HPO:iea	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000463	OMIM:166750	IEA				P		HPO:skoehler	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000589	OMIM:166750	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000668	OMIM:166750	IEA				P		HPO:iea	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0000679	OMIM:166750	IEA				P		HPO:iea	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0003771	OMIM:166750	IEA				P		HPO:skoehler	
OMIM	166750	OTODENTAL DYSPLASIA		HP:0031013	OMIM:166750	IEA				P		HPO:skoehler	
OMIM	166760	OTITIS MEDIA, SUSCEPTIBILITY TO		HP:0000403	PMID:26121085	PCS				P		HPO:iea	
OMIM	166760	OTITIS MEDIA, SUSCEPTIBILITY TO		HP:0010982	PMID:26121085	PCS				I		HP:probinson	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0000006	OMIM:166780	IEA				I		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0000276	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0000405	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0000460	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0000472	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0001256	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0003691	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0004467	OMIM:166780	IEA				P		HPO:iea	
OMIM	166780	OTOFACIOCERVICAL SYNDROME		HP:0200021	OMIM:166780	IEA				P		HPO:iea	
OMIM	166800	OTOSCLEROSIS		HP:0000006	OMIM:166800	IEA				I		HPO:iea	
OMIM	166800	OTOSCLEROSIS		HP:0000362	OMIM:166800	IEA				P		HPO:iea	
OMIM	166800	OTOSCLEROSIS		HP:0000405	OMIM:166800	IEA				P		HPO:iea	
OMIM	166900	OVALOCYTOSIS, HEREDITARY HEMOLYTIC		HP:0000006	OMIM:166900	IEA				I		HPO:iea	
OMIM	166900	OVALOCYTOSIS, HEREDITARY HEMOLYTIC		HP:0001878	OMIM:166900	IEA				P		HPO:iea	
OMIM	166900	OVALOCYTOSIS, HEREDITARY HEMOLYTIC		HP:0004445	PMID:5870194	PCS				P		HPO:lccarmody	
OMIM	166910	OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS		HP:0000006	OMIM:166910	TAS				I		HPO:probinson	
OMIM	166910	OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS		HP:0001878	OMIM:166910	TAS				P		HPO:probinson	
OMIM	166910	OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS		HP:0004445	OMIM:166910	TAS				P		HPO:probinson	
OMIM	166910	OVALOCYTOSIS, HEREDITARY HEMOLYTIC, WITH DEFECTIVE ERYTHROPOIESIS		HP:0010972	OMIM:166910	TAS				P		HPO:probinson	
OMIM	166950	TERATOMA, OVARIAN		HP:0000006	OMIM:166950	TAS				I		HPO:probinson	
OMIM	166950	TERATOMA, OVARIAN		HP:0012226	OMIM:166950	TAS				P		HPO:probinson	
OMIM	166970	OVARIAN FIBROMATA		HP:0000006	OMIM:166970	IEA				I		HPO:iea	
OMIM	166970	OVARIAN FIBROMATA		HP:0010618	OMIM:166970	IEA				P		HPO:skoehler	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0000006	OMIM:166990	IEA				I		HPO:iea	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0000238	OMIM:166990	IEA				P		HPO:iea	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0000822	OMIM:166990	IEA				P		HPO:iea	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0001274	OMIM:166990	IEA				P		HPO:iea	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0001873	OMIM:166990	IEA				P		HPO:iea	
OMIM	166990	OSTEOCHONDRODYSPLASIA, RHIZOMELIC, WITH CALLOSAL AGENESIS, THROMBOCYTOPENIA,HYDROCEPHALUS, AND HYPERTENSION		HP:0008905	OMIM:166990	TAS				P		HPO:probinson	
OMIM	167000	#167000 OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED		HP:0000006	OMIM:167000	IEA				I		HPO:iea	
OMIM	167000	#167000 OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED		HP:0001939	OMIM:167000	IEA				P		HPO:iea	
OMIM	167000	#167000 OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED		HP:0003002	OMIM:167000	IEA				P		HPO:iea	
OMIM	167000	#167000 OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED		HP:0006774	OMIM:167000	IEA				P		HPO:iea	
OMIM	167000	#167000 OVARIAN CANCEROVARIAN CANCER, EPITHELIAL, INCLUDED		HP:0100621	OMIM:167000	TAS				P		HPO:skoehler	
OMIM	167030	NEPHROLITHIASIS, CALCIUM OXALATE		HP:0000007	OMIM:167030	TAS				I		HPO:skoehler	
OMIM	167030	NEPHROLITHIASIS, CALCIUM OXALATE		HP:0000074	OMIM:167030	TAS				P		HPO:skoehler	
OMIM	167030	NEPHROLITHIASIS, CALCIUM OXALATE		HP:0001919	OMIM:167030	TAS				P		HPO:skoehler	
OMIM	167030	NEPHROLITHIASIS, CALCIUM OXALATE		HP:0003159	OMIM:167030	IEA				P		HPO:iea	
OMIM	167030	NEPHROLITHIASIS, CALCIUM OXALATE		HP:0008672	OMIM:167030	IEA				P		HPO:iea	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:167100	TAS				I		HPO:probinson	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0000508	OMIM:167100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0000975	OMIM:167100	TAS				P		HPO:probinson	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0001072	OMIM:167100	TAS				P		HPO:probinson	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0006465	OMIM:167100	TAS				P		HPO:probinson	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0010541	OMIM:167100	TAS				P		HPO:skoehler	
OMIM	167100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT		HP:0100759	OMIM:167100	TAS				P		HPO:skoehler	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0000006	OMIM:167200	IEA				I		HPO:iea	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0000972	OMIM:167200	IEA				P		HPO:iea	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0001425	OMIM:167200	IEA				I		HPO:iea	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0001805	OMIM:167200	IEA				P		HPO:iea	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0002745	OMIM:167200	IEA				P		HPO:skoehler	
OMIM	167200	PACHYONYCHIA CONGENITA, TYPE 1		HP:0007502	OMIM:167200	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0000006	OMIM:167210	IEA				I		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0000535	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0000695	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0000972	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0001425	OMIM:167210	TAS				I		HPO:skoehler	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0001609	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0002164	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0002209	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0007410	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0008392	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0008404	OMIM:167210	TAS				P		HPO:skoehler	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0011359	OMIM:167210	IEA				P		HPO:iea	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0012035	PMID:9618173	PCS				P		HPO:probinson	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0025084	OMIM:167210	TAS				P		HPO:skoehler	
OMIM	167210	PACHYONYCHIA CONGENITA 2		HP:0200040	OMIM:167210	TAS				P		HPO:skoehler	
OMIM	167220	PACMAN DYSPLASIA		HP:0000006	OMIM:167220	IEA				I		HPO:iea	
OMIM	167220	PACMAN DYSPLASIA		HP:0001939	OMIM:167220	IEA				P		HPO:iea	
OMIM	167220	PACMAN DYSPLASIA		HP:0005716	OMIM:167220	IEA				P		HPO:iea	
OMIM	167220	PACMAN DYSPLASIA		HP:0006487	OMIM:167220	IEA				P		HPO:skoehler	
OMIM	167220	PACMAN DYSPLASIA		HP:0010655	OMIM:167220	IEA				P		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0000006	OMIM:167250	TAS				I		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0000365	OMIM:167250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0002653	OMIM:167250	TAS				P		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0002669	OMIM:167250	TAS				P		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0002797	OMIM:167250	IEA				P		HPO:skoehler	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0003084	OMIM:167250	TAS				P		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0003155	OMIM:167250	TAS				P		HPO:iea	
OMIM	167250	PAGET DISEASE OF BONE 3; PDB3		HP:0005686	OMIM:167250	TAS				P		HPO:iea	
OMIM	167300	PAGET DISEASE, EXTRAMAMMARY		HP:0000976	OMIM:167300	TAS				P		HPO:iea	
OMIM	167300	PAGET DISEASE, EXTRAMAMMARY		HP:0002664	OMIM:167300	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0000006	OMIM:167320	IEA				I		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0000726	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0001288	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0001332	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0002145	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0002357	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0002644	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0002938	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003198	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003236	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003418	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003547	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003551	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003690	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003691	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003693	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003701	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003724	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003749	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0003805	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0006913	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0007112	OMIM:167320	IEA				P		HPO:iea	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0007354	OMIM:167320	IEA				P		HPO:skoehler	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0008946	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0008988	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0010628	OMIM:167320	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0010639	OMIM:167320	TAS				P		HPO:probinson	
OMIM	167320	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 1		HP:0030838	OMIM:167320	TAS				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0000006	OMIM:167400	IEA				I		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0000632	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0001649	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0001662	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0003623	OMIM:167400	TAS				C		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0007328	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0031284	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0200025	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0200026	OMIM:167400	IEA				P		HPO:skoehler	
OMIM	167400	PAROXYSMAL EXTREME PAIN DISORDER		HP:0500005	OMIM:167400	TAS				P		HPO:skoehler	
OMIM	167500	PALATOPHARYNGEAL INCOMPETENCE		HP:0000175	OMIM:167500	IEA				P		HPO:skoehler	
OMIM	167500	PALATOPHARYNGEAL INCOMPETENCE		HP:0000220	OMIM:167500	TAS				P		HPO:skoehler	
OMIM	167500	PALATOPHARYNGEAL INCOMPETENCE		HP:0001426	OMIM:167500	TAS				I		HPO:skoehler	
OMIM	167500	PALATOPHARYNGEAL INCOMPETENCE		HP:0001608	OMIM:167500	TAS				P		HPO:skoehler	
OMIM	167600	PALMARIS LONGUS MUSCLE, ABSENCE OF		HP:0000006	OMIM:167600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	167600	PALMARIS LONGUS MUSCLE, ABSENCE OF		HP:0000924	OMIM:167600	IEA				P		HPO:iea	
OMIM	167700	PALMOMENTAL REFLEX		HP:0000006	OMIM:167700	IEA				I		HPO:iea	
OMIM	167700	PALMOMENTAL REFLEX		HP:0000707	OMIM:167700	IEA				P		HPO:iea	
OMIM	167700	PALMOMENTAL REFLEX		HP:0030902	OMIM:167700	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000006	OMIM:167730	PCS				I		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000268	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000316	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000327	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000337	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000349	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000369	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000378	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000431	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000506	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000568	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000636	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0000652	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0001012	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0001092	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0004209	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0005280	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0009926	OMIM:167730	IEA				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0010748	OMIM:167730	PCS				P		HPO:probinson	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0030953	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167730	NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS		HP:0040164	OMIM:167730	TAS				P		HPO:skoehler	
OMIM	167750	PANCREAS, ANNULAR		HP:0000006	OMIM:167750	IEA				I		HPO:iea	
OMIM	167750	PANCREAS, ANNULAR		HP:0001734	OMIM:167750	IEA				P		HPO:iea	
OMIM	167750	PANCREAS, ANNULAR		HP:0005250	OMIM:167750	IEA				P		HPO:iea	
OMIM	167750	PANCREAS, ANNULAR		HP:0100867	OMIM:167750	IEA				P		HPO:skoehler	
OMIM	167755	167755 PANCREAS, DORSAL, AGENESIS OF		HP:0000006	OMIM:167755	IEA				I		HPO:skoehler	
OMIM	167755	167755 PANCREAS, DORSAL, AGENESIS OF		HP:0000819	OMIM:167755	IEA				P		HPO:skoehler	
OMIM	167755	167755 PANCREAS, DORSAL, AGENESIS OF		HP:0001732	OMIM:167755	TAS				P		HPO:skoehler	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0000006	OMIM:167800	IEA				I		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0000819	OMIM:167800	IEA				P		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0001733	OMIM:167800	IEA				P		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0001738	OMIM:167800	IEA				P		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0001945	OMIM:167800	TAS				P		HPO:probinson	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0001977	OMIM:167800	IEA				P		HPO:skoehler	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0002027	OMIM:167800	IEA				P		HPO:skoehler	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0002202	OMIM:167800	IEA				P		HPO:skoehler	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0002570	OMIM:167800	IEA				P		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0005206	OMIM:167800	IEA				P		HPO:iea	
OMIM	167800	PANCREATITIS, HEREDITARY		HP:0005213	OMIM:167800	IEA				P		HPO:iea	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0000006	OMIM:167850	TAS				I		HPO:probinson	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0001873	OMIM:167850	TAS				P		HPO:skoehler	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0001876	OMIM:167850	TAS				P		HPO:probinson	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0001882	OMIM:167850	TAS				P		HPO:skoehler	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0001903	OMIM:167850	TAS				P		HPO:skoehler	
OMIM	167850	167850 PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE		HP:0004950	OMIM:167850	TAS				P		HPO:probinson	
OMIM	167870	PANIC DISORDER 1		HP:0000006	OMIM:167870	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	167870	PANIC DISORDER 1		HP:0000739	OMIM:167870	IEA				P		HPO:skoehler	
OMIM	167900	PAPILLOMATOSIS, FAMILIAL CUTANEOUS		HP:0000006	OMIM:167900	TAS				I		HPO:probinson	
OMIM	167900	PAPILLOMATOSIS, FAMILIAL CUTANEOUS		HP:0000962	OMIM:167900	TAS				P		HPO:probinson	
OMIM	167950	PAPILLOMATOSIS, FLORID, OF NIPPLE		HP:0000006	OMIM:167950	IEA				I		HPO:iea	
OMIM	167950	PAPILLOMATOSIS, FLORID, OF NIPPLE		HP:0000951	OMIM:167950	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0000006	OMIM:168000	IEA				I		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0000405	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0000740	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0000975	OMIM:168000	TAS				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0001605	OMIM:168000	TAS				P		HPO:probinson	
OMIM	168000	PARAGANGLIOMAS 1		HP:0001609	OMIM:168000	TAS				P		HPO:probinson	
OMIM	168000	PARAGANGLIOMAS 1		HP:0001649	OMIM:168000	TAS				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0001686	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0001962	OMIM:168000	TAS				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0002331	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0002640	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0002886	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0003001	OMIM:168000	TAS				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0003334	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0003581	OMIM:168000	IEA				C		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0006715	OMIM:168000	IEA				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0006737	OMIM:168000	TAS		HP:0040284		P		HPO:probinson	21%
OMIM	168000	PARAGANGLIOMAS 1		HP:0006748	OMIM:168000	TAS		HP:0040284		P		HPO:probinson	53%
OMIM	168000	PARAGANGLIOMAS 1		HP:0006824	OMIM:168000	TAS				P		HPO:iea	
OMIM	168000	PARAGANGLIOMAS 1		HP:0008629	OMIM:168000	TAS				P		HPO:probinson	
OMIM	168000	PARAGANGLIOMAS 1		HP:0030074	OMIM:168000	TAS				P		HPO:skoehler	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0000006	OMIM:168100	IEA				I		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0000298	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001260	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001288	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001300	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001332	OMIM:168100	IEA				P		HPO:skoehler	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001337	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0001939	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0002063	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0002067	OMIM:168100	IEA				P		HPO:iea	
OMIM	168100	PARALYSIS AGITANS, JUVENILE, OF HUNT		HP:0003677	OMIM:168100	IEA				C		HPO:iea	
OMIM	168200	PARAMOLAR TUBERCLE OF BOLK		HP:0000006	OMIM:168200	IEA				I		HPO:iea	
OMIM	168200	PARAMOLAR TUBERCLE OF BOLK		HP:0000164	OMIM:168200	IEA				P		HPO:iea	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0000006	OMIM:168300	IEA				I		HPO:iea	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0001319	OMIM:168300	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0001324	OMIM:168300	TAS				P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0003326	OMIM:168300	IEA				P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0003552	OMIM:168300	IEA				P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0003593	OMIM:168300	IEA				C		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0003712	OMIM:168300	IEA				P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0005348	OMIM:168300	TAS	HP:0003621			P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0010548	OMIM:168300	IEA				P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0011809	OMIM:168300	TAS				P		HPO:probinson	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0011968	OMIM:168300	TAS	HP:0011463			P		HPO:skoehler	
OMIM	168300	#168300 PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC;;PARALYSIS PERIODICA PARAMYOTONICAPARAMYOTONIA CONGENITA WITHOUT COLD PARALYSIS, INCLUDED		HP:0012899	OMIM:168300	TAS				P		HPO:skoehler	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0000006	OMIM:168400	IEA				I		HPO:iea	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0000470	OMIM:168400	IEA				P		HPO:iea	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0001371	OMIM:168400	IEA				P		HPO:iea	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0002650	OMIM:168400	IEA				P		HPO:iea	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0002808	OMIM:168400	IEA				P		HPO:iea	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0002857	OMIM:168400	IEA				P		HPO:skoehler	
OMIM	168400	#168400 PARASTREMMATIC DWARFISM		HP:0003510	OMIM:168400	TAS				P		HPO:probinson	
OMIM	168500	PARIETAL FORAMINA		HP:0000006	OMIM:168500	IEA				I		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0000175	OMIM:168500	IEA				P		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0000204	OMIM:168500	IEA				P		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0001250	OMIM:168500	IEA				P		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0001425	OMIM:168500	IEA				I		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0002084	OMIM:168500	IEA				P		HPO:skoehler	
OMIM	168500	PARIETAL FORAMINA		HP:0002315	OMIM:168500	IEA				P		HPO:iea	
OMIM	168500	PARIETAL FORAMINA		HP:0002695	OMIM:168500	TAS				P		HPO:probinson	
OMIM	168500	PARIETAL FORAMINA		HP:0002697	OMIM:168500	TAS				P		HPO:probinson	
OMIM	168500	PARIETAL FORAMINA		HP:0007385	OMIM:168500	IEA				P		HPO:iea	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0000006	PMID:14571277	PCS				I		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0000256	PMID:14571277	PCS				P		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0000894	PMID:14571277	PCS				P		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0002695	OMIM:168550	IEA				P		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0002697	PMID:14571277	PCS				P		HPO:skoehler	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0004492	PMID:14571277	PCS				P		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0008551	PMID:14571277	PCS				P		HPO:probinson	
OMIM	168550	PARIETAL FORAMINA WITH CLEIDOCRANIAL DYSPLASIA		HP:0025247	PMID:14571277	PCS				P		HPO:probinson	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000012	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000298	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000716	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000726	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000738	OMIM:168600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0000751	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0001260	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0001300	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0001332	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0001337	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0001621	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002015	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002019	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002063	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002067	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002172	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002322	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002360	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0002529	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0003587	OMIM:168600	TAS				C		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0003676	OMIM:168600	TAS				C		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0003745	OMIM:168600	TAS				I		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0007311	OMIM:168600	IEA				P		HPO:iea	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0011960	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0012332	OMIM:168600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0031908	OMIM:168600	IEA				P		HPO:skoehler	
OMIM	168600	PARKINSON DISEASE, LATE-ONSET; PD		HP:0100315	OMIM:168600	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0000006	OMIM:168601	TAS				I		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0000012	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0000716	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0000726	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0000738	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0001260	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0001268	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0001300	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0001332	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0001336	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002015	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002063	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002067	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002171	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002172	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002322	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002360	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002362	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0002375	OMIM:168601	TAS				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0003587	OMIM:168601	TAS				C		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0003676	OMIM:168601	TAS				C		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0031908	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168601	PARKINSON DISEASE 1, AUTOSOMAL DOMINANT; PARK1		HP:0100315	OMIM:168601	IEA				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0000006	OMIM:168605	IEA				I		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0000298	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0000511	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0000716	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0000716	OMIM:168605	IEA				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0000719	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0000741	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0001260	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0001300	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0001337	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0001621	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0001824	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0001939	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0002063	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0002067	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0002093	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0002145	OMIM:168605	IEA				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0002360	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0002791	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0003678	OMIM:168605	TAS				C		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0007110	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168605	PERRY SYNDROME		HP:0007311	OMIM:168605	IEA				P		HPO:iea	
OMIM	168605	PERRY SYNDROME		HP:0100785	OMIM:168605	TAS				P		HPO:skoehler	
OMIM	168800	PAROTIDOMEGALY, HEREDITARY BILATERAL		HP:0000006	OMIM:168800	IEA				I		HPO:iea	
OMIM	168800	PAROTIDOMEGALY, HEREDITARY BILATERAL		HP:0000464	OMIM:168800	IEA				P		HPO:iea	
OMIM	168820	PARAOXONASE 1		HP:0000006	OMIM:168820	IEA				I		HPO:iea	
OMIM	168820	PARAOXONASE 1		HP:0001939	OMIM:168820	IEA				P		HPO:iea	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0000006	OMIM:168830	TAS				I		HPO:skoehler	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0000132	OMIM:168830	TAS				P		HPO:skoehler	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0000421	OMIM:168830	TAS				P		HPO:skoehler	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0000978	OMIM:168830	TAS				P		HPO:skoehler	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0001892	OMIM:168830	IEA				P		HPO:iea	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0003645	OMIM:168830	IEA				P		HPO:iea	
OMIM	168830	168830 PASSOVOY FACTOR DEFECT		HP:0003828	OMIM:168830	TAS				C		HPO:skoehler	
OMIM	168860	PATELLA APLASIA-HYPOPLASIA		HP:0000006	OMIM:168860	IEA				I		HPO:iea	
OMIM	168860	PATELLA APLASIA-HYPOPLASIA		HP:0000951	OMIM:168860	IEA				P		HPO:iea	
OMIM	168860	PATELLA APLASIA-HYPOPLASIA		HP:0003065	OMIM:168860	IEA				P		HPO:iea	
OMIM	168860	PATELLA APLASIA-HYPOPLASIA		HP:0006443	OMIM:168860	IEA				P		HPO:iea	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0000006	OMIM:168885	IEA				I		HPO:iea	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0000464	OMIM:168885	IEA				P		HPO:iea	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0001270	OMIM:168885	TAS				P		HPO:probinson	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0002131	OMIM:168885	TAS				P		HPO:skoehler	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0002312	OMIM:168885	IEA				P		HPO:iea	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0002548	OMIM:168885	TAS				P		HPO:skoehler	
OMIM	168885	PAROXYSMAL TONIC UPGAZE, BENIGN CHILDHOOD, WITH ATAXIA		HP:0031936	OMIM:168885	IEA				P		HPO:skoehler	
OMIM	168900	PATELLA, CHONDROMALACIA OF		HP:0000006	OMIM:168900	IEA				I		HPO:iea	
OMIM	168900	PATELLA, CHONDROMALACIA OF		HP:0003045	OMIM:168900	IEA				P		HPO:skoehler	
OMIM	169000	%169000 PATELLA, FAMILIAL RECURRENT DISLOCATION OF		HP:0000006	OMIM:169000	IEA				I		HPO:iea	
OMIM	169000	%169000 PATELLA, FAMILIAL RECURRENT DISLOCATION OF		HP:0005001	OMIM:169000	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000006	OMIM:169100	IEA				I		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000207	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000316	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000322	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000337	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000369	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000411	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000455	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000486	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000508	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0000574	OMIM:169100	PCS				P		HPO:probinson	
OMIM	169100	CHAR SYNDROME		HP:0001256	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0001263	OMIM:169100	TAS				P		HPO:skoehler	
OMIM	169100	CHAR SYNDROME		HP:0001643	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0002553	OMIM:169100	PCS				P		HPO:probinson	
OMIM	169100	CHAR SYNDROME		HP:0004209	OMIM:169100	IEA				P		HPO:iea	
OMIM	169100	CHAR SYNDROME		HP:0009244	OMIM:169100	PCS				P		HPO:probinson	
OMIM	169100	CHAR SYNDROME		HP:0025234	OMIM:169100	TAS				P		HPO:skoehler	
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0000006	OMIM:169150	IEA				I		HPO:iea	
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0000613	OMIM:169150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0000662	OMIM:169150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0007754	OMIM:169150	IEA				P		HPO:skoehler	
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0007913	OMIM:169150	IEA				P		HPO:iea	
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0011506	OMIM:169150	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0012508	OMIM:169150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	169150	MACULAR DYSTROPHY, PATTERNED, 1; MDPT1		HP:0025148	OMIM:169150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0000400	OMIM:169170	IEA				P		HPO:skoehler	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0000448	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0000819	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001007	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001176	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001250	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001386	OMIM:169170	TAS	HP:0003593			P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001507	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0001833	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0002684	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0002751	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0002857	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003026	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003118	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003180	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003309	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003311	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003745	OMIM:169170	IEA				I		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0003799	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0004558	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0004629	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0004684	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0006887	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0007517	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0007574	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0008476	OMIM:169170	IEA				P		HPO:iea	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0008833	OMIM:169170	TAS				P		HPO:probinson	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0010864	OMIM:169170	TAS				P		HPO:skoehler	
OMIM	169170	PATTERSON PSEUDOLEPRECHAUNISM SYNDROME		HP:0012412	OMIM:169170	TAS				P		HPO:skoehler	
OMIM	169200	PECHET FACTOR DEFICIENCY		HP:0000006	OMIM:169200	IEA				I		HPO:iea	
OMIM	169200	PECHET FACTOR DEFICIENCY		HP:0001892	OMIM:169200	IEA				P		HPO:skoehler	
OMIM	169300	169300 PECTUS EXCAVATUM;;FUNNEL CHEST		HP:0000006	OMIM:169300	TAS				I		HPO:skoehler	
OMIM	169300	169300 PECTUS EXCAVATUM;;FUNNEL CHEST		HP:0000767	OMIM:169300	IEA				P		HPO:iea	
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000006	PMID:16007606;PMID:19468205	PCS				I		HPO:sdoelken	
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000164	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000212	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000256	PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	2/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000316	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000403	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000486	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0000964	PMID:10457411;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001249	PMID:14684694,PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	3/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001263	OMIM:169400	TAS				P		HPO:skoehler	
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001508	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001537	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001629	PMID:12118250	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001761	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001873	PMID:10457411;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001875	PMID:10457411;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0001902	PMID:10457411	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0002007	PMID:16007606;PMID:12118250	PCS		HP:0040284		P		HPO:sdoelken	2/2
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0002069	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0002395	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0002808	PMID:10457411;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0002916	PMID:16007606;PMID:19468205	PCS		HP:0040281		P		HPO:sdoelken	HP:0040281
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0003502	PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	2/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0005280	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0006895	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0009027	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0009099	PMID:16007606	PCS		HP:0040284		P		HPO:sdoelken	1/1
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0009824	PMID:10457411;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0010041	PMID:12118250;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0010044	PMID:12118250;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0010047	PMID:12118250;PMID:14684694	PCS		HP:0040284		P		HPO:sdoelken	1/11
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0010442	OMIM:169400	TAS				P		HPO:skoehler	
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0011220	OMIM:169400	TAS				P		HPO:skoehler	
OMIM	169400	PELGER-HUET ANOMALY; PHA		HP:0011447	OMIM:169400	TAS				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000006	OMIM:169500	IEA				I		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000079	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000639	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000716	OMIM:169500	TAS				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000751	OMIM:169500	TAS				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0000802	OMIM:169500	TAS				P		HPO:probinson	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0001251	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0001257	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0001317	OMIM:169500	IEA				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0001347	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0002171	OMIM:169500	IEA				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0002344	OMIM:169500	IEA				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0002415	OMIM:169500	TAS				P		HPO:probinson	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0003487	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0003581	OMIM:169500	TAS				C		HPO:probinson	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0003676	OMIM:169500	IEA				C		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0004926	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0005341	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0006994	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0007024	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0007262	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0007371	OMIM:169500	TAS				P		HPO:skoehler	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0007480	OMIM:169500	IEA				P		HPO:iea	
OMIM	169500	LEUKODYSTROPHY, DEMYELINATING, ADULT-ONSET, AUTOSOMAL DOMINANT; ADLD		HP:0008652	OMIM:169500	IEA				P		HPO:iea	
OMIM	169545	PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA		HP:0000006	OMIM:169545	IEA				I		HPO:iea	
OMIM	169545	PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA		HP:0000086	OMIM:169545	IEA				P		HPO:iea	
OMIM	169545	PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA		HP:0001438	OMIM:169545	IEA				P		HPO:iea	
OMIM	169545	PELVIC LIPOMATOSIS WITH CROSSED RENAL ECTOPIA		HP:0001939	OMIM:169545	IEA				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000006	PMID:11146474	PCS				I		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000568	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000588	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000612	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000882	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000894	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0000946	PMID:9732492	PCS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0001374	PMID:9732492	PCS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0002938	PMID:9732492	PCS				P		HPO:probinson	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0003274	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0003298	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0003418	PMID:9732492	PCS				P		HPO:probinson	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0004209	PMID:9732492	PCS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0004322	OMIM:169550	TAS				P		HPO:iea	
OMIM	169550	PELVIS-SHOULDER DYSPLASIA		HP:0007759	OMIM:169550	TAS				P		HPO:iea	
OMIM	169600	BENIGN CHRONIC PEMPHIGUS		HP:0000006	OMIM:169600	IEA				I		HPO:iea	
OMIM	169600	BENIGN CHRONIC PEMPHIGUS		HP:0010783	OMIM:169600	IEA				P		HPO:skoehler	
OMIM	169610	PEMPHIGUS VULGARIS, FAMILIAL		HP:0000006	OMIM:169610	TAS				I		HPO:skoehler	
OMIM	169610	PEMPHIGUS VULGARIS, FAMILIAL		HP:0030057	OMIM:169610	TAS				P		HPO:probinson	
OMIM	169610	PEMPHIGUS VULGARIS, FAMILIAL		HP:0200097	OMIM:169610	TAS				P		HPO:probinson	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000007	OMIM:170100	IEA				I		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000316	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000444	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000508	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000520	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0000967	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001263	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001744	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001873	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001903	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001939	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0001999	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0002099	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0002162	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0002240	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0002719	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0002725	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0003196	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0005280	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0006528	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0006532	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0006579	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0007473	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0007489	OMIM:170100	IEA				P		HPO:iea	
OMIM	170100	#170100 PROLIDASE DEFICIENCY		HP:0011220	OMIM:170100	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000006	OMIM:170390	IEA				I		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000175	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000218	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000219	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000219	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000252	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000272	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000316	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS	HP:0012825	HP:0000324	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000325	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000327	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000337	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000369	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000414	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000581	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000677	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000696	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0000716	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001156	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001279	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS	HP:0012825	HP:0001328	OMIM:170390	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001388	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001507	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001657	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001770	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001773	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001864	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0001962	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0002650	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0002750	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0003100	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0003691	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0003778	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0003779	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0004209	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0004279	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0004467	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0005147	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0005478	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0006297	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0006335	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0008153	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0009803	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0010049	OMIM:170390	IEA				P		HPO:iea	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0010743	OMIM:170390	TAS				P		HPO:probinson	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0012745	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0025072	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170390	ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS		HP:0200055	OMIM:170390	TAS				P		HPO:skoehler	
OMIM	170400	#170400 HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1;;HYPOKALEMIC PERIODIC PARALYSIS; HOKPP		HP:0000006	OMIM:170400	TAS				I		HPO:probinson	
OMIM	170400	#170400 HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1;;HYPOKALEMIC PERIODIC PARALYSIS; HOKPP		HP:0002900	OMIM:170400	TAS				P		HPO:skoehler	
OMIM	170400	#170400 HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1;;HYPOKALEMIC PERIODIC PARALYSIS; HOKPP		HP:0003198	OMIM:170400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	170400	#170400 HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1;;HYPOKALEMIC PERIODIC PARALYSIS; HOKPP		HP:0003752	OMIM:170400	TAS				P		HPO:probinson	
OMIM	170400	#170400 HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1; HOKPP1;;HYPOKALEMIC PERIODIC PARALYSIS; HOKPP		HP:0003829	OMIM:170400	TAS				C		HPO:skoehler	
OMIM	170500	HYPERKALEMIC PERIODIC PARALYSIS		HP:0000006	OMIM:170500	TAS				I		HPO:probinson	
OMIM	170500	HYPERKALEMIC PERIODIC PARALYSIS		HP:0002486	OMIM:170500	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	170500	HYPERKALEMIC PERIODIC PARALYSIS		HP:0003593	OMIM:170500	IEA				C		HPO:iea	
OMIM	170500	HYPERKALEMIC PERIODIC PARALYSIS		HP:0003752	OMIM:170500	TAS				P		HPO:probinson	
OMIM	170500	HYPERKALEMIC PERIODIC PARALYSIS		HP:0007215	OMIM:170500	TAS				P		HPO:probinson	
OMIM	170600	NORMOKALEMIC PERIODIC PARALYSIS		HP:0000006	OMIM:170600	IEA				I		HPO:iea	
OMIM	170600	NORMOKALEMIC PERIODIC PARALYSIS		HP:0000157	OMIM:170600	IEA				P		HPO:iea	
OMIM	170600	NORMOKALEMIC PERIODIC PARALYSIS		HP:0001939	OMIM:170600	IEA				P		HPO:iea	
OMIM	170600	NORMOKALEMIC PERIODIC PARALYSIS		HP:0002486	OMIM:170600	IEA				P		HPO:skoehler	
OMIM	170600	NORMOKALEMIC PERIODIC PARALYSIS		HP:0003768	OMIM:170600	IEA				P		HPO:iea	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0000007	OMIM:170650	IEA				I		HPO:iea	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0000166	OMIM:170650	IEA	HP:0003593			P		HPO:iea	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0000951	OMIM:170650	IEA				P		HPO:iea	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0001425	OMIM:170650	IEA				I		HPO:skoehler	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0006480	OMIM:170650	IEA				P		HPO:iea	
OMIM	170650	PERIODONTITIS, AGGRESSIVE, 1		HP:0030816	OMIM:170650	TAS				P		HPO:skoehler	
OMIM	170700	PERIPHERAL DYSOSTOSIS		HP:0000006	OMIM:170700	IEA				I		HPO:iea	
OMIM	170700	PERIPHERAL DYSOSTOSIS		HP:0008843	OMIM:170700	TAS				P		HPO:skoehler	
OMIM	170700	PERIPHERAL DYSOSTOSIS		HP:0009803	OMIM:170700	IEA				P		HPO:iea	
OMIM	170700	PERIPHERAL DYSOSTOSIS		HP:0010230	OMIM:170700	IEA				P		HPO:iea	
OMIM	170900	PERNICIOUS ANEMIA		HP:0000006	OMIM:170900	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	170900	PERNICIOUS ANEMIA		HP:0001889	OMIM:170900	TAS				P		HPO:skoehler	
OMIM	170900	PERNICIOUS ANEMIA		HP:0200118	OMIM:170900	TAS				P		HPO:probinson	
OMIM	170980	PERONEAL NERVE, ACCESSORY DEEP		HP:0000006	OMIM:170980	IEA				I		HPO:iea	
OMIM	170980	PERONEAL NERVE, ACCESSORY DEEP		HP:0000707	OMIM:170980	IEA				P		HPO:iea	
OMIM	171000	PEYRONIE DISEASE		HP:0000119	OMIM:171000	IEA				P		HPO:iea	
OMIM	171000	PEYRONIE DISEASE		HP:0001475	OMIM:171000	TAS				I		HPO:nvasilevsky	
OMIM	171000	PEYRONIE DISEASE		HP:0005679	OMIM:171000	IEA				P		HPO:skoehler	
OMIM	171100	PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN		HP:0000006	OMIM:171100	TAS				I		HPO:nvasilevsky	
OMIM	171100	PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN		HP:0000007	OMIM:171100	TAS				I		HPO:nvasilevsky	
OMIM	171100	PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN		HP:0001871	OMIM:171100	IEA				P		HPO:iea	
OMIM	171100	PHAGOCYTOSIS, PLASMA-RELATED DEFECT IN		HP:0001939	OMIM:171100	IEA				P		HPO:iea	
OMIM	171200	THIOUREA TASTINGPHENYLTHIOCARBAMIDE TASTING, INCLUDED		HP:0000006	OMIM:171200	IEA				I		HPO:iea	
OMIM	171200	THIOUREA TASTINGPHENYLTHIOCARBAMIDE TASTING, INCLUDED		HP:0000818	OMIM:171200	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000006	OMIM:171300	IEA				I		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000093	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000519	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000875	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000957	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0000975	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001028	OMIM:171300	TAS				P		HPO:probinson	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001095	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001342	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001635	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001649	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0001920	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0002664	OMIM:171300	IEA				P		HPO:skoehler	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0002666	OMIM:171300	TAS				P		HPO:probinson	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0003072	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0003345	OMIM:171300	IEA				P		HPO:iea	
OMIM	171300	PHEOCHROMOCYTOMA		HP:0003574	OMIM:171300	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0000006	OMIM:171400	IEA				I		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0000822	PMID:18795243	PCS		HP:0040284		P		HPO:iea	13/54
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0000843	PMID:24152999	PCS				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0001574	OMIM:171400	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0001962	PMID:18795243	PCS		HP:0040284		P		HP:probinson	10/54
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002251	OMIM:171400	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002315	PMID:18795243	PCS		HP:0040284		P		HP:probinson	5/54
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002666	PMID:18795243,PMID:22274720	PCS		HP:0040284		P		HPO:iea	54/169
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002865	PMID:22274720	PCS		HP:0040284		P		HPO:iea	7/19
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002865	PMID:29465928	PCS		HP:0040281		P		HP:probinson	HP:0040281
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0002897	OMIM:171400	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0003118	OMIM:171400	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0003345	PMID:18795243	PCS		HP:0040284		P		HP:probinson	28/48
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0003528	OMIM:171400	IEA				P		HPO:iea	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0003639	PMID:18795243	PCS		HP:0040284		P		HPO:iea	36/48
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0011781	PMID:30085596	PCS				P		HP:probinson	
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0011978	PMID:18795243	IEA		HP:0040284		P		HP:probinson	28/48
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0011979	PMID:18795243	PCS		HP:0040284		P		HP:probinson	25/48
OMIM	171400	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA		HP:0100749	PMID:18795243	PCS		HP:0040284		P		HP:probinson	3/54
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000006	OMIM:171420	IEA				I		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000093	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000875	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000957	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000975	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0000997	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0001095	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0001342	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0001635	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0001649	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0002666	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0003072	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0003345	OMIM:171420	IEA				P		HPO:iea	
OMIM	171420	PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME		HP:0003574	OMIM:171420	IEA				P		HPO:iea	
OMIM	171450	PHLEBECTASIA OF LIPS		HP:0000006	OMIM:171450	IEA				I		HPO:iea	
OMIM	171450	PHLEBECTASIA OF LIPS		HP:0000159	OMIM:171450	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000006	OMIM:171480	IEA				I		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000272	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000343	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000402	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000405	OMIM:171480	TAS				P		HPO:skoehler	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000494	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000890	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0000895	OMIM:171480	TAS				P		HPO:skoehler	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0001171	OMIM:171480	TAS				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0002970	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0002974	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0003031	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0003038	OMIM:171480	TAS				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0003042	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0003834	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0003974	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0004322	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0004461	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0004557	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0005011	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0005792	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0006420	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0008551	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0009601	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0009829	OMIM:171480	TAS				P		HPO:skoehler	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0010038	OMIM:171480	IEA				P		HPO:iea	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0011675	OMIM:171480	IEA				P		HPO:skoehler	
OMIM	171480	171480 PHOCOMELIA-ECTRODACTYLY, EAR MALFORMATION, DEAFNESS, AND SINUS ARRHYTHMIA;;FACIOAURICULORADIAL DYSPLASIA		HP:0011800	OMIM:171480	TAS				P		HPO:skoehler	
OMIM	171720	ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1		HP:0000006	OMIM:171720	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	171720	ALKALINE PHOSPHATASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS 1		HP:0003155	OMIM:171720	TAS				P		HPO:probinson	
OMIM	172150	6-@PHOSPHOGLUCONOLACTONASE DEFICIENCY		HP:0000006	OMIM:172150	IEA				I		HPO:iea	
OMIM	172150	6-@PHOSPHOGLUCONOLACTONASE DEFICIENCY		HP:0001878	OMIM:172150	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000006	OMIM:172500	IEA				I		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000112	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000408	OMIM:172500	PCS				P		HPO:probinson	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000666	OMIM:172500	PCS				P		HPO:probinson	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000716	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000751	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0000819	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0001251	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0001289	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0001327	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0002446	OMIM:172500	PCS				P		HPO:probinson	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0005102	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0007164	OMIM:172500	IEA				P		HPO:iea	
OMIM	172500	172500 PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION;;HERRMANN SYNDROME		HP:0011153	OMIM:172500	TAS				P		HPO:skoehler	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000006	OMIM:172700	IEA				I		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000710	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000733	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000734	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000737	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000741	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000748	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0000751	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002145	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002171	OMIM:172700	IEA				P		HPO:skoehler	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002463	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002476	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002529	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0002591	OMIM:172700	IEA				P		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0003745	OMIM:172700	IEA				I		HPO:iea	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0010529	OMIM:172700	IEA				P		HPO:skoehler	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0030213	OMIM:172700	TAS				P		HPO:skoehler	
OMIM	172700	#172700 PICK DISEASE OF BRAIN;;LOBAR ATROPHY OF BRAIN;;DEMENTIA WITH LOBAR ATROPHY AND NEURONAL CYTOPLASMIC INCLUSIONS		HP:0030223	OMIM:172700	TAS				P		HPO:skoehler	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0000006	OMIM:172800	IEA				I		HPO:iea	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0000598	OMIM:172800	IEA				P		HPO:iea	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0001100	OMIM:172800	IEA				P		HPO:iea	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0002211	OMIM:172800	TAS				P		HPO:skoehler	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0002251	OMIM:172800	IEA				P		HPO:skoehler	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0002664	OMIM:172800	IEA				P		HPO:iea	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0007443	OMIM:172800	TAS				P		HPO:probinson	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0007542	OMIM:172800	TAS				P		HPO:skoehler	
OMIM	172800	#172800 PIEBALD TRAIT; PBT;;PIEBALDISM		HP:0007544	OMIM:172800	TAS				P		HPO:probinson	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0000006	OMIM:172850	IEA				I		HPO:iea	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0000365	OMIM:172850	IEA				P		HPO:iea	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0001249	OMIM:172850	IEA				P		HPO:iea	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0001251	OMIM:172850	IEA				P		HPO:iea	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0002211	OMIM:172850	IEA				P		HPO:iea	
OMIM	172850	PIEBALD TRAIT WITH NEUROLOGIC DEFECTS		HP:0007542	OMIM:172850	IEA				P		HPO:iea	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0000006	OMIM:172870	TAS				I		HPO:nvasilevsky	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0000540	OMIM:172870	TAS				P		HPO:probinson	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0000565	OMIM:172870	TAS				P		HPO:probinson	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0001417	OMIM:172870	TAS				I		HPO:nvasilevsky	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0007737	OMIM:172870	TAS				P		HPO:probinson	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0007773	OMIM:172870	TAS				P		HPO:probinson	
OMIM	172870	PIGMENTED PARAVENOUS CHORIORETINAL ATROPHY		HP:0007903	OMIM:172870	TAS				P		HPO:probinson	
OMIM	172880	PIERRE ROBIN SYNDROME AND OLIGODACTYLY		HP:0000006	OMIM:172880	IEA				I		HPO:iea	
OMIM	172880	PIERRE ROBIN SYNDROME AND OLIGODACTYLY		HP:0000175	OMIM:172880	IEA				P		HPO:skoehler	
OMIM	172880	PIERRE ROBIN SYNDROME AND OLIGODACTYLY		HP:0000201	OMIM:172880	IEA				P		HPO:iea	
OMIM	172880	PIERRE ROBIN SYNDROME AND OLIGODACTYLY		HP:0000347	OMIM:172880	IEA				P		HPO:iea	
OMIM	172880	PIERRE ROBIN SYNDROME AND OLIGODACTYLY		HP:0001180	OMIM:172880	IEA				P		HPO:iea	
OMIM	172900	PIGMENTED PURPURIC ERUPTION		HP:0000006	OMIM:172900	IEA				I		HPO:iea	
OMIM	172900	PIGMENTED PURPURIC ERUPTION		HP:0000951	OMIM:172900	IEA				P		HPO:iea	
OMIM	172900	PIGMENTED PURPURIC ERUPTION		HP:0003623	OMIM:172900	IEA				C		HPO:iea	
OMIM	173000	PILONIDAL SINUS		HP:0000006	OMIM:173000	IEA				I		HPO:iea	
OMIM	173000	PILONIDAL SINUS		HP:0000951	OMIM:173000	IEA				P		HPO:iea	
OMIM	173000	PILONIDAL SINUS		HP:0010769	OMIM:173000	IEA				P		HPO:skoehler	
OMIM	173100	#173100 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II; IGHD2;;IGHD II;;GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL DOMINANT;;PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMALDOMINANT		HP:0000006	OMIM:173100	TAS				I		HPO:skoehler	
OMIM	173100	#173100 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II; IGHD2;;IGHD II;;GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL DOMINANT;;PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMALDOMINANT		HP:0000824	OMIM:173100	TAS				P		HPO:iea	
OMIM	173100	#173100 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II; IGHD2;;IGHD II;;GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL DOMINANT;;PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMALDOMINANT		HP:0000839	OMIM:173100	IEA				P		HPO:iea	
OMIM	173100	#173100 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE II; IGHD2;;IGHD II;;GROWTH HORMONE DEFICIENCY, ISOLATED, AUTOSOMAL DOMINANT;;PITUITARY DWARFISM DUE TO ISOLATED GROWTH HORMONE DEFICIENCY, AUTOSOMALDOMINANT		HP:0003510	OMIM:173100	IEA				P		HPO:iea	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0000006	OMIM:173200	TAS				I		HPO:skoehler	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0000656	OMIM:173200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0000982	OMIM:173200	TAS				P		HPO:skoehler	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0001036	OMIM:173200	IEA				P		HPO:skoehler	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0008392	OMIM:173200	TAS				P		HPO:skoehler	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0025114	OMIM:173200	IEA				P		HPO:skoehler	
OMIM	173200	PITYRIASIS RUBRA PILARIS; PRP		HP:0040162	OMIM:173200	IEA				P		HPO:skoehler	
OMIM	173400	173400 PLATELET AGGREGATION, SPONTANEOUS		HP:0000006	OMIM:173400	TAS				I		HPO:probinson	
OMIM	173400	173400 PLATELET AGGREGATION, SPONTANEOUS		HP:0004419	OMIM:173400	TAS				P		HPO:probinson	
OMIM	173400	173400 PLATELET AGGREGATION, SPONTANEOUS		HP:0030403	OMIM:173400	TAS				P		HPO:skoehler	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0000006	OMIM:173420	IEA				I		HPO:iea	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0001873	OMIM:173420	IEA				P		HPO:iea	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0003006	OMIM:173420	TAS				P		HPO:skoehler	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0003010	OMIM:173420	IEA				P		HPO:iea	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0003540	OMIM:173420	IEA				P		HPO:iea	
OMIM	173420	PLATELET DISORDER, UNDEFINED		HP:0004377	OMIM:173420	TAS				P		HPO:skoehler	
OMIM	173450	PLATELET FACTOR 3 DEFICIENCY		HP:0000006	OMIM:173450	IEA				I		HPO:iea	
OMIM	173450	PLATELET FACTOR 3 DEFICIENCY		HP:0001892	OMIM:173450	IEA				P		HPO:iea	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000007	OMIM:173470	TAS				I	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000132	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000225	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000421	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000978	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0000979	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0001928	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0001975	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0002170	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0002239	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0003540	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0004809	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173470	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIa; GP3A;;GP IIIa;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED		HP:0004813	OMIM:173470	TAS				P	+173470 INTEGRIN, BETA-3; ITGB3;;PLATELET GLYCOPROTEIN IIIA; GP3A;;GP IIIA;;PLATELET FIBRINOGEN RECEPTOR, BETA SUBUNIT;;CD61THROMBOCYTOPENIA, NEONATAL ALLOIMMUNE, INCLUDED; NAIT, INCLUDED;;POSTTRANSFUSION PURPURA, INCLUDED; PTP, INCLUDED	HPO:skoehler	
OMIM	173580	PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED		HP:0000006	OMIM:173580	TAS				I		HPO:probinson	
OMIM	173580	PLATELET RESPONSIVENESS TO ADRENALINE, DEPRESSED		HP:0008148	OMIM:173580	TAS				P		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0000006	OMIM:173590	TAS				I		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0000421	OMIM:173590	TAS				P		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0001873	OMIM:173590	TAS				P		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0004866	OMIM:173590	TAS				P		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0008148	OMIM:173590	TAS				P		HPO:probinson	
OMIM	173590	PLATELET SIGNAL PROCESSING DEFECT		HP:0008320	OMIM:173590	TAS				P		HPO:probinson	
OMIM	173600	PNEUMOTHORAX, PRIMARY SPONTANEOUS		HP:0000006	OMIM:173600	IEA				I		HPO:iea	
OMIM	173600	PNEUMOTHORAX, PRIMARY SPONTANEOUS		HP:0002108	OMIM:173600	TAS				P		HPO:skoehler	
OMIM	173600	PNEUMOTHORAX, PRIMARY SPONTANEOUS		HP:0003829	OMIM:173600	IEA				C		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0000007	OMIM:173650	TAS				I		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0000670	OMIM:173650	TAS				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0000704	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0000972	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0000992	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0001030	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0001741	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0001807	OMIM:173650	TAS				P		HPO:probinson	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0004334	OMIM:173650	TAS				P		HPO:probinson	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0005585	OMIM:173650	TAS				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0005590	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0007488	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0007561	OMIM:173650	IEA				P		HPO:iea	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0009775	OMIM:173650	TAS				P		HPO:probinson	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0031045	OMIM:173650	IEA				P		HPO:skoehler	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0200020	PMID:21683471	PCS				P		HPO:probinson	
OMIM	173650	KINDLER SYNDROME; KNDLRS		HP:0430007	PMID:21683471	PCS				P		HPO:probinson	
OMIM	173700	173700 POIKILODERMA, HEREDITARY SCLEROSING		HP:0000006	OMIM:173700	TAS				I		HPO:iea	
OMIM	173700	173700 POIKILODERMA, HEREDITARY SCLEROSING		HP:0001029	OMIM:173700	TAS				P		HPO:iea	
OMIM	173700	173700 POIKILODERMA, HEREDITARY SCLEROSING		HP:0007618	OMIM:173700	TAS				P		HPO:iea	
OMIM	173700	173700 POIKILODERMA, HEREDITARY SCLEROSING		HP:0100759	OMIM:173700	TAS				P		HPO:skoehler	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0000006	OMIM:173800	IEA				I		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0000769	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0000773	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0000902	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0000912	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0001159	OMIM:173800	IEA				P		HPO:skoehler	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0001651	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0002937	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0005255	OMIM:173800	TAS				P		HPO:skoehler	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0005256	OMIM:173800	TAS				P		HPO:probinson	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0006008	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0006230	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0009011	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0009026	OMIM:173800	IEA				P		HPO:iea	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0011959	OMIM:173800	TAS				P		HPO:probinson	
OMIM	173800	%173800 POLAND SYNDROME;;POLAND SYNDACTYLY;;POLAND ANOMALY;;POLAND SEQUENCEPECTORALIS MUSCLE, ABSENCE OF, INCLUDED		HP:0030241	OMIM:173800	IEA				P		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0000006	OMIM:173900	IEA				I		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0000083	OMIM:173900	IEA				P		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0000113	OMIM:173900	IEA				P		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0000822	OMIM:173900	TAS				P		HPO:probinson	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0001407	OMIM:173900	IEA				P		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0001634	PMID:3419455	PCS		HP:0040284		P		HPO:iea	42/163
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0001653	OMIM:173900	PCS		HP:0040284		P		HPO:iea	51/163
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0002253	OMIM:173900	IEA				P		HPO:iea	
OMIM	173900	POLYCYSTIC KIDNEYS		HP:0007029	PMID:1513348	PCS		HP:0040284		P		HPO:iea	4/88
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000006	OMIM:174000	IEA				I		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000089	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000092	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000096	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000108	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000127	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0000822	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0001903	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0001970	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0001997	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0002048	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0002149	OMIM:174000	IEA				P		HPO:skoehler	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0002615	OMIM:174000	TAS				P		HPO:probinson	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0003259	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0003581	OMIM:174000	IEA				C		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0003774	OMIM:174000	TAS				P		HPO:probinson	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0004732	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0005576	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0005583	OMIM:174000	IEA				P		HPO:iea	
OMIM	174000	MEDULLARY CYSTIC KIDNEY DISEASE 1; MCKD1		HP:0012213	OMIM:174000	IEA				P		HPO:iea	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0000006	OMIM:174050	IEA				I		HPO:iea	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0000107	OMIM:174050	IEA				P		HPO:skoehler	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0000707	OMIM:174050	IEA				P		HPO:iea	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0001541	OMIM:174050	IEA				P		HPO:skoehler	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0001626	OMIM:174050	IEA				P		HPO:iea	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1	HP:0012825	HP:0003155	OMIM:174050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0003270	OMIM:174050	TAS				P		HPO:skoehler	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0003418	OMIM:174050	TAS				P		HPO:skoehler	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0003573	OMIM:174050	IEA				P		HPO:iea	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0003581	OMIM:174050	IEA				C		HPO:skoehler	
OMIM	174050	POLYCYSTIC LIVER DISEASE 1 WITH OR WITHOUT KIDNEY CYSTS; PCLD1		HP:0006557	OMIM:174050	TAS				P		HPO:skoehler	
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0000006	OMIM:174200	TAS				I		HPO:skoehler	
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0001159	OMIM:174200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0001162	OMIM:174200	IEA				P		HPO:iea	
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0001199	OMIM:174200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0011304	OMIM:174200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174200	POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1		HP:0100258	OMIM:174200	TAS				P		HPO:skoehler	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000007	OMIM:174300	IEA				I		HPO:iea	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000161	OMIM:174300	IEA				P		HPO:iea	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000175	OMIM:174300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000180	OMIM:174300	TAS				P		HPO:skoehler	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000193	OMIM:174300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0000316	OMIM:174300	TAS				P		HPO:skoehler	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0001162	OMIM:174300	IEA				P		HPO:iea	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0001249	OMIM:174300	TAS				P		HPO:skoehler	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0001274	OMIM:174300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0001830	OMIM:174300	IEA				P		HPO:iea	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0002007	OMIM:174300	TAS				P		HPO:skoehler	
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0002251	OMIM:174300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174300	#174300 OROFACIODIGITAL SYNDROME V; OFD5;;OFDS V;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE V;;OROFACIODIGITAL SYNDROME, THURSTON TYPE;;THURSTON SYNDROME;;POLYDACTYLY, POSTAXIAL, WITH MEDIAN CLEFT OF UPPER LIP		HP:0002650	OMIM:174300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	174310	POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA		HP:0000006	OMIM:174310	IEA				I		HPO:iea	
OMIM	174310	POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA		HP:0000545	OMIM:174310	IEA				P		HPO:iea	
OMIM	174310	POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA		HP:0001162	OMIM:174310	IEA				P		HPO:iea	
OMIM	174400	POLYDACTYLY, PREAXIAL I		HP:0000006	OMIM:174400	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	174400	POLYDACTYLY, PREAXIAL I		HP:0001177	OMIM:174400	IEA				P		HPO:iea	
OMIM	174400	POLYDACTYLY, PREAXIAL I		HP:0005895	OMIM:174400	IEA				P		HPO:iea	
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0000006	PMID:12837695	PCS				I		HPO:iea	
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0001159	PMID:18178630	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0001162	PMID:18178630	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0001177	PMID:18178630	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0001830	PMID:18178630	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0001841	PMID:18178630	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0005866	OMIM:174500	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0009606	OMIM:174500	TAS				P		HPO:skoehler	
OMIM	174500	#174500 POLYDACTYLY, PREAXIAL II; PPD2;;POLYDACTYLY OF TRIPHALANGEAL THUMB;;TRIPHALANGEAL THUMB-POLYDACTYLY SYNDROMETRIPHALANGEAL THUMB WITH POLYSYNDACTYLY, INCLUDED;;TRIPHALANGEAL THUMB-POLYSYNDACTYLY SYNDROME, INCLUDED;;TPT-PS SYNDROME, INCLUDED;;TRIPHALANGEAL THUMB, INCLUDED; TPT, INCLUDED		HP:0010066	OMIM:174500	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	174600	%174600 POLYDACTYLY, PREAXIAL III;;INDEX FINGER POLYDACTYLY		HP:0000006	OMIM:174600	IEA				I		HPO:iea	
OMIM	174600	%174600 POLYDACTYLY, PREAXIAL III;;INDEX FINGER POLYDACTYLY		HP:0001199	OMIM:174600	IEA				P		HPO:iea	
OMIM	174600	%174600 POLYDACTYLY, PREAXIAL III;;INDEX FINGER POLYDACTYLY		HP:0100258	OMIM:174600	TAS				P		HPO:skoehler	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0000006	OMIM:174700	TAS				I		HPO:probinson	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0000363	OMIM:174700	TAS				P		HPO:probinson	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0005688	OMIM:174700	TAS				P		HPO:probinson	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0006097	OMIM:174700	TAS				P		HPO:probinson	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0010713	OMIM:174700	TAS				P		HPO:probinson	
OMIM	174700	POLYDACTYLY, PREAXIAL IV		HP:0100258	OMIM:174700	TAS				P		HPO:probinson	
OMIM	174770	%174770 ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE;;JUVENILE SPRING ERUPTION OF EARS, INCLUDED		HP:0000006	OMIM:174770	IEA				I		HPO:iea	
OMIM	174770	%174770 ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE;;JUVENILE SPRING ERUPTION OF EARS, INCLUDED		HP:0000099	OMIM:174770	TAS				P		HPO:skoehler	
OMIM	174770	%174770 ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE;;JUVENILE SPRING ERUPTION OF EARS, INCLUDED		HP:0000992	OMIM:174770	TAS				P		HPO:iea	
OMIM	174770	%174770 ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE;;JUVENILE SPRING ERUPTION OF EARS, INCLUDED		HP:0000999	OMIM:174770	TAS				P		HPO:skoehler	
OMIM	174770	%174770 ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY; HPLE;;JUVENILE SPRING ERUPTION OF EARS, INCLUDED		HP:0100825	OMIM:174770	TAS				P		HPO:skoehler	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000324	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000365	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000618	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000826	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000836	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000843	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000845	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0000870	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0001442	OMIM:174800	IEA				I		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0002756	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0002893	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0003118	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0004493	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0005605	OMIM:174800	IEA				P		HPO:iea	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0010735	OMIM:174800	IEA				P		HPO:skoehler	
OMIM	174800	#174800 MCCUNE-ALBRIGHT SYNDROME; MAS;;ALBRIGHT SYNDROMEPOLYOSTOTIC FIBROUS DYSPLASIA, INCLUDED; PFD, INCLUDED; POFD, INCLUDED		HP:0200008	OMIM:174800	TAS				P		HPO:skoehler	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0000006	OMIM:174810	TAS				I		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0000405	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0002653	OMIM:174810	TAS				P		HPO:skoehler	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0002753	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0002756	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0002797	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0003080	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0003155	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0003676	OMIM:174810	TAS				C		HPO:skoehler	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0006480	OMIM:174810	TAS				P		HPO:probinson	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0006487	OMIM:174810	TAS				P		HPO:skoehler	
OMIM	174810	FAMILIAL EXPANSILE OSTEOLYSIS		HP:0025124	OMIM:174810	TAS				P		HPO:skoehler	
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0000006	OMIM:174900	PCS				I		HPO:iea	
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0001217	OMIM:174900	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0001508	OMIM:174900	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0001903	ISBN-10:0-19-262896-8	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0002027	ISBN-10:0-19-262896-8	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0002035	ISBN-10:0-19-262896-8	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0002573	ISBN-10:0-19-262896-8	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0002576	OMIM:174900	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0002900	OMIM:174900	TAS				P		HPO:skoehler	
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0003003	ISBN-10:0-19-262896-8	PCS		HP:0040284		P		HPO:iea	20%
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0003073	OMIM:174900	TAS				P		HPO:skoehler	
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0004394	OMIM:174900	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	174900	#174900 JUVENILE POLYPOSIS SYNDROME; JPS;;POLYPOSIS, JUVENILE INTESTINAL; PJI;;JUVENILE INTESTINAL POLYPOSIS; JIP;;POLYPOSIS, FAMILIAL, OF ENTIRE GASTROINTESTINAL TRACTJUVENILE POLYPOSIS OF STOMACH, INCLUDED;;JUVENILE POLYPOSIS COLI, INCLUDED		HP:0006771	ISBN-10:0-19-262896-8	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175020	POLYPOSIS, GASTRIC		HP:0000006	OMIM:175020	TAS				I		HPO:skoehler	
OMIM	175020	POLYPOSIS, GASTRIC		HP:0004394	OMIM:175020	IEA				P		HPO:iea	
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0000006	OMIM:175050	PCS				I		HPO:iea	
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0000421	PMID:15031030	PCS		HP:0040284		P		HPO:iea	10/16
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001009	PMID:15031030	PCS		HP:0040284		P		HPO:iea	14/20
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001217	PMID:15031030	PCS		HP:0040284		P		HPO:iea	17/25
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001297	PMID:15031030	PCS		HP:0040284		P		HPO:iea	3/25
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001634	OMIM:175050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001653	OMIM:175050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0001903	OMIM:175050	TAS				P		HPO:skoehler	
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0002408	PMID:15031030	PCS		HP:0040284		P		HPO:iea	3/25
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0002573	OMIM:175050	TAS				P		HPO:skoehler	
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0002647	OMIM:175050	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0002672	PMID:15031030	PCS		HP:0040284		P		HPO:iea	5/20
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0004390	OMIM:175050	TAS				P		HPO:skoehler	
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0004784	OMIM:175050	PCS		HP:0040284		P		HPO:iea	100%
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0004942	OMIM:175050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0006548	PMID:15031030	PCS		HP:0040284		P		HPO:iea	18/25
OMIM	175050	JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME; JPHT		HP:0006574	PMID:15031030	PCS		HP:0040284		P		HPO:iea	6/25
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0000006	OMIM:175100	PCS				I		HPO:iea	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0000670	OMIM:175100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0000706	OMIM:175100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0000953	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0001012	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0002884	PMID:1329510	PCS		HP:0040284		P		HPO:iea	2/470
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0002885	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=fap	PCS		HP:0040284		P		HPO:iea	1%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0002895	PMID:22425061	PCS		HP:0040284		P		HPO:iea	6%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0003003	OMIM:175100	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0003828	OMIM:175100	PCS				C		HPO:iea	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0004394	OMIM:175100	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0004783	https://www.ncbi.nlm.nih.gov/books/NBK1345/	PCS		HP:0040284		P		HPO:iea	90%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0005227	OMIM:175100	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0006722	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0006744	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0006771	PMID:14960520	PCS		HP:0040284		P		HPO:iea	5%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0007649	OMIM:175100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0008256	PMID:11156460	PCS		HP:0040284		P		HPO:iea	13%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0009592	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0010562	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0010619	OMIM:175100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0011068	OMIM:175100	TAS				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0011069	OMIM:175100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0030731	OMIM:175100	IEA				P		HPO:skoehler	
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0100245	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=fap	PCS		HP:0040284		P		HPO:iea	10%
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0100246	PMID:13946545;PMID:14933371	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175100	FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1		HP:0200040	PMID:13946545;PMID:14933371	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0000006	PMID:28445255	PCS				I		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0000069	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0000138	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0000153	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0000771	OMIM:175200	TAS				P		HPO:skoehler	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0001034	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0001080	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0001217	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0001891	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002027	OMIM:175200	IEA				P		HPO:skoehler	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002035	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002576	PMID:30699321	PCS				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002584	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002672	PMID:3587280	PCS		HP:0040284		P		HPO:iea	4/31
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0002894	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0003002	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0004390	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0008204	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0010784	OMIM:175200	IEA				P		HPO:skoehler	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0100582	OMIM:175200	IEA				P		HPO:iea	
OMIM	175200	PEUTZ-JEGHERS SYNDROME; PJS		HP:0100759	OMIM:175200	TAS				P		HPO:skoehler	
OMIM	175400	POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE		HP:0000006	OMIM:175400	IEA				I		HPO:iea	
OMIM	175400	POLYPOSIS, INTESTINAL, SCATTERED AND DISCRETE		HP:0005238	OMIM:175400	IEA				P		HPO:iea	
OMIM	175450	POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES		HP:0000006	OMIM:175450	IEA				I		HPO:iea	
OMIM	175450	POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES		HP:0002762	OMIM:175450	IEA				P		HPO:iea	
OMIM	175450	POLYPOSIS, INTESTINAL, WITH MULTIPLE EXOSTOSES		HP:0200008	OMIM:175450	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0000206	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0000217	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0000518	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0000953	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0001217	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0001324	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0001596	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0001903	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0001907	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002013	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002024	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002027	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002039	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002164	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002243	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002573	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002672	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002900	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002901	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0002917	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0003401	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0003745	OMIM:175500	IEA				I		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0004326	OMIM:175500	IEA				P		HPO:iea	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0004390	OMIM:175500	TAS				P		HPO:skoehler	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0008404	OMIM:175500	TAS				P		HPO:skoehler	
OMIM	175500	175500 POLYPOSIS, SKIN PIGMENTATION, ALOPECIA, AND FINGERNAIL CHANGES;;CRONKHITE-CANADA SYNDROME		HP:0100759	OMIM:175500	TAS				P		HPO:skoehler	
OMIM	175505	POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI		HP:0000006	OMIM:175505	TAS				I		HPO:probinson	
OMIM	175505	POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI		HP:0004295	OMIM:175505	TAS				P		HPO:probinson	
OMIM	175505	POLYPOSIS OF GASTRIC FUNDUS WITHOUT POLYPOSIS COLI		HP:0004394	OMIM:175505	TAS				P		HPO:probinson	
OMIM	175510	POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL		HP:0000006	OMIM:175510	TAS				I		HPO:probinson	
OMIM	175510	POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL		HP:0002576	OMIM:175510	TAS				P		HPO:probinson	
OMIM	175510	POLYPS, MULTIPLE AND RECURRENT INFLAMMATORY FIBROID, GASTROINTESTINAL		HP:0200008	OMIM:175510	TAS				P		HPO:iea	
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000006	OMIM:175700	TAS				I		HPO:iea	
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000023	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000028	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000047	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000238	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000243	OMIM:175700	TAS				P		HPO:skoehler	
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000256	PMID:15739154	PCS		HP:0040284		P		HPO:iea	53%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000270	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000316	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000348	PMID:15739154	PCS		HP:0040284		P		HPO:iea	70%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000431	PMID:15739154	PCS		HP:0040284		P		HPO:iea	79%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0000494	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001007	PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001162	PMID:15739154	PCS		HP:0040284		P		HPO:iea	78%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001177	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001250	ISBN-13:978-0721606156;PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001256	ISBN-13:978-0721606156;PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001274	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001363	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001459	PMID:15739154	PCS		HP:0040284		P		HPO:iea	90%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001537	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001627	ISBN-13:978-0721606156;PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001830	PMID:15739154	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001836	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0001841	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0002007	PMID:15739154	PCS		HP:0040284		P		HPO:iea	58%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0003074	PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0003828	OMIM:175700	TAS				C		HPO:skoehler	
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0004303	PMID:11484201	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0005616	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0006097	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0009473	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0010055	PMID:15739154	PCS		HP:0040284		P		HPO:iea	89%
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0010059	OMIM:175700	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0011304	OMIM:175700	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0011330	OMIM:175700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	175700	GREIG CEPHALOPOLYSYNDACTYLY SYNDROME		HP:0030799	OMIM:175700	TAS				P		HPO:skoehler	
OMIM	175750	POPLITEAL CYST		HP:0000006	OMIM:175750	IEA				I		HPO:iea	
OMIM	175750	POPLITEAL CYST		HP:0001386	PMID:5080689	PCS				P		HPO:lccarmody	
OMIM	175750	POPLITEAL CYST		HP:0002815	OMIM:175750	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0000006	OMIM:175780	IEA				I		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0000238	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0000577	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001123	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001249	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001250	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001257	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001272	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0001878	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002132	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002140	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002273	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002301	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002352	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0002451	OMIM:175780	IEA				P		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0003236	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0003487	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0003828	OMIM:175780	IEA				C		HPO:iea	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0007209	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0010636	OMIM:175780	TAS				P		HPO:skoehler	
OMIM	175780	PORENCEPHALY 1; POREN1		HP:0032046	OMIM:175780	IEA				P		HPO:skoehler	
OMIM	175800	POROKERATOSIS OF MIBELLI		HP:0000006	OMIM:175800	TAS				I		HPO:probinson	
OMIM	175800	POROKERATOSIS OF MIBELLI		HP:0003220	OMIM:175800	TAS				P		HPO:probinson	
OMIM	175800	POROKERATOSIS OF MIBELLI		HP:0003596	OMIM:175800	TAS				C		HPO:probinson	
OMIM	175800	POROKERATOSIS OF MIBELLI		HP:0008069	OMIM:175800	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	175800	POROKERATOSIS OF MIBELLI		HP:0200044	OMIM:175800	TAS				P		HPO:skoehler	
OMIM	175850	POROKERATOSIS PLANTARIS, PALMARIS, ET DISSEMINATA		HP:0000006	OMIM:175850	TAS				I		HPO:probinson	
OMIM	175850	POROKERATOSIS PLANTARIS, PALMARIS, ET DISSEMINATA		HP:0100869	OMIM:175850	TAS				P		HPO:probinson	
OMIM	175850	POROKERATOSIS PLANTARIS, PALMARIS, ET DISSEMINATA		HP:0100870	OMIM:175850	TAS				P		HPO:probinson	
OMIM	175850	POROKERATOSIS PLANTARIS, PALMARIS, ET DISSEMINATA		HP:0200044	OMIM:175850	TAS				P		HPO:skoehler	
OMIM	175860	POROKERATOSIS PUNCTATA PALMARIS ET PLANTARIS		HP:0000006	OMIM:175860	IEA				I		HPO:iea	
OMIM	175860	POROKERATOSIS PUNCTATA PALMARIS ET PLANTARIS		HP:0007613	OMIM:175860	IEA				P		HPO:iea	
OMIM	175860	POROKERATOSIS PUNCTATA PALMARIS ET PLANTARIS		HP:0200044	OMIM:175860	IEA				P		HPO:skoehler	
OMIM	175900	POROKERATOSIS 3, MULTIPLE TYPES; POROK3		HP:0000006	OMIM:175900	IEA				I		HPO:iea	
OMIM	175900	POROKERATOSIS 3, MULTIPLE TYPES; POROK3		HP:0001036	OMIM:175900	IEA				P		HPO:skoehler	
OMIM	175900	POROKERATOSIS 3, MULTIPLE TYPES; POROK3		HP:0008404	OMIM:175900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	175900	POROKERATOSIS 3, MULTIPLE TYPES; POROK3		HP:0200044	OMIM:175900	IEA				P		HPO:skoehler	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000006	OMIM:176000	IEA				I		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000016	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000020	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000716	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000725	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000739	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0000822	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0001250	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0001324	OMIM:176000	TAS				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0001402	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0001649	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002013	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002014	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002018	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002019	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002027	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002203	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0002590	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0003163	OMIM:176000	TAS				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0003401	OMIM:176000	TAS				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0003489	OMIM:176000	IEA				P		HPO:probinson	
OMIM	176000	#176000 PORPHYRIA, ACUTE INTERMITTENT;;AIP;;PORPHYRIA, SWEDISH TYPE;;PORPHOBILINOGEN DEAMINASE DEFICIENCY;;PBGD DEFICIENCY;;UROPORPHYRINOGEN SYNTHASE DEFICIENCY;;UPS DEFICIENCYPORPHYRIA, ACUTE INTERMITTENT, NONERYTHROID VARIANT, INCLUDED;;PORPHYRIA, CHESTER TYPE, INCLUDED; PORC, INCLUDED		HP:0100518	OMIM:176000	TAS				P		HPO:skoehler	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0000006	OMIM:176090	IEA				I		HPO:iea	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0000953	OMIM:176090	IEA				P		HPO:iea	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0000964	OMIM:176090	IEA				P		HPO:skoehler	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0000998	OMIM:176090	IEA				P		HPO:iea	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0001030	OMIM:176090	IEA				P		HPO:skoehler	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0001395	OMIM:176090	IEA				P		HPO:iea	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0001425	OMIM:176090	TAS				I		HPO:skoehler	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0010473	OMIM:176090	TAS				P		HPO:probinson	
OMIM	176090	PORPHYRIA CUTANEA TARDA, TYPE I		HP:0030955	OMIM:176090	IEA				P		HPO:skoehler	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0000006	OMIM:176100	IEA				I		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0000007	OMIM:176100	IEA				I		HPO:skoehler	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0000992	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0001030	OMIM:176100	IEA				P		HPO:skoehler	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0001394	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0001402	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0001596	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0001806	OMIM:176100	IEA				P		HPO:skoehler	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0002219	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0005586	OMIM:176100	IEA				P		HPO:iea	
OMIM	176100	PORPHYRIA CUTANEA TARDA		HP:0100324	OMIM:176100	TAS				P		HPO:skoehler	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0000006	OMIM:176200	TAS				I		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0000709	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0000992	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0001649	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0002013	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0002019	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0002027	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0003470	OMIM:176200	IEA				P		HPO:skoehler	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0009830	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176200	PORPHYRIA VARIEGATA		HP:0010473	OMIM:176200	TAS				P		HPO:probinson	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0000006	OMIM:176240	IEA				I		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0000954	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0001162	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0001830	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0002986	OMIM:176240	IEA				P		HPO:skoehler	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0004251	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0006209	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0006210	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0008079	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0010046	OMIM:176240	IEA				P		HPO:iea	
OMIM	176240	POSTAXIAL OLIGODACTYLY, TETRAMELIC		HP:0010579	OMIM:176240	IEA				P		HPO:iea	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0000006	OMIM:176250	TAS				I		HPO:probinson	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0001251	OMIM:176250	TAS				P		HPO:probinson	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0001315	OMIM:176250	TAS				P		HPO:probinson	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0002495	OMIM:176250	TAS				P		HPO:probinson	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0002650	OMIM:176250	TAS				P		HPO:probinson	
OMIM	176250	POSTERIOR COLUMN ATAXIA		HP:0010831	OMIM:176250	TAS				P		HPO:probinson	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000028	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	85%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000044	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000046	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	69%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000054	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000060	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000064	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000219	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000219	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000268	OMIM:176270	TAS				P		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000341	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000446	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000540	OMIM:176270	TAS				P		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000545	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000565	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000582	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000670	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000709	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	15%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000717	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	19%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000750	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000786	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	56%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000789	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000823	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000824	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000826	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	4%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000842	OMIM:176270	TAS				P		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000846	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	60%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000876	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000938	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000939	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0000992	ISBN-13:978-0721606156	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001159	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	15%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001270	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS	HP:0003623	HP:0040281		P		HPO:probinson	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001319	OMIM:176270	IEA				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001328	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001385	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	10%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001531	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001558	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS				P		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001611	ISBN-13:978-0721606156	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0001773	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002033	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002119	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002205	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002236	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002591	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS	HP:0003593	HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002714	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002791	OMIM:176270	TAS				P		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002808	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0002857	PMID:22043168	PCS				P		HP:probinson	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0003199	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS	HP:0003581	HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0003745	OMIM:176270	TAS				I		HPO:iea	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0004279	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0004283	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0004322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0005599	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	33%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0005968	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0005978	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS	HP:0011462	HP:0040284		P		HPO:iea	25%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007010	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007015	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007018	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS	HP:0003593	HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007328	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007513	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007730	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040284		P		HPO:iea	33%
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0007874	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0009466	ISBN-13:978-0721606156	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0010535	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pws	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0012743	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0030084	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0031878	PMID:22043168	PCS				P		HP:probinson	
OMIM	176270	PRADER-WILLI SYNDROME; PWS		HP:0200055	OMIM:176270	TAS				P		HPO:skoehler	
OMIM	176305	PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS		HP:0000006	OMIM:176305	IEA				I		HPO:iea	
OMIM	176305	PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS		HP:0000807	OMIM:176305	IEA				P		HPO:iea	
OMIM	176305	PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS		HP:0001162	OMIM:176305	IEA				P		HPO:iea	
OMIM	176305	PREAXIAL DEFICIENCY, POSTAXIAL POLYDACTYLY, AND HYPOSPADIAS		HP:0001885	OMIM:176305	TAS				P		HPO:probinson	
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0000006	OMIM:176400	TAS				I		HPO:iea	
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0000821	OMIM:176400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0004322	OMIM:176400	TAS	HP:0003581			P		HPO:iea	
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0008232	OMIM:176400	TAS				P		HPO:iea	
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0008236	OMIM:176400	TAS				P		HPO:iea	
OMIM	176400	PRECOCIOUS PUBERTY, CENTRAL		HP:0011969	OMIM:176400	TAS				P		HPO:iea	
OMIM	176410	PRECOCIOUS PUBERTY, MALE-LIMITED		HP:0001470	OMIM:176410	TAS				I		HPO:iea	
OMIM	176410	PRECOCIOUS PUBERTY, MALE-LIMITED		HP:0008185	OMIM:176410	TAS				P		HPO:iea	
OMIM	176410	PRECOCIOUS PUBERTY, MALE-LIMITED		HP:0008734	OMIM:176410	TAS				P		HPO:iea	
OMIM	176430	PREMATURE CHROMATID SEPARATION TRAIT		HP:0000006	OMIM:176430	IEA				I		HPO:iea	
OMIM	176430	PREMATURE CHROMATID SEPARATION TRAIT		HP:0200024	OMIM:176430	IEA				P		HPO:skoehler	
OMIM	176450	CURRARINO SYNDROME		HP:0000006	OMIM:176450	TAS				I		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000010	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000011	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000020	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000076	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000085	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000143	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0000813	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0001153	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0001263	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0002023	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0002025	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0002144	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0002617	OMIM:176450	IEA				P		HPO:skoehler	
OMIM	176450	CURRARINO SYNDROME		HP:0003270	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0003829	OMIM:176450	TAS				C		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0004796	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0007293	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0009789	OMIM:176450	TAS				P		HPO:probinson	
OMIM	176450	CURRARINO SYNDROME		HP:0009790	OMIM:176450	TAS		HP:0040284		P		HPO:probinson	75%
OMIM	176450	CURRARINO SYNDROME		HP:0009791	OMIM:176450	TAS		HP:0040284		P		HPO:probinson	22%
OMIM	176450	CURRARINO SYNDROME		HP:0009793	OMIM:176450	TAS				P		HPO:skoehler	
OMIM	176450	CURRARINO SYNDROME		HP:0010447	OMIM:176450	TAS				P		HPO:skoehler	
OMIM	176450	CURRARINO SYNDROME		HP:0012450	OMIM:176450	TAS				P		HPO:skoehler	
OMIM	176450	CURRARINO SYNDROME		HP:0100806	OMIM:176450	IEA				P		HPO:skoehler	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0000006	OMIM:176500	IEA				I		HPO:iea	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0000726	OMIM:176500	TAS				P		HPO:skoehler	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0001257	OMIM:176500	TAS				P		HPO:skoehler	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0001276	OMIM:176500	IEA				P		HPO:iea	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0001337	OMIM:176500	IEA				P		HPO:skoehler	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0002063	OMIM:176500	TAS				P		HPO:skoehler	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0002344	OMIM:176500	IEA				P		HPO:iea	
OMIM	176500	#176500 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1;;DEMENTIA, FAMILIAL BRITISH; FBD;;PRESENILE DEMENTIA WITH SPASTIC ATAXIA;;CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE		HP:0011970	OMIM:176500	TAS				P		HPO:skoehler	
OMIM	176600	PRESENILE DEMENTIA, KRAEPELIN TYPE		HP:0000006	OMIM:176600	IEA				I		HPO:iea	
OMIM	176600	PRESENILE DEMENTIA, KRAEPELIN TYPE		HP:0000726	OMIM:176600	TAS				P		HPO:skoehler	
OMIM	176620	176620 PRIAPISM, FAMILIAL IDIOPATHIC		HP:0000006	OMIM:176620	TAS				I		HPO:skoehler	
OMIM	176620	176620 PRIAPISM, FAMILIAL IDIOPATHIC		HP:0200023	OMIM:176620	IEA				P		HPO:skoehler	
OMIM	176630	176630 PRIMARY RELEASE DISORDER OF PLATELETS		HP:0000006	OMIM:176630	TAS				I		HPO:probinson	
OMIM	176630	176630 PRIMARY RELEASE DISORDER OF PLATELETS		HP:0000132	OMIM:176630	TAS				P		HPO:probinson	
OMIM	176630	176630 PRIMARY RELEASE DISORDER OF PLATELETS		HP:0000978	OMIM:176630	TAS				P		HPO:probinson	
OMIM	176630	176630 PRIMARY RELEASE DISORDER OF PLATELETS		HP:0004406	OMIM:176630	TAS				P		HPO:probinson	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0000006	OMIM:176670	IEA				I		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0000007	OMIM:176670	TAS				I		HPO:skoehler	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0000272	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0000347	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0001510	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0001596	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0001635	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0001658	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0001681	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0002797	PMID:16838330	PCS				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0004416	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0005181	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0007485	OMIM:176670	IEA				P		HPO:iea	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0011800	OMIM:176670	TAS				P		HPO:skoehler	
OMIM	176670	HUTCHINSON-GILFORD PROGERIA SYNDROME		HP:0040160	OMIM:176670	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000006	OMIM:176690	IEA				I		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000007	OMIM:176690	TAS				I		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000041	OMIM:176690	IEA				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000047	OMIM:176690	TAS				P		HPO:probinson	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000407	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000518	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000572	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000668	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000819	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0000823	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001054	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001249	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001367	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001518	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001518	OMIM:176690	TAS				P		HPO:probinson	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001620	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001647	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0001650	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0002013	OMIM:176690	IEA				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0002721	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0002943	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0003193	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0004322	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0004429	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0004791	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0005101	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0005320	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0005435	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0007879	OMIM:176690	IEA				P		HPO:iea	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0008209	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0040079	OMIM:176690	TAS				P		HPO:skoehler	
OMIM	176690	PROGEROID SHORT STATURE WITH PIGMENTED NEVI		HP:0100785	OMIM:176690	IEA				P		HPO:skoehler	
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0000006	OMIM:176700	TAS				I		HPO:skoehler	
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0000179	OMIM:176700	TAS				P		HPO:skoehler	
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0000303	OMIM:176700	IEA				P		HPO:iea	
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0001363	OMIM:176700	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0003829	OMIM:176700	TAS				C		HPO:skoehler	
OMIM	176700	PROGNATHISM, MANDIBULAR		HP:0007651	OMIM:176700	IEA				P		HPO:iea	
OMIM	176780	PELVIC ORGAN PROLAPSE		HP:0000006	OMIM:176780	IEA				I		HPO:iea	
OMIM	176780	PELVIC ORGAN PROLAPSE		HP:0002035	OMIM:176780	IEA				P		HPO:iea	
OMIM	176780	PELVIC ORGAN PROLAPSE		HP:0002607	OMIM:176780	IEA				P		HPO:skoehler	
OMIM	176800	176800 PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF		HP:0000006	OMIM:176800	TAS				I		HPO:probinson	
OMIM	176800	176800 PRONATION-SUPINATION OF THE FOREARM, IMPAIRMENT OF		HP:0006394	OMIM:176800	TAS				P		HPO:probinson	
OMIM	176807	PROSTATE CANCER		HP:0000006	OMIM:176807	TAS				I		HPO:skoehler	
OMIM	176807	PROSTATE CANCER		HP:0001428	OMIM:176807	IEA				I		HPO:skoehler	
OMIM	176807	PROSTATE CANCER		HP:0012125	OMIM:176807	TAS				P		HPO:probinson	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0000006	OMIM:176860	IEA				I		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0000478	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0000707	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0001038	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0002204	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0002625	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0002638	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0005305	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0005543	OMIM:176860	IEA				P		HPO:iea	
OMIM	176860	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN C DEFICIENCY, AUTOSOMALDOMINANT		HP:0100724	OMIM:176860	IEA				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000194	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000256	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0000268	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000276	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000494	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000508	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0000962	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0001012	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0001028	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0001140	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0001428	OMIM:176920	TAS				I		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0001528	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0001744	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0002176	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0002342	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0002625	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0002751	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0002753	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0003416	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0003593	OMIM:176920	TAS				C		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0003676	OMIM:176920	TAS				C		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0003745	OMIM:176920	IEA				I		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0003764	OMIM:176920	IEA				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0004472	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0004490	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0005280	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0005465	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0007403	OMIM:176920	IEA				P		HPO:iea	
OMIM	176920	PROTEUS SYNDROME		HP:0007483	OMIM:176920	TAS				P		HPO:probinson	
OMIM	176920	PROTEUS SYNDROME		HP:0010816	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0012032	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0012721	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0025092	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	176920	PROTEUS SYNDROME		HP:0100764	OMIM:176920	TAS				P		HPO:skoehler	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0000006	OMIM:177000	IEA				I		HPO:iea	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0000007	OMIM:177000	IEA				I		HPO:iea	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0000964	OMIM:177000	IEA				P		HPO:skoehler	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0000969	OMIM:177000	IEA				P		HPO:iea	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC	HP:0012825	HP:0000989	OMIM:177000	TAS				P		HPO:probinson	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC	HP:0012825	HP:0001081	OMIM:177000	TAS				P		HPO:probinson	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0001399	OMIM:177000	IEA				P		HPO:iea	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0001878	OMIM:177000	IEA				P		HPO:iea	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC	HP:0012825	HP:0002155	OMIM:177000	TAS				P		HPO:probinson	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC		HP:0010783	OMIM:177000	IEA				P		HPO:skoehler	
OMIM	177000	PROTOPORPHYRIA, ERYTHROPOIETIC	HP:0012825	HP:0011463	OMIM:177000	TAS				C		HPO:probinson	
OMIM	177050	PROTRUSIO ACETABULI		HP:0000006	OMIM:177050	IEA				I		HPO:iea	
OMIM	177050	PROTRUSIO ACETABULI		HP:0003179	PMID:629604	PCS				P		HPO:iea	
OMIM	177050	PROTRUSIO ACETABULI		HP:0003273	PMID:629604	PCS				P		HPO:iea	
OMIM	177050	PROTRUSIO ACETABULI		HP:0030838	PMID:629604	PCS				P		HPO:lccarmody	
OMIM	177050	PROTRUSIO ACETABULI		HP:0030838	OMIM:177050	IEA				P		HPO:skoehler	
OMIM	177100	PRURITUS, HEREDITARY LOCALIZED		HP:0000006	OMIM:177100	TAS				I		HPO:nvasilevsky	
OMIM	177100	PRURITUS, HEREDITARY LOCALIZED		HP:0000989	OMIM:177100	IEA				P		HPO:iea	
OMIM	177100	PRURITUS, HEREDITARY LOCALIZED		HP:0001423	OMIM:177100	TAS				I		HPO:nvasilevsky	
OMIM	177100	PRURITUS, HEREDITARY LOCALIZED		HP:0003581	OMIM:177100	IEA				C		HPO:iea	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0000006	OMIM:177170	TAS				I		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0000763	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0000926	PMID:27432013	PCS	HP:0011463	HP:0040284		P		HPO:probinson	5/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0001156	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0001377	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0001388	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0001498	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002341	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002515	PMID:20301660	PCS	HP:0011463			P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002650	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002663	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002758	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002758	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002808	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002816	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002829	PMID:20301660	PCS	HP:0011463			P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002834	PMID:21599986	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002857	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002938	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0002970	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0003026	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0003049	OMIM:177170	TAS				P		HPO:skoehler	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0003093	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0003311	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0003414	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0004019	PMID:21599986	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0004042	PMID:21599986	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0004236	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0004568	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0005063	OMIM:177170	TAS				P		HPO:skoehler	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0006467	PMID:27432013	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0008873	PMID:20301660	PCS	HP:0011463			P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0009487	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0009882	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0010049	PMID:20301660	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0010236	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0010582	PMID:27432013	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0011405	OMIM:177170	TAS				P		HPO:skoehler	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0012307	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177170	PSEUDOACHONDROPLASIA		HP:0100168	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0000006	OMIM:177200	IEA				I		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0000083	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0000822	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0001949	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0002900	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0003351	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0004319	OMIM:177200	IEA				P		HPO:iea	
OMIM	177200	LIDDLE SYNDROME 1; LIDLS1		HP:0200114	OMIM:177200	IEA				P		HPO:skoehler	
OMIM	177300	PSEUDOARTHROGRYPOSIS		HP:0000006	OMIM:177300	IEA				I		HPO:iea	
OMIM	177300	PSEUDOARTHROGRYPOSIS		HP:0002996	OMIM:177300	TAS				P		HPO:probinson	
OMIM	177300	PSEUDOARTHROGRYPOSIS		HP:0005892	OMIM:177300	IEA				P		HPO:iea	
OMIM	177300	PSEUDOARTHROGRYPOSIS		HP:0031013	OMIM:177300	IEA				P		HPO:skoehler	
OMIM	177350	PSEUDOATROPHODERMA COLLI		HP:0000006	OMIM:177350	IEA				I		HPO:iea	
OMIM	177350	PSEUDOATROPHODERMA COLLI		HP:0000951	OMIM:177350	IEA				P		HPO:iea	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0000007	OMIM:177400	TAS				I		HPO:probinson	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0000632	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0001649	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0002104	OMIM:177400	TAS				P		HPO:probinson	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0004302	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0004406	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0004972	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177400	BUTYRYLCHOLINESTERASE		HP:0011890	PMID:21637541	PCS				P		HPO:lccarmody	
OMIM	177600	PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF		HP:0000006	OMIM:177600	IEA				I		HPO:iea	
OMIM	177600	PSEUDOCHOLINESTERASE, INCREASE IN PLASMA LEVEL OF		HP:0001939	OMIM:177600	IEA				P		HPO:iea	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0000006	OMIM:177650	IEA				I		HPO:iea	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0000501	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0000518	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0001132	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0002063	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0009916	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0011499	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012627	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012629	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012631	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012633	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012635	OMIM:177650	IEA				P		HPO:skoehler	
OMIM	177650	EXFOLIATION SYNDROME; XFS		HP:0012636	OMIM:177650	TAS				P		HPO:skoehler	
OMIM	177700	#177700 GLAUCOMA 1, OPEN ANGLE, P; GLC1P		HP:0000006	OMIM:177700	IEA				I		HPO:iea	
OMIM	177700	#177700 GLAUCOMA 1, OPEN ANGLE, P; GLC1P		HP:0000501	OMIM:177700	IEA				P		HPO:skoehler	
OMIM	177700	#177700 GLAUCOMA 1, OPEN ANGLE, P; GLC1P		HP:0003581	OMIM:177700	TAS				C		HPO:probinson	
OMIM	177700	#177700 GLAUCOMA 1, OPEN ANGLE, P; GLC1P		HP:0007854	OMIM:177700	IEA				P		HPO:iea	
OMIM	177700	#177700 GLAUCOMA 1, OPEN ANGLE, P; GLC1P		HP:0012796	OMIM:177700	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0000006	OMIM:177735	TAS				I		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0000841	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0000848	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0000859	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0001508	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0001942	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0001944	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0002013	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0002014	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0002153	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0002615	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0002902	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0003593	OMIM:177735	TAS				C		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0008242	OMIM:177735	IEA				P		HPO:skoehler	
OMIM	177735	#177735 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL DOMINANT; PHA1A;;PHA I, AUTOSOMAL DOMINANT		HP:0011968	OMIM:177735	TAS				P		HPO:skoehler	
OMIM	177820	PSEUDO-VON WILLEBRAND DISEASE		HP:0000006	OMIM:177820	IEA				I		HPO:iea	
OMIM	177820	PSEUDO-VON WILLEBRAND DISEASE		HP:0003010	OMIM:177820	IEA				P		HPO:iea	
OMIM	177820	PSEUDO-VON WILLEBRAND DISEASE		HP:0004854	OMIM:177820	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000006	OMIM:177850	IEA				I		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000218	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000505	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000545	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000573	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000592	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000608	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0000766	OMIM:177850	TAS				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0001102	OMIM:177850	TAS				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0001342	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0001634	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0001681	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0002239	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0002634	OMIM:177850	IEA				P		HPO:skoehler	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0002650	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0002705	OMIM:177850	TAS				P		HPO:skoehler	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0002808	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0004966	OMIM:177850	TAS				P		HPO:probinson	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0005297	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0005462	OMIM:177850	IEA				P		HPO:iea	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0007663	OMIM:177850	TAS				P		HPO:skoehler	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0012457	OMIM:177850	TAS				P		HPO:probinson	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0025507	PMID:27933191	PCS				P		HPO:probinson	
OMIM	177850	PSEUDOXANTHOMA ELASTICUM, FORME FRUSTE		HP:0025533	OMIM:177850	TAS				P		HPO:skoehler	
OMIM	177900	PSORIASIS 1, SUSCEPTIBILITY TO		HP:0001369	OMIM:177900	IEA				P		HPO:iea	
OMIM	177900	PSORIASIS 1, SUSCEPTIBILITY TO		HP:0001426	OMIM:177900	IEA				I		HPO:iea	
OMIM	177900	PSORIASIS 1, SUSCEPTIBILITY TO		HP:0001803	OMIM:177900	IEA				P		HPO:iea	
OMIM	177900	PSORIASIS 1, SUSCEPTIBILITY TO		HP:0003765	OMIM:177900	TAS				P		HPO:iea	
OMIM	177900	PSORIASIS 1, SUSCEPTIBILITY TO		HP:0025088	OMIM:177900	TAS				P		HPO:skoehler	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000006	OMIM:177980	IEA				I		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000047	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000160	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000243	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000272	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000286	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000308	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000377	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0000767	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0001059	OMIM:177980	TAS				P		HPO:probinson	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0001249	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0001250	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0001547	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0001762	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0002007	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0002079	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0002536	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0002557	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0003241	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0004322	OMIM:177980	IEA				P		HPO:iea	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0011220	OMIM:177980	TAS				P		HPO:skoehler	
OMIM	177980	#177980 PTERYGIA, MENTAL RETARDATION, AND DISTINCTIVE CRANIOFACIAL FEATURES;;HASPESLAGH SYNDROME		HP:0012368	OMIM:177980	TAS				P		HPO:skoehler	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0000006	OMIM:177990	IEA				I		HPO:iea	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0000286	OMIM:177990	IEA				P		HPO:iea	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0000411	OMIM:177990	IEA				P		HPO:iea	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0000465	OMIM:177990	IEA				P		HPO:iea	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0002162	OMIM:177990	IEA				P		HPO:iea	
OMIM	177990	PTERYGIUM COLLI, ISOLATED		HP:0003196	OMIM:177990	IEA				P		HPO:iea	
OMIM	178000	PTERYGIUM OF CONJUNCTIVA AND CORNEA		HP:0000006	OMIM:178000	TAS				I		HPO:probinson	
OMIM	178000	PTERYGIUM OF CONJUNCTIVA AND CORNEA		HP:0000502	OMIM:178000	IEA				P		HPO:iea	
OMIM	178000	PTERYGIUM OF CONJUNCTIVA AND CORNEA		HP:0001059	OMIM:178000	TAS				P		HPO:probinson	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:178110	TAS				I		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000175	OMIM:178110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000368	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000470	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000494	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0000508	OMIM:178110	IEA				P		HPO:iea	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0001040	OMIM:178110	IEA				P		HPO:iea	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0001363	OMIM:178110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0002650	OMIM:178110	IEA				P		HPO:iea	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0002804	OMIM:178110	IEA				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0002937	OMIM:178110	IEA				P		HPO:iea	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0002948	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0002987	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0003273	OMIM:178110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0003302	OMIM:178110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0004322	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0006380	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178110	#178110 ARTHROGRYPOSIS, DISTAL, TYPE 8; DA8;;MULTIPLE PTERYGIUM SYNDROME, AUTOSOMAL DOMINANT;;PTERYGIUM SYNDROME, MULTIPLE, AUTOSOMAL DOMINANT		HP:0012385	OMIM:178110	TAS				P		HPO:skoehler	
OMIM	178200	PTERYGIUM, ANTECUBITAL		HP:0000006	OMIM:178200	IEA				I		HPO:iea	
OMIM	178200	PTERYGIUM, ANTECUBITAL		HP:0001377	OMIM:178200	IEA				P		HPO:iea	
OMIM	178200	PTERYGIUM, ANTECUBITAL		HP:0005739	OMIM:178200	IEA				P		HPO:iea	
OMIM	178200	PTERYGIUM, ANTECUBITAL		HP:0005829	OMIM:178200	IEA				P		HPO:iea	
OMIM	178200	PTERYGIUM, ANTECUBITAL		HP:0009760	OMIM:178200	TAS				P		HPO:probinson	
OMIM	178300	PTOSIS, HEREDITARY CONGENITAL 1		HP:0000006	OMIM:178300	IEA				I		HPO:iea	
OMIM	178300	PTOSIS, HEREDITARY CONGENITAL 1		HP:0007970	OMIM:178300	IEA				P		HPO:iea	
OMIM	178330	PTOSIS, STRABISMUS, AND ECTOPIC PUPILS		HP:0000006	OMIM:178330	IEA				I		HPO:iea	
OMIM	178330	PTOSIS, STRABISMUS, AND ECTOPIC PUPILS		HP:0000486	OMIM:178330	IEA				P		HPO:iea	
OMIM	178330	PTOSIS, STRABISMUS, AND ECTOPIC PUPILS		HP:0000508	OMIM:178330	IEA				P		HPO:iea	
OMIM	178350	PUBIC BONE DYSPLASIA		HP:0000006	OMIM:178350	IEA				I		HPO:iea	
OMIM	178350	PUBIC BONE DYSPLASIA		HP:0000924	OMIM:178350	IEA				P		HPO:iea	
OMIM	178370	PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT		HP:0000006	OMIM:178370	IEA				I		HPO:iea	
OMIM	178370	PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT		HP:0001629	OMIM:178370	IEA				P		HPO:iea	
OMIM	178370	PULMONARY ATRESIA WITH VENTRICULAR SEPTAL DEFECT		HP:0004935	OMIM:178370	IEA				P		HPO:iea	
OMIM	178400	PULMONARY EDEMA OF MOUNTAINEERS		HP:0000006	OMIM:178400	IEA				I		HPO:iea	
OMIM	178400	PULMONARY EDEMA OF MOUNTAINEERS		HP:0004890	OMIM:178400	IEA				P		HPO:iea	
OMIM	178400	PULMONARY EDEMA OF MOUNTAINEERS		HP:0100598	OMIM:178400	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0000006	OMIM:178500	IEA				I		HPO:iea	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0001217	OMIM:178500	IEA				P		HPO:iea	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0001394	OMIM:178500	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0002090	OMIM:178500	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0002092	OMIM:178500	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0002206	OMIM:178500	TAS				P		HPO:probinson	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0002875	OMIM:178500	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0006519	OMIM:178500	IEA				P		HPO:iea	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0010702	OMIM:178500	IEA				P		HPO:iea	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0012735	OMIM:178500	IEA				P		HPO:skoehler	
OMIM	178500	PULMONARY FIBROSIS, IDIOPATHIC; IPF		HP:0100759	OMIM:178500	TAS		HP:0040284		P		HPO:skoehler	50%
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0000006	OMIM:178550	IEA				I		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0001891	OMIM:178550	IEA				P		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0002093	OMIM:178550	IEA				P		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0002105	OMIM:178550	IEA				P		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0002206	OMIM:178550	IEA				P		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0005828	OMIM:178550	IEA				P		HPO:iea	
OMIM	178550	PULMONARY HEMOSIDEROSIS		HP:0006535	OMIM:178550	IEA				P		HPO:iea	
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0000006	OMIM:178600	PCS				I		HPO:iea	
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0000822	OMIM:178600	TAS				P		HPO:skoehler	
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0001009	OMIM:178600	TAS				P		HPO:skoehler	
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0001667	PMID:9729004	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0001708	PMID:9729004	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0001977	OMIM:178600	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0002092	PMID:9729004	PCS		HP:0040284		P		HPO:iea	100%
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0002094	OMIM:178600	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0003829	PMID:8988890	PCS				C		HPO:iea	
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0004964	OMIM:178600	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0005168	OMIM:178600	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0005308	OMIM:178600	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0005312	OMIM:178600	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0005317	PMID:9729004	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	178600	#178600 PULMONARY HYPERTENSION, PRIMARY, 1; PPH1;;PHT;;PULMONARY ARTERIAL HYPERTENSION; PAHPULMONARY HYPERTENSION, PRIMARY, DEXFENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, FENFLURAMINE-ASSOCIATED, INCLUDED;;PULMONARY HYPERTENSION, PRIMARY, 1, WITH HEREDITARY HEMORRHAGIC TELANGIECTASIA,INCLUDED;;PPH1 WITH HHT, INCLUDED		HP:0011353	OMIM:178600	TAS				P		HPO:skoehler	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0000006	OMIM:178610	IEA				I		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0000794	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0001217	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0001370	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0002086	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0002725	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0003493	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0003546	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0010702	OMIM:178610	IEA				P		HPO:iea	
OMIM	178610	178610 PULMONARY NODULAR LYMPHOID HYPERPLASIA, FAMILIAL		HP:0100759	OMIM:178610	TAS				P		HPO:skoehler	
OMIM	178650	PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES		HP:0000006	OMIM:178650	TAS				I		HPO:probinson	
OMIM	178650	PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES		HP:0001642	OMIM:178650	TAS				P		HPO:probinson	
OMIM	178650	PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES		HP:0001684	OMIM:178650	TAS				P		HPO:probinson	
OMIM	178650	PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES		HP:0003115	OMIM:178650	TAS				P		HPO:probinson	
OMIM	178651	PULMONIC STENOSIS AND DEAFNESS		HP:0000006	OMIM:178651	IEA				I		HPO:iea	
OMIM	178651	PULMONIC STENOSIS AND DEAFNESS		HP:0000365	OMIM:178651	IEA				P		HPO:iea	
OMIM	178651	PULMONIC STENOSIS AND DEAFNESS		HP:0001642	OMIM:178651	TAS				P		HPO:skoehler	
OMIM	178651	PULMONIC STENOSIS AND DEAFNESS		HP:0001714	OMIM:178651	TAS				P		HPO:skoehler	
OMIM	178800	PUPIL, EGG-SHAPED		HP:0000006	OMIM:178800	IEA				I		HPO:iea	
OMIM	178800	PUPIL, EGG-SHAPED		HP:0000478	OMIM:178800	IEA				P		HPO:iea	
OMIM	178900	PUPILLARY MEMBRANE, PERSISTENCE OF		HP:0000006	OMIM:178900	IEA				I		HPO:iea	
OMIM	178900	PUPILLARY MEMBRANE, PERSISTENCE OF		HP:0000485	OMIM:178900	IEA				P		HPO:iea	
OMIM	178900	PUPILLARY MEMBRANE, PERSISTENCE OF		HP:0000519	OMIM:178900	IEA				P		HPO:iea	
OMIM	178900	PUPILLARY MEMBRANE, PERSISTENCE OF		HP:0009917	OMIM:178900	IEA				P		HPO:skoehler	
OMIM	178995	PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY		HP:0000006	OMIM:178995	IEA				I		HPO:iea	
OMIM	178995	PRURITIC URTICARIAL PAPULES AND PLAQUES OF PREGNANCY		HP:0001065	OMIM:178995	IEA				P		HPO:skoehler	
OMIM	179000	PURPURA SIMPLEX		HP:0000006	OMIM:179000	IEA				I		HPO:iea	
OMIM	179000	PURPURA SIMPLEX		HP:0000132	OMIM:179000	IEA				P		HPO:iea	
OMIM	179000	PURPURA SIMPLEX		HP:0000421	OMIM:179000	IEA				P		HPO:iea	
OMIM	179000	PURPURA SIMPLEX		HP:0000508	OMIM:179000	IEA				P		HPO:iea	
OMIM	179000	PURPURA SIMPLEX		HP:0000978	OMIM:179000	TAS				P		HPO:probinson	
OMIM	179000	PURPURA SIMPLEX		HP:0000979	OMIM:179000	TAS				P		HPO:probinson	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0000006	OMIM:179010	IEA				I		HPO:iea	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0001426	OMIM:179010	IEA				I		HPO:iea	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0001508	OMIM:179010	IEA				P		HPO:iea	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0002021	OMIM:179010	TAS				P		HPO:probinson	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0002587	OMIM:179010	IEA				P		HPO:skoehler	
OMIM	179010	PYLORIC STENOSIS, INFANTILE HYPERTROPHIC 1		HP:0005977	OMIM:179010	TAS				P		HPO:probinson	
OMIM	179200	RADIAL HEADS, POSTERIOR DISLOCATION OF		HP:0000006	OMIM:179200	TAS				I		HPO:nvasilevsky	
OMIM	179200	RADIAL HEADS, POSTERIOR DISLOCATION OF		HP:0000007	OMIM:179200	TAS				I		HPO:nvasilevsky	
OMIM	179200	RADIAL HEADS, POSTERIOR DISLOCATION OF		HP:0001377	OMIM:179200	IEA				P		HPO:iea	
OMIM	179200	RADIAL HEADS, POSTERIOR DISLOCATION OF		HP:0005798	OMIM:179200	TAS	HP:0003577			P		HPO:probinson	
OMIM	179200	RADIAL HEADS, POSTERIOR DISLOCATION OF		HP:0009760	OMIM:179200	TAS				P		HPO:probinson	
OMIM	179250	RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARYDIASTEMA		HP:0000006	OMIM:179250	IEA				I		HPO:iea	
OMIM	179250	RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARYDIASTEMA		HP:0000047	OMIM:179250	TAS				P		HPO:skoehler	
OMIM	179250	RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARYDIASTEMA		HP:0000699	OMIM:179250	IEA				P		HPO:skoehler	
OMIM	179250	RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARYDIASTEMA		HP:0002984	OMIM:179250	IEA				P		HPO:iea	
OMIM	179250	RADIAL HYPOPLASIA, TRIPHALANGEAL THUMBS, HYPOSPADIAS, AND MAXILLARYDIASTEMA		HP:0005725	OMIM:179250	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0000006	OMIM:179270	IEA				I		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0000452	OMIM:179270	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0000453	OMIM:179270	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0000565	OMIM:179270	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0001245	OMIM:179270	TAS				P		HPO:probinson	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0002984	OMIM:179270	TAS				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0005280	OMIM:179270	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0009622	OMIM:179270	IEA				P		HPO:iea	
OMIM	179270	RADIAL RAY HYPOPLASIA WITH CHOANAL ATRESIA		HP:0009778	OMIM:179270	IEA				P		HPO:iea	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0000006	OMIM:179280	IEA				I		HPO:iea	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0000086	OMIM:179280	IEA				P		HPO:skoehler	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0000104	OMIM:179280	IEA				P		HPO:iea	
OMIM	179280	RADIAL-RENAL SYNDROME	HP:0012832	HP:0003974	OMIM:179280	TAS				P		HPO:probinson	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0004322	OMIM:179280	IEA				P		HPO:iea	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0008572	OMIM:179280	IEA				P		HPO:iea	
OMIM	179280	RADIAL-RENAL SYNDROME	HP:0012832	HP:0009777	OMIM:179280	TAS				P		HPO:probinson	
OMIM	179280	RADIAL-RENAL SYNDROME		HP:0040012	OMIM:179280	TAS				P		HPO:skoehler	
OMIM	179300	RADIOULNAR SYNOSTOSIS		HP:0000006	OMIM:179300	TAS				I		HPO:skoehler	
OMIM	179300	RADIOULNAR SYNOSTOSIS		HP:0001377	OMIM:179300	TAS				P		HPO:skoehler	
OMIM	179300	RADIOULNAR SYNOSTOSIS		HP:0002974	OMIM:179300	TAS				P		HPO:skoehler	
OMIM	179300	RADIOULNAR SYNOSTOSIS		HP:0003083	OMIM:179300	TAS	HP:0003577			P		HPO:skoehler	
OMIM	179400	RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE		HP:0000175	OMIM:179400	TAS				P		HPO:skoehler	
OMIM	179400	RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE		HP:0000204	OMIM:179400	TAS				P		HPO:skoehler	
OMIM	179400	RADIUS, APLASIA OF, WITH CLEFT LIP/PALATE		HP:0003974	OMIM:179400	TAS				P		HPO:skoehler	
OMIM	179450	RAGWEED SENSITIVITY		HP:0000006	OMIM:179450	IEA				I		HPO:iea	
OMIM	179450	RAGWEED SENSITIVITY		HP:0001945	OMIM:179450	IEA				P		HPO:skoehler	
OMIM	179450	RAGWEED SENSITIVITY		HP:0002715	OMIM:179450	IEA				P		HPO:iea	
OMIM	179500	RAINDROP HYPOPIGMENTATION		HP:0000006	OMIM:179500	IEA				I		HPO:iea	
OMIM	179500	RAINDROP HYPOPIGMENTATION		HP:0001010	OMIM:179500	IEA				P		HPO:skoehler	
OMIM	179600	RAYNAUD DISEASE		HP:0000006	OMIM:179600	IEA				I		HPO:iea	
OMIM	179600	RAYNAUD DISEASE		HP:0000924	OMIM:179600	IEA				P		HPO:iea	
OMIM	179600	RAYNAUD DISEASE		HP:0030880	OMIM:179600	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000006	OMIM:179613	IEA				I		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000028	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000126	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000164	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000179	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000212	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000219	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000219	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000248	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000272	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000283	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000316	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000347	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000358	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000365	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000369	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000463	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000486	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0000767	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001249	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001250	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001252	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001263	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001276	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001290	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001510	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001629	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001631	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001636	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001642	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001643	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0001719	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002059	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002119	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002162	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002188	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002650	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0002714	OMIM:179613	IEA				P		HPO:iea	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0004209	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0005280	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0005484	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0008897	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0009473	OMIM:179613	IEA				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0011800	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0012385	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179613	RECOMBINANT CHROMOSOME 8 SYNDROME		HP:0100876	OMIM:179613	TAS				P		HPO:skoehler	
OMIM	179650	RED CELL PERMEABILITY DEFECT		HP:0000006	OMIM:179650	TAS				I		HPO:probinson	
OMIM	179650	RED CELL PERMEABILITY DEFECT		HP:0004445	OMIM:179650	TAS				P		HPO:probinson	
OMIM	179700	RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS		HP:0000006	OMIM:179700	IEA				I		HPO:iea	
OMIM	179700	RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS		HP:0001046	PMID:3090825	PCS				P		HPO:lccarmody	
OMIM	179700	RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS	HP:0012826	HP:0001744	PMID:3090825	PCS				P		HPO:lccarmody	
OMIM	179700	RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS		HP:0001923	OMIM:179700	IEA				P		HPO:iea	
OMIM	179700	RED CELL PHOSPHOLIPID DEFECT WITH HEMOLYSIS		HP:0002904	OMIM:179700	IEA				P		HPO:skoehler	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0000006	OMIM:179800	TAS				I		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0000121	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0001324	OMIM:179800	IEA				P		HPO:skoehler	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0001947	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0002749	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0002756	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0002901	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0003768	OMIM:179800	IEA				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0008153	OMIM:179800	TAS				P		HPO:probinson	
OMIM	179800	RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL DOMINANT		HP:0008897	OMIM:179800	TAS				P		HPO:probinson	
OMIM	179830	179830 RENAL TUBULAR ACIDOSIS, PROXIMAL;;RENAL TUBULAR ACIDOSIS II;;RTA, PROXIMAL TYPE;;RTA, RATE TYPE		HP:0000006	OMIM:179830	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	179830	179830 RENAL TUBULAR ACIDOSIS, PROXIMAL;;RENAL TUBULAR ACIDOSIS II;;RTA, PROXIMAL TYPE;;RTA, RATE TYPE		HP:0001947	OMIM:179830	TAS				P		HPO:skoehler	
OMIM	179830	179830 RENAL TUBULAR ACIDOSIS, PROXIMAL;;RENAL TUBULAR ACIDOSIS II;;RTA, PROXIMAL TYPE;;RTA, RATE TYPE		HP:0001995	OMIM:179830	IEA				P		HPO:iea	
OMIM	179830	179830 RENAL TUBULAR ACIDOSIS, PROXIMAL;;RENAL TUBULAR ACIDOSIS II;;RTA, PROXIMAL TYPE;;RTA, RATE TYPE		HP:0002049	OMIM:179830	IEA				P		HPO:iea	
OMIM	179830	179830 RENAL TUBULAR ACIDOSIS, PROXIMAL;;RENAL TUBULAR ACIDOSIS II;;RTA, PROXIMAL TYPE;;RTA, RATE TYPE		HP:0004322	OMIM:179830	IEA				P		HPO:iea	
OMIM	179840	RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM		HP:0000006	OMIM:179840	TAS				I		HPO:skoehler	
OMIM	179840	RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM		HP:0000580	OMIM:179840	TAS				P		HPO:probinson	
OMIM	179840	RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM		HP:0000662	OMIM:179840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	179840	RETICULAR DYSTROPHY OF RETINAL PIGMENT EPITHELIUM		HP:0030454	OMIM:179840	TAS				P		HPO:probinson	
OMIM	179850	DOWLING-DEGOS DISEASE		HP:0000006	OMIM:179850	TAS				I		HPO:skoehler	
OMIM	179850	DOWLING-DEGOS DISEASE		HP:0007456	OMIM:179850	TAS				P		HPO:skoehler	
OMIM	179900	%179900 RETINAL APLASIA;;AMAUROSIS CONGENITA		HP:0000006	OMIM:179900	TAS				I		HPO:skoehler	
OMIM	179900	%179900 RETINAL APLASIA;;AMAUROSIS CONGENITA		HP:0001425	OMIM:179900	IEA				I		HPO:iea	
OMIM	179900	%179900 RETINAL APLASIA;;AMAUROSIS CONGENITA		HP:0007875	OMIM:179900	IEA				P		HPO:iea	
OMIM	180000	RETINAL ARTERIES, TORTUOSITY OF		HP:0000006	OMIM:180000	IEA				I		HPO:iea	
OMIM	180000	RETINAL ARTERIES, TORTUOSITY OF		HP:0000572	OMIM:180000	IEA				P		HPO:skoehler	
OMIM	180000	RETINAL ARTERIES, TORTUOSITY OF		HP:0000573	OMIM:180000	IEA				P		HPO:iea	
OMIM	180000	RETINAL ARTERIES, TORTUOSITY OF		HP:0001136	OMIM:180000	IEA				P		HPO:iea	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000006	OMIM:180020	TAS				I		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000512	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000529	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000546	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000548	OMIM:180020	IEA				P		HPO:skoehler	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000551	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0000613	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180020	RETINAL CONE DYSTROPHY 1; RCD1		HP:0011504	OMIM:180020	TAS				P		HPO:probinson	
OMIM	180050	%180050 RETINAL DETACHMENT		HP:0000006	OMIM:180050	IEA				I		HPO:iea	
OMIM	180050	%180050 RETINAL DETACHMENT		HP:0000541	OMIM:180050	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0000006	OMIM:180080	TAS				I		HPO:skoehler	
OMIM	180080	RETINAL VENOUS BEADING		HP:0000123	OMIM:180080	TAS				P		HPO:probinson	
OMIM	180080	RETINAL VENOUS BEADING		HP:0000365	OMIM:180080	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0000969	OMIM:180080	IEA				P		HPO:skoehler	
OMIM	180080	RETINAL VENOUS BEADING		HP:0001875	OMIM:180080	IEA				P		HPO:skoehler	
OMIM	180080	RETINAL VENOUS BEADING		HP:0007721	OMIM:180080	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0007815	OMIM:180080	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0007866	OMIM:180080	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0007902	OMIM:180080	IEA				P		HPO:iea	
OMIM	180080	RETINAL VENOUS BEADING		HP:0030666	OMIM:180080	IEA				P		HPO:skoehler	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0000006	OMIM:180100	TAS				I		HPO:skoehler	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0000007	OMIM:180100	TAS				I		HPO:skoehler	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0000510	OMIM:180100	IEA				P		HPO:iea	
OMIM	180100	RETINITIS PIGMENTOSA 1	HP:0012826	HP:0000545	OMIM:180100	TAS				P		HPO:skoehler	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0000662	OMIM:180100	IEA				P		HPO:iea	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0001133	OMIM:180100	IEA				P		HPO:iea	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0001425	OMIM:180100	TAS				I		HPO:skoehler	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0007688	OMIM:180100	IEA				P		HPO:iea	
OMIM	180100	RETINITIS PIGMENTOSA 1		HP:0007737	OMIM:180100	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0000006	OMIM:180104	TAS				I		HPO:skoehler	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0000510	OMIM:180104	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0000518	OMIM:180104	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0000662	OMIM:180104	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0001133	OMIM:180104	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0007401	OMIM:180104	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0007688	OMIM:180104	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0007737	OMIM:180104	TAS				P		HPO:probinson	
OMIM	180104	#180104 RETINITIS PIGMENTOSA 9; RP9		HP:0040049	OMIM:180104	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0000006	OMIM:180105	TAS				I		HPO:skoehler	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0000510	OMIM:180105	IEA				P		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0000543	OMIM:180105	IEA				P		HPO:skoehler	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0000662	OMIM:180105	IEA				P		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0001133	OMIM:180105	IEA				P		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0003593	OMIM:180105	IEA				C		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0007663	OMIM:180105	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0007688	OMIM:180105	IEA				P		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0007737	OMIM:180105	IEA				P		HPO:iea	
OMIM	180105	RETINITIS PIGMENTOSA 10; RP10		HP:0007787	OMIM:180105	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	180200	RETINOBLASTOMA; RB1		HP:0000006	OMIM:180200	IEA				I		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0000175	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0000555	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0001428	OMIM:180200	TAS				I		HPO:skoehler	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0001909	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0002665	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0002669	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0003745	OMIM:180200	IEA				I		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0007862	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0007902	OMIM:180200	IEA				P		HPO:iea	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0009919	OMIM:180200	IEA				P		HPO:skoehler	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0010799	OMIM:180200	TAS				P		HPO:skoehler	
OMIM	180200	RETINOBLASTOMA; RB1		HP:0011531	OMIM:180200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	180200	RETINOBLASTOMA; RB1		HP:0012254	OMIM:180200	TAS				P		HPO:skoehler	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000006	OMIM:180210	IEA				I		HPO:iea	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000488	OMIM:180210	IEA				P		HPO:skoehler	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000556	OMIM:180210	TAS				P		HPO:probinson	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000580	OMIM:180210	TAS				P		HPO:probinson	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000618	OMIM:180210	TAS	HP:0003584			P		HPO:skoehler	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0000662	OMIM:180210	IEA				P		HPO:iea	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0001105	OMIM:180210	IEA				P		HPO:iea	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0007737	OMIM:180210	IEA				P		HPO:iea	
OMIM	180210	RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT		HP:0007843	OMIM:180210	IEA				P		HPO:iea	
OMIM	180270	180270 RETINOSCHISIS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:180270	TAS				I		HPO:skoehler	
OMIM	180270	180270 RETINOSCHISIS, AUTOSOMAL DOMINANT		HP:0007769	OMIM:180270	IEA				P		HPO:iea	
OMIM	180270	180270 RETINOSCHISIS, AUTOSOMAL DOMINANT		HP:0008002	OMIM:180270	IEA				P		HPO:iea	
OMIM	180270	180270 RETINOSCHISIS, AUTOSOMAL DOMINANT		HP:0030502	OMIM:180270	TAS				P		HPO:skoehler	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0002667	PMID:21882293	PCS	HP:0011463			P		HPO:nvasilevsky	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0005987	PMID:21882293	PCS	HP:0003621			P		HPO:skoehler	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0006743	PMID:21882293	PCS				P		HPO:skoehler	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0025388	PMID:21882293	PCS	HP:0003621			P		HPO:nvasilevsky	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0030983	PMID:21882293	PCS				P		HPO:nvasilevsky	
OMIM	180295	#180295 RHABDOMYOSARCOMA, EMBRYONAL, 2; RMSE2		HP:0100528	PMID:21882293	PCS				P		HPO:nvasilevsky	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0000707	OMIM:180300	IEA				P		HPO:iea	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0001370	OMIM:180300	IEA				P		HPO:iea	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0001871	OMIM:180300	IEA				P		HPO:iea	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0002086	OMIM:180300	IEA				P		HPO:iea	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0002633	OMIM:180300	IEA				P		HPO:skoehler	
OMIM	180300	RHEUMATOID ARTHRITIS		HP:0002715	OMIM:180300	IEA				P		HPO:iea	
OMIM	180350	RHEUMATOID NODULOSIS		HP:0000006	OMIM:180350	TAS				I		HPO:iea	
OMIM	180350	RHEUMATOID NODULOSIS		HP:0001482	OMIM:180350	TAS				P		HPO:iea	
OMIM	180360	RHINY		HP:0000006	OMIM:180360	IEA				I		HPO:iea	
OMIM	180360	RHINY		HP:0000023	OMIM:180360	IEA				P		HPO:iea	
OMIM	180360	RHINY		HP:0000233	OMIM:180360	TAS				P		HPO:probinson	
OMIM	180360	RHINY		HP:0000463	OMIM:180360	IEA				P		HPO:iea	
OMIM	180360	RHINY		HP:0003196	OMIM:180360	TAS				P		HPO:skoehler	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000006	OMIM:180500	IEA				I		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000047	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000219	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000219	OMIM:180500	TAS				P		HPO:skoehler	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000322	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000327	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000336	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000431	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000482	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000485	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000486	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000501	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000526	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000558	OMIM:180500	TAS				P		HPO:probinson	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000627	OMIM:180500	IEA				P		HPO:skoehler	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000668	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0000824	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0001425	OMIM:180500	TAS				I		HPO:skoehler	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0002023	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0002025	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0003828	OMIM:180500	IEA				C		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0004298	OMIM:180500	IEA				P		HPO:iea	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0007676	OMIM:180500	IEA				P		HPO:skoehler	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0007873	OMIM:180500	TAS				P		HPO:probinson	
OMIM	180500	AXENFELD-RIEGER SYNDROME, TYPE 1; RIEG1		HP:0011500	OMIM:180500	TAS				P		HPO:skoehler	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0000006	OMIM:180550	TAS				I		HPO:skoehler	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0000481	OMIM:180550	TAS				P		HPO:skoehler	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0000502	OMIM:180550	TAS				P		HPO:skoehler	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0000646	PMID:7387508	PCS				P		HPO:lccarmody	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0025348	PMID:7387508	PCS				P		HPO:lccarmody	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0025612	PMID:7387508	PCS				P		HPO:lccarmody	
OMIM	180550	#180550 RING DERMOID OF CORNEA; RDC		HP:0500070	PMID:7387508	PCS				P		HPO:lccarmody	
OMIM	180600	RINGED HAIR		HP:0000006	OMIM:180600	IEA				I		HPO:iea	
OMIM	180600	RINGED HAIR		HP:0001595	OMIM:180600	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000006	OMIM:180700	IEA				I		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000023	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000028	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000054	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000059	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000060	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000075	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000126	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000158	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000189	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	46%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000202	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	35%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000207	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000212	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000218	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	52%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000219	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	50%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000219	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000256	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000260	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000272	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000278	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	44%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000286	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	39%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000316	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000343	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000347	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000358	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000369	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	28%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000431	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000463	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000463	OMIM:180700	TAS		HP:0040284		P		HPO:probinson	83%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000470	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	29%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000494	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000520	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000527	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	54%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000582	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	37%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000637	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000678	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000684	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0000767	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001052	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001156	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001249	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001263	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001537	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001705	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001837	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0001853	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0002007	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0002164	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	22%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0002714	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	63%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0002750	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0003027	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0003196	OMIM:180700	TAS		HP:0040284		P		HPO:probinson	83%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0004220	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0004279	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0005280	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	78%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0008905	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	35%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0009466	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0009883	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0010290	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0010297	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	39%
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0011304	OMIM:180700	IEA				P		HPO:iea	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0011800	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0012368	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0030084	OMIM:180700	TAS				P		HPO:skoehler	
OMIM	180700	#180700 ROBINOW SYNDROME, AUTOSOMAL DOMINANT; DRS;;ROBINOW DWARFISM;;FETAL FACE SYNDROME;;ACRAL DYSOSTOSIS WITH FACIAL AND GENITAL ABNORMALITIES		HP:0200055	OMIM:180700	TAS		HP:0040284		P		HPO:skoehler	62%
OMIM	180730	ROMBO SYNDROME		HP:0000006	OMIM:180730	IEA				I		HPO:iea	
OMIM	180730	ROMBO SYNDROME		HP:0000499	OMIM:180730	PCS				P		HPO:iea	
OMIM	180730	ROMBO SYNDROME		HP:0000534	OMIM:180730	PCS				P		HPO:iea	
OMIM	180730	ROMBO SYNDROME		HP:0002671	OMIM:180730	PCS				P		HPO:iea	
OMIM	180730	ROMBO SYNDROME		HP:0007380	OMIM:180730	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000006	OMIM:180750	IEA				I		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000272	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000316	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000460	OMIM:180750	TAS				P		HPO:probinson	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000486	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0000586	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0001357	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0003189	OMIM:180750	TAS				P		HPO:probinson	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0010055	OMIM:180750	IEA				P		HPO:iea	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0010066	OMIM:180750	TAS				P		HPO:probinson	
OMIM	180750	ROBINOW-SORAUF SYNDROME		HP:0012368	OMIM:180750	TAS				P		HPO:skoehler	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0000006	OMIM:180800	IEA				I		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0001265	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0001270	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0001284	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0001761	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0001765	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0002066	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0002460	OMIM:180800	TAS				P		HPO:probinson	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0002715	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0002751	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0002936	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003380	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003382	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003383	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003431	OMIM:180800	IEA				P		HPO:skoehler	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003481	OMIM:180800	IEA				P		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003621	OMIM:180800	IEA				C		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003677	OMIM:180800	IEA				C		HPO:iea	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0003693	OMIM:180800	TAS				P		HPO:probinson	
OMIM	180800	ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA		HP:0007351	OMIM:180800	IEA				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000006	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				I		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000028	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000047	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000049	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000077	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000136	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000160	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000189	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000218	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000252	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000260	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000270	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000273	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000278	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000286	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000294	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000327	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000347	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000365	PMID:16868563	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000369	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000377	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000431	PMID:17942008	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000444	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000481	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000490	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000494	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000501	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000508	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000518	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000520	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000527	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000539	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000574	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000579	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000589	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000678	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000689	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000717	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000733	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000736	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000742	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000750	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000752	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000756	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000767	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000954	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0000957	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001007	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001042	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001135	OMIM:180849	IEA				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001159	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001212	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001249	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001250	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001252	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001274	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001290	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001335	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001347	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001371	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001382	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001388	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001425	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				I		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001508	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS	HP:0003593			P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001561	PMID:16868563	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001601	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001629	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001631	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001643	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001763	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001909	OMIM:180849	IEA				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0001956	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS	HP:0003621			P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002007	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002019	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002098	http://www.ncbi.nlm.nih.gov/books/NBK1526/;PMID:16868563	PCS	HP:0003623			P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002144	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002162	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002183	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002236	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002251	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002317	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002353	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002370	ISBN-13:978-0721606156	TAS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002553	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002650	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002697	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002700	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002750	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002788	http://www.ncbi.nlm.nih.gov/books/NBK1526/;PMID:16868563	PCS	HP:0003593			P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002866	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002869	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002870	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0002999	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0003083	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0003298	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0003319	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0003745	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				I		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0003828	OMIM:180849	TAS				C		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0004209	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0004322	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0004411	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0005306	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0005743	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0005895	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0006297	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0006483	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0008107	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0008872	http://www.ncbi.nlm.nih.gov/books/NBK1526/;PMID:16868563	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0008897	OMIM:180849	TAS				P		HPO:skoehler	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0009715	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0009765	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0009921	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010055	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010066	http://www.ncbi.nlm.nih.gov/books/NBK1526/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010314	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010442	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010562	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0010775	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0011087	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0011304	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0011675	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	180849	RUBINSTEIN-TAYBI SYNDROME 1; RSTS1		HP:0100710	http://www.ncbi.nlm.nih.gov/books/NBK1526/	PCS				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000047	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000069	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000270	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000325	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000347	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000592	OMIM:180860	TAS				P		HPO:probinson	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000824	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0000957	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001159	OMIM:180860	IEA				P		HPO:skoehler	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001263	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001402	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001511	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001518	OMIM:180860	TAS				P		HPO:probinson	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001626	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0001760	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0002007	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0002667	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0002714	OMIM:180860	TAS				P		HPO:skoehler	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0002750	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0003162	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0003745	OMIM:180860	IEA				I		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0004209	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0004220	OMIM:180860	TAS				P		HPO:probinson	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0004227	OMIM:180860	TAS				P		HPO:probinson	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0005461	OMIM:180860	IEA				P		HPO:iea	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0010481	OMIM:180860	IEA				P		HPO:skoehler	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0010957	OMIM:180860	TAS				P		HPO:skoehler	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0030062	OMIM:180860	TAS				P		HPO:skoehler	
OMIM	180860	#180860 SILVER-RUSSELL SYNDROME; SRS;;RUSSELL-SILVER SYNDROME; RSS;;SILVER-RUSSELL DWARFISM		HP:0100617	OMIM:180860	TAS				P		HPO:skoehler	
OMIM	180870	RUVALCABA SYNDROME		HP:0000006	OMIM:180870	IEA				I		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000023	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000028	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000252	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000430	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000460	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000494	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000556	OMIM:180870	TAS				P		HPO:probinson	
OMIM	180870	RUVALCABA SYNDROME		HP:0000678	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000769	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000774	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0000823	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0001249	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0001377	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0001773	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0002650	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0002808	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0002983	OMIM:180870	TAS				P		HPO:skoehler	
OMIM	180870	RUVALCABA SYNDROME		HP:0004279	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0004322	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0009803	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0010049	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0010743	OMIM:180870	IEA				P		HPO:iea	
OMIM	180870	RUVALCABA SYNDROME		HP:0200055	OMIM:180870	TAS				P		HPO:skoehler	
OMIM	180900	RUTHERFURD SYNDROME		HP:0000006	OMIM:180900	IEA				I		HPO:iea	
OMIM	180900	RUTHERFURD SYNDROME		HP:0000680	OMIM:180900	IEA				P		HPO:iea	
OMIM	180900	RUTHERFURD SYNDROME		HP:0001131	OMIM:180900	IEA				P		HPO:iea	
OMIM	180900	RUTHERFURD SYNDROME		HP:0006352	OMIM:180900	IEA				P		HPO:iea	
OMIM	180900	RUTHERFURD SYNDROME		HP:0007759	OMIM:180900	IEA				P		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0000006	OMIM:180920	IEA				I		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0000217	OMIM:180920	IEA				P		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0000670	OMIM:180920	IEA				P		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0001092	OMIM:180920	IEA				P		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0007656	OMIM:180920	IEA				P		HPO:iea	
OMIM	180920	APLASIA OF LACRIMAL AND SALIVARY GLANDS		HP:0007732	OMIM:180920	IEA				P		HPO:iea	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0000501	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0000613	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0000622	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001094	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001138	OMIM:181000	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001369	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001744	OMIM:181000	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001824	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001876	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0001945	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0002037	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0002039	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0002094	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0002150	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0002240	OMIM:181000	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0003565	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0003745	OMIM:181000	TAS				I		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0006530	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0007734	OMIM:181000	IEA				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0008940	OMIM:181000	TAS				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0009926	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0010286	OMIM:181000	TAS				P		HP:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0010702	OMIM:181000	PCS				P		HPO:probinson	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0011840	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0012062	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0012424	OMIM:181000	IEA				P		HPO:skoehler	
OMIM	181000	SARCOIDOSIS, SUSCEPTIBILITY TO, 1; SS1		HP:0012735	OMIM:181000	TAS				P		HPO:skoehler	
OMIM	181010	SALIVARY DUCT CALCULI		HP:0000006	OMIM:181010	IEA				I		HPO:iea	
OMIM	181010	SALIVARY DUCT CALCULI		HP:0011850	OMIM:181010	IEA				P		HPO:skoehler	
OMIM	181030	SALIVARY GLAND ADENOMA, PLEOMORPHIC		HP:0000006	OMIM:181030	TAS				I		HPO:iea	
OMIM	181030	SALIVARY GLAND ADENOMA, PLEOMORPHIC		HP:0001428	OMIM:181030	TAS				I		HPO:skoehler	
OMIM	181030	SALIVARY GLAND ADENOMA, PLEOMORPHIC		HP:0100684	OMIM:181030	TAS				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000006	OMIM:181180	IEA				I		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000175	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000252	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000347	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000400	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000800	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0000951	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0001182	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0002049	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0004322	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0009463	OMIM:181180	IEA				P		HPO:iea	
OMIM	181180	SAY SYNDROME		HP:0009882	OMIM:181180	IEA				P		HPO:iea	
OMIM	181250	SCALP DEFECTS AND POSTAXIAL POLYDACTYLY		HP:0000006	OMIM:181250	TAS				I		HPO:skoehler	
OMIM	181250	SCALP DEFECTS AND POSTAXIAL POLYDACTYLY		HP:0005696	OMIM:181250	TAS				P		HPO:skoehler	
OMIM	181250	SCALP DEFECTS AND POSTAXIAL POLYDACTYLY		HP:0007385	OMIM:181250	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000006	OMIM:181270	IEA				I		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000083	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000089	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000104	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000286	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000303	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000369	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000378	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000385	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000411	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000463	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000519	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000581	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000601	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000612	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000765	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000818	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0000822	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0001057	OMIM:181270	IEA				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0001595	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0001597	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0002000	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0002164	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0002213	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0004691	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0005280	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0006349	OMIM:181270	TAS				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0006709	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0008070	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0008551	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0011251	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0011272	OMIM:181270	IEA				P		HPO:iea	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0011939	OMIM:181270	TAS				P		HPO:probinson	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0012330	OMIM:181270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0045025	OMIM:181270	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0100540	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181270	SCALP-EAR-NIPPLE SYNDROME; SENS		HP:0100783	OMIM:181270	TAS				P		HPO:skoehler	
OMIM	181300	SCAPULA, CONTOUR OF VERTEBRAL BORDER OF		HP:0000006	OMIM:181300	IEA				I		HPO:iea	
OMIM	181300	SCAPULA, CONTOUR OF VERTEBRAL BORDER OF		HP:0000924	OMIM:181300	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0000006	OMIM:181350	IEA				I		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0001644	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0001645	OMIM:181350	TAS				P		HPO:skoehler	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0001771	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0002987	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0003306	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0003325	OMIM:181350	TAS				P		HPO:probinson	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0003677	OMIM:181350	IEA				C		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0003691	OMIM:181350	TAS				P		HPO:skoehler	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0003828	OMIM:181350	TAS				C		HPO:skoehler	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0004631	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0005997	OMIM:181350	IEA				P		HPO:iea	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0006785	OMIM:181350	TAS				P		HPO:skoehler	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0008180	OMIM:181350	TAS				P		HPO:skoehler	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0008944	OMIM:181350	TAS				P		HPO:probinson	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0009049	OMIM:181350	TAS				P		HPO:probinson	
OMIM	181350	#181350 EMERY-DREIFUSS MUSCULAR DYSTROPHY 2, AUTOSOMAL DOMINANT; EDMD2;;EMD2;;EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT;;SCAPULOILIOPERONEAL ATROPHY WITH CARDIOPATHY;;MUSCULAR DYSTROPHY WITH EARLY CONTRACTURES AND CARDIOMYOPATHY, AUTOSOMALDOMINANT;;HAUPTMANN-THANNHAUSER MUSCULAR DYSTROPHYEMERY-DREIFUSS MUSCULAR DYSTROPHY, ATYPICAL, AUTOSOMAL RECESSIVE,INCLUDED;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE, INCLUDED;EDMD3, INCLUDED		HP:0011727	OMIM:181350	TAS				P		HPO:probinson	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0000006	OMIM:181400	IEA				I		HPO:iea	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0001762	OMIM:181400	IEA				P		HPO:iea	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0003704	OMIM:181400	IEA				P		HPO:iea	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0003724	OMIM:181400	IEA				P		HPO:iea	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0009027	OMIM:181400	IEA				P		HPO:skoehler	
OMIM	181400	SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE		HP:0009049	OMIM:181400	IEA				P		HPO:iea	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0000006	OMIM:181405	TAS				I		HPO:probinson	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0000473	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001265	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001270	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001284	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001385	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001762	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0001840	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0002093	OMIM:181405	IEA				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0002136	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0002650	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0002808	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0002936	OMIM:181405	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003307	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003391	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003555	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003634	OMIM:181405	TAS				P		HPO:probinson	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003691	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003697	OMIM:181405	TAS				P		HPO:probinson	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0003829	OMIM:181405	TAS				C		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0007178	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0008955	OMIM:181405	TAS				P		HPO:probinson	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0009049	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0009060	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0009063	OMIM:181405	TAS				P		HPO:probinson	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0009113	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0010307	OMIM:181405	IEA				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0010628	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0011349	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0011727	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0030084	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181405	SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY; SPSMA		HP:0200055	OMIM:181405	TAS				P		HPO:skoehler	
OMIM	181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM		HP:0000006	OMIM:181430	TAS				I		HPO:iea	
OMIM	181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM		HP:0003458	OMIM:181430	TAS				P		HPO:iea	
OMIM	181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM		HP:0003677	OMIM:181430	TAS				C		HPO:iea	
OMIM	181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM		HP:0009054	OMIM:181430	TAS				P		HPO:iea	
OMIM	181430	SCAPULOPERONEAL MYOPATHY, MYH7-RELATED; SPMM		HP:0030319	OMIM:181430	TAS				P		HPO:iea	
OMIM	181440	SCHEUERMANN DISEASE		HP:0000006	OMIM:181440	IEA				I		HPO:iea	
OMIM	181440	SCHEUERMANN DISEASE		HP:0002808	OMIM:181440	IEA				P		HPO:skoehler	
OMIM	181440	SCHEUERMANN DISEASE		HP:0010891	OMIM:181440	IEA				P		HPO:skoehler	
OMIM	181440	SCHEUERMANN DISEASE		HP:0040188	OMIM:181440	IEA				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000006	OMIM:181450	IEA				I		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000023	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000049	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000054	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000668	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000823	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000882	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0000894	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0001162	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0001513	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0001607	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0001629	OMIM:181450	TAS				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002021	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002023	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002025	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002215	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002557	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0002984	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003022	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003186	OMIM:181450	TAS				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003187	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003974	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003977	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0003982	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0005338	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0005792	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0007397	OMIM:181450	IEA				P		HPO:iea	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0008093	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0010627	OMIM:181450	TAS				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0011675	OMIM:181450	IEA				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0011755	OMIM:181450	TAS				P		HPO:skoehler	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0011917	OMIM:181450	TAS				P		HPO:probinson	
OMIM	181450	ULNAR-MAMMARY SYNDROME; UMS		HP:0030011	OMIM:181450	TAS				P		HPO:skoehler	
OMIM	181460	SCHISTOSOMA MANSONI INFECTION, SUSCEPTIBILITY/RESISTANCE TO		HP:0000006	OMIM:181460	IEA				I		HPO:iea	
OMIM	181460	SCHISTOSOMA MANSONI INFECTION, SUSCEPTIBILITY/RESISTANCE TO		HP:0002715	OMIM:181460	IEA				P		HPO:iea	
OMIM	181500	SCHIZOPHRENIA		HP:0000006	OMIM:181500	TAS				I		HPO:skoehler	
OMIM	181500	SCHIZOPHRENIA		HP:0000738	OMIM:181500	IEA				P		HPO:iea	
OMIM	181500	SCHIZOPHRENIA		HP:0000746	OMIM:181500	IEA				P		HPO:iea	
OMIM	181500	SCHIZOPHRENIA		HP:0001425	OMIM:181500	TAS				I		HPO:skoehler	
OMIM	181500	SCHIZOPHRENIA		HP:0002353	OMIM:181500	PCS		HP:0040284		P		HPO:iea	25%
OMIM	181500	SCHIZOPHRENIA		HP:0007086	OMIM:181500	IEA				P		HPO:iea	
OMIM	181500	SCHIZOPHRENIA		HP:0100753	OMIM:181500	TAS				P		HPO:skoehler	
OMIM	181500	SCHIZOPHRENIA		HP:0410291	PMID:7669819	PCS				P		HPO:nvasilevsky	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000006	OMIM:181510	TAS				I		HPO:skoehler	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000086	OMIM:181510	TAS				P		HPO:probinson	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000104	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000316	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000411	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000738	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0000746	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0001159	OMIM:181510	IEA				P		HPO:skoehler	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0002007	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0004322	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0005469	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0007086	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0008738	OMIM:181510	TAS				P		HPO:probinson	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0100396	OMIM:181510	IEA				P		HPO:iea	
OMIM	181510	SCHIZOPHRENIA 1; SCZD1		HP:0100753	OMIM:181510	TAS				P		HPO:probinson	
OMIM	181600	SCLEROTYLOSIS		HP:0000006	OMIM:181600	IEA				I		HPO:iea	
OMIM	181600	SCLEROTYLOSIS		HP:0001792	OMIM:181600	IEA				P		HPO:iea	
OMIM	181600	SCLEROTYLOSIS		HP:0002664	OMIM:181600	IEA				P		HPO:iea	
OMIM	181600	SCLEROTYLOSIS		HP:0007597	OMIM:181600	IEA				P		HPO:iea	
OMIM	181700	181700 SCLEROCORNEA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:181700	TAS				I		HPO:skoehler	
OMIM	181700	181700 SCLEROCORNEA, AUTOSOMAL DOMINANT		HP:0000647	OMIM:181700	TAS				P		HPO:skoehler	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0000006	OMIM:181750	TAS				I		HPO:skoehler	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0001009	OMIM:181750	IEA				P		HPO:iea	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0001438	OMIM:181750	IEA				P		HPO:iea	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0003220	OMIM:181750	IEA				P		HPO:iea	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0003761	OMIM:181750	IEA				P		HPO:iea	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0011838	OMIM:181750	TAS				P		HPO:skoehler	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0040012	OMIM:181750	TAS				P		HPO:skoehler	
OMIM	181750	SCLERODERMA, FAMILIAL PROGRESSIVE		HP:0100324	OMIM:181750	IEA				P		HPO:iea	
OMIM	181800	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:181800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	181800	SCOLIOSIS, IDIOPATHIC, SUSCEPTIBILITY TO, 1		HP:0002650	OMIM:181800	IEA				P		HPO:iea	
OMIM	182000	#182000 KERATOSIS, SEBORRHEIC		HP:0000006	OMIM:182000	TAS				I		HPO:skoehler	
OMIM	182000	#182000 KERATOSIS, SEBORRHEIC		HP:0200043	OMIM:182000	IEA				P		HPO:skoehler	
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000006	OMIM:182150	PCS				I		HPO:skoehler	
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000023	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000160	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000272	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000276	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000337	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000343	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000358	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000369	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000377	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000430	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000431	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000437	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000506	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000535	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000581	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0000951	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0001611	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0002553	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0002705	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0003189	OMIM:182150	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0010751	OMIM:182150	TAS				P		HPO:skoehler	
OMIM	182150	SIMOSA CRANIOFACIAL SYNDROME		HP:0012368	OMIM:182150	TAS				P		HPO:skoehler	
OMIM	182170	ANEMIA, SIDEROBLASTIC, AUTOSOMAL DOMINANT		HP:0000006	PMID:26491070	PCS				I		HPO:iea	
OMIM	182170	ANEMIA, SIDEROBLASTIC, AUTOSOMAL DOMINANT		HP:0001924	PMID:26491070	PCS				P		HPO:iea	
OMIM	182170	ANEMIA, SIDEROBLASTIC, AUTOSOMAL DOMINANT		HP:0004828	PMID:3653362	PCS				P		HPO:lccarmody	
OMIM	182190	SINUS NODE DISEASE AND MYOPIA		HP:0000006	OMIM:182190	TAS				I		HPO:probinson	
OMIM	182190	SINUS NODE DISEASE AND MYOPIA		HP:0011003	OMIM:182190	TAS				P		HPO:probinson	
OMIM	182190	SINUS NODE DISEASE AND MYOPIA		HP:0011704	OMIM:182190	TAS				P		HPO:probinson	
OMIM	182200	SELLA TURCICA, BRIDGED		HP:0000006	OMIM:182200	IEA				I		HPO:iea	
OMIM	182200	SELLA TURCICA, BRIDGED		HP:0005449	OMIM:182200	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000006	OMIM:182210	IEA				I		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000153	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000233	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000286	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000431	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000454	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000465	OMIM:182210	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0000774	OMIM:182210	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001195	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001252	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001290	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001328	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001539	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0001620	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME	HP:0012825	HP:0001999	OMIM:182210	TAS				P		HPO:probinson	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002000	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002023	OMIM:182210	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002643	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002650	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002808	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0002938	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0004322	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0004325	OMIM:182210	TAS				P		HPO:skoehler	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0005956	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0008749	OMIM:182210	IEA				P		HPO:iea	
OMIM	182210	SHPRINTZEN OMPHALOCELE SYNDROME		HP:0009555	OMIM:182210	TAS				P		HPO:probinson	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000006	OMIM:182212	TAS				I		HPO:skoehler	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000023	OMIM:182212	IEA		HP:0040284		P		HPO:iea	19/34
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000028	OMIM:182212	PCS		HP:0040284		P		HPO:iea	1/13
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000189	OMIM:182212	TAS				P		HPO:skoehler	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000218	PMID:15884042	PCS		HP:0040284		P		HPO:iea	30/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000238	PMID:15884042	PCS		HP:0040284		P		HPO:iea	13/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000244	OMIM:182212	IEA				P		HPO:skoehler	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000252	PMID:15884042	PCS		HP:0040284		P		HPO:iea	6/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000260	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000268	PMID:15884042	PCS		HP:0040284		P		HPO:iea	28/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000316	OMIM:182212	PCS		HP:0040284		P		HPO:iea	28/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000327	PMID:15884042	PCS		HP:0040284		P		HPO:iea	16/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000347	PMID:15884042	PCS		HP:0040284		P		HPO:iea	33/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000368	PMID:15884042	PCS		HP:0040284		P		HPO:iea	32/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000377	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000405	PMID:15884042	PCS		HP:0040284		P		HPO:iea	5/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000463	PMID:15884042	PCS		HP:0040284		P		HPO:iea	9/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000486	PMID:15884042	PCS		HP:0040284		P		HPO:iea	17/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000494	OMIM:182212	PCS		HP:0040284		P		HPO:iea	31/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000506	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000508	PMID:15884042	PCS		HP:0040284		P		HPO:iea	16/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000545	PMID:15884042	PCS		HP:0040284		P		HPO:iea	9/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000586	PMID:15884042	PCS		HP:0040284		P		HPO:iea	13/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000689	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000767	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000768	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000883	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000895	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000938	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0000974	OMIM:182212	PCS		HP:0040284		P		HPO:iea	7/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001166	PMID:15884042	PCS		HP:0040284		P		HPO:iea	34/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001249	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001252	PMID:15884042	PCS		HP:0040284		P		HPO:iea	26/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001263	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001290	OMIM:182212	IEA				P		HPO:skoehler	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001363	PMID:15884042	PCS		HP:0040284		P		HPO:iea	18/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001382	PMID:15884042	PCS		HP:0040284		P		HPO:iea	21/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001388	OMIM:182212	IEA				P		HPO:skoehler	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001537	PMID:15884042	PCS		HP:0040284		P		HPO:iea	13/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001634	PMID:15884042	PCS		HP:0040284		P		HPO:iea	13/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001762	OMIM:182212	PCS		HP:0040284		P		HPO:iea	13/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001763	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0001840	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002007	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002020	PMID:15884042	PCS		HP:0040284		P		HPO:iea	4/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002650	OMIM:182212	PCS		HP:0040284		P		HPO:iea	23/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002816	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002857	PMID:15884042	PCS		HP:0040284		P		HPO:iea	4/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0002870	OMIM:182212	PCS		HP:0040284		P		HPO:iea	6/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0003016	OMIM:182212	PCS		HP:0040284		P		HPO:iea	4/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0003083	PMID:15884042	PCS		HP:0040284		P		HPO:iea	5/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0003717	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0003745	OMIM:182212	IEA				I		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0004942	PMID:15884042	PCS		HP:0040284		P		HPO:iea	8/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0005815	OMIM:182212	PCS		HP:0040284		P		HPO:iea	5/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0007099	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0008440	OMIM:182212	IEA				P		HPO:iea	
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0008872	OMIM:182212	PCS		HP:0040284		P		HPO:iea	9/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0009023	PMID:15884042	PCS		HP:0040284		P		HPO:iea	5/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0009473	PMID:15884042	PCS		HP:0040284		P		HPO:iea	7/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0011220	PMID:15884042	PCS		HP:0040284		P		HPO:iea	17/37
OMIM	182212	SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS		HP:0012385	PMID:15884042	PCS		HP:0040284		P		HPO:skoehler	24/37
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0000006	OMIM:182230	TAS				I		HPO:skoehler	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0000007	OMIM:182230	TAS				I		HPO:skoehler	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0000609	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0000824	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0000873	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0001263	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0001274	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0001331	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0004322	OMIM:182230	TAS				P		HPO:skoehler	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0007766	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0009381	OMIM:182230	TAS				P		HPO:skoehler	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0010442	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0010627	OMIM:182230	PCS				P		HPO:probinson	
OMIM	182230	SEPTOOPTIC DYSPLASIA		HP:0025356	OMIM:182230	IEA				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000006	OMIM:182250	IEA				I		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000319	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000327	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000337	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000501	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000545	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000670	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000706	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000939	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0000992	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001252	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001290	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001324	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001635	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001640	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001650	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001682	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001761	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001762	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0001806	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0002205	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0002515	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0002673	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0002827	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0002857	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0003182	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0004322	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0004325	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0004380	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0004382	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0005303	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0006112	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0006232	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0006353	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0006386	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0008102	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0009771	OMIM:182250	IEA				P		HPO:iea	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0009890	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0030043	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0100295	OMIM:182250	IEA				P		HPO:skoehler	
OMIM	182250	SINGLETON-MERTEN SYNDROME 1; SGMRT1		HP:0100550	OMIM:182250	TAS				P		HPO:skoehler	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0000006	OMIM:182255	IEA				I		HPO:iea	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0001216	OMIM:182255	TAS				P		HPO:probinson	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0002652	OMIM:182255	IEA				P		HPO:iea	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0002663	OMIM:182255	TAS				P		HPO:probinson	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0004209	OMIM:182255	IEA				P		HPO:iea	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0004322	OMIM:182255	IEA				P		HPO:iea	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0005819	OMIM:182255	TAS				P		HPO:probinson	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0009844	OMIM:182255	TAS				P		HPO:probinson	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0010034	OMIM:182255	IEA				P		HPO:iea	
OMIM	182255	SKELETAL DYSPLASIA WITH DELAYED EPIPHYSEAL AND CARPAL BONE OSSIFICATION		HP:0010579	OMIM:182255	IEA				P		HPO:iea	
OMIM	182260	SLIPPED FEMORAL CAPITAL EPIPHYSES		HP:0000006	OMIM:182260	TAS				I		HPO:skoehler	
OMIM	182260	SLIPPED FEMORAL CAPITAL EPIPHYSES		HP:0006461	OMIM:182260	TAS				P		HPO:skoehler	
OMIM	182260	SLIPPED FEMORAL CAPITAL EPIPHYSES		HP:0008843	OMIM:182260	TAS				P		HPO:skoehler	
OMIM	182270	KETONE COMPOUNDS, ABILITY TO SMELL		HP:0003745	OMIM:182270	TAS				I		HPO:skoehler	
OMIM	182280	SMALL CELL CANCER OF THE LUNG		HP:0000006	OMIM:182280	TAS				I		HPO:iea	
OMIM	182280	SMALL CELL CANCER OF THE LUNG		HP:0100526	OMIM:182280	TAS				P		HPO:iea	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000006	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA				I		HPO:iea	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000079	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000164	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000202	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000220	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000248	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000272	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000283	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000303	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA	HP:0003584	HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000356	ISBN-13:978-0721606156	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000365	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000431	ISBN-13:978-0721606156	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000490	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000541	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000664	ISBN-13:978-0721606156	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000733	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA	HP:0003593	HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000742	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000750	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000752	OMIM:182290	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0000820	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001156	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001169	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001249	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001265	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001284	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA	HP:0003593	HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001600	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001609	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001627	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0001763	ISBN-13:978-0721606156	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002019	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002119	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002155	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002353	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002360	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002715	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0002973	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0003124	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0003745	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA				I		HPO:iea	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0004279	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0004322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0005607	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0007328	ISBN-13:978-0721606156	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0008609	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0010780	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0010803	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0011800	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0012168	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0012210	OMIM:182290	TAS				P		HPO:skoehler	
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0030680	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sms	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	182290	SMITH-MAGENIS SYNDROME SMITH-MAGENIS CHROMOSOME REGION, INCLUDED		HP:0031849	PMID:11445803	PCS				P		HPO:lccarmody	
OMIM	182410	SNEDDON SYNDROME		HP:0000006	OMIM:182410	IEA				I		HPO:iea	
OMIM	182410	SNEDDON SYNDROME		HP:0000007	OMIM:182410	TAS				I		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0000822	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0000965	OMIM:182410	IEA				P		HPO:iea	
OMIM	182410	SNEDDON SYNDROME		HP:0001250	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0001260	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0001268	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0001297	OMIM:182410	IEA				P		HPO:iea	
OMIM	182410	SNEDDON SYNDROME		HP:0001337	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0002301	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0002315	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0003613	OMIM:182410	IEA				P		HPO:iea	
OMIM	182410	SNEDDON SYNDROME		HP:0003676	OMIM:182410	IEA				C		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0003745	OMIM:182410	IEA				I		HPO:skoehler	
OMIM	182410	SNEDDON SYNDROME		HP:0010628	OMIM:182410	IEA				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0000006	OMIM:182600	IEA				I		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0000012	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0000020	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001256	OMIM:182600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001258	OMIM:182600	IEA				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001270	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001347	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001425	OMIM:182600	TAS				I		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0001761	OMIM:182600	IEA				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002064	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002079	OMIM:182600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002166	OMIM:182600	IEA				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002314	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002650	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0002839	OMIM:182600	IEA				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0003487	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0003587	OMIM:182600	IEA				C		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0003828	OMIM:182600	IEA				C		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0003829	OMIM:182600	IEA				C		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0007340	OMIM:182600	TAS				P		HPO:skoehler	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0008944	OMIM:182600	IEA				P		HPO:iea	
OMIM	182600	#182600 SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A;;SPG3;;STRUMPELL DISEASE;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 1; FSP1		HP:0010550	OMIM:182600	TAS				P		HPO:probinson	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000006	OMIM:182601	IEA				I		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000012	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000020	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000639	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000713	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000716	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000718	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000726	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000734	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0000741	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0001249	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0001258	OMIM:182601	IEA				P		HPO:skoehler	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0001347	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0002064	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0002166	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0002314	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0002354	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0002839	OMIM:182601	IEA				P		HPO:skoehler	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003419	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003487	OMIM:182601	IEA				P		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003587	OMIM:182601	IEA				C		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003676	OMIM:182601	IEA				C		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003743	OMIM:182601	IEA				I		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0003828	OMIM:182601	IEA				C		HPO:iea	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0007340	OMIM:182601	TAS				P		HPO:skoehler	
OMIM	182601	#182601 SPASTIC PARAPLEGIA 4, AUTOSOMAL DOMINANT; SPG4;;FAMILIAL SPASTIC PARAPLEGIA, AUTOSOMAL DOMINANT, 2; FSP2		HP:0010550	OMIM:182601	TAS				P		HPO:probinson	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0000006	OMIM:182610	IEA				I		HPO:iea	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0001249	OMIM:182610	IEA				P		HPO:iea	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0001250	OMIM:182610	IEA				P		HPO:iea	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0001258	OMIM:182610	IEA				P		HPO:skoehler	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0002313	OMIM:182610	IEA				P		HPO:iea	
OMIM	182610	182610 SPASTIC PARAPLEGIA, EPILEPSY, AND MENTAL RETARDATION; SPEMR		HP:0007340	OMIM:182610	TAS				P		HPO:skoehler	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0000006	OMIM:182690	TAS				I		HPO:iea	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0000097	OMIM:182690	TAS				P		HPO:iea	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0000112	OMIM:182690	TAS				P		HPO:skoehler	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0000794	OMIM:182690	TAS				P		HPO:skoehler	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0001249	OMIM:182690	TAS				P		HPO:iea	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0001258	OMIM:182690	TAS				P		HPO:iea	
OMIM	182690	SPASTIC PARAPLEGIA, SENSORINEURAL DEAFNESS, MENTAL RETARDATION, AND		HP:0008619	OMIM:182690	TAS				P		HPO:iea	
OMIM	182800	SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS		HP:0000006	OMIM:182800	IEA				I		HPO:iea	
OMIM	182800	SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS		HP:0001258	OMIM:182800	IEA				P		HPO:iea	
OMIM	182800	SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS		HP:0002071	OMIM:182800	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0000006	OMIM:182815	IEA				I		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0000561	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0001029	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0001258	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0002223	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0003383	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0003693	OMIM:182815	IEA				P		HPO:iea	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0007220	OMIM:182815	PCS				P		HPO:probinson	
OMIM	182815	SPASTIC PARAPLEGIA WITH NEUROPATHY AND POIKILODERMA		HP:0011402	OMIM:182815	PCS				P		HPO:probinson	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0000006	OMIM:182820	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0000826	OMIM:182820	IEA				P		HPO:iea	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0001249	OMIM:182820	IEA				P		HPO:iea	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0001258	OMIM:182820	IEA				P		HPO:iea	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0001260	OMIM:182820	IEA				P		HPO:iea	
OMIM	182820	SPASTIC PARAPLEGIA WITH PRECOCIOUS PUBERTY		HP:0001939	OMIM:182820	IEA				P		HPO:iea	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0000006	OMIM:182830	IEA				I		HPO:iea	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0000543	OMIM:182830	IEA				P		HPO:iea	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0000648	OMIM:182830	IEA				P		HPO:iea	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0000726	OMIM:182830	IEA				P		HPO:skoehler	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0001133	OMIM:182830	IEA				P		HPO:iea	
OMIM	182830	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND DEMENTIA		HP:0001258	OMIM:182830	IEA				P		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0000006	OMIM:182870	IEA				I		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0000952	OMIM:182870	IEA				P		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0001878	OMIM:182870	IEA				P		HPO:skoehler	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0002904	OMIM:182870	IEA				P		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0004444	OMIM:182870	IEA				P		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0004445	OMIM:182870	IEA				P		HPO:iea	
OMIM	182870	SPECTRIN, BETA, ERYTHROCYTIC		HP:0004839	OMIM:182870	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000006	OMIM:182875	IEA				I		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000324	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000343	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000369	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000486	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0000750	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0001328	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0007687	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0007946	OMIM:182875	IEA				P		HPO:iea	
OMIM	182875	SPEECH DEVELOPMENT, DELAYED, WITH FACIAL ASYMMETRY, STRABISMUS, ANDTRANSVERSE EARLOBE CREASE		HP:0009908	OMIM:182875	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0000006	OMIM:182900	IEA				I		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0000952	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0001081	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0001744	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0001878	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0001923	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0002904	OMIM:182900	IEA				P		HPO:iea	
OMIM	182900	SPHEROCYTOSIS, HEREDITARY		HP:0004444	OMIM:182900	IEA				P		HPO:iea	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0000006	OMIM:182920	IEA				I		HPO:iea	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0001337	OMIM:182920	IEA				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0001611	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0001939	OMIM:182920	IEA				P		HPO:iea	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0002015	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0002136	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0002460	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0002515	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003198	OMIM:182920	IEA				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003236	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003438	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003674	OMIM:182920	IEA				C		HPO:iea	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003677	OMIM:182920	TAS				C		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003701	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003722	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0003828	OMIM:182920	TAS				C		HPO:skoehler	
OMIM	182920	MYOPATHY, SPHEROID BODY		HP:0007126	OMIM:182920	TAS				P		HPO:skoehler	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0000006	OMIM:182940	TAS				I		HPO:skoehler	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0000020	OMIM:182940	IEA				P		HPO:iea	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0000238	OMIM:182940	IEA				P		HPO:iea	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0001012	OMIM:182940	IEA				P		HPO:skoehler	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0002323	OMIM:182940	IEA				P		HPO:iea	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0002475	OMIM:182940	TAS				P		HPO:skoehler	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0003298	OMIM:182940	IEA				P		HPO:iea	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0008482	OMIM:182940	IEA				P		HPO:iea	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0010305	OMIM:182940	IEA				P		HPO:skoehler	
OMIM	182940	NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO; NTD		HP:0012032	OMIM:182940	IEA				P		HPO:skoehler	
OMIM	182950	SPINAL ARACHNOIDITIS		HP:0000006	OMIM:182950	IEA				I		HPO:iea	
OMIM	182950	SPINAL ARACHNOIDITIS		HP:0000924	OMIM:182950	IEA				P		HPO:iea	
OMIM	182950	SPINAL ARACHNOIDITIS		HP:0001939	OMIM:182950	IEA				P		HPO:iea	
OMIM	182950	SPINAL ARACHNOIDITIS		HP:0002313	OMIM:182950	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0000006	OMIM:182960	TAS				I		HPO:probinson	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0001276	OMIM:182960	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0001761	OMIM:182960	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0001765	OMIM:182960	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0002460	OMIM:182960	PCS				P		HPO:probinson	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0003484	OMIM:182960	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0003484	OMIM:182960	PCS				P		HPO:probinson	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0003487	OMIM:182960	IEA				P		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0003676	OMIM:182960	IEA				C		HPO:iea	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0003693	OMIM:182960	PCS				P		HPO:probinson	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0006938	OMIM:182960	PCS				P		HPO:probinson	
OMIM	182960	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE I		HP:0007267	OMIM:182960	IEA				P		HPO:iea	
OMIM	182970	%182970 SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE;;FSHSMA		HP:0000006	OMIM:182970	TAS				I		HPO:skoehler	
OMIM	182970	%182970 SPINAL MUSCULAR ATROPHY, FACIOSCAPULOHUMERAL TYPE;;FSHSMA		HP:0007269	OMIM:182970	IEA				P		HPO:skoehler	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0000006	OMIM:182980	IEA				I		HPO:iea	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0001265	OMIM:182980	IEA				P		HPO:iea	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0002380	OMIM:182980	IEA				P		HPO:iea	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0003445	OMIM:182980	IEA				P		HPO:iea	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0003701	OMIM:182980	IEA				P		HPO:skoehler	
OMIM	182980	SPINAL MUSCULAR ATROPHY, PROXIMAL, ADULT, AUTOSOMAL DOMINANTSPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE, INCLUDED		HP:0007269	OMIM:182980	IEA				P		HPO:skoehler	
OMIM	182990	SPINAL INTRADURAL ARACHNOID CYSTS		HP:0000006	OMIM:182990	IEA				I		HPO:iea	
OMIM	182990	SPINAL INTRADURAL ARACHNOID CYSTS		HP:0000925	OMIM:182990	IEA				P		HPO:iea	
OMIM	182990	SPINAL INTRADURAL ARACHNOID CYSTS		HP:0010550	OMIM:182990	IEA				P		HPO:skoehler	
OMIM	182990	SPINAL INTRADURAL ARACHNOID CYSTS		HP:0100702	OMIM:182990	IEA				P		HPO:skoehler	
OMIM	183020	SPINAL MUSCULAR ATROPHY, SEGMENTAL		HP:0000006	OMIM:183020	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	183020	SPINAL MUSCULAR ATROPHY, SEGMENTAL		HP:0006802	OMIM:183020	IEA				P		HPO:iea	
OMIM	183020	SPINAL MUSCULAR ATROPHY, SEGMENTAL		HP:0009037	OMIM:183020	IEA				P		HPO:iea	
OMIM	183020	SPINAL MUSCULAR ATROPHY, SEGMENTAL		HP:0009130	OMIM:183020	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0000006	OMIM:183050	IEA				I		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0000762	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0001251	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0001257	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0001260	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0001271	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0002063	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0002067	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0002380	OMIM:183050	IEA				P		HPO:iea	
OMIM	183050	SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY		HP:0003202	OMIM:183050	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0000006	OMIM:183086	IEA				I		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0000640	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0000763	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0001260	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0001272	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0002015	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0002073	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0002076	OMIM:183086	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0003676	OMIM:183086	TAS				C		HPO:skoehler	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0003743	OMIM:183086	IEA				I		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0007670	OMIM:183086	IEA				P		HPO:iea	
OMIM	183086	#183086 SPINOCEREBELLAR ATAXIA 6; SCA6		HP:0007772	OMIM:183086	IEA				P		HPO:skoehler	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000006	OMIM:183090	IEA				I		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000510	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000514	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000602	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000640	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000641	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000657	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0000726	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001151	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001252	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001257	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001260	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001265	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001290	OMIM:183090	TAS				P		HPO:skoehler	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001300	OMIM:183090	IEA				P		HPO:skoehler	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001310	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0001336	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002015	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002063	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002067	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002070	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002073	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002075	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002172	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002174	OMIM:183090	TAS				P		HPO:probinson	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002198	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002380	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002495	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002503	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002542	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0002839	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0003693	OMIM:183090	IEA				P		HPO:iea	
OMIM	183090	SPINOCEREBELLAR ATAXIA 2; SCA2		HP:0003743	OMIM:183090	IEA				I		HPO:iea	
OMIM	183100	SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS		HP:0000006	OMIM:183100	IEA				I		HPO:iea	
OMIM	183100	SPINOCEREBELLAR ATROPHY WITH PUPILLARY PARALYSIS		HP:0007263	OMIM:183100	IEA				P		HPO:iea	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0000006	OMIM:183300	IEA				I		HPO:iea	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0000119	OMIM:183300	IEA				P		HPO:iea	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0000347	OMIM:183300	IEA				P		HPO:iea	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0003826	OMIM:183300	IEA				M		HPO:skoehler	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0006283	OMIM:183300	IEA				P		HPO:iea	
OMIM	183300	SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA		HP:0006333	OMIM:183300	IEA				P		HPO:iea	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0000006	OMIM:183350	IEA				I		HPO:iea	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0001744	OMIM:183350	IEA				P		HPO:iea	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0001876	OMIM:183350	IEA				P		HPO:iea	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0001971	OMIM:183350	TAS				P		HPO:probinson	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0002965	OMIM:183350	IEA				P		HPO:iea	
OMIM	183350	SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T-HELPER CELLS		HP:0008165	OMIM:183350	IEA				P		HPO:iea	
OMIM	183400	SPLIT LOWER LIP		HP:0000006	OMIM:183400	IEA				I		HPO:iea	
OMIM	183400	SPLIT LOWER LIP		HP:0000164	OMIM:183400	IEA				P		HPO:iea	
OMIM	183400	SPLIT LOWER LIP		HP:0000196	OMIM:183400	TAS				P		HPO:lccarmody	
OMIM	183400	SPLIT LOWER LIP		HP:0002010	OMIM:183400	IEA				P		HPO:iea	
OMIM	183500	SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA		HP:0000006	OMIM:183500	IEA				I		HPO:iea	
OMIM	183500	SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA		HP:0000668	OMIM:183500	IEA				P		HPO:iea	
OMIM	183500	SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA		HP:0001171	OMIM:183500	IEA				P		HPO:iea	
OMIM	183500	SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA		HP:0001839	OMIM:183500	IEA				P		HPO:iea	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0000006	PMID:16688749	PCS				I		HPO:iea	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0000175	OMIM:183600	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0000365	PMID:16688749	PCS		HP:0040284		P		HPO:iea	35%
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0000377	PMID:16688749	PCS		HP:0040284		P		HPO:iea	35%
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001159	PMID:16688749	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001171	OMIM:183600	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001180	PMID:16688749	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001199	OMIM:183600	TAS				P		HPO:skoehler	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001249	PMID:16688749	PCS		HP:0040284		P		HPO:iea	33%
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001839	OMIM:183600	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0001849	PMID:16688749	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0003828	OMIM:183600	TAS				C		HPO:skoehler	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0003829	OMIM:183600	TAS				C		HPO:skoehler	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0010055	OMIM:183600	TAS				P		HPO:skoehler	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0030084	OMIM:183600	TAS				P		HPO:skoehler	
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0030680	PMID:16688749	PCS		HP:0040284		P		HPO:iea	13%
OMIM	183600	SPLIT-HAND/FOOT MALFORMATION 1; SHFM1		HP:0100257	OMIM:183600	TAS				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0000006	OMIM:183700	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0000175	OMIM:183700	IEA				P		HPO:skoehler	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0000272	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0000347	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0000598	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0001171	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0001770	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0001839	OMIM:183700	IEA				P		HPO:iea	
OMIM	183700	SPLIT-FOOT DEFORMITY WITH MANDIBULOFACIAL DYSOSTOSIS		HP:0005321	OMIM:183700	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0000006	OMIM:183800	IEA				I		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0000486	OMIM:183800	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0000488	OMIM:183800	TAS				P		HPO:skoehler	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0000518	OMIM:183800	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0000639	PMID:9450888	PCS				P		HPO:probinson	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0001171	OMIM:183800	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0001839	OMIM:183800	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0004058	OMIM:183800	IEA				P		HPO:iea	
OMIM	183800	183800 SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS;;NYSTAGMUS-SPLIT HAND SYNDROME;;KARSCH-NEUGEBAUER SYNDROME; KNS		HP:0006934	OMIM:183800	IEA				P		HPO:skoehler	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0000006	OMIM:183802	IEA				I		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0000126	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0000238	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0000775	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0001171	OMIM:183802	IEA				P		HPO:skoehler	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0001839	OMIM:183802	IEA				P		HPO:skoehler	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0002475	OMIM:183802	TAS				P		HPO:skoehler	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0002944	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0003298	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0005999	OMIM:183802	IEA				P		HPO:iea	
OMIM	183802	183802 SPLIT-HAND WITH OBSTRUCTIVE UROPATHY, SPINA BIFIDA, AND DIAPHRAGMATICDEFECTS		HP:0010554	OMIM:183802	IEA				P		HPO:iea	
OMIM	183840	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:183840	IEA				I		HPO:iea	
OMIM	183840	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2		HP:0001367	OMIM:183840	IEA				P		HPO:iea	
OMIM	183840	SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2		HP:0001939	OMIM:183840	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0000006	OMIM:183849	IEA				I		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0001006	OMIM:183849	TAS				P		HPO:probinson	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002651	OMIM:183849	TAS				P		HPO:skoehler	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002663	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002812	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002834	OMIM:183849	TAS				P		HPO:probinson	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002869	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0002970	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0003184	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0003411	OMIM:183849	TAS				P		HPO:probinson	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0003911	OMIM:183849	TAS				P		HPO:probinson	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0004566	OMIM:183849	TAS				P		HPO:skoehler	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0004581	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0005043	OMIM:183849	TAS				P		HPO:probinson	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0005090	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0006599	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0008905	OMIM:183849	IEA				P		HPO:iea	
OMIM	183849	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH HYPOTRICHOSIS		HP:0100864	OMIM:183849	IEA				P		HPO:iea	
OMIM	183850	SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY		HP:0000006	OMIM:183850	IEA				I		HPO:iea	
OMIM	183850	SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY		HP:0001939	OMIM:183850	IEA				P		HPO:iea	
OMIM	183850	SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY		HP:0002655	OMIM:183850	IEA				P		HPO:iea	
OMIM	183850	SPONDYLOEPIPHYSEAL DYSPLASIA WITH PUNCTATE CORNEAL DYSTROPHY		HP:0007809	OMIM:183850	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000006	OMIM:183900	IEA				I		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000175	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000272	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000470	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000541	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000545	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000768	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0000926	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0001252	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0001290	OMIM:183900	TAS				P		HPO:skoehler	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0001552	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0001762	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002091	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002098	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002318	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002515	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002650	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002655	OMIM:183900	IEA				P		HPO:skoehler	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002808	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002812	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002827	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002938	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0002996	OMIM:183900	TAS				P		HPO:probinson	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0003071	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0003300	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0003311	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0007773	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0008142	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0008788	OMIM:183900	TAS				P		HPO:probinson	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0008800	OMIM:183900	TAS				P		HPO:probinson	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0008857	OMIM:183900	IEA				P		HPO:iea	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0010501	OMIM:183900	TAS				P		HPO:probinson	
OMIM	183900	SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA		HP:0012368	OMIM:183900	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000006	OMIM:184000	IEA				I		HPO:iea	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000407	OMIM:184000	IEA				P		HPO:iea	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000470	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000541	OMIM:184000	IEA				P		HPO:iea	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000545	OMIM:184000	IEA				P		HPO:iea	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000592	OMIM:184000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0000926	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0001763	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0002515	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0002655	OMIM:184000	IEA				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0002656	OMIM:184000	IEA				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS	HP:0012825	HP:0002938	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0003090	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0004322	OMIM:184000	IEA				P		HPO:iea	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0008812	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184000	184000 SPONDYLOEPIPHYSEAL DYSPLASIA, MYOPIA, AND SENSORINEURAL DEAFNESS		HP:0030084	OMIM:184000	TAS				P		HPO:skoehler	
OMIM	184095	#184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE;;SED, MAROTEAUX TYPE;;PSEUDO-MORQUIO SYNDROME, TYPE 2		HP:0000006	OMIM:184095	IEA				I		HPO:iea	
OMIM	184095	#184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE;;SED, MAROTEAUX TYPE;;PSEUDO-MORQUIO SYNDROME, TYPE 2		HP:0000478	OMIM:184095	IEA				P		HPO:iea	
OMIM	184095	#184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE;;SED, MAROTEAUX TYPE;;PSEUDO-MORQUIO SYNDROME, TYPE 2		HP:0000926	OMIM:184095	IEA				P		HPO:iea	
OMIM	184095	#184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE;;SED, MAROTEAUX TYPE;;PSEUDO-MORQUIO SYNDROME, TYPE 2		HP:0002655	OMIM:184095	IEA				P		HPO:iea	
OMIM	184095	#184095 SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE;;SED, MAROTEAUX TYPE;;PSEUDO-MORQUIO SYNDROME, TYPE 2		HP:0002857	OMIM:184095	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:184100	IEA				I		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0000272	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0000470	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0000768	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0000926	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0001369	OMIM:184100	TAS				P		HPO:skoehler	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0001552	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0002655	OMIM:184100	TAS				P		HPO:skoehler	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0002751	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0002938	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0003301	OMIM:184100	TAS				P		HPO:skoehler	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0003308	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0003311	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0005743	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0008922	OMIM:184100	IEA				P		HPO:iea	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0030838	OMIM:184100	IEA				P		HPO:skoehler	
OMIM	184100	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL DOMINANT		HP:0030839	OMIM:184100	IEA				P		HPO:skoehler	
OMIM	184200	SPONDYLOLISTHESIS		HP:0000006	OMIM:184200	IEA				I		HPO:iea	
OMIM	184200	SPONDYLOLISTHESIS		HP:0003304	OMIM:184200	IEA				P		HPO:iea	
OMIM	184200	SPONDYLOLISTHESIS		HP:0008489	OMIM:184200	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000006	OMIM:184250	IEA				I		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000023	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000175	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000545	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000768	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000907	OMIM:184250	TAS				P		HPO:probinson	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0000926	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0001156	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0001538	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0001763	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0002650	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0002651	OMIM:184250	IEA				P		HPO:skoehler	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0002812	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0002857	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003025	OMIM:184250	TAS				P		HPO:probinson	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003173	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003307	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003311	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003320	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003375	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0003510	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0006406	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0008788	OMIM:184250	IEA				P		HPO:iea	
OMIM	184250	#184250 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, STRUDWICK TYPE; SEMDSTWK;;SEMD, STRUDWICK TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA CONGENITA, STRUDWICK TYPE;;SMED, STRUDWICK TYPE;;SMED, TYPE I;;STRUDWICK SYNDROME;;DAPPLED METAPHYSIS SYNDROME;;SPONDYLOMETAPHYSEAL DYSPLASIA; SMD;;SEMDC		HP:0011860	OMIM:184250	TAS				P		HPO:probinson	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0000006	OMIM:184252	IEA				I		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0000271	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0000470	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0000768	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0000926	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0001498	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0001547	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0001760	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0002515	OMIM:184252	IEA				P		HPO:skoehler	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0002657	OMIM:184252	IEA				P		HPO:skoehler	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0002750	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0002751	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0002812	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0003015	OMIM:184252	TAS				P		HPO:skoehler	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0003037	OMIM:184252	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0003180	OMIM:184252	TAS				P		HPO:probinson	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0003311	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0003521	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0005042	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0006069	OMIM:184252	IEA				P		HPO:iea	
OMIM	184252	SPONDYLOMETAPHYSEAL DYSPLASIA, KOZLOWSKI TYPE		HP:0008833	OMIM:184252	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0000006	OMIM:184253	TAS				I		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0000545	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0000907	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0000926	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0001248	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0001498	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002657	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002751	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002812	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002834	PMID:23653587	PCS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002857	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0002938	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0003185	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0003510	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0003865	OMIM:184253	TAS				P		HPO:skoehler	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0006434	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0008839	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0030292	PMID:23653587	PCS				P		HPO:probinson	
OMIM	184253	SPONDYLOMETAPHYSEAL DYSPLASIA, ALGERIAN TYPE		HP:0100255	OMIM:184253	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0000006	OMIM:184255	TAS				I		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0002515	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0002650	OMIM:184255	IEA				P		HPO:skoehler	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0002657	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0002812	OMIM:184255	TAS				P		HPO:skoehler	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0002970	OMIM:184255	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0003025	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0003300	OMIM:184255	IEA				P		HPO:skoehler	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0003311	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0004322	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0004603	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184255	SPONDYLOMETAPHYSEAL DYSPLASIA, CORNER FRACTURE TYPE; SMDCF		HP:0100864	OMIM:184255	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000006	OMIM:184260	TAS				I		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000090	PMID:30728324	PCS		HP:0040284		P		HP:probinson	1/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000256	PMID:30728324	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000275	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000343	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000684	OMIM:184260	TAS				P		HPO:skoehler	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000703	PMID:30728324	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000768	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000774	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000926	OMIM:184260	TAS	HP:0003623			P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0000939	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0001156	PMID:30728324	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0001216	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0001270	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0001382	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0001522	PMID:30728324	PCS		HP:0040284		M		HP:probinson	3/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002089	PMID:30728324	PCS		HP:0040284		P		HP:probinson	4/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002098	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002205	PMID:30728324	PCS		HP:0040284		P		HP:probinson	1/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002650	PMID:30728324	PCS		HP:0040284		P		HPO:probinson	5/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002657	PMID:30728324	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002816	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002869	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002970	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0002983	PMID:30728324	PCS		HP:0040284		P		HP:probinson	1/10
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003016	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003021	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003026	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003027	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003180	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0003417	OMIM:184260	TAS	HP:0003623			P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0004625	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0008845	PMID:30728324	PCS				P		HP:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0009803	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0010049	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0010230	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0010582	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0010585	OMIM:184260	TAS				P		HPO:probinson	
OMIM	184260	SPONDYLOMETAPHYSEAL DYSPLASIA WITH DENTINOGENESIS IMPERFECTA		HP:0011220	OMIM:184260	TAS				P		HPO:skoehler	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0000006	OMIM:184300	IEA				I		HPO:iea	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0002758	OMIM:184300	IEA				P		HPO:iea	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0003298	OMIM:184300	IEA				P		HPO:iea	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0003302	OMIM:184300	IEA				P		HPO:iea	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0003304	OMIM:184300	IEA				P		HPO:iea	
OMIM	184300	SPONDYLOSIS, CERVICAL		HP:0008480	OMIM:184300	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0000006	OMIM:184400	IEA				I		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0000912	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0002650	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0002937	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0003298	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0003745	OMIM:184400	IEA				I		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0004632	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0006655	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0008952	OMIM:184400	IEA				P		HPO:iea	
OMIM	184400	SPRENGEL DEFORMITY		HP:0008984	OMIM:184400	IEA				P		HPO:iea	
OMIM	184450	%184450 STUTTERING, FAMILIAL PERSISTENT, 1; STUT1;;STAMMERING		HP:0000006	OMIM:184450	TAS				I		HPO:skoehler	
OMIM	184450	%184450 STUTTERING, FAMILIAL PERSISTENT, 1; STUT1;;STAMMERING		HP:0001608	OMIM:184450	IEA				P		HPO:iea	
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000006	OMIM:184460;PMID:2319886;PMID:10069712	PCS				I		HPO:iea	
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000381	OMIM:184460	TAS	HP:0003577	HP:0040281		P		HPO:probinson	HP:0040281
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000405	OMIM:184460	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000430	PMID:10069712	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000466	PMID:2319886;PMID:10069712	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0000540	OMIM:184460	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0001770	PMID:2319886;PMID:10069712	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0002949	PMID:2319886	PCS		HP:0040284		P		HPO:iea	2/5
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0003189	PMID:10069712	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0007943	OMIM:184460	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0009177	OMIM:184460	TAS				P		HPO:skoehler	
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0009765	PMID:2319886	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0009882	PMID:2319886	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0010055	OMIM:184460	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	184460	#184460 STAPES ANKYLOSIS WITH BROAD THUMB AND TOES;;ANKYLOSIS OF STAPES, HYPEROPIA, BROAD THUMBS, BROAD FIRST TOES, ANDSYNDACTYLY;;TEUNISSEN-CREMERS SYNDROME;;STAPES ANKYLOSIS SYNDROME WITHOUT SYMPHALANGISM		HP:0011304	OMIM:184460	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	184500	STEATOCYSTOMA MULTIPLEX		HP:0000006	OMIM:184500	TAS				I		HPO:probinson	
OMIM	184500	STEATOCYSTOMA MULTIPLEX		HP:0012035	OMIM:184500	TAS				P		HPO:probinson	
OMIM	184510	STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH		HP:0000006	OMIM:184510	IEA				I		HPO:iea	
OMIM	184510	STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH		HP:0000695	OMIM:184510	IEA				P		HPO:iea	
OMIM	184510	STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH		HP:0001597	OMIM:184510	IEA				P		HPO:iea	
OMIM	184510	STEATOCYSTOMA MULTIPLEX WITH NATAL TEETH		HP:0012035	OMIM:184510	IEA				P		HPO:skoehler	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0000006	OMIM:184700	IEA				I		HPO:iea	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0000141	OMIM:184700	IEA				P		HPO:iea	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0000876	OMIM:184700	IEA				P		HPO:iea	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0001007	OMIM:184700	TAS				P		HPO:probinson	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0001513	OMIM:184700	IEA				P		HPO:iea	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0001939	OMIM:184700	IEA				P		HPO:iea	
OMIM	184700	POLYCYSTIC OVARY SYNDROME 1		HP:0008675	OMIM:184700	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000006	OMIM:184705	IEA				I		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000193	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000365	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000377	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000480	PMID:8357025	PCS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000568	OMIM:184705	TAS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000612	PMID:8357025	PCS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0000921	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0001360	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0001627	OMIM:184705	TAS				P		HPO:skoehler	
OMIM	184705	184705 STEINFELD SYNDROME	HP:0012832	HP:0002984	OMIM:184705	TAS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME	HP:0012832	HP:0003022	OMIM:184705	TAS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0003468	OMIM:184705	TAS				P		HPO:skoehler	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0008501	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0008718	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0009601	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0009829	OMIM:184705	IEA				P		HPO:iea	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0009927	OMIM:184705	TAS				P		HPO:skoehler	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0011467	OMIM:184705	TAS				P		HPO:probinson	
OMIM	184705	184705 STEINFELD SYNDROME		HP:0030680	OMIM:184705	IEA				P		HPO:iea	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0000006	OMIM:184800	TAS				I		HPO:iea	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0000028	OMIM:184800	TAS				P		HPO:iea	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0000347	OMIM:184800	TAS				P		HPO:iea	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0000879	OMIM:184800	TAS				P		HPO:probinson	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0001627	OMIM:184800	TAS				P		HPO:skoehler	
OMIM	184800	184800 STERNUM, PREMATURE OBLITERATION OF SUTURES OF		HP:0006590	OMIM:184800	TAS				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000006	OMIM:184840	IEA				I		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000175	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000201	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000272	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000407	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000463	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000478	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0000926	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0002656	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0002829	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0002829	OMIM:184840	TAS				P		HP:probinson	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0003088	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0010580	OMIM:184840	IEA				P		HPO:iea	
OMIM	184840	STICKLER SYNDROME, TYPE III		HP:0011800	OMIM:184840	TAS				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000716	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000739	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000756	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000819	OMIM:184850	IEA				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000822	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0000975	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0001045	OMIM:184850	IEA				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0001347	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0001649	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0001903	OMIM:184850	IEA				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0001945	OMIM:184850	TAS				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002063	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002179	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002267	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002359	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002938	OMIM:184850	IEA				P		HPO:skoehler	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0002960	OMIM:184850	TAS				P		HPO:probinson	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0003581	OMIM:184850	IEA				C		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0003739	OMIM:184850	TAS				P		HPO:probinson	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0003745	OMIM:184850	IEA				I		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0006921	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0007066	OMIM:184850	IEA				P		HPO:iea	
OMIM	184850	STIFF-PERSON SYNDROME; SPS		HP:0007156	OMIM:184850	IEA				P		HPO:iea	
OMIM	184900	STIFF SKIN SYNDROME		HP:0000006	OMIM:184900	IEA				I		HPO:iea	
OMIM	184900	STIFF SKIN SYNDROME		HP:0001324	OMIM:184900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184900	STIFF SKIN SYNDROME		HP:0001371	OMIM:184900	IEA				P		HPO:iea	
OMIM	184900	STIFF SKIN SYNDROME		HP:0001376	OMIM:184900	IEA				P		HPO:iea	
OMIM	184900	STIFF SKIN SYNDROME		HP:0004322	OMIM:184900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184900	STIFF SKIN SYNDROME		HP:0009125	OMIM:184900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184900	STIFF SKIN SYNDROME		HP:0009830	OMIM:184900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	184900	STIFF SKIN SYNDROME		HP:0030053	OMIM:184900	IEA				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0000006	OMIM:185000	IEA				I		HPO:iea	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0000952	OMIM:185000	TAS				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0001744	OMIM:185000	TAS				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0001878	OMIM:185000	IEA				P		HPO:iea	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0001923	OMIM:185000	TAS				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0002240	OMIM:185000	TAS				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0002904	OMIM:185000	TAS				P		HPO:skoehler	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0003575	OMIM:185000	IEA				P		HPO:iea	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0004446	OMIM:185000	TAS				P		HPO:probinson	
OMIM	185000	#185000 OVERHYDRATED HEREDITARY STOMATOCYTOSIS; OHS;;POTASSIUM-SODIUM DISORDER OF ERYTHROCYTE		HP:0005502	OMIM:185000	IEA				P		HPO:iea	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0000006	OMIM:185020	IEA				I		HPO:iea	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0001744	OMIM:185020	TAS				P		HPO:skoehler	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0001878	OMIM:185020	IEA				P		HPO:iea	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0001923	OMIM:185020	TAS				P		HPO:skoehler	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0001939	OMIM:185020	IEA				P		HPO:iea	
OMIM	185020	#185020 CRYOHYDROCYTOSIS; CHC;;STOMATOCYTOSIS, COLD-SENSITIVE		HP:0004446	OMIM:185020	IEA				P		HPO:iea	
OMIM	185050	STORAGE POOL PLATELET DISEASE		HP:0000006	OMIM:185050	IEA				I		HPO:iea	
OMIM	185050	STORAGE POOL PLATELET DISEASE		HP:0002488	OMIM:185050	IEA				P		HPO:skoehler	
OMIM	185050	STORAGE POOL PLATELET DISEASE		HP:0002863	OMIM:185050	IEA				P		HPO:skoehler	
OMIM	185050	STORAGE POOL PLATELET DISEASE		HP:0003010	OMIM:185050	IEA				P		HPO:skoehler	
OMIM	185050	STORAGE POOL PLATELET DISEASE		HP:0005537	OMIM:185050	IEA				P		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0000006	OMIM:185069	IEA				I		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0000535	OMIM:185069	IEA				P		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0001650	OMIM:185069	IEA				P		HPO:skoehler	
OMIM	185069	STORM SYNDROME		HP:0001718	OMIM:185069	TAS				P		HPO:probinson	
OMIM	185069	STORM SYNDROME		HP:0002630	OMIM:185069	TAS				P		HPO:skoehler	
OMIM	185069	STORM SYNDROME		HP:0004380	OMIM:185069	TAS				P		HPO:skoehler	
OMIM	185069	STORM SYNDROME		HP:0004382	OMIM:185069	TAS				P		HPO:probinson	
OMIM	185069	STORM SYNDROME		HP:0004764	OMIM:185069	IEA				P		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0005195	OMIM:185069	IEA				P		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0006694	OMIM:185069	IEA				P		HPO:iea	
OMIM	185069	STORM SYNDROME		HP:0007605	OMIM:185069	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0000006	OMIM:185070	IEA				I		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0000421	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0000448	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0000490	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0000601	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0000616	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0001746	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0001873	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0001892	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0001903	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0002076	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0002401	OMIM:185070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	185070	STORMORKEN SYNDROME		HP:0003198	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0003236	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0003326	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0003676	OMIM:185070	TAS				C		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0003701	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0003750	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0004322	OMIM:185070	TAS				P		HPO:skoehler	
OMIM	185070	STORMORKEN SYNDROME		HP:0008064	OMIM:185070	IEA				P		HPO:iea	
OMIM	185070	STORMORKEN SYNDROME		HP:0010522	OMIM:185070	IEA				P		HPO:skoehler	
OMIM	185100	STRABISMUS, SUSCEPTIBILITY TO		HP:0031724	OMIM:185100	IEA				P		HPO:skoehler	
OMIM	185200	STRIAE DISTENSAE, FAMILIAL		HP:0000006	OMIM:185200	TAS				I		HPO:probinson	
OMIM	185200	STRIAE DISTENSAE, FAMILIAL		HP:0001065	OMIM:185200	TAS				P		HPO:probinson	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0000256	OMIM:185300	TAS				P		HPO:probinson	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0000329	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0000557	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0001249	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0001250	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0002120	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0003745	OMIM:185300	IEA				I		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0007872	OMIM:185300	IEA				P		HPO:iea	
OMIM	185300	STURGE-WEBER SYNDROME		HP:0012222	OMIM:185300	TAS				P		HPO:probinson	
OMIM	185460	SULFHEMOGLOBINEMIA, CONGENITAL		HP:0000006	OMIM:185460	IEA				I		HPO:iea	
OMIM	185460	SULFHEMOGLOBINEMIA, CONGENITAL		HP:0000961	OMIM:185460	IEA				P		HPO:skoehler	
OMIM	185460	SULFHEMOGLOBINEMIA, CONGENITAL		HP:0001871	OMIM:185460	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0000006	OMIM:185480	IEA				I		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0000252	OMIM:185480	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0001249	OMIM:185480	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0001250	OMIM:185480	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0001260	OMIM:185480	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0001324	OMIM:185480	IEA				P		HPO:skoehler	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0002307	OMIM:185480	IEA				P		HPO:iea	
OMIM	185480	SUPRABULBAR PARESIS, CONGENITAL		HP:0002353	OMIM:185480	IEA				P		HPO:iea	
OMIM	185500	SUPRAVALVULAR AORTIC STENOSIS		HP:0000006	OMIM:185500	TAS				I		HPO:skoehler	
OMIM	185500	SUPRAVALVULAR AORTIC STENOSIS		HP:0001642	OMIM:185500	TAS				P		HPO:probinson	
OMIM	185500	SUPRAVALVULAR AORTIC STENOSIS		HP:0004381	OMIM:185500	TAS				P		HPO:skoehler	
OMIM	185500	SUPRAVALVULAR AORTIC STENOSIS		HP:0004415	OMIM:185500	TAS				P		HPO:skoehler	
OMIM	185500	SUPRAVALVULAR AORTIC STENOSIS		HP:0004950	OMIM:185500	TAS				P		HPO:skoehler	
OMIM	185600	SYMPHALANGISM OF TOES		HP:0000006	OMIM:185600	TAS				I		HPO:probinson	
OMIM	185600	SYMPHALANGISM OF TOES		HP:0100235	OMIM:185600	TAS				P		HPO:probinson	
OMIM	185650	SYMPHALANGISM, C. S. LEWIS TYPE		HP:0000006	OMIM:185650	TAS				I		HPO:probinson	
OMIM	185650	SYMPHALANGISM, C. S. LEWIS TYPE		HP:0009703	OMIM:185650	TAS				P		HPO:probinson	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0000006	OMIM:185700	IEA				I		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001049	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001156	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001204	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001363	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001792	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001798	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0001859	OMIM:185700	IEA				P		HPO:iea	
OMIM	185700	SYMPHALANGISM, DISTAL		HP:0003828	OMIM:185700	IEA				C		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0000006	OMIM:185750	IEA				I		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0000256	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0000365	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0001049	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0001245	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0001770	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0001864	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0006019	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0006152	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0009778	OMIM:185750	IEA				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0009778	OMIM:185750	TAS				P		HPO:iea	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0010487	OMIM:185750	TAS				P		HPO:skoehler	
OMIM	185750	185750 SYMPHALANGISM WITH MULTIPLE ANOMALIES OF HANDS AND FEET		HP:0010554	OMIM:185750	IEA				P		HPO:iea	
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0000006	PMID:10080184;OMIM:185800	PCS				I		HPO:iea	
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0000381	PMID:10080184;OMIM:185800	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0000405	PMID:10080184;OMIM:185800	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0001204	PMID:10080184;OMIM:185800	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0005880	PMID:10080184;OMIM:185800	PCS		HP:0040284		P		HPO:iea	HP:0040284
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0006152	PMID:10080184;OMIM:185800	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0008368	PMID:10080184;OMIM:185800	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0009702	PMID:10080184;OMIM:185800	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0009843	OMIM:185800	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0010047	OMIM:185800	TAS				P		HPO:skoehler	
OMIM	185800	#185800 SYMPHALANGISM, PROXIMAL, 1A; SYM1A;;SYM1;;CUSHING SYMPHALANGISM;;HEREDITARY ABSENCE OF THE PROXIMAL INTERPHALANGEAL JOINTS		HP:0010194	OMIM:185800	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0000006	OMIM:185900	IEA				I	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:iea	
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0001204	OMIM:185900	IEA				P	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:iea	
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0004442	OMIM:185900	TAS		HP:0040283		P	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0004691	OMIM:185900	IEA				P	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:iea	
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0006097	OMIM:185900	IEA				P	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:iea	
OMIM	185900	CHROMOSOME 2q35 DUPLICATION SYNDROME		HP:0012725	OMIM:185900	IEA				P	CHROMOSOME 2Q35 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0000006	OMIM:186000	TAS				I		HPO:probinson	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0001501	OMIM:186000	TAS				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0001830	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0001841	OMIM:186000	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	186000	SYNPOLYDACTYLY 1		HP:0004209	OMIM:186000	TAS				P		HPO:probinson	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0004220	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0004692	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0006042	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0006097	OMIM:186000	TAS				P		HPO:probinson	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0006101	OMIM:186000	IEA				P		HPO:skoehler	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0006159	OMIM:186000	TAS				P		HPO:probinson	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0008083	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0009185	OMIM:186000	IEA				P		HPO:iea	
OMIM	186000	SYNPOLYDACTYLY 1		HP:0010055	OMIM:186000	TAS				P		HPO:skoehler	
OMIM	186100	SYNDACTYLY, TYPE III		HP:0000006	OMIM:186100	TAS				I		HPO:probinson	
OMIM	186100	SYNDACTYLY, TYPE III		HP:0009162	OMIM:186100	TAS				P		HPO:probinson	
OMIM	186100	SYNDACTYLY, TYPE III		HP:0009237	OMIM:186100	TAS				P		HPO:probinson	
OMIM	186100	SYNDACTYLY, TYPE III		HP:0010705	OMIM:186100	TAS				P		HPO:probinson	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0000006	PMID:18417549	PCS				I		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0001199	PMID:18417549	PCS				P		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0001501	OMIM:186200	TAS				P		HPO:skoehler	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0004691	OMIM:186200	IEA				P		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0005917	OMIM:18417549	PCS				P		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0006088	OMIM:186200	TAS				P		HPO:skoehler	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0010442	PMID:18417549	PCS				P		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0010708	PMID:18417549	PCS				P		HPO:iea	
OMIM	186200	SYNDACTYLY, TYPE IV; SDTY4		HP:0100259	OMIM:186200	IEA				P		HPO:skoehler	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0000006	OMIM:186300	IEA				I		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0001032	OMIM:186300	IEA				P		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0001156	OMIM:186300	TAS				P		HPO:probinson	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0004692	OMIM:186300	TAS				P		HPO:probinson	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0005867	OMIM:186300	TAS				P		HPO:probinson	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0006185	OMIM:186300	IEA				P		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0009473	OMIM:186300	IEA				P		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0009702	OMIM:186300	IEA				P		HPO:skoehler	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0009779	OMIM:186300	TAS				P		HPO:probinson	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0009882	OMIM:186300	IEA				P		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0010554	OMIM:186300	IEA				P		HPO:iea	
OMIM	186300	SYNDACTYLY, TYPE V		HP:0100490	OMIM:186300	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0000006	OMIM:186350	IEA				I		HPO:iea	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0000363	OMIM:186350	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0001177	OMIM:186350	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0001837	OMIM:186350	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0001841	OMIM:186350	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0001853	OMIM:186350	TAS				P		HPO:probinson	
OMIM	186350	SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME		HP:0005767	OMIM:186350	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0000006	OMIM:186400	IEA				I		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0000430	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0001798	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0003048	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0005880	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0008368	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0009702	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0009843	OMIM:186400	IEA				P		HPO:iea	
OMIM	186400	SYNOSTOSES, TARSAL, CARPAL, AND DIGITAL		HP:0010049	OMIM:186400	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000006	OMIM:186500	IEA				I		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000215	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000219	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000275	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000322	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000381	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000430	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000486	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000767	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000879	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000920	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0000954	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0001032	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0001156	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0001773	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0001798	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0002515	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0002967	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0003083	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0003416	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0003468	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0004691	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0005104	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0005792	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0005807	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0006152	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0006187	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0006385	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0008368	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0008460	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0008607	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0009466	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0009702	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0009816	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0009843	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0010109	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0010554	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0010624	OMIM:186500	IEA				P		HPO:iea	
OMIM	186500	#186500 MULTIPLE SYNOSTOSES SYNDROME 1; SYNS1;;SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY;;SYMPHALANGISM-BRACHYDACTYLY SYNDROME;;WL SYNDROME;;DEAFNESS-SYMPHALANGISM SYNDROME OF HERRMANN;;FACIOAUDIOSYMPHALANGISM SYNDROME		HP:0030084	OMIM:186500	TAS				P		HPO:skoehler	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0000006	OMIM:186550	IEA				I		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0001156	OMIM:186550	IEA				P		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0001191	OMIM:186550	TAS				P		HPO:skoehler	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0001233	OMIM:186550	IEA				P		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0002987	OMIM:186550	IEA				P		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0003016	OMIM:186550	TAS				P		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0006190	OMIM:186550	IEA				P		HPO:iea	
OMIM	186550	SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY		HP:0009183	OMIM:186550	IEA				P		HPO:iea	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0000006	OMIM:186579;PMID:11545688	PCS				I		HPO:iea	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0001156	OMIM:186570	TAS				P		HPO:skoehler	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0001204	OMIM:186579;PMID:11545688	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0002967	OMIM:186570	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0003041	OMIM:186579;PMID:11545688	PCS	HP:0011463	HP:0040283		P		HPO:iea	HP:0040283
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0004322	OMIM:186570	IEA				P		HPO:skoehler	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0006147	OMIM:186570	TAS				P		HPO:skoehler	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0006152	OMIM:186579;PMID:11545688	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0008368	OMIM:186579;PMID:11545688	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0009381	OMIM:186570	TAS				P		HPO:probinson	
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0009466	OMIM:186579;PMID:11545688	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0009702	OMIM:186579;PMID:11545688	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0010034	OMIM:186579;PMID:11545688	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	186570	#186570 TARSAL-CARPAL COALITION SYNDROME; TCC; SYNOSTOSIS OF TALUS AND CALCANEUS WITH SHORT STATURE, INCLUDED		HP:0030084	OMIM:186570	TAS				P		HPO:skoehler	
OMIM	186575	SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM		HP:0000006	OMIM:186575	IEA				I		HPO:iea	
OMIM	186575	SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM		HP:0002829	OMIM:186575	TAS				P		HPO:skoehler	
OMIM	186575	SYNOVIAL CHONDROMATOSIS, FAMILIAL, WITH DWARFISM		HP:0003510	PMID:1733839	PCS				P		HPO:iea	
OMIM	186580	BLAU SYNDROME		HP:0000006	OMIM:186580	TAS				I		HPO:probinson	
OMIM	186580	BLAU SYNDROME		HP:0000501	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0000518	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0000554	OMIM:186580	TAS				P		HPO:probinson	
OMIM	186580	BLAU SYNDROME		HP:0000585	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0000598	OMIM:186580	IEA				P		HPO:iea	
OMIM	186580	BLAU SYNDROME		HP:0000964	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0001101	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0001291	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0001369	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0001386	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0005830	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0007432	OMIM:186580	IEA				P		HPO:iea	
OMIM	186580	BLAU SYNDROME		HP:0007813	OMIM:186580	IEA				P		HPO:iea	
OMIM	186580	BLAU SYNDROME		HP:0011505	OMIM:186580	TAS				P		HPO:probinson	
OMIM	186580	BLAU SYNDROME		HP:0025230	OMIM:186580	TAS				P		HPO:skoehler	
OMIM	186580	BLAU SYNDROME		HP:0100490	OMIM:186580	TAS				P		HPO:iea	
OMIM	186580	BLAU SYNDROME		HP:0100769	OMIM:186580	TAS				P		HPO:probinson	
OMIM	186580	BLAU SYNDROME		HP:0200042	OMIM:186580	IEA				P		HPO:skoehler	
OMIM	186600	SYRINGOMAS, MULTIPLE		HP:0000006	OMIM:186600	IEA				I		HPO:iea	
OMIM	186600	SYRINGOMAS, MULTIPLE		HP:0000951	OMIM:186600	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0000006	OMIM:186700	IEA				I		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0000020	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0000639	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0001260	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002061	OMIM:186700	TAS				P		HPO:skoehler	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002066	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002277	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002317	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002395	OMIM:186700	TAS				P		HPO:skoehler	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002650	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0002699	OMIM:186700	TAS				P		HPO:skoehler	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0003396	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0003401	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0003487	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0003690	OMIM:186700	IEA				P		HPO:skoehler	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0005878	OMIM:186700	IEA				P		HPO:iea	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0007099	OMIM:186700	TAS				P		HPO:skoehler	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0012046	OMIM:186700	TAS				P		HPO:probinson	
OMIM	186700	SYRINGOMYELIA, ISOLATED		HP:0030833	OMIM:186700	TAS				P		HPO:skoehler	
OMIM	186750	TALONAVICULAR COALITION		HP:0000006	OMIM:186750	IEA				I		HPO:iea	
OMIM	186750	TALONAVICULAR COALITION		HP:0003028	PMID:29270563	PCS				P		HPO:lccarmody	
OMIM	186750	TALONAVICULAR COALITION		HP:0004209	OMIM:186750	IEA				P		HPO:iea	
OMIM	186750	TALONAVICULAR COALITION		HP:0005802	PMID:29270563	PCS				P		HPO:lccarmody	
OMIM	186750	TALONAVICULAR COALITION		HP:0009177	OMIM:186750	IEA				P		HPO:iea	
OMIM	186750	TALONAVICULAR COALITION		HP:0010109	PMID:29270563	PCS				P		HPO:lccarmody	
OMIM	186750	TALONAVICULAR COALITION		HP:0025238	PMID:29270563	PCS				P		HPO:lccarmody	
OMIM	186850	TARSAL FUSION		HP:0000006	OMIM:186850	IEA				I		HPO:iea	
OMIM	186850	TARSAL FUSION		HP:0008368	OMIM:186850	IEA				P		HPO:iea	
OMIM	187000	TEETH, ODD SHAPES OFLOBODONTIA, INCLUDED		HP:0000006	OMIM:187000	IEA				I		HPO:iea	
OMIM	187000	TEETH, ODD SHAPES OFLOBODONTIA, INCLUDED		HP:0000164	OMIM:187000	IEA				P		HPO:iea	
OMIM	187050	TEETH PRESENT AT BIRTH		HP:0000006	OMIM:187050	IEA				I		HPO:iea	
OMIM	187050	TEETH PRESENT AT BIRTH		HP:0000695	OMIM:187050	IEA				P		HPO:iea	
OMIM	187100	187100 TEETH, SUPERNUMERARY		HP:0000006	OMIM:187100	IEA				I		HPO:iea	
OMIM	187100	187100 TEETH, SUPERNUMERARY		HP:0011067	OMIM:187100	TAS				P		HPO:skoehler	
OMIM	187100	187100 TEETH, SUPERNUMERARY		HP:0011069	OMIM:187100	IEA				P		HPO:iea	
OMIM	187260	TELANGIECTASIA, HEREDITARY BENIGN		HP:0000006	PMID:14627680	PCS				I		HPO:probinson	
OMIM	187260	TELANGIECTASIA, HEREDITARY BENIGN		HP:0002617	OMIM:187260	IEA				P		HPO:skoehler	
OMIM	187260	TELANGIECTASIA, HEREDITARY BENIGN		HP:0007489	PMID:14627680	PCS				P		HPO:probinson	
OMIM	187260	TELANGIECTASIA, HEREDITARY BENIGN		HP:0011463	PMID:14627680	PCS				C		HPO:probinson	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000006	OMIM:187300	TAS				I		HPO:probinson	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000214	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000227	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000434	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000471	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000524	OMIM:187300	TAS				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0000961	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001217	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001232	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001250	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001342	OMIM:187300	TAS				P		HPO:probinson	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001394	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001425	OMIM:187300	TAS				I		HPO:skoehler	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001694	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001722	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001901	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0001903	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002076	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002094	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002138	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002140	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002248	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002249	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002326	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002390	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002408	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002573	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002604	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002626	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002629	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002642	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0002707	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0004406	OMIM:187300	IEA	HP:0003621			P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0006107	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0006548	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0006574	OMIM:187300	IEA				P		HPO:iea	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0011934	OMIM:187300	TAS				P		HPO:probinson	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0030049	OMIM:187300	TAS				P		HPO:skoehler	
OMIM	187300	#187300 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER;HHT;;OSLER-RENDU-WEBER DISEASE;;ORW DISEASETELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1, INCLUDED; HHT1, INCLUDED		HP:0100858	OMIM:187300	TAS				P		HPO:probinson	
OMIM	187350	TELECANTHUS		HP:0000006	OMIM:187350	IEA				I		HPO:iea	
OMIM	187350	TELECANTHUS		HP:0000506	OMIM:187350	IEA				P		HPO:iea	
OMIM	187350	TELECANTHUS		HP:0000674	OMIM:187350	IEA				P		HPO:iea	
OMIM	187350	TELECANTHUS		HP:0001249	OMIM:187350	IEA				P		HPO:iea	
OMIM	187350	TELECANTHUS		HP:0002744	OMIM:187350	IEA				P		HPO:iea	
OMIM	187360	TEMPORAL ARTERITIS		HP:0000006	OMIM:187360	IEA				I		HPO:iea	
OMIM	187360	TEMPORAL ARTERITIS		HP:0000618	OMIM:187360	IEA				P		HPO:iea	
OMIM	187360	TEMPORAL ARTERITIS		HP:0003565	OMIM:187360	IEA				P		HPO:iea	
OMIM	187360	TEMPORAL ARTERITIS		HP:0008030	OMIM:187360	IEA				P		HPO:iea	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0000006	OMIM:187370	TAS				I		HPO:skoehler	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0001239	OMIM:187370	TAS				P		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0002804	OMIM:187370	IEA				P		HPO:skoehler	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0002987	OMIM:187370	TAS				P		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0003089	OMIM:187370	TAS				P		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0003828	OMIM:187370	TAS				C		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0005684	OMIM:187370	TAS				P		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0008112	OMIM:187370	TAS				P		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0011463	OMIM:187370	TAS				C		HPO:probinson	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0040083	OMIM:187370	TAS				P		HPO:skoehler	
OMIM	187370	%187370 ARTHROGRYPOSIS, DISTAL, TYPE 10; DA10;;CONGENITAL PLANTAR CONTRACTURES;;TENDO CALCANEUS, SHORT		HP:0100490	OMIM:187370	TAS				P		HPO:skoehler	
OMIM	187390	TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF		HP:0000006	OMIM:187390	IEA				I		HPO:iea	
OMIM	187390	TENDONS, EXTENSOR, OF FINGERS, ANOMALOUS INSERTION OF		HP:0001167	OMIM:187390	TAS				P		HPO:iea	
OMIM	187395	TERATOCARCINOMA-DERIVED GROWTH FACTOR 1; TDGF1		HP:0000252	PMID:12073012	IEA				P		HPO:probinson	
OMIM	187395	TERATOCARCINOMA-DERIVED GROWTH FACTOR 1; TDGF1		HP:0001263	PMID:12073012	IEA				P		HPO:probinson	
OMIM	187395	TERATOCARCINOMA-DERIVED GROWTH FACTOR 1; TDGF1		HP:0001331	PMID:12073012	IEA				P		HPO:probinson	
OMIM	187395	TERATOCARCINOMA-DERIVED GROWTH FACTOR 1; TDGF1		HP:0002079	PMID:12073012	IEA				P		HPO:probinson	
OMIM	187400	TESTICULAR TORSION		HP:0000006	OMIM:187400	TAS				I		HPO:nvasilevsky	
OMIM	187400	TESTICULAR TORSION		HP:0000119	OMIM:187400	IEA				P		HPO:iea	
OMIM	187400	TESTICULAR TORSION		HP:0001450	OMIM:187400	TAS				I		HPO:nvasilevsky	
OMIM	187400	TESTICULAR TORSION		HP:0100813	OMIM:187400	TAS				P		HPO:skoehler	
OMIM	187500	TETRALOGY OF FALLOT		HP:0000006	OMIM:187500	IEA				I		HPO:iea	
OMIM	187500	TETRALOGY OF FALLOT		HP:0000337	OMIM:187500	IEA				P		HPO:iea	
OMIM	187500	TETRALOGY OF FALLOT		HP:0000520	OMIM:187500	IEA				P		HPO:iea	
OMIM	187500	TETRALOGY OF FALLOT		HP:0001636	OMIM:187500	IEA				P		HPO:iea	
OMIM	187500	TETRALOGY OF FALLOT		HP:0004209	OMIM:187500	IEA				P		HPO:iea	
OMIM	187500	TETRALOGY OF FALLOT		HP:0004467	OMIM:187500	IEA				P		HPO:iea	
OMIM	187501	TETRALOGY OF FALLOT AND GLAUCOMA		HP:0000006	OMIM:187501	IEA				I		HPO:iea	
OMIM	187501	TETRALOGY OF FALLOT AND GLAUCOMA		HP:0001087	OMIM:187501	IEA				P		HPO:iea	
OMIM	187501	TETRALOGY OF FALLOT AND GLAUCOMA		HP:0001636	OMIM:187501	IEA				P		HPO:iea	
OMIM	187510	TETRAMELIC MONODACTYLY		HP:0000006	OMIM:187510	TAS				I		HPO:probinson	
OMIM	187510	TETRAMELIC MONODACTYLY		HP:0001171	OMIM:187510	TAS				P		HPO:probinson	
OMIM	187510	TETRAMELIC MONODACTYLY		HP:0001839	OMIM:187510	TAS				P		HPO:probinson	
OMIM	187510	TETRAMELIC MONODACTYLY		HP:0004058	OMIM:187510	TAS				P		HPO:probinson	
OMIM	187510	TETRAMELIC MONODACTYLY		HP:0200054	OMIM:187510	TAS				P		HPO:probinson	
OMIM	187550	THALASSEMIA, BETA+, SILENT ALLELE		HP:0000006	OMIM:187550	IEA				I		HPO:iea	
OMIM	187550	THALASSEMIA, BETA+, SILENT ALLELE		HP:0011906	OMIM:187550	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000006	OMIM:187600	IEA				I		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000238	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000256	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000274	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000773	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000774	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000910	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0000946	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0001252	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0001263	OMIM:187600	IEA				P		HPO:skoehler	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0001558	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0001561	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002007	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002093	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002187	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002282	OMIM:187600	IEA				P		HPO:skoehler	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002676	OMIM:187600	IEA				P		HPO:skoehler	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0002677	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0003015	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0003025	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I	HP:0012828	HP:0003026	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0003185	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0003510	OMIM:187600	IEA				P		HPO:skoehler	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0003811	OMIM:187600	IEA				M		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0004565	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0006487	OMIM:187600	TAS				P		HPO:probinson	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0006584	OMIM:187600	IEA				P		HPO:iea	
OMIM	187600	THANATOPHORIC DYSPLASIA, TYPE I		HP:0008909	OMIM:187600	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000006	OMIM:187601	IEA				I		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000274	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000773	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000774	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000910	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000926	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0000946	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0001156	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0001558	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0001561	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0002093	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II	HP:0012828	HP:0002676	OMIM:187601	IEA				P		HPO:probinson	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0002677	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0003015	OMIM:187601	TAS				P		HPO:probinson	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0003025	OMIM:187601	TAS				P		HPO:probinson	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0003185	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0003811	OMIM:187601	IEA				M		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0006584	OMIM:187601	IEA				P		HPO:iea	
OMIM	187601	THANATOPHORIC DYSPLASIA, TYPE II		HP:0008909	OMIM:187601	TAS				P		HPO:probinson	
OMIM	187650	THEOPHYLLINE BIOTRANSFORMATION		HP:0000006	OMIM:187650	IEA				I		HPO:iea	
OMIM	187750	THORACIC DYSOSTOSIS, ISOLATED		HP:0000006	OMIM:187750	IEA				I		HPO:skoehler	
OMIM	187750	THORACIC DYSOSTOSIS, ISOLATED		HP:0000767	OMIM:187750	IEA				P		HPO:skoehler	
OMIM	187750	THORACIC DYSOSTOSIS, ISOLATED		HP:0000773	OMIM:187750	TAS				P		HPO:skoehler	
OMIM	187750	THORACIC DYSOSTOSIS, ISOLATED		HP:0001591	OMIM:187750	IEA				P		HPO:skoehler	
OMIM	187750	THORACIC DYSOSTOSIS, ISOLATED		HP:0002205	OMIM:187750	TAS				P		HPO:skoehler	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0000006	OMIM:187760	IEA				I		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0000773	OMIM:187760	TAS				P		HPO:probinson	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0000888	OMIM:187760	TAS				P		HPO:probinson	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0001533	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0001591	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0001602	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0002650	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0002686	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0002866	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0003016	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0003275	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0003301	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0006606	OMIM:187760	IEA				P		HPO:iea	
OMIM	187760	THORACOLARYNGOPELVIC DYSPLASIA		HP:0008839	OMIM:187760	IEA				P		HPO:skoehler	
OMIM	187770	THORACOPELVIC DYSOSTOSIS		HP:0000006	OMIM:187770	IEA				I		HPO:iea	
OMIM	187770	THORACOPELVIC DYSOSTOSIS		HP:0000773	OMIM:187770	IEA				P		HPO:iea	
OMIM	187770	THORACOPELVIC DYSOSTOSIS		HP:0002643	OMIM:187770	IEA				P		HPO:iea	
OMIM	187770	THORACOPELVIC DYSOSTOSIS		HP:0004322	OMIM:187770	IEA				P		HPO:iea	
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0000006	PMID:18065693	PCS				I		HPO:probinson	
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0000967	OMIM:187800	TAS				P		HPO:iea	
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0001902	PMID:18065693	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0001903	OMIM:187800	IEA				P		HPO:iea	
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0003540	OMIM:187800	TAS				P		HPO:probinson	
OMIM	187800	GLANZMANN THROMBASTHENIA, AUTOSOMAL DOMINANT		HP:0040185	PMID:18065693	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0000006	OMIM:187900	TAS				I		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0000007	OMIM:187900	TAS				I		HPO:probinson	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0000421	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0000967	OMIM:187900	IEA				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0000978	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0001873	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0002239	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0003010	OMIM:187900	TAS				P		HPO:probinson	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0003337	OMIM:187900	TAS				P		HPO:probinson	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0003593	OMIM:187900	TAS				C		HPO:probinson	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0003828	OMIM:187900	TAS				C		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0011974	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0012526	OMIM:187900	TAS				P		HPO:skoehler	
OMIM	187900	BLEEDING DISORDER, PLATELET-TYPE, 17; BDPLT17		HP:0031364	OMIM:187900	IEA				P		HPO:skoehler	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0000006	OMIM:187950	IEA				I		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0000822	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0000924	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0001063	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0001428	OMIM:187950	IEA				I		HPO:skoehler	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0001744	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0001894	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0003540	OMIM:187950	IEA				P		HPO:iea	
OMIM	187950	THROMBOCYTHEMIA, ESSENTIAL		HP:0005547	OMIM:187950	IEA				P		HPO:iea	
OMIM	188000	THROMBOCYTOPENIA 2		HP:0000006	OMIM:188000	IEA				I		HPO:iea	
OMIM	188000	THROMBOCYTOPENIA 2		HP:0000978	OMIM:188000	IEA				P		HPO:iea	
OMIM	188000	THROMBOCYTOPENIA 2		HP:0001873	OMIM:188000	IEA				P		HPO:iea	
OMIM	188020	THROMBOCYTOPENIA, CYCLIC		HP:0000006	OMIM:188020	IEA				I		HPO:iea	
OMIM	188020	THROMBOCYTOPENIA, CYCLIC		HP:0001873	OMIM:188020	IEA				P		HPO:iea	
OMIM	188020	THROMBOCYTOPENIA, CYCLIC		HP:0001875	OMIM:188020	IEA				P		HPO:skoehler	
OMIM	188020	THROMBOCYTOPENIA, CYCLIC		HP:0001892	OMIM:188020	IEA				P		HPO:iea	
OMIM	188020	THROMBOCYTOPENIA, CYCLIC		HP:0040289	OMIM:188020	TAS				P		HPO:skoehler	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0000243	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0000347	OMIM:188025	TAS				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:skoehler	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0000508	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0001249	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0001873	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0002021	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0003010	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0003745	OMIM:188025	IEA				I	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0009466	OMIM:188025	IEA				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:iea	
OMIM	188025	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11q23 DELETION SYNDROME		HP:0030084	OMIM:188025	TAS				P	#188025 THROMBOCYTOPENIA, PARIS-TROUSSEAU TYPE; TCPT;;CHROMOSOME 11Q23 DELETION SYNDROME	HPO:skoehler	
OMIM	188030	188030 THROMBOCYTOPENIC PURPURA, AUTOIMMUNE; AITP;;IMMUNE THROMBOCYTOPENIC PURPURA; ITP;;IDIOPATHIC THROMBOCYTOPENIC PURPURA		HP:0000006	OMIM:188030	TAS				I		HPO:skoehler	
OMIM	188030	188030 THROMBOCYTOPENIC PURPURA, AUTOIMMUNE; AITP;;IMMUNE THROMBOCYTOPENIC PURPURA; ITP;;IDIOPATHIC THROMBOCYTOPENIC PURPURA		HP:0001873	OMIM:188030	IEA				P		HPO:iea	
OMIM	188030	188030 THROMBOCYTOPENIC PURPURA, AUTOIMMUNE; AITP;;IMMUNE THROMBOCYTOPENIC PURPURA; ITP;;IDIOPATHIC THROMBOCYTOPENIC PURPURA		HP:0001892	OMIM:188030	IEA				P		HPO:iea	
OMIM	188030	188030 THROMBOCYTOPENIC PURPURA, AUTOIMMUNE; AITP;;IMMUNE THROMBOCYTOPENIC PURPURA; ITP;;IDIOPATHIC THROMBOCYTOPENIC PURPURA		HP:0003454	OMIM:188030	IEA				P		HPO:iea	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0000006	OMIM:188050	TAS				I		HPO:probinson	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0001907	OMIM:188050	IEA				P		HPO:skoehler	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0002204	OMIM:188050	TAS				P		HPO:probinson	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0002625	OMIM:188050	TAS				P		HPO:probinson	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0004419	OMIM:188050	TAS				P		HPO:probinson	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0005305	OMIM:188050	TAS				P		HPO:probinson	
OMIM	188050	THROMBOPHILIAVENOUS THROMBOEMBOLISM, INCLUDED		HP:0011463	OMIM:188050	TAS				C		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0000006	OMIM:188055	TAS				I		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0002625	OMIM:188055	TAS				P		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0003581	OMIM:188055	TAS				C		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0003645	OMIM:188055	TAS				P		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0012175	OMIM:188055	TAS				P		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0100602	OMIM:188055	TAS				P		HPO:probinson	
OMIM	188055	THROMBOPHILIA DUE TO DEFICIENCY OF ACTIVATED PROTEIN C COFACTOR		HP:0100724	OMIM:188055	IEA				P		HPO:skoehler	
OMIM	188100	THUMB DEFORMITY		HP:0000006	OMIM:188100	IEA				I		HPO:iea	
OMIM	188100	THUMB DEFORMITY		HP:0001626	OMIM:188100	IEA				P		HPO:iea	
OMIM	188100	THUMB DEFORMITY		HP:0009601	OMIM:188100	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0000006	OMIM:188150	IEA				I		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0001249	OMIM:188150	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0001596	OMIM:188150	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0004322	OMIM:188150	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0006315	OMIM:188150	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0007450	OMIM:188150	IEA				P		HPO:iea	
OMIM	188150	THUMB DEFORMITY AND ALOPECIA		HP:0009778	OMIM:188150	IEA				P		HPO:iea	
OMIM	188201	THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY		HP:0000006	OMIM:188201	TAS				I		HPO:skoehler	
OMIM	188201	THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY		HP:0001249	OMIM:188201	TAS				P		HPO:skoehler	
OMIM	188201	THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:188201	IEA				P		HPO:skoehler	
OMIM	188201	THUMBS, STIFF, WITH BRACHYDACTYLY TYPE A1 AND DEVELOPMENTAL DELAY		HP:0009371	OMIM:188201	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000006	OMIM:188400	IEA				I		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000023	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000110	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000122	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000126	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000175	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000193	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000218	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000316	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000322	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000347	PMID:28740581	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000369	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000370	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000577	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000581	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000627	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000646	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000647	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000750	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000777	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000821	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0000860	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001051	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001061	OMIM:188400	TAS		HP:0040284		P		HPO:probinson	23%
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001081	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001250	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001263	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001281	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001328	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001513	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001537	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001611	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001629	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001636	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001643	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0001660	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0002627	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0002650	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0002705	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0002719	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0002901	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0004322	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0005435	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0007018	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0007302	OMIM:188400	IEA				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0008211	PMID:28740581	PCS				P		HPO:iea	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0011611	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0012745	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0020046	OMIM:188400	IEA				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0025312	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0031817	PMID:28740581	PCS				P		HPO:lccarmody	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0100541	OMIM:188400	TAS				P		HPO:skoehler	
OMIM	188400	DIGEORGE SYNDROME; DGS		HP:0100753	OMIM:188400	TAS		HP:0040284		P		HPO:skoehler	22%
OMIM	188470	THYROID CANCER, NONMEDULLARY, 2; NMTC2		HP:0000006	OMIM:188470	IEA				I		HPO:iea	
OMIM	188470	THYROID CANCER, NONMEDULLARY, 2; NMTC2		HP:0001428	OMIM:188470	IEA				I		HPO:skoehler	
OMIM	188470	THYROID CANCER, NONMEDULLARY, 2; NMTC2		HP:0001939	OMIM:188470	IEA				P		HPO:iea	
OMIM	188470	THYROID CANCER, NONMEDULLARY, 2; NMTC2		HP:0006731	OMIM:188470	IEA				P		HPO:iea	
OMIM	188470	THYROID CANCER, NONMEDULLARY, 2; NMTC2		HP:0040198	OMIM:188470	TAS				P		HPO:skoehler	
OMIM	188550	THYROID CANCER, NONMEDULLARY, 1; NMTC1		HP:0000006	OMIM:188550	TAS				I		HPO:probinson	
OMIM	188550	THYROID CANCER, NONMEDULLARY, 1; NMTC1		HP:0000853	OMIM:188550	IEA				P		HPO:skoehler	
OMIM	188550	THYROID CANCER, NONMEDULLARY, 1; NMTC1		HP:0002895	OMIM:188550	TAS				P		HPO:probinson	
OMIM	188550	THYROID CANCER, NONMEDULLARY, 1; NMTC1		HP:0040198	OMIM:188550	TAS				P		HPO:skoehler	
OMIM	188560	THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT		HP:0000006	OMIM:188560	TAS				I		HPO:skoehler	
OMIM	188560	THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT		HP:0000853	OMIM:188560	TAS				P		HPO:skoehler	
OMIM	188560	THYROID HORMONE PLASMA MEMBRANE TRANSPORT DEFECT		HP:0008247	OMIM:188560	TAS				P		HPO:skoehler	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0000006	OMIM:188570	TAS				I		HPO:probinson	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0000750	OMIM:188570	IEA				P		HPO:iea	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0000853	OMIM:188570	IEA				P		HPO:iea	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0002930	OMIM:188570	IEA				P		HPO:iea	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0007018	OMIM:188570	IEA				P		HPO:iea	
OMIM	188570	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL DOMINANT		HP:0011788	OMIM:188570	TAS				P		HPO:probinson	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0000836	OMIM:188580	IEA				P		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0000853	OMIM:188580	TAS				P		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0001324	OMIM:188580	IEA				P		HPO:iea	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0001425	OMIM:188580	TAS				I		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0001649	OMIM:188580	IEA				P		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0001962	OMIM:188580	TAS				P		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0002900	OMIM:188580	IEA				P		HPO:iea	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0003201	OMIM:188580	IEA				P		HPO:iea	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0003745	OMIM:188580	TAS				I		HPO:skoehler	
OMIM	188580	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1; TTPP1		HP:0003768	OMIM:188580	IEA				P		HPO:skoehler	
OMIM	188700	TIBIA VARA		HP:0000006	OMIM:188700	TAS				I		HPO:probinson	
OMIM	188700	TIBIA VARA		HP:0002970	OMIM:188700	TAS				P		HPO:probinson	
OMIM	188700	TIBIA VARA		HP:0010591	OMIM:188700	TAS				P		HPO:probinson	
OMIM	188700	TIBIA VARA		HP:0010886	OMIM:188700	TAS				P		HPO:probinson	
OMIM	188740	TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY		HP:0000006	OMIM:188740	TAS				I		HPO:iea	
OMIM	188740	TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY		HP:0001627	OMIM:188740	TAS				P		HPO:skoehler	
OMIM	188740	TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY		HP:0009556	OMIM:188740	TAS				P		HPO:skoehler	
OMIM	188740	TIBIA, HYPOPLASIA OR APLASIA OF, WITH POLYDACTYLY		HP:0010442	OMIM:188740	TAS				P		HPO:probinson	
OMIM	188800	TIBIAL TORSION, BILATERAL MEDIAL		HP:0000006	OMIM:188800	TAS				I		HPO:iea	
OMIM	188800	TIBIAL TORSION, BILATERAL MEDIAL		HP:0002650	OMIM:188800	IEA				P		HPO:skoehler	
OMIM	188800	TIBIAL TORSION, BILATERAL MEDIAL		HP:0002979	OMIM:188800	TAS				P		HPO:probinson	
OMIM	188800	TIBIAL TORSION, BILATERAL MEDIAL		HP:0100694	OMIM:188800	TAS				P		HPO:skoehler	
OMIM	189000	TOE, FIFTH, NUMBER OF PHALANGES IN		HP:0000006	OMIM:189000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	189000	TOE, FIFTH, NUMBER OF PHALANGES IN		HP:0000924	OMIM:189000	IEA				P		HPO:iea	
OMIM	189100	TOE, MISSHAPEN		HP:0000006	OMIM:189100	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	189100	TOE, MISSHAPEN		HP:0000924	OMIM:189100	IEA				P		HPO:iea	
OMIM	189150	TOE, ROTATED FIFTH		HP:0000006	OMIM:189150	IEA				I		HPO:iea	
OMIM	189150	TOE, ROTATED FIFTH		HP:0001597	OMIM:189150	IEA				P		HPO:iea	
OMIM	189200	TOES, RELATIVE LENGTH OF FIRST AND SECOND		HP:0000006	OMIM:189200	IEA				I		HPO:iea	
OMIM	189200	TOES, RELATIVE LENGTH OF FIRST AND SECOND		HP:0000924	OMIM:189200	IEA				P		HPO:iea	
OMIM	189230	TOES, SPACE BETWEEN FIRST AND SECOND		HP:0000006	OMIM:189230	IEA				I		HPO:iea	
OMIM	189230	TOES, SPACE BETWEEN FIRST AND SECOND		HP:0001852	OMIM:189230	IEA				P		HPO:iea	
OMIM	189300	TONGUE CURLING, FOLDING, OR ROLLINGCLOVERLEAF TONGUE, INCLUDED		HP:0000006	OMIM:189300	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	189300	TONGUE CURLING, FOLDING, OR ROLLINGCLOVERLEAF TONGUE, INCLUDED		HP:0000153	OMIM:189300	IEA				P		HPO:iea	
OMIM	189490	TOOTH MALFORMATION		HP:0000006	OMIM:189490	IEA				I		HPO:iea	
OMIM	189490	TOOTH MALFORMATION		HP:0000668	OMIM:189490	IEA				P		HPO:iea	
OMIM	189490	TOOTH MALFORMATION		HP:0000692	OMIM:189490	IEA				P		HPO:iea	
OMIM	189490	TOOTH MALFORMATION		HP:0003828	OMIM:189490	IEA				C		HPO:skoehler	
OMIM	189490	TOOTH MALFORMATION		HP:0003829	OMIM:189490	IEA				C		HPO:skoehler	
OMIM	189500	WITKOP SYNDROME		HP:0000006	OMIM:189500	IEA				I		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0001598	OMIM:189500	IEA				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0001792	OMIM:189500	PCS				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0001803	OMIM:189500	IEA				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0001807	OMIM:189500	IEA				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0002213	OMIM:189500	PCS				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0006347	OMIM:189500	TAS				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0006349	OMIM:189500	IEA				P		HPO:probinson	
OMIM	189500	WITKOP SYNDROME		HP:0008070	OMIM:189500	PCS				P		HPO:probinson	
OMIM	189600	TORTICOLLIS		HP:0000006	OMIM:189600	IEA				I		HPO:iea	
OMIM	189600	TORTICOLLIS		HP:0000324	OMIM:189600	IEA				P		HPO:iea	
OMIM	189600	TORTICOLLIS		HP:0000473	OMIM:189600	IEA				P		HPO:iea	
OMIM	189700	%189700 TORUS PALATINUS AND TORUS MANDIBULARIS		HP:0000006	OMIM:189700	IEA				I		HPO:iea	
OMIM	189700	%189700 TORUS PALATINUS AND TORUS MANDIBULARIS		HP:0000153	OMIM:189700	IEA				P		HPO:iea	
OMIM	189700	%189700 TORUS PALATINUS AND TORUS MANDIBULARIS		HP:0100789	OMIM:189700	TAS				P		HPO:skoehler	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0000006	OMIM:189800	IEA				I		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0000093	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0000822	OMIM:189800	IEA				P		HPO:skoehler	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0000969	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0001250	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0001511	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0001873	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0002910	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0008071	OMIM:189800	IEA				P		HPO:iea	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0100601	OMIM:189800	TAS				P		HPO:skoehler	
OMIM	189800	PREECLAMPSIA/ECLAMPSIA 1		HP:0100602	OMIM:189800	TAS				P		HPO:skoehler	
OMIM	189960	TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA		HP:0002032	OMIM:189960	IEA				P		HPO:iea	
OMIM	189960	TRACHEOESOPHAGEAL FISTULA WITH OR WITHOUT ESOPHAGEAL ATRESIA		HP:0002575	OMIM:189960	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0000006	OMIM:189961	IEA				I		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0000924	OMIM:189961	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0001609	OMIM:189961	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0002094	OMIM:189961	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0002105	OMIM:189961	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0006532	OMIM:189961	IEA				P		HPO:iea	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0012735	OMIM:189961	TAS				P		HPO:skoehler	
OMIM	189961	TRACHEOPATHIA OSTEOPLASTICA		HP:0030828	OMIM:189961	TAS				P		HPO:skoehler	
OMIM	190100	GENIOSPASM 1; GSM1		HP:0000006	OMIM:190100	TAS				I		HPO:skoehler	
OMIM	190100	GENIOSPASM 1; GSM1		HP:0000739	OMIM:190100	IEA				P		HPO:skoehler	
OMIM	190100	GENIOSPASM 1; GSM1		HP:0012462	OMIM:190100	TAS				P		HPO:skoehler	
OMIM	190200	TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS		HP:0000006	OMIM:190200	IEA				I		HPO:iea	
OMIM	190200	TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS		HP:0001251	OMIM:190200	IEA				P		HPO:iea	
OMIM	190200	TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS		HP:0001939	OMIM:190200	IEA				P		HPO:iea	
OMIM	190200	TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS		HP:0002080	OMIM:190200	IEA				P		HPO:iea	
OMIM	190200	TREMOR OF INTENTION, ATAXIA, AND LIPOFUSCINOSIS		HP:0002216	OMIM:190200	IEA				P		HPO:iea	
OMIM	190300	TREMOR, HEREDITARY ESSENTIAL, 1		HP:0000006	OMIM:190300	IEA				I		HPO:iea	
OMIM	190300	TREMOR, HEREDITARY ESSENTIAL, 1		HP:0001260	OMIM:190300	TAS				P		HPO:probinson	
OMIM	190300	TREMOR, HEREDITARY ESSENTIAL, 1		HP:0002174	OMIM:190300	TAS				P		HPO:probinson	
OMIM	190300	TREMOR, HEREDITARY ESSENTIAL, 1		HP:0002378	OMIM:190300	TAS				P		HPO:probinson	
OMIM	190300	TREMOR, HEREDITARY ESSENTIAL, 1		HP:0003676	OMIM:190300	IEA				C		HPO:iea	
OMIM	190310	TREMOR, NYSTAGMUS, AND DUODENAL ULCER		HP:0000006	OMIM:190310	IEA				I		HPO:iea	
OMIM	190310	TREMOR, NYSTAGMUS, AND DUODENAL ULCER		HP:0000639	OMIM:190310	IEA				P		HPO:skoehler	
OMIM	190310	TREMOR, NYSTAGMUS, AND DUODENAL ULCER		HP:0001317	OMIM:190310	IEA				P		HPO:iea	
OMIM	190310	TREMOR, NYSTAGMUS, AND DUODENAL ULCER		HP:0002588	OMIM:190310	IEA				P		HPO:iea	
OMIM	190310	TREMOR, NYSTAGMUS, AND DUODENAL ULCER		HP:0030186	OMIM:190310	TAS				P		HPO:skoehler	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000006	OMIM:190320	TAS				I		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000264	OMIM:190320	TAS				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000268	OMIM:190320	TAS				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000679	OMIM:190320	TAS				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000687	OMIM:190320	TAS				P		HPO:probinson	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0000691	OMIM:190320	TAS				P		HPO:probinson	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0001595	OMIM:190320	IEA				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0001808	OMIM:190320	IEA				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0002007	OMIM:190320	TAS				P		HPO:iea	
OMIM	190320	TRICHODENTOOSSEOUS SYNDROME		HP:0011001	OMIM:190320	TAS				P		HPO:iea	
OMIM	190330	TRICHOMEGALY; TCMGLY		HP:0000006	OMIM:190330	IEA				I		HPO:iea	
OMIM	190330	TRICHOMEGALY; TCMGLY		HP:0000007	OMIM:190330	TAS				I		HPO:skoehler	
OMIM	190330	TRICHOMEGALY; TCMGLY		HP:0000518	OMIM:190330	IEA				P		HPO:iea	
OMIM	190330	TRICHOMEGALY; TCMGLY		HP:0000527	OMIM:190330	IEA				P		HPO:iea	
OMIM	190340	TRICHODISCOMAS, FAMILIAL MULTIPLE		HP:0000006	OMIM:190340	IEA				I		HPO:iea	
OMIM	190340	TRICHODISCOMAS, FAMILIAL MULTIPLE		HP:0001595	OMIM:190340	IEA				P		HPO:iea	
OMIM	190345	TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC		HP:0000006	OMIM:190345	IEA				I		HPO:iea	
OMIM	190345	TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC		HP:0025367	OMIM:190345	IEA				P		HPO:skoehler	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000006	OMIM:190350	TAS				I		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000189	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000219	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000343	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000347	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000400	OMIM:190350	TAS				P		HPO:skoehler	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000411	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000447	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000670	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000684	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000689	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000691	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000768	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0000938	OMIM:190350	TAS	HP:0003584			P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0001290	OMIM:190350	TAS				P		HPO:skoehler	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0001598	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0001763	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0001816	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0001820	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002002	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002205	OMIM:190350	TAS				P		HPO:skoehler	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002213	OMIM:190350	PCS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002217	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002650	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002750	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002758	OMIM:190350	TAS	HP:0003584			P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002805	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0002829	OMIM:190350	TAS	HP:0003584			P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0003279	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0003307	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0003370	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0003691	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0004322	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0005338	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0005743	OMIM:190350	TAS				P		HPO:skoehler	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0006253	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0008070	OMIM:190350	PCS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0008947	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010049	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010252	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010259	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010270	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010300	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0010743	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0011823	OMIM:190350	TAS				P		HPO:probinson	
OMIM	190350	TRICHORHINOPHALANGEAL SYNDROME, TYPE I		HP:0045074	OMIM:190350	TAS				P		HPO:skoehler	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000006	OMIM:190351	IEA				I		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000219	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000219	OMIM:190351	TAS				P		HPO:skoehler	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000319	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000343	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000411	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000430	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000447	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000678	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0000707	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3	HP:0012825	HP:0000938	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0001156	OMIM:190351	IEA				P		HPO:skoehler	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0001773	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0002650	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0002750	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0002805	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0003279	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0004279	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0004322	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0005338	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0005743	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0008070	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3	HP:0012828	HP:0009381	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0009803	OMIM:190351	IEA				P		HPO:iea	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0010049	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0010259	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0010743	OMIM:190351	TAS				P		HPO:probinson	
OMIM	190351	TRICHORHINOPHALANGEAL SYNDROME, TYPE III; TRPS3		HP:0011069	OMIM:190351	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0000006	OMIM:190360	IEA				I		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0000535	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0000653	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0000958	OMIM:190360	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0001006	OMIM:190360	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0001596	OMIM:190360	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002208	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002209	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002215	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002217	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002225	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002299	OMIM:190360	PCS				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0002552	OMIM:190360	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0003777	OMIM:190360	IEA				P		HPO:iea	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0009886	OMIM:190360	TAS				P		HPO:skoehler	
OMIM	190360	190360 TRICHODYSPLASIA-XERODERMA		HP:0011359	OMIM:190360	PCS				P		HPO:iea	
OMIM	190400	190400 TRIGEMINAL NEURALGIA;;TIC DOULOUREUX		HP:0000006	OMIM:190400	TAS				I		HPO:skoehler	
OMIM	190400	190400 TRIGEMINAL NEURALGIA;;TIC DOULOUREUX		HP:0000707	OMIM:190400	IEA				P		HPO:iea	
OMIM	190400	190400 TRIGEMINAL NEURALGIA;;TIC DOULOUREUX		HP:0100661	OMIM:190400	TAS				P		HPO:skoehler	
OMIM	190410	190410 TRIGGER THUMB		HP:0000006	OMIM:190410	TAS				I		HPO:skoehler	
OMIM	190410	190410 TRIGGER THUMB		HP:0001172	OMIM:190410	TAS				P		HPO:skoehler	
OMIM	190420	TRIGLYCERIDE STORAGE DISEASE, TYPE I		HP:0000252	OMIM:190420	TAS				P		HPO:probinson	
OMIM	190420	TRIGLYCERIDE STORAGE DISEASE, TYPE I		HP:0004325	OMIM:190420	TAS				P		HPO:probinson	
OMIM	190430	TRIGLYCERIDE STORAGE DISEASE, TYPE II		HP:0000006	OMIM:190430	TAS				I		HPO:probinson	
OMIM	190430	TRIGLYCERIDE STORAGE DISEASE, TYPE II		HP:0001513	OMIM:190430	TAS				P		HPO:probinson	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000006	OMIM:190440	IEA				I		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000040	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000243	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000252	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000384	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0000601	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC	HP:0012825	HP:0000664	OMIM:190440	TAS				P		HPO:skoehler	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0001363	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0001539	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0002245	OMIM:190440	IEA				P		HPO:iea	
OMIM	190440	#190440 TRIGONOCEPHALY 1; TRIGNO1;;CRANIOSYNOSTOSIS, METOPIC		HP:0008439	OMIM:190440	IEA				P		HPO:iea	
OMIM	190500	TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES		HP:0000006	OMIM:190500	IEA				I		HPO:iea	
OMIM	190500	TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES		HP:0001199	OMIM:190500	IEA				P		HPO:iea	
OMIM	190500	TRIPHALANGEAL THUMB WITH DOUBLE PHALANGES		HP:0009606	OMIM:190500	IEA				P		HPO:iea	
OMIM	190600	%190600 TRIPHALANGEAL THUMB, NONOPPOSABLE		HP:0000006	OMIM:190600	IEA				I		HPO:iea	
OMIM	190600	%190600 TRIPHALANGEAL THUMB, NONOPPOSABLE		HP:0001199	OMIM:190600	IEA				P		HPO:iea	
OMIM	190600	%190600 TRIPHALANGEAL THUMB, NONOPPOSABLE		HP:0010442	OMIM:190600	TAS				P		HPO:skoehler	
OMIM	190650	TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA		HP:0000006	OMIM:190650	IEA				I		HPO:iea	
OMIM	190650	TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA		HP:0001199	OMIM:190650	IEA				P		HPO:iea	
OMIM	190650	TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA		HP:0004322	OMIM:190650	IEA				P		HPO:iea	
OMIM	190650	TRIPHALANGEAL THUMBS AND DISLOCATION OF PATELLA		HP:0005001	OMIM:190650	TAS				P		HPO:skoehler	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0000006	OMIM:190680	IEA				I		HPO:iea	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0001156	OMIM:190680	IEA				P		HPO:skoehler	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0001171	OMIM:190680	TAS				P		HPO:probinson	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0001199	OMIM:190680	IEA				P		HPO:iea	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0001839	OMIM:190680	TAS				P		HPO:probinson	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0005643	OMIM:190680	IEA				P		HPO:iea	
OMIM	190680	TRIPHALANGEAL THUMBS WITH BRACHYECTRODACTYLY		HP:0009536	OMIM:190680	TAS				P		HPO:probinson	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000158	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000248	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000272	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000286	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000405	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000474	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000582	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000821	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0000954	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001088	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001169	OMIM:190685	TAS				P		HPO:probinson	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001249	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001252	OMIM:190685	TAS				P		HPO:skoehler	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001388	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0001674	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0002023	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0002251	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0002511	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0002866	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0003182	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0003467	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0003745	OMIM:190685	IEA				I		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0004220	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0004279	OMIM:190685	TAS				P		HPO:probinson	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0004322	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0005547	OMIM:190685	IEA				P		HPO:skoehler	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0006733	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0008551	OMIM:190685	IEA				P		HPO:iea	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0010808	OMIM:190685	TAS				P		HPO:skoehler	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0012368	OMIM:190685	TAS				P		HPO:skoehler	
OMIM	190685	#190685 DOWN SYNDROMETRISOMY 21, INCLUDED;;DOWN SYNDROME CHROMOSOME REGION, INCLUDED; DCR, INCLUDED;;DOWN SYNDROME CRITICAL REGION, INCLUDED; DSCR, INCLUDED;;TRANSIENT MYELOPROLIFERATIVE DISORDER OF DOWN SYNDROME, INCLUDED;;LEUKEMIA, MEGAKARYOBLASTIC, OF DOWN SYNDROME, INCLUDED		HP:0100867	OMIM:190685	IEA				P		HPO:iea	
OMIM	190800	TRISTICHIASIS		HP:0000006	OMIM:190800	IEA				I		HPO:iea	
OMIM	190800	TRISTICHIASIS		HP:0008009	OMIM:190800	IEA				P		HPO:iea	
OMIM	190900	TRITANOPIA		HP:0000006	OMIM:190900	IEA				I		HPO:iea	
OMIM	190900	TRITANOPIA		HP:0000552	OMIM:190900	IEA				P		HPO:probinson	
OMIM	190900	TRITANOPIA		HP:0007641	PMID:1531728	PCS				P		HPO:lccarmody	
OMIM	190900	TRITANOPIA		HP:0008275	OMIM:190900	IEA				P		HPO:iea	
OMIM	191000	TROCHLEA OF THE HUMERUS, APLASIA OF		HP:0000006	OMIM:191000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	191000	TROCHLEA OF THE HUMERUS, APLASIA OF		HP:0000175	OMIM:191000	IEA				P		HPO:iea	
OMIM	191000	TROCHLEA OF THE HUMERUS, APLASIA OF		HP:0005792	OMIM:191000	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000006	OMIM:191100	IEA				I		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000107	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000169	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000717	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000821	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000826	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0000957	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001249	OMIM:191100	TAS		HP:0040284		P		HPO:skoehler	30%
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001250	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001328	OMIM:191100	IEA				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001425	OMIM:191100	TAS				I		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001482	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0001716	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0002086	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0002514	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0002888	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0005584	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0006772	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0007018	OMIM:191100	IEA				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009554	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009592	OMIM:191100	IEA				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009716	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009717	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009717	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009719	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009720	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009720	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009721	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009722	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009724	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009727	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009729	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009729	OMIM:191100	IEA				P		HPO:iea	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0009734	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0010762	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0012469	OMIM:191100	TAS				P		HPO:skoehler	
OMIM	191100	TUBEROUS SCLEROSIS		HP:0200024	OMIM:191100	IEA				P		HPO:skoehler	
OMIM	191150	TUFTSIN DEFICIENCY		HP:0000006	OMIM:191150	IEA				I		HPO:iea	
OMIM	191150	TUFTSIN DEFICIENCY		HP:0001743	OMIM:191150	IEA				P		HPO:skoehler	
OMIM	191150	TUFTSIN DEFICIENCY		HP:0002719	OMIM:191150	IEA				P		HPO:skoehler	
OMIM	191200	TUNE DEAFNESS		HP:0000006	OMIM:191200	IEA				I		HPO:iea	
OMIM	191200	TUNE DEAFNESS		HP:0000365	OMIM:191200	IEA				P		HPO:skoehler	
OMIM	191250	TWINNING DUE TO SUPERFETATION		HP:0000006	OMIM:191250	IEA				I		HPO:iea	
OMIM	191390	INFLAMMATORY BOWEL DISEASE 11		HP:0001426	OMIM:191390	IEA				I		HPO:iea	
OMIM	191390	INFLAMMATORY BOWEL DISEASE 11		HP:0001824	OMIM:191390	IEA				P		HPO:iea	
OMIM	191390	INFLAMMATORY BOWEL DISEASE 11		HP:0002027	OMIM:191390	IEA				P		HPO:iea	
OMIM	191390	INFLAMMATORY BOWEL DISEASE 11		HP:0002037	OMIM:191390	TAS				P		HPO:probinson	
OMIM	191390	INFLAMMATORY BOWEL DISEASE 11		HP:0002573	OMIM:191390	IEA				P		HPO:iea	
OMIM	191400	191400 ULNA AND FIBULA, HYPOPLASIA OF;;MESOMELIC DWARFISM OF HYPOPLASTIC ULNA AND FIBULA TYPE;;REINHARDT-PFEIFFER MESOMELIC DYSPLASIA		HP:0000006	OMIM:191400	IEA				I		HPO:iea	
OMIM	191400	191400 ULNA AND FIBULA, HYPOPLASIA OF;;MESOMELIC DWARFISM OF HYPOPLASTIC ULNA AND FIBULA TYPE;;REINHARDT-PFEIFFER MESOMELIC DYSPLASIA		HP:0003022	OMIM:191400	IEA				P		HPO:iea	
OMIM	191400	191400 ULNA AND FIBULA, HYPOPLASIA OF;;MESOMELIC DWARFISM OF HYPOPLASTIC ULNA AND FIBULA TYPE;;REINHARDT-PFEIFFER MESOMELIC DYSPLASIA		HP:0003038	OMIM:191400	IEA				P		HPO:iea	
OMIM	191400	191400 ULNA AND FIBULA, HYPOPLASIA OF;;MESOMELIC DWARFISM OF HYPOPLASTIC ULNA AND FIBULA TYPE;;REINHARDT-PFEIFFER MESOMELIC DYSPLASIA		HP:0008921	OMIM:191400	TAS				P		HPO:iea	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0000006	OMIM:191420	IEA				I		HPO:iea	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0000925	OMIM:191420	IEA				P		HPO:iea	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0002673	OMIM:191420	IEA				P		HPO:iea	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0002750	OMIM:191420	IEA				P		HPO:iea	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0003072	OMIM:191420	TAS				P		HPO:probinson	
OMIM	191420	ULNA METAPHYSEAL DYSPLASIA SYNDROME		HP:0030836	OMIM:191420	TAS				P		HPO:skoehler	
OMIM	191440	ULNAR HYPOPLASIA		HP:0000006	OMIM:191440	TAS				I		HPO:probinson	
OMIM	191440	ULNAR HYPOPLASIA		HP:0002984	OMIM:191440	TAS				P		HPO:probinson	
OMIM	191440	ULNAR HYPOPLASIA		HP:0002986	OMIM:191440	TAS	HP:0003581			P		HPO:skoehler	
OMIM	191440	ULNAR HYPOPLASIA		HP:0005011	OMIM:191440	TAS				P		HPO:probinson	
OMIM	191440	ULNAR HYPOPLASIA		HP:0005033	OMIM:191440	TAS				P		HPO:probinson	
OMIM	191440	ULNAR HYPOPLASIA		HP:0006433	OMIM:191440	TAS				P		HPO:skoehler	
OMIM	191440	ULNAR HYPOPLASIA		HP:0009487	OMIM:191440	TAS				P		HPO:probinson	
OMIM	191480	UNCOMBABLE HAIR SYNDROME 1		HP:0000006	OMIM:191480	IEA				I		HPO:iea	
OMIM	191480	UNCOMBABLE HAIR SYNDROME 1		HP:0000007	OMIM:191480	TAS				I		HPO:skoehler	
OMIM	191480	UNCOMBABLE HAIR SYNDROME 1		HP:0002235	OMIM:191480	IEA				P		HPO:iea	
OMIM	191480	UNCOMBABLE HAIR SYNDROME 1		HP:0011359	OMIM:191480	TAS				P		HPO:skoehler	
OMIM	191480	UNCOMBABLE HAIR SYNDROME 1		HP:0030056	OMIM:191480	TAS				P		HPO:skoehler	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0000006	OMIM:191482	IEA				I		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0000047	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0000510	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0000677	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0000691	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0001118	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0001156	OMIM:191482	TAS				P		HPO:skoehler	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0001831	OMIM:191482	TAS				P		HPO:probinson	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0002235	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0010049	OMIM:191482	TAS				P		HPO:probinson	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0010241	OMIM:191482	TAS				P		HPO:probinson	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0011069	OMIM:191482	IEA				P		HPO:iea	
OMIM	191482	191482 UNCOMBABLE HAIR, RETINAL PIGMENTARY DYSTROPHY, DENTAL ANOMALIES, ANDBRACHYDACTYLY;;BORK SYNDROME		HP:0030056	OMIM:191482	TAS				P		HPO:skoehler	
OMIM	191500	UNDRITZ ANOMALY		HP:0000006	OMIM:191500	IEA				I		HPO:iea	
OMIM	191500	UNDRITZ ANOMALY		HP:0004821	OMIM:191500	IEA				P		HPO:iea	
OMIM	191520	UPINGTON DISEASE		HP:0000006	OMIM:191520	IEA				I		HPO:iea	
OMIM	191520	UPINGTON DISEASE		HP:0002829	OMIM:191520	IEA				P		HPO:iea	
OMIM	191520	UPINGTON DISEASE		HP:0003365	OMIM:191520	TAS				P		HPO:probinson	
OMIM	191520	UPINGTON DISEASE		HP:0005701	OMIM:191520	TAS				P		HPO:probinson	
OMIM	191520	UPINGTON DISEASE		HP:0006429	OMIM:191520	IEA				P		HPO:iea	
OMIM	191520	UPINGTON DISEASE		HP:0008812	OMIM:191520	IEA				P		HPO:iea	
OMIM	191530	URATE-BINDING GLOBULIN, DECREASE IN		HP:0000006	OMIM:191530	IEA				I		HPO:iea	
OMIM	191530	URATE-BINDING GLOBULIN, DECREASE IN		HP:0001939	OMIM:191530	IEA				P		HPO:iea	
OMIM	191550	URETER, BIFID OR DOUBLE		HP:0000006	OMIM:191550	IEA				I		HPO:iea	
OMIM	191550	URETER, BIFID OR DOUBLE		HP:0000073	OMIM:191550	IEA				P		HPO:skoehler	
OMIM	191600	URETER, CANCER OF		HP:0000006	OMIM:191600	IEA				I		HPO:iea	
OMIM	191600	URETER, CANCER OF		HP:0100516	OMIM:191600	IEA				P		HPO:skoehler	
OMIM	191650	URETEROCELE		HP:0000006	OMIM:191650	IEA				I		HPO:iea	
OMIM	191650	URETEROCELE		HP:0000070	OMIM:191650	IEA				P		HPO:iea	
OMIM	191650	URETEROCELE		HP:0000081	OMIM:191650	IEA				P		HPO:iea	
OMIM	191700	191700 UROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT;;NEPHROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT		HP:0000006	OMIM:191700	IEA				I		HPO:iea	
OMIM	191700	191700 UROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT;;NEPHROLITHIASIS, URIC ACID, AUTOSOMAL DOMINANT		HP:0008651	OMIM:191700	IEA				P		HPO:iea	
OMIM	191800	URINARY BLADDER, ATONY OF		HP:0000006	OMIM:191800	IEA				I		HPO:iea	
OMIM	191800	URINARY BLADDER, ATONY OF		HP:0000119	OMIM:191800	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000006	OMIM:191830	IEA				I		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000007	OMIM:191830	TAS				I		HPO:skoehler	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000093	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000104	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000104	OMIM:191830	TAS				P		HPO:probinson	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000110	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000110	OMIM:191830	TAS				P		HPO:probinson	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000148	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000278	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000316	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000369	OMIM:191830	TAS				P		HPO:skoehler	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000786	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000813	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0000822	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0001562	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0001762	OMIM:191830	TAS				P		HPO:skoehler	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0002009	OMIM:191830	TAS				P		HPO:skoehler	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0002089	OMIM:191830	IEA				P		HPO:iea	
OMIM	191830	#191830 RENAL HYPODYSPLASIA/APLASIA 1; RHDA1;;RENAL ADYSPLASIA;;RENAL AGENESIS;;RENAL APLASIA;;HEREDITARY RENAL APLASIA; HRA		HP:0003577	OMIM:191830	TAS				C		HPO:skoehler	
OMIM	191850	URTICARIA, AQUAGENIC		HP:0000006	OMIM:191850	IEA				I		HPO:iea	
OMIM	191850	URTICARIA, AQUAGENIC		HP:0001025	OMIM:191850	TAS				P		HPO:skoehler	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000006	OMIM:191900	IEA				I		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000083	OMIM:191900	IEA				P		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000153	OMIM:191900	IEA				P		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000365	OMIM:191900	IEA				P		HPO:skoehler	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000408	OMIM:191900	TAS	HP:0003584			P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000509	OMIM:191900	TAS				P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0000951	OMIM:191900	IEA				P		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0001917	OMIM:191900	TAS	HP:0003584			P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0001954	OMIM:191900	IEA				P		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0001974	OMIM:191900	IEA				P		HPO:skoehler	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0002829	OMIM:191900	TAS				P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0003326	OMIM:191900	TAS				P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0003565	OMIM:191900	TAS				P		HPO:probinson	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0003593	OMIM:191900	IEA				C		HPO:iea	
OMIM	191900	#191900 MUCKLE-WELLS SYNDROME; MWS;;URTICARIA-DEAFNESS-AMYLOIDOSIS SYNDROME;;UDA SYNDROME;;CRYOPYRIN-ASSOCIATED PERIODIC SYNDROME 2; CAPS2		HP:0011107	OMIM:191900	TAS				P		HPO:skoehler	
OMIM	191950	URTICARIA, FAMILIAL LOCALIZED HEAT		HP:0000006	OMIM:191950	IEA				I		HPO:iea	
OMIM	191950	URTICARIA, FAMILIAL LOCALIZED HEAT		HP:0001025	OMIM:191950	IEA				P		HPO:iea	
OMIM	192000	UTERINE ANOMALIES		HP:0000006	OMIM:192000	TAS				I		HPO:skoehler	
OMIM	192000	UTERINE ANOMALIES		HP:0000813	OMIM:192000	TAS				P		HPO:skoehler	
OMIM	192050	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS		HP:0000006	OMIM:192050	IEA				I		HPO:iea	
OMIM	192050	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS		HP:0000104	OMIM:192050	IEA				P		HPO:iea	
OMIM	192050	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS		HP:0003762	OMIM:192050	TAS				P		HPO:skoehler	
OMIM	192050	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS		HP:0008670	OMIM:192050	IEA				P		HPO:iea	
OMIM	192050	UTERUS BICORNIS BICOLLIS WITH PARTIAL VAGINAL SEPTUM AND UNILATERAL HEMATOCOLPOS WITH IPSILATERAL RENAL AGENESIS		HP:0031923	OMIM:192050	IEA				P		HPO:skoehler	
OMIM	192100	UVULA, BIFID		HP:0000006	OMIM:192100	IEA				I		HPO:iea	
OMIM	192100	UVULA, BIFID		HP:0000193	OMIM:192100	IEA				P		HPO:iea	
OMIM	192200	VARICOSE VEINS		HP:0001423	PMID:13561707	TAS				I		HPO:nvasilevsky	
OMIM	192200	VARICOSE VEINS		HP:0001426	PMID:4435791	TAS		HP:0040284		I		HPO:nvasilevsky	50%
OMIM	192200	VARICOSE VEINS		HP:0002619	OMIM:192200	IEA				P		HPO:iea	
OMIM	192310	VASCULITIS, LYMPHOCYTIC, NODULAR		HP:0000006	OMIM:192310	IEA				I		HPO:iea	
OMIM	192310	VASCULITIS, LYMPHOCYTIC, NODULAR		HP:0001939	OMIM:192310	IEA				P		HPO:iea	
OMIM	192310	VASCULITIS, LYMPHOCYTIC, NODULAR		HP:0005300	OMIM:192310	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000006	OMIM:192315	IEA				I		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000093	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000505	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000529	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000573	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000708	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000726	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0000790	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001009	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001147	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001250	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001260	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001269	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001297	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0001413	OMIM:192315	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0002076	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0002186	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0002395	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0002518	OMIM:192315	TAS				P		HPO:probinson	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0002910	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0003565	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0003581	OMIM:192315	TAS				C		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0003676	OMIM:192315	TAS				C		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0007009	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0007017	OMIM:192315	IEA				P		HPO:iea	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0009763	OMIM:192315	IEA				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0030880	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0031987	OMIM:192315	IEA				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0040049	OMIM:192315	TAS				P		HPO:skoehler	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0200029	OMIM:192315	TAS				P		HPO:probinson	
OMIM	192315	VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY; RVCL		HP:0200030	OMIM:192315	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000047	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000074	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000076	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000086	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000104	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000110	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000126	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000239	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000453	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000766	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0000772	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001159	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001195	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001199	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001508	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001511	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001602	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001629	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001636	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001643	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001669	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0001739	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002023	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002032	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002085	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002144	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002414	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002575	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002650	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002974	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0002984	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0003468	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0003745	OMIM:192350	IEA				I		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0003974	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0008897	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0009778	OMIM:192350	IEA				P		HPO:iea	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0010479	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192350	#192350 VATER ASSOCIATIONVACTERL ASSOCIATION, INCLUDED		HP:0100258	OMIM:192350	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000006	OMIM:192430	IEA				I		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000023	PMID:1956057	PCS		HP:0040284		P		HPO:iea	3/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000028	PMID:1956057	IEA	HP:0003577	HP:0040284		P		HP:probinson	3/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000176	PMID:1956057	PCS		HP:0040284		P		HP:probinson	15/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000194	OMIM:192430	IEA				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000201	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000220	PMID:1956057	PCS		HP:0040284		P		HPO:iea	38/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000252	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000278	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000414	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000430	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000581	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000598	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000627	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000718	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000720	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0000829	PMID:1956057	PCS		HP:0040284		P		HP:probinson	3/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001155	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001249	PMID:1956057	PCS		HP:0040284		P		HPO:skoehler	31/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001252	PMID:1956057	PCS		HP:0040284		P		HPO:skoehler	29/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001328	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001537	PMID:1956057	PCS		HP:0040284		P		HPO:iea	2/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001611	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001629	PMID:1956057	PCS				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001636	PMID:1956057	PCS		HP:0040284		P		HPO:iea	3/16
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0001883	PMID:1956057	PCS		HP:0040284		P		HP:probinson	4/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0002627	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0002719	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0002901	PMID:1956057	PCS		HP:0040284		P		HPO:skoehler	5/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0004322	PMID:1956057	PCS		HP:0040284		P		HPO:iea	24/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0004935	PMID:1956057	PCS		HP:0040284		P		HP:probinson	2/16
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0005435	PMID:1956057	PCS		HP:0040284		P		HPO:skoehler	2/38
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0006549	OMIM:192430	IEA				P		HPO:iea	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0011590	PMID:1956057	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/16
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0011611	PMID:1956057	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/16
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0011999	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0012841	OMIM:192430	TAS				P		HPO:skoehler	
OMIM	192430	VELOCARDIOFACIAL SYNDROME		HP:0045025	OMIM:192430	IEA				P		HPO:skoehler	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0000006	OMIM:192445	IEA				I		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0000176	OMIM:192445	IEA				P		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0000201	OMIM:192445	IEA				P		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0000494	OMIM:192445	IEA				P		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0001279	OMIM:192445	TAS				P		HPO:probinson	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0001649	OMIM:192445	IEA				P		HPO:skoehler	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0006682	OMIM:192445	IEA				P		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0009087	OMIM:192445	IEA				P		HPO:iea	
OMIM	192445	VENTRICULAR EXTRASYSTOLES WITH SYNCOPE, PERODACTYLY, AND ROBIN SEQUENCE		HP:0010185	OMIM:192445	IEA				P		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0000006	OMIM:192500	IEA				I		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0000598	OMIM:192500	IEA				P		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001279	OMIM:192500	IEA				P		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001425	OMIM:192500	TAS				I		HPO:skoehler	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001645	OMIM:192500	IEA				P		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001657	OMIM:192500	IEA				P		HPO:iea	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001663	OMIM:192500	TAS				P		HPO:skoehler	
OMIM	192500	#192500 LONG QT SYNDROME 1; LQT1;;WARD-ROMANO SYNDROME; WRS;;ROMANO-WARD SYNDROME; RWS;;VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVALLONG QT SYNDROME 1/2, DIGENIC, INCLUDED; LQT1/2, DIGENIC, INCLUDED;;LONG QT SYNDROME 1, ACQUIRED, SUSCEPTIBILITY TO, INCLUDED		HP:0001664	OMIM:192500	IEA				P		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0000006	OMIM:192600	TAS				I		HPO:skoehler	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0001635	OMIM:192600	IEA				P		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0001670	OMIM:192600	IEA				P		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0001682	OMIM:192600	IEA				P		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0001699	OMIM:192600	IEA				M		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0001939	OMIM:192600	IEA				P		HPO:iea	
OMIM	192600	#192600 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1;;CMH;;VENTRICULAR HYPERTROPHY, HEREDITARY;;ASYMMETRIC SEPTAL HYPERTROPHY; ASH;;HYPERTROPHIC SUBAORTIC STENOSIS, IDIOPATHIC		HP:0011675	OMIM:192600	TAS				P		HPO:skoehler	
OMIM	192605	VENTRICULAR TACHYCARDIA, FAMILIAL		HP:0000006	OMIM:192605	IEA				I		HPO:iea	
OMIM	192605	VENTRICULAR TACHYCARDIA, FAMILIAL		HP:0001645	OMIM:192605	IEA				P		HPO:iea	
OMIM	192605	VENTRICULAR TACHYCARDIA, FAMILIAL		HP:0001939	OMIM:192605	IEA				P		HPO:iea	
OMIM	192605	VENTRICULAR TACHYCARDIA, FAMILIAL		HP:0004751	OMIM:192605	IEA				P		HPO:iea	
OMIM	192605	VENTRICULAR TACHYCARDIA, FAMILIAL		HP:0011712	OMIM:192605	IEA				P		HPO:skoehler	
OMIM	192700	VENULAR INSUFFICIENCY, SYSTEMIC		HP:0000006	PMID:14117628,PMID:13561707	TAS				I		HPO:nvasilevsky	
OMIM	192700	VENULAR INSUFFICIENCY, SYSTEMIC		HP:0000961	OMIM:192700	IEA				P		HPO:skoehler	
OMIM	192700	VENULAR INSUFFICIENCY, SYSTEMIC		HP:0001626	OMIM:192700	IEA				P		HPO:iea	
OMIM	192800	VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS		HP:0000006	OMIM:192800	IEA				I		HPO:iea	
OMIM	192800	VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS		HP:0001939	OMIM:192800	IEA				P		HPO:iea	
OMIM	192800	VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS		HP:0005626	OMIM:192800	IEA				P		HPO:iea	
OMIM	192800	VERTEBRAL FUSION, POSTERIOR LUMBOSACRAL, WITH BLEPHAROPTOSIS		HP:0007970	OMIM:192800	IEA				P		HPO:iea	
OMIM	192900	VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS		HP:0000006	OMIM:192900	IEA				I		HPO:iea	
OMIM	192900	VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS		HP:0008417	OMIM:192900	IEA				P		HPO:skoehler	
OMIM	192900	VERTEBRAL HYPOPLASIA WITH LUMBAR KYPHOSIS		HP:0008454	OMIM:192900	IEA				P		HPO:iea	
OMIM	192950	VERTICAL TALUS, CONGENITAL		HP:0000006	OMIM:192950	IEA				I		HPO:iea	
OMIM	192950	VERTICAL TALUS, CONGENITAL		HP:0001369	OMIM:192950	IEA				P		HPO:skoehler	
OMIM	192950	VERTICAL TALUS, CONGENITAL		HP:0001838	OMIM:192950	IEA				P		HPO:iea	
OMIM	192950	VERTICAL TALUS, CONGENITAL		HP:0001848	OMIM:192950	IEA				P		HPO:iea	
OMIM	192950	VERTICAL TALUS, CONGENITAL		HP:0008138	OMIM:192950	IEA				P		HPO:iea	
OMIM	193000	VESICOURETERAL REFLUX 1		HP:0000006	OMIM:193000	TAS				I		HPO:nvasilevsky	
OMIM	193000	VESICOURETERAL REFLUX 1		HP:0000076	OMIM:193000	IEA				P		HPO:iea	
OMIM	193000	VESICOURETERAL REFLUX 1		HP:0000924	OMIM:193000	IEA				P		HPO:iea	
OMIM	193000	VESICOURETERAL REFLUX 1		HP:0001426	OMIM:193000	TAS				I		HPO:nvasilevsky	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0000006	OMIM:193003	IEA				I		HPO:iea	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0000486	OMIM:193003	IEA				P		HPO:iea	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0000640	OMIM:193003	IEA				P		HPO:iea	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0003680	OMIM:193003	IEA				C		HPO:iea	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0007179	OMIM:193003	IEA				P		HPO:iea	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0007670	OMIM:193003	IEA				P		HPO:probinson	
OMIM	193003	%193003 NYSTAGMUS 4, CONGENITAL, AUTOSOMAL DOMINANT; NYS4;;VESTIBULOCEREBELLAR DISORDER WITH PREDOMINANT OCULAR SIGNS		HP:0011477	OMIM:193003	TAS				P		HPO:skoehler	
OMIM	193005	VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE		HP:0000006	OMIM:193005	IEA				I		HPO:iea	
OMIM	193005	VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE		HP:0000360	OMIM:193005	IEA				P		HPO:iea	
OMIM	193005	VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE		HP:0000707	OMIM:193005	IEA				P		HPO:iea	
OMIM	193005	VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE		HP:0001730	OMIM:193005	IEA				P		HPO:iea	
OMIM	193005	VESTIBULOCOCHLEAR DYSFUNCTION, PROGRESSIVE		HP:0008568	OMIM:193005	IEA				P		HPO:iea	
OMIM	193007	VESTIBULOPATHY, FAMILIAL		HP:0000006	OMIM:193007	IEA				I		HPO:iea	
OMIM	193007	VESTIBULOPATHY, FAMILIAL		HP:0002141	OMIM:193007	IEA				P		HPO:iea	
OMIM	193007	VESTIBULOPATHY, FAMILIAL		HP:0002321	OMIM:193007	IEA				P		HPO:skoehler	
OMIM	193007	VESTIBULOPATHY, FAMILIAL		HP:0003677	OMIM:193007	IEA				C		HPO:iea	
OMIM	193090	%193090 TRANSCOBALAMIN I DEFICIENCY;;TCN1 DEFICIENCY;;COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY;;COBALAMIN R BINDER PROTEIN DEFICIENCYTRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED;;R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED		HP:0000006	OMIM:193090	IEA				I		HPO:iea	
OMIM	193090	%193090 TRANSCOBALAMIN I DEFICIENCY;;TCN1 DEFICIENCY;;COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY;;COBALAMIN R BINDER PROTEIN DEFICIENCYTRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED;;R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED		HP:0000007	OMIM:193090	TAS				I		HPO:skoehler	
OMIM	193090	%193090 TRANSCOBALAMIN I DEFICIENCY;;TCN1 DEFICIENCY;;COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY;;COBALAMIN R BINDER PROTEIN DEFICIENCYTRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED;;R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED		HP:0001315	OMIM:193090	IEA				P		HPO:iea	
OMIM	193090	%193090 TRANSCOBALAMIN I DEFICIENCY;;TCN1 DEFICIENCY;;COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY;;COBALAMIN R BINDER PROTEIN DEFICIENCYTRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED;;R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED		HP:0001939	OMIM:193090	IEA				P		HPO:iea	
OMIM	193090	%193090 TRANSCOBALAMIN I DEFICIENCY;;TCN1 DEFICIENCY;;COBALAMIN PSEUDODEFICIENCY DUE TO TRANSCOBALAMIN DEFICIENCY;;COBALAMIN R BINDER PROTEIN DEFICIENCYTRANSCOBALAMIN I DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED;;R BINDER DEFICIENCY WITH LACTOFERRIN DEFICIENCY, INCLUDED		HP:0003401	OMIM:193090	IEA				P		HPO:skoehler	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:193100	IEA				I		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0000117	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0000164	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0002653	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0002749	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0002814	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0003155	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0003324	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0003829	OMIM:193100	IEA				C		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0004322	OMIM:193100	IEA				P		HPO:iea	
OMIM	193100	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL DOMINANT		HP:0004912	OMIM:193100	IEA				P		HPO:skoehler	
OMIM	193200	VITILIGOVTLG		HP:0000007	OMIM:193200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	193200	VITILIGOVTLG		HP:0001045	OMIM:193200	IEA				P		HPO:iea	
OMIM	193200	VITILIGOVTLG		HP:0003764	OMIM:193200	IEA				P		HPO:skoehler	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000006	OMIM:193220	IEA				I		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000482	OMIM:193220	PCS				P		HPO:probinson	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000486	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000501	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000541	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000551	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000568	OMIM:193220	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000580	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000618	OMIM:193220	IEA				P		HPO:skoehler	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000639	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0000662	OMIM:193220	PCS				P		HPO:probinson	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0007641	OMIM:193220	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0007661	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0007902	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0007985	OMIM:193220	IEA				P		HPO:iea	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0008043	OMIM:193220	PCS				P		HPO:probinson	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0010693	OMIM:193220	PCS				P		HPO:probinson	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0030666	OMIM:193220	IEA				P		HPO:skoehler	
OMIM	193220	VITREORETINOCHOROIDOPATHY; VRCP		HP:0030856	OMIM:193220	IEA				P		HPO:skoehler	
OMIM	193230	VITREORETINAL DEGENERATION, SNOWFLAKE TYPE		HP:0000006	OMIM:193230	IEA				I		HPO:iea	
OMIM	193230	VITREORETINAL DEGENERATION, SNOWFLAKE TYPE		HP:0000518	OMIM:193230	IEA				P		HPO:iea	
OMIM	193230	VITREORETINAL DEGENERATION, SNOWFLAKE TYPE		HP:0007773	OMIM:193230	IEA				P		HPO:skoehler	
OMIM	193230	VITREORETINAL DEGENERATION, SNOWFLAKE TYPE		HP:0030663	OMIM:193230	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000006	OMIM:193235	PCS				I		HPO:probinson	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000512	OMIM:193235	PCS				P		HPO:probinson	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000541	OMIM:193235	IEA				P		HPO:iea	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000554	OMIM:193235	PCS				P		HPO:probinson	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000618	OMIM:193235	IEA				P		HPO:iea	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0000618	OMIM:193235	PCS				P		HPO:probinson	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0007658	OMIM:193235	IEA				P		HPO:iea	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0007773	OMIM:193235	IEA				P		HPO:skoehler	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0007778	OMIM:193235	IEA				P		HPO:skoehler	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0007902	OMIM:193235	IEA				P		HPO:iea	
OMIM	193235	VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY		HP:0030667	OMIM:193235	IEA				P		HPO:skoehler	
OMIM	193240	VOCAL CORD PARALYSIS AND PTOSIS		HP:0000006	OMIM:193240	IEA				I		HPO:iea	
OMIM	193240	VOCAL CORD PARALYSIS AND PTOSIS		HP:0001488	OMIM:193240	IEA				P		HPO:iea	
OMIM	193240	VOCAL CORD PARALYSIS AND PTOSIS		HP:0001605	OMIM:193240	TAS				P		HPO:skoehler	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0000006	OMIM:193250	IEA				I		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0000119	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0000348	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0000506	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0000637	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0002007	OMIM:193250	TAS				P		HPO:skoehler	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0002019	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0002566	OMIM:193250	IEA				P		HPO:iea	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0002580	OMIM:193250	TAS				P		HPO:probinson	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0003270	OMIM:193250	TAS				P		HPO:probinson	
OMIM	193250	%193250 VOLVULUS OF MIDGUT;;INTESTINAL MALROTATION, FAMILIAL		HP:0005234	OMIM:193250	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0000006	OMIM:193300	IEA				I		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0000360	OMIM:193300	IEA				P		HPO:skoehler	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0000407	OMIM:193300	IEA				P		HPO:skoehler	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0000822	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0001392	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0001737	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0001901	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0002321	OMIM:193300	IEA				P		HPO:skoehler	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0002666	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0002668	OMIM:193300	TAS				P		HPO:skoehler	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0002894	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0005562	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0005584	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0005954	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0006880	OMIM:193300	TAS				P		HPO:probinson	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0009711	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0009713	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0009715	OMIM:193300	IEA				P		HPO:iea	
OMIM	193300	#193300 VON HIPPEL-LINDAU SYNDROME; VHLVON HIPPEL-LINDAU SYNDROME, MODIFIERS OF, INCLUDED		HP:0030424	OMIM:193300	TAS				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000006	OMIM:193400	IEA				I		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000119	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000132	OMIM:193400	TAS				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000421	OMIM:193400	TAS				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000471	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0000978	OMIM:193400	IEA				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0001634	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0001650	OMIM:193400	IEA				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0002239	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0003010	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0003125	OMIM:193400	IEA				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0003540	OMIM:193400	IEA				P		HPO:iea	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0003829	OMIM:193400	TAS				C		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0005261	OMIM:193400	IEA				P		HPO:skoehler	
OMIM	193400	#193400 VON WILLEBRAND DISEASE, TYPE 1; VWD1;;VON WILLEBRAND DISEASE, TYPE I;;VWD, TYPE 1		HP:0005542	OMIM:193400	IEA				P		HPO:iea	
OMIM	193450	VULVOVAGINITIS, ALLERGIC SEMINAL		HP:0000006	OMIM:193450	IEA				I		HPO:iea	
OMIM	193450	VULVOVAGINITIS, ALLERGIC SEMINAL		HP:0001025	OMIM:193450	IEA				P		HPO:skoehler	
OMIM	193450	VULVOVAGINITIS, ALLERGIC SEMINAL		HP:0030683	OMIM:193450	IEA				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000006	OMIM:193500	IEA				I		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000202	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000303	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000316	OMIM:193500	TAS				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000319	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000430	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000431	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000506	OMIM:193500	TAS				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000574	OMIM:193500	TAS				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000581	OMIM:193500	TAS				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000635	OMIM:193500	IEA				P		HPO:skoehler	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000664	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0000912	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0001100	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002211	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002216	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002226	OMIM:193500	PCS				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002227	OMIM:193500	PCS				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002414	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002475	OMIM:193500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0002946	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0003250	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0005815	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0007443	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0007894	OMIM:193500	TAS				P		HPO:probinson	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0007990	OMIM:193500	IEA				P		HPO:iea	
OMIM	193500	WAARDENBURG SYNDROME, TYPE 1; WS1		HP:0008527	OMIM:193500	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0000006	OMIM:193510	IEA				I		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0000430	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0000431	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0000664	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0001022	OMIM:193510	TAS	HP:0003577			P		HPO:skoehler	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0001100	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0001425	OMIM:193510	TAS				I		HPO:skoehler	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0002211	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0002216	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0002226	OMIM:193510	PCS				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0002227	OMIM:193510	PCS				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0003828	OMIM:193510	TAS				C		HPO:skoehler	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0007443	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0007990	OMIM:193510	IEA				P		HPO:iea	
OMIM	193510	#193510 WAARDENBURG SYNDROME, TYPE 2A; WS2A;;WAARDENBURG SYNDROME, TYPE IIA;;WAARDENBURG SYNDROME WITHOUT DYSTOPIA CANTHORUM;;WS2		HP:0008527	OMIM:193510	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0000006	OMIM:193520	IEA				I		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0000997	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0001067	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0001626	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0004322	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0004482	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0007565	OMIM:193520	IEA				P		HPO:iea	
OMIM	193520	WATSON SYNDROME		HP:0009737	OMIM:193520	IEA				P		HPO:skoehler	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0000006	OMIM:193530	IEA				I		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0000395	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0000601	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0000698	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0001156	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0001162	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0001792	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0001830	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0002164	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0003502	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0004209	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0004279	OMIM:193530	IEA				P		HPO:iea	
OMIM	193530	WEYERS ACROFACIAL DYSOSTOSIS		HP:0006315	OMIM:193530	IEA				P		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0000006	OMIM:193670	IEA				I		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0000008	OMIM:193670	IEA				P		HPO:skoehler	
OMIM	193670	WHIM SYNDROME		HP:0000055	OMIM:193670	IEA				P		HPO:skoehler	
OMIM	193670	WHIM SYNDROME		HP:0001875	PMID:25662009	PCS				P		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0002110	PMID:25662009	PCS				P		HPO:probinson	
OMIM	193670	WHIM SYNDROME		HP:0002718	PMID:25662009	PCS				P		HPO:probinson	
OMIM	193670	WHIM SYNDROME		HP:0002788	OMIM:193670	IEA				P		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0003593	OMIM:193670	IEA				C		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0004313	PMID:25662009	PCS				P		HPO:probinson	
OMIM	193670	WHIM SYNDROME		HP:0004315	OMIM:193670	IEA				P		HPO:iea	
OMIM	193670	WHIM SYNDROME		HP:0005561	OMIM:193670	IEA				P		HPO:skoehler	
OMIM	193670	WHIM SYNDROME		HP:0031020	OMIM:193670	TAS				P		HPO:skoehler	
OMIM	193670	WHIM SYNDROME		HP:0031160	OMIM:193670	TAS				P		HPO:skoehler	
OMIM	193670	WHIM SYNDROME		HP:0200043	PMID:25662009	PCS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000006	PMID:25256237	PCS				I		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000023	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000028	PMID:16510655	PCS		HP:0040284		P		HPO:iea	5/12
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000160	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000218	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000252	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000272	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000286	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000298	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000303	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000343	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000346	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000365	PMID:16510655	PCS		HP:0040284		P		HP:probinson	8/27
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000430	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000431	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000470	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000486	PMID:16510655	PCS		HP:0040284		P		HPO:iea	11/26
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000490	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000506	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000508	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000581	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000678	PMID:16510655	PCS		HP:0040284		P		HP:probinson	14/14
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0000951	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001181	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001193	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001239	PMID:16510655	PCS	HP:0003577	HP:0040284		P		HP:probinson	23/27
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001249	OMIM:193700	TAS		HP:0040284		P		HPO:probinson	31%
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001250	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001270	PMID:16510655	PCS		HP:0040284		P		HP:probinson	28/28
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001272	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001324	OMIM:193700	TAS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001373	PMID:16510655	PCS		HP:0040284		P		HP:probinson	3/26
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001508	OMIM:193700	TAS				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001518	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001558	PMID:16510655	PCS		HP:0040284		P		HP:probinson	9/17
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001561	PMID:16510655	PCS		HP:0040284		P		HP:probinson	5/17
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001562	PMID:16510655	PCS		HP:0040284		P		HP:probinson	2/17
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001611	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001623	OMIM:193700	TAS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001762	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0001838	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002047	PMID:16510655	PCS		HP:0040284		P		HP:probinson	3/19
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002205	PMID:16510655	PCS		HP:0040284		P		HP:probinson	9/27
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002365	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002650	PMID:16510655	PCS		HP:0040284		P		HP:probinson	22/26
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002751	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002757	PMID:16510655	PCS		HP:0040284		P		HP:probinson	6/23
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002827	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002829	PMID:16510655	PCS		HP:0040284		P		HP:probinson	2/11
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0002987		PCS	HP:0003577	HP:0040284		P		HP:probinson	11/25
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0003044	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0003196	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0003273	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0003273	PMID:16510655	IEA	HP:0003577	HP:0040284		P		HP:probinson	15/26
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0003298	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0005830	OMIM:193700	TAS				P		HPO:probinson	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0005997	PMID:16510655	PCS	HP:0003577	HP:0040284		P		HP:probinson	24/27
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0006380	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0006380	PMID:16510655	PCS	HP:0003577	HP:0040284		P		HP:probinson	7/27
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0006958	OMIM:193700	IEA				P		HPO:iea	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0008872	PMID:16510655	PCS		HP:0040281		P		HP:probinson	HP:0040281
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0008897	OMIM:193700	TAS				P		HPO:probinson	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0009473	OMIM:193700	TAS				P		HPO:probinson	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0010751	OMIM:193700	TAS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0011220	OMIM:193700	TAS				P		HPO:probinson	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0011824	OMIM:193700	TAS				P		HPO:probinson	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0012368	OMIM:193700	TAS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0012385	OMIM:193700	TAS				P		HPO:skoehler	
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0012785	PMID:16510655	PCS	HP:0003577	HP:0040284		P		HP:probinson	28/28
OMIM	193700	ARTHROGRYPOSIS, DISTAL, TYPE 2A		HP:0100790	PMID:16510655	PCS		HP:0040284		P		HP:probinson	6/26
OMIM	193900	WHITE SPONGE NEVUS OF CANNON		HP:0000006	OMIM:193900	IEA				I		HPO:iea	
OMIM	193900	WHITE SPONGE NEVUS OF CANNON		HP:0001939	OMIM:193900	IEA				P		HPO:iea	
OMIM	193900	WHITE SPONGE NEVUS OF CANNON		HP:0002745	OMIM:193900	IEA				P		HPO:iea	
OMIM	194000	WIDOW'S PEAK		HP:0000006	OMIM:194000	IEA				I		HPO:iea	
OMIM	194000	WIDOW'S PEAK		HP:0000316	OMIM:194000	IEA				P		HPO:iea	
OMIM	194000	WIDOW'S PEAK		HP:0000349	OMIM:194000	IEA				P		HPO:skoehler	
OMIM	194000	WIDOW'S PEAK		HP:0004544	OMIM:194000	IEA				P		HPO:iea	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000006	PMID:20089974	PCS				I		HPO:iea	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000010	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000015	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000023	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000054	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000076	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000083	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000089	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000121	PMID:20089974	PCS		HP:0040284		P		HPO:iea	10%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000125	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000179	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000194	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000272	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000286	ISBN-13:978-0721606156	PCS	HP:0011463	HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000293	ISBN-13:978-0721606156	PCS	HP:0011463	HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000341	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000343	ISBN-13:978-0721606156,http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000403	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000407	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000455	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000486	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000539	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000581	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000601	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000629	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000635	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000646	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000668	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000689	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000691	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000739	PMID:20089974	PCS		HP:0040284		P		HPO:iea	80%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000767	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000805	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000819	PMID:20089974	PCS	HP:0003581	HP:0040284		P		HPO:iea	75%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000821	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	10%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000822	PMID:20089974	PCS		HP:0040284		P		HPO:iea	50%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000938	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000939	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000973	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0000977	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001136	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001249	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001252	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001290	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001297	PMID:20089974	PCS		HP:0040284		P		HPO:iea	HP:0040284
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001321	PMID:20089974	PCS		HP:0040284		P		HPO:iea	15%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001347	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001371	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001388	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001409	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001511	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001513	ISBN-13:978-0721606156	PCS	HP:0003581	HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001531	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	70%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001537	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001605	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001609	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001629	PMID:20089974	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001631	PMID:20089974	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001642	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS	HP:0003593	HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001647	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001653	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001699	PMID:20089974	PCS		HP:0040284		M		HPO:iea	HP:0040284
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001792	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001822	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001920	PMID:20089974	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0001952	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002019	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002020	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002035	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002141	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002150	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	30%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002183	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002216	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002253	PMID:20089974	PCS	HP:0011462	HP:0040284		P		HPO:iea	30%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002311	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002360	PMID:20089974	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002370	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002608	PMID:20089974	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002751	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0002974	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0003072	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	15%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0003196	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0004209	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0004322	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0004381	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	75%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0004764	PMID:20089974	PCS		HP:0040284		P		HPO:iea	20%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0004969	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0005145	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0005280	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0007018	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0007099	PMID:20089974	PCS		HP:0040284		P		HPO:iea	10%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0008661	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0008770	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0008872	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0009748	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0010747	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0010780	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0010794	PMID:20089974	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0011800	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0012450	OMIM:194050	TAS				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0012537	OMIM:194050	IEA				P		HPO:skoehler	
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0100000	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=williams	PCS		HP:0040284		P		HPO:iea	50%
OMIM	194050	WILLIAMS-BEUREN SYNDROME; WBS		HP:0200021	ISBN-13:978-0721606156	PCS	HP:0003581	HP:0040282		P		HPO:iea	HP:0040282
OMIM	194070	WILMS TUMOR 1		HP:0000006	OMIM:194070	IEA				I		HPO:iea	
OMIM	194070	WILMS TUMOR 1		HP:0001425	OMIM:194070	IEA				I		HPO:skoehler	
OMIM	194070	WILMS TUMOR 1		HP:0001428	OMIM:194070	IEA				I		HPO:iea	
OMIM	194070	WILMS TUMOR 1		HP:0002667	OMIM:194070	IEA				P		HPO:iea	
OMIM	194071	MULTIPLE TUMOR-ASSOCIATED CHROMOSOME REGION 1		HP:0000006	OMIM:194071	IEA				I		HPO:iea	
OMIM	194071	MULTIPLE TUMOR-ASSOCIATED CHROMOSOME REGION 1		HP:0001428	OMIM:194071	IEA				I		HPO:iea	
OMIM	194071	MULTIPLE TUMOR-ASSOCIATED CHROMOSOME REGION 1		HP:0002667	OMIM:194071	IEA				P		HPO:iea	
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000006	OMIM:194072	TAS				I	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000028	OMIM:194072	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000047	OMIM:194072	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000083	PMID:10945603	PCS	HP:0003581	HP:0040284		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	10/46
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000112	http://decipher.sanger.ac.uk/syndrome/35	TAS	HP:0003581	HP:0040284		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	40%
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000130	http://decipher.sanger.ac.uk/syndrome/35	TAS		HP:0040283		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040283
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000142	http://decipher.sanger.ac.uk/syndrome/35	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000150	http://decipher.sanger.ac.uk/syndrome/35	TAS		HP:0040283		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040283
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0000526	OMIM:194072	TAS		HP:0040281		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040281
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0001249	OMIM:194072	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0001428	OMIM:194072	TAS				I	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:skoehler	
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0001466	OMIM:194072	TAS				I	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:skoehler	
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0001513	http://decipher.sanger.ac.uk/syndrome/35,OMIM:194072	TAS		HP:0040283		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040283
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0002667	OMIM:194072	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194072	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11p13 DELETION SYNDROME		HP:0010464	http://decipher.sanger.ac.uk/syndrome/35	TAS		HP:0040282		P	#194072 WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME; WAGR;;WAGR SYNDROME;;CHROMOSOME 11P13 DELETION SYNDROME	HPO:iea	HP:0040282
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000006	OMIM:194080	IEA				I		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000033	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000037	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000061	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000097	OMIM:194080	TAS				P		HPO:skoehler	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000100	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000112	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000133	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000149	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000776	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0000822	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0001428	OMIM:194080	IEA				I		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0001967	OMIM:194080	TAS				P		HPO:probinson	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0002667	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0003248	OMIM:194080	IEA				P		HPO:iea	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0003774	OMIM:194080	TAS				P		HPO:probinson	
OMIM	194080	#194080 DENYS-DRASH SYNDROME; DDS;;DRASH SYNDROME;;WILMS TUMOR AND PSEUDO- OR TRUE HERMAPHRODITISM;;NEPHROPATHY, WILMS TUMOR, AND GENITAL ANOMALIES		HP:0010459	OMIM:194080	IEA				P		HPO:iea	
OMIM	194090	WILMS TUMOR 3		HP:0000006	OMIM:194090	IEA				I		HPO:iea	
OMIM	194090	WILMS TUMOR 3		HP:0002667	OMIM:194090	IEA				P		HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000006	OMIM:194190	TAS				I	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000028	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	50%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000047	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	50%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000151	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000175	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000188	OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000204	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000238	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000252	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000286	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000316	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000347	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000348	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000377	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000384	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000402	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000405	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	40%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000407	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	15%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000431	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000444	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000465	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000486	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000520	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000558	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000612	ISBN-13:978-3-7945-2657-4	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	30%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000639	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000668	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000733	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000826	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000902	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000954	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0000960	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001028	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001080	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001171	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001177	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040281
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001274	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040281
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001331	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001385	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001511	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040281		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040281
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040281
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001558	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001629	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001631	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	27%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001747	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001762	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001812	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001840	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0001841	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002020	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002057	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002119	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002144	OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002162	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002353	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	90%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002389	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002553	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002714	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002721	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040284		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	69%
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002750	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002808	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002827	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002948	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0002974	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0003199	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040281		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040281
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0003312	PMID:20301362	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0003745	OMIM:194190	TAS				I	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0004322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs;ISBN-13:978-3-7945-2657-4	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0004467	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0004484	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0004794	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0006655	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=whs	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0007109	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0007385	ISBN-13:978-3-7945-2657-4;OMIM:194190	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0008850	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040282
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0009193	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0009778	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0009918	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0010109	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	HP:0040283
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0010864	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:skoehler	
OMIM	194190	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4p16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME		HP:0011863	OMIM:194190	TAS				P	#194190 WOLF-HIRSCHHORN SYNDROME; WHS;;CHROMOSOME 4P16.3 DELETION SYNDROME;;PITT-ROGERS-DANKS SYNDROME; PRDS;;PITT SYNDROME	HPO:iea	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0000006	OMIM:194200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0001297	OMIM:194200	IEA				P		HPO:skoehler	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0001638	OMIM:194200	IEA				P		HPO:skoehler	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0001645	OMIM:194200	IEA				P		HPO:skoehler	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0001716	OMIM:194200	TAS				P		HPO:skoehler	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0001962	OMIM:194200	IEA				P		HPO:iea	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0004757	OMIM:194200	IEA				P		HPO:iea	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0004763	OMIM:194200	IEA				P		HPO:iea	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0005165	OMIM:194200	TAS				P		HPO:probinson	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0006677	OMIM:194200	IEA				P		HPO:iea	
OMIM	194200	WOLFF-PARKINSON-WHITE SYNDROME		HP:0006684	OMIM:194200	IEA				P		HPO:iea	
OMIM	194300	WOOLLY HAIR, AUTOSOMAL DOMINANT; ADWH		HP:0000006	OMIM:194300	IEA				I		HPO:iea	
OMIM	194300	WOOLLY HAIR, AUTOSOMAL DOMINANT; ADWH		HP:0002208	OMIM:194300	TAS				P		HPO:skoehler	
OMIM	194300	WOOLLY HAIR, AUTOSOMAL DOMINANT; ADWH		HP:0002217	OMIM:194300	TAS				P		HPO:skoehler	
OMIM	194300	WOOLLY HAIR, AUTOSOMAL DOMINANT; ADWH		HP:0002224	OMIM:194300	IEA				P		HPO:skoehler	
OMIM	194300	WOOLLY HAIR, AUTOSOMAL DOMINANT; ADWH		HP:0011359	OMIM:194300	TAS				P		HPO:skoehler	
OMIM	194320	WORONETS TRAIT		HP:0000006	OMIM:194320	IEA				I		HPO:iea	
OMIM	194320	WORONETS TRAIT		HP:0005540	OMIM:194320	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0000006	OMIM:194350	IEA				I		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0000028	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0000278	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0000347	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0000407	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0001873	OMIM:194350	TAS				P		HPO:skoehler	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0001876	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0001908	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0001909	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0002974	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0004209	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0006156	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0007400	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0009183	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0009463	OMIM:194350	TAS				P		HPO:probinson	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0009777	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0009778	OMIM:194350	IEA				P		HPO:iea	
OMIM	194350	WT LIMB-BLOOD SYNDROME		HP:0009803	OMIM:194350	IEA				P		HPO:iea	
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0000006	OMIM:194380	TAS				I		HPO:iea	
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0000952	OMIM:194380	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0000980	OMIM:194380	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0001081	OMIM:194380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0001744	OMIM:194380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0001923	OMIM:194380	TAS				P		HPO:skoehler	
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0002240	OMIM:194380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0003281	OMIM:194380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0003641	OMIM:194380	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0005535	OMIM:194380	IEA				P		HPO:iea	
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0008269	OMIM:194380	IEA				P		HPO:iea	
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0012115	OMIM:194380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	194380	DEHYDRATED HEREDITARY STOMATOCYTOSIS 1 WITH OR WITHOUT PSEUDOHYPERKALEMIA AND/OR PERINATAL EDEMA; DHS1		HP:0025548	OMIM:194380	IEA				P		HPO:skoehler	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0000006	OMIM:194400	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0000953	OMIM:194400	IEA				P		HPO:iea	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0001480	OMIM:194400	IEA				P		HPO:iea	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0003079	OMIM:194400	IEA				P		HPO:iea	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0008069	OMIM:194400	IEA				P		HPO:iea	
OMIM	194400	XERODERMA PIGMENTOSUM, AUTOSOMAL DOMINANT, MILD		HP:0010783	OMIM:194400	IEA				P		HPO:skoehler	
OMIM	194470	ZINC, ELEVATED PLASMA		HP:0000006	OMIM:194470	IEA				I		HPO:iea	
OMIM	194470	ZINC, ELEVATED PLASMA		HP:0001939	OMIM:194470	IEA				P		HPO:iea	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0000007	OMIM:200100	PCS				I		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0000488	OMIM:200100	TAS				P		HPO:skoehler	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0000546	PMID:24288038	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0001251	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0001927	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0002630	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0007305	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0008181	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200100	ABETALIPOPROTEINEMIA		HP:0011096	OMIM:200100	PCS				P		HPO:probinson	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000006	OMIM:200110	TAS				I		HPO:skoehler	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000007	OMIM:200110	IEA				I		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000062	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000153	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000154	OMIM:200110	PCS				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000188	OMIM:200110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000316	OMIM:200110	TAS				P		HPO:skoehler	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000561	OMIM:200110	PCS				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000750	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0000958	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0001126	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0001762	OMIM:200110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0001770	OMIM:200110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0002223	OMIM:200110	PCS				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0002933	OMIM:200110	PCS				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0005105	OMIM:200110	PCS				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0006709	OMIM:200110	IEA				P		HPO:iea	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0010049	OMIM:200110	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0011224	OMIM:200110	IEA				P		HPO:skoehler	
OMIM	200110	ABLEPHARON-MACROSTOMIA SYNDROME		HP:0011267	OMIM:200110	IEA				P		HPO:iea	
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0000007	OMIM:200130	PCS				I		HPO:probinson	
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0000252	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0000444	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0000501	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0000561	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0001249	OMIM:200130	IEA				P		HPO:skoehler	
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0002084	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	1/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0002223	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0002478	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200130	ABSENT EYEBROWS AND EYELASHES WITH MENTAL RETARDATION		HP:0003196	OMIM:200130	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000007	OMIM:200150	IEA				I		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000709	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000718	OMIM:200150	TAS				P		HPO:skoehler	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000726	OMIM:200150	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000734	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000739	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000751	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0000763	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001250	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001260	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001265	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001284	OMIM:200150	TAS				P		HPO:skoehler	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001300	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001332	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001575	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001761	OMIM:200150	TAS				P		HPO:skoehler	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0001927	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0002015	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0002307	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0002310	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0002340	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0003202	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0003236	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0003676	OMIM:200150	TAS				C		HPO:skoehler	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0003690	OMIM:200150	TAS				P		HPO:skoehler	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0007326	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0008767	OMIM:200150	IEA				P		HPO:iea	
OMIM	200150	#200150 CHOREOACANTHOCYTOSIS; CHAC;;LEVINE-CRITCHLEY SYNDROME;;ACANTHOCYTOSIS WITH NEUROLOGIC DISORDER;;NEUROACANTHOCYTOSIS;;CHOREA-ACANTHOCYTOSIS		HP:0100033	OMIM:200150	TAS				P		HPO:skoehler	
OMIM	200170	ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT		HP:0000007	OMIM:200170	IEA				I		HPO:iea	
OMIM	200170	ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT		HP:0000855	OMIM:200170	IEA				P		HPO:iea	
OMIM	200170	ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT		HP:0000956	OMIM:200170	IEA				P		HPO:iea	
OMIM	200170	ACANTHOSIS NIGRICANS WITH MUSCLE CRAMPS AND ACRAL ENLARGEMENT		HP:0003394	OMIM:200170	IEA				P		HPO:iea	
OMIM	200300	ACETOPHENETIDIN SENSITIVITY		HP:0000007	OMIM:200300	IEA				I		HPO:iea	
OMIM	200300	ACETOPHENETIDIN SENSITIVITY		HP:0001871	OMIM:200300	IEA				P		HPO:iea	
OMIM	200300	ACETOPHENETIDIN SENSITIVITY		HP:0001878	PMID:6015912	PCS				P		HPO:lccarmody	
OMIM	200300	ACETOPHENETIDIN SENSITIVITY		HP:0012119	PMID:6015912	PCS				P		HPO:skoehler	
OMIM	200400	ACHALASIA, FAMILIAL ESOPHAGEAL		HP:0000007	OMIM:200400	IEA				I		HPO:iea	
OMIM	200400	ACHALASIA, FAMILIAL ESOPHAGEAL		HP:0000217	OMIM:200400	IEA				P		HPO:iea	
OMIM	200400	ACHALASIA, FAMILIAL ESOPHAGEAL		HP:0001097	OMIM:200400	IEA				P		HPO:iea	
OMIM	200400	ACHALASIA, FAMILIAL ESOPHAGEAL		HP:0001370	OMIM:200400	IEA				P		HPO:iea	
OMIM	200400	ACHALASIA, FAMILIAL ESOPHAGEAL		HP:0002571	OMIM:200400	IEA				P		HPO:iea	
OMIM	200450	ACHALASIA-MICROCEPHALY SYNDROME		HP:0000007	OMIM:200450	IEA				I		HPO:iea	
OMIM	200450	ACHALASIA-MICROCEPHALY SYNDROME		HP:0000252	OMIM:200450	IEA				P		HPO:iea	
OMIM	200450	ACHALASIA-MICROCEPHALY SYNDROME		HP:0000565	OMIM:200450	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	200450	ACHALASIA-MICROCEPHALY SYNDROME		HP:0001249	OMIM:200450	IEA				P		HPO:iea	
OMIM	200450	ACHALASIA-MICROCEPHALY SYNDROME		HP:0002571	OMIM:200450	IEA				P		HPO:iea	
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0000007	PMID:11090342	PCS				I		HPO:iea	
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0002990	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0003974	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0003982	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0004050	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0004231	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0005632	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0005736	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0005792	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0009802	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0009820	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0010048	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0010509	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0010744	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200500	ACHEIROPODY ACHEIROPODIA ACHEIROPODY, BRAZILIAN TYPE		HP:0010760	OMIM:200500;PMID:11090342	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000007	OMIM:200600	TAS				I		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000463	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000470	OMIM:200600	TAS				P		HPO:skoehler	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000773	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000882	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000894	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000916	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0000923	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0001538	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0001552	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0001561	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0001789	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0002983	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0002984	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0003175	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0003196	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0003521	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0003826	OMIM:200600	TAS				M		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0004331	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0004606	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0005280	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0006489	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0010660	OMIM:200600	TAS				P		HPO:iea	
OMIM	200600	#200600 ACHONDROGENESIS, TYPE IA; ACG1A;;ACHONDROGENESIS, HOUSTON-HARRIS TYPE		HP:0010675	OMIM:200600	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000006	OMIM:200610	IEA				I		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000175	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000476	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000773	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000888	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0000969	OMIM:200610	IEA				P		HPO:skoehler	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0001248	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0001552	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0001561	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0001760	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0001789	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0002866	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED	HP:0012828	HP:0003026	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0003270	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0003521	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0003826	OMIM:200610	IEA				M		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0004605	OMIM:200610	IEA				P		HPO:iea	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0005622	OMIM:200610	TAS				P		HPO:probinson	
OMIM	200610	#200610 ACHONDROGENESIS, TYPE II; ACG2;;ACHONDROGENESIS, LANGER-SALDINO TYPE;;CHONDROGENESIS IMPERFECTA;;ACHONDROGENESIS, TYPE IB, FORMERLYHYPOCHONDROGENESIS, INCLUDED		HP:0008873	OMIM:200610	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0000007	OMIM:200700	IEA				I		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0001162	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0001371	OMIM:200700	IEA				P		HPO:skoehler	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0001522	OMIM:200700	IEA				M		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0001773	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0001964	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0002984	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0003022	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0003038	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0003086	OMIM:200700	IEA				P		HPO:skoehler	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0003097	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0003826	OMIM:200700	TAS				M		HPO:probinson	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0005736	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0005792	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0005914	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0006228	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0006498	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0008081	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0008873	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0009803	OMIM:200700	IEA				P		HPO:iea	
OMIM	200700	#200700 CHONDRODYSPLASIA, GREBE TYPE;;ACHONDROGENESIS, BRAZILIAN;;GREBE CHONDRODYSPLASIA;;GREBE DYSPLASIA;;ACROMESOMELIC DYSPLASIA, GREBE TYPE; AMDG;;ACHONDROGENESIS, TYPE II, FORMERLY		HP:0011927	OMIM:200700	TAS				P		HPO:skoehler	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0000007	OMIM:200900	TAS				I		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0000765	OMIM:200900	IEA				P		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0000778	OMIM:200900	TAS				P		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0001888	OMIM:200900	TAS				P		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0003819	OMIM:200900	TAS				M		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0004430	OMIM:200900	TAS				P		HPO:skoehler	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0004432	OMIM:200900	TAS				P		HPO:probinson	
OMIM	200900	ACHONDROPLASIA, SO-CALLED, AND SEVERE COMBINED IMMUNODEFICIENCY		HP:0005871	OMIM:200900	TAS				P		HPO:probinson	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0000007	OMIM:200950	IEA				I		HPO:iea	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0001252	OMIM:200950	IEA				P		HPO:iea	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0001290	OMIM:200950	TAS				P		HPO:skoehler	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0001892	OMIM:200950	IEA				P		HPO:iea	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0002013	OMIM:200950	IEA				P		HPO:iea	
OMIM	200950	ACID PHOSPHATASE DEFICIENCY		HP:0002179	OMIM:200950	IEA				P		HPO:iea	
OMIM	200970	ACKERMAN SYNDROME		HP:0000007	OMIM:200970	IEA				I		HPO:iea	
OMIM	200970	ACKERMAN SYNDROME		HP:0000289	OMIM:200970	TAS				P		HPO:probinson	
OMIM	200970	ACKERMAN SYNDROME		HP:0000501	OMIM:200970	TAS				P		HPO:skoehler	
OMIM	200970	ACKERMAN SYNDROME		HP:0000679	OMIM:200970	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000007	OMIM:200980	IEA				I		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000069	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000104	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000113	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000189	OMIM:200980	TAS				P		HPO:skoehler	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000218	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000268	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000286	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME	HP:0012828	HP:0000347	OMIM:200980	TAS				P		HPO:probinson	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000358	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000369	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000494	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000769	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000774	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000776	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000813	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000882	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000883	OMIM:200980	IEA				P		HPO:skoehler	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0000921	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001161	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001171	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001511	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001562	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001626	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001770	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001829	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0001839	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002089	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002561	OMIM:200980	TAS				P		HPO:skoehler	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002751	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002827	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002937	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002984	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0002987	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0003022	OMIM:200980	TAS				P		HPO:probinson	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0003316	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0003762	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0006381	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0006426	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0008468	OMIM:200980	IEA				P		HPO:iea	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0010477	OMIM:200980	TAS				P		HPO:skoehler	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0030799	OMIM:200980	TAS				P		HPO:skoehler	
OMIM	200980	ACRORENAL-MANDIBULAR SYNDROME		HP:0031909	OMIM:200980	IEA				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000006	OMIM:200990	PCS				I		HPO:iea	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000007	OMIM:200990	TAS				I		HPO:iea	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000023	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000028	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000047	PMID:1491747	PCS		HP:0040284		P		HPO:iea	10/18
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000054	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000143	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000175	PMID:19619433	PCS		HP:0040284		P		HPO:iea	21%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000194	PMID:19619433	PCS		HP:0040284		P		HPO:iea	16%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000204	PMID:19619433	PCS		HP:0040284		P		HPO:iea	21%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000207	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000218	PMID:19619433	PCS		HP:0040284		P		HPO:iea	31%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000233	PMID:19619433	PCS		HP:0040284		P		HPO:iea	9%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000256	PMID:1491747	PCS		HP:0040284		P		HPO:iea	25/27
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000260	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000269	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000286	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000308	PMID:19619433	PCS		HP:0040284		P		HPO:iea	14%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000316	PMID:1491747	PCS		HP:0040284		P		HPO:iea	24/26
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000319	PMID:19619433	PCS		HP:0040284		P		HPO:iea	2%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000322	PMID:19619433	PCS		HP:0040284		P		HPO:iea	31%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000337	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000343	PMID:19619433	PCS		HP:0040284		P		HPO:iea	9%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000358	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000365	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000377	PMID:1491747	PCS		HP:0040284		P		HPO:iea	19/23
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000384	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000431	PMID:1491747	PCS		HP:0040284		P		HPO:iea	24/26
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000486	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000494	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000589	OMIM:200990	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000639	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000648	OMIM:200990	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0000685	PMID:19619433	PCS		HP:0040284		P		HPO:iea	2%
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001156	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001162	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001177	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001182	PMID:19619433	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001249	PMID:1491747	PCS		HP:0040284		P		HPO:iea	23/25
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001250	PMID:1491747	PCS		HP:0040284		P		HPO:iea	9/27
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001274	OMIM:200990	IEA				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001290	PMID:1491747	PCS		HP:0040284		P		HPO:iea	20/23
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001425	OMIM:200990	PCS				I		HPO:iea	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001508	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001510	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001537	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001641	OMIM:200990	TAS				P		HPO:probinson	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001671	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001770	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001830	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0001841	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0002007	PMID:1491747	PCS		HP:0040284		P		HPO:probinson	23/26
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0002023	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0003196	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0004209	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0005148	OMIM:200990	IEA				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0006101	PMID:19619433	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0007370	PMID:19619433;OMIM:603099	PCS		HP:0040280		P		HPO:iea	HP:0040280
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0007894	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0008897	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0009611	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0009942	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0010066	PMID:19619433	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0010576	PMID:1491747	PCS		HP:0040284		P		HPO:iea	10/27
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0010864	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0011220	OMIM:200990	TAS				P		HPO:skoehler	
OMIM	200990	ACROCALLOSAL SYNDROME; ACLS		HP:0030680	PMID:1491747	PCS		HP:0040284		P		HPO:iea	5/22
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000007	OMIM:200995	IEA				I		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000105	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000263	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000286	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000316	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000369	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000377	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000470	OMIM:200995	TAS				P		HPO:probinson	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000582	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0000800	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001072	OMIM:200995	IEA				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001162	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001363	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001395	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001539	OMIM:200995	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001541	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0001748	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0002089	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0002240	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0002983	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0003196	OMIM:200995	TAS				P		HPO:skoehler	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0004790	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0005210	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0006544	OMIM:200995	IEA				P		HPO:iea	
OMIM	200995	ACROCEPHALOPOLYDACTYLOUS DYSPLASIA		HP:0100732	OMIM:200995	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000007	OMIM:201000;ISBN-13:978-0721606156	PCS				I		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000028	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000072	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000126	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000218	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000248	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000272	OMIM:201000	TAS				P		HPO:skoehler	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000286	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000327	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000347	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000369	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000377	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000405	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000407	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000470	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000482	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000506	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000648	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000826	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0000960	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001156	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001162	PMID:17503333	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001249	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001513	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001537	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001539	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001629	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001631	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001636	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001642	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001643	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001669	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001748	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001770	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001840	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0001841	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002059	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002650	OMIM:201000	TAS				P		HPO:skoehler	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002673	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002700	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002857	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002869	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0002970	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0003182	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0003241	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0003298	OMIM:201000	TAS				P		HPO:skoehler	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004209	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004322	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004440	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004442	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004443	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0004467	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0005280	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0006335	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0006349	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0006397	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0007370	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0007759	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0009473	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0009608	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0009843	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0009891	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0010093	PMID:17503333	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0010194	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0010275	PMID:17503333	PCS				P		HPO:iea	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0011800	OMIM:201000	TAS				P		HPO:skoehler	
OMIM	201000	#201000 CARPENTER SYNDROME 1; CRPT1;;CARPENTER SYNDROME;;ACROCEPHALOPOLYSYNDACTYLY TYPE II;;ACPS II		HP:0012385	OMIM:201000	TAS				P		HPO:skoehler	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0000007	OMIM:201020	IEA				I		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0000263	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0001159	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0001161	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0001193	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0009466	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0009473	OMIM:201020	IEA				P		HPO:iea	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0012385	OMIM:201020	TAS				P		HPO:skoehler	
OMIM	201020	201020 ACROCEPHALOPOLYSYNDACTYLY TYPE IV;;ACPS IV;;GOODMAN SYNDROME		HP:0030084	OMIM:201020	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000007	OMIM:201050	IEA				I		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000175	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000263	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000322	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000347	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000356	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000405	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000407	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000426	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000445	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000463	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000465	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000494	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000508	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000520	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000601	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000695	OMIM:201050	TAS				P		HPO:skoehler	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000767	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0000925	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0001363	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0001840	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0004322	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0004467	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0006958	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0010034	OMIM:201050	IEA				P		HPO:iea	
OMIM	201050	ACROCRANIOFACIAL DYSOSTOSIS		HP:0010105	OMIM:201050	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0000007	OMIM:201100	IEA				I		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0000135	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0000224	OMIM:201100	TAS				P		HPO:probinson	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0000712	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0000737	OMIM:201100	TAS				P		HPO:probinson	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001251	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001254	OMIM:201100	IEA				P		HPO:skoehler	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001337	OMIM:201100	TAS				P		HPO:probinson	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001508	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001744	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0001818	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0002014	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0002240	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0002293	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0003282	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0003593	OMIM:201100	IEA				C		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0004322	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0004396	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0005401	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0005435	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0008734	OMIM:201100	IEA				P		HPO:iea	
OMIM	201100	ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE		HP:0040171	OMIM:201100	TAS				P		HP:probinson	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000007	OMIM:201170	IEA				I		HPO:iea	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000160	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000218	OMIM:201170	IEA				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000260	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000316	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000322	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000347	OMIM:201170	IEA				P		HPO:iea	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000358	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000369	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000431	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000448	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000490	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000878	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000954	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0000963	OMIM:201170	IEA				P		HPO:iea	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0001199	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0001762	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0001814	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0001845	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0003038	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0004322	OMIM:201170	IEA				P		HPO:iea	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0005632	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0005736	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0012165	OMIM:201170	TAS				P		HPO:skoehler	
OMIM	201170	ACROFACIAL DYSOSTOSIS SYNDROME OF RODRIGUEZ		HP:0030084	OMIM:201170	IEA				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000007	OMIM:201180	TAS				I		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000154	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000175	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000204	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000248	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000272	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000303	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000316	OMIM:201180	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000337	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000349	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000410	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000431	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000508	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000527	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000568	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000648	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000677	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0000767	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0001089	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0001249	OMIM:201180	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0001250	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0001792	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0004322	OMIM:201180	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0004523	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0007835	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0008807	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0009882	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0010049	OMIM:201180	TAS				P		HPO:skoehler	
OMIM	201180	ACROFRONTOFACIONASAL DYSOSTOSIS 1		HP:0011304	OMIM:201180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0000007	OMIM:201250	IEA				I		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0000954	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0001773	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0002827	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0002984	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0002986	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0003022	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0003038	OMIM:201250	IEA				P		HPO:skoehler	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0003038	OMIM:201250	TAS				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0003042	OMIM:201250	TAS				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0003086	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0005096	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0005736	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0006011	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0006014	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0006110	OMIM:201250	TAS				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0006144	OMIM:201250	TAS				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0008890	OMIM:201250	IEA				P		HPO:iea	
OMIM	201250	ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE		HP:0009778	OMIM:201250	TAS				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0000007	OMIM:201300	IEA				I		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0000224	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0000762	OMIM:201300	TAS				P		HPO:probinson	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0000970	PMID:16534117	TAS				P		HPO:probinson	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001069	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001252	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001265	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001284	PMID:16534117	PCS				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001290	OMIM:201300	TAS				P		HPO:skoehler	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001818	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001842	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0001939	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0002020	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0002661	OMIM:201300	TAS				P		HPO:probinson	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0003380	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0003448	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0003593	OMIM:201300	IEA				C		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0003677	OMIM:201300	PCS				C		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0006121	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0007460	OMIM:201300	TAS				P		HP:probinson	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0008000	OMIM:201300	TAS				P		HP:probinson	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0008872	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0009771	OMIM:201300	IEA				P		HPO:iea	
OMIM	201300	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE II		HP:0009830	OMIM:201300	IEA				P		HPO:skoehler	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:201310	IEA				I		HPO:iea	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000083	OMIM:201310	IEA				P		HPO:iea	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000089	OMIM:201310	TAS				P		HPO:probinson	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001171	OMIM:201310	TAS				P		HPO:probinson	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001839	OMIM:201310	TAS				P		HPO:probinson	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0005563	OMIM:201310	TAS				P		HPO:probinson	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0009466	OMIM:201310	IEA				P		HPO:iea	
OMIM	201310	201310 ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0030084	OMIM:201310	TAS				P		HPO:skoehler	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0000007	OMIM:201400	IEA				I		HPO:iea	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0000835	OMIM:201400	IEA				P		HPO:iea	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0001250	OMIM:201400	IEA				P		HPO:skoehler	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0003162	OMIM:201400	IEA				P		HPO:iea	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0003593	OMIM:201400	IEA				C		HPO:skoehler	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0008163	OMIM:201400	IEA				P		HPO:iea	
OMIM	201400	ACTH DEFICIENCY, ISOLATED; IAD		HP:0011748	OMIM:201400	TAS				P		HPO:skoehler	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0000007	OMIM:201450	IEA				I		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001250	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001252	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001254	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001259	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001263	OMIM:201450	TAS				P		HPO:probinson	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001290	OMIM:201450	TAS				P		HPO:skoehler	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001397	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001942	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF	HP:0012825	HP:0001942	OMIM:201450	TAS				P		HPO:probinson	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0001943	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0002013	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0002181	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0002240	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0002910	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0003108	OMIM:201450	IEA				P		HPO:skoehler	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0003234	OMIM:201450	IEA				P		HPO:iea	
OMIM	201450	ACYL-COA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF		HP:0008309	OMIM:201450	TAS				P		HPO:skoehler	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0000007	OMIM:201470	IEA				I		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0000590	OMIM:201470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0000709	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0000750	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001250	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001252	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001254	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001263	OMIM:201470	TAS				P		HPO:skoehler	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001290	OMIM:201470	TAS				P		HPO:skoehler	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001371	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001508	OMIM:201470	IEA				P		HPO:skoehler	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0001638	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0002500	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0002650	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0003198	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0003219	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0003623	OMIM:201470	TAS				C		HPO:skoehler	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0004911	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0008872	OMIM:201470	IEA				P		HPO:iea	
OMIM	201470	ACYL-COA DEHYDROGENASE, SHORT-CHAIN, DEFICIENCY OF		HP:0010628	OMIM:201470	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0000007	OMIM:201475	IEA				I		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001252	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001254	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001290	OMIM:201475	TAS				P		HPO:skoehler	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001324	OMIM:201475	TAS				P		HPO:probinson	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001397	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001404	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001639	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001645	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0001958	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0002013	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0002240	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0002789	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0003215	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0003234	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0003236	OMIM:201475	TAS				P		HPO:skoehler	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0003552	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0003738	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0008305	OMIM:201475	IEA				P		HPO:iea	
OMIM	201475	ACYL-COA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF		HP:0009045	OMIM:201475	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000007	OMIM:201550	IEA				I		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000175	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000218	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000220	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000252	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0000998	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0001290	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0001363	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0002015	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0002058	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0002093	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0002705	OMIM:201550	TAS				P		HPO:skoehler	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0002804	OMIM:201550	IEA				P		HPO:skoehler	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0003198	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0006990	OMIM:201550	IEA				P		HPO:iea	
OMIM	201550	ADDUCTED THUMBS SYNDROME		HP:0007266	OMIM:201550	PCS				P		HPO:probinson	
OMIM	201710	LIPOID CONGENITAL ADRENAL HYPERPLASIA		HP:0000007	OMIM:201710	IEA				I		HPO:iea	
OMIM	201710	LIPOID CONGENITAL ADRENAL HYPERPLASIA		HP:0000047	OMIM:201710	IEA				P		HPO:iea	
OMIM	201710	LIPOID CONGENITAL ADRENAL HYPERPLASIA		HP:0000127	OMIM:201710	IEA				P		HPO:iea	
OMIM	201710	LIPOID CONGENITAL ADRENAL HYPERPLASIA		HP:0000840	OMIM:201710	IEA				P		HPO:iea	
OMIM	201710	LIPOID CONGENITAL ADRENAL HYPERPLASIA		HP:0008258	OMIM:201710	IEA				P		HPO:skoehler	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000007	OMIM:201750	IEA				I		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000028	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000041	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000046	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000047	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000048	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000054	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000062	OMIM:201750	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000066	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000085	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000147	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000248	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000252	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000272	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000316	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000377	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000405	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000452	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000453	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000520	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0000818	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001166	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001194	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001363	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001438	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001518	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001562	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001586	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001601	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001838	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0001939	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002007	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002308	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002650	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002676	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002780	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002937	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002974	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0002980	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0003031	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0003041	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0005280	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0008072	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0008073	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0008368	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0008665	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0009473	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0009702	OMIM:201750	IEA				P		HPO:iea	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0011800	OMIM:201750	TAS				P		HPO:skoehler	
OMIM	201750	#201750 ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS;ABS1		HP:0012385	OMIM:201750	TAS				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000007	OMIM:201810	TAS				I		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000037	OMIM:201810	IEA				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000047	OMIM:201810	IEA				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000048	OMIM:201810	TAS				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000054	OMIM:201810	TAS				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0000062	OMIM:201810	TAS				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0008221	OMIM:201810	IEA				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0008707	OMIM:201810	TAS				P		HPO:skoehler	
OMIM	201810	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 DEFICIENCY		HP:0012411	OMIM:201810	TAS				P		HPO:skoehler	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000007	OMIM:201910	IEA				I		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000047	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000127	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000765	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000771	OMIM:201910	TAS	HP:0003581			P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000822	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0000840	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0001507	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0001943	OMIM:201910	IEA				P		HPO:iea	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0001945	OMIM:201910	IEA				P		HPO:skoehler	
OMIM	201910	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY		HP:0008221	OMIM:201910	IEA				P		HPO:skoehler	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000007	OMIM:202010	IEA				I		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000013	OMIM:202010	TAS				P		HPO:probinson	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000040	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000061	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000079	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000822	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000840	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0000953	OMIM:202010	TAS				P		HPO:skoehler	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0002900	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0003351	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0003623	OMIM:202010	IEA				C		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0004319	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0004322	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0005616	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0008185	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0008258	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0008665	OMIM:202010	IEA				P		HPO:iea	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0008726	OMIM:202010	TAS				P		HPO:probinson	
OMIM	202010	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASEDEFICIENCY		HP:0008734	OMIM:202010	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000007	OMIM:202110	IEA				I		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000037	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000062	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000771	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000786	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000822	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0000840	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0001949	OMIM:202110	IEA				P		HPO:iea	
OMIM	202110	ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY		HP:0008221	OMIM:202110	IEA				P		HPO:skoehler	
OMIM	202150	ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZINGHORMONE		HP:0000007	OMIM:202150	IEA				I		HPO:iea	
OMIM	202150	ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZINGHORMONE		HP:0000028	OMIM:202150	IEA				P		HPO:iea	
OMIM	202150	ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZINGHORMONE		HP:0000054	OMIM:202150	IEA				P		HPO:iea	
OMIM	202150	ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZINGHORMONE		HP:0001939	OMIM:202150	IEA				P		HPO:iea	
OMIM	202150	ADRENAL HYPOPLASIA, CONGENITAL, WITH ABSENT PITUITARY LUTEINIZINGHORMONE		HP:0008244	OMIM:202150	IEA				P		HPO:iea	
OMIM	202155	202155 ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE		HP:0000007	OMIM:202155	TAS				I		HPO:skoehler	
OMIM	202155	202155 ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE		HP:0001507	OMIM:202155	IEA				P		HPO:iea	
OMIM	202155	202155 ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE		HP:0008207	OMIM:202155	IEA				P		HPO:iea	
OMIM	202155	202155 ADRENAL HYPOPLASIA, CYTOMEGALIC TYPE		HP:0008244	OMIM:202155	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0000007	OMIM:202200	IEA				I		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0000098	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0000953	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0001250	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0001259	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0001508	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0001988	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0002719	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0003154	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0005616	OMIM:202200	IEA				P		HPO:iea	
OMIM	202200	#202200 GLUCOCORTICOID DEFICIENCY 1; GCCD1;;FAMILIAL GLUCOCORTICOID DEFICIENCY 1; FGD1;;ADRENAL UNRESPONSIVENESS TO ACTH;;ACTH RESISTANCE		HP:0008163	OMIM:202200	IEA				P		HPO:iea	
OMIM	202300	ADRENOCORTICAL CARCINOMA, HEREDITARY		HP:0000007	OMIM:202300	IEA				I		HPO:iea	
OMIM	202300	ADRENOCORTICAL CARCINOMA, HEREDITARY		HP:0006744	OMIM:202300	IEA				P		HPO:iea	
OMIM	202355	ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT		HP:0000007	OMIM:202355	IEA				I		HPO:iea	
OMIM	202355	ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT		HP:0000953	OMIM:202355	IEA				P		HPO:iea	
OMIM	202355	ADRENOCORTICAL UNRESPONSIVENESS TO ACTH WITH POSTRECEPTOR DEFECT		HP:0003154	OMIM:202355	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000007	OMIM:202370	IEA				I		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000218	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000268	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000286	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000348	OMIM:202370	IEA				P		HPO:skoehler	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000369	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000431	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000463	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000565	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0000846	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0001249	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0001250	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0001999	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0002007	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0002705	OMIM:202370	TAS				P		HPO:skoehler	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0003455	OMIM:202370	IEA				P		HPO:iea	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0010696	OMIM:202370	TAS	HP:0003623			P		HPO:probinson	
OMIM	202370	PEROXISOME BIOGENESIS DISORDER 2B; PBD2B		HP:0011220	OMIM:202370	IEA				P		HPO:skoehler	
OMIM	202400	AFIBRINOGENEMIA, CONGENITALHYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED		HP:0000007	OMIM:202400	TAS				I		HPO:probinson	
OMIM	202400	AFIBRINOGENEMIA, CONGENITALHYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED		HP:0001892	OMIM:202400	TAS				P		HPO:probinson	
OMIM	202400	AFIBRINOGENEMIA, CONGENITALHYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED		HP:0011900	OMIM:202400	TAS				P		HPO:probinson	
OMIM	202400	AFIBRINOGENEMIA, CONGENITALHYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED		HP:0012223	OMIM:202400	TAS				P		HPO:probinson	
OMIM	202550	AGANGLIONOSIS, TOTAL INTESTINAL		HP:0000007	OMIM:202550	IEA				I		HPO:iea	
OMIM	202550	AGANGLIONOSIS, TOTAL INTESTINAL		HP:0005241	OMIM:202550	IEA				P		HPO:iea	
OMIM	202600	AGENESIS OF CEREBRAL WHITE MATTER		HP:0000007	OMIM:202600	IEA				I		HPO:iea	
OMIM	202600	AGENESIS OF CEREBRAL WHITE MATTER		HP:0001249	OMIM:202600	IEA				P		HPO:iea	
OMIM	202600	AGENESIS OF CEREBRAL WHITE MATTER		HP:0200017	OMIM:202600	IEA				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000006	OMIM:202650	IEA				I		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000007	OMIM:202650	TAS				I		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000160	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000171	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000175	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000347	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000356	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000405	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000478	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0000494	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0001274	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0001360	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0001696	OMIM:202650	IEA				P		HPO:iea	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0002098	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0002779	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0005349	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0008749	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0009939	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0012730	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202650	AGNATHIA-OTOCEPHALY COMPLEX		HP:0100663	OMIM:202650	TAS				P		HPO:skoehler	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0000006	PMID:14962902	PCS				I		HPO:skoehler	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0001507	OMIM:202700	IEA				P		HPO:iea	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0001875	PMID:14962902	PCS				P		HPO:probinson	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0001880	OMIM:202700	IEA				P		HPO:iea	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0001894	OMIM:202700	IEA				P		HPO:iea	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1	HP:0012825	HP:0001903	OMIM:202700	TAS				P		HPO:skoehler	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0002718	OMIM:202700	TAS				P		HPO:probinson	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0003593	OMIM:202700	TAS				C		HPO:skoehler	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0004845	OMIM:202700	IEA				P		HPO:iea	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0005541	OMIM:202700	TAS				P		HPO:probinson	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0010702	OMIM:202700	IEA				P		HPO:iea	
OMIM	202700	#202700 NEUTROPENIA, SEVERE CONGENITAL, 1, AUTOSOMAL DOMINANT; SCN1		HP:0012311	OMIM:202700	TAS				P		HPO:skoehler	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0000007	OMIM:202900	IEA				I		HPO:iea	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0000252	OMIM:202900	IEA				P		HPO:iea	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0000819	OMIM:202900	IEA				P		HPO:iea	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0003128	OMIM:202900	IEA				P		HPO:iea	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0003510	OMIM:202900	IEA				P		HPO:iea	
OMIM	202900	ALANINURIA WITH MICROCEPHALY, DWARFISM, ENAMEL HYPOPLASIA, AND DIABETESMELLITUS		HP:0006297	OMIM:202900	IEA				P		HPO:iea	
OMIM	203000	FRONTONASAL DYSPLASIA WITH ALAR CLEFTS		HP:0000007	OMIM:203000	IEA				I		HPO:iea	
OMIM	203000	FRONTONASAL DYSPLASIA WITH ALAR CLEFTS		HP:0000430	OMIM:203000	IEA				P		HPO:iea	
OMIM	203000	FRONTONASAL DYSPLASIA WITH ALAR CLEFTS		HP:0000506	OMIM:203000	IEA				P		HPO:iea	
OMIM	203000	FRONTONASAL DYSPLASIA WITH ALAR CLEFTS		HP:0003191	OMIM:203000	IEA				P		HPO:iea	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000007	OMIM:203100	TAS				I		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000483	OMIM:203100	TAS				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000486	OMIM:203100	TAS				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000545	OMIM:203100	TAS				P		HPO:probinson	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000577	OMIM:203100	IEA				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000613	OMIM:203100	TAS				P		HPO:probinson	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000635	OMIM:203100	TAS				P		HPO:probinson	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0000639	OMIM:203100	TAS				P		HPO:probinson	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0001022	OMIM:203100	IEA				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0001107	OMIM:203100	TAS				P		HPO:probinson	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0003577	OMIM:203100	TAS				C		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0007663	OMIM:203100	TAS				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0007750	OMIM:203100	TAS				P		HPO:iea	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0011364	OMIM:203100	TAS				P		HPO:skoehler	
OMIM	203100	ALBINISM, OCULOCUTANEOUS, TYPE IA; OCA1A		HP:0200098	OMIM:203100	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000007	OMIM:203200	TAS				I		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000486	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000545	OMIM:203200	IEA				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000577	OMIM:203200	IEA				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000635	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0000639	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0001022	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0002297	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0007603	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0007663	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0007750	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203200	ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2		HP:0007894	OMIM:203200	TAS				P		HPO:skoehler	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0000007	OMIM:203290	IEA				I		HPO:skoehler	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0000486	OMIM:203290	IEA				P		HPO:iea	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0000639	OMIM:203290	TAS				P		HPO:probinson	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0001022	OMIM:203290	IEA				P		HPO:skoehler	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0002297	OMIM:203290	IEA				P		HPO:skoehler	
OMIM	203290	ALBINISM, OCULOCUTANEOUS, TYPE III		HP:0007443	OMIM:203290	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000007	OMIM:203300	IEA				I		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000083	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000225	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000421	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000618	OMIM:203300	IEA				P		HPO:skoehler	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000639	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000978	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0000995	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001022	OMIM:203300	TAS				P		HPO:skoehler	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001107	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001141	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001425	OMIM:203300	IEA				I		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001480	OMIM:203300	TAS				P		HPO:skoehler	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001595	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0001638	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0002027	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0002091	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0002206	OMIM:203300	TAS				P		HPO:skoehler	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0002573	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0002583	OMIM:203300	IEA				P		HPO:skoehler	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0003010	OMIM:203300	IEA				P		HPO:iea	
OMIM	203300	HERMANSKY-PUDLAK SYNDROME 1; HPS1		HP:0007603	OMIM:203300	IEA				P		HPO:iea	
OMIM	203330	PSEUDOHYPOPARATHYROIDISM, TYPE II		HP:0000852	OMIM:203330	IEA				P		HPO:iea	
OMIM	203330	PSEUDOHYPOPARATHYROIDISM, TYPE II		HP:0002901	OMIM:203330	IEA				P		HPO:iea	
OMIM	203330	PSEUDOHYPOPARATHYROIDISM, TYPE II		HP:0002905	OMIM:203330	IEA				P		HPO:iea	
OMIM	203330	PSEUDOHYPOPARATHYROIDISM, TYPE II		HP:0003165	OMIM:203330	IEA				P		HPO:iea	
OMIM	203330	PSEUDOHYPOPARATHYROIDISM, TYPE II		HP:0003745	OMIM:203330	IEA				I		HPO:iea	
OMIM	203340	MICROCEPHALY - ALBINISM - DIGITAL ANOMALIES		HP:0001022	OMIM:203340	IEA				P		HPO:skoehler	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0000007	OMIM:203400	IEA				I		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0000127	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0000848	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0001508	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0001510	OMIM:203400	TAS				P		HPO:skoehler	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0001944	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0001954	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0002013	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0002153	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0002615	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0002902	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0003623	OMIM:203400	IEA				C		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0004319	OMIM:203400	IEA				P		HPO:iea	
OMIM	203400	#203400 CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY;;CMO I DEFICIENCY;;ALDOSTERONE DEFICIENCY I;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1A;;ALDOSTERONE DEFICIENCY DUE TO DEFECT IN STEROID 18-HYDROXYLASE;;18-@HYDROXYLASE DEFICIENCY;;STEROID 18-@HYDROXYLASE DEFICIENCY		HP:0008872	OMIM:203400	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0000006	OMIM:203450	IEA				I		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0000238	OMIM:203450	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0001250	OMIM:203450	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0001251	PMID:12975300	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	203450	ALEXANDER DISEASE		HP:0001257	OMIM:203450	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0002376	OMIM:203450	TAS				P		HPO:probinson	
OMIM	203450	ALEXANDER DISEASE		HP:0002483	OMIM:203450	TAS				P		HPO:probinson	
OMIM	203450	ALEXANDER DISEASE		HP:0002922	OMIM:203450	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0003593	OMIM:203450	TAS				C		HPO:probinson	
OMIM	203450	ALEXANDER DISEASE		HP:0004481	OMIM:203450	IEA				P		HPO:iea	
OMIM	203450	ALEXANDER DISEASE		HP:0007162	OMIM:203450	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0000007	OMIM:203500	IEA				I		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0000079	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0000598	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0001369	OMIM:203500	IEA				P		HPO:skoehler	
OMIM	203500	ALKAPTONURIA		HP:0001507	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0001717	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0001939	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0002808	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0002829	OMIM:203500	IEA				P		HPO:skoehler	
OMIM	203500	ALKAPTONURIA		HP:0002948	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0003040	OMIM:203500	IEA				P		HPO:skoehler	
OMIM	203500	ALKAPTONURIA		HP:0003418	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0004380	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0004382	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0004690	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0004942	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0007832	OMIM:203500	IEA				P		HPO:iea	
OMIM	203500	ALKAPTONURIA		HP:0008419	OMIM:203500	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:203550	IEA				I		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000262	OMIM:203550	TAS				P		HPO:probinson	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000268	OMIM:203550	TAS				P		HPO:probinson	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000448	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000506	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000545	OMIM:203550	IEA				P		HPO:skoehler	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0000670	OMIM:203550	IEA				P		HPO:skoehler	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0001371	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0001371	OMIM:203550	TAS				P		HPO:skoehler	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0001596	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0002265	OMIM:203550	TAS				P		HPO:probinson	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0002827	OMIM:203550	IEA				P		HPO:skoehler	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0003510	OMIM:203550	IEA				P		HPO:skoehler	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0004220	OMIM:203550	TAS				P		HPO:probinson	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0005659	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0006282	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0006887	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0008850	OMIM:203550	IEA				P		HPO:iea	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME	HP:0012825	HP:0010554	OMIM:203550	TAS				P		HPO:probinson	
OMIM	203550	ALOPECIA-CONTRACTURES-DWARFISM MENTAL RETARDATION SYNDROME		HP:0010864	OMIM:203550	TAS				P		HPO:skoehler	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0000007	OMIM:203600	IEA				I		HPO:iea	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0000252	OMIM:203600	TAS				P		HPO:skoehler	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0001249	OMIM:203600	IEA				P		HPO:iea	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0001250	OMIM:203600	IEA				P		HPO:iea	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0001596	OMIM:203600	IEA				P		HPO:iea	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0002353	OMIM:203600	IEA				P		HPO:iea	
OMIM	203600	203600 ALOPECIA-EPILEPSY-OLIGOPHRENIA SYNDROME OF MOYNAHAN;;MOYNAHAN ALOPECIA SYNDROME		HP:0008070	OMIM:203600	TAS				P		HPO:skoehler	
OMIM	203650	%203650 ALOPECIA-MENTAL RETARDATION SYNDROME 1; APMR1;;AMR SYNDROME		HP:0000007	OMIM:203650	IEA				I		HPO:iea	
OMIM	203650	%203650 ALOPECIA-MENTAL RETARDATION SYNDROME 1; APMR1;;AMR SYNDROME		HP:0002289	OMIM:203650	IEA				P		HPO:iea	
OMIM	203650	%203650 ALOPECIA-MENTAL RETARDATION SYNDROME 1; APMR1;;AMR SYNDROME		HP:0006887	OMIM:203650	IEA				P		HPO:iea	
OMIM	203650	%203650 ALOPECIA-MENTAL RETARDATION SYNDROME 1; APMR1;;AMR SYNDROME		HP:0010864	OMIM:203650	TAS				P		HPO:skoehler	
OMIM	203655	#203655 ALOPECIA UNIVERSALIS CONGENITA; ALUNC;;ATRICHIA, GENERALIZED		HP:0000007	OMIM:203655	IEA				I		HPO:iea	
OMIM	203655	#203655 ALOPECIA UNIVERSALIS CONGENITA; ALUNC;;ATRICHIA, GENERALIZED		HP:0001596	OMIM:203655	IEA				P		HPO:skoehler	
OMIM	203655	#203655 ALOPECIA UNIVERSALIS CONGENITA; ALUNC;;ATRICHIA, GENERALIZED		HP:0001939	OMIM:203655	IEA				P		HPO:iea	
OMIM	203655	#203655 ALOPECIA UNIVERSALIS CONGENITA; ALUNC;;ATRICHIA, GENERALIZED		HP:0002289	OMIM:203655	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0000007	OMIM:203700	IEA				I		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0000572	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0000649	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0000726	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001251	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001252	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001263	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001272	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001276	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001290	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001336	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001399	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001408	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001413	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001414	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0001508	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002013	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002133	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002151	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002171	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002240	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002376	OMIM:203700	PCS				P		HPO:probinson	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002446	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002529	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002910	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0002922	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0003219	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0003470	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0003535	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0003593	OMIM:203700	PCS				C		HPO:probinson	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0003678	OMIM:203700	IEA				C		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0006964	OMIM:203700	IEA				P		HPO:iea	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0012847	OMIM:203700	TAS				P		HPO:skoehler	
OMIM	203700	MITOCHONDRIAL DNA DEPLETION SYNDROME 4A (ALPERS TYPE)		HP:0100704	OMIM:203700	IEA				P		HPO:iea	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:203740	IEA				I		HPO:iea	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0001252	OMIM:203740	IEA				P		HPO:iea	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:203740	TAS				P		HPO:skoehler	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0001942	OMIM:203740	IEA				P		HPO:iea	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0002151	OMIM:203740	TAS				P		HPO:probinson	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0003819	OMIM:203740	TAS				M		HPO:probinson	
OMIM	203740	ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY		HP:0004902	OMIM:203740	IEA				P		HPO:iea	
OMIM	203750	ALPHA-METHYLACETOACETIC ACIDURIA		HP:0000007	OMIM:203750	IEA				I		HPO:iea	
OMIM	203750	ALPHA-METHYLACETOACETIC ACIDURIA		HP:0001249	OMIM:203750	IEA				P		HPO:iea	
OMIM	203750	ALPHA-METHYLACETOACETIC ACIDURIA		HP:0001944	OMIM:203750	IEA				P		HPO:iea	
OMIM	203750	ALPHA-METHYLACETOACETIC ACIDURIA		HP:0002013	OMIM:203750	IEA				P		HPO:iea	
OMIM	203750	ALPHA-METHYLACETOACETIC ACIDURIA		HP:0005974	OMIM:203750	IEA				P		HPO:iea	
OMIM	203760	ALPHA-2-DEFICIENT COLLAGEN DISEASE		HP:0000007	OMIM:203760	IEA				I		HPO:iea	
OMIM	203760	ALPHA-2-DEFICIENT COLLAGEN DISEASE		HP:0001166	OMIM:203760	IEA				P		HPO:iea	
OMIM	203760	ALPHA-2-DEFICIENT COLLAGEN DISEASE		HP:0001519	OMIM:203760	IEA				P		HPO:iea	
OMIM	203760	ALPHA-2-DEFICIENT COLLAGEN DISEASE		HP:0001939	OMIM:203760	IEA				P		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:203780	TAS				I		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000083	OMIM:203780	IEA				P		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000093	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000100	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000123	OMIM:203780	IEA				P		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000365	OMIM:203780	IEA				P		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000545	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000790	OMIM:203780	IEA				P		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0000822	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0001425	OMIM:203780	IEA				I		HPO:iea	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:203780	TAS				C		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0003774	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0004722	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0011501	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0030034	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203780	ALPORT SYNDROME, AUTOSOMAL RECESSIVE		HP:0200020	OMIM:203780	TAS				P		HPO:skoehler	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000007	OMIM:203800	IEA				I		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000083	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS	HP:0011010	HP:0000123	OMIM:203800	TAS				P		HPO:skoehler	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000164	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000230	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000388	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000408	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000523	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000548	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000572	OMIM:203800	IEA				P		HPO:skoehler	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000580	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000613	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000618	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000639	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000771	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000815	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000821	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000822	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000824	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000831	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000842	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000858	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000873	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0000956	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001133	OMIM:203800	TAS				P		HPO:skoehler	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001155	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001263	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001397	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001596	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001635	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001644	OMIM:203800	IEA	HP:0003593			P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001763	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001956	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0001970	PMID:21358663	PCS				P		HPO:probinson	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002099	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002149	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002155	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002240	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002621	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002650	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002808	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0002910	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0003233	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0004322	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0004438	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0005616	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0005987	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0006532	OMIM:203800	IEA				P		HPO:iea	
OMIM	203800	ALSTROM SYNDROME; ALMS		HP:0200120	OMIM:203800	TAS				P		HPO:skoehler	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000007	OMIM:204000	IEA				I		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000407	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000518	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000563	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000580	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000613	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000618	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000639	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0000654	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0001099	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0001249	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0001483	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0001510	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0002240	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0003296	OMIM:204000	IEA				P		HPO:iea	
OMIM	204000	LEBER CONGENITAL AMAUROSIS, TYPE I		HP:0003354	OMIM:204000	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000007	OMIM:204100	IEA				I		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000518	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000563	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000580	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000613	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000618	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0000654	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0001099	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0001249	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0001320	OMIM:204100	IEA				P		HPO:iea	
OMIM	204100	LEBER CONGENITAL AMAUROSIS, TYPE II		HP:0001483	OMIM:204100	IEA				P		HPO:iea	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000007	PMID:2769722	PCS				I		HPO:iea	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000505	PMID:2769722	PCS	HP:0003577			P		HP:probinson	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000556	PMID:2769722	PCS				P		HPO:iea	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000574	PMID:2769722	PCS				P		HPO:iea	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000613	PMID:2769722	PCS				P		HPO:skoehler	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0000664	PMID:2769722	PCS				P		HPO:iea	
OMIM	204110	AMAUROSIS CONGENITA, CONE-ROD TYPE, WITH CONGENITAL HYPERTRICHOSIS		HP:0001007	PMID:2769722	PCS	HP:0003577			P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000007	OMIM:204200	IEA				I		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000501	OMIM:204200	IEA				P		HPO:skoehler	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000510	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000518	OMIM:204200	IEA				P		HPO:skoehler	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000529	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000550	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000608	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000618	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000648	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000709	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000726	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0000739	OMIM:204200	TAS				P		HPO:probinson	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001249	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001250	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001260	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001300	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001317	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001336	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0001922	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0002059	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0002074	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0002361	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0002505	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0003205	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0003208	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0003463	OMIM:204200	IEA				P		HPO:iea	
OMIM	204200	CEROID LIPOFUSCINOSIS, NEURONAL, 3; CLN3		HP:0005157	OMIM:204200	TAS				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:204300	IEA				I		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0000716	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0000726	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:204300	IEA				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0001251	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0001336	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0002059	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0002071	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0002074	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0002352	OMIM:204300	IEA				P		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0002367	OMIM:204300	TAS				P		HPO:probinson	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0003205	OMIM:204300	IEA				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0003208	OMIM:204300	IEA				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0003226	OMIM:204300	IEA				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0003581	OMIM:204300	IEA				C		HPO:iea	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0003657	OMIM:204300	IEA				P		HPO:skoehler	
OMIM	204300	CEROID LIPOFUSCINOSIS, NEURONAL, 4A, AUTOSOMAL RECESSIVE		HP:0008765	OMIM:204300	TAS				P		HPO:probinson	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0000007	OMIM:204500	IEA				I		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0000529	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0000546	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0000550	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0000750	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0001250	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0001251	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0001311	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0001336	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0002059	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0002074	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0002376	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0003205	OMIM:204500	IEA				P		HPO:iea	
OMIM	204500	CEROID LIPOFUSCINOSIS, NEURONAL, 2		HP:0003463	OMIM:204500	IEA				P		HPO:iea	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0000007	OMIM:204650	IEA				I		HPO:iea	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0000705	OMIM:204650	TAS				P		HPO:skoehler	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0001425	OMIM:204650	IEA				I		HPO:iea	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0006285	OMIM:204650	IEA				P		HPO:iea	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0006286	OMIM:204650	IEA				P		HPO:iea	
OMIM	204650	AMELOGENESIS IMPERFECTA, TYPE IC		HP:0009102	OMIM:204650	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000007	OMIM:204690	IEA				I		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000083	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000103	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000121	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000212	OMIM:204690	TAS				P		HPO:skoehler	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000696	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000705	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0000805	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0001548	OMIM:204690	IEA				P		HPO:skoehler	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0004727	OMIM:204690	IEA				P		HPO:iea	
OMIM	204690	204690 ENAMEL-RENAL SYNDROME; ERS;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS;;AMELOGENESIS IMPERFECTA, TYPE IG; AI1G		HP:0006302	OMIM:204690	IEA				P		HPO:iea	
OMIM	204700	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1		HP:0000007	OMIM:204700	TAS				I		HPO:skoehler	
OMIM	204700	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1		HP:0000670	OMIM:204700	TAS				P		HPO:skoehler	
OMIM	204700	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1		HP:0000705	OMIM:204700	TAS				P		HPO:skoehler	
OMIM	204700	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1; AI2A1		HP:0009102	OMIM:204700	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0000007	OMIM:204730	IEA				I		HPO:iea	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0000939	OMIM:204730	IEA				P		HPO:iea	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0001249	OMIM:204730	TAS				P		HPO:skoehler	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0001941	OMIM:204730	IEA				P		HPO:iea	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0003355	OMIM:204730	IEA				P		HPO:iea	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0003510	OMIM:204730	IEA				P		HPO:iea	
OMIM	204730	AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS		HP:0003560	OMIM:204730	IEA				P		HPO:iea	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0000007	OMIM:204750	IEA				I		HPO:iea	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0000252	OMIM:204750	TAS				P		HPO:skoehler	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0000750	OMIM:204750	TAS				P		HPO:skoehler	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0001256	OMIM:204750	IEA				P		HPO:iea	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0001263	OMIM:204750	TAS				P		HPO:skoehler	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0001290	OMIM:204750	TAS				P		HPO:skoehler	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0003355	OMIM:204750	IEA				P		HPO:skoehler	
OMIM	204750	2-AMINOADIPIC 2-OXOADIPIC ACIDURIA		HP:0007018	OMIM:204750	TAS				P		HPO:skoehler	
OMIM	204800	AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF		HP:0000007	OMIM:204800	IEA				I		HPO:iea	
OMIM	204800	AMOBARBITAL, DEFICIENT N-HYDROXYLATION OF		HP:0001939	OMIM:204800	IEA				P		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0000007	OMIM:204850	IEA				I		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0000153	OMIM:204850	IEA				P		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0000618	OMIM:204850	IEA				P		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0001249	OMIM:204850	IEA				P		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0007759	OMIM:204850	TAS				P		HPO:iea	
OMIM	204850	AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION		HP:0011034	OMIM:204850	IEA				P		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0000007	OMIM:204870	TAS				I		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0000613	OMIM:204870	TAS				P		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0000622	OMIM:204870	TAS				P		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0001131	OMIM:204870	TAS				P		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0007663	OMIM:204870	TAS				P		HPO:skoehler	
OMIM	204870	#204870 CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD;;CDGDL;;AMYLOIDOSIS, CORNEAL;;AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE;;CORNEAL DYSTROPHY, LATTICE TYPE III;;LATTICE CORNEAL DYSTROPHY, TYPE III		HP:0011463	OMIM:204870	TAS				C		HPO:skoehler	
OMIM	204900	AMYLOIDOSIS, CUTANEOUS BULLOUS		HP:0000007	OMIM:204900	IEA				I		HPO:iea	
OMIM	204900	AMYLOIDOSIS, CUTANEOUS BULLOUS		HP:0000951	OMIM:204900	IEA				P		HPO:iea	
OMIM	204900	AMYLOIDOSIS, CUTANEOUS BULLOUS		HP:0011034	OMIM:204900	IEA				P		HPO:skoehler	
OMIM	205000	AMYOTONIA CONGENITA		HP:0000007	OMIM:205000	IEA				I		HPO:iea	
OMIM	205000	AMYOTONIA CONGENITA		HP:0003202	OMIM:205000	IEA				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0000007	PMID:24562058	PCS				I		HPO:probinson	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0000183	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0001285	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0001332	OMIM:205100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0001347	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002015	OMIM:205100	IEA				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002061	OMIM:205100	TAS				P		HPO:probinson	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002064	OMIM:205100	TAS				P		HPO:probinson	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002127	OMIM:205100	IEA				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002193	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002307	OMIM:205100	TAS				P		HPO:skoehler	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002366	OMIM:205100	IEA				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002425	OMIM:205100	TAS				P		HPO:skoehler	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002464	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002491	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0002501	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0003444	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0003487	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0003676	OMIM:205100	TAS				C		HPO:skoehler	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0003677	OMIM:205100	TAS				C		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0003693	OMIM:205100	TAS				P		HPO:iea	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0006986	OMIM:205100	TAS				P		HPO:probinson	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0007354	OMIM:205100	TAS				P		HPO:probinson	
OMIM	205100	AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2		HP:0009130	OMIM:205100	IEA				P		HPO:iea	
OMIM	205200	AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA		HP:0000007	OMIM:205200	IEA				I		HPO:iea	
OMIM	205200	AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA		HP:0000726	OMIM:205200	IEA				P		HPO:iea	
OMIM	205200	AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA		HP:0003693	OMIM:205200	IEA				P		HPO:iea	
OMIM	205200	AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA		HP:0007354	OMIM:205200	TAS				P		HPO:skoehler	
OMIM	205250	AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES		HP:0000007	OMIM:205250	TAS				I		HPO:probinson	
OMIM	205250	AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES		HP:0002460	OMIM:205250	TAS				P		HPO:probinson	
OMIM	205250	AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES		HP:0002483	OMIM:205250	TAS				P		HPO:probinson	
OMIM	205250	AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES		HP:0003202	OMIM:205250	TAS				P		HPO:probinson	
OMIM	205250	AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES		HP:0007354	OMIM:205250	TAS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0000007	OMIM:205400	PCS				I		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0000505	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0000656	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0000958	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001265	OMIM:205400	TAS				P		HPO:skoehler	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001349	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001658	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001677	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001712	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0001744	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0002164	OMIM:205400	TAS				P		HPO:skoehler	
OMIM	205400	TANGIER DISEASE; TGD		HP:0002240	OMIM:205400	TAS				P		HPO:skoehler	
OMIM	205400	TANGIER DISEASE; TGD		HP:0003233	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0003477	OMIM:205400	TAS				P		HPO:skoehler	
OMIM	205400	TANGIER DISEASE; TGD		HP:0003693	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0007328	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0007759	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0008404	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0010829	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0011096	OMIM:205400	PCS				P		HPO:probinson	
OMIM	205400	TANGIER DISEASE; TGD		HP:0025608	OMIM:205400	IEA				P		HPO:skoehler	
OMIM	205700	ANEMIA, AUTOIMMUNE HEMOLYTIC		HP:0000007	OMIM:205700	IEA				I		HPO:iea	
OMIM	205700	ANEMIA, AUTOIMMUNE HEMOLYTIC		HP:0001890	OMIM:205700	IEA				P		HPO:iea	
OMIM	205700	ANEMIA, AUTOIMMUNE HEMOLYTIC		HP:0001939	OMIM:205700	IEA				P		HPO:iea	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0000007	OMIM:205950	IEA				I		HPO:iea	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0001425	OMIM:205950	IEA				I		HPO:skoehler	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0003281	OMIM:205950	IEA				P		HPO:skoehler	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0003593	OMIM:205950	IEA				C		HPO:skoehler	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0025066	OMIM:205950	TAS				P		HPO:skoehler	
OMIM	205950	ANEMIA, SIDEROBLASTIC, 2, PYRIDOXINE-REFRACTORY; SIDBA2		HP:0032231	OMIM:205950	IEA				P		HPO:skoehler	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:206000	IEA				I		HPO:iea	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0001417	OMIM:206000	IEA				I		HPO:iea	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0001433	OMIM:206000	IEA				P		HPO:iea	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0005522	OMIM:206000	IEA				P		HPO:iea	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0025066	OMIM:206000	TAS				P		HPO:skoehler	
OMIM	206000	ANEMIA, SIDEROBLASTIC, PYRIDOXINE-RESPONSIVE, AUTOSOMAL RECESSIVE		HP:0032231	OMIM:206000	IEA				P		HPO:skoehler	
OMIM	206100	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1		HP:0000007	OMIM:206100	IEA				I		HPO:iea	
OMIM	206100	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1		HP:0001392	OMIM:206100	IEA				P		HPO:iea	
OMIM	206100	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1		HP:0001939	OMIM:206100	IEA				P		HPO:iea	
OMIM	206100	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1		HP:0025066	OMIM:206100	TAS				P		HPO:skoehler	
OMIM	206100	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1; AHMIO1		HP:0032231	OMIM:206100	IEA				P		HPO:skoehler	
OMIM	206200	IRON-REFRACTORY IRON DEFICIENCY ANEMIA		HP:0000007	PMID:18408718	PCS				I		HPO:skoehler	
OMIM	206200	IRON-REFRACTORY IRON DEFICIENCY ANEMIA		HP:0004447	PMID:18408718	PCS				P		HPO:probinson	
OMIM	206200	IRON-REFRACTORY IRON DEFICIENCY ANEMIA		HP:0004840	PMID:18408718	PCS				P		HPO:probinson	
OMIM	206200	IRON-REFRACTORY IRON DEFICIENCY ANEMIA		HP:0011273	PMID:18408718	PCS				P		HPO:probinson	
OMIM	206200	IRON-REFRACTORY IRON DEFICIENCY ANEMIA		HP:0031877	PMID:23729726	PCS				P		HPO:lccarmody	
OMIM	206300	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF REDCELL MEMBRANE		HP:0000007	OMIM:206300	IEA				I		HPO:iea	
OMIM	206300	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF REDCELL MEMBRANE		HP:0001930	OMIM:206300	IEA				P		HPO:iea	
OMIM	206300	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, ASSOCIATED WITH ABNORMALITY OF REDCELL MEMBRANE		HP:0001939	OMIM:206300	IEA				P		HPO:iea	
OMIM	206400	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM		HP:0000007	OMIM:206400	IEA				I		HPO:iea	
OMIM	206400	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM		HP:0000952	OMIM:206400	IEA				P		HPO:iea	
OMIM	206400	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM		HP:0001744	OMIM:206400	IEA				P		HPO:iea	
OMIM	206400	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM		HP:0001930	OMIM:206400	IEA				P		HPO:iea	
OMIM	206400	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, POSSIBLY DUE TO DEFECT IN PORPHYRINMETABOLISM		HP:0003163	OMIM:206400	IEA				P		HPO:iea	
OMIM	206500	ANENCEPHALY; ANPH		HP:0002323	OMIM:206500	IEA				P		HPO:iea	
OMIM	206500	ANENCEPHALY; ANPH		HP:0002414	OMIM:206500	IEA				P		HPO:iea	
OMIM	206500	ANENCEPHALY; ANPH		HP:0003577	OMIM:206500	IEA				C		HPO:skoehler	
OMIM	206550	ANGIOLIPOMATOSIS, FAMILIAL		HP:0000007	OMIM:206550	TAS				I		HPO:probinson	
OMIM	206550	ANGIOLIPOMATOSIS, FAMILIAL		HP:0006773	OMIM:206550	TAS				P		HPO:probinson	
OMIM	206550	ANGIOLIPOMATOSIS, FAMILIAL		HP:0011462	OMIM:206550	TAS				C		HPO:probinson	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0000007	OMIM:206570	IEA				I		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0000712	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0000726	OMIM:206570	IEA				P		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0000822	OMIM:206570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0000965	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0001123	OMIM:206570	IEA				P		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0001250	OMIM:206570	IEA				P		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0001251	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0001260	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0002076	OMIM:206570	IEA				P		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0002119	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0002136	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0002200	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0002977	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0003745	OMIM:206570	TAS				I		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0007586	OMIM:206570	IEA				P		HPO:iea	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0012377	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206570	ANGIOMATOSIS, DIFFUSE CORTICOMENINGEAL, OF DIVRY AND VAN BOGAERT		HP:0012444	OMIM:206570	TAS				P		HPO:skoehler	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000007	OMIM:206600	IEA				I		HPO:iea	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000164	OMIM:206600	IEA				P		HPO:iea	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000707	OMIM:206600	IEA				P		HPO:iea	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000958	OMIM:206600	TAS				P		HPO:skoehler	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000970	OMIM:206600	IEA				P		HPO:iea	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0000972	OMIM:206600	TAS				P		HPO:skoehler	
OMIM	206600	206600 ANHIDROSIS, FAMILIAL GENERALIZED, WITH ABNORMAL OR ABSENT SWEAT GLANDS		HP:0011136	OMIM:206600	IEA				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0000006	OMIM:206700	IEA				I		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0000007	OMIM:206700	IEA				I		HPO:iea	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0000505	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0000526	OMIM:206700	IEA				P		HPO:iea	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0000639	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0001249	OMIM:206700	IEA				P		HPO:iea	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0001251	OMIM:206700	IEA				P		HPO:iea	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0001270	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0001321	OMIM:206700	IEA				P		HPO:iea	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0001350	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0002174	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206700	GILLESPIE SYNDROME; GLSP		HP:0007676	OMIM:206700	TAS				P		HPO:skoehler	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0000007	OMIM:206750	IEA				I		HPO:iea	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0000122	OMIM:206750	IEA				P		HPO:iea	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0000506	OMIM:206750	IEA				P		HPO:iea	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0000526	OMIM:206750	TAS				P		HPO:probinson	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0001087	OMIM:206750	IEA				P		HPO:iea	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0001249	OMIM:206750	IEA				P		HPO:iea	
OMIM	206750	ANIRIDIA, PARTIAL, WITH UNILATERAL RENAL AGENESIS AND PSYCHOMOTORRETARDATION		HP:0002007	OMIM:206750	IEA				P		HPO:iea	
OMIM	206780	ANODONTIA OF PERMANENT DENTITION		HP:0000007	OMIM:206780	IEA				I		HPO:iea	
OMIM	206780	ANODONTIA OF PERMANENT DENTITION		HP:0000674	OMIM:206780	TAS				P		HPO:probinson	
OMIM	206800	ANONYCHIA CONGENITA		HP:0000007	OMIM:206800	IEA				I		HPO:iea	
OMIM	206800	ANONYCHIA CONGENITA		HP:0001798	OMIM:206800	TAS	HP:0003577			P		HPO:probinson	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000006	OMIM:206900	IEA				I		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000028	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000044	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000047	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000054	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000252	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000407	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000528	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000568	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000589	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000609	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000902	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0000921	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001252	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001263	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001264	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001274	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001290	OMIM:206900	TAS				P		HPO:skoehler	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001328	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001629	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0001643	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002007	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002032	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002079	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002444	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002510	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002937	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0002948	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0003316	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0004322	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0005815	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0008417	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0008897	OMIM:206900	IEA				P		HPO:iea	
OMIM	206900	MICROPHTHALMIA, SYNDROMIC 3		HP:0010627	OMIM:206900	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000007	OMIM:206920	IEA				I		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000175	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000204	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000218	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000278	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000358	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000369	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000454	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000494	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000528	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000568	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000581	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0000954	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001162	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001180	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001215	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001249	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001510	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001595	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001626	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001762	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001770	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001830	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001849	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0001852	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0002002	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0002007	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0002827	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0002982	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0003038	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0003196	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0005280	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0005867	OMIM:206920	IEA				P		HPO:iea	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0008897	OMIM:206920	TAS				P		HPO:skoehler	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0011220	OMIM:206920	TAS				P		HPO:skoehler	
OMIM	206920	#206920 MICROPHTHALMIA WITH LIMB ANOMALIES;;WAARDENBURG ANOPHTHALMIA SYNDROME;;ANOPHTHALMIA-SYNDACTYLY;;OPHTHALMOACROMELIC SYNDROME; OAS		HP:0012745	OMIM:206920	TAS				P		HPO:skoehler	
OMIM	207000	ANOSMIA FOR ISOBUTYRIC ACID		HP:0000007	OMIM:207000	IEA				I		HPO:iea	
OMIM	207000	ANOSMIA FOR ISOBUTYRIC ACID		HP:0010633	OMIM:207000	TAS				P		HPO:probinson	
OMIM	207300	ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO		HP:0000007	OMIM:207300	TAS				I		HPO:probinson	
OMIM	207300	ANTITHROMBIN, FAMILIAL HEMORRHAGIC DIATHESIS DUE TO		HP:0001892	OMIM:207300	TAS				P		HPO:probinson	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000007	OMIM:207410	IEA				I		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000059	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000063	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000148	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000238	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000248	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000260	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000272	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000343	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000377	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000402	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000452	OMIM:207410	TAS				P		HPO:skoehler	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000453	OMIM:207410	TAS				P		HPO:probinson	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000520	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0000774	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0001166	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0001249	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0001371	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0001631	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0001838	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0002007	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0002781	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0002980	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0003031	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0003041	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0003275	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0004440	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0004443	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0005280	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0011800	OMIM:207410	TAS				P		HPO:skoehler	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0012210	OMIM:207410	IEA				P		HPO:iea	
OMIM	207410	#207410 ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS;ABS2;;TRAPEZOIDOCEPHALY-SYNOSTOSIS SYNDROME;;MULTISYNOSTOTIC OSTEODYSGENESIS WITH LONG BONE FRACTURES;;OSTEODYSGENESIS, MULTISYNOSTOTIC, WITH FRACTURES		HP:0012385	OMIM:207410	TAS				P		HPO:skoehler	
OMIM	207500	ANUS, IMPERFORATE		HP:0000007	OMIM:207500	TAS				I		HPO:nvasilevsky	
OMIM	207500	ANUS, IMPERFORATE		HP:0001426	PMID:4852015	TAS				I		HPO:nvasilevsky	
OMIM	207500	ANUS, IMPERFORATE		HP:0002023	OMIM:207500	IEA				P		HPO:iea	
OMIM	207600	TAKAYASU ARTERITIS		HP:0000007	OMIM:207600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	207600	TAKAYASU ARTERITIS		HP:0012089	OMIM:207600	TAS				P		HPO:probinson	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0000007	OMIM:207620	IEA				I		HPO:iea	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0000119	OMIM:207620	TAS				P		HPO:probinson	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0001629	OMIM:207620	IEA				P		HPO:iea	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0002089	OMIM:207620	IEA				P		HPO:iea	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0002937	OMIM:207620	IEA				P		HPO:iea	
OMIM	207620	207620 APHALANGY WITH HEMIVERTEBRAE		HP:0200113	OMIM:207620	TAS				P		HPO:skoehler	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0000007	OMIM:207720	IEA				I		HPO:iea	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0000020	OMIM:207720	TAS				P		HPO:iea	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0000961	OMIM:207720	TAS				P		HPO:iea	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0002793	OMIM:207720	IEA				P		HPO:iea	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0003128	OMIM:207720	TAS				P		HPO:iea	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0010535	OMIM:207720	TAS				P		HPO:skoehler	
OMIM	207720	207720 APNEA, CENTRAL SLEEP;;SLEEP APNEA, LETHAL CENTRAL		HP:0012195	OMIM:207720	TAS				P		HPO:skoehler	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0000007	OMIM:207731	IEA				I		HPO:iea	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0000245	OMIM:207731	IEA				P		HPO:skoehler	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0001888	OMIM:207731	IEA				P		HPO:iea	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0001892	OMIM:207731	IEA				P		HPO:skoehler	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0002593	OMIM:207731	IEA				P		HPO:iea	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0003075	OMIM:207731	IEA				P		HPO:iea	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0004471	OMIM:207731	IEA				P		HPO:iea	
OMIM	207731	APLASIA CUTIS CONGENITA WITH INTESTINAL LYMPHANGIECTASIA		HP:0007430	OMIM:207731	IEA				P		HPO:iea	
OMIM	207740	APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZEDPOLYNEUROPATHY		HP:0000007	OMIM:207740	IEA				I		HPO:iea	
OMIM	207740	APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZEDPOLYNEUROPATHY		HP:0000966	OMIM:207740	IEA				P		HPO:iea	
OMIM	207740	APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZEDPOLYNEUROPATHY		HP:0001271	OMIM:207740	IEA				P		HPO:iea	
OMIM	207740	APLASIA OF EXTENSOR MUSCLES OF FINGERS, UNILATERAL, WITH GENERALIZEDPOLYNEUROPATHY		HP:0003011	OMIM:207740	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0000007	OMIM:207750	IEA				I		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0000660	OMIM:207750	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0001013	OMIM:207750	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0001733	OMIM:207750	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0001744	OMIM:207750	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0002155	OMIM:207750	IEA				P		HPO:iea	
OMIM	207750	APOLIPOPROTEIN C-II DEFICIENCY		HP:0002240	OMIM:207750	IEA				P		HPO:iea	
OMIM	207770	APROSENCEPHALY SYNDROME		HP:0000007	OMIM:207770	IEA				I		HPO:iea	
OMIM	207770	APROSENCEPHALY SYNDROME		HP:0001180	OMIM:207770	IEA				P		HPO:iea	
OMIM	207770	APROSENCEPHALY SYNDROME		HP:0002323	OMIM:207770	IEA				P		HPO:iea	
OMIM	207770	APROSENCEPHALY SYNDROME		HP:0007268	OMIM:207770	IEA				P		HPO:iea	
OMIM	207780	AREDYLD		HP:0000007	OMIM:207780	TAS				I		HPO:skoehler	
OMIM	207780	AREDYLD		HP:0000303	OMIM:207780	IEA				P		HPO:iea	
OMIM	207780	AREDYLD		HP:0000598	OMIM:207780	IEA				P		HPO:iea	
OMIM	207780	AREDYLD		HP:0000968	OMIM:207780	IEA				P		HPO:skoehler	
OMIM	207780	AREDYLD		HP:0001939	OMIM:207780	IEA				P		HPO:iea	
OMIM	207780	AREDYLD		HP:0004528	OMIM:207780	IEA				P		HPO:iea	
OMIM	207790	207790 ARACHNOID CYSTS, INTRACRANIAL		HP:0000007	OMIM:207790	IEA				I		HPO:iea	
OMIM	207790	207790 ARACHNOID CYSTS, INTRACRANIAL		HP:0000252	OMIM:207790	IEA				P		HPO:iea	
OMIM	207790	207790 ARACHNOID CYSTS, INTRACRANIAL		HP:0000256	OMIM:207790	IEA				P		HPO:iea	
OMIM	207790	207790 ARACHNOID CYSTS, INTRACRANIAL		HP:0001249	OMIM:207790	IEA				P		HPO:iea	
OMIM	207790	207790 ARACHNOID CYSTS, INTRACRANIAL		HP:0100702	OMIM:207790	TAS				P		HPO:skoehler	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0000007	OMIM:207800	IEA				I		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0000737	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0000752	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0001249	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0001250	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0001263	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0001987	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0002013	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0002039	OMIM:207800	TAS				P		HPO:skoehler	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0002478	OMIM:207800	IEA				P		HPO:iea	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0003218	OMIM:207800	PCS				P		HPO:probinson	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0008339	OMIM:207800	IEA				P		HPO:probinson	
OMIM	207800	#207800 ARGININEMIA;;ARGINASE DEFICIENCY;;HYPERARGININEMIA;;ARG1 DEFICIENCY		HP:0008897	OMIM:207800	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0000007	OMIM:207900	IEA				I		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0000737	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001249	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001250	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001251	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001254	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001259	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001263	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001395	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001508	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001950	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001951	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0001987	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0002013	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0002038	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0002181	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0002240	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0002299	OMIM:207900	IEA				P		HPO:skoehler	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0003217	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0003218	OMIM:207900	TAS				P		HPO:skoehler	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0003355	OMIM:207900	IEA				P		HPO:skoehler	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0003623	OMIM:207900	TAS				C		HPO:probinson	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0005961	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0008872	OMIM:207900	IEA				P		HPO:iea	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0009886	OMIM:207900	IEA				P		HPO:skoehler	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0011359	OMIM:207900	TAS				P		HPO:skoehler	
OMIM	207900	ARGININOSUCCINIC ACIDURIA		HP:0031956	OMIM:207900	IEA				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0000238	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0000639	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0000961	OMIM:207950	IEA				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0001251	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0001252	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0001274	OMIM:207950	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0001290	OMIM:207950	TAS				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0001426	OMIM:207950	IEA				I		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002015	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002179	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002282	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002308	OMIM:207950	TAS				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002318	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002475	OMIM:207950	IEA				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0002483	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0003396	OMIM:207950	IEA				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0003690	OMIM:207950	IEA				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0005348	OMIM:207950	IEA				P		HPO:iea	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0011968	OMIM:207950	TAS				P		HPO:skoehler	
OMIM	207950	CHIARI MALFORMATION TYPE II		HP:0012318	OMIM:207950	TAS				P		HPO:probinson	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0000007	OMIM:208000	IEA				I		HPO:iea	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0000822	OMIM:208000	TAS				P		HPO:skoehler	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0001507	OMIM:208000	IEA				P		HPO:iea	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0001635	OMIM:208000	TAS				P		HPO:skoehler	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0001658	OMIM:208000	IEA				P		HPO:iea	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0001717	OMIM:208000	IEA				P		HPO:iea	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0004322	OMIM:208000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0004912	OMIM:208000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0004940	OMIM:208000	IEA				P		HPO:iea	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0025477	OMIM:208000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0031013	OMIM:208000	IEA				P		HPO:skoehler	
OMIM	208000	ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1		HP:0100545	OMIM:208000	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000007	OMIM:208050	IEA				I		HPO:iea	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000023	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000218	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000276	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000316	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000343	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000347	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000444	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000494	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000563	OMIM:208050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000581	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000767	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000768	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000776	OMIM:208050	TAS				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000822	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000973	OMIM:208050	IEA				P		HPO:iea	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0000978	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001027	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001166	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001249	OMIM:208050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001252	OMIM:208050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001290	OMIM:208050	TAS				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001371	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001388	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001537	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001650	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001659	OMIM:208050	IEA				P		HPO:iea	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001714	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0001977	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0002036	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0002140	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0003577	OMIM:208050	IEA				C		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0004415	OMIM:208050	TAS				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0004415	OMIM:208050	IEA				P		HPO:skoehler	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0004955	OMIM:208050	TAS				P		HPO:probinson	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0006687	OMIM:208050	IEA				P		HPO:iea	
OMIM	208050	ARTERIAL TORTUOSITY SYNDROME		HP:0007421	OMIM:208050	IEA				P		HPO:iea	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0000007	OMIM:208060	IEA				I		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0000822	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0000823	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0000951	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0001385	OMIM:208060	TAS				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0001658	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0001903	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0002592	OMIM:208060	IEA				P		HPO:skoehler	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0002634	OMIM:208060	TAS				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0004322	OMIM:208060	TAS				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0004589	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0004963	OMIM:208060	TAS				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0007768	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0008014	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0009803	OMIM:208060	IEA				P		HPO:probinson	
OMIM	208060	ARTERIOSCLEROSIS, SEVERE JUVENILE		HP:0012622	OMIM:208060	TAS				P		HPO:probinson	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0000007	OMIM:208080	IEA				I		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0000293	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0000321	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0000347	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0000824	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0001765	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES	HP:0012839	HP:0002804	OMIM:208080	TAS				P		HPO:skoehler	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0005684	OMIM:208080	TAS				P		HPO:probinson	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0006887	OMIM:208080	IEA				P		HPO:iea	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0010864	OMIM:208080	TAS				P		HPO:skoehler	
OMIM	208080	208080 ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES		HP:0100490	OMIM:208080	TAS				P		HPO:probinson	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0000007	OMIM:208081	IEA				I		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0000271	OMIM:208081	IEA				P		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0000774	OMIM:208081	IEA				P		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0001249	OMIM:208081	IEA				P		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0002093	OMIM:208081	IEA				P		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES	HP:0012839	HP:0002804	OMIM:208081	TAS				P		HPO:skoehler	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0002878	OMIM:208081	TAS				P		HPO:skoehler	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0003199	OMIM:208081	IEA				P		HPO:iea	
OMIM	208081	208081 ARTHROGRYPOSIS, DISTAL, WITH MENTAL RETARDATION AND CHARACTERISTICFACIES		HP:0005684	OMIM:208081	TAS				P		HPO:probinson	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000007	OMIM:208085	IEA				I		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000112	OMIM:208085	IEA				P		HPO:iea	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000121	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000252	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000340	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000347	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000369	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0000952	OMIM:208085	IEA				P		HPO:iea	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001252	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001263	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001290	OMIM:208085	TAS				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001339	OMIM:208085	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001385	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001508	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001522	OMIM:208085	IEA				M		HPO:iea	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001629	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001631	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001667	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001884	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001892	OMIM:208085	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001942	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001944	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0001947	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0002611	OMIM:208085	IEA				P		HPO:iea	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0002804	OMIM:208085	IEA				P		HPO:iea	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0002908	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0002910	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0008064	OMIM:208085	IEA				P		HPO:skoehler	
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0009806	OMIM:208085	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208085	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1		HP:0200084	OMIM:208085	TAS				P		HPO:skoehler	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0000007	OMIM:208100	IEA				I		HPO:iea	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0002803	OMIM:208100	IEA				P		HPO:skoehler	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0002804	OMIM:208100	TAS				P		HPO:probinson	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0003198	OMIM:208100	IEA				P		HPO:iea	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0003577	OMIM:208100	IEA				C		HPO:skoehler	
OMIM	208100	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE; AMCN		HP:0030680	OMIM:208100	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000007	OMIM:208150	IEA				I		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000028	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000160	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000175	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000218	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000238	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000316	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000343	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000347	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000358	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000437	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000470	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000506	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000508	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000520	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000581	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0000883	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001193	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001196	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001321	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001331	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001438	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001511	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001518	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001561	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001622	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001762	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001838	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0001989	OMIM:208150	TAS				P		HPO:skoehler	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0002089	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0002389	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0002644	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0002705	OMIM:208150	TAS				P		HPO:skoehler	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0002804	OMIM:208150	IEA				P		HPO:skoehler	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0003070	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0003100	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0003700	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0003826	OMIM:208150	TAS		HP:0040284		M		HPO:probinson	30%
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0005257	OMIM:208150	TAS				P		HPO:probinson	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0006266	OMIM:208150	IEA				P		HPO:iea	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0009487	OMIM:208150	TAS				P		HPO:skoehler	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0012745	OMIM:208150	TAS				P		HPO:skoehler	
OMIM	208150	FETAL AKINESIA DEFORMATION SEQUENCE; FADS		HP:0100490	OMIM:208150	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0000007	OMIM:208155	IEA				I		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0000201	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0000346	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0000707	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0001662	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0002104	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0002804	OMIM:208155	TAS				P		HPO:probinson	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0003761	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0003781	OMIM:208155	IEA				P		HPO:iea	
OMIM	208155	ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE		HP:0005968	OMIM:208155	IEA				P		HPO:iea	
OMIM	208158	ARTHROGRYPOSIS - HYPERKERATOSIS, LETHAL FORM		HP:0002804	OMIM:208158	IEA				P		HPO:skoehler	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0000007	OMIM:208230	IEA				I		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0000926	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0000939	OMIM:208230	IEA				P		HPO:skoehler	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0001324	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0001386	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0001387	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0001760	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002355	OMIM:208230	TAS				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002515	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002751	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002758	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002812	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0002970	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0003016	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0003040	OMIM:208230	TAS				P		HPO:skoehler	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0003071	OMIM:208230	TAS				P		HPO:probinson	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0003371	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0004576	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0004637	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0006163	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0006247	OMIM:208230	IEA				P		HPO:iea	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0010580	OMIM:208230	TAS				P		HPO:probinson	
OMIM	208230	ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD		HP:0100490	OMIM:208230	TAS				P		HPO:skoehler	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0000007	OMIM:208250	IEA				I		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0001239	OMIM:208250	IEA				P		HPO:skoehler	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0001369	OMIM:208250	IEA				P		HPO:skoehler	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0002563	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0002812	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0003040	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0005186	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0005194	OMIM:208250	TAS				P		HPO:probinson	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0005197	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0005879	OMIM:208250	IEA				P		HPO:iea	
OMIM	208250	CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME		HP:0011909	OMIM:208250	TAS				P		HPO:probinson	
OMIM	208300	ASCITES, CHYLOUS		HP:0000007	OMIM:208300	IEA				I		HPO:iea	
OMIM	208300	ASCITES, CHYLOUS		HP:0000501	OMIM:208300	TAS				P		HPO:skoehler	
OMIM	208300	ASCITES, CHYLOUS		HP:0012281	OMIM:208300	TAS	HP:0003577			P		HPO:probinson	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000007	OMIM:208400	IEA				I		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000053	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000154	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000158	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000179	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000248	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000252	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000280	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000283	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000463	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000518	OMIM:208400	IEA				P		HPO:skoehler	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000750	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000926	OMIM:208400	TAS				P		HPO:probinson	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0000943	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001061	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001071	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001249	OMIM:208400	TAS				P		HPO:skoehler	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001250	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001252	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001257	OMIM:208400	TAS				P		HPO:skoehler	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001290	OMIM:208400	TAS				P		HPO:skoehler	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001388	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001609	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001653	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001875	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001922	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0001939	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002014	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002059	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002205	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002240	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002376	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002650	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002684	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002738	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002750	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002756	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0002808	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0003302	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0003304	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0004322	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0004568	OMIM:208400	TAS				P		HPO:probinson	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0005280	OMIM:208400	IEA				P		HPO:iea	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0012068	OMIM:208400	TAS				P		HPO:probinson	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0032198	OMIM:208400	IEA				P		HPO:skoehler	
OMIM	208400	ASPARTYLGLUCOSAMINURIA; AGU		HP:0100790	OMIM:208400	TAS				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000007	OMIM:208500	IEA				I		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000083	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000093	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000107	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000123	OMIM:208500	IEA				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000546	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000773	OMIM:208500	TAS				P		HPO:probinson	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000774	OMIM:208500	IEA				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000888	OMIM:208500	TAS				P		HPO:probinson	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0000952	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001156	OMIM:208500	TAS				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001161	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001395	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001408	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001522	OMIM:208500	TAS		HP:0040283		M		HPO:probinson	HP:0040283
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001737	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0001829	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0002089	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0002093	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0002205	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0002866	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0002908	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0003022	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0003025	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0003038	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0003828	OMIM:208500	TAS				C		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0004322	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0006557	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0006644	OMIM:208500	IEA				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0008797	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0008839	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0009803	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0010230	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0010444	OMIM:208500	IEA				P		HPO:skoehler	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0010582	OMIM:208500	IEA				P		HPO:iea	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0012622	OMIM:208500	TAS				P		HPO:probinson	
OMIM	208500	SHORT-RIB THORACIC DYSPLASIA 1 WITH OR WITHOUT POLYDACTYLY; SRTD1		HP:0100732	OMIM:208500	TAS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0000007	PMID:20413652	PCS				I		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0000023	PMID:28991257	PCS		HP:0040284		P		HP:probinson	2/10
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001274	OMIM:208530	IEA				P		HPO:iea	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001629	OMIM:208530	TAS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001631	OMIM:208530	TAS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001636	PMID:28991257	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/10
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001642	OMIM:208530	IEA				P		HPO:iea	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001669	PMID:28991257	PCS		HP:0040284		P		HP:probinson	7/10
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001674	OMIM:208530	IEA				P		HPO:iea	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001696	PMID:20413652	PCS		HP:0040284		P		HPO:skoehler	2/5
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001746	PMID:20413652	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001748	OMIM:208530	IEA				P		HPO:iea	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0001750	PMID:20413652	PCS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0002101	OMIM:208530	TAS				P		HPO:probinson	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0004935	PMID:20413652	PCS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0005160	PMID:20413652	PCS	HP:0003577	HP:0040284		P		HP:probinson	5/5
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0011536	PMID:20413652	PCS				P		HPO:skoehler	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0011565	PMID:20413652	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0031565	PMID:17924340	PCS				P		HP:probinson	
OMIM	208530	ASPLENIA WITH CARDIOVASCULAR ANOMALIES		HP:0031834	PMID:20413652	PCS		HP:0040284		P		HP:probinson	1/5
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0000007	OMIM:208540	IEA				I		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0000083	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0000105	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0000110	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0000113	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001305	OMIM:208540	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001394	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001395	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001396	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001407	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001408	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001562	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001631	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001643	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001650	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001737	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001746	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0001748	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0002009	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0002089	OMIM:208540	TAS				P		HPO:probinson	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0002240	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0002566	OMIM:208540	TAS				P		HPO:probinson	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0002613	OMIM:208540	IEA				P		HPO:iea	
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0005999	OMIM:208540	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	208540	#208540 RENAL-HEPATIC-PANCREATIC DYSPLASIA; RHPD		HP:0100732	OMIM:208540	TAS				P		HPO:skoehler	
OMIM	208550	ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE		HP:0000007	OMIM:208550	IEA				I		HPO:iea	
OMIM	208550	ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE		HP:0002099	OMIM:208550	IEA				P		HPO:iea	
OMIM	208550	ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE		HP:0012042	OMIM:208550	TAS				P		HPO:probinson	
OMIM	208550	ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE		HP:0100582	OMIM:208550	TAS				P		HPO:skoehler	
OMIM	208600	ASTHMA, SHORT STATURE, AND ELEVATED IGA		HP:0000007	OMIM:208600	IEA				I		HPO:iea	
OMIM	208600	ASTHMA, SHORT STATURE, AND ELEVATED IGA		HP:0002099	OMIM:208600	IEA				P		HPO:iea	
OMIM	208600	ASTHMA, SHORT STATURE, AND ELEVATED IGA		HP:0003261	OMIM:208600	IEA				P		HPO:iea	
OMIM	208600	ASTHMA, SHORT STATURE, AND ELEVATED IGA		HP:0004322	OMIM:208600	IEA				P		HPO:iea	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0000007	OMIM:208700	IEA				I		HPO:iea	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0000726	OMIM:208700	IEA				P		HPO:iea	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0001250	OMIM:208700	IEA				P		HPO:skoehler	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0001251	OMIM:208700	IEA				P		HPO:iea	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0001271	OMIM:208700	IEA				P		HPO:iea	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0001336	OMIM:208700	IEA				P		HPO:skoehler	
OMIM	208700	ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA		HP:0002123	OMIM:208700	TAS				P		HPO:skoehler	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0000007	OMIM:208750	IEA				I		HPO:iea	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0000407	OMIM:208750	IEA				P		HPO:iea	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0000951	OMIM:208750	IEA				P		HPO:iea	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0001249	OMIM:208750	IEA				P		HPO:iea	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0001251	OMIM:208750	IEA				P		HPO:iea	
OMIM	208750	ATAXIA, DEAFNESS, AND CARDIOMYOPATHY		HP:0001638	OMIM:208750	IEA				P		HPO:iea	
OMIM	208850	ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0000007	OMIM:208850	IEA				I		HPO:iea	
OMIM	208850	ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0000408	OMIM:208850	IEA				P		HPO:iea	
OMIM	208850	ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001249	OMIM:208850	IEA				P		HPO:iea	
OMIM	208850	ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001251	OMIM:208850	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0000007	OMIM:208870	IEA				I		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0000252	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0000519	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0000639	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0001249	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0001251	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0001252	OMIM:208870	IEA				P		HPO:iea	
OMIM	208870	ATAXIA-MICROCEPHALY-CATARACT SYNDROME		HP:0001290	OMIM:208870	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000007	OMIM:208900	IEA				I		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000134	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000246	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000486	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000524	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000639	OMIM:208900	IEA				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000778	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000819	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000823	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0000957	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001250	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001251	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001260	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001266	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001315	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001332	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001336	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001337	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001595	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001909	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0001952	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0002110	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0002665	OMIM:208900	IEA				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0002720	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0002837	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0004322	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0005357	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0005407	OMIM:208900	TAS				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0006254	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0008348	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0008669	OMIM:208900	IEA				P		HPO:iea	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0012189	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208900	#208900 ATAXIA-TELANGIECTASIA; AT;;AT1;;LOUIS-BAR SYNDROMEAT, COMPLEMENTATION GROUP A, INCLUDED; ATA, INCLUDED;;AT, COMPLEMENTATION GROUP C, INCLUDED; ATC, INCLUDED;;AT, COMPLEMENTATION GROUP D, INCLUDED; ATD, INCLUDED;;AT, COMPLEMENTATION GROUP E, INCLUDED; ATE, INCLUDED;;ATAXIA-TELANGIECTASIA VARIANT, INCLUDED		HP:0012539	OMIM:208900	TAS				P		HPO:skoehler	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0000007	OMIM:208910	IEA				I		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0000524	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0000657	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0000777	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0001251	OMIM:208910	IEA				P		HPO:skoehler	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0001332	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0001522	OMIM:208910	IEA				M		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0001909	OMIM:208910	IEA				P		HPO:skoehler	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0001952	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0002720	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0003220	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0006254	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0007181	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0007380	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0007440	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0009067	OMIM:208910	IEA				P		HPO:iea	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0009473	OMIM:208910	IEA				P		HPO:skoehler	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0040012	OMIM:208910	TAS				P		HPO:skoehler	
OMIM	208910	ATAXIA-TELANGIECTASIA WITH GENERALIZED SKIN PIGMENTATION AND EARLY DEATH		HP:0040270	OMIM:208910	TAS				P		HPO:skoehler	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000007	OMIM:208920	TAS				I		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000571	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000590	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000640	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000657	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000726	OMIM:208920	TAS				P		HPO:skoehler	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0000764	OMIM:208920	PCS				P		HPO:probinson	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001251	PMID:14506070	PCS				P		HPO:probinson	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001260	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001265	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001266	PMID:14506070	PCS		HP:0040284		P		HPO:probinson	79%
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001268	OMIM:208920	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001272	OMIM:208920	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001284	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001324	OMIM:208920	TAS				P		HPO:skoehler	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001332	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001337	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0001761	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0002066	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0002070	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0002078	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0002650	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0002936	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003073	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003124	PMID:14506070	PCS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003387	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003581	OMIM:208920	TAS				C		HPO:skoehler	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003621	OMIM:208920	PCS				C		HPO:probinson	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0003693	OMIM:208920	TAS				P		HPO:iea	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0040078	OMIM:208920	IEA				P		HPO:skoehler	
OMIM	208920	ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA; EAOH		HP:0100543	PMID:14506070	PCS				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0000007	OMIM:209010	IEA				I		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0000093	OMIM:209010	IEA				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0000112	OMIM:209010	TAS				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0000407	OMIM:209010	IEA				P		HPO:skoehler	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0000819	OMIM:209010	IEA				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0001317	OMIM:209010	IEA				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0001327	OMIM:209010	IEA				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0001677	OMIM:209010	IEA				P		HPO:skoehler	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0001920	OMIM:209010	IEA				P		HPO:iea	
OMIM	209010	ATHEROSCLEROSIS, PREMATURE, WITH DEAFNESS, NEPHROPATHY, DIABETES MELLITUS,PHOTOMYOCLONUS, AND DEGENERATIVE NEUROLOGIC DISEASE		HP:0007201	OMIM:209010	IEA				P		HPO:iea	
OMIM	209050	ATHROMBIA, ESSENTIAL		HP:0000007	OMIM:209050	IEA				I		HPO:iea	
OMIM	209050	ATHROMBIA, ESSENTIAL		HP:0001892	OMIM:209050	IEA				P		HPO:skoehler	
OMIM	209050	ATHROMBIA, ESSENTIAL		HP:0003010	OMIM:209050	TAS				P		HPO:probinson	
OMIM	209050	ATHROMBIA, ESSENTIAL		HP:0003540	OMIM:209050	TAS				P		HPO:probinson	
OMIM	209050	ATHROMBIA, ESSENTIAL		HP:0008352	OMIM:209050	IEA				P		HPO:iea	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0000007	OMIM:209100	IEA				I		HPO:iea	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0001251	OMIM:209100	IEA				P		HPO:iea	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0001252	OMIM:209100	IEA				P		HPO:iea	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0001290	OMIM:209100	TAS				P		HPO:skoehler	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0002540	OMIM:209100	TAS				P		HPO:skoehler	
OMIM	209100	ATONIC-ASTATIC SYNDROME OF FOERSTER		HP:0012651	OMIM:209100	TAS				P		HPO:skoehler	
OMIM	209300	ATRANSFERRINEMIA		HP:0000007	OMIM:209300	TAS				I		HPO:probinson	
OMIM	209300	ATRANSFERRINEMIA		HP:0001392	OMIM:209300	IEA				P		HPO:iea	
OMIM	209300	ATRANSFERRINEMIA		HP:0001635	OMIM:209300	TAS				P		HPO:probinson	
OMIM	209300	ATRANSFERRINEMIA		HP:0001931	OMIM:209300	TAS				P		HPO:probinson	
OMIM	209300	ATRANSFERRINEMIA		HP:0012239	OMIM:209300	TAS				P		HPO:probinson	
OMIM	209500	ATRICHIA WITH PAPULAR LESIONS		HP:0000007	OMIM:209500	IEA				I		HPO:iea	
OMIM	209500	ATRICHIA WITH PAPULAR LESIONS		HP:0001006	OMIM:209500	IEA				P		HPO:iea	
OMIM	209500	ATRICHIA WITH PAPULAR LESIONS		HP:0007482	OMIM:209500	IEA				P		HPO:iea	
OMIM	209600	ATRIOVENTRICULAR DISSOCIATION		HP:0000007	OMIM:209600	IEA				I		HPO:iea	
OMIM	209600	ATRIOVENTRICULAR DISSOCIATION		HP:0004752	OMIM:209600	IEA				P		HPO:iea	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0000006	OMIM:209700	TAS				I		HPO:skoehler	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0000007	OMIM:209700	IEA				I		HPO:iea	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0001056	OMIM:209700	TAS				P		HPO:skoehler	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0001626	OMIM:209700	IEA				P		HPO:iea	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0001820	OMIM:209700	TAS				P		HPO:skoehler	
OMIM	209700	ATROPHODERMA VERMICULATA; AVA		HP:0100837	OMIM:209700	IEA				P		HPO:skoehler	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0000007	OMIM:209770	IEA				I		HPO:iea	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0000413	OMIM:209770	IEA				P		HPO:iea	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0001249	OMIM:209770	IEA				P		HPO:iea	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0001438	OMIM:209770	IEA				P		HPO:iea	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0001629	OMIM:209770	IEA				P		HPO:iea	
OMIM	209770	AURAL ATRESIA, MULTIPLE CONGENITAL ANOMALIES, AND MENTAL RETARDATION		HP:0001762	OMIM:209770	IEA				P		HPO:iea	
OMIM	209800	AUSTRALIA ANTIGEN		HP:0000007	PMID:14239025	TAS				I		HPO:nvasilevsky	
OMIM	209800	AUSTRALIA ANTIGEN		HP:0000717	OMIM:209800	IEA				P		HPO:iea	
OMIM	209800	AUSTRALIA ANTIGEN		HP:0001263	OMIM:209800	TAS				P		HPO:nvasilevsky	
OMIM	209800	AUSTRALIA ANTIGEN		HP:0001426	OMIM:209800	TAS				I		HPO:nvasilevsky	
OMIM	209850	AUTISM		HP:0000717	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0000721	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0000723	OMIM:209850	TAS				P		HPO:skoehler	
OMIM	209850	AUTISM		HP:0000728	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0000732	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0000733	OMIM:209850	TAS				P		HPO:skoehler	
OMIM	209850	AUTISM		HP:0000750	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0000758	OMIM:209850	TAS				P		HPO:probinson	
OMIM	209850	AUTISM		HP:0001249	OMIM:209850	IEA				P		HPO:iea	
OMIM	209850	AUTISM		HP:0001250	OMIM:209850	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	209850	AUTISM		HP:0001425	OMIM:209850	TAS				I		HPO:skoehler	
OMIM	209850	AUTISM		HP:0001426	OMIM:209850	IEA				I		HPO:iea	
OMIM	209850	AUTISM		HP:0002353	OMIM:209850	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	209850	AUTISM		HP:0003144	OMIM:209850	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	209850	AUTISM		HP:0003745	OMIM:209850	IEA				I		HPO:iea	
OMIM	209850	AUTISM		HP:0011463	OMIM:209850	IEA				C		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000006	OMIM:209880	TAS				I		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000153	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000358	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000369	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000494	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0000975	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0001626	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0002019	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0002104	OMIM:209880	IEA				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0002251	OMIM:209880	IEA				P		HPO:iea	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0002791	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0003005	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0004370	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0006747	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0007110	OMIM:209880	IEA				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0011968	OMIM:209880	TAS				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0012416	OMIM:209880	IEA				P		HPO:skoehler	
OMIM	209880	CENTRAL HYPOVENTILATION SYNDROME, CONGENITAL; CCHS		HP:0012418	OMIM:209880	IEA				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000006	OMIM:209885	TAS				I		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000032	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000055	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000154	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000233	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000303	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000316	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000347	OMIM:209885	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000365	OMIM:209885	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000369	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000377	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000414	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000430	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000506	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000535	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000656	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000684	OMIM:209885	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000958	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0000998	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0001249	OMIM:209885	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0001582	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0002557	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0002561	OMIM:209885	IEA				P		HPO:skoehler	
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0002705	OMIM:209885	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209885	BARBER-SAY SYNDROME; BBRSAY		HP:0004334	OMIM:209885	TAS				P		HPO:skoehler	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000007	PMID:9039982	PCS				I		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000054	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000077	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000135	PMID:26762677	PCS				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000137	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000148	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000218	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000256	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000365	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000483	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000486	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000501	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000510	PMID:26762677	PCS				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000518	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000545	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000546	OMIM:209900	TAS				P		HPO:skoehler	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000556	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000639	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000668	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000678	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000750	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000819	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0000822	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001007	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001080	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001156	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001159	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001162	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001249	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001251	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001263	OMIM:209900	TAS				P		HPO:skoehler	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001328	PMID:26762677	PCS				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001395	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001513	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001712	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001769	OMIM:209900	TAS				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001773	OMIM:209900	TAS				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0001829	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002099	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002141	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002167	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002251	OMIM:209900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002370	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0002705	OMIM:209900	TAS				P		HPO:skoehler	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0008734	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0009466	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0009806	OMIM:209900	IEA				P		HPO:iea	
OMIM	209900	BARDET-BIEDL SYNDROME 1; BBS1		HP:0012393	PMID:26762677	PCS				P		HP:probinson	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0000006	OMIM:209920	IEA				I		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0000007	OMIM:209920	TAS				I		HPO:skoehler	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0000010	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0001508	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0001875	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002024	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002383	OMIM:209920	IEA				P		HPO:skoehler	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002583	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002718	OMIM:209920	TAS				P		HPO:probinson	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002728	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002783	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002788	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002841	OMIM:209920	TAS				P		HPO:probinson	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0002965	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0003139	OMIM:209920	TAS				P		HPO:probinson	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0004385	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0004429	OMIM:209920	TAS				P		HPO:probinson	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0004432	OMIM:209920	IEA				P		HPO:skoehler	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0005386	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0006562	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0007041	OMIM:209920	IEA				P		HPO:iea	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0011473	OMIM:209920	TAS				P		HPO:skoehler	
OMIM	209920	BARE LYMPHOCYTE SYNDROME, TYPE II		HP:0030151	OMIM:209920	IEA				P		HPO:skoehler	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0000007	PMID:7815885	PCS				I		HPO:iea	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001433	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001438	OMIM:209950	IEA				P		HPO:iea	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001744	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001824	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001894	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001903	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001945	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0001974	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002014	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002039	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002090	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002113	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002716	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0002923	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0003073	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0003237	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0003496	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0003565	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0005661	OMIM:209950	IEA				P		HPO:iea	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0008802	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0025043	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0025427	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0030166	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209950	ATYPICAL MYCOBACTERIOSIS, FAMILIAL		HP:0100727	PMID:7815885	PCS				P		HPO:lccarmody	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0000007	OMIM:209970	IEA				I		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0000062	OMIM:209970	IEA				P		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0000238	OMIM:209970	IEA				P		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0000431	OMIM:209970	IEA				P		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0000924	OMIM:209970	IEA				P		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0001873	OMIM:209970	IEA				P		HPO:iea	
OMIM	209970	BEEMER LETHAL MALFORMATION SYNDROME		HP:0030680	OMIM:209970	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0000007	OMIM:210000	IEA				I		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0000529	OMIM:210000	TAS				P		HPO:skoehler	
OMIM	210000	BEHR SYNDROME		HP:0000639	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0000648	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0001249	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0001270	OMIM:210000	TAS				P		HPO:skoehler	
OMIM	210000	BEHR SYNDROME		HP:0001272	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0001288	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0001310	OMIM:210000	TAS				P		HPO:skoehler	
OMIM	210000	BEHR SYNDROME		HP:0001337	OMIM:210000	TAS				P		HPO:skoehler	
OMIM	210000	BEHR SYNDROME		HP:0001347	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0001771	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0002191	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0003089	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0003487	OMIM:210000	IEA				P		HPO:iea	
OMIM	210000	BEHR SYNDROME		HP:0003676	OMIM:210000	TAS				C		HPO:skoehler	
OMIM	210000	BEHR SYNDROME		HP:0006366	OMIM:210000	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0000007	OMIM:210050	IEA				I		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0001250	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0001263	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0001394	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0001399	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0001409	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0002097	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0004322	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0007029	OMIM:210050	IEA				P		HPO:iea	
OMIM	210050	BERRY ANEURYSM, CIRRHOSIS, PULMONARY EMPHYSEMA, AND CEREBRAL CALCIFICATION		HP:0007238	OMIM:210050	IEA				P		HPO:iea	
OMIM	210100	BETA-AMINOISOBUTYRIC ACID, URINARY EXCRETION OF		HP:0000007	OMIM:210100	IEA				I		HPO:iea	
OMIM	210100	BETA-AMINOISOBUTYRIC ACID, URINARY EXCRETION OF		HP:0003355	OMIM:210100	IEA				P		HPO:skoehler	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0000007	OMIM:210200	IEA				I	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001249	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:skoehler	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001250	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001252	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001254	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001259	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001263	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001290	OMIM:210200	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:skoehler	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001347	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001425	OMIM:210200	TAS				I	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:skoehler	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001508	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0001943	OMIM:210200	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:probinson	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0002013	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0002179	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0002919	OMIM:210200	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:probinson	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0004911	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0006573	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0008281	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0008872	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:iea	
OMIM	210200	3-METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY; MCC1D		HP:0025356	OMIM:210200	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 1 DEFICIENCY; MCC1D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0000007	OMIM:210210	IEA				I	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001051	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001249	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001250	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001252	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001254	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001259	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001263	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001290	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001347	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001425	OMIM:210210	TAS				I	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001508	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001596	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001942	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001943	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001992	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0001993	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0002013	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0002179	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0002919	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0003108	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0003202	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0003353	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:iea	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0008281	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0011968	OMIM:210210	TAS				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210210	3-METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY; MCC2D		HP:0025356	OMIM:210210	IEA				P	3-METHYLCROTONYL-COA CARBOXYLASE 2 DEFICIENCY; MCC2D	HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0000007	OMIM:210250	IEA				I		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001369	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001392	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001574	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001677	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001744	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001892	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001902	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0001923	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0002027	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0002829	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0003124	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0003540	OMIM:210250	TAS				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0004446	OMIM:210250	IEA				P		HPO:skoehler	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0004802	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0004870	OMIM:210250	IEA				P		HPO:iea	
OMIM	210250	#210250 SITOSTEROLEMIA;;STSL;;PHYTOSTEROLEMIAMACROTHROMBOCYTOPENIA/STOMATOCYTOSIS, MEDITERRANEAN, INCLUDED		HP:0008158	OMIM:210250	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0000007	OMIM:210350	IEA				I		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0000238	OMIM:210350	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0000612	OMIM:210350	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0000818	OMIM:210350	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0001177	OMIM:210350	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0001249	OMIM:210350	IEA				P		HPO:iea	
OMIM	210350	BIEMOND SYNDROME II		HP:0004322	OMIM:210350	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0000007	OMIM:210370	IEA				I		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0000529	OMIM:210370	TAS				P		HPO:skoehler	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0000533	OMIM:210370	TAS				P		HPO:probinson	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0000546	OMIM:210370	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0001133	OMIM:210370	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0001871	OMIM:210370	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0007675	OMIM:210370	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0007880	OMIM:210370	IEA				P		HPO:iea	
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0011003	OMIM:210370	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210370	BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD		HP:0030528	OMIM:210370	IEA				P		HPO:skoehler	
OMIM	210400	210400 BIFID NOSE, AUTOSOMAL RECESSIVE;;MEDIAN FISSURE OF NOSE;;NOSE, MEDIAN CLEFT OF		HP:0000007	OMIM:210400	IEA				I		HPO:iea	
OMIM	210400	210400 BIFID NOSE, AUTOSOMAL RECESSIVE;;MEDIAN FISSURE OF NOSE;;NOSE, MEDIAN CLEFT OF		HP:0004122	OMIM:210400	IEA				P		HPO:iea	
OMIM	210400	210400 BIFID NOSE, AUTOSOMAL RECESSIVE;;MEDIAN FISSURE OF NOSE;;NOSE, MEDIAN CLEFT OF		HP:0011803	OMIM:210400	TAS				P		HPO:skoehler	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0000952	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0001394	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0001408	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0002240	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0002910	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0003573	OMIM:210500	TAS				P		HPO:skoehler	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0003593	OMIM:210500	TAS				C		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0003676	OMIM:210500	TAS				C		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0005242	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0006580	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0008282	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0011984	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210500	%210500 BILIARY ATRESIA, EXTRAHEPATIC; EHBA		HP:0011985	OMIM:210500	TAS				P		HPO:probinson	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000006	OMIM:210550	TAS				I		HPO:nvasilevsky	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000093	OMIM:210550	TAS				P		HPO:probinson	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000124	OMIM:210550	TAS				P		HPO:skoehler	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000218	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000347	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000369	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000952	OMIM:210550	IEA				P		HPO:skoehler	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0000954	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001252	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001290	OMIM:210550	TAS				P		HPO:skoehler	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001419	OMIM:210550	TAS				I		HPO:nvasilevsky	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001508	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001552	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001762	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0001996	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0002719	OMIM:210550	TAS				P		HPO:skoehler	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0002827	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0002908	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0002909	OMIM:210550	IEA				P		HPO:iea	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0003076	OMIM:210550	TAS				P		HPO:probinson	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0003355	OMIM:210550	TAS				P		HPO:probinson	
OMIM	210550	BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY		HP:0006560	OMIM:210550	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000007	OMIM:210600	IEA				I		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000028	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000047	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000175	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000218	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000237	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000252	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000324	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000340	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000347	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000369	OMIM:210600	TAS				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000377	OMIM:210600	IEA				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000444	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000448	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000486	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000494	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000581	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000678	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000689	OMIM:210600	IEA				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000752	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000878	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0000954	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001090	OMIM:210600	IEA				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001249	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001250	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001302	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001320	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001511	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001592	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001763	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001852	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001876	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0001883	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0002650	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0002750	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0002827	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0002987	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0003083	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0003508	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0004209	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0006143	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0006297	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0006434	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0006442	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0007048	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0008665	OMIM:210600	IEA				P		HPO:iea	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0008897	OMIM:210600	TAS				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0010230	OMIM:210600	TAS				P		HPO:skoehler	
OMIM	210600	SECKEL SYNDROME 1; SCKL1		HP:0010583	OMIM:210600	IEA				P		HPO:skoehler	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000007	OMIM:210700	IEA				I		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000028	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000275	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000278	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000444	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0000508	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0001090	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0001249	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0002216	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0002293	OMIM:210700	TAS				P		HPO:skoehler	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0003510	OMIM:210700	IEA				P		HPO:iea	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0006872	PMID:5458566	PCS				P		HP:probinson	
OMIM	210700	MICROCEPHALIC PRIMORDIAL DWARFISM, MONTREAL TYPE		HP:0007605	OMIM:210700	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000007	OMIM:210710	IEA				I		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000028	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000054	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000089	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000107	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000237	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000252	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000269	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000340	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000347	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000369	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000377	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000448	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000470	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000520	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000535	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000653	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000878	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000890	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000926	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000946	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000954	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000958	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0000962	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001156	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001176	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001249	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001250	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001274	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001302	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001508	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001511	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001562	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001631	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001636	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001680	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0001833	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002209	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002282	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002335	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002750	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002827	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002980	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002983	OMIM:210710	TAS				P		HPO:skoehler	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0002987	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003042	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003044	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003051	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003097	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003273	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003498	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003826	OMIM:210710	IEA				M		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0003865	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0004616	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0005792	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0006380	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0006400	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0006579	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0007333	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0008551	OMIM:210710	TAS				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0009826	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210710	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I		HP:0010049	OMIM:210710	IEA				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000007	OMIM:210720	TAS				I		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000047	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000252	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000278	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000340	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000426	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000448	OMIM:210720	TAS				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000540	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000582	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000691	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000774	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000826	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000882	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000890	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0000957	OMIM:210720	TAS				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001156	OMIM:210720	TAS				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001249	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001263	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001377	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001511	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001620	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0001956	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002209	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002690	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002750	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002812	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002866	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002982	OMIM:210720	IEA				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0002986	OMIM:210720	IEA				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0003015	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0003031	OMIM:210720	IEA				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0003100	PMID:15372530	PCS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0003275	OMIM:210720	IEA				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0003498	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0004209	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0004944	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0005819	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0005978	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0006297	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0006461	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0006587	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0006645	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0007402	OMIM:210720	TAS				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0008551	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2	HP:0012828	HP:0008897	OMIM:210720	TAS				P		HPO:skoehler	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0009193	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0009882	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0010034	OMIM:210720	IEA				P		HPO:iea	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0010579	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0010583	OMIM:210720	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0011834	OMIM:210720	TAS				P		HPO:probinson	
OMIM	210720	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2		HP:0100263	OMIM:210720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000007	OMIM:210730	IEA				I		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000047	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000215	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000218	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000219	OMIM:210730	TAS				P		HPO:skoehler	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000252	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000270	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000340	OMIM:210730	TAS				P		HPO:probinson	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000341	OMIM:210730	TAS				P		HPO:probinson	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000347	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000486	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000501	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000520	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000540	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000567	OMIM:210730	TAS				P		HPO:probinson	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000613	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000648	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000677	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0000768	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001249	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001252	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001272	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001290	OMIM:210730	TAS				P		HPO:skoehler	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001511	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001620	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0001883	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0002690	OMIM:210730	TAS				P		HPO:probinson	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0002751	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0002836	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003090	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003100	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003173	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003175	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003273	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003510	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0003717	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0004209	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0005832	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0005897	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0006380	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0006470	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0008826	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0009465	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0010230	OMIM:210730	IEA				P		HPO:iea	
OMIM	210730	MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III		HP:0100857	OMIM:210730	TAS				P		HPO:probinson	
OMIM	210740	Bangstad syndrome		HP:0000007	OMIM:210740	IEA				I	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0000275	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0000278	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0000444	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0000831	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0000853	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0001090	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0001249	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0001518	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0001876	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0002073	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210740	Bangstad syndrome		HP:0003510	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:skoehler	
OMIM	210740	Bangstad syndrome		HP:0006872	OMIM:210740	TAS				P	BANGSTAD SYNDROME	HPO:probinson	
OMIM	210740	Bangstad syndrome		HP:0006872	PMID:2662702	PCS				P	BANGSTAD SYNDROME	HP:probinson	
OMIM	210740	Bangstad syndrome		HP:0008193	OMIM:210740	IEA				P	BANGSTAD SYNDROME	HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000007	OMIM:210745	IEA				I		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000179	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000303	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000431	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000458	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000508	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000565	OMIM:210745	IEA				P		HPO:skoehler	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000574	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000581	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0000664	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0001760	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0004322	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0004661	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0006889	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0007715	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0010554	OMIM:210745	IEA				P		HPO:iea	
OMIM	210745	BLEPHAROPHIMOSIS WITH PTOSIS, SYNDACTYLY, AND SHORT STATURE		HP:0025586	OMIM:210745	IEA				P		HPO:skoehler	
OMIM	210750	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6		HP:0000007	OMIM:210750	IEA				I		HPO:iea	
OMIM	210750	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6		HP:0001595	OMIM:210750	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000007	OMIM:210900	IEA				I		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000027	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000028	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000252	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000268	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000272	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000275	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000411	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000448	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000690	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000868	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000957	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000992	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0000998	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0001159	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0001161	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0001256	OMIM:210900	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	210900	BLOOM SYNDROME		HP:0001328	OMIM:210900	TAS				P		HPO:probinson	
OMIM	210900	BLOOM SYNDROME		HP:0001511	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0001620	OMIM:210900	TAS				P		HPO:probinson	
OMIM	210900	BLOOM SYNDROME		HP:0001909	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0002110	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0002665	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0002720	OMIM:210900	TAS				P		HPO:probinson	
OMIM	210900	BLOOM SYNDROME		HP:0002850	OMIM:210900	TAS				P		HPO:probinson	
OMIM	210900	BLOOM SYNDROME		HP:0002860	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0003220	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0004209	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0004315	OMIM:210900	TAS				P		HPO:probinson	
OMIM	210900	BLOOM SYNDROME		HP:0005585	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0005590	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0005598	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0005978	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0006528	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0008897	OMIM:210900	IEA				P		HPO:iea	
OMIM	210900	BLOOM SYNDROME		HP:0040012	OMIM:210900	TAS				P		HPO:skoehler	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0000007	OMIM:211000	TAS				I		HPO:nvasilevsky	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0000121	OMIM:211000	IEA				P		HPO:iea	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0001417	PMID:14246093	TAS				I		HPO:nvasilevsky	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0001438	OMIM:211000	IEA				P		HPO:iea	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0003072	OMIM:211000	IEA				P		HPO:iea	
OMIM	211000	BLUE DIAPER SYNDROME		HP:0004365	PMID:14246093	TAS				P		HPO:nvasilevsky	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0000007	OMIM:211120	IEA				I		HPO:iea	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0000773	OMIM:211120	TAS				P		HPO:skoehler	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0000774	OMIM:211120	TAS				P		HPO:skoehler	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0001591	OMIM:211120	TAS				P		HPO:skoehler	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0002093	OMIM:211120	TAS				P		HPO:skoehler	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0002652	OMIM:211120	IEA				P		HPO:iea	
OMIM	211120	211120 BONE DYSPLASIA, LETHAL, HOLMGREN TYPE		HP:0004322	OMIM:211120	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0000007	OMIM:211180	IEA				I		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0000252	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0000347	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0000448	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0001367	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0001518	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0001838	OMIM:211180	IEA				P		HPO:iea	
OMIM	211180	BOWEN-CONRADI SYNDROME		HP:0004209	OMIM:211180	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0000007	OMIM:211200	IEA				I		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0000047	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0000347	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0000598	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0001087	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0001274	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0001508	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0001627	OMIM:211200	TAS				P		HPO:skoehler	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0003819	OMIM:211200	IEA				M		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0008872	OMIM:211200	IEA				P		HPO:iea	
OMIM	211200	211200 BOWEN SYNDROME OF MULTIPLE MALFORMATIONS		HP:0030680	OMIM:211200	IEA				P		HPO:iea	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000007	OMIM:211350	TAS				I		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000175	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000204	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000347	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000348	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000369	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000895	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000907	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0000926	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0001059	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0001376	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0001762	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0002980	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0002982	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA	HP:0012828	HP:0002983	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0002986	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003015	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003031	PMID:11140840	PCS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003097	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003180	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003498	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0003865	PMID:11140840	PCS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0005009	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0005257	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0005280	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0005792	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0010049	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0010561	OMIM:211350	TAS				P		HPO:probinson	
OMIM	211350	KYPHOMELIC DYSPLASIA		HP:0012368	OMIM:211350	TAS				P		HPO:skoehler	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0000007	OMIM:211369	IEA				I		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0000252	OMIM:211369	IEA				P		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0000819	OMIM:211369	IEA				P		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0001250	OMIM:211369	IEA				P		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0005726	OMIM:211369	IEA				P		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0005824	OMIM:211369	IEA				P		HPO:iea	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0009372	OMIM:211369	IEA				P		HPO:probinson	
OMIM	211369	BRACHYDACTYLY, TYPE A2, WITH MICROCEPHALY		HP:0009576	OMIM:211369	TAS				P		HPO:probinson	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000007	OMIM:211370	IEA				I		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000066	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000327	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000369	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000486	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000494	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000518	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000545	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000639	OMIM:211370	IEA				P		HPO:skoehler	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000653	OMIM:211370	TAS				P		HPO:skoehler	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0000674	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0001006	OMIM:211370	IEA				P		HPO:skoehler	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0001831	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0002213	OMIM:211370	TAS				P		HPO:skoehler	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0002221	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0002555	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0002557	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0004322	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0007759	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0008070	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0009743	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0009803	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0010049	OMIM:211370	IEA				P		HPO:iea	
OMIM	211370	BRACHYMETAPODY-ANODONTIA-HYPOTRICHOSIS-ALBINOIDISM		HP:0010743	OMIM:211370	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000007	OMIM:211380	IEA				I		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000048	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000179	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000193	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000218	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000219	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000272	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000289	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000303	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000316	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000324	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000327	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000337	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000341	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000343	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000358	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000369	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000431	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000463	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000485	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000494	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000501	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000518	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000520	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000574	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000664	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000667	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000684	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000689	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000767	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000808	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0000925	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0001156	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0001249	OMIM:211380	IEA				P		HPO:iea	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0001263	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0001545	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0001571	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0002025	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0006610	OMIM:211380	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0009765	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0011800	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211380	ELSAHY-WATERS SYNDROME; ESWS		HP:0020049	OMIM:211380	IEA				P		HPO:skoehler	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0000007	OMIM:211390	IEA				I		HPO:iea	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0001006	OMIM:211390	IEA				P		HPO:iea	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0001249	OMIM:211390	IEA				P		HPO:iea	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0002164	OMIM:211390	IEA				P		HPO:iea	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0002299	OMIM:211390	TAS				P		HPO:skoehler	
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0008404	OMIM:211390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	211390	%211390 SABINAS BRITTLE HAIR SYNDROME;;BRITTLE HAIR AND MENTAL DEFICIT		HP:0011359	OMIM:211390	TAS				P		HPO:skoehler	
OMIM	211400	#211400 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1; BESC1;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0000006	OMIM:211400	TAS				I		HPO:skoehler	
OMIM	211400	#211400 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1; BESC1;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0002110	OMIM:211400	TAS				P		HPO:skoehler	
OMIM	211400	#211400 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1; BESC1;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0004469	OMIM:211400	TAS				P		HPO:skoehler	
OMIM	211400	#211400 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 1; BESC1;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0012236	OMIM:211400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	211480	BUERGER DISEASE		HP:0000007	OMIM:211480	IEA				I		HPO:iea	
OMIM	211480	BUERGER DISEASE		HP:0000975	OMIM:211480	IEA				P		HPO:skoehler	
OMIM	211480	BUERGER DISEASE		HP:0009763	OMIM:211480	IEA				P		HPO:skoehler	
OMIM	211480	BUERGER DISEASE		HP:0012531	OMIM:211480	TAS				P		HPO:skoehler	
OMIM	211480	BUERGER DISEASE		HP:0030880	OMIM:211480	TAS				P		HPO:skoehler	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0000007	OMIM:211500	IEA				I		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0000508	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0001283	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0001349	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0002015	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0005951	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0007034	OMIM:211500	IEA				P		HPO:iea	
OMIM	211500	BULBAR PALSY, PROGRESSIVE, OF CHILDHOOD		HP:0009113	OMIM:211500	IEA				P		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0000007	OMIM:211530	IEA				I		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0000407	OMIM:211530	TAS				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0000467	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0000508	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0000544	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001251	OMIM:211530	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001252	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001283	OMIM:211530	IEA				P		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001308	OMIM:211530	IEA				P		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001317	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001605	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0001621	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002015	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002058	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002093	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002098	OMIM:211530	TAS				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002205	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002312	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002650	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002808	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0002877	OMIM:211530	IEA				P		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0003621	OMIM:211530	IEA				C		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0003676	OMIM:211530	IEA				C		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0003701	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0007097	OMIM:211530	IEA				P		HPO:iea	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0009113	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0009130	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0009830	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0010307	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0010628	OMIM:211530	TAS				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0011448	OMIM:211530	TAS				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0011449	OMIM:211530	IEA				P		HPO:skoehler	
OMIM	211530	BROWN-VIALETTO-VAN LAERE SYNDROME 1; BVVLS1		HP:0012473	OMIM:211530	TAS				P		HPO:skoehler	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0000007	OMIM:211600	IEA				I		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0000952	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0000989	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0001394	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0001508	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0001744	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0002014	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0002240	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0002630	OMIM:211600	TAS				P		HPO:probinson	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0002908	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0003510	OMIM:211600	IEA				P		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0003593	OMIM:211600	IEA				C		HPO:iea	
OMIM	211600	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1		HP:0006575	OMIM:211600	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000007	OMIM:211750	IEA				I		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000028	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000154	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000191	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000218	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000243	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000252	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000286	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000347	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000358	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000369	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000431	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000463	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000486	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000582	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000803	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0000973	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001162	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001250	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001252	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001263	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001290	OMIM:211750	TAS				P		HPO:skoehler	
OMIM	211750	C SYNDROME		HP:0001508	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001539	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001629	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001643	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001770	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0001830	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0002240	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0002650	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0002750	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0002827	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0002983	OMIM:211750	TAS				P		HPO:skoehler	
OMIM	211750	C SYNDROME		HP:0003083	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0003196	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0004322	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0006643	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0008665	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0009100	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0009465	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0009466	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0009826	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0010049	OMIM:211750	IEA				P		HPO:iea	
OMIM	211750	C SYNDROME		HP:0025356	OMIM:211750	IEA				P		HPO:skoehler	
OMIM	211750	C SYNDROME		HP:0030084	OMIM:211750	TAS				P		HPO:skoehler	
OMIM	211770	CAHMR SYNDROME		HP:0000007	OMIM:211770	IEA				I		HPO:iea	
OMIM	211770	CAHMR SYNDROME		HP:0001249	OMIM:211770	IEA				P		HPO:iea	
OMIM	211770	CAHMR SYNDROME		HP:0004554	OMIM:211770	IEA				P		HPO:iea	
OMIM	211770	CAHMR SYNDROME		HP:0007971	OMIM:211770	IEA				P		HPO:iea	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0000007	OMIM:211800	IEA				I		HPO:iea	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0000925	OMIM:211800	IEA				P		HPO:iea	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0001367	OMIM:211800	IEA				P		HPO:iea	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0003207	OMIM:211800	IEA				P		HPO:iea	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0011986	OMIM:211800	TAS				P		HPO:skoehler	
OMIM	211800	CALCIFICATION OF JOINTS AND ARTERIES; CALJA		HP:0025477	OMIM:211800	IEA				P		HPO:skoehler	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0000007	OMIM:211890	TAS				I		HPO:iea	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0000113	OMIM:211890	TAS				P		HPO:skoehler	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0000476	OMIM:211890	IEA				P		HPO:skoehler	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0001004	OMIM:211890	IEA				P		HPO:skoehler	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0001737	OMIM:211890	TAS				P		HPO:iea	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0001748	OMIM:211890	IEA				P		HPO:iea	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0004322	OMIM:211890	IEA				P		HPO:iea	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0006487	OMIM:211890	TAS				P		HPO:iea	
OMIM	211890	%211890 CAMPOMELIA, CUMMING TYPE;;CERVICAL LYMPHOCELE WITH BOWED LONG BONES;;CUMMING SYNDROME		HP:0006557	OMIM:211890	TAS				P		HPO:iea	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0000007	OMIM:211900	TAS				I		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0000121	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0000679	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0000951	OMIM:211900	IEA				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0001102	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0002905	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0003621	OMIM:211900	IEA				C		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0003761	OMIM:211900	IEA				P		HPO:skoehler	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0003771	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0004934	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0005571	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0005572	OMIM:211900	TAS				P		HPO:skoehler	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0006297	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0007799	OMIM:211900	TAS				P		HPO:probinson	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0031485	OMIM:211900	IEA				P		HPO:skoehler	
OMIM	211900	TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1; HFTC1		HP:0100774	OMIM:211900	IEA				P		HPO:skoehler	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000007	OMIM:211910	IEA				I		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000160	OMIM:211910	TAS				P		HPO:probinson	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000193	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000218	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000248	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000252	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000272	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000286	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000316	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000358	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000369	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000385	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000463	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000472	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000482	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000506	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000581	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000582	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000664	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000689	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000767	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000768	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000960	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0000995	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001156	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001215	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001249	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001250	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001511	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001770	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001773	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0001822	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002645	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002688	OMIM:211910	TAS				P		HPO:probinson	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002714	OMIM:211910	TAS				P		HPO:probinson	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002750	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002866	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002938	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0002967	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0003038	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0003196	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0003298	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0003440	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0003691	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0004279	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0004322	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0004453	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0005280	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0005456	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0006166	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0006292	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0006668	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0008424	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0008551	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0010743	OMIM:211910	IEA				P		HPO:iea	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0011800	OMIM:211910	TAS				P		HPO:skoehler	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0012368	OMIM:211910	TAS				P		HPO:skoehler	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0012745	OMIM:211910	TAS				P		HPO:skoehler	
OMIM	211910	211910 CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE I; GCS1;;FACIOTHORACOSKELETAL SYNDROME; FTSS		HP:0100864	OMIM:211910	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000007	OMIM:211920	IEA				I		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000066	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000252	OMIM:211920	TAS				P		HPO:skoehler	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000343	OMIM:211920	TAS				P		HPO:skoehler	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000347	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000369	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000400	OMIM:211920	TAS				P		HPO:skoehler	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000464	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000470	OMIM:211920	TAS				P		HPO:skoehler	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000601	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000767	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000938	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0000954	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0001156	OMIM:211920	IEA				P		HPO:skoehler	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0001511	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0001762	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0001822	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0001885	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0003065	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0003100	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0004322	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0004634	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0005643	OMIM:211920	TAS				P		HPO:probinson	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0005819	OMIM:211920	TAS				P		HPO:probinson	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0006610	OMIM:211920	IEA				P		HPO:iea	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0008093	OMIM:211920	TAS				P		HPO:probinson	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0011917	OMIM:211920	TAS				P		HPO:probinson	
OMIM	211920	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE II		HP:0100490	OMIM:211920	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0000007	OMIM:211930	IEA				I		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0000271	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0001166	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0001643	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0001765	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0002650	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0002652	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0009473	OMIM:211930	IEA				P		HPO:iea	
OMIM	211930	211930 CAMPTODACTYLY WITH FIBROUS TISSUE HYPERPLASIA AND SKELETAL DYSPLASIA		HP:0012385	OMIM:211930	TAS				P		HPO:skoehler	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0000007	OMIM:211960	IEA				I		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0000023	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0000316	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0000343	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0001245	OMIM:211960	TAS				P		HPO:probinson	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0001634	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0001762	OMIM:211960	TAS				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0002414	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0002652	OMIM:211960	IEA				P		HPO:skoehler	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0003236	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0003457	OMIM:211960	TAS				P		HPO:skoehler	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0005689	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0007477	OMIM:211960	TAS				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0009473	OMIM:211960	IEA				P		HPO:iea	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0010487	OMIM:211960	TAS				P		HPO:probinson	
OMIM	211960	%211960 CAMPTODACTYLY WITH MUSCULAR HYPOPLASIA, SKELETAL DYSPLASIA, AND ABNORMALPALMAR CREASES;;TEL HASHOMER CAMPTODACTYLY SYNDROME		HP:0012385	OMIM:211960	TAS				P		HPO:skoehler	
OMIM	211980	LUNG CANCER		HP:0000006	OMIM:211980	IEA				I		HPO:skoehler	
OMIM	211980	LUNG CANCER		HP:0000007	OMIM:211980	IEA				I		HPO:iea	
OMIM	211980	LUNG CANCER		HP:0001428	OMIM:211980	IEA				I		HPO:skoehler	
OMIM	211980	LUNG CANCER		HP:0006519	OMIM:211980	IEA				P		HPO:iea	
OMIM	211990	CAMPTOMELIC SYNDROME, LONG-LIMB TYPE		HP:0000007	OMIM:211990	TAS				I		HPO:probinson	
OMIM	211990	CAMPTOMELIC SYNDROME, LONG-LIMB TYPE	HP:0012825	HP:0002983	OMIM:211990	TAS				P		HPO:probinson	
OMIM	211990	CAMPTOMELIC SYNDROME, LONG-LIMB TYPE		HP:0006487	OMIM:211990	TAS				P		HPO:probinson	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0000007	OMIM:212050	IEA				I		HPO:iea	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0001287	OMIM:212050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0001597	OMIM:212050	IEA				P		HPO:iea	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0001871	OMIM:212050	IEA				P		HPO:iea	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0002721	OMIM:212050	TAS				P		HPO:skoehler	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0009098	OMIM:212050	IEA				P		HPO:iea	
OMIM	212050	#212050 CANDIDIASIS, FAMILIAL, 2; CANDF2;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE;;CARD9 IMMUNODEFICIENCY		HP:0012203	OMIM:212050	TAS				P		HPO:skoehler	
OMIM	212060	CARBIMAZOLE SENSITIVITY		HP:0000007	OMIM:212060	IEA				I		HPO:iea	
OMIM	212060	CARBIMAZOLE SENSITIVITY		HP:0012235	OMIM:212060	TAS				P		HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000007	OMIM:212065	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000093	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000100	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000107	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000114	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000219	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000219	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000252	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000400	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000510	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000565	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000639	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000815	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000821	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0000938	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001250	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001251	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001252	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001263	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001265	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001271	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001290	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001324	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001324	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001371	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001395	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001397	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001508	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001560	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001638	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001698	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001790	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001894	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001929	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0001976	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002013	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002014	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002240	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002401	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002720	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002808	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0002910	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0003073	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0003146	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0003186	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0003642	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0003645	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0004315	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0005280	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0006955	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0007552	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0008151	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0008209	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0008872	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0011220	OMIM:212065	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:probinson	
OMIM	212065	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A		HP:0025356	OMIM:212065	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IA; CDG1A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000007	OMIM:212066	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000154	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000164	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000194	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000212	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000232	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000233	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000248	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000252	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000256	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000278	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000358	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000400	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:probinson	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000407	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000426	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000470	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000494	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000527	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000574	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000699	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000718	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000733	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000742	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000767	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0000938	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001007	OMIM:212066	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	HP:0040283
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001250	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001276	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001290	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001508	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001547	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001572	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001629	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001763	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001929	PMID:11228641	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:probinson	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0001976	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0002317	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0002673	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0003100	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0003160	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0003423	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0004322	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0004841	PMID:11228641	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:probinson	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0006887	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0007466	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0008070	OMIM:212066	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	HP:0040283
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0008897	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0009623	OMIM:212066	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:iea	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0009765	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0010808	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0010864	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0011858	PMID:11228641	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:probinson	
OMIM	212066	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIa; CDG2A		HP:0012301	OMIM:212066	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIA; CDG2A	HPO:skoehler	
OMIM	212067	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx;;CDG-x		HP:0000007	OMIM:212067	IEA				I	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIX;;CDG-X	HPO:iea	
OMIM	212067	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx;;CDG-x		HP:0001000	OMIM:212067	IEA				P	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIX;;CDG-X	HPO:iea	
OMIM	212067	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx;;CDG-x		HP:0001250	OMIM:212067	IEA				P	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIX;;CDG-X	HPO:iea	
OMIM	212067	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx;;CDG-x		HP:0001939	OMIM:212067	IEA				P	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIX;;CDG-X	HPO:iea	
OMIM	212067	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIx;;CDG-x		HP:0012469	OMIM:212067	TAS				P	212067 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE I/IIX;;CDG-X	HPO:skoehler	
OMIM	212070	CARBOXYPEPTIDASE N DEFICIENCY		HP:0000007	OMIM:212070	IEA				I		HPO:iea	
OMIM	212070	CARBOXYPEPTIDASE N DEFICIENCY		HP:0100665	OMIM:212070	IEA				P		HPO:skoehler	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0000007	OMIM:212080	IEA				I		HPO:iea	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0000252	OMIM:212080	IEA				P		HPO:iea	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0001522	OMIM:212080	IEA				M		HPO:iea	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0001635	OMIM:212080	IEA				P		HPO:iea	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0001638	OMIM:212080	IEA				P		HPO:skoehler	
OMIM	212080	CARDIAC LIPIDOSIS, FAMILIAL		HP:0001939	OMIM:212080	IEA				P		HPO:iea	
OMIM	212090	CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA		HP:0000007	OMIM:212090	TAS				I		HPO:skoehler	
OMIM	212090	CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA		HP:0001680	OMIM:212090	TAS				P		HPO:skoehler	
OMIM	212090	CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA		HP:0001684	OMIM:212090	TAS				P		HPO:skoehler	
OMIM	212090	CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA		HP:0011682	OMIM:212090	TAS				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0000007	OMIM:212093	IEA				I		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0000023	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0000072	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0000126	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0000969	OMIM:212093	IEA				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0001634	OMIM:212093	TAS				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0001655	OMIM:212093	TAS				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0001704	OMIM:212093	TAS				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0001718	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0001789	OMIM:212093	TAS				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0005180	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0008722	OMIM:212093	IEA				P		HPO:iea	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0011662	OMIM:212093	IEA				P		HPO:skoehler	
OMIM	212093	CARDIAC VALVULAR DEFECT, DEVELOPMENTAL; CVDD		HP:0031014	OMIM:212093	TAS				P		HPO:skoehler	
OMIM	212100	CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS		HP:0000007	OMIM:212100	IEA				I		HPO:iea	
OMIM	212100	CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS		HP:0000365	OMIM:212100	IEA				P		HPO:iea	
OMIM	212100	CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS		HP:0001714	OMIM:212100	IEA				P		HPO:iea	
OMIM	212100	CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS		HP:0005875	OMIM:212100	IEA				P		HPO:iea	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000006	OMIM:212112	TAS				I		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000007	OMIM:212112	TAS				I		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000278	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000508	OMIM:212112	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000815	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0000894	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0001249	OMIM:212112	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0001644	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0001653	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0009125	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212112	CARDIOMYOPATHY, DILATED, WITH HYPERGONADOTROPIC HYPOGONADISM		HP:0200021	OMIM:212112	TAS				P		HPO:skoehler	
OMIM	212130	CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH		HP:0000007	OMIM:212130	IEA				I		HPO:iea	
OMIM	212130	CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH		HP:0001670	OMIM:212130	IEA				P		HPO:iea	
OMIM	212130	CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH		HP:0003198	OMIM:212130	IEA				P		HPO:iea	
OMIM	212135	212135 CARDIOSKELETAL SYNDROME, KUWAITI TYPE		HP:0000007	OMIM:212135	IEA				I		HPO:iea	
OMIM	212135	212135 CARDIOSKELETAL SYNDROME, KUWAITI TYPE		HP:0001627	OMIM:212135	TAS				P		HPO:skoehler	
OMIM	212135	212135 CARDIOSKELETAL SYNDROME, KUWAITI TYPE		HP:0002652	OMIM:212135	IEA				P		HPO:iea	
OMIM	212135	212135 CARDIOSKELETAL SYNDROME, KUWAITI TYPE		HP:0004322	OMIM:212135	IEA				P		HPO:iea	
OMIM	212135	212135 CARDIOSKELETAL SYNDROME, KUWAITI TYPE		HP:0030680	OMIM:212135	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0000007	OMIM:212138	IEA				I		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0000737	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001250	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001254	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001259	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001290	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001324	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001638	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001662	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001678	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY	HP:0012825	HP:0001714	OMIM:212138	PCS				P		HPO:probinson	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001943	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0001987	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0002240	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0002615	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0002910	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0003201	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0003215	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0003236	OMIM:212138	TAS				P		HPO:skoehler	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0004756	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0006543	OMIM:212138	IEA				P		HPO:iea	
OMIM	212138	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY		HP:0006682	OMIM:212138	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0000007	OMIM:212140	TAS				I		HPO:probinson	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001252	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001254	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001259	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001262	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001289	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001290	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001298	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001324	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001324	OMIM:212140	TAS				P		HPO:probinson	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001397	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001508	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001635	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001639	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001640	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001706	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001943	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001987	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0001988	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0002013	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0002240	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0002910	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0003198	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0003234	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0005959	OMIM:212140	IEA				P		HPO:iea	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0030362	OMIM:212140	TAS				P		HPO:probinson	
OMIM	212140	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY		HP:0045061	OMIM:212140	TAS				P		HPO:skoehler	
OMIM	212160	CARNITINE DEFICIENCY, MYOPATHIC		HP:0000007	OMIM:212160	TAS				I		HPO:probinson	
OMIM	212160	CARNITINE DEFICIENCY, MYOPATHIC		HP:0003198	OMIM:212160	TAS				P		HPO:probinson	
OMIM	212160	CARNITINE DEFICIENCY, MYOPATHIC		HP:0003234	OMIM:212160	IEA				P		HPO:skoehler	
OMIM	212160	CARNITINE DEFICIENCY, MYOPATHIC		HP:0030362	OMIM:212160	TAS				P		HPO:probinson	
OMIM	212200	CARNOSINEMIA		HP:0000007	OMIM:212200	IEA				I		HPO:iea	
OMIM	212200	CARNOSINEMIA		HP:0001249	OMIM:212200	IEA				P		HPO:iea	
OMIM	212200	CARNOSINEMIA		HP:0002123	OMIM:212200	IEA				P		HPO:iea	
OMIM	212200	CARNOSINEMIA		HP:0003167	OMIM:212200	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0000007	OMIM:212350	IEA				I		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0000486	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0000501	OMIM:212350	TAS				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0000519	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0000545	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0000639	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0001252	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0001270	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0001290	OMIM:212350	TAS				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0001324	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0001510	OMIM:212350	TAS				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0001639	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0001873	OMIM:212350	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212350	SENGERS SYNDROME		HP:0002093	OMIM:212350	TAS				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0002151	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0003198	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0003388	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0003535	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0003546	OMIM:212350	IEA				P		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0003593	OMIM:212350	IEA				C		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0003737	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0003828	OMIM:212350	TAS				C		HPO:skoehler	
OMIM	212350	SENGERS SYNDROME		HP:0004901	OMIM:212350	IEA				P		HPO:iea	
OMIM	212350	SENGERS SYNDROME		HP:0012378	OMIM:212350	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0000007	OMIM:212360	IEA				I		HPO:iea	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0000519	OMIM:212360	IEA				P		HPO:iea	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0000958	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0000962	OMIM:212360	IEA				P		HPO:iea	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0000972	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0001041	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0002164	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0007418	OMIM:212360	TAS	HP:0003577			P		HPO:probinson	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0008404	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0009775	OMIM:212360	IEA				P		HPO:iea	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0011838	OMIM:212360	TAS				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0032152	OMIM:212360	IEA				P		HPO:skoehler	
OMIM	212360	PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 2; PPKCA2		HP:0100490	OMIM:212360	TAS				P		HPO:probinson	
OMIM	212400	CATARACT AND CONGENITAL ICHTHYOSIS		HP:0000007	OMIM:212400	IEA				I		HPO:iea	
OMIM	212400	CATARACT AND CONGENITAL ICHTHYOSIS		HP:0000518	OMIM:212400	IEA				P		HPO:iea	
OMIM	212400	CATARACT AND CONGENITAL ICHTHYOSIS		HP:0007431	OMIM:212400	IEA				P		HPO:iea	
OMIM	212500	CATARACT, CONGENITAL OR JUVENILECATARACT, JUVENILE, HUTTERITE TYPE, INCLUDED		HP:0000007	OMIM:212500	IEA				I		HPO:iea	
OMIM	212500	CATARACT, CONGENITAL OR JUVENILECATARACT, JUVENILE, HUTTERITE TYPE, INCLUDED		HP:0000519	OMIM:212500	IEA				P		HPO:iea	
OMIM	212500	CATARACT, CONGENITAL OR JUVENILECATARACT, JUVENILE, HUTTERITE TYPE, INCLUDED		HP:0001118	OMIM:212500	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0000007	OMIM:212540	IEA				I		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0000252	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0000271	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0000518	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0001257	OMIM:212540	IEA				P		HPO:skoehler	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0001508	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0001518	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0002751	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0002804	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0002827	OMIM:212540	IEA				P		HPO:skoehler	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0006887	OMIM:212540	IEA				P		HPO:iea	
OMIM	212540	212540 CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME;;CAMFAK SYNDROMECATARACT, MICROCEPHALY, ARTHROGRYPOSIS, KYPHOSIS SYNDROME, INCLUDED;;CAMAK SYNDROME, INCLUDED		HP:0010864	OMIM:212540	TAS				P		HPO:skoehler	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000007	OMIM:212550	IEA				I		HPO:iea	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000501	OMIM:212550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000518	OMIM:212550	IEA				P		HPO:iea	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000541	OMIM:212550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000556	OMIM:212550	TAS				P		HPO:skoehler	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000567	OMIM:212550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000568	OMIM:212550	IEA				P		HPO:iea	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000612	OMIM:212550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000616	OMIM:212550	IEA				P		HPO:iea	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000639	OMIM:212550	IEA				P		HPO:iea	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0000666	OMIM:212550	TAS				P		HPO:skoehler	
OMIM	212550	OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY; ODRMD		HP:0007401	OMIM:212550	IEA				P		HPO:skoehler	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0000007	OMIM:212710	IEA				I		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0000519	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001251	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001256	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001271	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0001284	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0002936	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0004322	OMIM:212710	IEA				P		HPO:iea	
OMIM	212710	CATARACT-ATAXIA-DEAFNESS-RETARDATION SYNDROME		HP:0008615	OMIM:212710	IEA	HP:0003584			P		HPO:iea	
OMIM	212720	MARTSOLF SYNDROME		HP:0000007	OMIM:212720	IEA				I		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000028	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000044	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000054	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000218	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000248	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000252	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000286	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000322	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME	HP:0012825	HP:0000327	OMIM:212720	PCS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000347	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000358	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000455	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000494	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000518	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000692	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000767	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0000768	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001388	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001635	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001638	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001762	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001831	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0001840	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0002205	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0002779	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0002938	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0003992	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0004279	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0004322	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0004405	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0004684	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0005280	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0006887	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0008388	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0008593	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0008872	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0009803	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0010049	OMIM:212720	IEA				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0010864	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212720	MARTSOLF SYNDROME		HP:0011300	OMIM:212720	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000007	OMIM:212750	IEA				I		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000716	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000739	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000789	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000823	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000939	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0000964	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001250	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001251	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001271	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001425	OMIM:212750	TAS				I		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001426	OMIM:212750	IEA				I		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001508	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001596	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001824	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001891	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001894	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0001972	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002013	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002014	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002027	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002514	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002514	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002570	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002608	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002665	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002720	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002748	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002829	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002901	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0002910	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0003256	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0003270	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0003645	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0004298	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0004322	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0006297	OMIM:212750	IEA				P		HPO:iea	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0008151	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0008897	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0010280	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0011107	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0011892	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0100502	OMIM:212750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0100507	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0100512	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0100646	OMIM:212750	IEA				P		HPO:skoehler	
OMIM	212750	CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1		HP:0100651	OMIM:212750	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000007	OMIM:212780	IEA				I		HPO:iea	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000089	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000104	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000316	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000347	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0000494	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0001159	OMIM:212780	IEA				P		HPO:iea	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0002984	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0003022	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212780	#212780 CENANI-LENZ SYNDACTYLY SYNDROME; CLSS;;CENANI SYNDACTYLISM;;CENANI-LENZ SYNDACTYLY;;SYNDACTYLY, TYPE VII		HP:0011220	OMIM:212780	TAS				P		HPO:skoehler	
OMIM	212790	PREMATURE CENTROMERE DIVISION; PCD		HP:0000007	OMIM:212790	IEA				I		HPO:iea	
OMIM	212790	PREMATURE CENTROMERE DIVISION; PCD		HP:0001939	OMIM:212790	IEA				P		HPO:iea	
OMIM	212790	PREMATURE CENTROMERE DIVISION; PCD		HP:0003745	OMIM:212790	TAS				I		HPO:skoehler	
OMIM	212800	CEPHALIN LIPIDOSIS		HP:0000007	OMIM:212800	IEA				I		HPO:iea	
OMIM	212800	CEPHALIN LIPIDOSIS		HP:0001249	OMIM:212800	IEA				P		HPO:iea	
OMIM	212800	CEPHALIN LIPIDOSIS		HP:0001743	OMIM:212800	IEA				P		HPO:iea	
OMIM	212800	CEPHALIN LIPIDOSIS		HP:0001939	OMIM:212800	IEA				P		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0000007	OMIM:212835	IEA				I		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0000968	OMIM:212835	IEA				P		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0001006	OMIM:212835	IEA				P		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0001251	OMIM:212835	IEA				P		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0001596	OMIM:212835	IEA				P		HPO:iea	
OMIM	212835	212835 CEREBELLAR ATAXIA AND ECTODERMAL DYSPLASIA		HP:0006349	OMIM:212835	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000007	OMIM:212840	IEA				I		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000044	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000726	OMIM:212840	TAS				P		HPO:skoehler	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000789	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000876	OMIM:212840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0000924	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0001135	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0001251	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0001260	OMIM:212840	TAS				P		HPO:skoehler	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0001272	OMIM:212840	TAS				P		HPO:skoehler	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0001939	OMIM:212840	IEA				P		HPO:iea	
OMIM	212840	#212840 CEREBELLAR ATAXIA AND HYPOGONADOTROPIC HYPOGONADISM; CAHH;;GORDON HOLMES SYNDROME;;LUTEINIZING HORMONE-RELEASING HORMONE, DEFICIENCY OF, WITH ATAXIA;;LHRH DEFICIENCY AND ATAXIA		HP:0002059	OMIM:212840	TAS				P		HPO:skoehler	
OMIM	212850	CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS		HP:0000007	OMIM:212850	IEA				I		HPO:iea	
OMIM	212850	CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS		HP:0000407	OMIM:212850	IEA				P		HPO:iea	
OMIM	212850	CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS		HP:0001251	OMIM:212850	IEA	HP:0003581			P		HPO:iea	
OMIM	212850	CEREBELLAR ATAXIA AND NEUROSENSORY DEAFNESS		HP:0001761	OMIM:212850	IEA				P		HPO:iea	
OMIM	212890	CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA		HP:0000007	OMIM:212890	IEA				I		HPO:iea	
OMIM	212890	CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA		HP:0002073	OMIM:212890	IEA	HP:0003584			P		HPO:iea	
OMIM	212890	CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA		HP:0003447	OMIM:212890	TAS				P		HPO:skoehler	
OMIM	212890	CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA		HP:0003584	OMIM:212890	TAS				C		HPO:skoehler	
OMIM	212890	CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA		HP:0010829	OMIM:212890	TAS	HP:0003584			P		HPO:probinson	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0000007	OMIM:213000	IEA				I		HPO:iea	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0000639	OMIM:213000	IEA				P		HPO:iea	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0001251	OMIM:213000	IEA				P		HPO:iea	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0001252	OMIM:213000	IEA				P		HPO:iea	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0001290	OMIM:213000	TAS				P		HPO:skoehler	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0001321	OMIM:213000	IEA				P		HPO:iea	
OMIM	213000	CEREBELLAR HYPOPLASIA		HP:0001337	OMIM:213000	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0000007	OMIM:213002	IEA				I		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0000252	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0000486	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0000639	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0000677	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0001251	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0001263	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0001321	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0001374	OMIM:213002	IEA				P		HPO:iea	
OMIM	213002	CEREBELLAR HYPOPLASIA WITH ENDOSTEAL SCLEROSIS		HP:0004322	OMIM:213002	IEA				P		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0000007	OMIM:213010	IEA				I		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0000079	OMIM:213010	IEA				P		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0001405	OMIM:213010	IEA				P		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0002085	OMIM:213010	IEA				P		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0002335	OMIM:213010	IEA				P		HPO:iea	
OMIM	213010	CEREBELLAR VERMIS APLASIA WITH ASSOCIATED FEATURES SUGGESTING SMITH-LEMLI-OPITZSYNDROME AND MECKEL SYNDROME		HP:0100259	OMIM:213010	IEA				P		HPO:iea	
OMIM	213100	CEREBELLOPARENCHYMAL DISORDER II		HP:0000007	OMIM:213100	IEA				I		HPO:iea	
OMIM	213100	CEREBELLOPARENCHYMAL DISORDER II		HP:0001250	OMIM:213100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213100	CEREBELLOPARENCHYMAL DISORDER II		HP:0001251	OMIM:213100	IEA				P		HPO:iea	
OMIM	213100	CEREBELLOPARENCHYMAL DISORDER II		HP:0001260	OMIM:213100	IEA				P		HPO:iea	
OMIM	213100	CEREBELLOPARENCHYMAL DISORDER II		HP:0002317	OMIM:213100	IEA				P		HPO:iea	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0000007	OMIM:213200	TAS				I		HPO:probinson	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0000639	OMIM:213200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0000750	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001152	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001249	OMIM:213200	TAS				P		HPO:probinson	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001257	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001260	OMIM:213200	TAS				P		HPO:probinson	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001263	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001265	OMIM:213200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001290	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001310	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001321	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001337	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001347	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0001761	OMIM:213200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0002066	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0002070	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0002171	OMIM:213200	IEA				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0002311	OMIM:213200	TAS				P		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0002317	OMIM:213200	TAS				P		HPO:probinson	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0003593	OMIM:213200	TAS				C		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0003680	OMIM:213200	TAS				C		HPO:skoehler	
OMIM	213200	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2		HP:0004322	OMIM:213200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213300	JOUBERT SYNDROME 1		HP:0000007	OMIM:213300	IEA				I		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000107	OMIM:213300	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	213300	JOUBERT SYNDROME 1		HP:0000158	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000256	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000286	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000369	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000463	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000508	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000556	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000567	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000570	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000588	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000617	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000657	OMIM:213300	PCS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000718	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000742	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0000752	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001162	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001249	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001251	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001252	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001263	OMIM:213300	PCS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001290	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001320	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001395	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001425	OMIM:213300	TAS				I		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0001760	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002195	OMIM:213300	TAS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002335	OMIM:213300	TAS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002365	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002419	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002508	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002553	OMIM:213300	PCS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002790	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002871	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0002876	OMIM:213300	IEA				P		HPO:iea	
OMIM	213300	JOUBERT SYNDROME 1		HP:0007271	OMIM:213300	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	213300	JOUBERT SYNDROME 1		HP:0007772	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0007973	OMIM:213300	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	213300	JOUBERT SYNDROME 1		HP:0010808	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0010828	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213300	JOUBERT SYNDROME 1		HP:0011220	OMIM:213300	PCS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0011933	OMIM:213300	TAS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0100951	OMIM:213300	PCS				P		HPO:probinson	
OMIM	213300	JOUBERT SYNDROME 1		HP:0200096	OMIM:213300	TAS				P		HPO:skoehler	
OMIM	213400	CEREBELLOPARENCHYMAL DISORDER V		HP:0000007	OMIM:213400	IEA				I		HPO:iea	
OMIM	213400	CEREBELLOPARENCHYMAL DISORDER V		HP:0001251	OMIM:213400	IEA				P		HPO:iea	
OMIM	213400	CEREBELLOPARENCHYMAL DISORDER V		HP:0001336	OMIM:213400	IEA				P		HPO:iea	
OMIM	213400	CEREBELLOPARENCHYMAL DISORDER V		HP:0001939	OMIM:213400	IEA				P		HPO:iea	
OMIM	213500	CEREBRAL ANGIOPATHY, DYSPHORIC		HP:0000007	OMIM:213500	IEA				I		HPO:iea	
OMIM	213500	CEREBRAL ANGIOPATHY, DYSPHORIC		HP:0000707	OMIM:213500	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0000006	OMIM:213600	IEA				I		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0000020	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0000298	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0000709	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0000716	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001260	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001268	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001288	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001300	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001332	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001337	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0001347	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002063	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002067	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002072	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002075	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002135	OMIM:213600	TAS				P		HPO:probinson	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002172	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002305	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002354	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002406	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002461	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0002504	OMIM:213600	IEA				P		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0003581	OMIM:213600	IEA				C		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0003676	OMIM:213600	IEA				C		HPO:iea	
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0007256	OMIM:213600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213600	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1; IBGC1		HP:0031908	OMIM:213600	IEA				P		HPO:skoehler	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000007	OMIM:213700	TAS				I		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000518	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000543	PMID:11804206	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000726	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000738	OMIM:213700	TAS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000746	OMIM:213700	TAS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0000939	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001081	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ctx	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001114	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ctx	TAS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001249	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001250	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001251	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001257	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001272	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001658	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0001681	OMIM:213700	TAS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0002014	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0002059	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0002093	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0002518	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0003107	OMIM:213700	TAS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0003482	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0007024	OMIM:213700	IEA				P		HPO:iea	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0007256	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0009830	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0010845	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0010874	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0031290	OMIM:213700	IEA				P		HPO:skoehler	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0100291	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213700	CEREBROTENDINOUS XANTHOMATOSIS; CTX		HP:0100321	PMID:10775536	PCS				P		HPO:probinson	
OMIM	213900	CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE		HP:0000007	OMIM:213900	IEA				I		HPO:iea	
OMIM	213900	CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE		HP:0000707	OMIM:213900	IEA				P		HPO:iea	
OMIM	213900	CEREBRAL SCLEROSIS SIMILAR TO PELIZAEUS-MERZBACHER DISEASE		HP:0001939	OMIM:213900	IEA				P		HPO:iea	
OMIM	213950	CEREBROCORTICAL DEGENERATION OF INFANCY		HP:0000007	OMIM:213950	IEA				I		HPO:iea	
OMIM	213950	CEREBROCORTICAL DEGENERATION OF INFANCY		HP:0002063	OMIM:213950	IEA				P		HPO:skoehler	
OMIM	213950	CEREBROCORTICAL DEGENERATION OF INFANCY		HP:0002120	OMIM:213950	IEA				P		HPO:iea	
OMIM	213950	CEREBROCORTICAL DEGENERATION OF INFANCY		HP:0007281	OMIM:213950	IEA				P		HPO:iea	
OMIM	213950	CEREBROCORTICAL DEGENERATION OF INFANCY		HP:0025013	OMIM:213950	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:213980	IEA				I		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000023	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000049	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000077	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000175	OMIM:213980	TAS				P		HPO:probinson	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000204	OMIM:213980	TAS				P		HPO:probinson	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000212	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000218	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000248	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000252	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000256	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000294	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000327	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000341	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000347	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000358	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000368	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000369	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000445	OMIM:213980	TAS				P		HPO:probinson	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000470	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000486	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000508	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000527	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000535	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000574	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000582	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000653	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000664	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000739	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000742	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000774	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000824	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000892	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000902	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0000960	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001162	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001252	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001270	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001319	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001344	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001363	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001382	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001520	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001558	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001561	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001631	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001643	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001762	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001763	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0001845	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002079	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002162	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002290	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002553	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002558	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002650	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0002937	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0003196	OMIM:213980	TAS				P		HPO:probinson	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0004322	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0004568	OMIM:213980	IEA				P		HPO:iea	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0006347	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0006610	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0007018	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0008897	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0011504	OMIM:213980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0011968	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	213980	CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME		HP:0012368	OMIM:213980	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000007	OMIM:214100	IEA				I		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000028	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000047	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000126	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000158	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000218	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000244	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000256	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000272	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000286	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000311	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000316	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000347	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000348	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000358	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000407	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000463	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000501	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000512	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000518	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000543	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000580	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000582	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000639	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000835	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0000954	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001088	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001193	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001250	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001252	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001265	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001284	OMIM:214100	IEA				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001290	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001401	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001425	OMIM:214100	IEA				I		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001508	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001591	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001623	OMIM:214100	IEA				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001629	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001643	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001762	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001838	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0001840	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002089	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002126	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002240	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002282	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002416	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002705	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002750	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0002967	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0003355	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0003455	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0004492	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0004734	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0005469	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0005989	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0005989	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0006579	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0006887	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0006894	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0007370	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0007759	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0008665	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0009487	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0010655	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0010808	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0010864	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0011039	OMIM:214100	IEA				P		HPO:iea	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0012368	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214100	PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)		HP:0012592	OMIM:214100	TAS				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000007	OMIM:214110	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000028	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000113	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000175	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000239	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000262	OMIM:214110	TAS				P		HPO:probinson	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000268	OMIM:214110	TAS				P		HPO:probinson	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000286	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000316	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000347	OMIM:214110	IEA				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000348	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000518	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000580	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000582	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000778	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000952	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0000954	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001088	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001093	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001249	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001250	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001252	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001284	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001290	OMIM:214110	TAS				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001401	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001508	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001511	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001627	OMIM:214110	TAS				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001762	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0001840	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0002033	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0002104	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0002240	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0002764	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0002967	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0003355	OMIM:214110	IEA				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0003455	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0003819	OMIM:214110	IEA				M		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0007759	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0008665	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0009473	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0011039	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0012103	OMIM:214110	TAS				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0012385	OMIM:214110	TAS				P		HPO:skoehler	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0030680	OMIM:214110	IEA				P		HPO:iea	
OMIM	214110	PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER); PBD2A		HP:0100540	OMIM:214110	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000007	OMIM:214150	IEA				I		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000233	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000252	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000340	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000343	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000347	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000407	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000426	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000490	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000518	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000568	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000581	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000598	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000639	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0000939	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001007	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001249	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001250	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001252	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001274	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001290	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001321	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001508	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0001838	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002171	OMIM:214150	IEA				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002187	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002673	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002751	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002804	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0002987	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0003819	OMIM:214150	TAS				M		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0004681	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0006380	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0006610	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0008125	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0009473	OMIM:214150	IEA				P		HPO:iea	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0012385	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214150	CEREBROOCULOFACIOSKELETAL SYNDROME 1		HP:0012448	OMIM:214150	TAS				P		HPO:skoehler	
OMIM	214200	CEROID STORAGE DISEASE		HP:0000007	OMIM:214200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	214200	CEROID STORAGE DISEASE		HP:0001399	OMIM:214200	IEA				P		HPO:iea	
OMIM	214200	CEROID STORAGE DISEASE		HP:0001743	OMIM:214200	IEA				P		HPO:iea	
OMIM	214290	CERVICAL VERTEBRAE, AGENESIS OF		HP:0000007	OMIM:214290	IEA				I		HPO:iea	
OMIM	214290	CERVICAL VERTEBRAE, AGENESIS OF		HP:0000464	OMIM:214290	IEA				P		HPO:iea	
OMIM	214290	CERVICAL VERTEBRAE, AGENESIS OF		HP:0008459	OMIM:214290	IEA				P		HPO:iea	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:214300	TAS				I		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000175	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000204	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000377	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000405	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000407	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000466	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000470	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000912	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001629	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0002162	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0002650	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0002949	OMIM:214300	TAS				P		HPO:probinson	
OMIM	214300	KLIPPEL-FEIL SYNDROME, AUTOSOMAL RECESSIVE		HP:0004602	OMIM:214300	IEA				P		HPO:skoehler	
OMIM	214350	CHANDS		HP:0000007	OMIM:214350	IEA				I		HPO:iea	
OMIM	214350	CHANDS		HP:0002164	OMIM:214350	IEA				P		HPO:iea	
OMIM	214350	CHANDS		HP:0002212	OMIM:214350	IEA				P		HPO:iea	
OMIM	214350	CHANDS		HP:0002710	OMIM:214350	IEA				P		HPO:iea	
OMIM	214350	CHANDS		HP:0009755	OMIM:214350	IEA				P		HPO:skoehler	
OMIM	214370	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION,AND ABSENT SENSORY LARGE MYELINATED FIBERS		HP:0000007	OMIM:214370	TAS				I		HPO:skoehler	
OMIM	214370	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION,AND ABSENT SENSORY LARGE MYELINATED FIBERS		HP:0000407	OMIM:214370	TAS				P		HPO:skoehler	
OMIM	214370	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION,AND ABSENT SENSORY LARGE MYELINATED FIBERS		HP:0001249	OMIM:214370	IEA				P		HPO:skoehler	
OMIM	214370	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, MENTAL RETARDATION,AND ABSENT SENSORY LARGE MYELINATED FIBERS		HP:0009830	OMIM:214370	TAS				P		HPO:skoehler	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0000007	OMIM:214400	IEA				I		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0000764	OMIM:214400	PCS				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001171	OMIM:214400	TAS				P		HPO:skoehler	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001178	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001265	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001270	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001284	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001425	OMIM:214400	TAS				I		HPO:skoehler	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0001765	OMIM:214400	TAS				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0002460	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0002460	OMIM:214400	TAS				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0002751	OMIM:214400	IEA		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0002936	OMIM:214400	TAS				P		HPO:skoehler	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003380	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003382	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003400	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003429	OMIM:214400	TAS				P		HPO:skoehler	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003431	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003593	OMIM:214400	IEA				C		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003678	OMIM:214400	TAS				C		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0003693	OMIM:214400	TAS				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0006915	OMIM:214400	IEA				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0007182	OMIM:214400	TAS				P		HPO:probinson	
OMIM	214400	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A; CMT4A		HP:0040078	OMIM:214400	IEA				P		HPO:skoehler	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0000007	OMIM:214450	IEA				I		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001008	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001010	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001249	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001250	OMIM:214450	IEA				P		HPO:skoehler	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001252	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001263	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0001290	OMIM:214450	TAS				P		HPO:skoehler	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0002218	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0002220	OMIM:214450	IEA				P		HPO:iea	
OMIM	214450	GRISCELLI SYNDROME, TYPE 1		HP:0003593	OMIM:214450	IEA				C		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000007	OMIM:214500	IEA				I		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000230	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000486	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000505	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000613	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000639	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000762	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0000952	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001010	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001104	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001249	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001250	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001265	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001288	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001337	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001744	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001873	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001882	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0001903	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0002180	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0002240	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0002716	OMIM:214500	TAS				P		HPO:probinson	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0005406	OMIM:214500	TAS				P		HPO:probinson	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0005429	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0005592	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0005599	OMIM:214500	IEA				P		HPO:skoehler	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0006824	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0007133	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0007663	OMIM:214500	TAS				P		HPO:skoehler	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0007730	OMIM:214500	IEA				P		HPO:iea	
OMIM	214500	#214500 CHEDIAK-HIGASHI SYNDROME; CHS		HP:0009027	OMIM:214500	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0000007	OMIM:214700	IEA				I		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0000841	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0000859	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001507	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001508	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001510	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001561	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001622	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001626	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001944	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0001948	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0002014	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0002900	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0002902	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0003113	OMIM:214700	IEA				P		HPO:iea	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0003270	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214700	#214700 DIARRHEA 1, SECRETORY CHLORIDE, CONGENITAL; DIAR1;;CHLORIDE DIARRHEA, CONGENITAL, FINNISH TYPE;;CHLORIDORRHEA, CONGENITAL		HP:0200114	OMIM:214700	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0000006	OMIM:214800	IEA				I		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000028	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000044	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000054	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000066	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000085	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000089	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000104	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000126	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000175	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000204	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000252	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000272	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0000316	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000321	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000324	PMID:16400610	PCS		HP:0040284		P		HPO:iea	36/56
OMIM	214800	CHARGE SYNDROME		HP:0000347	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000378	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000394	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000410	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000453	PMID:2260555	PCS		HP:0040284		P		HPO:iea	27/47
OMIM	214800	CHARGE SYNDROME		HP:0000458	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0000465	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000480	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000494	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000508	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000528	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000568	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0000612	PMID:9556299	PCS		HP:0040284		P		HPO:iea	79%
OMIM	214800	CHARGE SYNDROME		HP:0000772	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000821	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0000823	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000824	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0000860	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001018	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001161	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001249	PMID:2260555	PCS		HP:0040284		P		HPO:iea	47/47
OMIM	214800	CHARGE SYNDROME		HP:0001360	PMID:2260555	PCS		HP:0040284		P		HPO:iea	2/144
OMIM	214800	CHARGE SYNDROME		HP:0001537	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001539	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001629	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0001631	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001636	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001642	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0001643	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0001719	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0001888	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0002015	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0002023	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0002025	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0002032	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0002139	PMID:2260555	PCS		HP:0040284		P		HPO:iea	11/144
OMIM	214800	CHARGE SYNDROME		HP:0002247	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0002575	PMID:16400610	PCS		HP:0040284		P		HPO:iea	10/55
OMIM	214800	CHARGE SYNDROME		HP:0002650	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0002901	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0002937	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0003022	OMIM:214800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	214800	CHARGE SYNDROME		HP:0003745	OMIM:214800	IEA				I		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0003974	OMIM:214800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	214800	CHARGE SYNDROME		HP:0004058	OMIM:214800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	214800	CHARGE SYNDROME		HP:0004496	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0008213	OMIM:214800	IEA				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0008551	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0008897	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0009778	OMIM:214800	IEA				P		HPO:iea	
OMIM	214800	CHARGE SYNDROME		HP:0010443	OMIM:214800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	214800	CHARGE SYNDROME		HP:0010515	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0010628	https://www.ncbi.nlm.nih.gov/books/NBK1117/	TAS		HP:0040284		P		HPO:iea	40%
OMIM	214800	CHARGE SYNDROME		HP:0011968	OMIM:214800	TAS				P		HPO:skoehler	
OMIM	214800	CHARGE SYNDROME		HP:0200021	OMIM:214800	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0000007	OMIM:214900	IEA				I		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0000952	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0001004	OMIM:214900	TAS				P		HPO:skoehler	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0001055	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0001394	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0001744	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0002024	OMIM:214900	IEA				P		HPO:skoehler	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0002240	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0002908	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0002910	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0003077	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0003155	OMIM:214900	IEA				P		HPO:iea	
OMIM	214900	CHOLESTASIS-LYMPHEDEMA SYNDROME		HP:0006566	OMIM:214900	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0000007	OMIM:214950	IEA				I		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0001399	OMIM:214950	IEA				P		HPO:skoehler	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0001406	OMIM:214950	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0001508	OMIM:214950	IEA				P		HPO:skoehler	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0002240	OMIM:214950	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0002630	OMIM:214950	TAS				P		HPO:probinson	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0002904	OMIM:214950	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0002910	OMIM:214950	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0003256	OMIM:214950	TAS				P		HPO:skoehler	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0003623	OMIM:214950	IEA				C		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0006579	OMIM:214950	IEA				P		HPO:iea	
OMIM	214950	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 4		HP:0200084	OMIM:214950	TAS				P		HPO:skoehler	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0000007	OMIM:214980	TAS				I		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0000546	OMIM:214980	TAS				P		HPO:skoehler	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0000648	OMIM:214980	TAS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0000952	OMIM:214980	TAS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0000989	OMIM:214980	TAS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0001081	OMIM:214980	TAS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0001251	OMIM:214980	PCS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0001488	OMIM:214980	TAS				P		HPO:skoehler	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0100490	OMIM:214980	PCS				P		HPO:probinson	
OMIM	214980	CHOLESTASIS WITH GALLSTONE, ATAXIA, AND VISUAL DISTURBANCE		HP:0200084	OMIM:214980	TAS				P		HPO:probinson	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0000007	OMIM:215030	IEA				I		HPO:iea	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0000961	OMIM:215030	IEA				P		HPO:iea	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0001522	OMIM:215030	IEA				M		HPO:iea	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0002090	OMIM:215030	IEA				P		HPO:skoehler	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0002789	OMIM:215030	IEA				P		HPO:iea	
OMIM	215030	215030 CHOLESTEROL PNEUMONIA		HP:0012735	OMIM:215030	TAS				P		HPO:skoehler	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0000007	OMIM:215045	TAS				I		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD	HP:0012828	HP:0000272	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0000347	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0000773	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0001561	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0001622	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0001789	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0002983	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD	HP:0012828	HP:0003015	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0003177	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0003826	OMIM:215045	TAS				M		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0004233	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0005616	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0005789	OMIM:215045	TAS	HP:0003577			P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0008108	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215045	#215045 CHONDRODYSPLASIA, BLOMSTRAND TYPE; BOCD		HP:0008754	OMIM:215045	TAS				P		HPO:probinson	
OMIM	215050	CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS		HP:0000007	OMIM:215050	TAS				I		HPO:probinson	
OMIM	215050	CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS		HP:0003510	OMIM:215050	TAS				P		HPO:probinson	
OMIM	215050	CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS		HP:0005871	OMIM:215050	TAS				P		HPO:probinson	
OMIM	215050	CHONDRODYSPLASIA CALCIFICANS METAPHYSEALIS		HP:0008155	OMIM:215050	TAS				P		HPO:probinson	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000007	OMIM:215100	IEA				I		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000175	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000252	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000272	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000347	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000407	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000519	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0000582	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001249	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001250	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001257	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001371	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001525	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001596	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0001939	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0002007	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0002093	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0002120	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0002188	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0002751	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0003015	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0003417	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0003510	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0005280	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0005841	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0008064	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0008905	OMIM:215100	IEA				P		HPO:iea	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0010655	OMIM:215100	TAS				P		HPO:probinson	
OMIM	215100	#215100 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 1; RCDP1;;PEROXISOME BIOGENESIS DISORDER 9; PBD9;;CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC FORM; CDPR;;CHONDRODYSTROPHIA CALCIFICANS PUNCTATA		HP:0012368	OMIM:215100	TAS				P		HPO:skoehler	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000007	PMID:11113916;PMID:14684694	PCS				I		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000256	PMID:18382993;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000272	PMID:11180245;PMID:3377005;PMID:8213919;PMID:14684697;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000315	PMID:11180245;PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000316	PMID:18382993;PMID:14684697	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000327	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000347	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000348	PMID:14684697	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000369	PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000476	PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000692	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000773	PMID:11113916;PMID:11180245;PMID:3377005;PMID:8213919;PMID:14684697;PMID:12618959;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000774	PMID:11180245;PMID:3377005;PMID:18382993;PMID:14684697;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000782	PMID:11180245;PMID:3377005;PMID:12618959	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000878	PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000890	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0000941	PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001162	PMID:8213919;PMID:14684697;PMID:12618959	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001169	PMID:11180245;PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001367	PMID:12618959	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001433	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001539	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001552	PMID:11180245;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001561	PMID:18382993;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001640	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001790	PMID:18382993;PMID:14684697;PMID:12618959;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001802	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001804	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001830	PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001852	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0001978	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002089	PMID:11113916;PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002101	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002202	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002240	PMID:18382993;PMID:14684697	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002566	PMID:11113916	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002694	PMID:11180245;PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002787	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0002983	PMID:11113916;PMID:14684694	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003015	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003021	PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003027	OMIM:215140	TAS				P		HPO:skoehler	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003107	PMID:14684697;PMID:12618959	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003440	PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003811	PMID:14684697	PCS				M		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0003826	OMIM:215140	TAS				M		HPO:skoehler	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0004331	PMID:11180245;PMID:3377005;PMID:8213919;PMID:14684697;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0004510	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0004598	OMIM:215140	TAS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0004599	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005019	PMID:8213919	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005099	OMIM:215140	TAS				P		HPO:skoehler	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005280	PMID:18382993;PMID:14684697	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005528	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005716	PMID:14684697	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0005855	PMID:11113916;PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0006487	PMID:12618959;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0006559	PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0006619	PMID:11180245;PMID:3377005;PMID:8213919;PMID:18382993;PMID:14684697;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0006637	PMID:3377005;PMID:8213919	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008364	PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008420	PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008479	PMID:3377005	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008516	PMID:3377005;PMID:8213919	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008754	PMID:3377005;PMID:14684697;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008873	PMID:18382993;PMID:14684694	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0008905	OMIM:215140	TAS				P		HPO:skoehler	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0009106	PMID:11180245;PMID:3377005;PMID:8213919;PMID:14684697;PMID:12618959;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0009107	PMID:3377005;PMID:18382993	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0009487	PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0009803	PMID:11113916;PMID:11180245;PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0010655	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0010659	OMIM:215140	IEA				P		HPO:iea	
OMIM	215140	#215140 GREENBERG DYSPLASIA; GRBGD;;HYDROPS-ECTOPIC CALCIFICATION-MOTH-EATEN SKELETAL DYSPLASIA;;HEM SKELETAL DYSPLASIA;;MOTH-EATEN SKELETAL DYSPLASIA;;CHONDRODYSTROPHY, HYDROPIC AND PRENATALLY LETHAL TYPE		HP:0010675	PMID:3377005;PMID:8213919;PMID:12210303	PCS				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000007	OMIM:215150	TAS				I		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000175	OMIM:215150	TAS				P		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000201	OMIM:215150	TAS				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000272	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000347	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000407	OMIM:215150	TAS				P		HPO:skoehler	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000410	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000414	OMIM:215150	TAS				P		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000463	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0000926	OMIM:215150	TAS	HP:0011463			P		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0001371	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0002656	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0002829	OMIM:215150	TAS				P		HPO:skoehler	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0002938	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0003015	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0003026	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0003037	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0003088	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0003417	OMIM:215150	TAS	HP:0011463			P		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0004279	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0004322	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0004568	OMIM:215150	TAS				P		HPO:probinson	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0004679	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0005003	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0006237	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0006532	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0009803	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0010049	OMIM:215150	IEA				P		HPO:iea	
OMIM	215150	#215150 OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA; OSMED;;CHONDRODYSTROPHY WITH SENSORINEURAL DEAFNESS;;NANCE-INSLEY SYNDROME;;NANCE-SWEENEY CHONDRODYSPLASIA		HP:0011800	OMIM:215150	TAS				P		HPO:skoehler	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0000007	OMIM:215250	IEA				I		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0000093	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0000100	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0001518	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0001648	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0002086	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0002720	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0002721	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0002843	OMIM:215250	IEA				P		HPO:skoehler	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0004322	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0006462	OMIM:215250	TAS				P		HPO:probinson	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0006577	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0007759	OMIM:215250	IEA				P		HPO:iea	
OMIM	215250	CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME		HP:0008155	OMIM:215250	IEA				P		HPO:iea	
OMIM	215300	#215300 CHONDROSARCOMA		HP:0000007	OMIM:215300	IEA				I		HPO:iea	
OMIM	215300	#215300 CHONDROSARCOMA		HP:0000924	OMIM:215300	IEA				P		HPO:iea	
OMIM	215300	#215300 CHONDROSARCOMA		HP:0006765	OMIM:215300	TAS				P		HPO:skoehler	
OMIM	215400	#215400 CHORDOMA, SUSCEPTIBILITY TO; CHDM		HP:0000006	OMIM:215400	IEA				I		HPO:iea	
OMIM	215400	#215400 CHORDOMA, SUSCEPTIBILITY TO; CHDM		HP:0000234	OMIM:215400	IEA				P		HPO:iea	
OMIM	215400	#215400 CHORDOMA, SUSCEPTIBILITY TO; CHDM		HP:0000925	OMIM:215400	IEA				P		HPO:iea	
OMIM	215400	#215400 CHORDOMA, SUSCEPTIBILITY TO; CHDM		HP:0010762	OMIM:215400	TAS				P		HPO:skoehler	
OMIM	215450	CHOREA, BENIGN FAMILIAL		HP:0000007	OMIM:215450	IEA				I		HPO:iea	
OMIM	215450	CHOREA, BENIGN FAMILIAL		HP:0002072	OMIM:215450	IEA				P		HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0000007	PMID:24355708	PCS				I	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0000044	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	9/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0000529	PMID:24355708	PCS				P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0000556	OMIM:215470	IEA				P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0000613	OMIM:215470	IEA				P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001135	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	8/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001251	OMIM:215470	TAS				P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001256	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HP:probinson	6/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001257	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	3/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001265	PMID:24355708	PCS				P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001272	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	9/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0001284	OMIM:215470	TAS				P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0002066	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HP:probinson	9/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0002080	OMIM:215470	IEA				P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0002127	OMIM:215470	TAS		HP:0040283		P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	HP:0040283
OMIM	215470	Boucher-Neuhauser syndrome		HP:0002168	OMIM:215470	IEA				P	BOUCHER-NEUHAUSER SYNDROME	HPO:iea	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0003621	OMIM:215470	TAS				C	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0003676	PMID:24355708	PCS				C	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0003693	PMID:24355708	PCS		HP:0040284		P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	5/9
OMIM	215470	Boucher-Neuhauser syndrome		HP:0007263	OMIM:215470	TAS				P	BOUCHER-NEUHAUSER SYNDROME	HPO:skoehler	
OMIM	215470	Boucher-Neuhauser syndrome		HP:0030339	PMID:25299038	PCS				P	BOUCHER-NEUHAUSER SYNDROME	HP:probinson	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0000007	OMIM:215480	IEA				I		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0000486	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0001250	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0001608	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0001939	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0002922	OMIM:215480	TAS				P		HPO:skoehler	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0003487	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0006801	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0006887	OMIM:215480	IEA				P		HPO:iea	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0006960	OMIM:215480	TAS				P		HPO:skoehler	
OMIM	215480	215480 CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION		HP:0010864	OMIM:215480	TAS				P		HPO:skoehler	
OMIM	215500	%215500 CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 1; CACD1;;CHOROIDAL DYSTROPHY, CENTRAL AREOLAR; CACD;;CHOROIDAL SCLEROSIS		HP:0000007	OMIM:215500	IEA				I		HPO:iea	
OMIM	215500	%215500 CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, 1; CACD1;;CHOROIDAL DYSTROPHY, CENTRAL AREOLAR; CACD;;CHOROIDAL SCLEROSIS		HP:0030491	OMIM:215500	TAS				P		HPO:skoehler	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0000007	OMIM:215510	IEA				I		HPO:iea	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0000252	OMIM:215510	IEA				P		HPO:iea	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0001252	OMIM:215510	IEA				P		HPO:iea	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0001263	OMIM:215510	IEA				P		HPO:iea	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0001290	OMIM:215510	TAS				P		HPO:skoehler	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0002664	OMIM:215510	TAS				P		HPO:skoehler	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0003220	OMIM:215510	TAS				P		HPO:probinson	
OMIM	215510	CHROMOSOMAL INSTABILITY WITH TISSUE-SPECIFIC RADIOSENSITIVITY		HP:0011133	OMIM:215510	TAS				P		HPO:probinson	
OMIM	215518	CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION		HP:0000007	OMIM:215518	IEA				I		HPO:iea	
OMIM	215518	CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION		HP:0001939	OMIM:215518	IEA				P		HPO:iea	
OMIM	215518	CILIARY DISCOORDINATION DUE TO RANDOM CILIARY ORIENTATION		HP:0002719	OMIM:215518	IEA				P		HPO:iea	
OMIM	215520	CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES		HP:0000007	OMIM:215520	IEA				I		HPO:iea	
OMIM	215520	CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES		HP:0005425	OMIM:215520	TAS				P		HPO:probinson	
OMIM	215520	CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES		HP:0005938	OMIM:215520	TAS				P		HPO:probinson	
OMIM	215520	CILIARY DYSKINESIA DUE TO TRANSPOSITION OF CILIARY MICROTUBULES		HP:0012265	OMIM:215520	TAS				P		HPO:probinson	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0000007	OMIM:215550	IEA				I		HPO:iea	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0000924	OMIM:215550	IEA				P		HPO:iea	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0000951	OMIM:215550	IEA				P		HPO:iea	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0001561	OMIM:215550	IEA				P		HPO:iea	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0002093	OMIM:215550	IEA				P		HPO:iea	
OMIM	215550	CIRCUMVALLATE PLACENTA SYNDROME		HP:0002170	OMIM:215550	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0000007	OMIM:215600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0000822	OMIM:215600	IEA				P		HPO:skoehler	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0000952	OMIM:215600	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0001254	OMIM:215600	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0001413	OMIM:215600	TAS				P		HPO:skoehler	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0001945	OMIM:215600	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0002040	OMIM:215600	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0002092	OMIM:215600	IEA				P		HPO:skoehler	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0003270	OMIM:215600	IEA				P		HPO:iea	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0410067	PMID:2311216	PCS				P		HPO:NicoleVasilevsky	
OMIM	215600	CIRRHOSIS, FAMILIAL		HP:0410069	PMID:3426740	PCS				P		HPO:NicoleVasilevsky	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0000007	OMIM:215700	PCS				I		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0000737	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001249	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001250	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001251	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001254	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001259	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001263	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001297	OMIM:215700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001394	OMIM:215700	TAS				P		HPO:skoehler	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001508	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001950	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001951	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0001987	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0002013	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0002038	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0002181	OMIM:215700	IEA				P		HPO:iea	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0002240	OMIM:215700	TAS				P		HPO:skoehler	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0003217	OMIM:215700	TAS				P		HPO:probinson	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0003218	OMIM:215700	TAS				P		HPO:probinson	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0003623	OMIM:215700	TAS				C		HPO:skoehler	
OMIM	215700	CITRULLINEMIA, CLASSIC		HP:0005961	OMIM:215700	TAS				P		HPO:probinson	
OMIM	215720	CITRULLINE TRANSPORT DEFECT		HP:0000007	OMIM:215720	IEA				I		HPO:iea	
OMIM	215720	CITRULLINE TRANSPORT DEFECT		HP:0001510	OMIM:215720	IEA				P		HPO:iea	
OMIM	215720	CITRULLINE TRANSPORT DEFECT		HP:0001939	OMIM:215720	IEA				P		HPO:iea	
OMIM	215800	CLEFT LARYNX, POSTERIORSTRIDOR, CONGENITAL, INCLUDED		HP:0000007	OMIM:215800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	215800	CLEFT LARYNX, POSTERIORSTRIDOR, CONGENITAL, INCLUDED		HP:0000961	OMIM:215800	IEA				P		HPO:iea	
OMIM	215800	CLEFT LARYNX, POSTERIORSTRIDOR, CONGENITAL, INCLUDED		HP:0001608	OMIM:215800	IEA				P		HPO:iea	
OMIM	215800	CLEFT LARYNX, POSTERIORSTRIDOR, CONGENITAL, INCLUDED		HP:0002835	OMIM:215800	IEA				P		HPO:iea	
OMIM	215800	CLEFT LARYNX, POSTERIORSTRIDOR, CONGENITAL, INCLUDED		HP:0006511	OMIM:215800	IEA				P		HPO:iea	
OMIM	215850	CLEFT-LIMB-HEART MALFORMATION SYNDROME		HP:0000007	OMIM:215850	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	215850	CLEFT-LIMB-HEART MALFORMATION SYNDROME		HP:0001159	OMIM:215850	IEA				P		HPO:skoehler	
OMIM	215850	CLEFT-LIMB-HEART MALFORMATION SYNDROME		HP:0001507	OMIM:215850	IEA				P		HPO:iea	
OMIM	215850	CLEFT-LIMB-HEART MALFORMATION SYNDROME		HP:0001660	OMIM:215850	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000007	OMIM:216100	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000085	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000204	OMIM:216100	TAS				P		HPO:probinson	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000252	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000316	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000508	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0000824	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001191	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001249	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001377	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001438	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001545	OMIM:216100	TAS				P		HPO:probinson	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0001780	OMIM:216100	TAS				P		HPO:probinson	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0002553	OMIM:216100	TAS				P		HPO:probinson	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0003995	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0004322	OMIM:216100	IEA				P		HPO:iea	
OMIM	216100	CLEFT LIP/PALATE WITH ABNORMAL THUMBS AND MICROCEPHALY		HP:0009601	OMIM:216100	IEA				P		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0000007	OMIM:216300	IEA				I		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0000185	OMIM:216300	IEA				P		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0001852	OMIM:216300	IEA				P		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0008498	OMIM:216300	TAS				P		HPO:probinson	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0008513	OMIM:216300	IEA				P		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0010109	OMIM:216300	IEA				P		HPO:iea	
OMIM	216300	CLEFT PALATE, DEAFNESS, AND OLIGODONTIA		HP:0012225	OMIM:216300	TAS				P		HPO:probinson	
OMIM	216330	CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM		HP:0000007	OMIM:216330	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	216330	CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM		HP:0000248	OMIM:216330	IEA				P		HPO:iea	
OMIM	216330	CLEIDOCRANIAL DYSPLASIA, RECESSIVE FORM		HP:0003510	OMIM:216330	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000007	OMIM:216340	IEA				I		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000028	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000047	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000054	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000188	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000216	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000233	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000239	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000252	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000268	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000316	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000322	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000347	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000365	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000369	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000385	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000463	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000464	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000518	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000520	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000535	OMIM:216340	PCS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000582	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000647	OMIM:216340	IEA				P		HPO:iea	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000653	OMIM:216340	PCS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000782	OMIM:216340	TAS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000894	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0000954	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001182	OMIM:216340	TAS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001274	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001290	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001302	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001321	OMIM:216340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001511	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001525	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001561	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001622	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001629	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001636	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001638	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001770	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001789	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001831	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0001871	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002021	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002092	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002139	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002209	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002561	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002692	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0002827	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0004331	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0006323	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0006628	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0006660	OMIM:216340	TAS				P		HPO:skoehler	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0008362	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0008386	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0009381	OMIM:216340	TAS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0009777	OMIM:216340	TAS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0009835	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0009843	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0011309	OMIM:216340	IEA				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0011309	OMIM:216340	TAS				P		HPO:probinson	
OMIM	216340	YUNIS-VARON SYNDROME		HP:0011344	OMIM:216340	PCS				P		HPO:probinson	
OMIM	216360	COACH SYNDROME		HP:0000007	OMIM:216360	IEA				I		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000083	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0000090	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0000154	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000311	OMIM:216360	IEA				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0000316	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000463	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000508	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000589	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0000639	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0000657	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0000822	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001162	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0001250	OMIM:216360	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216360	COACH SYNDROME		HP:0001251	OMIM:216360	IEA				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001252	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0001257	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0001263	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001290	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001320	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001347	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001394	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001395	OMIM:216360	TAS	HP:0003577			P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001409	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001425	OMIM:216360	TAS				I		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001438	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0001510	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0001744	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0002085	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0002240	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0002342	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0002419	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0002617	OMIM:216360	IEA				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0002910	OMIM:216360	TAS				P		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0003593	OMIM:216360	TAS				C		HPO:skoehler	
OMIM	216360	COACH SYNDROME		HP:0006817	OMIM:216360	IEA				P		HPO:iea	
OMIM	216360	COACH SYNDROME		HP:0008659	OMIM:216360	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000007	PMID:16865293	PCS				I		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000028	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000054	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000083	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000093	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000135	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000252	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000292	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000303	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000377	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000407	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000417	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000486	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000518	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000540	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000580	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000633	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000639	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000648	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000649	OMIM:216400	TAS				P		HPO:probinson	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000670	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000680	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000685	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000689	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000726	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000762	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000822	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000858	OMIM:216400	TAS				P		HPO:skoehler	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000958	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000970	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000987	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0000992	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001000	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001249	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001250	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001251	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001260	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001271	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001288	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001324	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001337	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001376	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001425	OMIM:216400	TAS				I		HPO:skoehler	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001511	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0001744	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002059	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002135	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002240	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002343	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002545	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002684	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002808	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0002866	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0003224	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0003278	OMIM:216400	TAS				P		HPO:probinson	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0003357	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0003469	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0003758	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0005328	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0006958	OMIM:216400	TAS				P		HPO:probinson	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0007759	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0007814	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0008070	OMIM:216400	TAS				P		HPO:skoehler	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0008839	OMIM:216400	TAS				P		HPO:probinson	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0008850	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0010234	OMIM:216400	IEA				P		HPO:iea	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0011359	OMIM:216400	TAS				P		HPO:skoehler	
OMIM	216400	COCKAYNE SYNDROME A; CSA		HP:0011675	OMIM:216400	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000007	OMIM:216550	IEA				I		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000194	OMIM:216550	IEA				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0000252	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000297	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0000322	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000327	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME	HP:0012825	HP:0000347	OMIM:216550	TAS				P		HPO:probinson	
OMIM	216550	COHEN SYNDROME		HP:0000426	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000444	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000494	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000505	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000545	PMID:12446373	PCS		HP:0040280		P		HPO:probinson	HP:0040280
OMIM	216550	COHEN SYNDROME		HP:0000574	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000648	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000662	PMID:12446373	PCS		HP:0040284		P		HPO:probinson	18/22
OMIM	216550	COHEN SYNDROME		HP:0000675	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000823	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000824	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0000954	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001135	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001182	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001249	OMIM:216550	IEA				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0001250	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001270	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001290	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0001319	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001321	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0001382	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001518	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001601	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001634	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001763	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0001875	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0001882	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0002705	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0002857	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0002938	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME	HP:0012825	HP:0002943	OMIM:216550	TAS				P		HPO:probinson	
OMIM	216550	COHEN SYNDROME		HP:0002967	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0004283	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0004283	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0004322	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0007074	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0007663	OMIM:216550	TAS				P		HPO:skoehler	
OMIM	216550	COHEN SYNDROME		HP:0007737	PMID:12446373	PCS		HP:0040284		P		HPO:probinson	11/13
OMIM	216550	COHEN SYNDROME		HP:0008872	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0008915	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0010049	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0010743	OMIM:216550	IEA				P		HPO:iea	
OMIM	216550	COHEN SYNDROME		HP:0011504	PMID:12446373	PCS	HP:0011463	HP:0040284		P		HPO:probinson	5/9
OMIM	216700	COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING		HP:0000007	OMIM:216700	IEA				I		HPO:iea	
OMIM	216700	COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING		HP:0000951	OMIM:216700	IEA				P		HPO:iea	
OMIM	216700	COLLAGENOSIS, FAMILIAL REACTIVE PERFORATING		HP:0001939	OMIM:216700	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0000007	OMIM:216800	IEA				I		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0000175	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0000340	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0000540	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0000639	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0001116	OMIM:216800	TAS				P		HPO:probinson	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0001822	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0002673	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0002857	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0005001	OMIM:216800	IEA				P		HPO:iea	
OMIM	216800	COLOBOMA OF MACULA AND SKELETAL ANOMALIES		HP:0009184	OMIM:216800	TAS				P		HPO:probinson	
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:216820	TAS				I		HPO:skoehler	
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:216820	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000565	OMIM:216820	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000577	OMIM:216820	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000589	OMIM:216820	IEA				P		HPO:iea	
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:216820	IEA				P		HPO:skoehler	
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0001132	OMIM:216820	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0007663	OMIM:216820	TAS				P		HPO:skoehler	
OMIM	216820	COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE		HP:0025586	OMIM:216820	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0000007	OMIM:216900	IEA				I		HPO:iea	
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0000613	OMIM:216900	IEA				P		HPO:iea	
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0000618	OMIM:216900	IEA				P		HPO:skoehler	
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0000639	OMIM:216900	IEA				P		HPO:skoehler	
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0011516	OMIM:216900	TAS				P		HPO:skoehler	
OMIM	216900	#216900 ACHROMATOPSIA 2; ACHM2;;COLORBLINDNESS, TOTAL;;ROD MONOCHROMATISM 2;;ROD MONOCHROMACY 2; RMCH2		HP:0012047	OMIM:216900	TAS				P		HPO:skoehler	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0000007	OMIM:216920	IEA				I		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0001507	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0001875	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0001880	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0002718	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0002733	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0002972	OMIM:216920	IEA				P		HPO:iea	
OMIM	216920	COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT		HP:0003261	OMIM:216920	IEA				P		HPO:iea	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0000007	OMIM:216950	IEA				I		HPO:iea	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY	HP:0012825	HP:0000123	OMIM:216950	TAS				P		HPO:skoehler	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0001369	OMIM:216950	TAS				P		HPO:probinson	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0002829	OMIM:216950	IEA				P		HPO:iea	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0002837	OMIM:216950	TAS				P		HPO:probinson	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0002960	OMIM:216950	IEA				P		HPO:iea	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0004431	OMIM:216950	IEA				P		HPO:iea	
OMIM	216950	COMPLEMENT COMPONENT C1R DEFICIENCY		HP:0007417	OMIM:216950	IEA				P		HPO:iea	
OMIM	217000	COMPLEMENT COMPONENT 2 DEFICIENCY		HP:0000007	OMIM:217000	IEA				I		HPO:iea	
OMIM	217000	COMPLEMENT COMPONENT 2 DEFICIENCY		HP:0000979	OMIM:217000	IEA				P		HPO:skoehler	
OMIM	217000	COMPLEMENT COMPONENT 2 DEFICIENCY		HP:0002725	OMIM:217000	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000007	OMIM:217080	IEA				I		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000543	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000548	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000613	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000639	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000662	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000670	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0000705	OMIM:217080	IEA				P		HPO:iea	
OMIM	217080	#217080 JALILI SYNDROME;;CONE-ROD DYSTROPHY AND AMELOGENESIS IMPERFECTA		HP:0007803	OMIM:217080	TAS				P		HPO:skoehler	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0000007	OMIM:217085	TAS				I		HPO:skoehler	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0000316	OMIM:217085	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0001162	OMIM:217085	IEA				P		HPO:iea	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0001233	OMIM:217085	TAS				P		HPO:probinson	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0001674	OMIM:217085	IEA				P		HPO:iea	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0001680	OMIM:217085	IEA				P		HPO:iea	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0001682	OMIM:217085	TAS				P		HPO:skoehler	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY	HP:0012832	HP:0010055	OMIM:217085	TAS				P		HPO:skoehler	
OMIM	217085	CONGENITAL HEART DEFECTS, HAMARTOMAS OF TONGUE, AND POLYSYNDACTYLY		HP:0011802	OMIM:217085	TAS				P		HPO:probinson	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000007	OMIM:217090	IEA				I		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000123	OMIM:217090	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000212	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000230	OMIM:217090	IEA				P		HPO:skoehler	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000238	OMIM:217090	IEA				P		HPO:skoehler	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000256	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000509	OMIM:217090	IEA				P		HPO:skoehler	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000598	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000618	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000704	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000787	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0000951	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0001305	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0001321	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0001600	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0001939	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0002588	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0002788	OMIM:217090	IEA				P		HPO:iea	
OMIM	217090	PLASMINOGEN DEFICIENCY, TYPE ILIGNEOUS CONJUNCTIVITIS, INCLUDED		HP:0003593	OMIM:217090	IEA				C		HPO:iea	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0000007	OMIM:217095	IEA				I		HPO:iea	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0000316	OMIM:217095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001660	OMIM:217095	IEA				P		HPO:skoehler	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001669	OMIM:217095	TAS				P		HPO:skoehler	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001674	OMIM:217095	TAS				P		HPO:skoehler	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001680	OMIM:217095	TAS				P		HPO:skoehler	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001719	OMIM:217095	IEA				P		HPO:iea	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0001939	OMIM:217095	IEA				P		HPO:iea	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED	HP:0012832	HP:0010055	OMIM:217095	TAS				P		HPO:skoehler	
OMIM	217095	#217095 CONOTRUNCAL HEART MALFORMATIONS; CTHMTRUNCUS ARTERIOSUS COMMUNIS, INCLUDED;;CONOTRUNCAL ANOMALY FACE SYNDROME, INCLUDED; CAFS, INCLUDED;;DOUBLE-OUTLET RIGHT VENTRICLE, INCLUDED; DORV, INCLUDED;;PERSISTENT TRUNCUS ARTERIOSUS, INCLUDED; PTA, INCLUDED;;INTERRUPTED AORTIC ARCH, INCLUDED		HP:0100259	OMIM:217095	TAS				P		HPO:skoehler	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0000175	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0000204	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0000625	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001159	OMIM:217100	IEA				P		HPO:skoehler	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001161	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001539	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001543	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001547	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001683	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0001762	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0002006	OMIM:217100	TAS				P		HPO:skoehler	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0002084	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0002101	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0002650	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0002836	OMIM:217100	IEA				P		HPO:iea	
OMIM	217100	%217100 CONSTRICTING BANDS, CONGENITAL;;AMNIOTIC BAND SEQUENCE; ABS;;STREETER ANOMALYADAM COMPLEX, INCLUDED;;TERMINAL TRANSVERSE DEFECTS OF ARM, INCLUDED;;AMPUTATION, CONGENITAL, INCLUDED		HP:0003745	OMIM:217100	IEA				I		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0000007	OMIM:217150	IEA				I		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0000175	OMIM:217150	IEA				P		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0000277	OMIM:217150	IEA				P		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0000473	OMIM:217150	IEA				P		HPO:skoehler	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0000695	OMIM:217150	IEA				P		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0002047	OMIM:217150	IEA				P		HPO:iea	
OMIM	217150	CONTRACTURES, CONGENITAL, TORTICOLLIS, AND MALIGNANT HYPERTHERMIA		HP:0002804	OMIM:217150	IEA				P		HPO:iea	
OMIM	217200	CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET		HP:0000007	OMIM:217200	IEA				I		HPO:iea	
OMIM	217200	CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET		HP:0001249	OMIM:217200	IEA				P		HPO:iea	
OMIM	217200	CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET		HP:0001250	OMIM:217200	IEA				P		HPO:skoehler	
OMIM	217200	CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET		HP:0001336	OMIM:217200	IEA				P		HPO:skoehler	
OMIM	217200	CONVULSIVE DISORDER, FAMILIAL, WITH PRENATAL OR EARLY ONSET		HP:0001522	OMIM:217200	IEA				M		HPO:iea	
OMIM	217300	#217300 CORNEA PLANA 2; CNA2		HP:0000007	OMIM:217300	IEA				I		HPO:iea	
OMIM	217300	#217300 CORNEA PLANA 2; CNA2		HP:0000540	OMIM:217300	IEA				P		HPO:skoehler	
OMIM	217300	#217300 CORNEA PLANA 2; CNA2		HP:0001084	OMIM:217300	IEA				P		HPO:skoehler	
OMIM	217300	#217300 CORNEA PLANA 2; CNA2		HP:0007720	OMIM:217300	TAS				P		HPO:skoehler	
OMIM	217300	#217300 CORNEA PLANA 2; CNA2		HP:0100689	OMIM:217300	TAS				P		HPO:skoehler	
OMIM	217400	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS		HP:0000007	PMID:11836359	PCS				I		HPO:iea	
OMIM	217400	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS		HP:0000407	PMID:17220209	PCS				P		HPO:probinson	
OMIM	217400	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS		HP:0001131	OMIM:217400	IEA				P		HPO:iea	
OMIM	217400	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS		HP:0007663	PMID:17220209	PCS				P		HP:probinson	
OMIM	217400	CORNEAL DYSTROPHY AND PERCEPTIVE DEAFNESS		HP:0007759	OMIM:217400	IEA				P		HPO:iea	
OMIM	217500	CORNEAL DYSTROPHY, BAND-SHAPED		HP:0000007	OMIM:217500	IEA				I		HPO:iea	
OMIM	217500	CORNEAL DYSTROPHY, BAND-SHAPED		HP:0007709	OMIM:217500	IEA				P		HPO:iea	
OMIM	217520	217520 CORNEAL DEGENERATION, BAND-SHAPED SPHEROID		HP:0000007	OMIM:217520	TAS				I		HPO:skoehler	
OMIM	217520	217520 CORNEAL DEGENERATION, BAND-SHAPED SPHEROID		HP:0007705	OMIM:217520	IEA				P		HPO:skoehler	
OMIM	217600	CORNEAL DYSTROPHY, CENTRAL TYPE		HP:0000007	OMIM:217600	IEA				I		HPO:iea	
OMIM	217600	CORNEAL DYSTROPHY, CENTRAL TYPE		HP:0001131	OMIM:217600	IEA				P		HPO:skoehler	
OMIM	217600	CORNEAL DYSTROPHY, CENTRAL TYPE		HP:0007881	OMIM:217600	IEA				P		HPO:iea	
OMIM	217700	CORNEAL ENDOTHELIAL DYSTROPHY 2		HP:0000007	OMIM:217700	IEA				I		HPO:iea	
OMIM	217700	CORNEAL ENDOTHELIAL DYSTROPHY 2		HP:0007759	OMIM:217700	IEA				P		HPO:iea	
OMIM	217700	CORNEAL ENDOTHELIAL DYSTROPHY 2		HP:0008005	OMIM:217700	IEA				P		HPO:iea	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0000007	OMIM:217800	IEA				I		HPO:iea	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0000495	OMIM:217800	IEA				P		HPO:skoehler	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0000613	OMIM:217800	IEA				P		HPO:iea	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0001131	OMIM:217800	IEA				P		HPO:skoehler	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0001939	OMIM:217800	IEA				P		HPO:iea	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0003621	OMIM:217800	IEA				C		HPO:iea	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0007754	OMIM:217800	TAS				P		HPO:skoehler	
OMIM	217800	MACULAR DYSTROPHY, CORNEAL, 1		HP:0007856	OMIM:217800	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000007	OMIM:217980	IEA				I		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000028	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000047	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000175	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000201	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000252	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000260	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000293	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000316	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000347	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000377	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000463	OMIM:217980	IEA				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000470	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000506	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000508	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000581	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0000774	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001156	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001159	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001249	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001252	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001274	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001290	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001321	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001545	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001600	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001638	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001643	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0001671	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0002098	OMIM:217980	TAS	HP:0003623			P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0002643	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0002714	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0002777	OMIM:217980	TAS	HP:0003577			P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0002779	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0003196	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0004279	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0005280	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0005989	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0008749	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0009623	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0012745	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0030084	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0030680	OMIM:217980	IEA				P		HPO:iea	
OMIM	217980	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE		HP:0100790	OMIM:217980	TAS				P		HPO:skoehler	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0000007	OMIM:217990	IEA				I		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0000252	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0000256	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0000384	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0001249	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0001274	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0001510	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0002007	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0009473	OMIM:217990	IEA				P		HPO:iea	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0011220	OMIM:217990	TAS				P		HPO:skoehler	
OMIM	217990	%217990 CORPUS CALLOSUM, AGENESIS OF;;ACC		HP:0012385	OMIM:217990	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000007	OMIM:218000	IEA				I		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000218	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000248	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000276	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000294	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000316	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000324	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000327	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000341	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000400	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000431	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000508	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000709	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0000763	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001182	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001249	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001250	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001263	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001270	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001271	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001274	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001284	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001290	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001319	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001349	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0001371	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0002111	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0002119	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0002650	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0002922	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003196	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003202	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003378	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003383	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003431	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003444	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003448	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003477	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003676	OMIM:218000	IEA				C		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0003690	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0004691	OMIM:218000	TAS				P		HPO:probinson	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0007178	OMIM:218000	IEA				P		HPO:iea	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0011947	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218000	#218000 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN;;CHARLEVOIX DISEASE;;ANDERMANN SYNDROME;;POLYNEUROPATHY, SENSORIMOTOR, WITH OR WITHOUT AGENESIS OF THE CORPUSCALLOSUM;;CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY		HP:0200085	OMIM:218000	TAS				P		HPO:skoehler	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0000007	OMIM:218010	IEA				I		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0000308	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0000343	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0001263	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0001507	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0002007	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0003196	OMIM:218010	IEA				P		HPO:iea	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0011220	OMIM:218010	TAS				P		HPO:skoehler	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0025356	OMIM:218010	IEA				P		HPO:skoehler	
OMIM	218010	CORTICAL BLINDNESS, RETARDATION, AND POSTAXIAL POLYDACTYLY		HP:0100704	OMIM:218010	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0000007	OMIM:218030	IEA				I		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0000822	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0001095	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0001508	OMIM:218030	TAS				P		HPO:skoehler	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0001510	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0001518	OMIM:218030	TAS				P		HPO:skoehler	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0002900	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0003351	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0003828	OMIM:218030	TAS				C		HPO:skoehler	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0004319	OMIM:218030	IEA				P		HPO:iea	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0004319	OMIM:218030	TAS				P		HPO:skoehler	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0004322	OMIM:218030	TAS				P		HPO:skoehler	
OMIM	218030	#218030 APPARENT MINERALOCORTICOID EXCESS; AME;;AME1;;CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY		HP:0200114	OMIM:218030	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000006	OMIM:218040	IEA				I		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000083	OMIM:218040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000158	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000179	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000218	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000238	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000256	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000260	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000280	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000286	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000293	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000307	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000316	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000347	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000358	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000369	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000463	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000465	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000470	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000486	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000494	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000508	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000768	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000953	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0000956	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001187	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001249	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001263	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001508	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001548	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001552	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001561	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001598	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001609	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001622	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001629	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001631	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001634	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001639	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001642	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001699	OMIM:218040	IEA				M		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001762	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001771	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001808	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001814	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001816	OMIM:218040	TAS				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001869	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0001943	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002021	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002033	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002059	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002093	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002107	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002119	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002212	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002779	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002780	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002859	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002862	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002870	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002878	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0002996	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0003745	OMIM:218040	IEA				I		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0003764	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0004322	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0005280	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0005989	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0006191	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0007099	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0008070	OMIM:218040	IEA				P		HPO:iea	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0009588	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0011675	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0012081	OMIM:218040	TAS				P		HPO:skoehler	
OMIM	218040	COSTELLO SYNDROME; CSTLO		HP:0031842	OMIM:218040	IEA				P		HPO:skoehler	
OMIM	218050	CRAMPS, FAMILIAL ADOLESCENT		HP:0000007	OMIM:218050	IEA				I		HPO:iea	
OMIM	218050	CRAMPS, FAMILIAL ADOLESCENT		HP:0003011	OMIM:218050	IEA				P		HPO:iea	
OMIM	218050	CRAMPS, FAMILIAL ADOLESCENT		HP:0003236	OMIM:218050	IEA				P		HPO:iea	
OMIM	218100	CRANIAL NERVES, CONGENITAL PARESIS OF		HP:0000007	OMIM:218100	IEA				I		HPO:iea	
OMIM	218100	CRANIAL NERVES, CONGENITAL PARESIS OF		HP:0000377	OMIM:218100	IEA				P		HPO:iea	
OMIM	218100	CRANIAL NERVES, CONGENITAL PARESIS OF		HP:0010628	OMIM:218100	IEA				P		HPO:iea	
OMIM	218200	CRANIAL NERVES, RECURRENT PARESIS OF		HP:0000007	OMIM:218200	TAS				I		HPO:nvasilevsky	
OMIM	218200	CRANIAL NERVES, RECURRENT PARESIS OF		HP:0000819	OMIM:218200	IEA				P		HPO:iea	
OMIM	218200	CRANIAL NERVES, RECURRENT PARESIS OF		HP:0007250	OMIM:218200	IEA				P		HPO:iea	
OMIM	218200	CRANIAL NERVES, RECURRENT PARESIS OF		HP:0009830	OMIM:218200	IEA				P		HPO:skoehler	
OMIM	218200	CRANIAL NERVES, RECURRENT PARESIS OF		HP:0010628	OMIM:218200	IEA				P		HPO:iea	
OMIM	218300	218300 CRANIODIAPHYSEAL DYSPLASIA; CDD		HP:0000007	OMIM:218300	TAS				I		HPO:probinson	
OMIM	218300	218300 CRANIODIAPHYSEAL DYSPLASIA; CDD		HP:0001249	OMIM:218300	TAS				P		HPO:iea	
OMIM	218300	218300 CRANIODIAPHYSEAL DYSPLASIA; CDD		HP:0003034	OMIM:218300	TAS				P		HPO:iea	
OMIM	218300	218300 CRANIODIAPHYSEAL DYSPLASIA; CDD		HP:0005465	OMIM:218300	TAS				P		HPO:iea	
OMIM	218300	218300 CRANIODIAPHYSEAL DYSPLASIA; CDD		HP:0100252	OMIM:218300	TAS				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000007	OMIM:218330	IEA				I		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000218	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000232	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000268	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000286	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000293	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000431	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000463	OMIM:218330	IEA				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000506	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000545	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000556	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000601	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000639	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000668	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000674	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000687	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000691	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000767	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000773	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000774	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000939	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000954	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0000968	OMIM:218330	IEA				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001156	OMIM:218330	TAS				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001388	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001395	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001399	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001407	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001538	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001647	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001799	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001816	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001831	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001837	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0001970	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002007	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002213	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002217	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002240	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002705	OMIM:218330	TAS				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0002901	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0003038	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0003071	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0004298	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0004442	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0005567	OMIM:218330	TAS				P		HPO:probinson	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0005792	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0006297	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0006563	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0008070	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0008905	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0009466	OMIM:218330	IEA				P		HPO:iea	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0009880	OMIM:218330	TAS				P		HPO:probinson	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0009882	OMIM:218330	TAS				P		HPO:probinson	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0012622	OMIM:218330	TAS				P		HPO:probinson	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0030084	OMIM:218330	TAS				P		HPO:skoehler	
OMIM	218330	CRANIOECTODERMAL DYSPLASIA 1		HP:0030799	OMIM:218330	TAS				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000007	OMIM:218340	IEA				I		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000276	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000316	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000343	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000347	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000369	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000394	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000444	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000494	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000545	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000567	OMIM:218340	TAS				P		HPO:probinson	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000612	OMIM:218340	TAS				P		HPO:probinson	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000678	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0000685	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001156	OMIM:218340	TAS				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001250	OMIM:218340	IEA				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001256	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001263	OMIM:218340	TAS				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001274	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001290	OMIM:218340	TAS				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001659	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001762	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001763	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0001885	OMIM:218340	IEA				P		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0002007	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0002119	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0002553	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0002827	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0003593	OMIM:218340	TAS				C		HPO:skoehler	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0004942	OMIM:218340	IEA				P		HPO:iea	
OMIM	218340	TEMTAMY SYNDROME; TEMTYS		HP:0012019	OMIM:218340	IEA				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000028	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000047	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000085	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000238	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000244	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000272	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000341	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000348	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000357	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0000565	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001249	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001250	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001274	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001290	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001629	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0001643	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0002007	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0002021	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0002079	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0002280	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0003745	OMIM:218350	TAS				I		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0004322	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0007099	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE		HP:0011217	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218350	CRANIOFACIAL DYSSYNOSTOSIS WITH SHORT STATURE	HP:0012825	HP:0011800	OMIM:218350	TAS				P		HPO:skoehler	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000007	OMIM:218400	IEA				I		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000187	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000256	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000280	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000303	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000316	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000410	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000431	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000506	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000648	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000696	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0000765	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0001739	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0001742	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0003015	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0004407	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0005465	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0006384	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0009772	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0010628	OMIM:218400	IEA				P		HPO:iea	
OMIM	218400	#218400 CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; CMDR		HP:0100255	OMIM:218400	IEA				P		HPO:skoehler	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0000007	OMIM:218450	IEA				I		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0000028	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0000054	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0000211	OMIM:218450	TAS				P		HPO:skoehler	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0000347	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0001249	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0001510	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0001627	OMIM:218450	TAS				P		HPO:skoehler	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0004442	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0005607	OMIM:218450	IEA				P		HPO:iea	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0030260	OMIM:218450	TAS				P		HPO:skoehler	
OMIM	218450	CRANIOSTENOSIS, SAGITTAL, WITH CONGENITAL HEART DISEASE, MENTAL DEFICIENCY, AND MANDIBULAR ANKYLOSIS		HP:0030680	OMIM:218450	IEA				P		HPO:iea	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0000007	OMIM:218530	IEA				I		HPO:iea	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0001363	OMIM:218530	IEA				P		HPO:iea	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0001841	OMIM:218530	IEA				P		HPO:iea	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0009162	OMIM:218530	TAS				P		HPO:probinson	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0009576	OMIM:218530	TAS				P		HPO:probinson	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0009623	OMIM:218530	TAS				P		HPO:skoehler	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0009777	OMIM:218530	IEA				P		HPO:iea	
OMIM	218530	CRANIOSYNOSTOSIS WITH ANOMALIES OF THE CRANIAL BASE AND DIGITS		HP:0011926	OMIM:218530	IEA				P		HPO:skoehler	
OMIM	218550	CRANIOSYNOSTOSIS WITH FIBULAR APLASIA		HP:0000007	PMID:8100584	PCS				I		HPO:iea	
OMIM	218550	CRANIOSYNOSTOSIS WITH FIBULAR APLASIA		HP:0000028	PMID:8100584	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	218550	CRANIOSYNOSTOSIS WITH FIBULAR APLASIA	HP:0012832	HP:0000954	PMID:8100584	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	218550	CRANIOSYNOSTOSIS WITH FIBULAR APLASIA		HP:0001363	PMID:8100584	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	218550	CRANIOSYNOSTOSIS WITH FIBULAR APLASIA		HP:0002990	PMID:8100584	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000007	OMIM:218600	IEA				I		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000077	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000143	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000160	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000175	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000193	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000218	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000238	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000244	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000286	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000316	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000347	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000368	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000405	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000426	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000430	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000452	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000486	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000494	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000545	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000648	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0000902	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0001249	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0001250	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0001274	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0001545	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0001627	OMIM:218600	TAS				P		HPO:skoehler	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0002023	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0002126	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0002650	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0002984	OMIM:218600	TAS				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0002996	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003022	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003031	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003065	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003298	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003468	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0003974	OMIM:218600	TAS				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004231	OMIM:218600	TAS				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004322	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004425	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004440	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004442	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004443	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0004871	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0005201	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0005792	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0005886	OMIM:218600	IEA				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0006467	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0007452	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0009601	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0009702	OMIM:218600	IEA				P		HPO:iea	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0010048	OMIM:218600	TAS				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0011318	PMID:1583650	PCS				P		HPO:probinson	
OMIM	218600	#218600 BALLER-GEROLD SYNDROME; BGS;;CRANIOSYNOSTOSIS WITH RADIAL DEFECTS;;CRANIOSYNOSTOSIS-RADIAL APLASIA SYNDROME		HP:0030680	OMIM:218600	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000007	OMIM:218649	TAS				I		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000023	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000028	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000033	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000047	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000054	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000076	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000126	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000175	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000233	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000243	OMIM:218649	TAS				P		HPO:skoehler	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000262	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000268	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000272	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000286	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000316	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000319	OMIM:218649	TAS				P		HPO:probinson	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000343	OMIM:218649	TAS				P		HPO:probinson	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG	HP:0012825	HP:0000347	OMIM:218649	TAS				P		HPO:probinson	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000369	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000402	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000407	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000486	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000494	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000508	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000581	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000582	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000601	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000767	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000768	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0000774	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001076	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001188	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001238	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001274	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001276	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001363	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001537	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001539	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0001629	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0002000	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0002558	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0002566	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0002828	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0003196	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0004797	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0005326	OMIM:218649	TAS				P		HPO:skoehler	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0006184	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0006610	OMIM:218649	TAS				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0006887	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0007099	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0008551	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0008872	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0009473	OMIM:218649	IEA				P		HPO:iea	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0010864	OMIM:218649	TAS				P		HPO:skoehler	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0011800	OMIM:218649	TAS				P		HPO:skoehler	
OMIM	218649	CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG		HP:0012385	OMIM:218649	TAS				P		HPO:skoehler	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000007	OMIM:218650	IEA				I		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000110	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000202	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000252	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000337	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000444	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000567	OMIM:218650	TAS				P		HPO:probinson	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0000958	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0001249	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0001250	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME		HP:0001363	OMIM:218650	IEA				P		HPO:iea	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME	HP:0012825	HP:0009816	OMIM:218650	TAS				P		HPO:probinson	
OMIM	218650	CRANIOSYNOSTOSIS-MENTAL RETARDATION-CLEFTING SYNDROME	HP:0012825	HP:0009821	OMIM:218650	TAS				P		HPO:probinson	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0000007	OMIM:218670	IEA				I		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0000384	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0000568	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0000601	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0000609	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001263	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001274	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001321	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001331	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001339	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0001363	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0002139	OMIM:218670	IEA				P		HPO:iea	
OMIM	218670	CRANIOTELENCEPHALIC DYSPLASIA		HP:0007330	OMIM:218670	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0000006	OMIM:218700	TAS				I		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0000158	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0000851	OMIM:218700	IEA				P		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0000853	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0000958	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001252	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001254	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001290	OMIM:218700	TAS				P		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001510	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001537	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001615	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0001662	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0002019	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0002045	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0002750	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0002904	OMIM:218700	IEA				P		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0002925	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0003270	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0004491	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0005990	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0008191	OMIM:218700	TAS				P		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0008872	OMIM:218700	IEA				P		HPO:iea	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0010307	OMIM:218700	TAS				P		HPO:skoehler	
OMIM	218700	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2		HP:0100028	OMIM:218700	IEA				P		HPO:skoehler	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0000007	OMIM:218800	IEA				I		HPO:iea	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0000952	OMIM:218800	IEA				P		HPO:skoehler	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0001298	OMIM:218800	IEA				P		HPO:skoehler	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0001343	OMIM:218800	IEA				P		HPO:iea	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0008282	OMIM:218800	IEA				P		HPO:iea	
OMIM	218800	CRIGLER-NAJJAR SYNDROME, TYPE I		HP:0040284	OMIM:218800	IEA						HPO:skoehler	
OMIM	218900	CROME SYNDROME		HP:0000007	OMIM:218900	IEA				I		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0000519	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0000639	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0001249	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0001250	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0001298	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0004322	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0007033	OMIM:218900	IEA				P		HPO:iea	
OMIM	218900	CROME SYNDROME		HP:0008682	OMIM:218900	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000007	OMIM:219000	IEA				I		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000028	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000047	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000054	OMIM:219000	PCS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000089	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000148	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000175	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000183	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000204	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000238	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000252	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000316	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000369	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000377	OMIM:219000	PCS				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000378	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000405	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000413	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000430	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000430	OMIM:219000	TAS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000431	OMIM:219000	PCS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000445	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000452	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000528	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000561	OMIM:219000	PCS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000618	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000636	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000678	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000689	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000777	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0000813	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001126	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001249	OMIM:219000	PCS				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001362	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001551	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001602	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001607	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0001627	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002006	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002084	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002089	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002223	OMIM:219000	PCS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002244	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002475	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0002536	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0003183	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0003191	OMIM:219000	TAS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0004112	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0004378	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0005280	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0005280	OMIM:219000	PCS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0005325	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0005352	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0005950	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0006610	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0006714	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0007633	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0007925	OMIM:219000	TAS				P		HPO:probinson	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0007957	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0007993	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0008559	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0008609	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0008665	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0008678	OMIM:219000	PCS				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0008750	OMIM:219000	TAS				P		HPO:skoehler	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0009601	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0009767	OMIM:219000	IEA				P		HPO:iea	
OMIM	219000	#219000 FRASER SYNDROME;;CRYPTOPHTHALMOS WITH OTHER MALFORMATIONSCRYPTOPHTHALMOS-SYNDACTYLY SYNDROME, INCLUDED		HP:0010554	OMIM:219000	IEA				P		HPO:iea	
OMIM	219050	CRYPTORCHIDISM, UNILATERAL OR BILATERAL		HP:0000006	OMIM:219050	TAS				I		HPO:skoehler	
OMIM	219050	CRYPTORCHIDISM, UNILATERAL OR BILATERAL		HP:0000104	OMIM:219050	IEA				P		HPO:iea	
OMIM	219050	CRYPTORCHIDISM, UNILATERAL OR BILATERAL		HP:0012741	OMIM:219050	IEA				P		HPO:skoehler	
OMIM	219070	CURVED NAIL OF FOURTH TOE		HP:0000007	OMIM:219070	IEA				I		HPO:iea	
OMIM	219070	CURVED NAIL OF FOURTH TOE		HP:0001812	OMIM:219070	IEA				P		HPO:iea	
OMIM	219070	CURVED NAIL OF FOURTH TOE		HP:0008393	OMIM:219070	IEA				P		HPO:iea	
OMIM	219070	CURVED NAIL OF FOURTH TOE		HP:0009882	OMIM:219070	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000006	OMIM:219080	IEA				I		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000311	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000709	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000713	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000716	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000739	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000822	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000938	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000939	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000963	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0000978	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0001065	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0001268	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0001575	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0001579	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0001956	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0002664	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0002808	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0002920	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0003202	OMIM:219080	IEA				P		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0003581	OMIM:219080	IEA				C		HPO:iea	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0003745	OMIM:219080	IEA				I		HPO:skoehler	
OMIM	219080	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA		HP:0008231	OMIM:219080	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000006	OMIM:219090	TAS				I		HPO:nvasilevsky	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000007	OMIM:219090	TAS				I		HPO:nvasilevsky	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000787	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000822	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000876	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000939	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000963	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000969	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0000978	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001007	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001041	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001058	OMIM:219090	IEA				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001065	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001345	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001513	OMIM:219090	IEA				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001575	OMIM:219090	TAS				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001948	OMIM:219090	IEA				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0001952	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0002808	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0002893	OMIM:219090	IEA				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0002900	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0002953	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0003154	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0003202	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0004586	OMIM:219090	IEA				P		HPO:iea	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0012743	OMIM:219090	TAS				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0031364	OMIM:219090	IEA				P		HPO:skoehler	
OMIM	219090	PITUITARY ADENOMA, ACTH-SECRETING		HP:0100852	OMIM:219090	IEA				P		HPO:iea	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0000007	OMIM:219095	IEA				I		HPO:iea	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0001522	OMIM:219095	IEA				M		HPO:iea	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0002014	OMIM:219095	IEA				P		HPO:skoehler	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0002583	OMIM:219095	IEA				P		HPO:iea	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0007396	OMIM:219095	IEA				P		HPO:iea	
OMIM	219095	CUTANEOUS PHOTOSENSITIVITY AND COLITIS, LETHAL		HP:0010783	OMIM:219095	IEA				P		HPO:skoehler	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:219100	IEA				I		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000015	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000023	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:219100	TAS				P		HPO:skoehler	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000271	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000767	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0000776	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001166	OMIM:219100	TAS				P		HPO:skoehler	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001388	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001425	OMIM:219100	IEA				I		HPO:skoehler	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001537	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001548	OMIM:219100	TAS				P		HPO:skoehler	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001562	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0001582	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0002097	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0002205	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0004381	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0004948	OMIM:219100	IEA				P		HPO:iea	
OMIM	219100	#219100 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA; ARCL1A;;ARCL1;;CUTIS LAXA, AUTOSOMAL RECESSIVE		HP:0004970	OMIM:219100	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000007	OMIM:219150	IEA				I		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000023	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000028	OMIM:219150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000160	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000239	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000248	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000316	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000369	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000400	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000418	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000486	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000518	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000545	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000601	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000767	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000963	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0000973	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001084	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001181	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001249	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001250	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001252	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001263	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001290	OMIM:219150	TAS				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001347	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001374	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001382	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001508	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001511	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001537	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0001762	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0002007	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0002305	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0002645	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0002650	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0002750	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0003510	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0003745	OMIM:219150	IEA				I		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0007394	OMIM:219150	IEA				P		HPO:iea	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0008070	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0010537	OMIM:219150	IEA				P		HPO:skoehler	
OMIM	219150	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIA		HP:0011220	OMIM:219150	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000007	OMIM:219200	IEA				I		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000023	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000160	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000218	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000252	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000260	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000272	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000343	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000369	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000463	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000486	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000494	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000545	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000670	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0000973	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001249	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001250	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001252	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001270	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001290	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001302	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001305	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001374	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001382	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001508	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001511	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001582	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0001763	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0002007	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0002126	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0002208	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0002299	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0002650	OMIM:219200	IEA				P		HPO:iea	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0003160	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0003196	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0008872	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0009125	OMIM:219200	IEA				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0011800	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219200	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIA; ARCL2A		HP:0012368	OMIM:219200	TAS				P		HPO:skoehler	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000007	OMIM:219250	IEA				I		HPO:iea	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000501	OMIM:219250	TAS				P		HPO:skoehler	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000541	OMIM:219250	TAS	HP:0003577			P		HPO:skoehler	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000555	OMIM:219250	TAS				P		HPO:skoehler	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000822	OMIM:219250	IEA				P		HPO:iea	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0000965	OMIM:219250	IEA				P		HPO:iea	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0001009	OMIM:219250	IEA				P		HPO:iea	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0002979	OMIM:219250	IEA				P		HPO:iea	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0006385	OMIM:219250	TAS				P		HPO:skoehler	
OMIM	219250	CUTIS MARMORATA TELANGIECTATICA CONGENITA		HP:0025107	OMIM:219250	TAS				P		HPO:skoehler	
OMIM	219300	CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY		HP:0000007	OMIM:219300	IEA				I		HPO:iea	
OMIM	219300	CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY		HP:0001249	OMIM:219300	IEA				P		HPO:iea	
OMIM	219300	CUTIS VERTICIS GYRATA AND MENTAL DEFICIENCY		HP:0010541	OMIM:219300	IEA				P		HPO:skoehler	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0000007	OMIM:219400	IEA				I		HPO:iea	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0000961	OMIM:219400	IEA				P		HPO:iea	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0001217	OMIM:219400	IEA				P		HPO:iea	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0001438	OMIM:219400	IEA				P		HPO:iea	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0002094	OMIM:219400	IEA				P		HPO:iea	
OMIM	219400	219400 CYANOSIS AND HEPATIC DISEASE		HP:0012115	OMIM:219400	TAS				P		HPO:skoehler	
OMIM	219500	CYSTATHIONINURIA		HP:0000007	OMIM:219500	TAS				I		HPO:probinson	
OMIM	219500	CYSTATHIONINURIA		HP:0003153	OMIM:219500	TAS				P		HPO:probinson	
OMIM	219550	CYSTEINE PEPTIDURIA		HP:0000007	OMIM:219550	IEA				I		HPO:iea	
OMIM	219550	CYSTEINE PEPTIDURIA		HP:0001249	PMID:4730204	PCS				P		HPO:iea	
OMIM	219550	CYSTEINE PEPTIDURIA		HP:0010895	PMID:4730204	PCS				P		HPO:lccarmody	
OMIM	219550	CYSTEINE PEPTIDURIA		HP:0010918	PMID:4730204	PCS				P		HPO:lccarmody	
OMIM	219600	CYSTIC DISEASE OF LUNG		HP:0000007	OMIM:219600	TAS				I		HPO:skoehler	
OMIM	219600	CYSTIC DISEASE OF LUNG		HP:0002719	OMIM:219600	TAS				P		HPO:skoehler	
OMIM	219600	CYSTIC DISEASE OF LUNG		HP:0004876	OMIM:219600	TAS				P		HPO:skoehler	
OMIM	219600	CYSTIC DISEASE OF LUNG		HP:0005948	OMIM:219600	TAS				P		HPO:skoehler	
OMIM	219700	CYSTIC FIBROSIS		HP:0000007	OMIM:219700	IEA				I		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0001508	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0001648	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0001738	OMIM:219700	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	219700	CYSTIC FIBROSIS		HP:0001944	OMIM:219700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	219700	CYSTIC FIBROSIS		HP:0002035	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0002099	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0002110	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0002150	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0002613	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0003251	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0004401	OMIM:219700	IEA				P		HPO:iea	
OMIM	219700	CYSTIC FIBROSIS		HP:0006528	OMIM:219700	IEA				P		HPO:skoehler	
OMIM	219700	CYSTIC FIBROSIS		HP:0006532	OMIM:219700	IEA				P		HPO:skoehler	
OMIM	219700	CYSTIC FIBROSIS		HP:0006538	OMIM:219700	IEA				P		HPO:skoehler	
OMIM	219700	CYSTIC FIBROSIS		HP:0012236	OMIM:219700	TAS				P		HPO:probinson	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000007	OMIM:219721	IEA				I		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000047	OMIM:219721	IEA				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000049	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000276	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION	HP:0012825	HP:0000347	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000431	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000506	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0000789	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0001249	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0001648	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0001738	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0001889	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0002007	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0002014	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0002097	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0002150	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0002613	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0004401	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0005230	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0005263	OMIM:219721	IEA				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0006532	OMIM:219721	IEA				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0006538	OMIM:219721	IEA				P		HPO:skoehler	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0008327	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0009748	OMIM:219721	IEA				P		HPO:iea	
OMIM	219721	CYSTIC FIBROSIS WITH HELICOBACTER PYLORI GASTRITIS, MEGALOBLASTIC ANEMIA, AND MENTAL RETARDATION		HP:0100507	OMIM:219721	TAS				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0000007	OMIM:219730	IEA				I		HPO:iea	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0000083	OMIM:219730	TAS				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0000108	OMIM:219730	IEA				P		HPO:iea	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0000238	OMIM:219730	IEA				P		HPO:iea	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0001250	OMIM:219730	TAS				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0001561	OMIM:219730	TAS				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0001622	OMIM:219730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0001629	OMIM:219730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0002119	OMIM:219730	TAS				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0002617	OMIM:219730	IEA				P		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0003577	OMIM:219730	TAS				C		HPO:skoehler	
OMIM	219730	VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE; VMCKD		HP:0100259	OMIM:219730	TAS				P		HPO:skoehler	
OMIM	219750	#219750 CYSTINOSIS, ADULT NONNEPHROPATHIC;;CYSTINOSIS, OCULAR NONNEPHROPATHIC;;CYSTINOSIS, BENIGN NONNEPHROPATHIC		HP:0000007	OMIM:219750	TAS				I		HPO:probinson	
OMIM	219750	#219750 CYSTINOSIS, ADULT NONNEPHROPATHIC;;CYSTINOSIS, OCULAR NONNEPHROPATHIC;;CYSTINOSIS, BENIGN NONNEPHROPATHIC		HP:0000531	OMIM:219750	TAS				P		HPO:probinson	
OMIM	219750	#219750 CYSTINOSIS, ADULT NONNEPHROPATHIC;;CYSTINOSIS, OCULAR NONNEPHROPATHIC;;CYSTINOSIS, BENIGN NONNEPHROPATHIC	HP:0012825	HP:0000613	OMIM:219750	TAS				P		HPO:skoehler	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000007	PMID:12110740	PCS				I		HPO:lccarmody	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000026	PMID:12110740	PCS	HP:0003581	HP:0040284		P		HPO:lccarmody	70%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000083	OMIM:219800	TAS		HP:0040284		P		HPO:probinson	50%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000093	PMID:12110740	PCS				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000103	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000488	OMIM:219800	IEA				P		HPO:skoehler	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000495	OMIM:219800	IEA				P		HPO:skoehler	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000531	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000580	OMIM:219800	TAS				P		HPO:probinson	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000613	PMID:12110740	PCS	HP:0003621	HP:0040284		P		HPO:lccarmody	50%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000618	PMID:12110740	PCS	HP:0011462	HP:0040284		P		HPO:lccarmody	10%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000787	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000819	PMID:12110740	PCS	HP:0003581	HP:0040284		P		HPO:lccarmody	5%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000823	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000832	PMID:12110740	PCS	HP:0011463	HP:0040284		P		HPO:lccarmody	50%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000897	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0000966	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001010	OMIM:219800	TAS				P		HPO:probinson	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001531	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001738	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001744	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001944	PMID:12110740	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	95%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001959	PMID:12110740	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	95%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0001994	PMID:12110740	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	95%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002007	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002015	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002059	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002240	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002344	OMIM:219800	TAS				P		HPO:skoehler	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002514	PMID:12110740	PCS	HP:0003581	HP:0040284		P		HPO:lccarmody	15%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002748	PMID:12110740	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	95%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002750	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002857	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002902	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002907	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0002909	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003016	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003076	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003198	PMID:12110740	PCS	HP:0011462	HP:0040284		P		HPO:lccarmody	20%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003202	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003234	OMIM:219800	TAS				P		HPO:skoehler	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003251	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003358	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0003774	PMID:12110740	PCS	HP:0003621	HP:0040284		P		HPO:lccarmody	95%
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0004322	PMID:12110740	PCS	HP:0003593			P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0004911	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0004912	OMIM:219800	IEA				P		HPO:iea	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0005599	OMIM:219800	TAS				P		HPO:probinson	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0007814	PMID:16603246	PCS				P		HPO:probinson	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0030190	PMID:2381441	PCS				P		HPO:lccarmody	
OMIM	219800	CYSTINOSIS, NEPHROPATHIC; CTNS		HP:0200136	PMID:12110740	PCS	HP:0011462	HP:0040284		P		HPO:lccarmody	20%
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0000007	OMIM:219900	IEA				I		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0000093	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0000488	OMIM:219900	TAS				P		HPO:skoehler	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0000531	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0001507	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0002748	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0003358	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0003621	OMIM:219900	TAS				C		HPO:probinson	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0003774	OMIM:219900	IEA				P		HPO:iea	
OMIM	219900	#219900 CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE;;CYSTINOSIS, INTERMEDIATE		HP:0007814	PMID:6866439	TAS				P		HPO:probinson	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000006	OMIM:220100	TAS				I		HPO:skoehler	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000007	OMIM:220100	TAS				I		HPO:skoehler	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000010	OMIM:220100	TAS				P		HPO:skoehler	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000083	OMIM:220100	TAS				P		HPO:skoehler	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000707	OMIM:220100	IEA				P		HPO:iea	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0000787	OMIM:220100	IEA				P		HPO:iea	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0003131	OMIM:220100	TAS				P		HPO:probinson	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0003268	OMIM:220100	TAS				P		HPO:probinson	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0003297	OMIM:220100	TAS				P		HPO:probinson	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0003532	OMIM:220100	TAS				P		HPO:probinson	
OMIM	220100	#220100 CYSTINURIA;;CSNU;;CYSTINURIA, TYPE I, FORMERLY; CSNU1, FORMERLY;;CYSTINURIA, TYPE II, FORMERLY;;CYSTINURIA, TYPE III, FORMERLY; CSNU3, FORMERLY;;CYSTINURIA, TYPE NON-I, FORMERLYCYSTINURIA, TYPE A, INCLUDED;;CYSTINURIA, TYPE B, INCLUDED;;CYSTINURIA, TYPE A/B, INCLUDED		HP:0003828	OMIM:220100	TAS				C		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000007	OMIM:220110	IEA				I		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000093	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000124	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000407	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000508	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000580	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0000648	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001249	OMIM:220110	IEA				P		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001250	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001251	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001252	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001263	OMIM:220110	TAS				P		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001270	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001290	OMIM:220110	TAS				P		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001410	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001425	OMIM:220110	TAS				I		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001427	OMIM:220110	IEA				I		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001508	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001639	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001903	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0001994	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002098	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002151	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002240	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002352	OMIM:220110	IEA				P		HPO:skoehler	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002490	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002747	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0002875	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003076	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003109	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003128	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003355	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003546	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0003688	OMIM:220110	IEA				P		HPO:iea	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0006565	OMIM:220110	TAS				P		HPO:probinson	
OMIM	220110	MITOCHONDRIAL COMPLEX IV DEFICIENCY		HP:0012240	OMIM:220110	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000007	OMIM:220111	IEA				I		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000272	OMIM:220111	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000294	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000316	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000431	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000463	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000486	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0000750	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001007	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001250	OMIM:220111	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001251	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001252	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001263	OMIM:220111	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001290	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001337	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001414	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001508	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0001943	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0002151	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0002171	OMIM:220111	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0002490	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0002553	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0002789	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0003074	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0003128	OMIM:220111	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0003593	OMIM:220111	TAS				C		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0006565	OMIM:220111	IEA				P		HPO:iea	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0007305	OMIM:220111	TAS				P		HPO:probinson	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0011096	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0011220	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0011800	OMIM:220111	TAS				P		HPO:skoehler	
OMIM	220111	LEIGH SYNDROME, FRENCH CANADIAN TYPE; LSFC		HP:0025356	OMIM:220111	IEA				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0000007	OMIM:220120	IEA				I		HPO:iea	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0000252	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0000407	OMIM:220120	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001249	OMIM:220120	IEA				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001250	OMIM:220120	IEA				P		HPO:iea	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001263	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001298	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001319	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001336	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001347	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001508	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001510	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0001942	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0002120	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0002179	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0002510	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0002521	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0003355	OMIM:220120	IEA				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0008288	OMIM:220120	IEA				P		HPO:iea	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0008936	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220120	#220120 D-GLYCERIC ACIDURIA;;D-GLYCERIC ACIDEMIA;;GLYCERATE KINASE DEFICIENCY		HP:0012448	OMIM:220120	TAS				P		HPO:skoehler	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0000007	OMIM:220150	IEA				I		HPO:iea	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0000791	OMIM:220150	IEA				P		HPO:iea	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0001919	OMIM:220150	IEA				P		HPO:skoehler	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0003537	OMIM:220150	IEA				P		HPO:iea	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0008682	OMIM:220150	IEA				P		HPO:skoehler	
OMIM	220150	HYPOURICEMIA, RENAL, 1; RHUC1		HP:0012611	OMIM:220150	TAS				P		HPO:skoehler	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0000238	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0000639	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0000930	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0000931	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0000933	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0001425	OMIM:220200	TAS				I		HPO:skoehler	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0002078	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0002198	OMIM:220200	IEA				P		HPO:iea	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0002335	OMIM:220200	TAS				P		HPO:probinson	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0002951	OMIM:220200	TAS				P		HPO:probinson	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0003745	OMIM:220200	TAS				I		HPO:skoehler	
OMIM	220200	DANDY-WALKER SYNDROME		HP:0006824	OMIM:220200	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000007	OMIM:220210	IEA				I		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000047	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000126	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000175	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000238	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000248	OMIM:220210	TAS				P		HPO:skoehler	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000269	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000316	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000337	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000337	OMIM:220210	TAS				P		HPO:probinson	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000347	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000348	OMIM:220210	TAS				P		HPO:probinson	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000369	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000494	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000589	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000824	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000835	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0000921	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001159	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001195	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001252	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001263	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001290	OMIM:220210	TAS				P		HPO:skoehler	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001305	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001511	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001629	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001631	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001636	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001642	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001650	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0001719	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0002023	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0002162	OMIM:220210	TAS				P		HPO:skoehler	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0002937	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0004383	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0005280	OMIM:220210	IEA				P		HPO:iea	
OMIM	220210	RITSCHER-SCHINZEL SYNDROME 1		HP:0007291	OMIM:220210	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000007	OMIM:220219	IEA				I		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000238	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000256	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000545	OMIM:220219	IEA				P		HPO:skoehler	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000639	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000930	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000931	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0000933	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0001305	OMIM:220219	PCS				P		HPO:probinson	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0001799	OMIM:220219	PCS				P		HPO:probinson	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0001821	OMIM:220219	PCS				P		HPO:probinson	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0002078	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0002198	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0002335	OMIM:220219	TAS				P		HPO:probinson	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0002951	OMIM:220219	TAS				P		HPO:probinson	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0006118	OMIM:220219	TAS				P		HPO:skoehler	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0006824	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0006887	OMIM:220219	IEA				P		HPO:iea	
OMIM	220219	DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, MACROCEPHALY, MYOPIA, AND BRACHYTELEPHALANGY		HP:0010864	OMIM:220219	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000007	OMIM:220220	TAS				I		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000238	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000256	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000268	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000308	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000369	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000431	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000533	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000627	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000639	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000930	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000931	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0000933	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0001162	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0001305	OMIM:220220	TAS				P		HPO:probinson	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0001643	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY	HP:0012825	HP:0001650	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002007	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002078	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002198	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002335	OMIM:220220	TAS				P		HPO:probinson	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002617	OMIM:220220	IEA				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0002951	OMIM:220220	TAS				P		HPO:probinson	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0005280	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0006824	OMIM:220220	IEA				P		HPO:iea	
OMIM	220220	DANDY-WALKER MALFORMATION WITH POSTAXIAL POLYDACTYLY		HP:0045025	OMIM:220220	TAS				P		HPO:skoehler	
OMIM	220290	#220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1ADEAFNESS, DIGENIC, GJB2/GJB6, INCLUDED;;DEAFNESS, DIGENIC, GJB2/GJB3, INCLUDED		HP:0000007	OMIM:220290	TAS				I		HPO:skoehler	
OMIM	220290	#220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1ADEAFNESS, DIGENIC, GJB2/GJB6, INCLUDED;;DEAFNESS, DIGENIC, GJB2/GJB3, INCLUDED		HP:0000407	OMIM:220290	TAS				P		HPO:skoehler	
OMIM	220290	#220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1ADEAFNESS, DIGENIC, GJB2/GJB6, INCLUDED;;DEAFNESS, DIGENIC, GJB2/GJB3, INCLUDED		HP:0001751	OMIM:220290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220290	#220290 DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1ADEAFNESS, DIGENIC, GJB2/GJB6, INCLUDED;;DEAFNESS, DIGENIC, GJB2/GJB3, INCLUDED		HP:0010984	OMIM:220290	TAS				I		HPO:skoehler	
OMIM	220300	DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY		HP:0000007	OMIM:220300	TAS				I		HPO:iea	
OMIM	220300	DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY		HP:0000365	OMIM:220300	TAS	HP:0003577			P		HPO:iea	
OMIM	220300	DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY		HP:0001336	OMIM:220300	IEA				P		HPO:skoehler	
OMIM	220300	DEAFNESS, CONGENITAL, AND FAMILIAL MYOCLONIC EPILEPSY		HP:0002123	OMIM:220300	TAS				P		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0000007	OMIM:220400	IEA				I		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0001279	OMIM:220400	IEA				P		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0001425	OMIM:220400	TAS				I		HPO:skoehler	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0001645	OMIM:220400	IEA				P		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0001657	OMIM:220400	IEA				P		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0001664	OMIM:220400	IEA				P		HPO:iea	
OMIM	220400	JERVELL AND LANGE-NIELSEN SYNDROME 1		HP:0008527	OMIM:220400	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000007	OMIM:220500	TAS				I		HPO:probinson	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000104	OMIM:220500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000218	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000232	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000252	OMIM:220500	TAS				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000280	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000343	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000369	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000407	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000414	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000431	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000448	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000463	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000518	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000618	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000648	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000800	OMIM:220500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0000951	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001156	OMIM:220500	IEA				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001199	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001249	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001250	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001252	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001265	OMIM:220500	TAS				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001271	OMIM:220500	IEA				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001290	OMIM:220500	TAS				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001305	OMIM:220500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001627	OMIM:220500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001798	OMIM:220500	TAS				P		HPO:probinson	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0001798	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0002059	OMIM:220500	TAS				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0002164	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0002714	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0003676	OMIM:220500	TAS				C		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0008404	OMIM:220500	IEA				P		HPO:skoehler	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0008619	OMIM:220500	TAS				P		HPO:probinson	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0009882	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0011003	OMIM:220500	IEA				P		HPO:iea	
OMIM	220500	DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS		HP:0011476	OMIM:220500	TAS				P		HPO:probinson	
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0000007	OMIM:220600	TAS				I		HPO:skoehler	
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0000407	OMIM:220600	TAS				P		HPO:skoehler	
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0001171	OMIM:220600	TAS				P		HPO:skoehler	
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0001182	OMIM:220600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0001597	OMIM:220600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0001839	OMIM:220600	TAS				P		HPO:skoehler	
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0002650	OMIM:220600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220600	#220600 SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS; SHFM1D;;DEAFNESS, CONGENITAL, AND SPLIT HANDS AND FEET		HP:0003510	OMIM:220600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	220900	DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM		HP:0000007	OMIM:220900	IEA				I		HPO:iea	
OMIM	220900	DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM		HP:0000135	OMIM:220900	IEA				P		HPO:iea	
OMIM	220900	DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM		HP:0000365	OMIM:220900	IEA				P		HPO:iea	
OMIM	220900	DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM		HP:0001022	OMIM:220900	IEA				P		HPO:iea	
OMIM	220900	DEAFNESS, CONGENITAL, WITH TOTAL ALBINISM		HP:0001249	OMIM:220900	IEA				P		HPO:iea	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0000007	OMIM:221200	TAS				I		HPO:probinson	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0000093	OMIM:221200	TAS				P		HPO:probinson	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0000405	OMIM:221200	TAS				P		HPO:skoehler	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0000790	OMIM:221200	TAS				P		HPO:probinson	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0001249	OMIM:221200	TAS				P		HPO:probinson	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0011003	OMIM:221200	TAS				P		HPO:skoehler	
OMIM	221200	DEAFNESS AND MYOPIA; DFNMYP		HP:0012715	OMIM:221200	IEA				P		HPO:skoehler	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0000007	OMIM:221300	TAS				I		HPO:probinson	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0000135	OMIM:221300	TAS				P		HPO:probinson	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0000369	OMIM:221300	TAS				P		HPO:probinson	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0000377	OMIM:221300	TAS				P		HPO:probinson	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0000405	OMIM:221300	TAS				P		HPO:skoehler	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0001249	OMIM:221300	TAS				P		HPO:probinson	
OMIM	221300	DEAFNESS, CONDUCTIVE, WITH MALFORMED EXTERNAL EAR		HP:0004452	OMIM:221300	TAS				P		HPO:probinson	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000007	OMIM:221320	IEA				I		HPO:iea	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000164	OMIM:221320	TAS				P		HPO:probinson	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000389	OMIM:221320	IEA				P		HPO:iea	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000405	OMIM:221320	IEA				P		HPO:skoehler	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000413	OMIM:221320	IEA				P		HPO:iea	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000508	OMIM:221320	IEA				P		HPO:iea	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0000968	OMIM:221320	IEA				P		HPO:iea	
OMIM	221320	DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES		HP:0004209	OMIM:221320	IEA				P		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0000007	OMIM:221350	IEA				I		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0000365	OMIM:221350	IEA				P		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0001045	OMIM:221350	IEA				P		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0002571	OMIM:221350	IEA				P		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0003202	OMIM:221350	IEA				P		HPO:iea	
OMIM	221350	DEAFNESS, CONGENITAL, WITH VITILIGO AND ACHALASIA		HP:0004322	OMIM:221350	IEA				P		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0000007	OMIM:221400	IEA				I		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0000407	OMIM:221400	TAS				P		HPO:probinson	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0001649	OMIM:221400	IEA				P		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0002256	OMIM:221400	IEA				P		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0002630	OMIM:221400	IEA				P		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0003075	OMIM:221400	TAS				P		HPO:probinson	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0005229	OMIM:221400	IEA				P		HPO:iea	
OMIM	221400	DEAFNESS, NERVE TYPE, WITH MESENTERIC DIVERTICULA OF SMALL BOWEL ANDPROGRESSIVE SENSORY NEUROPATHY		HP:0009830	OMIM:221400	IEA				P		HPO:skoehler	
OMIM	221500	DEAFNESS, NEURAL, CONGENITAL MODERATE		HP:0000007	OMIM:221500	TAS				I		HPO:skoehler	
OMIM	221500	DEAFNESS, NEURAL, CONGENITAL MODERATE		HP:0000407	OMIM:221500	TAS	HP:0003577			P		HPO:skoehler	
OMIM	221700	DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS		HP:0000007	OMIM:221700	TAS				I		HPO:skoehler	
OMIM	221700	DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS		HP:0000407	OMIM:221700	TAS				P		HPO:skoehler	
OMIM	221700	DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS		HP:0003212	OMIM:221700	TAS				P		HPO:probinson	
OMIM	221700	DEAFNESS, NEURAL, WITH ATYPICAL ATOPIC DERMATITIS		HP:0007573	OMIM:221700	TAS				P		HPO:skoehler	
OMIM	221740	DEAFNESS-OLIGODONTIA SYNDROME		HP:0000007	OMIM:221740	IEA				I		HPO:iea	
OMIM	221740	DEAFNESS-OLIGODONTIA SYNDROME		HP:0000677	OMIM:221740	IEA				P		HPO:iea	
OMIM	221740	DEAFNESS-OLIGODONTIA SYNDROME		HP:0000699	OMIM:221740	IEA				P		HPO:iea	
OMIM	221740	DEAFNESS-OLIGODONTIA SYNDROME		HP:0008527	OMIM:221740	IEA				P		HPO:iea	
OMIM	221745	221745 DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE		HP:0000007	OMIM:221745	IEA				I		HPO:iea	
OMIM	221745	221745 DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE		HP:0000407	OMIM:221745	IEA				P		HPO:skoehler	
OMIM	221745	221745 DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE		HP:0000408	OMIM:221745	TAS				P		HPO:skoehler	
OMIM	221745	221745 DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE		HP:0001427	OMIM:221745	TAS				I		HPO:skoehler	
OMIM	221745	221745 DEAFNESS, SENSORINEURAL, AUTOSOMAL-MITOCHONDRIAL TYPE		HP:0003621	OMIM:221745	IEA				C		HPO:iea	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0000007	OMIM:221750	IEA				I		HPO:iea	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0000407	OMIM:221750	TAS				P		HPO:skoehler	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0000470	OMIM:221750	IEA				P		HPO:skoehler	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0000824	OMIM:221750	IEA				P		HPO:iea	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0000839	OMIM:221750	TAS				P		HPO:skoehler	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0001249	OMIM:221750	IEA				P		HPO:skoehler	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0004322	OMIM:221750	IEA				P		HPO:skoehler	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0008213	OMIM:221750	IEA				P		HPO:iea	
OMIM	221750	DEAFNESS, SENSORINEURAL, WITH PITUITARY DWARFISM		HP:0010627	OMIM:221750	IEA				P		HPO:skoehler	
OMIM	221760	DERMATOGLYPHICS--PALMAR TRIRADIUS D, ABSENCE OF		HP:0000007	OMIM:221760	IEA				I		HPO:iea	
OMIM	221760	DERMATOGLYPHICS--PALMAR TRIRADIUS D, ABSENCE OF		HP:0007477	OMIM:221760	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000007	OMIM:221770	TAS				I		HPO:probinson	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000020	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000718	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000719	OMIM:221770	IEA				P		HPO:skoehler	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000727	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000734	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000751	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0000757	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001155	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001250	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001257	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001288	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001336	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0001760	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002059	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002079	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002127	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002135	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002167	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002171	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002186	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002340	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002352	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002353	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002354	OMIM:221770	IEA				P		HPO:skoehler	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002476	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0002756	OMIM:221770	TAS				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0003447	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0003487	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0010524	OMIM:221770	IEA				P		HPO:skoehler	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0011096	OMIM:221770	IEA				P		HPO:iea	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0012062	OMIM:221770	TAS				P		HPO:probinson	
OMIM	221770	POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY; PLOSL		HP:0031844	OMIM:221770	IEA				P		HPO:skoehler	
OMIM	221780	DERMATOGLYPHICS--HYPOTHENAR RADIAL ARCH		HP:0000007	OMIM:221780	IEA				I		HPO:iea	
OMIM	221780	DERMATOGLYPHICS--HYPOTHENAR RADIAL ARCH		HP:0001018	OMIM:221780	IEA				P		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0000007	OMIM:221790	IEA				I		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0000400	OMIM:221790	IEA				P		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0000448	OMIM:221790	IEA				P		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001072	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001176	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001249	OMIM:221790	IEA				P		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001249	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001833	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0001939	OMIM:221790	IEA				P		HPO:iea	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0002415	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0005328	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221790	DERMATOLEUKODYSTROPHY		HP:0100678	OMIM:221790	PCS				P		HPO:probinson	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0000007	OMIM:221800	IEA				I		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0000212	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0001131	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0001155	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0007795	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0008039	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0008134	OMIM:221800	IEA				P		HPO:iea	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0032153	OMIM:221800	IEA				P		HPO:skoehler	
OMIM	221800	DERMOCHONDROCORNEAL DYSTROPHY		HP:0200036	OMIM:221800	IEA				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0000007	OMIM:221810	IEA				I		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0000491	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0000618	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0000677	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0001171	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0001371	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0001769	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0001785	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0001945	OMIM:221810	IEA				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0002164	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0002650	OMIM:221810	TAS				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0002797	OMIM:221810	TAS				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0002829	OMIM:221810	IEA				P		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0003593	OMIM:221810	IEA				C		HPO:iea	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0008404	OMIM:221810	TAS				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0009473	OMIM:221810	TAS				P		HPO:skoehler	
OMIM	221810	221810 DERMATOOSTEOLYSIS, KIRGHIZIAN TYPE;;KIRGHIZIAN DERMATOOSTEOLYSIS		HP:0200042	OMIM:221810	IEA				P		HPO:skoehler	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0000006	OMIM:221820	TAS				I		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0000716	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0000727	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0001257	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0001347	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002063	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002067	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002171	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002172	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002186	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002300	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002352	OMIM:221820	IEA				P		HPO:skoehler	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002354	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002362	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002500	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0002529	OMIM:221820	TAS				P		HPO:skoehler	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0003581	OMIM:221820	TAS				C		HPO:probinson	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0003678	OMIM:221820	TAS				C		HPO:skoehler	
OMIM	221820	#221820 LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS;;LEUKOENCEPHALOPATHY WITH NEUROAXONAL SPHEROIDS, AUTOSOMAL DOMINANT;;GLIOSIS, FAMILIAL PROGRESSIVE SUBCORTICAL; GPSC;;DEMENTIA, FAMILIAL, NEUMANN TYPE;;SUBCORTICAL GLIOSIS OF NEUMANN		HP:0007305	OMIM:221820	TAS				P		HPO:probinson	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000007	OMIM:221900	TAS				I		HPO:probinson	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000482	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000518	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000554	OMIM:221900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000555	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000557	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000565	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000568	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000594	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000612	OMIM:221900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0000667	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0007899	OMIM:221900	TAS	HP:0003577			P		HPO:probinson	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0007957	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0007968	OMIM:221900	IEA				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0008052	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0009917	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0011484	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0011886	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221900	#221900 PERSISTENT HYPERPLASTIC PRIMARY VITREOUS, AUTOSOMAL RECESSIVE; PHPVAR;;RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC; NCRNA;;RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT;;PERSISTENT FETAL VASCULATURE		HP:0012043	OMIM:221900	TAS				P		HPO:skoehler	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000007	OMIM:221950	IEA				I		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000175	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000340	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000347	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000400	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000448	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000528	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0000568	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0001249	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0001266	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0001651	OMIM:221950	IEA				P		HPO:iea	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0001999	OMIM:221950	IEA				P		HPO:skoehler	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0002948	OMIM:221950	IEA				P		HPO:skoehler	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0003422	OMIM:221950	TAS				P		HPO:probinson	
OMIM	221950	DEXTROCARDIA WITH UNUSUAL FACIES AND MICROPHTHALMIA		HP:0005815	OMIM:221950	IEA				P		HPO:iea	
OMIM	221995	NEPHROGENIC DIABETES INSIPIDUS - INTRACRANIAL CALCIFICATION		HP:0009806	OMIM:221995	IEA				P		HPO:skoehler	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0000103	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0000819	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0001425	OMIM:222100	IEA				I		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0001959	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0001993	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0002591	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0002960	OMIM:222100	IEA				P		HPO:skoehler	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0003074	OMIM:222100	IEA				P		HPO:iea	
OMIM	222100	DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM		HP:0410050	PMID:9357814,PMID:17659063,PMID:16731998	PCS				P		HPO:NicoleVasilevsky	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000007	OMIM:222300	IEA				I		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000011	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000029	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000072	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000126	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000407	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000508	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000580	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000639	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000648	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000708	OMIM:222300	TAS				P		HPO:skoehler	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000819	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000821	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0000873	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001249	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001250	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001251	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001260	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001337	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001510	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001638	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001873	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001889	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0001924	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0002015	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0002059	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0002401	OMIM:222300	IEA				P		HPO:iea	
OMIM	222300	#222300 WOLFRAM SYNDROME 1; WFS1;;WFS;;DIABETES INSIPIDUS AND MELLITUS WITH OPTIC ATROPHY AND DEAFNESS; DIDMOAD		HP:0006217	OMIM:222300	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0000007	OMIM:222350	IEA				I		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0001250	OMIM:222350	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0001251	OMIM:222350	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0001257	OMIM:222350	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0002180	OMIM:222350	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0003131	OMIM:222350	IEA				P		HPO:iea	
OMIM	222350	DIAMINOPENTANURIA		HP:0003297	OMIM:222350	IEA				P		HPO:iea	
OMIM	222400	DIAPHRAGMATIC HERNIA 2		HP:0000007	OMIM:222400	TAS				I		HPO:nvasilevsky	
OMIM	222400	DIAPHRAGMATIC HERNIA 2		HP:0000776	OMIM:222400	IEA				P		HPO:skoehler	
OMIM	222400	DIAPHRAGMATIC HERNIA 2		HP:0001426	OMIM:222400	TAS				I		HPO:nvasilevsky	
OMIM	222400	DIAPHRAGMATIC HERNIA 2		HP:0008986	OMIM:222400	IEA				P		HPO:iea	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000007	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai;ISBN-13:0-19-262896-8	PCS				I		HPO:iea	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000256	OMIM:222448	TAS				P		HPO:skoehler	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000260	PMID:12923867	PCS		HP:0040284		P		HPO:iea	9/12
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000272	OMIM:222448	TAS				P		HPO:skoehler	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000316	PMID:12923867	PCS		HP:0040284		P		HPO:iea	12/12
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000358	PMID:12923867	PCS		HP:0040284		P		HPO:iea	7/11
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000369	PMID:12923867	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000407	PMID:12923867	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000455	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai;PMID:12923867	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000494	PMID:12923867	PCS		HP:0040284		P		HPO:iea	8/11
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000518	PMID:9066882	PCS		HP:0040284		P		HPO:iea	HP:0040284
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000520	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000529	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000541	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000556	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000612	PMID:12923867	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000776	PMID:12923867	PCS		HP:0040284		P		HPO:iea	9/13
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0000813	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS	HP:0003674	HP:0040283		P		HPO:iea	HP:0040283
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001263	PMID:12923867	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001338	OMIM:222448	TAS				P		HPO:skoehler	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001537	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040284		P		HPO:iea	50%
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001539	PMID:12923867	PCS		HP:0040284		P		HPO:iea	6/12
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0001629	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0002566	PMID:12923867	PCS		HP:0040284		P		HPO:iea	3/13
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0003126	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040284		P		HPO:iea	100%
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0003196	PMID:12923867	PCS		HP:0040284		P		HPO:iea	9/11
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0005280	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0005574	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040284		P		HPO:iea	100%
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0007370	PMID:12923867	PCS		HP:0040284		P		HPO:iea	11/11
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0007676	OMIM:222448	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0009110	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040284		P		HPO:iea	50%
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0011003	PMID:12923867	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0011800	OMIM:222448	TAS				P		HPO:skoehler	
OMIM	222448	#222448 DONNAI-BARROW SYNDROME;;FACIOOCULOACOUSTICORENAL SYNDROME;;DBS/FOAR SYNDROME;;DIAPHRAGMATIC HERNIA, EXOMPHALOS, ABSENT CORPUS CALLOSUM, HYPERTELORISM,MYOPIA, SENSORINEURAL DEAFNESS, AND PROTEINURIA		HP:0100876	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=donnai	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000007	OMIM:222470	IEA				I		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000154	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000160	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000193	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000316	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000343	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000369	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000445	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000457	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000463	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000494	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000520	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0000952	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001194	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001394	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001395	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001399	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001508	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001511	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001518	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001561	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001629	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001636	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001642	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001659	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001732	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0001894	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002007	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002041	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002212	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002213	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002224	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002240	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002299	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0002715	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0003073	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0003235	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0003452	OMIM:222470	IEA				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0004322	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0004734	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0006267	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0008070	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0008551	OMIM:222470	IEA				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0009886	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0009891	OMIM:222470	TAS				P		HPO:iea	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0011031	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0011220	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0011473	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0011877	OMIM:222470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0012023	OMIM:222470	TAS				P		HPO:skoehler	
OMIM	222470	TRICHOHEPATOENTERIC SYNDROME 1; THES1		HP:0100543	OMIM:222470	IEA				P		HPO:iea	
OMIM	222500	DIASTEMATOMYELIA		HP:0000007	OMIM:222500	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	222500	DIASTEMATOMYELIA		HP:0000707	OMIM:222500	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0000007	OMIM:222600	IEA				I		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0000175	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0000365	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0001076	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0001234	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0001609	OMIM:222600	IEA				P		HPO:skoehler	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0001762	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0002176	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0002751	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0002947	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0003026	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0003071	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0003273	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0004894	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0006646	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0008434	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0008608	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0008873	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0008921	OMIM:222600	IEA				P		HPO:iea	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0009381	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0009465	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0010582	OMIM:222600	TAS				P		HPO:probinson	
OMIM	222600	#222600 DIASTROPHIC DYSPLASIA;;DTD;;DDDIASTROPHIC DYSPLASIA, BROAD BONE-PLATYSPONDYLIC VARIANT, INCLUDED		HP:0010723	OMIM:222600	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0000007	OMIM:222690	IEA				I		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0001249	OMIM:222690	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0002024	OMIM:222690	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0003168	OMIM:222690	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0003268	OMIM:222690	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0003297	OMIM:222690	IEA				P		HPO:iea	
OMIM	222690	DIBASIC AMINO ACIDURIA I		HP:0003532	OMIM:222690	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0000007	OMIM:222700	IEA				I		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0000725	OMIM:222700	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0000939	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0000973	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0000974	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001252	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001259	OMIM:222700	IEA				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001290	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001324	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001508	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001733	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001744	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001873	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001882	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001903	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001956	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0001987	OMIM:222700	TAS				P		HPO:probinson	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002013	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002014	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002018	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002093	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002151	OMIM:222700	IEA				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002213	OMIM:222700	TAS				P		HPO:probinson	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002240	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002750	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0002757	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003202	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003218	OMIM:222700	TAS				P		HPO:probinson	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003281	OMIM:222700	IEA				P		HPO:iea	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003355	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003593	OMIM:222700	TAS				C		HPO:probinson	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0003774	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0004322	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0004395	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0006517	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0008070	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0012156	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222700	LYSINURIC PROTEIN INTOLERANCE; LPI		HP:0040223	OMIM:222700	TAS				P		HPO:skoehler	
OMIM	222730	DICARBOXYLICAMINO ACIDURIA		HP:0000007	OMIM:222730	IEA				I		HPO:iea	
OMIM	222730	DICARBOXYLICAMINO ACIDURIA		HP:0001249	OMIM:222730	IEA				P		HPO:iea	
OMIM	222730	DICARBOXYLICAMINO ACIDURIA		HP:0003162	OMIM:222730	IEA				P		HPO:iea	
OMIM	222730	DICARBOXYLICAMINO ACIDURIA		HP:0003355	OMIM:222730	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0000007	OMIM:222748	IEA				I		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0000750	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001249	OMIM:222748	TAS				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001250	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001254	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001262	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001357	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001510	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001762	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001942	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0001999	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0002023	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0002062	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0002500	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0003654	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0007256	OMIM:222748	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0007308	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0008872	OMIM:222748	IEA				P		HPO:iea	
OMIM	222748	#222748 DIHYDROPYRIMIDINASE DEFICIENCY;;DIHYDROPYRIMIDINURIA;;DPYS DEFICIENCY;;DPH DEFICIENCY		HP:0009803	OMIM:222748	IEA				P		HPO:skoehler	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000007	OMIM:222765	IEA				I		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000218	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000239	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000252	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000347	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000348	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000431	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000463	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000518	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0000938	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0001249	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0001252	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0001290	OMIM:222765	TAS				P		HPO:skoehler	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0001371	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0001508	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0002644	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0002650	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0002832	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0003301	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0005280	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0005792	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0008838	OMIM:222765	IEA				P		HPO:iea	
OMIM	222765	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 2		HP:0008905	OMIM:222765	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0000007	OMIM:222800	IEA				I		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0000952	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001081	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001082	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001744	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001895	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001897	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001901	OMIM:222800	IEA				P		HPO:skoehler	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001930	OMIM:222800	IEA				P		HPO:iea	
OMIM	222800	ERYTHROCYTOSIS, FAMILIAL, 8; ECYT8		HP:0001939	OMIM:222800	IEA				P		HPO:iea	
OMIM	222900	SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL		HP:0000007	OMIM:222900	IEA				I		HPO:iea	
OMIM	222900	SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL		HP:0000787	OMIM:222900	IEA				P		HPO:iea	
OMIM	222900	SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL		HP:0001939	OMIM:222900	IEA				P		HPO:iea	
OMIM	222900	SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL		HP:0002014	OMIM:222900	IEA				P		HPO:iea	
OMIM	222900	SUCRASE-ISOMALTASE DEFICIENCY, CONGENITAL		HP:0002024	OMIM:222900	IEA				P		HPO:iea	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0000007	OMIM:223000	IEA				I		HPO:iea	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0001942	OMIM:223000	IEA				P		HPO:iea	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0001944	OMIM:223000	IEA				P		HPO:iea	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0002014	OMIM:223000	IEA				P		HPO:skoehler	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0004789	OMIM:223000	TAS				P		HPO:probinson	
OMIM	223000	LACTASE DEFICIENCY, CONGENITAL		HP:0025130	OMIM:223000	TAS	HP:0003577			P		HPO:skoehler	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0000006	OMIM:223100	TAS				I		HPO:skoehler	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0000007	OMIM:223100	IEA				I		HPO:iea	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0001939	OMIM:223100	IEA				P		HPO:iea	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0002014	OMIM:223100	IEA				P		HPO:iea	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0002027	OMIM:223100	TAS				P		HPO:skoehler	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0004789	OMIM:223100	IEA				P		HPO:iea	
OMIM	223100	LACTOSE INTOLERANCE, ADULT TYPE		HP:0025130	OMIM:223100	TAS				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0000007	OMIM:223200	IEA				I		HPO:iea	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0000175	OMIM:223200	TAS				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0000204	OMIM:223200	TAS				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0000407	OMIM:223200	IEA				P		HPO:iea	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0001012	OMIM:223200	IEA				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0001161	OMIM:223200	IEA				P		HPO:iea	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0002827	OMIM:223200	TAS				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0005217	OMIM:223200	IEA				P		HPO:iea	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0005765	OMIM:223200	IEA				P		HPO:iea	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0012033	OMIM:223200	TAS				P		HPO:skoehler	
OMIM	223200	%223200 DISORGANIZATION, MOUSE, HOMOLOG OF;;DS		HP:0100524	OMIM:223200	TAS				P		HPO:skoehler	
OMIM	223300	223300 DISSEMINATED SCLEROSIS WITH NARCOLEPSY		HP:0000007	OMIM:223300	IEA				I		HPO:iea	
OMIM	223300	223300 DISSEMINATED SCLEROSIS WITH NARCOLEPSY		HP:0000707	OMIM:223300	IEA				P		HPO:iea	
OMIM	223300	223300 DISSEMINATED SCLEROSIS WITH NARCOLEPSY		HP:0002524	OMIM:223300	TAS				P		HPO:skoehler	
OMIM	223300	223300 DISSEMINATED SCLEROSIS WITH NARCOLEPSY		HP:0030050	OMIM:223300	TAS				P		HPO:skoehler	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0000007	OMIM:223320	IEA				I		HPO:iea	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0001370	OMIM:223320	IEA				P		HPO:iea	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0004786	OMIM:223320	IEA				P		HPO:iea	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0004799	OMIM:223320	IEA				P		HPO:iea	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0004800	OMIM:223320	IEA				P		HPO:iea	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0100279	OMIM:223320	TAS				P		HPO:skoehler	
OMIM	223320	DIVERTICULOSIS, SMALL-INTESTINAL		HP:0100646	OMIM:223320	IEA				P		HPO:skoehler	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000007	OMIM:223330	IEA				I		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000015	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000023	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000486	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000541	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0000545	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0002253	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0002256	OMIM:223330	IEA				P		HPO:iea	
OMIM	223330	223330 DIVERTICULOSIS OF BOWEL, HERNIA, AND RETINAL DETACHMENT		HP:0100541	OMIM:223330	TAS				P		HPO:skoehler	
OMIM	223340	DK PHOCOMELIA SYNDROME		HP:0000007	OMIM:223340	IEA				I		HPO:iea	
OMIM	223340	DK PHOCOMELIA SYNDROME		HP:0000119	OMIM:223340	IEA				P		HPO:iea	
OMIM	223340	DK PHOCOMELIA SYNDROME		HP:0001873	OMIM:223340	IEA				P		HPO:iea	
OMIM	223340	DK PHOCOMELIA SYNDROME		HP:0002084	OMIM:223340	IEA				P		HPO:iea	
OMIM	223340	DK PHOCOMELIA SYNDROME		HP:0009829	OMIM:223340	IEA				P		HPO:iea	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0000007	OMIM:223350	IEA				I		HPO:iea	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0001004	PMID:5280989	PCS				P		HPO:lccarmody	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0001684	PMID:5280989	PCS				P		HPO:lccarmody	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0001903	PMID:5280989	IEA				P		HPO:skoehler	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0001954	PMID:5280989	PCS				P		HPO:lccarmody	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0004808	PMID:5280989	PCS				P		HPO:lccarmody	
OMIM	223350	DOHLE BODIES AND LEUKEMIA		HP:0040235	PMID:5280989	PCS				P		HPO:lccarmody	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0000007	OMIM:223360	IEA				I		HPO:iea	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0000017	OMIM:223360	IEA				P		HPO:iea	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0000218	OMIM:223360	IEA				P		HPO:iea	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0000508	OMIM:223360	IEA				P		HPO:iea	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0001250	OMIM:223360	IEA				P		HPO:skoehler	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY	HP:0012828	HP:0001278	OMIM:223360	TAS				P		HPO:probinson	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0001998	OMIM:223360	TAS				P		HPO:probinson	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0005964	OMIM:223360	IEA				P		HPO:iea	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0005964	OMIM:223360	TAS	HP:0003623			P		HPO:probinson	
OMIM	223360	#223360 DOPAMINE BETA-HYDROXYLASE DEFICIENCY, CONGENITAL;;NOREPINEPHRINE DEFICIENCY;;NORADRENALINE DEFICIENCY		HP:0012877	OMIM:223360	TAS				P		HPO:skoehler	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000007	OMIM:223370	IEA				I		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000023	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000028	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000047	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000176	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000218	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000220	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000252	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000274	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000286	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000324	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000340	OMIM:223370	TAS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000347	OMIM:223370	PCS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000348	OMIM:223370	TAS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000369	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000388	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000411	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000431	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000455	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000485	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000486	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000506	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000508	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000510	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000540	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000568	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000581	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000581	OMIM:223370	PCS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000612	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000670	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000684	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000736	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000750	OMIM:223370	TAS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000752	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000960	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0000964	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001159	OMIM:223370	IEA				P		HPO:skoehler	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001249	OMIM:223370	PCS		HP:0040284		P		HPO:probinson	10%
OMIM	223370	DUBOWITZ SYNDROME		HP:0001252	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001290	OMIM:223370	TAS				P		HPO:skoehler	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001511	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001620	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001763	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0001915	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002020	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002028	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002209	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002572	OMIM:223370	TAS				P		HPO:skoehler	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002665	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002719	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002720	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0002750	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0003006	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0004209	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0004315	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0005338	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0006349	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0006721	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0007676	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0008872	OMIM:223370	IEA				P		HPO:iea	
OMIM	223370	DUBOWITZ SYNDROME		HP:0008897	OMIM:223370	PCS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0009891	OMIM:223370	TAS				P		HPO:probinson	
OMIM	223370	DUBOWITZ SYNDROME		HP:0012745	OMIM:223370	TAS				P		HPO:skoehler	
OMIM	223380	DOPAMINE BETA-HYDROXYLASE, PLASMA, THERMOLABILITY OF		HP:0000007	OMIM:223380	IEA				I		HPO:iea	
OMIM	223380	DOPAMINE BETA-HYDROXYLASE, PLASMA, THERMOLABILITY OF		HP:0001939	OMIM:223380	IEA				P		HPO:iea	
OMIM	223400	DUODENAL ATRESIA		HP:0000007	OMIM:223400	IEA				I		HPO:iea	
OMIM	223400	DUODENAL ATRESIA		HP:0002247	OMIM:223400	IEA				P		HPO:iea	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0000007	OMIM:223500	TAS				I		HPO:nvasilevsky	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0000365	OMIM:223500	IEA				P		HPO:iea	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0001249	OMIM:223500	IEA				P		HPO:iea	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0001419	OMIM:223500	TAS				I		HPO:nvasilevsky	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0001511	OMIM:223500	IEA				P		HPO:iea	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0001943	OMIM:223500	IEA				P		HPO:skoehler	
OMIM	223500	DWARFISM, LOW-BIRTH-WEIGHT TYPE, WITH UNRESPONSIVENESS TO GROWTH HORMONE		HP:0003510	OMIM:223500	IEA				P		HPO:iea	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0000007	OMIM:223540	IEA				I		HPO:iea	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0000252	OMIM:223540	TAS				P		HPO:skoehler	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0000315	OMIM:223540	TAS				P		HPO:skoehler	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0001249	OMIM:223540	IEA				P		HPO:iea	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0003510	OMIM:223540	IEA				P		HPO:skoehler	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0007676	OMIM:223540	IEA				P		HPO:iea	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0011003	OMIM:223540	IEA				P		HPO:iea	
OMIM	223540	223540 DWARFISM, MENTAL RETARDATION, AND EYE ABNORMALITY;;MOLLICA SYNDROME		HP:0100018	OMIM:223540	IEA				P		HPO:skoehler	
OMIM	223550	DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION		HP:0000007	OMIM:223550	IEA				I		HPO:iea	
OMIM	223550	DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION		HP:0002827	OMIM:223550	IEA				P		HPO:iea	
OMIM	223550	DWARFISM, PROPORTIONATE, WITH HIP DISLOCATION		HP:0003510	OMIM:223550	IEA				P		HPO:iea	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000007	OMIM:223800	TAS				I		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000252	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000280	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000303	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000470	PMID:19816730	PCS		HP:0040284		P		HPO:probinson	14/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000768	PMID:19816730	PCS		HP:0040284		P		HP:probinson	13/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000882	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000884	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000911	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000914	PMID:19816730	PCS		HP:0040284		P		HPO:skoehler	14/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000920	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0000926	PMID:12491225	PCS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001156	PMID:19816730	PCS		HP:0040284		P		HP:probinson	15/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001169	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001376	PMID:19816730	PCS		HP:0040284		P		HP:probinson	7/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001498	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001552	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001762	PMID:19816730	PCS		HP:0040284		P		HP:probinson	1/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001763	PMID:19816730	PCS		HP:0040284		P		HP:probinson	3/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0001769	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002515	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002650	PMID:19816730	PCS		HP:0040284		P		HPO:probinson	11/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002681	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002684	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002692	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002808	PMID:19816730	PCS		HP:0040284		P		HP:probinson	8/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002857	PMID:19816730	PCS		HP:0040284		P		HPO:skoehler	14/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002866	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002938	PMID:19816730	PCS		HP:0040284		P		HPO:probinson	15/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002942	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002970	PMID:19816730	PCS		HP:0040284		P		HP:probinson	1/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002980	PMID:19816730	PCS		HP:0040284		P		HP:probinson	1/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0002982	PMID:19816730	PCS		HP:0040284		P		HP:probinson	1/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003016	PMID:19816730	PCS		HP:0040284		P		HP:probinson	15/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003180	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003183	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003311	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003375	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0003521	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0004209	PMID:19816730	PCS		HP:0040284		P		HP:probinson	5/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0004568	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0004991	PMID:19816730	PCS		HP:0040284		P		HP:probinson	14/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0004997	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0006450	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0006589	PMID:19816730	PCS		HP:0040284		P		HP:probinson	15/15
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0008786	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0008897	OMIM:223800	TAS				P		HPO:skoehler	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0010049	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0010230	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0010743	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0011344	OMIM:223800	TAS				P		HPO:probinson	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0012385	OMIM:223800	TAS				P		HPO:skoehler	
OMIM	223800	DYGGVE-MELCHIOR-CLAUSEN DISEASE		HP:0012428	PMID:19816730	PCS		HP:0040284		P		HP:probinson	3/15
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000007	OMIM:223900	IEA				I		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000096	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000224	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000495	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000522	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000712	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0000822	OMIM:223900	IEA				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001063	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001069	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001252	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001265	OMIM:223900	TAS				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001278	OMIM:223900	IEA				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001290	OMIM:223900	TAS				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001510	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001649	OMIM:223900	IEA				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0001954	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002013	OMIM:223900	IEA				P		HPO:skoehler	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002014	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002019	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002020	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002311	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002650	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0002821	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0003138	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0003259	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0003387	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0003577	OMIM:223900	IEA				C		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0003676	OMIM:223900	IEA				C		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0004891	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0005947	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0008000	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0008872	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0012211	OMIM:223900	IEA				P		HPO:iea	
OMIM	223900	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III		HP:0012804	OMIM:223900	TAS				P		HPO:skoehler	
OMIM	224000	DYSAUTONOMIA-LIKE DISORDER		HP:0000007	OMIM:224000	IEA				I		HPO:iea	
OMIM	224000	DYSAUTONOMIA-LIKE DISORDER		HP:0001249	OMIM:224000	IEA				P		HPO:iea	
OMIM	224000	DYSAUTONOMIA-LIKE DISORDER		HP:0009830	OMIM:224000	IEA				P		HPO:skoehler	
OMIM	224000	DYSAUTONOMIA-LIKE DISORDER		HP:0012332	OMIM:224000	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0000007	OMIM:224050	IEA				I		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0000486	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0000518	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0000640	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0000750	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001249	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001250	OMIM:224050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001252	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001260	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001263	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001272	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001290	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001302	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001310	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001321	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001347	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001763	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0001939	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002066	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002075	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002078	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002080	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002136	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002365	OMIM:224050	TAS				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0002465	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0003577	OMIM:224050	TAS				C		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0003680	OMIM:224050	IEA				C		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0004322	OMIM:224050	IEA				P		HPO:iea	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0009879	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224050	CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME 1; CAMRQ1		HP:0025356	OMIM:224050	IEA				P		HPO:skoehler	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0000007	OMIM:224100	IEA				I		HPO:iea	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0000952	OMIM:224100	IEA				P		HPO:skoehler	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0001081	OMIM:224100	IEA				P		HPO:skoehler	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0001744	OMIM:224100	IEA				P		HPO:skoehler	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0001923	OMIM:224100	IEA				P		HPO:skoehler	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0003352	OMIM:224100	IEA				P		HPO:iea	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0003655	OMIM:224100	IEA				P		HPO:iea	
OMIM	224100	ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE II		HP:0010972	OMIM:224100	IEA				P		HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0000007	OMIM:224120	IEA				I	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0001159	OMIM:224120	TAS		HP:0040283		P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	HP:0040283
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0001530	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0001744	OMIM:224120	TAS				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0001789	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0001923	OMIM:224120	TAS				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0003352	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0003655	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0004447	OMIM:224120	TAS				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0005532	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0006579	OMIM:224120	IEA				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:iea	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0011273	OMIM:224120	TAS				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	
OMIM	224120	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ia; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE Ia;;CDA Ia;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I		HP:0012132	OMIM:224120	TAS				P	#224120 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IA; CDAN1A;;DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE IA;;CDA IA;;ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE I	HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000007	OMIM:224230	IEA				I		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000252	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000579	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000653	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000670	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000691	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000939	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0000953	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001059	OMIM:224230	IEA				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001249	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001395	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001792	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001873	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0001915	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002043	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002164	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002165	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002206	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002209	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0002745	OMIM:224230	IEA				P		HPO:iea	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0005528	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0008404	OMIM:224230	TAS				P		HPO:skoehler	
OMIM	224230	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1		HP:0009926	OMIM:224230	IEA				P		HPO:iea	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0000007	OMIM:224250	IEA				I		HPO:iea	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0000028	OMIM:224250	TAS				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0000072	OMIM:224250	TAS				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0000126	OMIM:224250	TAS				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0000952	OMIM:224250	IEA				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0001249	OMIM:224250	IEA				P		HPO:iea	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0001250	OMIM:224250	IEA				P		HPO:iea	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0002719	OMIM:224250	TAS				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0008736	OMIM:224250	TAS				P		HPO:skoehler	
OMIM	224250	224250 DYSMYELINATION WITH JAUNDICE		HP:0100021	OMIM:224250	IEA				P		HPO:skoehler	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000007	OMIM:224300	TAS				I		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000218	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000242	OMIM:224300	IEA				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000311	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000347	OMIM:224300	IEA				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000365	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000618	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000648	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000677	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000684	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000695	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000773	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000774	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000879	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000885	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000926	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000938	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0000941	OMIM:224300	TAS				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0001249	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0001250	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0001474	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0001476	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002007	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002376	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002659	OMIM:224300	IEA				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002688	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002689	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002694	OMIM:224300	TAS				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002868	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0002870	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0003015	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0003301	OMIM:224300	IEA				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0003498	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0004054	OMIM:224300	IEA				P		HPO:iea	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0004334	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0005019	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0005089	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0006383	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0006429	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0006480	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0007209	OMIM:224300	TAS				P		HPO:skoehler	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0008479	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0011220	OMIM:224300	TAS				P		HPO:skoehler	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0011349	OMIM:224300	TAS				P		HPO:skoehler	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0030320	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224300	DYSOSTEOSCLEROSIS		HP:0100923	OMIM:224300	TAS				P		HPO:probinson	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000007	OMIM:224400	IEA				I		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000175	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000238	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000272	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000311	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000347	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000470	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000501	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000586	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000773	OMIM:224400	TAS				P		HPO:probinson	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0000774	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0001007	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0001181	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0001376	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0002084	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0002983	OMIM:224400	IEA				P		HPO:skoehler	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0003016	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0003026	OMIM:224400	TAS				P		HPO:probinson	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0003375	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0003510	OMIM:224400	IEA				P		HPO:skoehler	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0004233	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0005622	OMIM:224400	TAS				P		HPO:probinson	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0006487	OMIM:224400	TAS				P		HPO:probinson	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0008110	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0008921	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0009473	OMIM:224400	IEA				P		HPO:iea	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0011800	OMIM:224400	TAS				P		HPO:skoehler	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0012019	OMIM:224400	IEA				P		HPO:skoehler	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0012368	OMIM:224400	TAS				P		HPO:skoehler	
OMIM	224400	DYSSEGMENTAL DYSPLASIA, ROLLAND-DESBUQUOIS TYPE		HP:0012385	OMIM:224400	TAS				P		HPO:skoehler	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000007	OMIM:224410	IEA				I		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000028	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000160	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000272	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000347	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000358	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0000431	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0001362	OMIM:224410	IEA				P		HPO:skoehler	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0001548	OMIM:224410	IEA				P		HPO:skoehler	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0001762	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0002089	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0002879	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0003026	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0003026	OMIM:224410	TAS				P		HPO:probinson	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0003811	OMIM:224410	IEA				M		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0004298	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0005257	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0006487	OMIM:224410	TAS				P		HPO:probinson	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0008873	OMIM:224410	IEA				P		HPO:iea	
OMIM	224410	#224410 DYSSEGMENTAL DYSPLASIA, SILVERMAN-HANDMAKER TYPE; DDSH;;DYSSEGMENTAL DWARFISM, SILVERMAN-HANDMAKER TYPE;;ANISOSPONDYLIC CAMPTOMICROMELIC DWARFISM, SILVERMAN-HANDMAKER TYPE		HP:0012368	OMIM:224410	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0000007	OMIM:224500	IEA				I		HPO:iea	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0000473	OMIM:224500	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0000643	OMIM:224500	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0001260	OMIM:224500	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0001304	OMIM:224500	IEA				P		HPO:iea	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0001337	OMIM:224500	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0002015	OMIM:224500	TAS				P		HPO:skoehler	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0003621	OMIM:224500	IEA				C		HPO:iea	
OMIM	224500	DYSTONIA 2, TORSION, AUTOSOMAL RECESSIVE; DYT2		HP:0003677	OMIM:224500	TAS				C		HPO:skoehler	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0000007	OMIM:224550	IEA				I		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0000750	OMIM:224550	IEA				P		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0001288	OMIM:224550	IEA				P		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0001332	OMIM:224550	IEA				P		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0001347	OMIM:224550	IEA				P		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0002072	OMIM:224550	IEA				P		HPO:skoehler	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0003307	OMIM:224550	IEA				P		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0003621	OMIM:224550	IEA				C		HPO:iea	
OMIM	224550	224550 DYSTONIA WITH RINGBINDEN		HP:0011463	OMIM:224550	TAS				C		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000007	OMIM:224690	IEA				I		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000028	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000049	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000054	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000059	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000064	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000160	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000175	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000179	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000218	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000237	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000252	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000327	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000347	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000365	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000369	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000376	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000413	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000486	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000527	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000581	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000691	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000768	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000773	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000883	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000895	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000911	OMIM:224690	TAS				P		HPO:probinson	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0000963	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001249	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001388	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001425	OMIM:224690	TAS				I		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001508	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001511	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001518	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001623	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001762	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0001795	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002007	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002020	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002098	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002644	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002673	OMIM:224690	IEA				P		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002750	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002857	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002937	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0002970	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0003042	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0003100	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0003187	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0003561	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0004209	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0004279	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0006498	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0006591	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0006628	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0008551	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0008665	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0008872	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0009473	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0010554	OMIM:224690	IEA				P		HPO:iea	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0010886	OMIM:224690	IEA				P		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0012385	OMIM:224690	TAS				P		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0012745	OMIM:224690	TAS				P		HPO:skoehler	
OMIM	224690	MEIER-GORLIN SYNDROME 1; MGORS1		HP:0200055	OMIM:224690	TAS				P		HPO:skoehler	
OMIM	224700	EBSTEIN ANOMALY		HP:0000007	OMIM:224700	IEA				I		HPO:iea	
OMIM	224700	EBSTEIN ANOMALY		HP:0001631	OMIM:224700	IEA				P		HPO:iea	
OMIM	224700	EBSTEIN ANOMALY		HP:0001645	OMIM:224700	IEA				P		HPO:skoehler	
OMIM	224700	EBSTEIN ANOMALY		HP:0004309	OMIM:224700	TAS				P		HPO:skoehler	
OMIM	224700	EBSTEIN ANOMALY		HP:0005110	OMIM:224700	IEA				P		HPO:iea	
OMIM	224700	EBSTEIN ANOMALY		HP:0010316	OMIM:224700	IEA				P		HPO:iea	
OMIM	224700	EBSTEIN ANOMALY		HP:0011712	OMIM:224700	TAS				P		HPO:skoehler	
OMIM	224700	EBSTEIN ANOMALY		HP:0025478	OMIM:224700	TAS				P		HPO:skoehler	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000007	OMIM:224750	IEA				I		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000320	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000478	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000668	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000968	OMIM:224750	TAS				P		HPO:skoehler	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0000982	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0001006	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0001792	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0001806	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0001807	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0001816	OMIM:224750	TAS				P		HPO:skoehler	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0002671	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0002860	OMIM:224750	IEA				P		HPO:iea	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0011313	OMIM:224750	TAS				P		HPO:skoehler	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0031405	OMIM:224750	IEA				P		HPO:skoehler	
OMIM	224750	SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS		HP:0031454	OMIM:224750	IEA				P		HPO:skoehler	
OMIM	224800	ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS		HP:0000007	OMIM:224800	IEA				I		HPO:iea	
OMIM	224800	ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS		HP:0000407	OMIM:224800	IEA				P		HPO:iea	
OMIM	224800	ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS		HP:0002943	OMIM:224800	IEA				P		HPO:iea	
OMIM	224800	ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS		HP:0007529	OMIM:224800	IEA				P		HPO:iea	
OMIM	224800	ECTODERMAL DYSPLASIA AND NEUROSENSORY DEAFNESS		HP:0009473	OMIM:224800	IEA				P		HPO:skoehler	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000007	OMIM:224900	IEA				I		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000232	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000535	OMIM:224900	PCS				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000607	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000653	OMIM:224900	PCS				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000668	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000674	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000691	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000966	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0000970	OMIM:224900	TAS				P		HPO:skoehler	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0001006	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0001106	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0001425	OMIM:224900	TAS				I		HPO:skoehler	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0002007	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0002046	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0005280	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0007607	OMIM:224900	IEA				P		HPO:skoehler	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0010803	OMIM:224900	IEA				P		HPO:iea	
OMIM	224900	ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B		HP:0012471	OMIM:224900	TAS				P		HPO:skoehler	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000007	OMIM:225000	IEA				I		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000175	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000204	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000288	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000535	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000598	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000653	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000668	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000674	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000691	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000966	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0000972	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0001263	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0002164	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0002296	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0010554	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0010621	OMIM:225000	IEA				P		HPO:iea	
OMIM	225000	%225000 ROSSELLI-GULIENETTI SYNDROME		HP:0040080	OMIM:225000	TAS				P		HPO:skoehler	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0000832	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0000853	OMIM:225040	IEA				P		HPO:skoehler	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0000924	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0001274	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0001417	OMIM:225040	TAS				I		HPO:nvasilevsky	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0001466	OMIM:225040	TAS				I		HPO:nvasilevsky	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0001939	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0006887	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0007607	OMIM:225040	IEA				P		HPO:iea	
OMIM	225040	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND AGENESISOF THE CORPUS CALLOSUM		HP:0010864	OMIM:225040	TAS				P		HPO:skoehler	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0000007	OMIM:225050	IEA				I		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0000535	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0000832	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0001000	OMIM:225050	IEA				P		HPO:skoehler	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0001025	OMIM:225050	IEA				P		HPO:skoehler	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0002164	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0002209	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0002719	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0005938	OMIM:225050	TAS				P		HPO:probinson	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0007607	OMIM:225050	IEA				P		HPO:iea	
OMIM	225050	ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH HYPOTHYROIDISM AND CILIARYDYSKINESIA		HP:0012265	OMIM:225050	TAS				P		HPO:probinson	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000007	OMIM:225060	IEA				I		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000175	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000204	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000272	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000288	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000325	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000535	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000598	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000653	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000668	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000674	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000691	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000968	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0000972	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0002164	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0002296	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0002299	OMIM:225060	IEA				P		HPO:skoehler	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0010554	OMIM:225060	IEA				P		HPO:iea	
OMIM	225060	CLEFT LIP/PALATE-ECTODERMAL DYSPLASIA SYNDROME; CLPED1		HP:0010621	OMIM:225060	IEA				P		HPO:iea	
OMIM	225100	ECTOPIA LENTIS		HP:0000007	OMIM:225100	IEA				I		HPO:iea	
OMIM	225100	ECTOPIA LENTIS		HP:0001083	OMIM:225100	IEA				P		HPO:iea	
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0000007	OMIM:225200	IEA				I		HPO:iea	
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0000518	OMIM:225200	TAS				P		HPO:skoehler	
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0000541	OMIM:225200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0001083	OMIM:225200	IEA				P		HPO:skoehler	
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0009917	OMIM:225200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	225200	%225200 ECTOPIA LENTIS ET PUPILLAE;;ECTOPIA LENTIS WITH ECTOPIA OF PUPIL		HP:0011003	OMIM:225200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0000006	OMIM:225250	IEA				I		HPO:iea	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0000851	OMIM:225250	IEA				P		HPO:skoehler	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0001510	OMIM:225250	IEA				P		HPO:skoehler	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0001939	OMIM:225250	IEA				P		HPO:iea	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0005990	OMIM:225250	IEA				P		HPO:skoehler	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0006887	OMIM:225250	IEA				P		HPO:iea	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0010864	OMIM:225250	TAS				P		HPO:skoehler	
OMIM	225250	#225250 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 5; CHNG5		HP:0100028	OMIM:225250	IEA				P		HPO:skoehler	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000007	OMIM:225280	IEA				I		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000535	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000653	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000687	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000691	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0000968	OMIM:225280	IEA				P		HPO:skoehler	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0001159	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0001171	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0001592	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0002209	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0007754	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0009473	OMIM:225280	IEA				P		HPO:iea	
OMIM	225280	ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME		HP:0012385	OMIM:225280	TAS				P		HPO:skoehler	
OMIM	225290	ECTRODACTYLY-POLYDACTYLY		HP:0000007	OMIM:225290	IEA				I		HPO:iea	
OMIM	225290	ECTRODACTYLY-POLYDACTYLY		HP:0001162	OMIM:225290	IEA				P		HPO:iea	
OMIM	225290	ECTRODACTYLY-POLYDACTYLY		HP:0001171	OMIM:225290	IEA				P		HPO:iea	
OMIM	225290	ECTRODACTYLY-POLYDACTYLY		HP:0001839	OMIM:225290	IEA				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0000007	PMID:18515319;OMIM:225300	PCS				I		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0001171	PMID:18515319	PCS				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0001180	PMID:18515319	PCS				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0001770	PMID:18515319	PCS				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0001839	PMID:18515319	PCS				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0001849	PMID:18515319	PCS				P		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0003829	PMID:18515319	PCS				C		HPO:iea	
OMIM	225300	SPLIT-HAND/FOOT MALFORMATION 6		HP:0006101	PMID:18515319	PCS				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000007	OMIM:225310	IEA				I		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000963	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000967	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000974	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000978	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0000987	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0001065	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0001388	OMIM:225310	IEA				P		HPO:iea	
OMIM	225310	EHLERS-DANLOS SYNDROME WITH PLATELET DYSFUNCTION FROM FIBRONECTINABNORMALITY		HP:0001634	OMIM:225310	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000007	OMIM:225320	IEA				I		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000023	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000767	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000963	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000974	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000977	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0000978	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001075	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001388	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001634	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001653	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001659	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001763	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0001848	OMIM:225320	IEA				P		HPO:iea	
OMIM	225320	EHLERS-DANLOS SYNDROME, AUTOSOMAL RECESSIVE, CARDIAC VALVULAR FORM		HP:0002816	OMIM:225320	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000007	OMIM:225400	IEA				I		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000015	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000023	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI	HP:0012825	HP:0000098	OMIM:225400	TAS				P		HPO:probinson	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000286	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000482	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000501	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000541	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000545	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000563	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000592	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000618	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000678	OMIM:225400	TAS				P		HPO:probinson	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000939	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000963	OMIM:225400	TAS				P		HPO:probinson	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000974	OMIM:225400	TAS				P		HPO:skoehler	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000977	OMIM:225400	TAS				P		HPO:probinson	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000978	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0000993	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001166	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001252	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001270	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001290	OMIM:225400	TAS				P		HPO:skoehler	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001373	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001388	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001519	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001558	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001635	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001762	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001763	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001788	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0001939	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0002093	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0002239	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0002808	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0005280	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0005952	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0006532	OMIM:225400	TAS				P		HPO:probinson	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0007517	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0008458	OMIM:225400	IEA				P		HPO:iea	
OMIM	225400	EHLERS-DANLOS SYNDROME, TYPE VI		HP:0025019	OMIM:225400	TAS				P		HPO:skoehler	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000007	OMIM:225410	IEA				I		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000023	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000212	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000222	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000225	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000232	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000260	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000286	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000347	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000494	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000545	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000592	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000668	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000938	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0000978	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C	HP:0012825	HP:0001007	OMIM:225410	TAS				P		HPO:probinson	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001027	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001030	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001270	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C	HP:0012828	HP:0001388	OMIM:225410	TAS				P		HPO:probinson	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001476	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001537	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001582	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001622	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001788	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0001831	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0002983	OMIM:225410	TAS				P		HPO:skoehler	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0004322	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0004876	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0005332	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0006344	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0009803	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0009826	OMIM:225410	IEA				P		HPO:iea	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0010749	OMIM:225410	IEA				P		HPO:skoehler	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0012471	OMIM:225410	TAS				P		HPO:skoehler	
OMIM	225410	#225410 EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE;;EHLERS-DANLOS SYNDROME, DERMATOSPARAXIS TYPE;;DERMATOSPARAXIS;;EDS VIIC;;EDS7C		HP:0200094	OMIM:225410	TAS				P		HPO:skoehler	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000007	OMIM:225500	TAS				I		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000028	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000039	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000047	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000204	OMIM:225500	TAS				P		HPO:skoehler	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000668	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000684	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000695	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000768	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000773	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000774	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000888	ISBN:3642035590	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0000968	OMIM:225500	TAS				P		HPO:skoehler	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001162	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001241	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001249	OMIM:225500	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001305	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001631	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001762	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0001830	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0002164	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0002857	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0002866	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0003026	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0006035	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0006477	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0008921	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0010454	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225500	ELLIS-VAN CREVELD SYNDROME		HP:0011565	OMIM:225500	TAS				P		HPO:probinson	
OMIM	225700	ENCEPHALOMALACIA, MULTILOCULAR		HP:0000007	OMIM:225700	IEA				I		HPO:iea	
OMIM	225700	ENCEPHALOMALACIA, MULTILOCULAR		HP:0000252	OMIM:225700	IEA				P		HPO:iea	
OMIM	225700	ENCEPHALOMALACIA, MULTILOCULAR		HP:0001249	OMIM:225700	IEA				P		HPO:iea	
OMIM	225700	ENCEPHALOMALACIA, MULTILOCULAR		HP:0001264	OMIM:225700	IEA				P		HPO:iea	
OMIM	225700	ENCEPHALOMALACIA, MULTILOCULAR		HP:0040197	OMIM:225700	IEA				P		HPO:skoehler	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0000007	OMIM:225740	IEA				I		HPO:iea	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0000518	OMIM:225740	IEA				P		HPO:iea	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0001252	OMIM:225740	IEA				P		HPO:iea	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0001290	OMIM:225740	TAS				P		HPO:skoehler	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0001638	OMIM:225740	IEA				P		HPO:iea	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0007239	OMIM:225740	IEA				P		HPO:iea	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0007371	OMIM:225740	TAS				P		HPO:probinson	
OMIM	225740	ENCEPHALOPATHY, AXONAL, WITH NECROTIZING MYOPATHY, CARDIOMYOPATHY, AND CATARACTS		HP:0008978	OMIM:225740	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000006	OMIM:225750	IEA				I		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000007	OMIM:225750	IEA				I		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000253	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000486	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000639	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0000967	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001063	OMIM:225750	TAS				P		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001250	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001257	OMIM:225750	IEA				P		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001263	OMIM:225750	TAS				P		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001332	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001433	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001744	OMIM:225750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001873	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0001945	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002059	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002062	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002071	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002135	OMIM:225750	TAS				P		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002135	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002187	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002240	OMIM:225750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002352	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002421	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002448	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0002910	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0004394	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0006579	OMIM:225750	TAS				P		HPO:skoehler	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0007321	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0008872	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0008936	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0009704	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0009709	OMIM:225750	IEA				P		HPO:iea	
OMIM	225750	#225750 AICARDI-GOUTIERES SYNDROME 1; AGS1;;AGS;;ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH INTRACRANIAL CALCIFICATIONAND CHRONIC CEREBROSPINAL FLUID LYMPHOCYTOSIS;;CREE ENCEPHALITIS;;PSEUDOTOXOPLASMOSIS SYNDROMEAICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT, INCLUDED		HP:0009710	OMIM:225750	IEA				P		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0000007	OMIM:225753	TAS				I		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0000252	OMIM:225753	IEA				P		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001250	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001257	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001321	OMIM:225753	IEA				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001321	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001336	OMIM:225753	IEA				P		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001522	OMIM:225753	IEA				M		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001561	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0001939	OMIM:225753	IEA				P		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0002171	OMIM:225753	IEA				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0002365	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0002803	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0002878	OMIM:225753	IEA				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0003577	OMIM:225753	TAS				C		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0007001	OMIM:225753	TAS				P		HPO:probinson	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0007105	OMIM:225753	IEA				P		HPO:iea	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0011344	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225753	PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4		HP:0012110	OMIM:225753	TAS				P		HPO:skoehler	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0000007	OMIM:225755	IEA				I		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0000546	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0000824	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0001251	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0001256	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0001257	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0001298	OMIM:225755	TAS				P		HPO:skoehler	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0001363	OMIM:225755	IEA				P		HPO:iea	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0002119	OMIM:225755	TAS				P		HPO:skoehler	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0002514	OMIM:225755	TAS				P		HPO:skoehler	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0002617	OMIM:225755	IEA				P		HPO:skoehler	
OMIM	225755	ENCEPHALOPATHY WITH INTRACRANIAL CALCIFICATION, GROWTH HORMONE DEFICIENCY, MICROCEPHALY, AND RETINAL DEGENERATION		HP:0003510	OMIM:225755	IEA				P		HPO:iea	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0000007	OMIM:225790	IEA				I		HPO:iea	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0000238	OMIM:225790	IEA				P		HPO:iea	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0000347	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001250	OMIM:225790	IEA				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001263	OMIM:225790	IEA				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001274	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001305	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001321	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001371	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001511	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001561	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001622	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0001939	OMIM:225790	IEA				P		HPO:iea	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0002304	OMIM:225790	IEA				P		HPO:skoehler	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0002324	OMIM:225790	IEA				P		HPO:iea	
OMIM	225790	PROLIFERATIVE VASCULOPATHY AND HYDRANENCEPHALY-HYDROCEPHALY SYNDROME; PVHH		HP:0002365	OMIM:225790	TAS				P		HPO:skoehler	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0000007	OMIM:226000	IEA				I		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0000028	OMIM:226000	IEA				P		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0000707	OMIM:226000	IEA				P		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0001425	OMIM:226000	IEA				I		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0001635	OMIM:226000	IEA				P		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0001638	OMIM:226000	IEA				P		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0001706	OMIM:226000	IEA				P		HPO:iea	
OMIM	226000	ENDOCARDIAL FIBROELASTOSIS		HP:0001999	OMIM:226000	IEA				P		HPO:iea	
OMIM	226100	ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA		HP:0000007	OMIM:226100	IEA				I		HPO:iea	
OMIM	226100	ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA		HP:0001638	OMIM:226100	IEA				P		HPO:iea	
OMIM	226100	ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA		HP:0001653	OMIM:226100	IEA				P		HPO:iea	
OMIM	226100	ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA		HP:0001706	OMIM:226100	IEA				P		HPO:iea	
OMIM	226100	ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA		HP:0004974	OMIM:226100	IEA				P		HPO:iea	
OMIM	226150	226150 ENTEROCOLITIS		HP:0000007	OMIM:226150	IEA				I		HPO:iea	
OMIM	226150	226150 ENTEROCOLITIS		HP:0002573	OMIM:226150	IEA				P		HPO:iea	
OMIM	226150	226150 ENTEROCOLITIS		HP:0003270	OMIM:226150	IEA				P		HPO:iea	
OMIM	226150	226150 ENTEROCOLITIS		HP:0004387	OMIM:226150	IEA				P		HPO:iea	
OMIM	226150	226150 ENTEROCOLITIS		HP:0100279	OMIM:226150	TAS				P		HPO:skoehler	
OMIM	226200	ENTEROKINASE DEFICIENCY		HP:0000007	OMIM:226200	TAS				I		HPO:probinson	
OMIM	226200	ENTEROKINASE DEFICIENCY		HP:0001508	OMIM:226200	TAS				P		HPO:probinson	
OMIM	226200	ENTEROKINASE DEFICIENCY		HP:0002014	OMIM:226200	IEA				P		HPO:probinson	
OMIM	226200	ENTEROKINASE DEFICIENCY		HP:0003075	OMIM:226200	TAS				P		HPO:probinson	
OMIM	226200	ENTEROKINASE DEFICIENCY		HP:0007609	OMIM:226200	TAS				P		HPO:probinson	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0000007	OMIM:226300	IEA				I		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0001217	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0001510	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0001541	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0001891	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0001894	OMIM:226300	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002013	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002014	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002024	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002027	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002204	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002240	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002242	OMIM:226300	TAS				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0002639	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0003073	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0003075	OMIM:226300	IEA				P		HPO:iea	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0005214	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0007430	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226300	COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE		HP:0030243	OMIM:226300	IEA				P		HPO:skoehler	
OMIM	226350	EOSINOPHILIC FASCIITIS		HP:0000007	OMIM:226350	IEA				I		HPO:iea	
OMIM	226350	EOSINOPHILIC FASCIITIS		HP:0045029	OMIM:226350	TAS				P		HPO:skoehler	
OMIM	226400	EPIDERMODYSPLASIA VERRUCIFORMIS		HP:0001939	OMIM:226400	IEA				P		HPO:iea	
OMIM	226400	EPIDERMODYSPLASIA VERRUCIFORMIS		HP:0002671	OMIM:226400	IEA				P		HPO:iea	
OMIM	226400	EPIDERMODYSPLASIA VERRUCIFORMIS		HP:0200043	OMIM:226400	IEA				P		HPO:skoehler	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000007	OMIM:226440	IEA				I		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000164	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000175	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000215	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000219	OMIM:226440	TAS				P		HPO:skoehler	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000303	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0000322	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0001132	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0001249	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0001810	OMIM:226440	IEA				P		HPO:iea	
OMIM	226440	226440 EPIDERMOLYSIS BULLOSA, LATE-ONSET LOCALIZED JUNCTIONAL, WITH MENTALRETARDATION		HP:0003584	OMIM:226440	TAS				C		HPO:probinson	
OMIM	226500	%226500 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA;;EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS;;EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE; EBR3		HP:0000007	OMIM:226500	IEA				I		HPO:iea	
OMIM	226500	%226500 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA;;EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS;;EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE; EBR3		HP:0002164	OMIM:226500	IEA				P		HPO:iea	
OMIM	226500	%226500 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA;;EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS;;EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE; EBR3		HP:0007504	OMIM:226500	IEA				P		HPO:iea	
OMIM	226500	%226500 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA;;EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS;;EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE; EBR3		HP:0008404	OMIM:226500	TAS				P		HPO:skoehler	
OMIM	226500	%226500 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA;;EPIDERMOLYSIS BULLOSA WITH CONGENITAL DEAFNESS;;EPIDERMOLYSIS BULLOSA PROGRESSIVA, RECESSIVE; EBR3		HP:0008527	OMIM:226500	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000007	OMIM:226600	IEA				I		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000160	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000509	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000518	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000559	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001030	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001056	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001075	OMIM:226600	TAS				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001371	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001510	OMIM:226600	TAS				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001596	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001903	OMIM:226600	TAS				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002015	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002019	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002043	OMIM:226600	TAS				P		HPO:probinson	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002164	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002860	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0003577	OMIM:226600	TAS				C		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0004057	OMIM:226600	TAS				P		HPO:probinson	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0004395	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0005203	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0006297	OMIM:226600	IEA				P		HPO:iea	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0008066	OMIM:226600	TAS				P		HPO:skoehler	
OMIM	226600	#226600 EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE; RDEB;;DYSTROPHIC EPIDERMOLYSIS BULLOSA, AUTOSOMAL RECESSIVE;;EPIDERMOLYSIS BULLOSA DYSTROPHICA, HALLOPEAU-SIEMENS TYPE; EBR1EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL RECESSIVE, LOCALISATAVARIANT, INCLUDED;;EPIDERMOLYSIS BULLOSA DYSTROPHICA INVERSA, AUTOSOMAL RECESSIVE, INCLUDED		HP:0008404	OMIM:226600	TAS				P		HPO:skoehler	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0000007	OMIM:226650	IEA				I		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0000668	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0000670	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0001425	OMIM:226650	IEA				I		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0001808	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0002164	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0006089	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0007556	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0008404	OMIM:226650	TAS				P		HPO:skoehler	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0100490	OMIM:226650	IEA				P		HPO:iea	
OMIM	226650	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, NON-HERLITZ TYPE		HP:0200097	OMIM:226650	TAS				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0000007	OMIM:226670	IEA				I		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0000491	OMIM:226670	IEA				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0000670	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0000972	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0001056	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0001903	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0002164	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0002643	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0003560	OMIM:226670	TAS				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0004322	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0004552	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0006297	OMIM:226670	IEA				P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0008066	OMIM:226670	IEA	HP:0003623			P		HPO:iea	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0008404	OMIM:226670	TAS				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0009025	OMIM:226670	IEA				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0011859	OMIM:226670	TAS				P		HPO:skoehler	
OMIM	226670	#226670 EPIDERMOLYSIS BULLOSA SIMPLEX WITH MUSCULAR DYSTROPHY;;EBS-MD;;EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY;;MD-EBS; MDEBS		HP:0012227	OMIM:226670	TAS				P		HPO:probinson	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0000007	OMIM:226700	IEA				I		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0000670	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0001056	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0001075	OMIM:226700	TAS				P		HPO:skoehler	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0001508	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0001522	OMIM:226700	IEA				M		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0002021	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0002164	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0003341	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0003577	OMIM:226700	IEA				C		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0006297	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0007383	OMIM:226700	IEA				P		HPO:iea	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0008066	OMIM:226700	TAS				P		HP:probinson	
OMIM	226700	EPIDERMOLYSIS BULLOSA, JUNCTIONAL, HERLITZ TYPE		HP:0008404	OMIM:226700	TAS				P		HPO:skoehler	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0000007	OMIM:226730	IEA				I		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0000119	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0000656	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001030	OMIM:226730	IEA				P		HPO:skoehler	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001056	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001057	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001060	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001075	OMIM:226730	TAS				P		HPO:probinson	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001522	OMIM:226730	IEA				M		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001561	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0001798	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0002032	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0002041	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0002164	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0002804	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0003341	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0003577	OMIM:226730	IEA				C		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0004399	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0005984	OMIM:226730	TAS				P		HPO:probinson	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0006297	OMIM:226730	IEA				P		HPO:iea	
OMIM	226730	#226730 EPIDERMOLYSIS BULLOSA JUNCTIONALIS WITH PYLORIC ATRESIA;;EPIDERMOLYSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA;;JUNCTIONAL EPIDERMOLYSIS BULLOSA WITH PYLORIC ATRESIA;;JEB-PA;;EPIDERMYLOSIS BULLOSA, JUNCTIONAL, WITH PYLORIC ATRESIA AND APLASIACUTIS CONGENITA;;EB-PA-ACC;;CARMI SYNDROME;;APLASIA CUTIS CONGENITA WITH GASTROINTESTINAL ATRESIA		HP:0008404	OMIM:226730	TAS				P		HPO:skoehler	
OMIM	226735	EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA		HP:0000007	OMIM:226735	IEA				I		HPO:iea	
OMIM	226735	EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA		HP:0000776	OMIM:226735	IEA				P		HPO:skoehler	
OMIM	226735	EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA		HP:0003811	OMIM:226735	IEA				M		HPO:iea	
OMIM	226735	EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA		HP:0007446	OMIM:226735	IEA				P		HPO:skoehler	
OMIM	226735	EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA		HP:0008066	OMIM:226735	IEA				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0000007	OMIM:226750	IEA				I		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0000705	OMIM:226750	IEA				P		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0000726	OMIM:226750	IEA				P		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001249	OMIM:226750	IEA				P		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001250	OMIM:226750	IEA				P		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001251	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001257	OMIM:226750	IEA				P		HPO:iea	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001263	OMIM:226750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0001321	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0002059	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0002119	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0002376	OMIM:226750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0002521	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0003828	OMIM:226750	TAS				C		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0006297	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0010864	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226750	#226750 KOHLSCHUTTER-TONZ SYNDROME; KTZS;;EPILEPSY AND YELLOW TEETH;;EPILEPSY, DEMENTIA, AND AMELOGENESIS IMPERFECTA;;KOHLSCHUTTER SYNDROME		HP:0200134	OMIM:226750	TAS				P		HPO:skoehler	
OMIM	226800	EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION		HP:0000007	OMIM:226800	TAS				I		HPO:probinson	
OMIM	226800	EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION		HP:0001249	OMIM:226800	TAS				P		HPO:probinson	
OMIM	226800	EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION		HP:0001264	OMIM:226800	TAS				P		HPO:probinson	
OMIM	226800	EPILEPSY, PHOTOGENIC, WITH SPASTIC DIPLEGIA AND MENTAL RETARDATION		HP:0007207	OMIM:226800	TAS				P		HPO:probinson	
OMIM	226810	CELIAC DISEASE, EPILEPSY AND CEREBRAL CALCIFICATION SYNDROME		HP:0002608	OMIM:226810	IEA				P		HPO:skoehler	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0000007	OMIM:226850	IEA				I		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0000524	OMIM:226850	IEA				P		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0000664	OMIM:226850	IEA				P		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0001249	OMIM:226850	IEA				P		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0001250	OMIM:226850	IEA				P		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0001939	OMIM:226850	IEA				P		HPO:iea	
OMIM	226850	EPILEPSY-TELANGIECTASIA		HP:0001999	OMIM:226850	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0000007	OMIM:226900	IEA				I		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0001156	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0001385	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0001762	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0002650	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0002654	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0002656	OMIM:226900	IEA				P		HPO:skoehler	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0002829	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0003370	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0004322	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0006376	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0008802	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0010049	OMIM:226900	IEA				P		HPO:iea	
OMIM	226900	EPIPHYSEAL DYSPLASIA, MULTIPLE, 4		HP:0031174	PMID:12525546	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	226950	EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS		HP:0000007	OMIM:226950	IEA				I		HPO:iea	
OMIM	226950	EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS		HP:0000365	OMIM:226950	IEA				P		HPO:iea	
OMIM	226950	EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS		HP:0002656	OMIM:226950	IEA				P		HPO:skoehler	
OMIM	226950	EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS		HP:0010574	OMIM:226950	IEA				P		HPO:skoehler	
OMIM	226950	EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS		HP:0011003	OMIM:226950	IEA				P		HPO:iea	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0000007	OMIM:226960	TAS				I		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0000252	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0000639	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0001256	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0001518	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0002656	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0003177	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0003182	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0004322	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0010582	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226960	EPIPHYSEAL DYSPLASIA, MICROCEPHALY, AND NYSTAGMUS		HP:0010585	OMIM:226960	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000007	OMIM:226980	TAS				I		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000083	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000218	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000252	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000316	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000582	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000831	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000926	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0000939	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0001263	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0001276	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0001498	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0001552	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002240	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002654	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002656	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002673	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002827	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002857	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0002868	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0003071	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0003301	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0003307	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0003311	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0003593	OMIM:226980	TAS				C		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0004236	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0004322	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0004467	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0005280	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0006110	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0006274	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0008134	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0010168	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0010230	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0010234	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0010585	OMIM:226980	TAS				P		HPO:probinson	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0030043	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226980	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS		HP:0100651	OMIM:226980	TAS				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0000007	OMIM:226990	IEA				I		HPO:iea	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0000246	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0001744	OMIM:226990	IEA				P		HPO:iea	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0001945	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0002090	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0002110	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0002719	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	226990	IMMUNODEFICIENCY 32B; IMD32B		HP:0002721	OMIM:226990	IEA				P		HPO:skoehler	
OMIM	227000	ERYTHEMA OF ACRAL REGIONS		HP:0000007	OMIM:227000	IEA				I		HPO:iea	
OMIM	227000	ERYTHEMA OF ACRAL REGIONS		HP:0000164	OMIM:227000	IEA				P		HPO:iea	
OMIM	227000	ERYTHEMA OF ACRAL REGIONS		HP:0001762	OMIM:227000	IEA				P		HPO:iea	
OMIM	227000	ERYTHEMA OF ACRAL REGIONS		HP:0010783	OMIM:227000	IEA				P		HPO:skoehler	
OMIM	227010	ERMINE PHENOTYPE		HP:0000007	OMIM:227010	IEA				I		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0000407	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0001022	OMIM:227010	IEA				P		HPO:skoehler	
OMIM	227010	ERMINE PHENOTYPE		HP:0001045	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0001256	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0002226	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0002227	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0005585	OMIM:227010	IEA				P		HPO:iea	
OMIM	227010	ERMINE PHENOTYPE		HP:0011364	OMIM:227010	IEA				P		HPO:skoehler	
OMIM	227050	TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD		HP:0000007	OMIM:227050	IEA				I		HPO:iea	
OMIM	227050	TRANSIENT ERYTHROBLASTOPENIA OF CHILDHOOD		HP:0005510	OMIM:227050	IEA				P		HPO:iea	
OMIM	227090	ERYTHRODERMA, LETHAL CONGENITAL		HP:0000007	OMIM:227090	IEA				I		HPO:iea	
OMIM	227090	ERYTHRODERMA, LETHAL CONGENITAL		HP:0001508	OMIM:227090	IEA				P		HPO:iea	
OMIM	227090	ERYTHRODERMA, LETHAL CONGENITAL		HP:0001522	OMIM:227090	IEA				M		HPO:iea	
OMIM	227090	ERYTHRODERMA, LETHAL CONGENITAL		HP:0003073	OMIM:227090	IEA				P		HPO:iea	
OMIM	227090	ERYTHRODERMA, LETHAL CONGENITAL		HP:0007381	OMIM:227090	IEA				P		HPO:iea	
OMIM	227150	ETHANOLAMINOSIS		HP:0000007	OMIM:227150	IEA				I		HPO:iea	
OMIM	227150	ETHANOLAMINOSIS		HP:0001290	OMIM:227150	IEA				P		HPO:iea	
OMIM	227150	ETHANOLAMINOSIS		HP:0001522	OMIM:227150	IEA				M		HPO:iea	
OMIM	227150	ETHANOLAMINOSIS		HP:0001640	OMIM:227150	IEA				P		HPO:iea	
OMIM	227150	ETHANOLAMINOSIS		HP:0001939	OMIM:227150	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0000007	OMIM:227210	IEA				I		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0000527	OMIM:227210	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0000607	OMIM:227210	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0004691	OMIM:227210	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0005620	OMIM:227210	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0007425	OMIM:227210	TAS				P		HPO:probinson	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0010709	OMIM:227210	IEA				P		HPO:iea	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0011930	OMIM:227210	TAS				P		HPO:probinson	
OMIM	227210	227210 EYEBROWS, DUPLICATION OF, WITH STRETCHABLE SKIN AND SYNDACTYLY		HP:0045018	OMIM:227210	TAS				P		HPO:skoehler	
OMIM	227220	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1		HP:0000007	OMIM:227220	TAS				I		HPO:nvasilevsky	
OMIM	227220	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1		HP:0000478	OMIM:227220	IEA				P		HPO:iea	
OMIM	227220	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 1		HP:0010982	OMIM:227220	TAS				I		HPO:nvasilevsky	
OMIM	227240	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5		HP:0000007	OMIM:227240	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	227240	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5		HP:0000478	OMIM:227240	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0000007	OMIM:227250	IEA				I		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0000158	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0000256	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0000316	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0000494	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0001249	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0002355	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0002751	OMIM:227250	IEA				P		HPO:iea	
OMIM	227250	227250 FACIAL ABNORMALITIES, KYPHOSCOLIOSIS, AND MENTAL RETARDATION		HP:0010808	OMIM:227250	TAS				P		HPO:skoehler	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000007	OMIM:227255	IEA				I		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000126	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000143	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000160	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000238	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000316	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000358	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000414	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000431	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000465	OMIM:227255	IEA				P		HPO:skoehler	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000494	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0000637	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001194	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001252	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001274	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001290	OMIM:227255	TAS				P		HPO:skoehler	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001511	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001629	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001636	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001669	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0001999	OMIM:227255	TAS				P		HPO:skoehler	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0002023	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0002162	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0002714	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0002937	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0003196	OMIM:227255	IEA				P		HPO:iea	
OMIM	227255	FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS		HP:0400004	OMIM:227255	TAS				P		HPO:skoehler	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0000007	OMIM:227260	IEA				I		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0000414	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0000561	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0000629	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0000968	OMIM:227260	IEA				P		HPO:skoehler	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0002023	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0005280	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0008496	OMIM:227260	IEA				P		HPO:iea	
OMIM	227260	FACIAL ECTODERMAL DYSPLASIA		HP:0008509	OMIM:227260	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000007	OMIM:227270	IEA				I		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000160	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000171	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000278	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000347	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0000954	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0001518	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0001883	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0002984	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0003022	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0003038	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0003811	OMIM:227270	IEA				M		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0009237	OMIM:227270	TAS				P		HPO:probinson	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0009486	OMIM:227270	IEA				P		HPO:iea	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0009778	OMIM:227270	TAS				P		HPO:probinson	
OMIM	227270	FACIOCARDIOMELIC DYSPLASIA, LETHAL		HP:0030680	OMIM:227270	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000007	OMIM:227280	IEA				I		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000023	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000028	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000072	OMIM:227280	TAS				P		HPO:probinson	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000085	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000175	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000272	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000347	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000431	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0000668	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0001357	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0001706	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0001770	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0001792	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0002515	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0002650	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0003199	OMIM:227280	TAS				P		HPO:probinson	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0003764	OMIM:227280	IEA				P		HPO:skoehler	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0005326	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0006887	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0008551	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0010055	OMIM:227280	IEA				P		HPO:iea	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0010864	OMIM:227280	TAS				P		HPO:skoehler	
OMIM	227280	FACIOCARDIORENAL SYNDROME		HP:0030084	OMIM:227280	IEA				P		HPO:skoehler	
OMIM	227300	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0000007	OMIM:227300	IEA				I		HPO:iea	
OMIM	227300	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0001892	OMIM:227300	IEA				P		HPO:iea	
OMIM	227300	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0003125	OMIM:227300	IEA				P		HPO:iea	
OMIM	227300	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF		HP:0003225	OMIM:227300	IEA				P		HPO:iea	
OMIM	227310	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR		HP:0000007	OMIM:227310	IEA				I		HPO:iea	
OMIM	227310	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR		HP:0001892	OMIM:227310	IEA				P		HPO:iea	
OMIM	227310	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR		HP:0003125	OMIM:227310	IEA				P		HPO:iea	
OMIM	227310	FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, WITH NORMAL PROTEINC AND PROTEIN C INHIBITOR		HP:0003225	OMIM:227310	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000007	OMIM:227320	IEA				I		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000049	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000219	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000219	OMIM:227320	TAS				P		HPO:skoehler	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000319	OMIM:227320	TAS				P		HPO:probinson	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000343	OMIM:227320	TAS				P		HPO:probinson	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000347	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000463	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000568	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000767	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0000807	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0001792	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0003246	OMIM:227320	IEA				P		HPO:iea	
OMIM	227320	227320 FACIOTHORACOGENITAL SYNDROME		HP:0006610	OMIM:227320	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:227330	IEA				I		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000023	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000028	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000049	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000154	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000189	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000211	OMIM:227330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000218	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000248	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000316	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000325	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000349	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000358	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000365	OMIM:227330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000426	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000463	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000472	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000494	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000637	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000689	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0000767	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001159	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001169	OMIM:227330	IEA				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:227330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001547	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001773	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0001840	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0002002	OMIM:227330	IEA				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0002948	OMIM:227330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0003196	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0003508	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0004209	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0005639	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0008551	OMIM:227330	IEA				P		HPO:iea	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0012385	OMIM:227330	TAS				P		HPO:skoehler	
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0100515	OMIM:227330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	227330	FACIODIGITOGENITAL SYNDROME, AUTOSOMAL RECESSIVE		HP:0200021	OMIM:227330	IEA				P		HPO:iea	
OMIM	227400	FACTOR V DEFICIENCY		HP:0000007	OMIM:227400	IEA				I		HPO:iea	
OMIM	227400	FACTOR V DEFICIENCY		HP:0000132	OMIM:227400	TAS				P		HPO:probinson	
OMIM	227400	FACTOR V DEFICIENCY		HP:0000421	OMIM:227400	TAS				P		HPO:probinson	
OMIM	227400	FACTOR V DEFICIENCY		HP:0000978	OMIM:227400	TAS				P		HPO:probinson	
OMIM	227400	FACTOR V DEFICIENCY		HP:0003010	OMIM:227400	IEA				P		HPO:iea	
OMIM	227400	FACTOR V DEFICIENCY		HP:0003225	OMIM:227400	IEA				P		HPO:iea	
OMIM	227400	FACTOR V DEFICIENCY		HP:0003645	OMIM:227400	TAS				P		HPO:probinson	
OMIM	227400	FACTOR V DEFICIENCY		HP:0005542	OMIM:227400	IEA				P		HPO:iea	
OMIM	227400	FACTOR V DEFICIENCY		HP:0008151	OMIM:227400	TAS				P		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0000007	OMIM:227500	IEA				I		HPO:iea	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0000132	OMIM:227500	TAS				P		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0000421	OMIM:227500	TAS				P		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0001892	OMIM:227500	IEA				P		HPO:iea	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0002170	OMIM:227500	TAS				P		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0003828	OMIM:227500	TAS				C		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0005261	OMIM:227500	TAS				P		HPO:skoehler	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0008169	OMIM:227500	IEA				P		HPO:iea	
OMIM	227500	#227500 FACTOR VII DEFICIENCY;;F7 DEFICIENCY;;HYPOPROCONVERTINEMIA		HP:0012233	OMIM:227500	TAS				P		HPO:skoehler	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0000007	OMIM:227600	IEA				I		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0000132	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0000225	OMIM:227600	TAS				P		HPO:probinson	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0000421	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0002170	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0003011	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0003645	OMIM:227600	TAS				P		HPO:probinson	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0003828	OMIM:227600	TAS				C		HPO:skoehler	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0005261	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0008151	OMIM:227600	TAS				P		HPO:probinson	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0008321	OMIM:227600	IEA				P		HPO:iea	
OMIM	227600	#227600 FACTOR X DEFICIENCY;;F10 DEFICIENCY;;STUART-PROWER FACTOR DEFICIENCY		HP:0012233	OMIM:227600	TAS				P		HPO:skoehler	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000007	OMIM:227645	IEA				I		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000028	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000081	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000085	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000086	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000104	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000252	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000365	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000486	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000568	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000815	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000957	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0000978	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001000	OMIM:227645	TAS				P		HPO:skoehler	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001017	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001249	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001518	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001627	OMIM:227645	TAS				P		HPO:skoehler	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001873	OMIM:227645	TAS				P		HPO:skoehler	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001875	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001876	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001896	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001903	OMIM:227645	TAS				P		HPO:skoehler	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0001909	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0003213	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0003214	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0003221	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0003974	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0004322	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0009777	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0009778	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0009943	OMIM:227645	IEA				P		HPO:iea	
OMIM	227645	#227645 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FANCC;;FACC; FAC;;FANCONI PANCYTOPENIA, TYPE 3; FA3		HP:0030680	OMIM:227645	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000007	OMIM:227646	IEA				I		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000028	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000081	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000085	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000086	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000104	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000252	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000365	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000486	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000568	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000815	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000957	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0000978	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001000	OMIM:227646	TAS				P		HPO:skoehler	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001017	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001249	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001518	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001627	OMIM:227646	TAS				P		HPO:skoehler	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001873	OMIM:227646	TAS				P		HPO:skoehler	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001875	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001876	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001896	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001903	OMIM:227646	TAS				P		HPO:skoehler	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0001909	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0003213	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0003214	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0003221	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0003974	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0004322	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0009777	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0009778	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0009943	OMIM:227646	IEA				P		HPO:iea	
OMIM	227646	#227646 FANCONI ANEMIA, COMPLEMENTATION GROUP D2; FANCD2;;FAD2;;FANCONI ANEMIA, COMPLEMENTATION GROUP D; FANCD; FACD;;FANCONI PANCYTOPENIA, TYPE 4; FA4		HP:0030680	OMIM:227646	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000007	OMIM:227650	TAS				I		HPO:skoehler	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000028	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000081	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000085	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000086	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000104	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000252	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000365	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000486	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000568	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000815	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000957	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0000978	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001000	OMIM:227650	TAS				P		HPO:skoehler	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001017	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001249	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001518	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001627	OMIM:227650	TAS				P		HPO:skoehler	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001873	OMIM:227650	TAS				P		HPO:skoehler	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001875	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001876	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001896	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001903	OMIM:227650	TAS				P		HPO:skoehler	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0001909	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0003213	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0003214	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0003221	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0003974	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0004322	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0009777	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0009778	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0009943	OMIM:227650	IEA				P		HPO:iea	
OMIM	227650	FANCONI ANEMIA, COMPLEMENTATION GROUP A		HP:0030680	OMIM:227650	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0000007	OMIM:227810	IEA				I		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0000124	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0001263	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0001508	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0001941	OMIM:227810	IEA				P		HPO:skoehler	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0002024	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0002148	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0002749	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0002900	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0002909	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003076	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003109	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003155	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003270	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003537	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0003758	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0004396	OMIM:227810	IEA				P		HPO:iea	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0004915	OMIM:227810	TAS				P		HPO:probinson	
OMIM	227810	#227810 FANCONI-BICKEL SYNDROME; FBS;;HEPATORENAL GLYCOGENOSIS WITH RENAL FANCONI SYNDROME;;HEPATIC GLYCOGENOSIS WITH FANCONI NEPHROPATHY;;HEPATIC GLYCOGENOSIS WITH AMINO ACIDURIA AND GLUCOSURIA;;FANCONI SYNDROME WITH INTESTINAL MALABSORPTION AND GALACTOSE INTOLERANCE;;PSEUDO-PHLORIZIN DIABETES;;GLYCOGENOSIS, FANCONI TYPE;;GLYCOGEN STORAGE DISEASE XI		HP:0012468	OMIM:227810	TAS				P		HPO:skoehler	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0000007	OMIM:227850	IEA				I		HPO:iea	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0001876	OMIM:227850	IEA				P		HPO:iea	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0002754	OMIM:227850	IEA				P		HPO:iea	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0002783	OMIM:227850	IEA				P		HPO:iea	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0005939	OMIM:227850	IEA				P		HPO:iea	
OMIM	227850	FANCONI-LIKE SYNDROME		HP:0007606	OMIM:227850	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0000007	OMIM:228000	IEA				I		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0000737	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001249	OMIM:228000	IEA				P		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001270	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001369	OMIM:228000	TAS				P		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001386	OMIM:228000	IEA				P		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001508	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001615	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0001744	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0002093	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0002240	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0003676	OMIM:228000	TAS				C		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0003828	OMIM:228000	TAS				C		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0007470	OMIM:228000	IEA				P		HPO:iea	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0010729	OMIM:228000	IEA				P		HPO:skoehler	
OMIM	228000	#228000 FARBER LIPOGRANULOMATOSIS;;FARBER DISEASE;;CERAMIDASE DEFICIENCY;;ACID CERAMIDASE DEFICIENCY;;AC DEFICIENCY;;N-LAURYLSPHINGOSINE DEACYLASE DEFICIENCY		HP:0040139	OMIM:228000	IEA				P		HPO:skoehler	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0000007	OMIM:228020	IEA				I		HPO:iea	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0000765	OMIM:228020	IEA				P		HPO:iea	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0000951	OMIM:228020	IEA				P		HPO:iea	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0001376	OMIM:228020	IEA				P		HPO:iea	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0002086	OMIM:228020	IEA				P		HPO:iea	
OMIM	228020	FASCIAL DYSTROPHY, CONGENITAL		HP:0005750	OMIM:228020	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0000007	OMIM:228100	IEA				I		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0000119	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0000799	OMIM:228100	TAS				P		HPO:probinson	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0000952	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001250	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001252	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001254	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001259	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001290	OMIM:228100	TAS				P		HPO:skoehler	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001343	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001397	OMIM:228100	TAS				P		HPO:skoehler	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001892	OMIM:228100	IEA				P		HPO:probinson	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0001943	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0002901	OMIM:228100	IEA				P		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0003811	OMIM:228100	IEA				M		HPO:iea	
OMIM	228100	VISCERAL STEATOSIS, CONGENITAL		HP:0006693	OMIM:228100	IEA				P		HPO:iea	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0000007	OMIM:228250	TAS				I		HPO:probinson	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0001171	OMIM:228250	TAS				P		HPO:skoehler	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0003982	OMIM:228250	TAS				P		HPO:skoehler	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0004058	OMIM:228250	TAS				P		HPO:skoehler	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0009556	OMIM:228250	TAS				P		HPO:skoehler	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0010443	OMIM:228250	TAS				P		HPO:probinson	
OMIM	228250	FEMUR, UNILATERAL BIFID, WITH MONODACTYLOUS ECTRODACTYLY		HP:0200054	OMIM:228250	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000007	OMIM:228300	TAS				I		HPO:iea	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000044	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000054	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000138	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000771	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000869	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0000876	OMIM:228300	IEA				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0001939	OMIM:228300	IEA				P		HPO:iea	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0002215	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0002225	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0008226	OMIM:228300	IEA				P		HPO:iea	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0008669	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0010789	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0012215	OMIM:228300	TAS				P		HPO:skoehler	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0030344	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228300	HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA; HH23		HP:0040171	OMIM:228300	TAS				P		HPO:probinson	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0000007	OMIM:228355	IEA				I		HPO:iea	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0000365	OMIM:228355	IEA				P		HPO:iea	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0000851	OMIM:228355	TAS				P		HPO:probinson	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0001249	OMIM:228355	IEA				P		HPO:iea	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0001264	OMIM:228355	IEA				P		HPO:iea	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0001939	OMIM:228355	IEA				P		HPO:iea	
OMIM	228355	FETAL IODINE DEFICIENCY DISORDER		HP:0008251	OMIM:228355	TAS				P		HPO:probinson	
OMIM	228400	FEVER, FAMILIAL LIFELONG PERSISTENT		HP:0000007	OMIM:228400	TAS				I		HPO:probinson	
OMIM	228400	FEVER, FAMILIAL LIFELONG PERSISTENT		HP:0001945	OMIM:228400	TAS		HP:0040280		P		HPO:probinson	HP:0040280
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000007	OMIM:228520	IEA				I		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000160	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000175	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000260	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000272	OMIM:228520	IEA				P		HPO:skoehler	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000343	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000369	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000377	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000463	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000470	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000485	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000520	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000773	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000882	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000883	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000890	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000907	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000922	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000926	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0000947	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001538	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001539	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001655	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001773	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001789	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001800	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0001804	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0002007	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003026	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003038	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003175	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003196	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003375	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0003826	OMIM:228520	IEA				M		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0004209	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0004279	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0005257	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0005280	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0005442	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0005476	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0005622	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0006645	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0008451	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0008905	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0009473	OMIM:228520	IEA				P		HPO:iea	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0012368	OMIM:228520	IEA				P		HPO:skoehler	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0012385	OMIM:228520	TAS				P		HPO:skoehler	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0100865	OMIM:228520	TAS				P		HPO:probinson	
OMIM	228520	FIBROCHONDROGENESIS 1; FBCG1		HP:0200055	OMIM:228520	TAS				P		HPO:skoehler	
OMIM	228550	#228550 MYOFIBROMATOSIS, INFANTILE, 1; IMF1;;MYOFIBROMATOSIS, JUVENILE;;FIBROMATOSIS, CONGENITAL GENERALIZED; CGF		HP:0000006	OMIM:228550	TAS				I		HPO:skoehler	
OMIM	228550	#228550 MYOFIBROMATOSIS, INFANTILE, 1; IMF1;;MYOFIBROMATOSIS, JUVENILE;;FIBROMATOSIS, CONGENITAL GENERALIZED; CGF		HP:0003549	OMIM:228550	TAS				P		HPO:skoehler	
OMIM	228550	#228550 MYOFIBROMATOSIS, INFANTILE, 1; IMF1;;MYOFIBROMATOSIS, JUVENILE;;FIBROMATOSIS, CONGENITAL GENERALIZED; CGF		HP:0010614	OMIM:228550	TAS				P		HPO:skoehler	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000007	OMIM:228560	IEA				I		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000169	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000218	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000232	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000256	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000316	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000430	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000494	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000574	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000664	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000696	OMIM:228560	TAS				P		HPO:probinson	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0000951	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0001999	OMIM:228560	IEA				P		HPO:skoehler	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0005280	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0006335	OMIM:228560	IEA				P		HPO:iea	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0012471	OMIM:228560	TAS				P		HPO:skoehler	
OMIM	228560	228560 FIBROMATOSIS, GINGIVAL, WITH DISTINCTIVE FACIES		HP:0040079	OMIM:228560	TAS				P		HPO:skoehler	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000007	OMIM:228600	IEA				I		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000169	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000212	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000280	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000938	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0000939	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0001482	PMID:12214284	PCS				P		HPO:probinson	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0002014	OMIM:228600	TAS				P		HPO:skoehler	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0002719	OMIM:228600	TAS				P		HPO:skoehler	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0002797	OMIM:228600	IEA				P		HPO:iea	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0003676	OMIM:228600	TAS				C		HPO:skoehler	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0003828	OMIM:228600	TAS				C		HPO:skoehler	
OMIM	228600	HYALINE FIBROMATOSIS SYNDROME; HFS		HP:0005876	OMIM:228600	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0000007	OMIM:228800	IEA				I		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0000464	OMIM:228800	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0000765	OMIM:228800	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0001392	OMIM:228800	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0005200	OMIM:228800	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0009473	OMIM:228800	IEA				P		HPO:iea	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0030991	OMIM:228800	TAS				P		HPO:skoehler	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0100490	OMIM:228800	TAS				P		HPO:skoehler	
OMIM	228800	FIBROSCLEROSIS, MULTIFOCAL		HP:0100646	OMIM:228800	IEA				P		HPO:skoehler	
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0000007	OMIM:228900	PCS				I		HPO:iea	
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0001156	PMID:12121354	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0001772	OMIM:228900	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0001792	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0002990	PMID:2363425	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0002999	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0003038	OMIM:228900	IEA				P		HPO:skoehler	
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0004097	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0006092	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0008119	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0008905	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0009803	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0010049	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0010624	OMIM:228900	TAS				P		HPO:skoehler	
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0010743	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228900	#228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY;;DU PAN SYNDROME		HP:0010760	PMID:12121354	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0000007	PMID:16826533	PCS				I		HPO:iea	
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0000141	OMIM:228930	TAS				P		HPO:skoehler	
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001162	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001180	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001374	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001762	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001770	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001802	OMIM:228930	TAS				P		HPO:skoehler	
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001849	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0001964	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0002866	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0002980	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0002984	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0002986	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0002990	OMIM:228930	IEA				P		HPO:skoehler	
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0004322	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0005613	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0005914	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006101	PMID:9128926	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006143	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006262	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006443	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006492	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0006495	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0008839	PMID:9128926	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0009465	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0009767	OMIM:228930	TAS				P		HPO:skoehler	
OMIM	228930	FIBULAR APLASIA OR HYPOPLASIA, FEMORAL BOWING AND POLY-, SYN-, AND OLIGODACTYLY		HP:0030084	OMIM:228930	TAS				P		HPO:skoehler	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0000007	OMIM:228940	IEA				I		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0000089	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0000107	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0000347	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0000377	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0001159	OMIM:228940	IEA				P		HPO:skoehler	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0001629	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0001660	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0002093	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0002878	OMIM:228940	TAS				P		HPO:skoehler	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0003022	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0003027	OMIM:228940	IEA				P		HPO:iea	
OMIM	228940	228940 FIBULOULNAR APLASIA OR HYPOPLASIA WITH RENAL ABNORMALITIES		HP:0003811	OMIM:228940	IEA				M		HPO:iea	
OMIM	228960	FLAUJEAC FACTOR DEFICIENCY		HP:0000007	OMIM:228960	IEA				I		HPO:iea	
OMIM	228960	FLAUJEAC FACTOR DEFICIENCY		HP:0003645	OMIM:228960	IEA				P		HPO:iea	
OMIM	228960	FLAUJEAC FACTOR DEFICIENCY		HP:0005527	OMIM:228960	IEA				P		HPO:iea	
OMIM	228980	FLECK RETINA, FAMILIAL BENIGN; FRFB		HP:0000007	OMIM:228980	TAS				I		HPO:probinson	
OMIM	228980	FLECK RETINA, FAMILIAL BENIGN; FRFB		HP:0000618	OMIM:228980	IEA				P		HPO:skoehler	
OMIM	228980	FLECK RETINA, FAMILIAL BENIGN; FRFB		HP:0012045	OMIM:228980	TAS				P		HPO:probinson	
OMIM	228990	FLECK RETINA OF KANDORI		HP:0000007	OMIM:228990	IEA				I		HPO:iea	
OMIM	228990	FLECK RETINA OF KANDORI		HP:0000618	OMIM:228990	IEA				P		HPO:skoehler	
OMIM	228990	FLECK RETINA OF KANDORI		HP:0000662	OMIM:228990	IEA				P		HPO:iea	
OMIM	228990	FLECK RETINA OF KANDORI		HP:0012045	OMIM:228990	IEA				P		HPO:skoehler	
OMIM	229045	FOCAL EPITHELIAL HYPERPLASIA, ORAL		HP:0000007	OMIM:229045	IEA				I		HPO:iea	
OMIM	229045	FOCAL EPITHELIAL HYPERPLASIA, ORAL		HP:0000153	OMIM:229045	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0000007	OMIM:229050	IEA				I		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0000155	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0000737	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001249	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001250	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001251	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001252	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001263	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001290	OMIM:229050	TAS				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001508	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001873	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001875	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0001882	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002014	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002024	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002135	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002305	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002719	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0002719	OMIM:229050	TAS				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0003593	OMIM:229050	IEA				C		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0004851	OMIM:229050	IEA				P		HPO:iea	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0008872	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0009830	OMIM:229050	IEA				P		HPO:skoehler	
OMIM	229050	FOLATE MALABSORPTION, HEREDITARY		HP:0100660	OMIM:229050	TAS				P		HPO:skoehler	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0000007	OMIM:229070	IEA				I		HPO:iea	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0000027	OMIM:229070	IEA				P		HPO:skoehler	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0000135	OMIM:229070	IEA				P		HPO:skoehler	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0000786	OMIM:229070	IEA				P		HPO:iea	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0000789	OMIM:229070	TAS				P		HPO:skoehler	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0001939	OMIM:229070	IEA				P		HPO:iea	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0002750	OMIM:229070	TAS				P		HPO:skoehler	
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0003199	OMIM:229070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	229070	HYPOGONADOTROPIC HYPOGONADISM 24 WITHOUT ANOSMIA; HH24		HP:0008734	OMIM:229070	TAS				P		HPO:skoehler	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0000007	OMIM:229100	IEA				I		HPO:iea	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0001249	OMIM:229100	IEA				P		HPO:iea	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0001510	OMIM:229100	IEA				P		HPO:iea	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0001889	OMIM:229100	IEA				P		HPO:iea	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0003355	OMIM:229100	IEA				P		HPO:skoehler	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0003612	OMIM:229100	IEA				P		HPO:iea	
OMIM	229100	FORMIMINOTRANSFERASE DEFICIENCY		HP:0004821	OMIM:229100	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0000007	OMIM:229120	IEA				I		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0000179	OMIM:229120	IEA				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0000280	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0000282	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0000407	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0001169	OMIM:229120	IEA				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0001249	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0001250	OMIM:229120	IEA				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0002684	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0004279	OMIM:229120	TAS				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0004279	OMIM:229120	IEA				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0004322	OMIM:229120	IEA				P		HPO:skoehler	
OMIM	229120	FOUNTAIN SYNDROME		HP:0009836	OMIM:229120	IEA				P		HPO:iea	
OMIM	229120	FOUNTAIN SYNDROME		HP:0009836	OMIM:229120	TAS				P		HPO:probinson	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000007	OMIM:229200	IEA				I		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000256	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000286	OMIM:229200	TAS				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000365	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000545	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000563	OMIM:229200	TAS				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000572	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000592	OMIM:229200	TAS				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000703	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000987	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0000993	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0001119	OMIM:229200	TAS				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0001374	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0001388	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0001519	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0001634	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0002297	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0002650	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0003302	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0007517	OMIM:229200	IEA				P		HPO:iea	
OMIM	229200	BRITTLE CORNEA SYNDROME		HP:0100689	PMID:23642083	PCS				P		HPO:probinson	
OMIM	229230	FRASER-LIKE SYNDROME		HP:0000007	OMIM:229230	TAS				I		HPO:probinson	
OMIM	229230	FRASER-LIKE SYNDROME		HP:0000138	OMIM:229230	TAS				P		HPO:probinson	
OMIM	229230	FRASER-LIKE SYNDROME		HP:0001607	OMIM:229230	TAS				P		HPO:probinson	
OMIM	229230	FRASER-LIKE SYNDROME		HP:0001845	OMIM:229230	TAS				P		HPO:probinson	
OMIM	229230	FRASER-LIKE SYNDROME		HP:0009540	OMIM:229230	TAS				P		HPO:probinson	
OMIM	229250	FREESIA FLOWERS, INABILITY TO SMELL		HP:0000007	OMIM:229250	TAS				I		HPO:probinson	
OMIM	229250	FREESIA FLOWERS, INABILITY TO SMELL		HP:0000618	OMIM:229250	IEA				P		HPO:skoehler	
OMIM	229250	FREESIA FLOWERS, INABILITY TO SMELL		HP:0012247	OMIM:229250	TAS				P		HPO:probinson	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000007	OMIM:229300	IEA				I		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000639	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000648	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000649	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000763	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0000819	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0001123	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0001260	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0001635	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0001639	OMIM:229300	TAS				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0001761	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0002066	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0002070	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0002495	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0002522	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0002650	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003115	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003116	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003209	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003232	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003448	PMID:6231891	PCS				P		HPO:probinson	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003487	OMIM:229300	IEA				P		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0003621	OMIM:229300	IEA				C		HPO:iea	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0007078	PMID:6231891	PCS				P		HPO:probinson	
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0007663	OMIM:229300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	229300	#229300 FRIEDREICH ATAXIA 1; FRDA;;FRDA1;;FAFRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED		HP:0010831	OMIM:229300	TAS				P		HPO:skoehler	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0000007	OMIM:229310	IEA				I		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0000639	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001087	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001251	OMIM:229310	PCS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001260	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001315	OMIM:229310	TAS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001635	OMIM:229310	TAS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001691	OMIM:229310	TAS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001761	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001765	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0001953	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0002062	OMIM:229310	PCS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0002495	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0002650	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003115	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003116	OMIM:229310	TAS				P		HPO:skoehler	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003133	OMIM:229310	PCS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003209	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003232	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003487	OMIM:229310	IEA				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0003621	OMIM:229310	TAS				C		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0005157	OMIM:229310	TAS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0007078	OMIM:229310	PCS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0011397	OMIM:229310	PCS				P		HPO:iea	
OMIM	229310	229310 FRIEDREICH ATAXIA AND CONGENITAL GLAUCOMA		HP:0011441	OMIM:229310	PCS				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000007	OMIM:229400	IEA				I		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000193	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000202	OMIM:229400	IEA				P		HPO:skoehler	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000204	OMIM:229400	TAS				P		HPO:probinson	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000248	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000272	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000316	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000430	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000482	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000506	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000508	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000518	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000568	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000581	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000612	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0000625	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0003196	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0004122	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0004423	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0005466	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0007541	OMIM:229400	TAS				P		HPO:probinson	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0007708	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0007835	OMIM:229400	IEA				P		HPO:iea	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0009755	OMIM:229400	IEA				P		HPO:skoehler	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0011800	OMIM:229400	TAS				P		HPO:skoehler	
OMIM	229400	%229400 FRONTOFACIONASAL DYSPLASIA;;FFND;;FRONTOFACIONASAL DYSOSTOSIS		HP:0011803	OMIM:229400	TAS				P		HPO:skoehler	
OMIM	229500	FRUCTOSE AND GALACTOSE INTOLERANCE		HP:0000007	OMIM:229500	IEA				I		HPO:iea	
OMIM	229500	FRUCTOSE AND GALACTOSE INTOLERANCE		HP:0001250	OMIM:229500	IEA				P		HPO:iea	
OMIM	229500	FRUCTOSE AND GALACTOSE INTOLERANCE		HP:0001943	OMIM:229500	IEA				P		HPO:skoehler	
OMIM	229500	FRUCTOSE AND GALACTOSE INTOLERANCE		HP:0004919	OMIM:229500	TAS				P		HPO:probinson	
OMIM	229500	FRUCTOSE AND GALACTOSE INTOLERANCE		HP:0005973	OMIM:229500	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0000007	OMIM:229600	IEA				I		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0000114	OMIM:229600	TAS				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0000952	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001249	OMIM:229600	TAS				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001250	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001254	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001259	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001394	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001397	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001508	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001942	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0001943	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002013	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002018	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002027	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002049	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002148	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002149	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002239	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002240	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002904	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0002910	OMIM:229600	IEA				P		HPO:skoehler	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0003076	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0003109	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0003128	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0003149	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0003646	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0004395	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0005973	OMIM:229600	IEA				P		HPO:iea	
OMIM	229600	#229600 FRUCTOSE INTOLERANCE, HEREDITARY;;FRUCTOSEMIA;;FRUCTOSE-1-PHOSPHATE ALDOLASE DEFICIENCY;;FRUCTOSE-1,6-BISPHOSPHATE ALDOLASE B DEFICIENCY;;ALDOLASE B DEFICIENCY;;ALDOB DEFICIENCY		HP:0008273	OMIM:229600	IEA				P		HPO:iea	
OMIM	229650	FRUCTOSE UTILIZATION		HP:0000007	OMIM:229650	IEA				I		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0000007	OMIM:229700	IEA				I		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0000737	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001250	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001252	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001254	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001259	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001290	OMIM:229700	TAS				P		HPO:skoehler	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001649	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001942	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001943	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001945	OMIM:229700	IEA				P		HPO:skoehler	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0001946	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0002094	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0002104	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0002240	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0002883	OMIM:229700	IEA				P		HPO:iea	
OMIM	229700	FRUCTOSE-1,6-BISPHOSPHATASE DEFICIENCY		HP:0040301	OMIM:229700	TAS				P		HPO:skoehler	
OMIM	229800	FRUCTOSURIA, ESSENTIAL		HP:0000007	OMIM:229800	TAS				I		HPO:iea	
OMIM	229800	FRUCTOSURIA, ESSENTIAL		HP:0011033	OMIM:229800	TAS				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000007	OMIM:229850	IEA				I		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000028	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000047	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000048	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000049	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000073	OMIM:229850	TAS				P		HPO:probinson	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000104	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000107	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000126	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000154	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000175	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000204	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000280	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000308	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000316	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000343	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000369	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000431	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000463	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000470	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000475	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000475	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000568	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000581	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000813	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000883	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000885	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0000954	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001212	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001249	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001250	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001274	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001305	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001520	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001539	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001561	OMIM:229850	IEA		HP:0040284		P		HPO:skoehler	14%
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001629	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001631	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001748	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001792	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001798	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0001838	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002023	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002032	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002089	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002139	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002245	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002247	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002251	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0002566	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0003826	OMIM:229850	IEA				M		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0005257	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0006278	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0007036	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0007096	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0007759	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009112	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009473	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009623	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009778	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009882	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0009937	OMIM:229850	TAS				P		HPO:probinson	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0010310	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0010804	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0011039	OMIM:229850	IEA				P		HPO:iea	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0012385	OMIM:229850	TAS				P		HPO:skoehler	
OMIM	229850	FRYNS SYNDROME; FRNS		HP:0045025	OMIM:229850	IEA				P		HPO:skoehler	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000007	OMIM:230000	IEA				I		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000158	OMIM:230000	TAS				P		HPO:probinson	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000179	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000280	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000316	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000365	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000445	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000503	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000574	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000914	OMIM:230000	TAS				P		HPO:skoehler	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000943	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000958	OMIM:230000	IEA				P		HPO:skoehler	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0000970	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001014	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001249	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001250	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001271	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001371	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001552	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001640	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001744	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0001922	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002007	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002059	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002205	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002240	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002510	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002650	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002673	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0002938	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0004298	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0004322	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0004558	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0004630	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0005453	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0008430	OMIM:230000	TAS				P		HPO:probinson	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0008436	OMIM:230000	IEA				P		HPO:iea	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0010471	OMIM:230000	TAS				P		HPO:probinson	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0011220	OMIM:230000	TAS				P		HPO:skoehler	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0012236	OMIM:230000	TAS				P		HPO:probinson	
OMIM	230000	#230000 FUCOSIDOSIS;;ALPHA-L-FUCOSIDASE DEFICIENCY		HP:0100790	OMIM:230000	TAS				P		HPO:skoehler	
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0000007	OMIM:230200	TAS				I		HPO:probinson	
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0000518	OMIM:230200	TAS				P		HPO:probinson	
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0002516	OMIM:230200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0006579	OMIM:230200	IEA				P		HPO:iea	
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0012023	OMIM:230200	TAS				P		HPO:probinson	
OMIM	230200	GALACTOKINASE DEFICIENCY		HP:0012024	OMIM:230200	TAS				P		HPO:probinson	
OMIM	230300	GALACTORRHEA		HP:0000007	OMIM:230300	IEA				I		HPO:iea	
OMIM	230300	GALACTORRHEA		HP:0000119	OMIM:230300	IEA				P		HPO:iea	
OMIM	230300	GALACTORRHEA		HP:0000765	OMIM:230300	IEA				P		HPO:iea	
OMIM	230300	GALACTORRHEA		HP:0100829	OMIM:230300	IEA				P		HPO:skoehler	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0000007	OMIM:230350	IEA				I		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0000407	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0000750	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0000952	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001249	OMIM:230350	TAS				P		HPO:skoehler	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001252	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001263	OMIM:230350	TAS				P		HPO:skoehler	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001290	OMIM:230350	TAS				P		HPO:skoehler	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001508	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0001744	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0002013	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0002194	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0002240	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0003355	OMIM:230350	IEA				P		HPO:iea	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0012023	OMIM:230350	TAS				P		HPO:probinson	
OMIM	230350	GALACTOSE EPIMERASE DEFICIENCY		HP:0012024	OMIM:230350	TAS				P		HPO:probinson	
OMIM	230400	GALACTOSEMIA		HP:0000007	OMIM:230400	IEA				I		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0000518	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0000815	OMIM:230400	IEA				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0001249	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0001394	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0001410	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0001508	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0001878	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0001942	OMIM:230400	IEA				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0002013	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0002014	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0002240	OMIM:230400	IEA				P		HPO:iea	
OMIM	230400	GALACTOSEMIA		HP:0003355	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0004918	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0008209	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0012023	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0012024	OMIM:230400	TAS				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0012592	OMIM:230400	IEA				P		HPO:skoehler	
OMIM	230400	GALACTOSEMIA		HP:0410061	PMID:11092512,PMID:7671965	PCS				P		HPO:NicoleVasilevsky	
OMIM	230400	GALACTOSEMIA		HP:0410062	PMID:11092512	PCS				P		HPO:NicoleVasilevsky	
OMIM	230400	GALACTOSEMIA		HP:0410063	PMID:14680973	PCS				P		HPO:NicoleVasilevsky	
OMIM	230400	GALACTOSEMIA		HP:0410064	PMID:14680973	PCS				P		HPO:NicoleVasilevsky	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0000007	OMIM:230450	IEA				I		HPO:iea	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0001271	OMIM:230450	IEA				P		HPO:iea	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0001878	OMIM:230450	IEA				P		HPO:iea	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0001939	OMIM:230450	IEA				P		HPO:iea	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0003198	OMIM:230450	IEA				P		HPO:iea	
OMIM	230450	GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUETO		HP:0006904	OMIM:230450	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000007	OMIM:230500	IEA				I		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000023	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000079	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000212	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000280	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000316	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000457	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000470	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000900	OMIM:230500	TAS				P		HPO:probinson	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0000998	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001071	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001249	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001387	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001522	OMIM:230500	IEA				M		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001635	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001639	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001644	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001654	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001744	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0001922	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0002007	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0002240	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0002650	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0002808	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0003510	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0004568	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0007313	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0008166	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0008479	OMIM:230500	IEA				P		HPO:iea	
OMIM	230500	#230500 GM1-GANGLIOSIDOSIS, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I;;GANGLIOSIDOSIS, GENERALIZED GM1, INFANTILE FORM;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 1;;BETA-GALACTOSIDASE-1 DEFICIENCY;;GLB1 DEFICIENCYGM1-GANGLIOSIDOSIS, TYPE I, WITH CARDIAC INVOLVEMENT, INCLUDED;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I, WITH CARDIAC INVOLVEMENT,INCLUDED		HP:0010729	OMIM:230500	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0000007	OMIM:230600	IEA				I		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0000271	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0000648	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0000926	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0001251	OMIM:230600	IEA				P		HPO:skoehler	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0001288	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0001392	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0001743	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0001982	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0002059	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0002119	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0002123	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0002510	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0002673	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0007272	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0007281	OMIM:230600	IEA				P		HPO:iea	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0007281	OMIM:230600	TAS				P		HPO:probinson	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0008166	OMIM:230600	TAS				P		HPO:probinson	
OMIM	230600	#230600 GM1-GANGLIOSIDOSIS, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 2GANGLIOSIDOSIS, GENERALIZED GM1, LATE-INFANTILE TYPE, INCLUDED		HP:0008166	OMIM:230600	IEA				P		HPO:skoehler	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0000007	OMIM:230650	IEA				I		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0000271	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0000926	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0001256	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0001332	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0001350	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0001871	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0002506	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0002650	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0002808	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0002869	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0003202	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0003274	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0003651	OMIM:230650	TAS				P		HPO:skoehler	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0004322	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0007759	OMIM:230650	IEA				P		HPO:iea	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0008166	OMIM:230650	TAS				P		HPO:skoehler	
OMIM	230650	#230650 GM1-GANGLIOSIDOSIS, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, ADULT TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, CHRONIC TYPE;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE III;;GANGLIOSIDOSIS, GENERALIZED GM1, TYPE 3		HP:0008430	OMIM:230650	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000007	OMIM:230740	IEA				I		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000164	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000179	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000260	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000270	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000316	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000347	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000411	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000486	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000501	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000563	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000613	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000639	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000648	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000653	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0000706	OMIM:230740	TAS				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001006	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001043	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001249	OMIM:230740	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001250	OMIM:230740	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001270	OMIM:230740	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001382	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001510	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001537	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001582	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001591	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001596	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0001939	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002007	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002119	OMIM:230740	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002353	OMIM:230740	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002557	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002650	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002705	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0002750	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0003187	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0005280	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0005576	OMIM:230740	IEA				P		HPO:iea	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0045075	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230740	GAPO SYNDROME; GAPOS		HP:0200040	OMIM:230740	IEA				P		HPO:skoehler	
OMIM	230750	GASTROSCHISISABDOMINAL WALL DEFECTS, INCLUDED		HP:0000007	OMIM:230750	TAS				I		HPO:nvasilevsky	
OMIM	230750	GASTROSCHISISABDOMINAL WALL DEFECTS, INCLUDED		HP:0001426	OMIM:230750	TAS				I		HPO:nvasilevsky	
OMIM	230750	GASTROSCHISISABDOMINAL WALL DEFECTS, INCLUDED		HP:0001543	OMIM:230750	IEA				P		HPO:iea	
OMIM	230750	GASTROSCHISISABDOMINAL WALL DEFECTS, INCLUDED		HP:0010866	OMIM:230750	TAS				P		HPO:nvasilevsky	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0000007	OMIM:230800	IEA				I		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0000421	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0000478	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0000822	OMIM:230800	IEA				P		HPO:skoehler	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0000953	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0001744	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0001873	OMIM:230800	TAS				P		HPO:skoehler	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0001876	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0001903	OMIM:230800	TAS				P		HPO:skoehler	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0001971	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002092	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002094	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002113	OMIM:230800	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002240	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002653	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002756	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0002953	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0004975	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0006530	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0006775	OMIM:230800	IEA				P		HPO:iea	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0007401	OMIM:230800	TAS				P		HPO:skoehler	
OMIM	230800	GAUCHER DISEASE, TYPE I		HP:0010885	OMIM:230800	TAS				P		HPO:skoehler	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0000007	OMIM:230900	IEA				I		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0000211	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0000486	OMIM:230900	IEA				P		HPO:skoehler	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0000565	OMIM:230900	TAS				P		HPO:skoehler	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0000657	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001250	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001257	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001263	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001347	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001508	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001538	OMIM:230900	TAS				P		HPO:probinson	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001744	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001873	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0001903	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002015	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002059	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002063	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002100	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002104	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002240	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002344	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0002483	OMIM:230900	IEA				P		HPO:iea	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0011968	OMIM:230900	TAS				P		HPO:skoehler	
OMIM	230900	GAUCHER DISEASE, TYPE II		HP:0025356	OMIM:230900	IEA				P		HPO:skoehler	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0000007	OMIM:231000	IEA				I		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0000486	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0000716	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0000726	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001251	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001270	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001336	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001744	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001873	OMIM:231000	TAS				P		HPO:skoehler	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0001876	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0002123	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0002167	OMIM:231000	TAS				P		HPO:probinson	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0002240	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0002313	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0002344	OMIM:231000	IEA				P		HPO:skoehler	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0003581	OMIM:231000	IEA				C		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0003656	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0004322	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0004325	OMIM:231000	IEA				P		HPO:iea	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0004934	OMIM:231000	IEA				P		HPO:skoehler	
OMIM	231000	#231000 GAUCHER DISEASE, TYPE III;;GD III;;GAUCHER DISEASE, SUBACUTE NEURONOPATHIC TYPE;;GAUCHER DISEASE, CHRONIC NEURONOPATHIC TYPE;;GAUCHER DISEASE, JUVENILE AND ADULT, CEREBRALGAUCHER DISEASE, TYPE IIIA, INCLUDED;;GAUCHER DISEASE, TYPE IIIB, INCLUDED;;GAUCHER DISEASE, NORRBOTTNIAN TYPE, INCLUDED		HP:0007817	OMIM:231000	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0000007	OMIM:231005	IEA				I		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0000238	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0000486	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0000623	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0000666	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001250	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001640	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001718	OMIM:231005	IEA				P		HPO:skoehler	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001744	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001761	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0001876	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0002240	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0004380	OMIM:231005	PCS				P		HPO:probinson	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0004382	PMID:1333717	PCS				P		HPO:probinson	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0004963	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0007759	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0007885	OMIM:231005	IEA				P		HPO:iea	
OMIM	231005	GAUCHER DISEASE, TYPE IIIC		HP:0007975	OMIM:231005	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000007	OMIM:231050	IEA				I		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000154	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000311	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000319	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000343	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000391	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000463	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000582	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000767	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0000938	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001072	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001239	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001250	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001263	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001387	PMID:21415077	PCS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001620	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001635	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001650	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001718	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001773	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0001792	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0002240	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0002673	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0002680	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0002777	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0003026	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0003090	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0003196	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0004279	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0004322	OMIM:231050	TAS				P		HPO:probinson	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0005041	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0006161	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0009473	OMIM:231050	IEA				P		HPO:iea	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0010446	OMIM:231050	IEA				P		HPO:skoehler	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0100490	OMIM:231050	TAS				P		HPO:skoehler	
OMIM	231050	#231050 GELEOPHYSIC DYSPLASIA 1; GPHYSD1		HP:0100679	OMIM:231050	TAS				P		HPO:skoehler	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000007	OMIM:231060	IEA				I		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000047	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000107	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000175	OMIM:231060	TAS				P		HPO:skoehler	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000204	OMIM:231060	TAS				P		HPO:skoehler	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000347	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0000369	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0001629	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0001669	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0001719	OMIM:231060	TAS				P		HPO:skoehler	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0008668	OMIM:231060	IEA				P		HPO:iea	
OMIM	231060	GENITOPALATOCARDIAC SYNDROME		HP:0012020	OMIM:231060	TAS				P		HPO:probinson	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000007	OMIM:231070	IEA				I		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000252	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000272	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000303	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000327	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000490	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000704	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000750	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000926	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000938	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000939	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0000973	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0001187	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0001249	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002645	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002751	OMIM:231070	IEA				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002757	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002953	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002980	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0002982	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0003301	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0003510	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0004568	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0004586	OMIM:231070	IEA				P		HPO:iea	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0005328	OMIM:231070	IEA				P		HPO:skoehler	
OMIM	231070	GERODERMA OSTEODYSPLASTICUM; GO		HP:0012385	OMIM:231070	TAS				P		HPO:skoehler	
OMIM	231080	GERMAN SYNDROME		HP:0000007	OMIM:231080	IEA				I		HPO:iea	
OMIM	231080	GERMAN SYNDROME		HP:0001004	OMIM:231080	IEA				P		HPO:iea	
OMIM	231080	GERMAN SYNDROME		HP:0001319	OMIM:231080	TAS				P		HPO:probinson	
OMIM	231080	GERMAN SYNDROME		HP:0001648	OMIM:231080	TAS				P		HPO:skoehler	
OMIM	231080	GERMAN SYNDROME		HP:0002375	OMIM:231080	IEA				P		HPO:skoehler	
OMIM	231080	GERMAN SYNDROME		HP:0002804	OMIM:231080	IEA				P		HPO:iea	
OMIM	231090	HYDATIDIFORM MOLE, RECURRENT, 1; HYDM1		HP:0000007	OMIM:231090	IEA				I		HPO:iea	
OMIM	231090	HYDATIDIFORM MOLE, RECURRENT, 1; HYDM1		HP:0000119	OMIM:231090	IEA				P		HPO:iea	
OMIM	231090	HYDATIDIFORM MOLE, RECURRENT, 1; HYDM1		HP:0032192	OMIM:231090	IEA				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0000007	OMIM:231095	TAS				I		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0001873	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0001882	OMIM:231095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0005505	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0005528	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0005890	OMIM:231095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0005890	OMIM:231095	IEA				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0011001	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0011974	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231095	#231095 GHOSAL HEMATODIAPHYSEAL DYSPLASIA; GHDD;;GHOSAL SYNDROME		HP:0100252	OMIM:231095	TAS				P		HPO:skoehler	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0000007	OMIM:231100	IEA				I		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001394	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001395	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001396	OMIM:231100	IEA				P		HPO:skoehler	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001399	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001404	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001511	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001562	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001790	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001892	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0001943	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0003281	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0003452	OMIM:231100	IEA				P		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0003577	OMIM:231100	IEA				C		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0003678	OMIM:231100	IEA				C		HPO:iea	
OMIM	231100	HEMOCHROMATOSIS, NEONATAL		HP:0006579	OMIM:231100	TAS				P		HPO:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0000007	PMID:9616133	PCS				I	BERNARD-SOULIER SYNDROME	HPO:iea	
OMIM	231200	Bernard-Soulier syndrome		HP:0000132	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HPO:iea	
OMIM	231200	Bernard-Soulier syndrome		HP:0000225	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0000421	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HPO:iea	
OMIM	231200	Bernard-Soulier syndrome		HP:0000979	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HPO:iea	
OMIM	231200	Bernard-Soulier syndrome	HP:0012825	HP:0001873	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HPO:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0001902	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0002239	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0003010	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HPO:iea	
OMIM	231200	Bernard-Soulier syndrome		HP:0004846	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0006298	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231200	Bernard-Soulier syndrome		HP:0011871	PMID:9616133	PCS				P	BERNARD-SOULIER SYNDROME	HP:probinson	
OMIM	231300	GLAUCOMA 3, PRIMARY CONGENITAL, A		HP:0000007	OMIM:231300	IEA				I		HPO:iea	
OMIM	231300	GLAUCOMA 3, PRIMARY CONGENITAL, A		HP:0000557	OMIM:231300	IEA				P		HPO:iea	
OMIM	231300	GLAUCOMA 3, PRIMARY CONGENITAL, A		HP:0001425	OMIM:231300	IEA				I		HPO:iea	
OMIM	231300	GLAUCOMA 3, PRIMARY CONGENITAL, A		HP:0007906	OMIM:231300	IEA				P		HPO:iea	
OMIM	231300	GLAUCOMA 3, PRIMARY CONGENITAL, A		HP:0008041	OMIM:231300	IEA				P		HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:231530	TAS				I	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:probinson	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:231530	TAS				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:skoehler	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001397	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001510	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001639	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001644	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0001985	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0002173	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0002605	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0002913	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0003215	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0004448	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0006929	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0008872	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:iea	
OMIM	231530	3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY		HP:0100950	OMIM:231530	IEA				P	3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY	HPO:skoehler	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000007	OMIM:231550	IEA				I		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000252	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000522	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000522	OMIM:231550	TAS				P		HPO:probinson	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000648	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000649	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000953	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0000972	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001249	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001251	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001260	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001263	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001278	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001324	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0001347	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0002571	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0003487	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0003676	OMIM:231550	IEA				C		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0004319	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0004322	OMIM:231550	TAS				P		HPO:probinson	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0007002	OMIM:231550	TAS				P		HPO:skoehler	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0008163	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0008259	OMIM:231550	IEA				P		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0009916	OMIM:231550	TAS				P		HPO:skoehler	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0011463	OMIM:231550	IEA				C		HPO:iea	
OMIM	231550	#231550 ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME; AAAS;;TRIPLE-A SYNDROME;;ALACRIMA-ACHALASIA-ADRENAL INSUFFICIENCY NEUROLOGIC DISORDER;;GLUCOCORTICOID DEFICIENCY AND ACHALASIA;;ALLGROVE SYNDROME;;ADDISONIAN-ACHALASIA SYNDROME;;HYPOADRENALISM WITH ACHALASIA;;ALACRIMA-ACHALASIA-ADDISONIANISM;;ACTH-RESISTANT ADRENAL INSUFFICIENCY, ACHALASIA AND ALACRIMAACHALASIA-ALACRIMA SYNDROME, INCLUDED		HP:0012332	OMIM:231550	TAS				P		HPO:probinson	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0000007	OMIM:231630	IEA				I		HPO:iea	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0001962	PMID:942671	PCS	HP:0003581			P		HPO:nvasilevsky	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0002018	OMIM:231630	IEA				P		HPO:iea	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0002094	PMID:942671	PCS	HP:0003581			P		HPO:nvasilevsky	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0002315	PMID:4117590	PCS				P		HPO:probinson	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0031284	PMID:942671	PCS	HP:0003581			P		HPO:nvasilevsky	
OMIM	231630	GLUTAMATE MONOSODIUM SENSITIVITY		HP:0100749	PMID:942671	PCS	HP:0003581			P		HPO:nvasilevsky	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0000007	OMIM:231670	IEA				I		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0000256	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001250	OMIM:231670	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001252	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001264	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001266	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001290	OMIM:231670	TAS				P		HPO:skoehler	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001332	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001508	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001942	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0001943	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0002063	OMIM:231670	TAS				P		HPO:skoehler	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0002179	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0002240	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0002919	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0003150	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0003530	OMIM:231670	IEA				P		HPO:skoehler	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0006873	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0006956	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0007105	OMIM:231670	IEA				P		HPO:iea	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0012448	OMIM:231670	TAS				P		HPO:skoehler	
OMIM	231670	GLUTARIC ACIDEMIA I; GA1		HP:0410175	OMIM:231670	IEA				P		HPO:skoehler	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:231680	IEA				I		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000078	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000113	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000114	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000256	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000260	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000348	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000377	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000506	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000519	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000803	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0000952	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001252	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001302	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001324	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001325	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001397	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001943	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0001999	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002013	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002018	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002089	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002098	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002171	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002240	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002614	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0002909	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003076	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003150	OMIM:231680	TAS				P		HPO:probinson	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003150	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003219	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003530	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003647	OMIM:231680	IEA				P		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0003811	OMIM:231680	IEA				M		HPO:iea	
OMIM	231680	MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY		HP:0005280	OMIM:231680	IEA				P		HPO:iea	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0000007	OMIM:231690	IEA				I	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:iea	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0000822	OMIM:231690	TAS				P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:skoehler	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0000836	OMIM:231690	TAS		HP:0040283		P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:skoehler	HP:0040283
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0000853	OMIM:231690	TAS		HP:0040283		P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:skoehler	HP:0040283
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0001508	OMIM:231690	IEA				P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:iea	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0002013	OMIM:231690	TAS				P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:skoehler	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0002014	OMIM:231690	TAS				P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:skoehler	
OMIM	231690	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-CoA OXIDASE DEFICIENCY		HP:0003150	OMIM:231690	IEA				P	#231690 GLUTARIC ACIDURIA III;;GA III;;GLUTARYL-COA OXIDASE DEFICIENCY	HPO:iea	
OMIM	231900	GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIADUE TO		HP:0000007	OMIM:231900	TAS				I		HPO:probinson	
OMIM	231900	GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIADUE TO		HP:0001878	OMIM:231900	TAS				P		HPO:probinson	
OMIM	231900	GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIADUE TO		HP:0003258	OMIM:231900	TAS				P		HPO:probinson	
OMIM	231900	GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIADUE TO		HP:0003343	OMIM:231900	TAS				P		HPO:probinson	
OMIM	231950	GLUTATHIONURIA		HP:0000007	OMIM:231950	IEA				I		HPO:iea	
OMIM	231950	GLUTATHIONURIA		HP:0001249	OMIM:231950	IEA				P		HPO:iea	
OMIM	231950	GLUTATHIONURIA		HP:0001337	OMIM:231950	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	231950	GLUTATHIONURIA		HP:0001939	OMIM:231950	IEA				P		HPO:iea	
OMIM	231970	231970 GLUTEAL MUSCLES, ABSENCE OF		HP:0000007	OMIM:231970	IEA				I		HPO:iea	
OMIM	231970	231970 GLUTEAL MUSCLES, ABSENCE OF		HP:0000609	OMIM:231970	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	231970	231970 GLUTEAL MUSCLES, ABSENCE OF		HP:0002650	OMIM:231970	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	231970	231970 GLUTEAL MUSCLES, ABSENCE OF		HP:0003298	OMIM:231970	IEA				P		HPO:iea	
OMIM	231970	231970 GLUTEAL MUSCLES, ABSENCE OF		HP:0009013	OMIM:231970	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000007	OMIM:232200	IEA				I		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000093	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000097	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000105	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000295	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000660	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000787	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000822	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000823	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000939	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0000991	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001114	OMIM:232200	TAS				P		HPO:skoehler	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001402	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001538	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001733	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001892	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001943	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0001997	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0002149	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0002240	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0002254	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA	HP:0012825	HP:0002910	OMIM:232200	PCS				P		HPO:probinson	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0003077	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0003128	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0003199	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0004322	OMIM:232200	IEA				P		HPO:iea	
OMIM	232200	GLYCOGEN STORAGE DISEASE IA		HP:0012213	OMIM:232200	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000007	OMIM:232220	IEA				I		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000093	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000097	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000105	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000155	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000295	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000660	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000787	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000822	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000823	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000939	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0000991	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001114	OMIM:232220	TAS				P		HPO:skoehler	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001402	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001538	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001733	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001875	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001943	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0001997	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0002149	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0002240	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0002718	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB	HP:0012825	HP:0002910	OMIM:232220	PCS				P		HPO:probinson	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0003077	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0003128	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0004322	OMIM:232220	IEA				P		HPO:iea	
OMIM	232220	GLYCOGEN STORAGE DISEASE IB		HP:0012213	OMIM:232220	IEA				P		HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000007	OMIM:232240	IEA				I	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000083	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000093	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000097	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000790	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000822	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000823	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0000991	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0001114	OMIM:232240	TAS				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:skoehler	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0001402	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0001942	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0001943	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0001997	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0002092	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0002149	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:skoehler	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0002240	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0002884	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0003077	OMIM:232240	TAS				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:probinson	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0003128	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0006280	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0012213	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:iea	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0012522	OMIM:232240	TAS				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:probinson	
OMIM	232240	GLYCOGEN STORAGE DISEASE Ic; GSD1C		HP:0410175	OMIM:232240	IEA				P	GLYCOGEN STORAGE DISEASE IC; GSD1C	HPO:skoehler	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0000007	OMIM:232300	IEA				I		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0000158	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0000365	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001252	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001284	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001290	OMIM:232300	TAS				P		HPO:skoehler	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001640	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001716	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001744	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0001945	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0002093	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0002094	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0002205	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0002240	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0002747	OMIM:232300	TAS				P		HPO:skoehler	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0003236	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0003701	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0003725	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0004944	OMIM:232300	IEA				P		HPO:iea	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0005165	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0006597	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232300	GLYCOGEN STORAGE DISEASE II		HP:0011400	OMIM:232300	TAS				P		HPO:probinson	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000007	OMIM:232400	IEA				I	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000219	OMIM:232400	TAS				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:skoehler	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000233	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000272	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000455	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0000490	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0001324	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0001395	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0001638	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0001714	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0001943	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0002240	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0002910	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0003077	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0003198	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0003236	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0003693	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0004322	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0005280	OMIM:232400	IEA				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:iea	
OMIM	232400	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIa, INCLUDED; GSD IIIa, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIb, INCLUDED; GSD IIIb, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIc, INCLUDED; GSD IIIc, INCLUDED;;GLYCOGEN STORAGE DISEASE IIId, INCLUDED; GSD IIId, INCLUDED		HP:0011800	OMIM:232400	TAS				P	#232400 GLYCOGEN STORAGE DISEASE III;;GSD III; GSD3;;FORBES DISEASE;;CORI DISEASE;;LIMIT DEXTRINOSIS;;AMYLO-1,6-GLUCOSIDASE DEFICIENCY;;AGL DEFICIENCY;;GLYCOGEN DEBRANCHER DEFICIENCY;;GDE DEFICIENCYGLYCOGEN STORAGE DISEASE IIIA, INCLUDED; GSD IIIA, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIB, INCLUDED; GSD IIIB, INCLUDED;;GLYCOGEN STORAGE DISEASE IIIC, INCLUDED; GSD IIIC, INCLUDED;;GLYCOGEN STORAGE DISEASE IIID, INCLUDED; GSD IIID, INCLUDED	HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0000007	OMIM:232500	IEA				I		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0000969	OMIM:232500	IEA				P		HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001252	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001290	OMIM:232500	TAS				P		HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001315	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001324	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001394	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001399	OMIM:232500	TAS				P		HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001409	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001433	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001508	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001541	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001558	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001561	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001638	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0001789	OMIM:232500	TAS				P		HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0002040	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0002804	OMIM:232500	IEA				P		HPO:skoehler	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0003202	OMIM:232500	IEA				P		HPO:iea	
OMIM	232500	GLYCOGEN STORAGE DISEASE IV		HP:0005576	OMIM:232500	IEA				P		HPO:skoehler	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0000007	PMID:8316268	PCS				I		HPO:iea	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0001324	PMID:22250184	PCS		HP:0040284		P		HPO:skoehler	49/196
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0002913	PMID:22250184	PCS		HP:0040284		P		HPO:iea	98/196
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0003236	PMID:22250184	PCS		HP:0040284		P		HPO:probinson	166/168
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0003621	PMID:22250184	PCS				C		HP:probinson	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0003710	PMID:8316268	PCS				P		HPO:probinson	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0003738	PMID:8316268	PCS				P		HPO:probinson	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0009045	PMID:8316268	PCS				P		HP:probinson	
OMIM	232600	GLYCOGEN STORAGE DISEASE V; GSD5		HP:0040319	OMIM:232600	IEA				P		HPO:skoehler	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0000007	PMID:25266922	PCS				I		HPO:iea	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0001531	PMID:25266922	PCS				P		HP:probinson	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0001943	PMID:25266922	PCS				P		HPO:skoehler	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0002155	PMID:25266922	PCS				P		HP:probinson	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0002240	PMID:25266922	PCS	HP:0003593	HP:0040284		P		HPO:iea	4/4
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0002910	PMID:25266922	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	232700	GLYCOGEN STORAGE DISEASE VI	HP:0012825	HP:0003077	OMIM:232700	TAS				P		HPO:probinson	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0003124	PMID:25266922	PCS				P		HP:probinson	
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0006568	PMID:25266922	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	232700	GLYCOGEN STORAGE DISEASE VI		HP:0008897	OMIM:232700	IEA				P		HPO:iea	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0000007	OMIM:232800	TAS				I		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0000952	OMIM:232800	TAS				P		HPO:skoehler	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0001081	OMIM:232800	TAS				P		HPO:skoehler	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0001324	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0001878	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0001923	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0001997	OMIM:232800	TAS				P		HPO:skoehler	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0002149	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0003546	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0003573	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0003710	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0003828	OMIM:232800	TAS				C		HPO:skoehler	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0008305	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0009051	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232800	GLYCOGEN STORAGE DISEASE VII		HP:0030271	OMIM:232800	TAS				P		HPO:probinson	
OMIM	232900	GLYCOPROTEIN STORAGE DISEASE		HP:0000007	OMIM:232900	IEA				I		HPO:iea	
OMIM	232900	GLYCOPROTEIN STORAGE DISEASE		HP:0001744	OMIM:232900	IEA				P		HPO:iea	
OMIM	232900	GLYCOPROTEIN STORAGE DISEASE		HP:0001997	OMIM:232900	IEA				P		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0000006	OMIM:233100	TAS				I		HPO:skoehler	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0000007	OMIM:233100	IEA				I		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0000103	OMIM:233100	IEA				P		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0001959	OMIM:233100	IEA				P		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0002591	OMIM:233100	IEA				P		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0003076	OMIM:233100	IEA				P		HPO:iea	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0003828	OMIM:233100	TAS				C		HPO:skoehler	
OMIM	233100	#233100 RENAL GLUCOSURIA; GLYS1;;GLYCOSURIA, RENAL		HP:0010677	OMIM:233100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0000007	OMIM:233270	IEA				I		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0000252	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0000568	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0000823	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0001156	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0001627	OMIM:233270	TAS				P		HPO:skoehler	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0006887	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0009466	OMIM:233270	IEA				P		HPO:iea	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0010864	OMIM:233270	TAS				P		HPO:skoehler	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0030084	OMIM:233270	TAS				P		HPO:skoehler	
OMIM	233270	233270 GOMBO SYNDROME;;GROWTH RETARDATION, OCULAR ABNORMALITIES, MICROCEPHALY, BRACHYDACTYLY,AND OLIGOPHRENIA		HP:0030680	OMIM:233270	IEA				P		HPO:iea	
OMIM	233300	OVARIAN DYSGENESIS 1		HP:0000007	OMIM:233300	IEA				I		HPO:iea	
OMIM	233300	OVARIAN DYSGENESIS 1		HP:0000133	OMIM:233300	IEA				P		HPO:iea	
OMIM	233300	OVARIAN DYSGENESIS 1		HP:0000786	OMIM:233300	IEA				P		HPO:iea	
OMIM	233300	OVARIAN DYSGENESIS 1		HP:0000837	OMIM:233300	IEA				P		HPO:iea	
OMIM	233300	OVARIAN DYSGENESIS 1		HP:0000939	OMIM:233300	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000007	OMIM:233400	IEA				I		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000133	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000218	OMIM:233400	TAS				P		HPO:skoehler	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000407	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000639	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000786	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000837	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0000939	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001260	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001264	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001265	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001270	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001272	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001284	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001761	OMIM:233400	TAS				P		HPO:skoehler	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0001762	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0002066	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0002650	OMIM:233400	TAS				P		HPO:skoehler	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0004322	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0007141	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0007941	OMIM:233400	IEA				P		HPO:iea	
OMIM	233400	#233400 PERRAULT SYNDROME 1; PRLTS1;;OVARIAN DYSGENESIS WITH SENSORINEURAL DEAFNESS;;GONADAL DYSGENESIS, XX TYPE, WITH DEAFNESS		HP:0100543	OMIM:233400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	233420	46,XY SEX REVERSAL 7		HP:0000007	OMIM:233420	TAS				I		HPO:iea	
OMIM	233420	46,XY SEX REVERSAL 7		HP:0000013	OMIM:233420	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	233420	46,XY SEX REVERSAL 7		HP:0000150	OMIM:233420	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	233420	46,XY SEX REVERSAL 7		HP:0000786	OMIM:233420	TAS				P		HPO:skoehler	
OMIM	233420	46,XY SEX REVERSAL 7		HP:0001425	OMIM:233420	TAS				I		HPO:iea	
OMIM	233420	46,XY SEX REVERSAL 7		HP:0008668	OMIM:233420	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	233420	46,XY SEX REVERSAL 7		HP:0008697	OMIM:233420	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	233420	46,XY SEX REVERSAL 7		HP:0009714	OMIM:233420	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	233420	46,XY SEX REVERSAL 7		HP:0010464	OMIM:233420	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	233420	46,XY SEX REVERSAL 7		HP:0012245	OMIM:233420	TAS				P		HPO:probinson	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0000007	OMIM:233430	IEA				I		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0000133	OMIM:233430	IEA				P		HPO:skoehler	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0000202	OMIM:233430	IEA				P		HPO:skoehler	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0000204	OMIM:233430	TAS				P		HPO:skoehler	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0000786	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0001169	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0001256	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0001627	OMIM:233430	TAS				P		HPO:skoehler	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0001769	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0001999	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0002000	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0004322	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0004467	OMIM:233430	IEA				P		HPO:iea	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0010884	OMIM:233430	TAS				P		HPO:skoehler	
OMIM	233430	233430 GONADAL DYSGENESIS, XY TYPE, WITH ASSOCIATED ANOMALIES		HP:0030680	OMIM:233430	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0000007	OMIM:233450	IEA				I		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0000083	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0000093	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0000099	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0000790	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0002094	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0002105	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0002113	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0002960	OMIM:233450	IEA				P		HPO:iea	
OMIM	233450	GOODPASTURE SYNDROME		HP:0040223	OMIM:233450	TAS				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000007	OMIM:233600	TAS				I		HPO:probinson	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000218	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000275	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000300	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000347	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0000431	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0001581	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0001913	OMIM:233600	TAS				P		HPO:probinson	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0001974	OMIM:233600	TAS				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0002014	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0002024	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0003819	OMIM:233600	TAS				M		HPO:skoehler	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0004313	OMIM:233600	TAS				P		HPO:probinson	
OMIM	233600	IMMUNODEFICIENCY 59 AND HYPOGLYCEMIA; IMD59		HP:0040154	OMIM:233600	IEA				P		HPO:skoehler	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0000007	OMIM:233650	IEA				I		HPO:iea	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0002205	OMIM:233650	IEA				P		HPO:iea	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0003593	OMIM:233650	IEA				C		HPO:iea	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0004315	OMIM:233650	TAS				P		HPO:probinson	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0005387	OMIM:233650	TAS				P		HPO:probinson	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0005403	OMIM:233650	TAS				P		HPO:probinson	
OMIM	233650	COMBINED CELLULAR AND HUMORAL IMMUNE DEFECTS WITH GRANULOMAS		HP:0010976	OMIM:233650	TAS				P		HPO:probinson	
OMIM	233670	GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS		HP:0000007	OMIM:233670	IEA				I		HPO:iea	
OMIM	233670	GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS		HP:0005512	OMIM:233670	IEA				P		HPO:iea	
OMIM	233670	GRANULOMATOUS DISEASE WITH DEFECT IN NEUTROPHIL CHEMOTAXIS		HP:0007499	OMIM:233670	IEA				P		HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0000007	OMIM:233690	IEA				I	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0000976	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0001744	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002240	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002716	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002721	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:skoehler	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002723	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002724	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002726	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002740	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002741	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002742	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002754	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002840	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002842	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0002955	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003203	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003206	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003514	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0003621	OMIM:233690	IEA				C	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0005224	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0005406	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0006532	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0007417	OMIM:233690	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:iea	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0100523	PMID:18422995	PCS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:probinson	
OMIM	233690	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE		HP:0100658	OMIM:233690	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-NEGATIVE	HPO:probinson	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0000007	OMIM:233700	IEA				I	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0000976	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0001744	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002240	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002716	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002721	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:skoehler	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002723	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002724	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002726	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002740	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002741	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002742	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002754	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002840	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002842	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0002955	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0003203	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0003206	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0003621	OMIM:233700	IEA				C	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0005224	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0005406	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0006532	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0007417	OMIM:233700	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:iea	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0100523	PMID:19329991	PCS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:probinson	
OMIM	233700	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE I; CDG1		HP:0100658	OMIM:233700	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE I; CDG1	HPO:probinson	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0000007	OMIM:233710	IEA				I	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0000976	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0001744	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002240	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002716	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002721	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:skoehler	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002723	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002724	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002726	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002740	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002741	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002742	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002754	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002840	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002842	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0002955	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0003203	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0003206	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0003621	OMIM:233710	IEA				C	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0005224	OMIM:233710	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:skoehler	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0005406	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0006532	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0007417	OMIM:233710	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:iea	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0100523	PMID:7795241	PCS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:probinson	
OMIM	233710	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE II; CDG2		HP:0100658	OMIM:233710	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE II; CDG2	HPO:probinson	
OMIM	233800	GROUPED PIGMENTATION OF THE MACULA		HP:0000007	OMIM:233800	TAS				I		HPO:probinson	
OMIM	233800	GROUPED PIGMENTATION OF THE MACULA		HP:0007703	OMIM:233800	TAS				P		HPO:probinson	
OMIM	233800	GROUPED PIGMENTATION OF THE MACULA		HP:0012508	OMIM:233800	TAS				P		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000007	OMIM:233805	TAS				I		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000160	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000347	OMIM:233805	IEA				P		HPO:skoehler	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000444	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF	HP:0012825	HP:0000767	OMIM:233805	TAS				P		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000831	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0000963	OMIM:233805	TAS				P		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0001371	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0001763	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0003758	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0004334	OMIM:233805	TAS				P		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0007556	OMIM:233805	IEA				P		HPO:iea	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0009125	OMIM:233805	TAS				P		HPO:probinson	
OMIM	233805	GROWTH FACTORS, COMBINED DEFECT OF		HP:0100324	OMIM:233805	IEA				P		HPO:skoehler	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0000007	OMIM:233810	TAS				I		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0000687	OMIM:233810	TAS				P		HPO:skoehler	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0000691	OMIM:233810	TAS				P		HPO:skoehler	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0000750	OMIM:233810	TAS				P		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0000964	OMIM:233810	TAS				P		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0001263	OMIM:233810	TAS				P		HPO:skoehler	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0001290	OMIM:233810	TAS				P		HPO:skoehler	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0001338	OMIM:233810	TAS				P		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0001511	OMIM:233810	TAS				P		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0008897	OMIM:233810	TAS				P		HPO:probinson	
OMIM	233810	GROWTH RETARDATION, SMALL AND PUFFY HANDS AND FEET, AND ECZEMA		HP:0025356	OMIM:233810	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0000007	OMIM:233910	IEA				I		HPO:iea	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0000496	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0000737	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001250	OMIM:233910	IEA				P		HPO:iea	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001254	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001263	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001266	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001332	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001337	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0001954	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0002015	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0002063	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0002344	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0002487	OMIM:233910	TAS				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0002509	OMIM:233910	IEA				P		HPO:iea	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0003593	OMIM:233910	IEA				C		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0003781	OMIM:233910	TAS				P		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0003828	OMIM:233910	TAS				C		HPO:skoehler	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0004923	OMIM:233910	TAS				P		HPO:probinson	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0006829	OMIM:233910	IEA				P		HPO:iea	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0006887	OMIM:233910	IEA				P		HPO:iea	
OMIM	233910	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, B; HPABH4B		HP:0025356	OMIM:233910	IEA				P		HPO:skoehler	
OMIM	234000	FACTOR XII DEFICIENCY		HP:0000007	OMIM:234000	IEA				I		HPO:iea	
OMIM	234000	FACTOR XII DEFICIENCY		HP:0003645	OMIM:234000	IEA				P		HPO:iea	
OMIM	234000	FACTOR XII DEFICIENCY		HP:0004841	OMIM:234000	IEA				P		HPO:iea	
OMIM	234000	FACTOR XII DEFICIENCY		HP:0005542	OMIM:234000	IEA				P		HPO:iea	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0000007	OMIM:234030	TAS				I		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0000535	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0000653	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0000992	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0001249	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0002208	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234030	HAIR DEFECT WITH PHOTOSENSITIVITY AND MENTAL RETARDATION		HP:0002299	OMIM:234030	TAS				P		HPO:probinson	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000007	OMIM:234050	IEA				I		HPO:iea	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000144	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000252	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000278	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000286	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000400	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000463	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000482	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000568	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000639	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000648	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000653	OMIM:234050	IEA				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0000685	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001097	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001249	OMIM:234050	IEA				P		HPO:iea	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001263	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001338	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001510	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001598	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001629	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0001792	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0002120	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0002224	OMIM:234050	IEA				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0002299	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0003196	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0006829	OMIM:234050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0008070	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0009886	OMIM:234050	TAS				P		HPO:skoehler	
OMIM	234050	TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4		HP:0025356	OMIM:234050	IEA				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000028	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000160	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000218	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000232	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000233	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000242	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000248	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000252	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000268	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000272	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000347	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000369	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000426	PMID:15347328	PCS				P		HPO:lccarmody	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000430	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000460	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000486	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000494	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000518	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000535	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000567	OMIM:234100	TAS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000568	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000588	OMIM:234100	TAS				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000592	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000612	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000639	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000653	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000689	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000695	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000752	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000767	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000822	OMIM:234100	IEA				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000883	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0000958	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001009	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001155	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001249	OMIM:234100	IEA		HP:0040284		P		HPO:probinson	15%
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001266	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001382	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001518	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0001592	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002007	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002069	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002092	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002205	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002213	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002414	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002645	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002650	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002691	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002705	OMIM:234100	TAS				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002779	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0002870	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0003016	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0003100	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0003307	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0003508	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0003745	OMIM:234100	IEA				I		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0004334	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0004782	OMIM:234100	TAS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0006532	OMIM:234100	TAS				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0006611	OMIM:234100	IEA				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0008070	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0010539	OMIM:234100	TAS				P		HPO:skoehler	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0011069	OMIM:234100	PCS				P		HPO:probinson	
OMIM	234100	HALLERMANN-STREIFF SYNDROME; HSS		HP:0030799	OMIM:234100	TAS				P		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000007	OMIM:234200	IEA				I		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000020	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000273	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000546	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000580	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000643	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000648	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000658	OMIM:234200	TAS				P		HPO:probinson	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000716	OMIM:234200	TAS				P		HPO:probinson	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000726	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000752	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0000953	OMIM:234200	TAS				P		HPO:probinson	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001251	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001257	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001260	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001263	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001266	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001288	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001300	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001337	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001618	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001760	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0001927	OMIM:234200	TAS				P		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002015	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002063	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002067	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002180	OMIM:234200	TAS				P		HPO:probinson	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002283	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002304	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002310	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0002454	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0003198	OMIM:234200	TAS				P		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0003199	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0003678	OMIM:234200	TAS				C		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0007256	OMIM:234200	TAS				P		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0007313	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0008770	OMIM:234200	TAS				P		HPO:probinson	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0008872	OMIM:234200	IEA				P		HPO:iea	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0031814	OMIM:234200	IEA				P		HPO:skoehler	
OMIM	234200	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1		HP:0100034	OMIM:234200	TAS				P		HPO:skoehler	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:234250	IEA				I		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000179	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000252	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000448	OMIM:234250	TAS				P		HPO:skoehler	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000463	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000926	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0000939	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001156	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001250	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001344	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001508	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0001511	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0002650	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0002750	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0002808	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0003301	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0005280	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0006297	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0006334	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0006347	OMIM:234250	TAS				P		HPO:skoehler	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0008872	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0010806	OMIM:234250	IEA				P		HPO:iea	
OMIM	234250	234250 HALL-RIGGS MENTAL RETARDATION SYNDROME		HP:0100255	OMIM:234250	IEA				P		HPO:iea	
OMIM	234280	HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY		HP:0000007	OMIM:234280	IEA				I		HPO:iea	
OMIM	234280	HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY		HP:0001159	OMIM:234280	IEA				P		HPO:skoehler	
OMIM	234280	HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY		HP:0001177	OMIM:234280	IEA				P		HPO:iea	
OMIM	234280	HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY		HP:0008080	OMIM:234280	IEA				P		HPO:skoehler	
OMIM	234280	HALLUX VARUS AND PREAXIAL POLYSYNDACTYLY		HP:0010055	OMIM:234280	IEA				P		HPO:iea	
OMIM	234350	HALOTHANE HEPATITIS		HP:0000007	OMIM:234350	TAS				I		HPO:nvasilevsky	
OMIM	234350	HALOTHANE HEPATITIS		HP:0000952	OMIM:234350	IEA				P		HPO:iea	
OMIM	234350	HALOTHANE HEPATITIS		HP:0001426	OMIM:234350	TAS				I		HPO:nvasilevsky	
OMIM	234350	HALOTHANE HEPATITIS		HP:0001513	OMIM:234350	TAS				P		HPO:skoehler	
OMIM	234350	HALOTHANE HEPATITIS		HP:0001880	OMIM:234350	IEA				P		HPO:iea	
OMIM	234350	HALOTHANE HEPATITIS		HP:0001945	OMIM:234350	IEA				P		HPO:iea	
OMIM	234350	HALOTHANE HEPATITIS		HP:0006562	OMIM:234350	IEA				P		HPO:skoehler	
OMIM	234350	HALOTHANE HEPATITIS		HP:0012115	OMIM:234350	TAS				P		HPO:skoehler	
OMIM	234500	HARTNUP DISORDER		HP:0000007	OMIM:234500	TAS				I		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0000206	OMIM:234500	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234500	HARTNUP DISORDER		HP:0000709	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0000712	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0000992	OMIM:234500	TAS				P		HPO:skoehler	
OMIM	234500	HARTNUP DISORDER		HP:0001250	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0001263	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0001276	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0001347	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234500	HARTNUP DISORDER		HP:0002131	OMIM:234500	TAS				P		HPO:skoehler	
OMIM	234500	HARTNUP DISORDER		HP:0004322	OMIM:234500	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	234500	HARTNUP DISORDER		HP:0008353	OMIM:234500	TAS				P		HPO:probinson	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0000007	OMIM:234580	TAS				I		HPO:probinson	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0000407	OMIM:234580	IEA				P		HPO:iea	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0000705	OMIM:234580	IEA				P		HPO:iea	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0001820	OMIM:234580	IEA				P		HPO:skoehler	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0006297	OMIM:234580	TAS				P		HPO:probinson	
OMIM	234580	#234580 HEIMLER SYNDROME 1; HMLR1;;HEARING LOSS, SENSORINEURAL, WITH ENAMEL HYPOPLASIA AND NAIL DEFECTS;;PEROXISOME BIOGENESIS DISORDER 1C; PBD1C		HP:0007754	OMIM:234580	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0000007	OMIM:234700	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0001638	OMIM:234700	IEA				P		HPO:iea	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0001653	OMIM:234700	IEA				P		HPO:iea	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0001685	OMIM:234700	IEA				P		HPO:iea	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0001692	OMIM:234700	PCS				P		HPO:probinson	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0006681	OMIM:234700	IEA				P		HPO:iea	
OMIM	234700	HEART BLOCK, CONGENITAL		HP:0006690	OMIM:234700	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0000007	OMIM:234800	IEA				I		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0000316	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0000925	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0001063	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0001388	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0001741	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0003468	OMIM:234800	TAS				P		HPO:skoehler	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0005692	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0007461	OMIM:234800	IEA				P		HPO:iea	
OMIM	234800	234800 HEMANGIOMATOSIS, CUTANEOUS, WITH ASSOCIATED FEATURES		HP:0010302	OMIM:234800	IEA				P		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0000007	OMIM:234810	TAS				I		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0002092	OMIM:234810	TAS				P		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0002094	OMIM:234810	TAS				P		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0005954	OMIM:234810	TAS				P		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0006518	OMIM:234810	IEA				P		HPO:skoehler	
OMIM	234810	#234810 PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD2;;HEMANGIOMATOSIS, FAMILIAL PULMONARY CAPILLARY		HP:0012735	OMIM:234810	TAS				P		HPO:skoehler	
OMIM	234820	HEMANGIOPERICYTOMA, MALIGNANT		HP:0000007	OMIM:234820	IEA				I		HPO:iea	
OMIM	234820	HEMANGIOPERICYTOMA, MALIGNANT		HP:0001626	OMIM:234820	IEA				P		HPO:iea	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0000006	OMIM:235000	IEA				I		HPO:iea	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0001256	OMIM:235000	IEA		HP:0040284		P		HPO:skoehler	20%
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0001528	OMIM:235000	IEA				P		HPO:iea	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0002475	OMIM:235000	TAS				P		HPO:probinson	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0002650	OMIM:235000	IEA				P		HPO:iea	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0002667	OMIM:235000	TAS				P		HPO:probinson	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0002898	OMIM:235000	IEA				P		HPO:skoehler	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0003712	OMIM:235000	TAS				P		HPO:probinson	
OMIM	235000	HEMIHYPERPLASIA, ISOLATED		HP:0003829	OMIM:235000	IEA				C		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000007	OMIM:235200	IEA				I		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000027	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000029	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000044	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000141	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000802	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000819	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000939	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0000953	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001009	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001394	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001402	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001541	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001596	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001635	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001638	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001640	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001744	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0001952	OMIM:235200	TAS				P		HPO:skoehler	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0002027	OMIM:235200	TAS				P		HPO:skoehler	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0002202	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0002240	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0002910	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0003040	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0003281	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0003452	OMIM:235200	IEA				P		HPO:iea	
OMIM	235200	HEMOCHROMATOSIS, TYPE 1		HP:0011675	OMIM:235200	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000007	OMIM:235255	IEA				I		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000023	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000028	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000054	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000126	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000175	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000218	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000219	OMIM:235255	IEA				P		HPO:skoehler	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000272	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000316	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000319	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000347	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000369	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000431	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000470	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000474	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000494	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000520	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000774	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0000998	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001004	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001162	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001252	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001290	OMIM:235255	TAS				P		HPO:skoehler	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001399	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001522	OMIM:235255	IEA				M		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001541	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001561	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001629	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0001744	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0002119	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0002240	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0002243	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0002901	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0003075	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0003270	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0005469	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0005989	OMIM:235255	TAS				P		HPO:skoehler	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0006273	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0006521	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0008229	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0009085	OMIM:235255	IEA				P		HPO:iea	
OMIM	235255	MULLERIAN DERIVATIVES, PERSISTENCE OF, WITH LYMPHANGIECTASIA AND POSTAXIAL POLYDACTYLY		HP:0011800	OMIM:235255	TAS				P		HPO:skoehler	
OMIM	235370	HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS		HP:0000007	OMIM:235370	IEA				I		HPO:iea	
OMIM	235370	HEMOLYTIC ANEMIA WITH THERMAL SENSITIVITY OF RED CELLS		HP:0004804	OMIM:235370	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0000006	OMIM:235400	IEA				I		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0000007	OMIM:235400	IEA				I		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0000822	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0000979	OMIM:235400	IEA				P		HPO:skoehler	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001250	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001259	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001269	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001873	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001919	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001923	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001937	OMIM:235400	TAS				P		HPO:probinson	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001945	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0001981	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0002014	OMIM:235400	TAS				P		HPO:skoehler	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0002357	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0003077	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0003138	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0003259	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0005356	OMIM:235400	TAS				P		HPO:skoehler	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0005369	OMIM:235400	TAS				P		HPO:skoehler	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0005416	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0005421	OMIM:235400	IEA				P		HPO:iea	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0005575	OMIM:235400	TAS				P		HPO:probinson	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0100519	OMIM:235400	TAS				P		HPO:skoehler	
OMIM	235400	#235400 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1; AHUS1;;AHUS, SUSCEPTIBILITY TO, 1HEMOLYTIC UREMIC SYNDROME, TYPICAL, INCLUDED		HP:0100543	OMIM:235400	IEA				P		HPO:iea	
OMIM	235500	HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN		HP:0000007	OMIM:235500	IEA				I		HPO:iea	
OMIM	235500	HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN		HP:0002086	OMIM:235500	IEA				P		HPO:iea	
OMIM	235500	HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN		HP:0002720	OMIM:235500	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000007	OMIM:235510	IEA				I		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000028	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000076	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000085	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000086	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000126	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000160	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000189	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000212	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000272	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000278	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000286	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000316	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000319	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000337	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000369	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000405	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000407	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000431	OMIM:235510	TAS				P		HPO:probinson	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000501	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000677	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000684	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000752	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0000767	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001004	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001007	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001055	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001249	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001250	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001302	OMIM:235510	IEA				P		HPO:skoehler	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001530	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001537	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001629	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001631	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001698	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001762	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0001773	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002035	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002202	OMIM:235510	TAS				P		HPO:probinson	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002243	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002593	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002650	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002750	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0002866	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0003073	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0003298	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0004279	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0004440	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0005183	OMIM:235510	TAS				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0005280	OMIM:235510	TAS				P		HPO:probinson	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0006531	OMIM:235510	TAS				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0007598	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0008229	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0009473	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0010554	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0011065	OMIM:235510	IEA				P		HPO:iea	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0012368	OMIM:235510	TAS				P		HPO:skoehler	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0012385	OMIM:235510	TAS				P		HPO:skoehler	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0100539	OMIM:235510	TAS				P		HPO:skoehler	
OMIM	235510	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME		HP:0200055	OMIM:235510	TAS				P		HPO:skoehler	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0000007	OMIM:235550	IEA				I		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0000252	OMIM:235550	IEA				P		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0001392	OMIM:235550	IEA				P		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0002721	OMIM:235550	IEA				P		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0002849	OMIM:235550	IEA				P		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0004315	OMIM:235550	IEA				P		HPO:iea	
OMIM	235550	HEPATIC VENOOCCLUSIVE DISEASE WITH IMMUNODEFICIENCY		HP:0006685	OMIM:235550	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0000007	OMIM:235555	IEA				I		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0000952	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0001399	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0001406	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0001508	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0001744	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0002014	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0002240	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0002570	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0002904	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0002910	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0003155	OMIM:235555	IEA				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0003256	OMIM:235555	TAS				P		HPO:iea	
OMIM	235555	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 2		HP:0003623	OMIM:235555	IEA				C		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0000007	OMIM:235700	IEA				I		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0000952	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001081	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001082	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001744	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001895	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001897	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001923	OMIM:235700	TAS				P		HPO:skoehler	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001930	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0001939	OMIM:235700	IEA				P		HPO:iea	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0002904	OMIM:235700	TAS				P		HPO:skoehler	
OMIM	235700	#235700 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY		HP:0003577	OMIM:235700	TAS				C		HPO:skoehler	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000006	PMID:17958891	PCS				I		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000028	PMID:17958891	IEA		HP:0040284		P		HPO:iea	23/63
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000028	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	51/123
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000047	PMID:12920073,PMID:29300384	PCS		HP:0040284		P		HPO:iea	3/22
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000048	PMID:17958891	IEA		HP:0040284		P		HPO:iea	3/63
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000077	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	59/233
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000175	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	5/170
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000176	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000252	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	135/166
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000307	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000316	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000378	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000403	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	34.6%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000431	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000486	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	56.8%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000490	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000494	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000508	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000565	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000612	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000684	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000684	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	47.7%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000687	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000692	OMIM:235730	TAS				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000692	PMID:29300384	PCS				P		HPO:lccarmody	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000767	OMIM:235730	TAS				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0000768	OMIM:235730	TAS				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001250	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	102/139
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001270	PMID:12920073	PCS				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001274	PMID:12920073	PCS		HP:0040284		P		HPO:iea	5/22
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001290	OMIM:235730	TAS				P		HPO:skoehler	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001290	PMID:29300384	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	79.1%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001344	OMIM:235730	TAS				P		HPO:skoehler	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001344	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	58/86
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001627	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	193/332
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001629	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001631	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001642	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0001643	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002013	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002019	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	19/73
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002021	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	14/190
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002079	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002119	OMIM:235730	IEA				P		HPO:skoehler	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002251	PMID:12920073,PMID:26156877,PMID:29300384	PCS		HP:0040284		P		HPO:iea	13/22
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002307	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0002558	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0003270	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0003720	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0004322	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	34/73
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0004415	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0004961	PMID:17958891,PMID:29300384	PCS		HP:0040284		P		HPO:iea	5/167
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0005274	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0007048	OMIM:235730	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0009748	OMIM:235730	IEA				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0009765	PMID:17103451	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0009909	PMID:17958891	PCS				P		HPO:iea	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0010864	PMID:12920073	PCS		HP:0040284		P		HPO:iea	22/22
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0011229	OMIM:235730	TAS				P		HPO:skoehler	
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0012372	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	22/221
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0012429	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	40.7%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0025100	PMID:29300384	PCS		HP:0040284		P		HPO:lccarmody	77.8%
OMIM	235730	MOWAT-WILSON SYNDROME; MOWS		HP:0040082	OMIM:235730	TAS				P		HPO:skoehler	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0000007	OMIM:235740	IEA				I		HPO:iea	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0000122	OMIM:235740	IEA				P		HPO:iea	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0000316	OMIM:235740	IEA				P		HPO:iea	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0000365	OMIM:235740	IEA				P		HPO:iea	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0001161	OMIM:235740	IEA				P		HPO:iea	
OMIM	235740	HIRSCHSPRUNG DISEASE WITH POLYDACTYLY, RENAL AGENESIS, AND DEAFNESS		HP:0002251	OMIM:235740	IEA				P		HPO:iea	
OMIM	235750	HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT		HP:0000007	OMIM:235750	IEA				I		HPO:iea	
OMIM	235750	HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT		HP:0001629	OMIM:235750	IEA				P		HPO:iea	
OMIM	235750	HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT		HP:0001841	OMIM:235750	TAS				P		HPO:probinson	
OMIM	235750	HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT		HP:0002251	OMIM:235750	IEA				P		HPO:iea	
OMIM	235750	HIRSCHSPRUNG DISEASE WITH ULNAR POLYDACTYLY, POLYSYNDACTYLY OF BIGTOES, AND VENTRICULAR SEPTAL DEFECT		HP:0005873	OMIM:235750	IEA				P		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0000007	OMIM:235760	IEA				I		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0000023	OMIM:235760	IEA				P		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0000126	OMIM:235760	IEA				P		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0001792	OMIM:235760	IEA				P		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES	HP:0012825	HP:0001999	OMIM:235760	IEA				P		HPO:probinson	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0002023	OMIM:235760	IEA				P		HPO:iea	
OMIM	235760	HIRSCHSPRUNG DISEASE WITH HYPOPLASTIC NAILS AND DYSMORPHIC FACIALFEATURES		HP:0002251	OMIM:235760	IEA				P		HPO:iea	
OMIM	235800	HISTIDINEMIA		HP:0000006	OMIM:235800	TAS				I		HPO:skoehler	
OMIM	235800	HISTIDINEMIA		HP:0000007	OMIM:235800	PCS				I		HPO:iea	
OMIM	235800	HISTIDINEMIA		HP:0000708	OMIM:235800	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	235800	HISTIDINEMIA		HP:0001249	OMIM:235800	PCS		HP:0040284		P		HPO:iea	HP:0040284
OMIM	235800	HISTIDINEMIA		HP:0002167	OMIM:235800	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	235800	HISTIDINEMIA		HP:0002927	OMIM:235800	PCS				P		HPO:iea	
OMIM	235800	HISTIDINEMIA		HP:0010906	OMIM:235800	PCS				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000007	OMIM:235830	IEA				I		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000219	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000219	OMIM:235830	TAS				P		HPO:skoehler	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000319	OMIM:235830	TAS				P		HPO:skoehler	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000343	OMIM:235830	TAS				P		HPO:skoehler	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000400	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000407	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0000431	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0001249	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0001800	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0002123	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0002927	OMIM:235830	IEA				P		HPO:iea	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0005819	OMIM:235830	TAS				P		HPO:probinson	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0005844	OMIM:235830	TAS				P		HPO:probinson	
OMIM	235830	%235830 HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT		HP:0008666	OMIM:235830	IEA				P		HPO:iea	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0000007	OMIM:235900	TAS				I		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0002113	OMIM:235900	TAS				P		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0002719	OMIM:235900	TAS				P		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0005413	OMIM:235900	TAS				P		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0005764	OMIM:235900	TAS				P		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0010702	OMIM:235900	TAS				P		HPO:probinson	
OMIM	235900	HISTIOCYTOSIS, FAMILIAL LIPOCHROME		HP:0100727	OMIM:235900	IEA				P		HPO:skoehler	
OMIM	236000	#236000 LYMPHOMA, HODGKIN;;HODGKIN DISEASE		HP:0000007	OMIM:236000	IEA				I		HPO:iea	
OMIM	236000	#236000 LYMPHOMA, HODGKIN;;HODGKIN DISEASE		HP:0003347	OMIM:236000	IEA				P		HPO:iea	
OMIM	236000	#236000 LYMPHOMA, HODGKIN;;HODGKIN DISEASE		HP:0003459	OMIM:236000	IEA				P		HPO:iea	
OMIM	236000	#236000 LYMPHOMA, HODGKIN;;HODGKIN DISEASE		HP:0012189	OMIM:236000	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000006	OMIM:236100	TAS				I		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000007	OMIM:236100	IEA				I		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000054	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000252	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000568	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000601	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000835	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0000873	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001249	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001250	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001263	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001274	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001290	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001321	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001425	OMIM:236100	TAS				I		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001750	OMIM:236100	IEA				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0001943	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0002006	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0003745	OMIM:236100	TAS				I		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0003828	OMIM:236100	TAS				C		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0003829	OMIM:236100	TAS				C		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0004322	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0006988	OMIM:236100	IEA				P		HPO:iea	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0008501	OMIM:236100	TAS				P		HPO:probinson	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0009914	OMIM:236100	IEA				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0009927	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0011800	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0012806	OMIM:236100	IEA				P		HPO:skoehler	
OMIM	236100	HOLOPROSENCEPHALY 1; HPE1		HP:0030779	OMIM:236100	TAS				P		HPO:skoehler	
OMIM	236110	HOLZGREVE SYNDROME		HP:0000007	OMIM:236110	IEA				I		HPO:iea	
OMIM	236110	HOLZGREVE SYNDROME		HP:0000089	OMIM:236110	IEA				P		HPO:iea	
OMIM	236110	HOLZGREVE SYNDROME		HP:0000104	OMIM:236110	IEA				P		HPO:iea	
OMIM	236110	HOLZGREVE SYNDROME		HP:0000175	OMIM:236110	IEA				P		HPO:iea	
OMIM	236110	HOLZGREVE SYNDROME		HP:0000204	OMIM:236110	TAS				P		HPO:skoehler	
OMIM	236110	HOLZGREVE SYNDROME		HP:0001161	OMIM:236110	IEA				P		HPO:iea	
OMIM	236110	HOLZGREVE SYNDROME		HP:0004383	OMIM:236110	IEA				P		HPO:skoehler	
OMIM	236130	HOMOCARNOSINOSIS		HP:0000007	OMIM:236130	IEA				I		HPO:iea	
OMIM	236130	HOMOCARNOSINOSIS		HP:0001000	OMIM:236130	IEA				P		HPO:skoehler	
OMIM	236130	HOMOCARNOSINOSIS		HP:0001249	OMIM:236130	IEA				P		HPO:iea	
OMIM	236130	HOMOCARNOSINOSIS		HP:0001258	OMIM:236130	IEA				P		HPO:iea	
OMIM	236130	HOMOCARNOSINOSIS		HP:0003167	PMID:3736769	PCS				P		HPO:probinson	
OMIM	236130	HOMOCARNOSINOSIS		HP:0007703	OMIM:236130	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000007	PMID:20301697	PCS				I		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000023	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY	HP:0012825	HP:0000098	OMIM:236200	TAS				P		HPO:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000218	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000501	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000505	PMID:9775245	PCS		HP:0040284		P		HP:probinson	4/19
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000545	PMID:9775245	PCS		HP:0040284		P		HPO:iea	8/19
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000678	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000708	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000716	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000767	PMID:20301697	PCS				P		HPO:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000768	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000939	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0000965	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001010	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001132	PMID:9775245	PCS		HP:0040284		P		HP:probinson	13/19
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001166	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001249	PMID:20301697	PCS				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001250	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001263	PMID:20301697	IEA				P		HP:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001297	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001376	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001397	OMIM:236200	TAS				P		HPO:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001508	OMIM:236200	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001519	PMID:20301697	PCS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001634	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001658	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001733	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0001907	PMID:20301697	PCS				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0002156	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0002160	PMID:20301697	PCS				P		HP:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0002299	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0002650	PMID:20301697	PCS				P		HP:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0002751	OMIM:236200	IEA				P		HPO:iea	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0003235	PMID:20301697	PCS				P		HP:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0004586	OMIM:236200	TAS				P		HPO:probinson	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0012075	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236200	HOMOCYSTINURIA DUE TO CYSTATHIONINE BETA-SYNTHASE DEFICIENCY		HP:0040160	OMIM:236200	TAS				P		HPO:skoehler	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0000007	OMIM:236250	IEA				I		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0000252	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0000708	OMIM:236250	TAS				P		HPO:skoehler	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0001250	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0001263	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0001288	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0001297	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0001324	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0002156	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0002160	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0002311	OMIM:236250	IEA				P		HPO:iea	
OMIM	236250	#236250 HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATEREDUCTASE ACTIVITY;;METHYLENETETRAHYDROFOLATE REDUCTASE DEFICIENCY;;MTHFR DEFICIENCYMTHFR DEFICIENCY, THERMOLABILE TYPE, INCLUDED		HP:0003401	OMIM:236250	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0000007	OMIM:236270	IEA				I		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0000618	OMIM:236270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0000639	OMIM:236270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001250	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001252	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001254	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001263	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001288	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001290	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001508	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0001889	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0002059	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0002156	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0002160	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0003223	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0003524	OMIM:236270	IEA				P		HPO:iea	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0003593	OMIM:236270	TAS				C		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0003658	OMIM:236270	TAS				P		HPO:skoehler	
OMIM	236270	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLE COMPLEMENTATION TYPE		HP:0006887	OMIM:236270	IEA				P		HPO:iea	
OMIM	236300	HOOFT DISEASE		HP:0000007	OMIM:236300	IEA				I		HPO:iea	
OMIM	236300	HOOFT DISEASE		HP:0000510	OMIM:236300	IEA				P		HPO:iea	
OMIM	236300	HOOFT DISEASE		HP:0001249	OMIM:236300	IEA				P		HPO:iea	
OMIM	236300	HOOFT DISEASE		HP:0001507	OMIM:236300	IEA				P		HPO:iea	
OMIM	236300	HOOFT DISEASE		HP:0001820	OMIM:236300	IEA				P		HPO:skoehler	
OMIM	236300	HOOFT DISEASE		HP:0001939	OMIM:236300	IEA				P		HPO:iea	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0000007	OMIM:236400	IEA				I		HPO:iea	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0000083	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0000248	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0000385	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0000431	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0003041	OMIM:236400	IEA				P		HPO:iea	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0008551	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236400	HUMERORADIAL SYNOSTOSISHUMERORADIAL/MULTIPLE SYNOSTOSIS SYNDROME		HP:0011220	PMID:2669480	PCS				P		HPO:lccarmody	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0000007	OMIM:236410	IEA				I		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0000248	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0000385	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0000431	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0001357	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0002007	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0003041	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0008368	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0008551	OMIM:236410	PCS				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0009702	OMIM:236410	IEA				P		HPO:iea	
OMIM	236410	236410 HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES		HP:0011220	OMIM:236410	TAS				P		HPO:skoehler	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0000007	OMIM:236450	IEA				I		HPO:iea	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0000007	OMIM:236450	PCS				I		HPO:probinson	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0000100	OMIM:236450	PCS				P		HPO:probinson	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0004322	OMIM:236450	PCS				P		HPO:probinson	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0008872	OMIM:236450	PCS				P		HPO:probinson	
OMIM	236450	236450 HUTTERITE CEREBROOSTEONEPHRODYSPLASIA SYNDROME;;COND;;CEREBROOSTEONEPHOSIS SYNDROME		HP:0010864	OMIM:236450	TAS				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000007	OMIM:236500	IEA				I		HPO:iea	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000089	OMIM:236500	IEA				P		HPO:iea	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000104	OMIM:236500	TAS				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000107	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000110	OMIM:236500	IEA				P		HPO:iea	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000308	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000418	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000476	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0000954	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0001321	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0001562	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0001762	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0002009	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0002324	OMIM:236500	IEA				P		HPO:iea	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0002365	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0004209	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0004691	OMIM:236500	TAS				P		HPO:probinson	
OMIM	236500	MULTINUCLEATED NEURONS, ANHYDRAMNIOS, RENAL DYSPLASIA, CEREBELLAR HYPOPLASIA, AND HYDRANENCEPHALY; MARCH		HP:0005989	OMIM:236500	IEA				P		HPO:skoehler	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0000007	OMIM:236600	TAS				I		HPO:skoehler	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0000238	OMIM:236600	IEA				P		HPO:iea	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0001249	OMIM:236600	TAS				P		HPO:skoehler	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0001250	OMIM:236600	TAS				P		HPO:skoehler	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0002119	OMIM:236600	IEA				P		HPO:iea	
OMIM	236600	#236600 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1; HYC1;;HYDROCEPHALY;;VENTRICULOMEGALY		HP:0003577	OMIM:236600	TAS				C		HPO:skoehler	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0000007	OMIM:236640	IEA				I		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0000238	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0000347	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0001511	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0001539	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0001760	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0002089	OMIM:236640	TAS				P		HPO:skoehler	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0002566	OMIM:236640	IEA				P		HPO:iea	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0002982	OMIM:236640	TAS				P		HPO:skoehler	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0006385	OMIM:236640	TAS				P		HPO:skoehler	
OMIM	236640	236640 HYDROCEPHALUS WITH ASSOCIATED MALFORMATIONS		HP:0009816	OMIM:236640	IEA				P		HPO:iea	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0000007	OMIM:236660	IEA				I		HPO:iea	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0000098	OMIM:236660	IEA				P		HPO:iea	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0000238	OMIM:236660	IEA				P		HPO:iea	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0001388	OMIM:236660	IEA				P		HPO:iea	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0002751	OMIM:236660	IEA				P		HPO:skoehler	
OMIM	236660	HYDROCEPHALUS, TALL STATURE, JOINT LAXITY, AND KYPHOSCOLIOSIS		HP:0005619	OMIM:236660	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000007	OMIM:236670	IEA				I		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000050	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000110	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000175	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000204	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000238	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000252	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000413	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000485	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000501	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000518	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000541	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000545	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000557	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000568	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000589	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000609	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000618	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0000659	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001105	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001250	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001252	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001263	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001274	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001302	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001305	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001321	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0001425	OMIM:236670	TAS				I		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002023	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002079	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002085	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002126	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002187	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002189	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002365	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0002803	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0003236	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0003741	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0006829	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0006888	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0007033	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0007260	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0007291	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0007957	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0007973	OMIM:236670	TAS				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0008551	OMIM:236670	IEA				P		HPO:iea	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0010864	OMIM:236670	TAS				P		HPO:skoehler	
OMIM	236670	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE		HP:0031882	OMIM:236670	IEA				P		HPO:skoehler	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000007	OMIM:236680	IEA				I		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000047	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000126	PMID:2074561	PCS				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000136	OMIM:236680	IEA		HP:0040284		P		HPO:iea	50%
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000142	PMID:2074561	PCS				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000161	OMIM:236680	IEA				P		HPO:skoehler	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000175	PMID:2074561	PCS				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000347	PMID:2074561	PCS		HP:0040284		P		HPO:iea	56/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000369	PMID:2074561	PCS		HP:0040284		P		HPO:iea	36/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000377	PMID:2074561	PCS		HP:0040284		P		HPO:iea	36/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000475	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0000568	PMID:2074561	PCS		HP:0040284		P		HPO:iea	49/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001162	PMID:2074561	PCS		HP:0040284		P		HPO:iea	29/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001177	PMID:2074561	PCS		HP:0040284		P		HPO:iea	36/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001274	PMID:2074561	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001305	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001331	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001511	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001539	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001561	PMID:2074561	PCS		HP:0040284		P		HPO:iea	51/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001629	PMID:2074561	PCS				P		HPO:skoehler	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001674	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001747	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0001762	PMID:2074561	PCS		HP:0040284		P		HPO:iea	27/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002101	PMID:2074561	PCS		HP:0040284		P		HPO:iea	35/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002139	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002282	OMIM:236680	IEA				P		HPO:skoehler	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002323	PMID:2074561	PCS		HP:0040284		P		HPO:iea	3/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002536	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0002777	PMID:3321994	PCS		HP:0040284		P		HPO:iea	29/38
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0003826	PMID:2074561	PCS		HP:0040284		M		HPO:iea	41/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0006379	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0006882	PMID:2074561	IEA	HP:0003577	HP:0040284		P		HPO:iea	47/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0008216	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0008749	PMID:2074561	PCS		HP:0040284		P		HPO:iea	32/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0008986	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0009752	PMID:2074561	PCS		HP:0040284		P		HPO:iea	42/56
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0009824	OMIM:236680	IEA				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0010066	PMID:2074561	PCS				P		HPO:iea	
OMIM	236680	HYDROLETHALUS SYNDROME 1		HP:0011803	PMID:2074561	PCS				P		HPO:skoehler	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0000007	OMIM:236690	IEA				I		HPO:iea	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0000020	OMIM:236690	TAS				P		HPO:probinson	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0000726	OMIM:236690	IEA				P		HPO:skoehler	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0001263	OMIM:236690	IEA				P		HPO:iea	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0001288	OMIM:236690	IEA				P		HPO:iea	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0002343	OMIM:236690	IEA				P		HPO:iea	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0002607	OMIM:236690	TAS				P		HPO:probinson	
OMIM	236690	HYDROCEPHALUS, NORMAL-PRESSURE		HP:0025356	OMIM:236690	IEA				P		HPO:skoehler	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000007	OMIM:236700	IEA				I		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000028	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000072	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000113	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000126	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000143	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000145	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000148	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0000969	OMIM:236700	IEA				P		HPO:skoehler	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0001159	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0001162	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0001374	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0001586	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0002023	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0002089	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0002251	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0006159	OMIM:236700	IEA				P		HPO:iea	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0010741	OMIM:236700	TAS				P		HPO:probinson	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0030010	OMIM:236700	TAS				P		HPO:skoehler	
OMIM	236700	#236700 MCKUSICK-KAUFMAN SYNDROME; MKKS;;HYDROMETROCOLPOS SYNDROME;;HYDROMETROCOLPOS, POSTAXIAL POLYDACTYLY, AND CONGENITAL HEART MALFORMATION;HMCS;;KAUFMAN-MCKUSICK SYNDROME		HP:0030680	OMIM:236700	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000007	OMIM:236730	IEA				I		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000010	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000028	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000072	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000126	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0000805	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0001999	OMIM:236730	IEA				P		HPO:iea	
OMIM	236730	UROFACIAL SYNDROME		HP:0002019	OMIM:236730	IEA				P		HPO:skoehler	
OMIM	236730	UROFACIAL SYNDROME		HP:0005346	OMIM:236730	TAS				P		HPO:skoehler	
OMIM	236730	UROFACIAL SYNDROME		HP:0010481	OMIM:236730	TAS				P		HPO:skoehler	
OMIM	236750	HYDROPS FETALIS, NONIMMUNE		HP:0001635	OMIM:236750	TAS	HP:0003577			P		HPO:iea	
OMIM	236750	HYDROPS FETALIS, NONIMMUNE		HP:0001790	OMIM:236750	TAS				P		HPO:skoehler	
OMIM	236750	HYDROPS FETALIS, NONIMMUNE		HP:0001903	OMIM:236750	TAS	HP:0003577			P		HPO:iea	
OMIM	236750	HYDROPS FETALIS, NONIMMUNE		HP:0003577	OMIM:236750	TAS				C		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0000007	OMIM:236792	IEA				I		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0000365	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0000486	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0000639	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0000648	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0001250	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0001272	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0001285	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002062	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002071	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002171	OMIM:236792	IEA				P		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002283	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002352	OMIM:236792	IEA				P		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002357	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0002376	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0003593	OMIM:236792	IEA				C		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0006887	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0007256	OMIM:236792	TAS				P		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0007258	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0007371	OMIM:236792	IEA				P		HPO:iea	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0010864	OMIM:236792	TAS				P		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0040144	OMIM:236792	IEA				P		HPO:skoehler	
OMIM	236792	#236792 L-2-HYDROXYGLUTARIC ACIDURIA;;L-2-HYDROXYGLUTARIC ACIDEMIA		HP:0040147	OMIM:236792	IEA				P		HPO:skoehler	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0000007	OMIM:236795	IEA				I		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0000252	OMIM:236795	IEA				P		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0001508	OMIM:236795	IEA				P		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0001993	OMIM:236795	IEA				P		HPO:skoehler	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0001999	OMIM:236795	IEA				P		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0002269	OMIM:236795	IEA				P		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0003128	OMIM:236795	IEA				P		HPO:iea	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0003355	OMIM:236795	IEA				P		HPO:skoehler	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0005974	OMIM:236795	TAS				P		HPO:skoehler	
OMIM	236795	%236795 3-@HYDROXYISOBUTYRIC ACIDURIA		HP:0006906	OMIM:236795	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0000007	OMIM:236800	IEA				I		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0000124	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0000365	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001249	OMIM:236800	IEA				P		HPO:skoehler	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001259	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001263	OMIM:236800	TAS				P		HPO:skoehler	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001276	OMIM:236800	TAS				P		HPO:probinson	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001649	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0001942	OMIM:236800	IEA				P		HPO:skoehler	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0002086	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0002615	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0003011	OMIM:236800	IEA				P		HPO:iea	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0003355	OMIM:236800	IEA				P		HPO:skoehler	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0007030	OMIM:236800	TAS				P		HPO:skoehler	
OMIM	236800	HYDROXYKYNURENINURIA		HP:0025356	OMIM:236800	IEA				P		HPO:skoehler	
OMIM	236900	HYDROXYLYSINURIA		HP:0000007	OMIM:236900	IEA				I		HPO:iea	
OMIM	236900	HYDROXYLYSINURIA		HP:0001249	OMIM:236900	IEA				P		HPO:iea	
OMIM	236900	HYDROXYLYSINURIA		HP:0002123	OMIM:236900	IEA				P		HPO:iea	
OMIM	236900	HYDROXYLYSINURIA		HP:0003297	OMIM:236900	IEA				P		HPO:skoehler	
OMIM	237000	HYDROXYPROLINEMIA		HP:0000007	OMIM:237000	IEA				I		HPO:iea	
OMIM	237000	HYDROXYPROLINEMIA		HP:0001249	OMIM:237000	IEA				P		HPO:iea	
OMIM	237000	HYDROXYPROLINEMIA		HP:0002907	OMIM:237000	IEA				P		HPO:iea	
OMIM	237000	HYDROXYPROLINEMIA		HP:0003260	OMIM:237000	IEA				P		HPO:iea	
OMIM	237100	HYMEN, IMPERFORATE		HP:0000007	OMIM:237100	IEA				I		HPO:iea	
OMIM	237100	HYMEN, IMPERFORATE		HP:0000141	OMIM:237100	IEA				P		HPO:iea	
OMIM	237100	HYMEN, IMPERFORATE		HP:0030011	OMIM:237100	TAS				P		HPO:skoehler	
OMIM	237100	HYMEN, IMPERFORATE		HP:0030711	OMIM:237100	TAS				P		HPO:skoehler	
OMIM	237100	HYMEN, IMPERFORATE		HP:0031923	OMIM:237100	IEA				P		HPO:skoehler	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0000007	OMIM:237300	PCS				I		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0000737	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001249	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001250	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001251	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001254	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001259	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001263	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001297	OMIM:237300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001508	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001950	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001951	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0001987	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0002013	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0002038	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0002181	OMIM:237300	IEA				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0003572	OMIM:237300	PCS				P		HPO:iea	
OMIM	237300	#237300 CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO;;CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY;;CPS I DEFICIENCY		HP:0005961	OMIM:237300	PCS				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0000007	OMIM:237310	IEA				I		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0000718	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001250	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001254	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001259	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001289	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001508	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0001987	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0002013	OMIM:237310	TAS				P		HPO:skoehler	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0002098	OMIM:237310	IEA				P		HPO:iea	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0100543	OMIM:237310	TAS				P		HPO:skoehler	
OMIM	237310	N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY		HP:0410068	PMID:7623444	PCS				P		HPO:NicoleVasilevsky	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0000007	OMIM:237400	IEA				I		HPO:iea	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0001250	OMIM:237400	IEA				P		HPO:iea	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0001262	OMIM:237400	IEA				P		HPO:iea	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0001508	OMIM:237400	IEA				P		HPO:iea	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0002643	OMIM:237400	IEA				P		HPO:iea	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0003166	OMIM:237400	TAS				P		HPO:probinson	
OMIM	237400	HYPER-BETA-ALANINEMIA		HP:0012556	OMIM:237400	TAS				P		HPO:probinson	
OMIM	237450	HYPERBILIRUBINEMIA, ROTOR TYPE		HP:0000007	OMIM:237450	IEA				I		HPO:iea	
OMIM	237450	HYPERBILIRUBINEMIA, ROTOR TYPE		HP:0000924	OMIM:237450	IEA				P		HPO:iea	
OMIM	237450	HYPERBILIRUBINEMIA, ROTOR TYPE		HP:0000952	OMIM:237450	IEA				P		HPO:iea	
OMIM	237450	HYPERBILIRUBINEMIA, ROTOR TYPE		HP:0001000	OMIM:237450	IEA				P		HPO:skoehler	
OMIM	237450	HYPERBILIRUBINEMIA, ROTOR TYPE		HP:0002908	OMIM:237450	IEA				P		HPO:iea	
OMIM	237500	DUBIN-JOHNSON SYNDROME		HP:0000007	OMIM:237500	IEA				I		HPO:iea	
OMIM	237500	DUBIN-JOHNSON SYNDROME		HP:0000952	OMIM:237500	IEA				P		HPO:iea	
OMIM	237500	DUBIN-JOHNSON SYNDROME		HP:0001080	OMIM:237500	IEA				P		HPO:iea	
OMIM	237500	DUBIN-JOHNSON SYNDROME		HP:0002908	OMIM:237500	IEA				P		HPO:iea	
OMIM	237550	HYPERBILIRUBINEMIA, CONJUGATED, TYPE III		HP:0000007	OMIM:237550	IEA				I		HPO:iea	
OMIM	237550	HYPERBILIRUBINEMIA, CONJUGATED, TYPE III		HP:0000952	OMIM:237550	IEA				P		HPO:iea	
OMIM	237550	HYPERBILIRUBINEMIA, CONJUGATED, TYPE III		HP:0002908	OMIM:237550	IEA				P		HPO:iea	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0000006	OMIM:237800	TAS				I		HPO:skoehler	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0000007	OMIM:237800	IEA				I		HPO:iea	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0000952	OMIM:237800	IEA				P		HPO:iea	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0001744	OMIM:237800	IEA				P		HPO:iea	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0001923	OMIM:237800	TAS				P		HPO:skoehler	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0002240	OMIM:237800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0002904	OMIM:237800	IEA				P		HPO:iea	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0010972	OMIM:237800	TAS				P		HPO:skoehler	
OMIM	237800	HYPERBILIRUBINEMIA, SHUNT, PRIMARY; PSHB		HP:0012132	OMIM:237800	IEA				P		HPO:skoehler	
OMIM	237900	HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATALBREASTFEEDING JAUNDICE, INCLUDED		HP:0000007	OMIM:237900	IEA				I		HPO:iea	
OMIM	237900	HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATALBREASTFEEDING JAUNDICE, INCLUDED		HP:0000952	OMIM:237900	IEA				P		HPO:iea	
OMIM	237900	HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATALBREASTFEEDING JAUNDICE, INCLUDED		HP:0001343	OMIM:237900	IEA				P		HPO:iea	
OMIM	237900	HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATALBREASTFEEDING JAUNDICE, INCLUDED		HP:0008176	OMIM:237900	IEA				P		HPO:iea	
OMIM	237900	HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATALBREASTFEEDING JAUNDICE, INCLUDED		HP:0100021	OMIM:237900	IEA				P		HPO:skoehler	
OMIM	238320	HYPERGONADOTROPIC HYPOGONADISM		HP:0000007	OMIM:238320	IEA				I		HPO:iea	
OMIM	238320	HYPERGONADOTROPIC HYPOGONADISM		HP:0000815	OMIM:238320	IEA				P		HPO:iea	
OMIM	238320	HYPERGONADOTROPIC HYPOGONADISM		HP:0000837	OMIM:238320	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000007	OMIM:238340	IEA				I		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000407	OMIM:238340	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0000546	OMIM:238340	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001249	OMIM:238340	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001250	OMIM:238340	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001508	OMIM:238340	IEA				P		HPO:iea	
OMIM	238340	HYPERLEUCINE-ISOLEUCINEMIA		HP:0001939	OMIM:238340	IEA				P		HPO:iea	
OMIM	238350	HYPERLEXIA		HP:0000007	OMIM:238350	IEA				I		HPO:iea	
OMIM	238350	HYPERLEXIA		HP:0000717	OMIM:238350	IEA				P		HPO:iea	
OMIM	238350	HYPERLEXIA		HP:0001426	OMIM:238350	IEA				I		HPO:iea	
OMIM	238350	HYPERLEXIA		HP:0003745	OMIM:238350	IEA				I		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0000007	OMIM:238600	IEA				I		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0000660	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0000952	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0001013	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0001433	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0001733	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0001744	OMIM:238600	TAS				P		HPO:skoehler	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0002013	OMIM:238600	TAS				P		HPO:skoehler	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0002018	OMIM:238600	TAS				P		HPO:skoehler	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0002574	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0003077	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0003124	OMIM:238600	IEA				P		HPO:iea	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0012238	OMIM:238600	TAS				P		HPO:skoehler	
OMIM	238600	HYPERLIPOPROTEINEMIA, TYPE I		HP:0031028	OMIM:238600	TAS				P		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0000007	OMIM:238700	IEA				I		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0000119	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0000736	OMIM:238700	TAS				P		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0000750	OMIM:238700	TAS				P		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0000752	OMIM:238700	TAS				P		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001083	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001249	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001250	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001252	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001256	OMIM:238700	TAS				P		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0001903	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0002161	OMIM:238700	IEA				P		HPO:iea	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0003593	OMIM:238700	TAS				C		HPO:skoehler	
OMIM	238700	HYPERLYSINEMIA, TYPE I		HP:0100543	OMIM:238700	TAS				P		HPO:skoehler	
OMIM	238710	HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA		HP:0000007	OMIM:238710	IEA				I		HPO:iea	
OMIM	238710	HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA		HP:0001249	OMIM:238710	IEA				P		HPO:iea	
OMIM	238710	HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA		HP:0002161	OMIM:238710	IEA				P		HPO:iea	
OMIM	238710	HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA		HP:0008265	OMIM:238710	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0000007	OMIM:238750	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0001249	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0001254	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0001259	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0001510	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0001987	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0002024	OMIM:238750	IEA				P		HPO:skoehler	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0002161	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0003168	OMIM:238750	IEA				P		HPO:iea	
OMIM	238750	HYPERLYSINURIA WITH HYPERAMMONEMIA		HP:0003297	OMIM:238750	IEA				P		HPO:iea	
OMIM	238800	238800 HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA		HP:0000007	OMIM:238800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	238800	238800 HYPERMETABOLISM DUE TO DEFECT IN MITOCHONDRIA		HP:0001939	OMIM:238800	IEA				P		HPO:iea	
OMIM	238950	HYPEROPIA, HIGH		HP:0000007	OMIM:238950	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	238950	HYPEROPIA, HIGH		HP:0008499	OMIM:238950	TAS				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0000007	OMIM:238970	IEA				I		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0000533	OMIM:238970	IEA		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0000762	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001249	OMIM:238970	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001254	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001259	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001263	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001289	OMIM:238970	IEA				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001290	OMIM:238970	TAS				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001328	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001410	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001508	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0001987	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002038	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002062	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002120	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002123	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002169	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002240	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002313	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002370	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002495	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0002572	OMIM:238970	TAS				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0006846	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0007256	OMIM:238970	TAS				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0007894	OMIM:238970	IEA				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0012026	OMIM:238970	TAS				P		HPO:probinson	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0025356	OMIM:238970	IEA				P		HPO:skoehler	
OMIM	238970	HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME		HP:0200119	OMIM:238970	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0000007	OMIM:239000	IEA				I		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0000256	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0000407	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0000488	OMIM:239000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0000939	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0001102	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0001270	OMIM:239000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0001324	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0001552	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0002149	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0002684	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0002757	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0002808	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0002905	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003080	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003148	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003155	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003260	OMIM:23900	TAS				P		HPO:probinson	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003676	OMIM:239000	TAS				C		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0003828	OMIM:239000	TAS				C		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0004322	OMIM:239000	TAS				P		HPO:probinson	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0006480	OMIM:239000	IEA				P		HPO:iea	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0006487	OMIM:239000	TAS				P		HPO:probinson	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0011001	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0031013	OMIM:239000	TAS				P		HPO:skoehler	
OMIM	239000	PAGET DISEASE OF BONE 5, JUVENILE-ONSET		HP:0200056	OMIM:239000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:239100	IEA				I		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0000365	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0000935	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0002315	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0003155	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0004437	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0006824	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0007958	OMIM:239100	IEA				P		HPO:iea	
OMIM	239100	#239100 HYPEROSTOSIS CORTICALIS GENERALISATA;;VAN BUCHEM DISEASE; VBCH;;HYPERPHOSPHATASEMIA TARDA;;ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL RECESSIVE		HP:0011001	OMIM:239100	TAS				P		HPO:skoehler	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0000007	OMIM:239199	IEA				I		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0000121	OMIM:239199	IEA				P		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0000843	OMIM:239199	TAS				P		HPO:probinson	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0001508	OMIM:239199	IEA				P		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0001947	OMIM:239199	IEA				P		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0002013	OMIM:239199	IEA				P		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0002150	OMIM:239199	IEA				P		HPO:iea	
OMIM	239199	HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA		HP:0003072	OMIM:239199	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0000006	OMIM:239200	TAS				I		HPO:skoehler	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0000007	OMIM:239200	TAS				I		HPO:skoehler	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0000103	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0000774	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001252	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001290	OMIM:239200	TAS				P		HPO:skoehler	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001508	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001744	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001903	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0001959	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002019	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002094	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002148	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002150	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002240	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002757	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0002789	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003025	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003072	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003109	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003165	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003355	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0003761	OMIM:239200	IEA				P		HPO:skoehler	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0008200	OMIM:239200	IEA				P		HPO:iea	
OMIM	239200	HYPERPARATHYROIDISM, NEONATAL SEVERE		HP:0008872	OMIM:239200	IEA				P		HPO:iea	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000007	PMID:20080219	PCS				I		HPO:iea	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000175	OMIM:239300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000204	PMID:20080219	PCS		HP:0040284		P		HPO:iea	1/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000219	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000238	PMID:20080219	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000272	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000303	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000316	PMID:20080219	PCS		HP:0040284		P		HPO:iea	6/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000322	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000358	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000365	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000407	PMID:20080219	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000431	PMID:20080219	PCS		HP:0040284		P		HPO:iea	6/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000455	PMID:20080219	PCS		HP:0040284		P		HPO:iea	6/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000582	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0000637	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001090	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001182	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001216	PMID:20080219	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001249	PMID:20080219	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001250	PMID:20080219	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001252	PMID:20080219	PCS	HP:0003593	HP:0040284		P		HPO:iea	5/5
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001290	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001344	OMIM:239300	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001357	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001545	PMID:20080219	PCS		HP:0040284		P		HPO:iea	2/5
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001627	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001792	PMID:20080219	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001795	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0001831	OMIM:239300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002019	PMID:20080219	PCS		HP:0040284		P		HPO:iea	2/5
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002034	PMID:20080219	TAS		HP:0040284		P		HPO:nvasilevsky	4/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002120	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002251	PMID:20080219	PCS		HP:0040284		P		HPO:iea	1/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002305	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002553	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0002714	PMID:20080219	PCS		HP:0040284		P		HPO:iea	6/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0003155	PMID:20080219	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0003196	OMIM:239300	IEA				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0009882	PMID:20080219	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0010804	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0010864	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0011800	OMIM:239300	TAS				P		HPO:skoehler	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0011968	OMIM:239300	TAS		HP:0040283		P		HPO:nvasilevsky	Occasional
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0012210	OMIM:239300	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0012448	PMID:17351347	TAS				P		HPO:nvasilevsky	
OMIM	239300	HYPERPHOSPHATASIA WITH MENTAL RETARDATION		HP:0025356	PMID:20080219	TAS		HP:0040284		P		HPO:nvasilevsky	7/7
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0000007	OMIM:239350	IEA				I		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0000103	OMIM:239350	TAS				P		HPO:skoehler	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0000737	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0001250	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0001281	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0001608	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0001945	OMIM:239350	IEA				P		HPO:skoehler	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0002013	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0002014	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0002905	OMIM:239350	IEA				P		HPO:iea	
OMIM	239350	HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES		HP:0025430	OMIM:239350	TAS				P		HPO:skoehler	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000007	OMIM:239500	IEA				I		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000718	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000729	PMID:20524212	PCS		HP:0040284		P		HP:probinson	3/19
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000733	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000750	PMID:17412540	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0000752	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001249	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001249	OMIM:239500	TAS				P		HPO:probinson	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001250	PMID:20524212	PCS		HP:0040284		P		HP:probinson	13/19
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001251	PMID:20524212,PMID:17412540	PCS		HP:0040284		P		HP:probinson	4/19
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001252	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001263	PMID:20524212,PMID:17412540	PCS		HP:0040284		P		HPO:skoehler	10/19
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0001290	OMIM:239500	TAS				P		HPO:skoehler	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0002133	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0002353	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0003080	OMIM:239500	IEA				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0003108	PMID:23462603	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0003137	PMID:11510941	PCS				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0008358	PMID:20524212	PCS				P		HPO:iea	
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0008358	PMID:17412540	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	239500	HYPERPROLINEMIA, TYPE I		HP:0100753	OMIM:239500	IEA				P		HPO:skoehler	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0000007	OMIM:239510	IEA				I		HPO:iea	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0001249	OMIM:239510	IEA				P		HPO:iea	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0001250	OMIM:239510	IEA				P		HPO:skoehler	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0003080	OMIM:239510	IEA				P		HPO:iea	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0003108	OMIM:239510	IEA				P		HPO:iea	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0003137	OMIM:239510	IEA				P		HPO:iea	
OMIM	239510	HYPERPROLINEMIA, TYPE II		HP:0008358	OMIM:239510	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000007	OMIM:239710	IEA				I		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000047	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000048	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000049	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000218	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000248	OMIM:239710	TAS				P		HPO:probinson	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000252	OMIM:239710	TAS				P		HPO:probinson	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000260	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000316	OMIM:239710	TAS				P		HPO:probinson	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000337	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000349	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000358	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000369	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000396	OMIM:239710	PCS				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000445	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000474	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000494	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000508	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000520	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0000960	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0001159	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0001161	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0004322	OMIM:239710	TAS				P		HPO:probinson	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0005989	OMIM:239710	TAS				P		HPO:skoehler	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0010055	OMIM:239710	IEA				P		HPO:iea	
OMIM	239710	239710 ACROFRONTOFACIONASAL DYSOSTOSIS 2;;AFFN DYSOSTOSIS 2; AFFND2;;ACROFRONTOFACIONASAL DYSOSTOSIS WITH GENITOURINARY ANOMALIES;;NAGUIB-RICHIERI-COSTA SYNDROME;;HYPERTELORISM, HYPOSPADIAS, AND POLYSYNDACTYLY SYNDROME		HP:0011304	OMIM:239710	TAS				P		HPO:probinson	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000007	OMIM:239711	IEA				I		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000047	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000286	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000316	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000343	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000358	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000369	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0000581	OMIM:239711	PCS				P		HPO:probinson	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0001256	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0001636	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0001643	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0001655	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0001762	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0003298	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0005280	OMIM:239711	IEA				P		HPO:iea	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0011659	OMIM:239711	PCS				P		HPO:probinson	
OMIM	239711	HYPERTELORISM AND TETRALOGY OF FALLOT		HP:0045025	OMIM:239711	IEA				P		HPO:skoehler	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000007	OMIM:239800	IEA				I		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000086	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000160	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000175	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000204	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000252	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000316	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME	HP:0012825	HP:0000347	OMIM:239800	TAS				P		HPO:probinson	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000405	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000413	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000455	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0000925	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0001245	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0001263	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0001627	OMIM:239800	TAS				P		HPO:skoehler	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0002006	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0003468	OMIM:239800	TAS				P		HPO:skoehler	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0004691	OMIM:239800	TAS				P		HPO:probinson	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0008551	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0009237	OMIM:239800	IEA				P		HPO:iea	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0011803	OMIM:239800	TAS				P		HPO:probinson	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0025356	OMIM:239800	IEA				P		HPO:skoehler	
OMIM	239800	HYPERTELORISM, MICROTIA, FACIAL CLEFTING SYNDROME		HP:0030680	OMIM:239800	IEA				P		HPO:iea	
OMIM	239840	HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY		HP:0000007	OMIM:239840	IEA				I		HPO:iea	
OMIM	239840	HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY		HP:0000763	OMIM:239840	PCS				P		HPO:probinson	
OMIM	239840	HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY		HP:0002754	OMIM:239840	IEA				P		HPO:iea	
OMIM	239840	HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY		HP:0004535	OMIM:239840	PCS				P		HPO:probinson	
OMIM	239840	HYPERTRICHOSIS, CONGENITAL ANTERIOR CERVICAL, WITH PERIPHERAL SENSORY		HP:0007178	OMIM:239840	PCS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000006	OMIM:239850	IEA				I		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000179	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000212	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000215	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000256	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000280	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000286	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000343	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000431	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000463	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000470	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000527	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000774	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000926	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0000939	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001004	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001256	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001520	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001537	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001640	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001643	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001647	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0001698	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0002673	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0002690	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0002750	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0003016	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0003300	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0004540	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0004634	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0004975	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0005129	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0005280	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0005445	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0007665	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0008822	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0010055	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0010068	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0010109	OMIM:239850	TAS				P		HPO:probinson	
OMIM	239850	HYPERTRICHOTIC OSTEOCHONDRODYSPLASIA		HP:0011220	OMIM:239850	IEA				P		HPO:probinson	
OMIM	239900	HYPERTROPHIC NEUROPATHY AND CATARACT		HP:0000007	OMIM:239900	TAS				I		HPO:skoehler	
OMIM	239900	HYPERTROPHIC NEUROPATHY AND CATARACT		HP:0000518	OMIM:239900	TAS				P		HPO:skoehler	
OMIM	239900	HYPERTROPHIC NEUROPATHY AND CATARACT		HP:0002922	OMIM:239900	TAS				P		HPO:skoehler	
OMIM	239900	HYPERTROPHIC NEUROPATHY AND CATARACT		HP:0002936	OMIM:239900	TAS				P		HPO:skoehler	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0000007	OMIM:240000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0000164	OMIM:240000	TAS				P		HPO:skoehler	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0000522	OMIM:240000	TAS				P		HPO:probinson	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0000717	OMIM:240000	TAS				P		HPO:skoehler	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0001249	OMIM:240000	TAS				P		HPO:probinson	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0001344	OMIM:240000	TAS				P		HPO:probinson	
OMIM	240000	HYPERURICEMIA, INFANTILE, WITH ABNORMAL BEHAVIOR AND NORMAL HYPOXANTHINEGUANINE PHOSPHORIBOSYLTRANSFERASE		HP:0002149	OMIM:240000	TAS				P		HPO:skoehler	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0000007	OMIM:240150	IEA				I		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0000083	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0001085	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0001392	OMIM:240150	TAS				P		HPO:skoehler	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0001541	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0002018	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0002516	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0003072	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0003256	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0007418	OMIM:240150	IEA				P		HPO:iea	
OMIM	240150	HYPERVITAMINOSIS A, SUSCEPTIBILITY TO		HP:0012514	OMIM:240150	IEA				P		HPO:skoehler	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0000007	OMIM:240200	IEA				I		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0000835	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0000846	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0000961	OMIM:240200	IEA				P		HPO:skoehler	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0001000	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0001250	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0001626	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0001943	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0002013	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0002104	OMIM:240200	IEA				P		HPO:skoehler	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0002153	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0002902	OMIM:240200	IEA				P		HPO:iea	
OMIM	240200	HYPOADRENOCORTICISM, FAMILIAL		HP:0008872	OMIM:240200	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000006	OMIM:240300	TAS				I		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000007	PMID:11836330	PCS				I		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000026	PMID:11836330	PCS				P		HP:probinson	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000121	PMID:11836330	PCS		HP:0040284		P		HP:probinson	3/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000134	PMID:11836330	PCS				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000518	PMID:11836330	PCS		HP:0040284		P		HP:probinson	6/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000580	OMIM:240300	TAS				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000819	OMIM:240300	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000821	PMID:11836330	PCS		HP:0040284		P		HP:probinson	4/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000829	PMID:11836330	PCS		HP:0040284		P		HPO:iea	11/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0000980	OMIM:240300	IEA				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001045	PMID:11836330	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001081	OMIM:240300	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001096	PMID:11836330	PCS		HP:0040284		P		HPO:iea	2/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001133	OMIM:240300	TAS				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001596	PMID:11836330	PCS		HP:0040284		P		HPO:iea	7/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001746	OMIM:240300	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0001903	OMIM:240300	IEA				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0002014	OMIM:240300	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0002024	PMID:11836330	PCS		HP:0040284		P		HPO:iea	3/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0002582	PMID:11836330	PCS		HP:0040284		P		HPO:iea	3/10
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0002728	PMID:11836330	PCS		HP:0040284		P		HPO:iea	11/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0003621	OMIM:240300	IEA				C		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0004319	PMID:28740581	IEA				P		HPO:iea	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0006297	PMID:11836330	PCS		HP:0040284		P		HPO:iea	11/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0007663	OMIM:240300	TAS				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0008207	PMID:11836330	PCS		HP:0040284		P		HPO:skoehler	9/11
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0031817	PMID:28740581	PCS				P		HPO:lccarmody	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0100651	OMIM:240300	TAS				P		HPO:skoehler	
OMIM	240300	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I		HP:0200120	OMIM:240300	TAS				P		HPO:skoehler	
OMIM	240400	HYPOASCORBEMIA		HP:0000007	OMIM:240400	IEA				I		HPO:iea	
OMIM	240400	HYPOASCORBEMIA		HP:0001939	OMIM:240400	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0000006	OMIM:240500	IEA				I		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0000007	OMIM:240500	IEA				I		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0000403	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0000509	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0001287	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0001744	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002014	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002110	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002240	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002664	OMIM:240500	IEA				P		HPO:skoehler	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002665	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002718	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002720	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002721	OMIM:240500	IEA				P		HPO:skoehler	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002729	OMIM:240500	IEA				P		HPO:skoehler	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002837	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002850	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0002960	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0004315	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0005435	OMIM:240500	IEA				P		HPO:iea	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0006532	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240500	IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2		HP:0011108	OMIM:240500	TAS				P		HPO:probinson	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0000007	OMIM:240600	IEA				I		HPO:iea	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0001250	OMIM:240600	IEA				P		HPO:iea	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0001946	OMIM:240600	IEA				P		HPO:skoehler	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0001998	OMIM:240600	IEA				P		HPO:iea	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0002151	OMIM:240600	TAS				P		HPO:probinson	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0003162	OMIM:240600	IEA				P		HPO:iea	
OMIM	240600	GLYCOGEN STORAGE DISEASE 0, LIVER		HP:0011998	OMIM:240600	TAS				P		HPO:probinson	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0000006	OMIM:240800	TAS				I		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0000007	OMIM:240800	IEA				I		HPO:iea	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0000486	OMIM:240800	IEA				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0000737	OMIM:240800	TAS				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0000825	OMIM:240800	TAS				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001249	OMIM:240800	IEA				P		HPO:iea	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001250	OMIM:240800	IEA				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001251	OMIM:240800	IEA				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001257	OMIM:240800	IEA				P		HPO:iea	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001259	OMIM:240800	IEA				P		HPO:iea	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001347	OMIM:240800	TAS				P		HPO:skoehler	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0001943	OMIM:240800	IEA				P		HPO:iea	
OMIM	240800	HYPOGLYCEMIA, LEUCINE-INDUCED; LIH		HP:0002329	OMIM:240800	IEA				P		HPO:iea	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0000006	OMIM:240900	TAS				I		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0000007	OMIM:240900	IEA				I		HPO:iea	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0000771	OMIM:240900	TAS				P		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0001250	OMIM:240900	TAS				P		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0001520	OMIM:240900	TAS				P		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0001528	OMIM:240900	TAS				P		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0001956	OMIM:240900	TAS				P		HPO:skoehler	
OMIM	240900	#240900 HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH		HP:0001998	OMIM:240900	IEA				P		HPO:iea	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0000007	OMIM:240950	IEA				I		HPO:iea	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0000026	OMIM:240950	TAS				P		HPO:iea	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0000135	OMIM:240950	IEA				P		HPO:skoehler	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0000518	OMIM:240950	IEA				P		HPO:iea	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0000789	OMIM:240950	IEA				P		HPO:iea	
OMIM	240950	HYPOGONADISM-CATARACT SYNDROME		HP:0008232	OMIM:240950	TAS				P		HPO:iea	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0000007	OMIM:241000	TAS				I		HPO:probinson	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0000026	OMIM:241000	TAS				P		HPO:probinson	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0000027	OMIM:241000	TAS				P		HPO:probinson	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0000252	OMIM:241000	TAS				P		HPO:probinson	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0001249	OMIM:241000	TAS				P		HPO:skoehler	
OMIM	241000	HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY		HP:0010714	OMIM:241000	TAS				P		HPO:probinson	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000007	OMIM:241080	IEA				I		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000013	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000044	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000054	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000325	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000407	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000411	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000426	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000674	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000709	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000738	OMIM:241080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000815	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0000819	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0001249	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0001260	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0001266	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0001332	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0001596	OMIM:241080	TAS				P		HPO:skoehler	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0002071	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0002213	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0002925	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0003077	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0005135	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0008070	OMIM:241080	PCS				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0008209	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0008697	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0008734	OMIM:241080	IEA				P		HPO:iea	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0030353	OMIM:241080	TAS				P		HPO:skoehler	
OMIM	241080	WOODHOUSE-SAKATI SYNDROME		HP:0040171	OMIM:241080	TAS				P		HPO:skoehler	
OMIM	241090	HYPOGONADISM, PRIMARY, AND PARTIAL ALOPECIA		HP:0000007	OMIM:241090	TAS				I		HPO:skoehler	
OMIM	241090	HYPOGONADISM, PRIMARY, AND PARTIAL ALOPECIA		HP:0000815	OMIM:241090	TAS				P		HPO:probinson	
OMIM	241090	HYPOGONADISM, PRIMARY, AND PARTIAL ALOPECIA		HP:0001596	OMIM:241090	TAS				P		HPO:skoehler	
OMIM	241090	HYPOGONADISM, PRIMARY, AND PARTIAL ALOPECIA		HP:0010464	OMIM:241090	TAS				P		HPO:probinson	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000007	OMIM:241100	IEA				I		HPO:iea	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000026	OMIM:241100	IEA				P		HPO:iea	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000029	OMIM:241100	IEA				P		HPO:skoehler	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000047	OMIM:241100	IEA				P		HPO:iea	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000054	OMIM:241100	IEA				P		HPO:iea	
OMIM	241100	HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED		HP:0000771	OMIM:241100	IEA				P		HPO:iea	
OMIM	241120	HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES		HP:0000007	OMIM:241120	IEA				I		HPO:iea	
OMIM	241120	HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES		HP:0000966	OMIM:241120	IEA				P		HPO:iea	
OMIM	241120	HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES		HP:0001945	OMIM:241120	TAS				P		HPO:probinson	
OMIM	241120	HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES		HP:0007500	OMIM:241120	IEA				P		HPO:iea	
OMIM	241120	HYPOHIDROSIS WITH ABNORMAL PALMAR DERMAL RIDGES		HP:0007608	OMIM:241120	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0000007	OMIM:241150	IEA				I		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0000114	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0000848	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0001949	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0002013	OMIM:241150	IEA				P		HPO:skoehler	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0002018	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0002900	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0003394	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0003566	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0004921	OMIM:241150	IEA				P		HPO:iea	
OMIM	241150	%241150 HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY;;HYPOKALEMIA, FAMILIAL;;GULLNER SYNDROME		HP:0012378	OMIM:241150	TAS				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000007	OMIM:241200	IEA				I		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000103	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000111	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000121	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000127	OMIM:241200	TAS				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000128	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000256	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000325	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000400	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000841	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000848	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000859	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000934	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0000938	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001090	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001249	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001250	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001263	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001281	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001425	OMIM:241200	TAS				I		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001508	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001518	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001561	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001563	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001622	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001944	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001945	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001959	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0001960	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002007	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002013	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002014	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002019	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002150	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002632	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002900	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002914	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0002917	OMIM:241200	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003081	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003113	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003158	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003324	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003394	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003401	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003527	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003540	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0003566	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0004322	OMIM:241200	IEA				P		HPO:skoehler	
OMIM	241200	BARTTER SYNDROME, ANTENATAL, TYPE 2		HP:0011220	OMIM:241200	TAS				P		HPO:skoehler	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000007	OMIM:241310	IEA				I		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000205	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000272	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000327	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000347	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000452	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0000588	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0001631	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0001643	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0004440	OMIM:241310	IEA				P		HPO:iea	
OMIM	241310	%241310 HYPOMANDIBULAR FACIOCRANIAL DYSOSTOSIS		HP:0012730	OMIM:241310	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000007	OMIM:241410	IEA				I		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000028	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000054	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000193	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000233	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000252	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000343	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000347	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000358	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000369	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000444	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000490	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0000824	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0001249	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0001250	OMIM:241410	IEA				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0001281	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0001773	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002007	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002079	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002119	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002199	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002718	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002750	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002901	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0002905	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0004279	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0005280	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0005686	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0008198	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0008846	OMIM:241410	IEA				P		HPO:iea	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0008897	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0011220	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0012448	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241410	HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME		HP:0200055	OMIM:241410	TAS				P		HPO:skoehler	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000007	OMIM:241500	IEA				I		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000121	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000164	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000592	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000737	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000773	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000897	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0000926	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001024	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001250	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001252	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001290	OMIM:241500	TAS				P		HPO:skoehler	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001363	OMIM:241500	TAS				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001508	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001522	OMIM:241500	IEA				M		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001561	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001608	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001903	OMIM:241500	IEA				P		HPO:skoehler	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0001945	OMIM:241500	TAS				P		HPO:probinson	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002013	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002019	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002039	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002104	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002150	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002170	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002205	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002659	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002979	OMIM:241500	TAS				P		HPO:probinson	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0002983	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0003021	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0003072	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0003239	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0003491	OMIM:241500	TAS				P		HPO:probinson	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0003826	OMIM:241500	TAS				M		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0004492	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0004606	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0005474	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0006385	OMIM:241500	TAS				P		HPO:probinson	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0008428	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0008873	OMIM:241500	IEA				P		HPO:iea	
OMIM	241500	HYPOPHOSPHATASIA, INFANTILE		HP:0011864	OMIM:241500	TAS				P		HPO:probinson	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0000007	OMIM:241510	IEA				I		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0000268	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0000520	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0000670	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0000897	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0001024	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0001250	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0001363	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0002007	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0002515	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0002979	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0003198	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0003239	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0003282	OMIM:241510	TAS				P		HPO:probinson	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0003491	OMIM:241510	TAS				P		HPO:probinson	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0004322	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0006323	OMIM:241510	IEA				P		HPO:iea	
OMIM	241510	HYPOPHOSPHATASIA, CHILDHOOD		HP:0011864	OMIM:241510	TAS				P		HPO:probinson	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0000007	OMIM:241519	IEA				I		HPO:iea	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0000117	OMIM:241519	IEA				P		HPO:iea	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0002514	OMIM:241519	IEA				P		HPO:iea	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0008491	OMIM:241519	IEA				P		HPO:iea	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0008732	OMIM:241519	IEA				P		HPO:iea	
OMIM	241519	241519 HYPOPHOSPHATEMIA, RENAL, WITH INTRACEREBRAL CALCIFICATIONS		HP:0009882	OMIM:241519	IEA				P		HPO:iea	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:241520	IEA				I		HPO:iea	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0000407	OMIM:241520	IEA				P		HPO:iea	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0001363	OMIM:241520	IEA				P		HPO:iea	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0002148	OMIM:241520	IEA				P		HPO:skoehler	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0002748	OMIM:241520	IEA				P		HPO:skoehler	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0004912	OMIM:241520	TAS				P		HPO:probinson	
OMIM	241520	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE		HP:0011001	OMIM:241520	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000007	OMIM:241530	IEA				I		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000117	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000124	OMIM:241530	TAS				P		HPO:skoehler	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000886	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000893	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0000920	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001252	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001290	OMIM:241530	TAS				P		HPO:skoehler	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001324	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001438	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001508	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0001510	OMIM:241530	TAS				P		HPO:skoehler	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002007	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002148	OMIM:241530	IEA				P		HPO:skoehler	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002150	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002355	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002653	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002663	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002748	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002752	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002753	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002757	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002979	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002980	OMIM:241530	TAS				P		HPO:probinson	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0002982	OMIM:241530	TAS				P		HPO:probinson	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003013	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003020	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003025	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003029	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003152	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003155	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003593	OMIM:241530	IEA				C		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0003698	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0004492	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0004724	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0004912	OMIM:241530	TAS				P		HPO:probinson	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0005469	OMIM:241530	IEA				P		HPO:iea	
OMIM	241530	HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY		HP:0010502	OMIM:241530	TAS				P		HPO:probinson	
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0000007	PMID:5111754	TAS				I		HPO:nvasilevsky	
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0001650	PMID:15690347	TAS		HP:0040284		P		HPO:nvasilevsky	32/413
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0001680	PMID:15690347	TAS		HP:0040284		P		HPO:nvasilevsky	32/413
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0004383	OMIM:241550	IEA				P		HPO:iea	
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0004383	PMID:15690347	TAS		HP:0040284		P		HPO:nvasilevsky	32/413
OMIM	241550	HYPOPLASTIC LEFT HEART SYNDROME		HP:0010983	PMID:15690347	TAS				I		HPO:nvasilevsky	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0000007	OMIM:241600	IEA				I		HPO:iea	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0002110	OMIM:241600	TAS				P		HPO:skoehler	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0002205	OMIM:241600	TAS				P		HPO:skoehler	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0002986	OMIM:241600	TAS				P		HPO:probinson	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0003022	OMIM:241600	IEA				P		HPO:iea	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0003073	OMIM:241600	TAS				P		HPO:probinson	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0003075	OMIM:241600	TAS				P		HPO:skoehler	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0003828	OMIM:241600	TAS				C		HPO:skoehler	
OMIM	241600	IMMUNODEFICIENCY 43		HP:0004315	OMIM:241600	TAS				P		HPO:probinson	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:241760	IEA				I		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0000047	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0000243	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0000252	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0001388	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0001597	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0001999	OMIM:241760	IEA				P		HPO:iea	
OMIM	241760	HYPOSPADIAS-MENTAL RETARDATION SYNDROME		HP:0030817	OMIM:241760	TAS				P		HPO:skoehler	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000007	OMIM:241800	IEA				I		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000054	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000110	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000161	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000171	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000175	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000238	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000256	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000347	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000773	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0000830	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0001162	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0001522	OMIM:241800	TAS		HP:0040282		M		HPO:probinson	HP:0040282
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0001627	OMIM:241800	TAS				P		HPO:skoehler	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002085	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002089	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002444	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002652	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002827	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0002983	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0003196	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0005280	OMIM:241800	IEA				P		HPO:iea	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0009733	OMIM:241800	IEA				P		HPO:skoehler	
OMIM	241800	241800 HYPOTHALAMIC HAMARTOMASCONGENITAL HYPOTHALAMIC HAMARTOMA SYNDROME, INCLUDED; CHHS, INCLUDED		HP:0030680	OMIM:241800	IEA				P		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0000007	OMIM:241850	IEA				I		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0000175	OMIM:241850	IEA				P		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0000453	OMIM:241850	IEA				P		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0001561	OMIM:241850	IEA				P		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0008191	OMIM:241850	IEA				P		HPO:iea	
OMIM	241850	HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE		HP:0010564	OMIM:241850	IEA				P		HPO:skoehler	
OMIM	242050	HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY		HP:0000007	OMIM:242050	IEA				I		HPO:iea	
OMIM	242050	HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY		HP:0000924	OMIM:242050	IEA				P		HPO:iea	
OMIM	242050	HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY		HP:0002150	OMIM:242050	IEA				P		HPO:iea	
OMIM	242050	HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY		HP:0003537	OMIM:242050	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0000007	OMIM:242100	IEA				I		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0000232	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0000656	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0000966	OMIM:242100	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0000982	OMIM:242100	TAS				P		HPO:skoehler	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001249	OMIM:242100	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001510	OMIM:242100	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001595	OMIM:242100	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001596	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001792	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001816	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0001831	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0003241	OMIM:242100	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0003470	OMIM:242100	IEA				P		HPO:skoehler	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0007431	OMIM:242100	TAS				P		HPO:skoehler	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0007479	OMIM:242100	IEA				P		HPO:iea	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0009381	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0010783	OMIM:242100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0025092	OMIM:242100	TAS				P		HPO:skoehler	
OMIM	242100	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 2		HP:0025114	OMIM:242100	TAS				P		HPO:skoehler	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000007	OMIM:242150	IEA				I		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000407	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000509	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000545	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000563	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000613	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0000633	OMIM:242150	TAS				P		HPO:probinson	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001019	OMIM:242150	IEA				P		HPO:skoehler	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001249	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001394	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001508	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001596	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0001808	OMIM:242150	IEA				P		HPO:skoehler	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0004322	OMIM:242150	IEA				P		HPO:iea	
OMIM	242150	ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS		HP:0008064	OMIM:242150	IEA				P		HPO:iea	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0000007	OMIM:242300	IEA				I		HPO:iea	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0000232	OMIM:242300	TAS				P		HPO:skoehler	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0000656	OMIM:242300	TAS				P		HPO:skoehler	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0000972	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0001006	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0001019	OMIM:242300	TAS				P		HPO:skoehler	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0001036	OMIM:242300	IEA				P		HPO:skoehler	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0001371	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0001596	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0002164	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0007431	OMIM:242300	TAS				P		HPO:skoehler	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0007549	OMIM:242300	TAS				P		HPO:probinson	
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0008404	OMIM:242300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242300	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 1; ARCI1		HP:0025092	OMIM:242300	TAS				P		HPO:skoehler	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0000007	OMIM:242500	IEA				I		HPO:iea	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0000232	OMIM:242500	IEA				P		HPO:iea	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0000520	OMIM:242500	TAS				P		HPO:iea	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0000656	OMIM:242500	IEA				P		HPO:skoehler	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0001622	OMIM:242500	TAS				P		HPO:skoehler	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0002063	OMIM:242500	TAS				P		HPO:iea	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0007431	OMIM:242500	TAS				P		HPO:iea	
OMIM	242500	#242500 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4B; ARCI4B;;ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE;;HARLEQUIN ICHTHYOSIS; HI;;'HARLEQUIN FETUS'		HP:0009381	OMIM:242500	IEA				P		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0000007	OMIM:242510	IEA				I		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0000232	OMIM:242510	IEA				P		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0000656	OMIM:242510	IEA				P		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0001249	OMIM:242510	IEA				P		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0001596	OMIM:242510	IEA				P		HPO:iea	
OMIM	242510	ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION		HP:0008064	OMIM:242510	IEA				P		HPO:iea	
OMIM	242520	ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION		HP:0000007	OMIM:242520	IEA				I		HPO:iea	
OMIM	242520	ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION		HP:0001251	OMIM:242520	IEA				P		HPO:iea	
OMIM	242520	ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION		HP:0001260	OMIM:242520	IEA				P		HPO:iea	
OMIM	242520	ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION		HP:0001433	OMIM:242520	IEA				P		HPO:iea	
OMIM	242520	ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION		HP:0008064	OMIM:242520	IEA				P		HPO:iea	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0000007	OMIM:242530	TAS				I		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0000112	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0001249	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0003259	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0003510	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0007479	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242530	ICHTHYOSIS, MENTAL RETARDATION, DWARFISM, AND RENAL IMPAIRMENT		HP:0012213	OMIM:242530	TAS				P		HPO:probinson	
OMIM	242550	ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA		HP:0000007	OMIM:242550	IEA				I		HPO:iea	
OMIM	242550	ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA		HP:0001249	OMIM:242550	IEA				P		HPO:iea	
OMIM	242550	ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA		HP:0001595	OMIM:242550	IEA				P		HPO:iea	
OMIM	242550	ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA		HP:0003355	OMIM:242550	IEA				P		HPO:iea	
OMIM	242550	ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA		HP:0007431	OMIM:242550	TAS				P		HPO:skoehler	
OMIM	242600	IMINOGLYCINURIA		HP:0000007	OMIM:242600	IEA				I		HPO:iea	
OMIM	242600	IMINOGLYCINURIA		HP:0000478	OMIM:242600	IEA				P		HPO:iea	
OMIM	242600	IMINOGLYCINURIA		HP:0001249	OMIM:242600	IEA				P		HPO:iea	
OMIM	242600	IMINOGLYCINURIA		HP:0003080	OMIM:242600	IEA				P		HPO:iea	
OMIM	242600	IMINOGLYCINURIA		HP:0003108	OMIM:242600	IEA				P		HPO:skoehler	
OMIM	242600	IMINOGLYCINURIA		HP:0003137	OMIM:242600	IEA				P		HPO:iea	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0000007	OMIM:242670	TAS				I		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0000246	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0002257	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0012208	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0012263	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0012265	OMIM:242670	IEA				P		HPO:skoehler	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0012267	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242670	CILIARY DYSKINESIA WITH DEFECTIVE RADIAL SPOKES		HP:0100582	OMIM:242670	TAS				P		HPO:probinson	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0000007	OMIM:242680	IEA				I		HPO:iea	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0000246	OMIM:242680	IEA				P		HPO:iea	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0002257	OMIM:242680	IEA				P		HPO:iea	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0002837	OMIM:242680	IEA				P		HPO:iea	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0005938	OMIM:242680	TAS				P		HPO:probinson	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0006536	OMIM:242680	IEA				P		HPO:iea	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0012263	OMIM:242680	TAS				P		HPO:skoehler	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0012265	OMIM:242680	IEA				P		HPO:skoehler	
OMIM	242680	242680 CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA;;IMMOTILE CILIA SYNDROME DUE TO EXCESSIVELY LONG CILIA		HP:0100582	OMIM:242680	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0000007	OMIM:242700	IEA				I		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0000976	OMIM:242700	TAS				P		HPO:skoehler	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0000999	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0001433	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0001508	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0001888	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0002028	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0002097	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0002110	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0002843	OMIM:242700	IEA				P		HPO:skoehler	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0002972	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0005359	OMIM:242700	TAS				P		HPO:skoehler	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0005899	OMIM:242700	IEA				P		HPO:iea	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0006532	OMIM:242700	IEA				P		HPO:skoehler	
OMIM	242700	IMMUNE DEFECT DUE TO ABSENCE OF THYMUS		HP:0006538	OMIM:242700	IEA				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0000007	OMIM:242840	IEA				I		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000175	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000204	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000252	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000316	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000347	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000369	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0000407	OMIM:242840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	242840	VICI SYNDROME		HP:0000519	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0000639	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0000777	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001010	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001022	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001107	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001250	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001252	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001263	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001270	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001274	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001290	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001320	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001508	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001510	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001635	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001638	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0001644	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001712	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0001941	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0002205	OMIM:242840	IEA				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0002282	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0002533	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0002718	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0002721	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0002728	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0002841	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0002965	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0003198	OMIM:242840	TAS				P		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0003244	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0003577	OMIM:242840	TAS				C		HPO:skoehler	
OMIM	242840	VICI SYNDROME		HP:0004315	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0004429	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0005407	OMIM:242840	TAS				P		HPO:probinson	
OMIM	242840	VICI SYNDROME		HP:0005419	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0005599	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0007894	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0008348	OMIM:242840	IEA				P		HPO:iea	
OMIM	242840	VICI SYNDROME		HP:0010636	OMIM:242840	IEA				P		HPO:skoehler	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0000007	OMIM:242850	IEA				I		HPO:iea	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0002718	OMIM:242850	TAS				P		HPO:probinson	
OMIM	242850	IMMUNE DEFICIENCY DISEASE	HP:0012828	HP:0002850	OMIM:242850	IEA				P		HPO:probinson	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0004429	OMIM:242850	TAS				P		HPO:probinson	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0004787	OMIM:242850	IEA				P		HPO:iea	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0005363	OMIM:242850	IEA				P		HPO:iea	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0005374	OMIM:242850	TAS				P		HPO:probinson	
OMIM	242850	IMMUNE DEFICIENCY DISEASE		HP:0030151	OMIM:242850	IEA				P		HPO:skoehler	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000007	PMID:10588719	PCS				I		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000158	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000246	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000272	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000286	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000316	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000347	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000369	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0000463	OMIM:242860	TAS				P		HPO:probinson	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0001249	OMIM:242860	TAS				P		HPO:probinson	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0001508	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002014	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002024	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002090	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002110	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002720	OMIM:242860	TAS				P		HP:probinson	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0002721	OMIM:242860	IEA				P		HPO:skoehler	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0003196	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0003196	OMIM:242860	TAS				P		HPO:probinson	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0003496	OMIM:242860	TAS				P		HP:probinson	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0004322	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0004469	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0005280	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0005403	OMIM:242860	IEA				P		HPO:iea	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0010808	OMIM:242860	TAS				P		HPO:skoehler	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0012368	OMIM:242860	TAS				P		HPO:skoehler	
OMIM	242860	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME		HP:0040218	OMIM:242860	TAS				P		HP:probinson	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0000007	OMIM:242870	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0002718	OMIM:242870	TAS				P		HPO:probinson	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0002721	OMIM:242870	TAS				P		HPO:probinson	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0004315	OMIM:242870	IEA				P		HPO:probinson	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0005401	OMIM:242870	TAS				P		HPO:probinson	
OMIM	242870	IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES		HP:0005403	OMIM:242870	TAS				P		HPO:probinson	
OMIM	242880	IMMUNOERYTHROMYELOID HYPOPLASIA		HP:0000007	OMIM:242880	IEA				I		HPO:iea	
OMIM	242880	IMMUNOERYTHROMYELOID HYPOPLASIA		HP:0004315	OMIM:242880	IEA				P		HPO:iea	
OMIM	242880	IMMUNOERYTHROMYELOID HYPOPLASIA		HP:0005523	OMIM:242880	IEA				P		HPO:iea	
OMIM	242880	IMMUNOERYTHROMYELOID HYPOPLASIA		HP:0008161	OMIM:242880	IEA				P		HPO:iea	
OMIM	242880	IMMUNOERYTHROMYELOID HYPOPLASIA		HP:0012133	OMIM:242880	TAS				P		HPO:probinson	
OMIM	242890	IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW		HP:0000007	OMIM:242890	IEA				I		HPO:iea	
OMIM	242890	IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW		HP:0002715	OMIM:242890	IEA				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000007	OMIM:242900	TAS				I		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000083	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000093	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000097	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000100	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000414	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000470	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000483	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000545	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000691	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000822	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000926	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0000938	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001034	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001270	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001511	OMIM:242900	TAS		HP:0040284		P		HPO:probinson	50%
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001538	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001620	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001873	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001875	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001888	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0001903	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002208	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002213	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002326	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002515	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002634	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002655	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002719	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002843	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002925	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002938	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0002942	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0003090	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0003182	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0003300	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0003521	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0005280	OMIM:242900	TAS				P		HPO:iea	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0006453	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0007759	OMIM:242900	TAS				P		HPO:probinson	
OMIM	242900	IMMUNOOSSEOUS DYSPLASIA, SCHIMKE TYPE		HP:0010701	OMIM:242900	TAS				P		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0000007	OMIM:243000	TAS				I		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0000020	OMIM:243000	TAS				P		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0000458	OMIM:243000	TAS				P		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0000966	OMIM:243000	TAS				P		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0000970	OMIM:243000	TAS				P		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0001265	OMIM:243000	TAS				P		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0002661	OMIM:243000	TAS				P		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0003593	OMIM:243000	TAS				C		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0003828	OMIM:243000	TAS				C		HPO:skoehler	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0004409	OMIM:243000	TAS				P		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0007021	OMIM:243000	TAS				P		HPO:probinson	
OMIM	243000	INDIFFERENCE TO PAIN, CONGENITAL, AUTOSOMAL RECESSIVE; CIP		HP:0012332	OMIM:243000	TAS				P		HPO:skoehler	
OMIM	243050	INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION		HP:0000007	OMIM:243050	IEA				I		HPO:iea	
OMIM	243050	INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION		HP:0001249	OMIM:243050	IEA				P		HPO:iea	
OMIM	243050	INDOLYLACROYL GLYCINURIA WITH MENTAL RETARDATION		HP:0003108	OMIM:243050	TAS				P		HPO:skoehler	
OMIM	243060	MALE INFERTILITY WITH LARGE-HEADED, MULTIFLAGELLAR, POLYPLOID SPERMATOZOA		HP:0000007	OMIM:243060	IEA				I		HPO:iea	
OMIM	243060	MALE INFERTILITY WITH LARGE-HEADED, MULTIFLAGELLAR, POLYPLOID SPERMATOZOA		HP:0000025	OMIM:243060	IEA				P		HPO:skoehler	
OMIM	243060	MALE INFERTILITY WITH LARGE-HEADED, MULTIFLAGELLAR, POLYPLOID SPERMATOZOA		HP:0003251	OMIM:243060	IEA				P		HPO:skoehler	
OMIM	243080	INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO		HP:0000007	OMIM:243080	IEA				I		HPO:iea	
OMIM	243080	INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO		HP:0001939	OMIM:243080	IEA				P		HPO:iea	
OMIM	243080	INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO		HP:0002715	OMIM:243080	IEA				P		HPO:iea	
OMIM	243100	INTERNAL CAROTID ARTERIES, HYPOPLASIA OF		HP:0000007	OMIM:243100	IEA				I		HPO:iea	
OMIM	243100	INTERNAL CAROTID ARTERIES, HYPOPLASIA OF		HP:0000726	OMIM:243100	IEA				P		HPO:iea	
OMIM	243100	INTERNAL CAROTID ARTERIES, HYPOPLASIA OF		HP:0002637	OMIM:243100	IEA				P		HPO:iea	
OMIM	243100	INTERNAL CAROTID ARTERIES, HYPOPLASIA OF		HP:0005290	OMIM:243100	IEA				P		HPO:iea	
OMIM	243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0000007	OMIM:243110	TAS				I		HPO:nvasilevsky	
OMIM	243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0000403	PMID:6611555	PCS				P		HPO:iea	
OMIM	243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0001417	OMIM:243110	TAS				I		HPO:nvasilevsky	
OMIM	243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0001510	PMID:6611555	PCS				P		HPO:iea	
OMIM	243110	INTERLEUKIN 1, DEFECTIVE T-CELL RESPONSE TO		HP:0006532	PMID:6611555	PCS				P		HPO:iea	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0000007	OMIM:243150	IEA				I		HPO:iea	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0000778	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0000924	OMIM:243150	IEA				P		HPO:iea	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001438	OMIM:243150	IEA				P		HPO:iea	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001511	OMIM:243150	TAS				P		HPO:skoehler	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001539	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001561	OMIM:243150	TAS				P		HPO:skoehler	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001629	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0001890	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0002566	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0002573	OMIM:243150	TAS				P		HPO:skoehler	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0003765	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0004430	OMIM:243150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0011100	OMIM:243150	IEA				P		HPO:skoehler	
OMIM	243150	GASTROINTESTINAL DEFECTS AND IMMUNODEFICIENCY SYNDROME; GIDID		HP:0032220	OMIM:243150	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:243180	IEA				I		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0001284	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002013	OMIM:243180	IEA				P		HPO:skoehler	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002066	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002253	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002495	OMIM:243180	TAS				P		HPO:probinson	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002566	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0002574	OMIM:243180	TAS				P		HPO:probinson	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0005249	OMIM:243180	IEA				P		HPO:iea	
OMIM	243180	VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE		HP:0010831	OMIM:243180	TAS				P		HPO:probinson	
OMIM	243185	NATAL TEETH - INTESTINAL PSEUDOOBSTRUCTION - PATENT DUCTUS		HP:0000695	OMIM:243185	IEA				P		HPO:skoehler	
OMIM	243200	INTRACRANIAL HYPERTENSION, IDIOPATHIC		HP:0000007	OMIM:243200	TAS				I		HPO:skoehler	
OMIM	243200	INTRACRANIAL HYPERTENSION, IDIOPATHIC		HP:0000822	OMIM:243200	TAS				P		HPO:skoehler	
OMIM	243200	INTRACRANIAL HYPERTENSION, IDIOPATHIC		HP:0001085	OMIM:243200	TAS				P		HPO:skoehler	
OMIM	243200	INTRACRANIAL HYPERTENSION, IDIOPATHIC		HP:0002516	OMIM:243200	TAS				P		HPO:skoehler	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0000007	OMIM:243300	TAS				I		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0000365	PMID:19478059	PCS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0000989	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0001046	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0001733	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0002240	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0002908	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0006575	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243300	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC 1		HP:0012202	OMIM:243300	TAS				P		HPO:probinson	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000006	OMIM:243310	TAS				I		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000007	OMIM:243310	IEA				I		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000028	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000054	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000154	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000202	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000204	OMIM:243310	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000219	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000219	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000243	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000252	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000278	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000286	PMID:26583190	PCS				P		HPO:probinson	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000307	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000316	PMID:3351890	PCS				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000343	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000369	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000396	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000407	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000431	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000463	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000470	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000508	PMID:3351890	PCS				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000567	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000568	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000612	PMID:3351890	PCS				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0000637	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001249	PMID:3351890	PCS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001250	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001252	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001263	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001274	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001290	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001302	OMIM:243310	IEA				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001508	OMIM:243310	IEA				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001643	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001647	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001650	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0001939	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0002119	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0002162	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0002553	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0003196	OMIM:243310	IEA				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0004322	PMID:3351890	PCS				P		HPO:iea	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0008897	OMIM:243310	TAS				P		HPO:skoehler	
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0010066	OMIM:243310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243310	BARAITSER-WINTER SYNDROME 1; BRWS1		HP:0011800	OMIM:243310	IEA				P		HPO:skoehler	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0000007	OMIM:243320	IEA				I		HPO:iea	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0000707	OMIM:243320	IEA				P		HPO:iea	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0001510	OMIM:243320	IEA				P		HPO:iea	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0001889	OMIM:243320	IEA				P		HPO:iea	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0001939	OMIM:243320	IEA				P		HPO:iea	
OMIM	243320	INTRINSIC FACTOR AND R BINDER, COMBINED CONGENITAL DEFICIENCY OF		HP:0005219	OMIM:243320	IEA				P		HPO:iea	
OMIM	243400	ACETYLATION, SLOW		HP:0000007	OMIM:243400	IEA				I		HPO:iea	
OMIM	243400	ACETYLATION, SLOW		HP:0001939	OMIM:243400	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0000007	OMIM:243440	IEA				I		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0000175	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0000238	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0000347	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0000932	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0001710	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0008551	OMIM:243440	IEA				P		HPO:iea	
OMIM	243440	243440 ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME;;MICROTIA-AORTIC ARCH SYNDROME		HP:0009892	OMIM:243440	TAS				P		HPO:skoehler	
OMIM	243450	ISOVALERIC ACID, INABILITY TO SMELL		HP:0000007	OMIM:243450	IEA				I		HPO:iea	
OMIM	243450	ISOVALERIC ACID, INABILITY TO SMELL		HP:0000458	OMIM:243450	TAS				P		HPO:probinson	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0000007	OMIM:243500	IEA				I	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001250	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001254	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001259	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001263	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001873	OMIM:243500	TAS				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:skoehler	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001876	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001882	OMIM:243500	TAS				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:skoehler	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001942	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001944	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0001993	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0002013	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0003108	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:skoehler	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0005528	OMIM:243500	IEA				P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:iea	
OMIM	243500	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY		HP:0011695	OMIM:243500	TAS		HP:0040283		P	#243500 ISOVALERIC ACIDEMIA; IVA;;ISOVALERIC ACID COA DEHYDROGENASE DEFICIENCY;;IVD DEFICIENCY	HPO:skoehler	HP:0040283
OMIM	243600	%243600 JEJUNAL ATRESIA;;APPLE PEEL SYNDROME;;APPLE PEEL SMALL BOWEL SYNDROME; APSB		HP:0000007	OMIM:243600	IEA				I		HPO:iea	
OMIM	243600	%243600 JEJUNAL ATRESIA;;APPLE PEEL SYNDROME;;APPLE PEEL SMALL BOWEL SYNDROME; APSB		HP:0001438	OMIM:243600	IEA				P		HPO:iea	
OMIM	243600	%243600 JEJUNAL ATRESIA;;APPLE PEEL SYNDROME;;APPLE PEEL SMALL BOWEL SYNDROME; APSB		HP:0005235	OMIM:243600	TAS				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000007	PMID:25564561	PCS				I		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000126	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000154	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000175	PMID:25564561	PCS				P		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000238	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000316	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000426	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000431	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000482	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000490	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000518	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000568	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000609	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000612	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000647	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0000659	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0001274	PMID:25564561	PCS				P		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0001320	PMID:25564561	PCS				P		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0001321	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0002000	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0002247	PMID:25564561	PCS				P		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0002566	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0003198	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0003577	OMIM:243605	IEA				C		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0003826	PMID:25564561	PCS				M		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0005235	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0012584	PMID:25564561	PCS				P		HPO:probinson	
OMIM	243605	STROMME SYNDROME; STROMS		HP:0012841	OMIM:243605	IEA				P		HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:243700	IEA				I	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HP:0012828	HP:0000964	OMIM:243700	TAS				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0001047	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0001880	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002099	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002138	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002301	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002664	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002718	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0002841	OMIM:243700	TAS				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:243700	IEA				C	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0004429	OMIM:243700	TAS				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0005318	OMIM:243700	IEA				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:iea	
OMIM	243700	#243700 HYPER-IgE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IgE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE		HP:0005425	OMIM:243700	TAS				P	#243700 HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL RECESSIVE;;HYPER-IGE SYNDROME, AUTOSOMAL RECESSIVE;;HIES, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000007	OMIM:243800	IEA				I		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000028	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000047	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000054	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000126	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000143	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000252	OMIM:243800	PCS				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000407	OMIM:243800	PCS				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000430	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000444	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000486	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000819	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000821	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000954	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0000957	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001092	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001153	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001249	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001252	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001290	OMIM:243800	TAS				P		HPO:skoehler	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001362	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001388	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001396	OMIM:243800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001399	OMIM:243800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001508	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001511	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001518	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001545	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001597	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001629	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001631	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001644	OMIM:243800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001696	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0001738	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002023	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002024	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002209	OMIM:243800	TAS				P		HPO:probinson	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002236	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002253	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002286	OMIM:243800	PCS				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002557	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002617	OMIM:243800	IEA				P		HPO:skoehler	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002750	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0002901	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0003362	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0003819	OMIM:243800	PCS				M		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0004209	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0004322	OMIM:243800	PCS				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0005498	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0006334	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0006349	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0007385	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0008665	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0008716	OMIM:243800	IEA				P		HPO:iea	
OMIM	243800	JOHANSON-BLIZZARD SYNDROME; JBS		HP:0012050	OMIM:243800	TAS				P		HPO:probinson	
OMIM	243910	ARIMA SYNDROME		HP:0000007	OMIM:243910	IEA				I		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000090	OMIM:243910	TAS	HP:0003621			P		HPO:probinson	
OMIM	243910	ARIMA SYNDROME		HP:0000092	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000108	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000113	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000154	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000508	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000550	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000556	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000567	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000618	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0000639	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001162	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001251	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001252	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001263	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001290	OMIM:243910	TAS				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0001395	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001397	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0001830	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0002094	OMIM:243910	IEA				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0002198	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0002240	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0002282	OMIM:243910	IEA				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0002335	OMIM:243910	TAS				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0002365	OMIM:243910	TAS				P		HPO:probinson	
OMIM	243910	ARIMA SYNDROME		HP:0002419	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0002436	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0002508	OMIM:243910	TAS				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0002789	OMIM:243910	IEA				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0003774	OMIM:243910	TAS	HP:0011463			P		HPO:probinson	
OMIM	243910	ARIMA SYNDROME		HP:0005576	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0006817	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0006887	OMIM:243910	IEA				P		HPO:iea	
OMIM	243910	ARIMA SYNDROME		HP:0010864	OMIM:243910	TAS				P		HPO:skoehler	
OMIM	243910	ARIMA SYNDROME		HP:0025356	OMIM:243910	IEA				P		HPO:skoehler	
OMIM	244100	JUMPING FRENCHMAN OF MAINE		HP:0000007	OMIM:244100	IEA				I		HPO:iea	
OMIM	244100	JUMPING FRENCHMAN OF MAINE		HP:0000707	OMIM:244100	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000006	OMIM:244200	TAS				I		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000007	OMIM:244200	IEA				I		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000028	OMIM:244200	TAS				P		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000044	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000054	OMIM:244200	TAS				P		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000122	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000175	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000204	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000365	OMIM:244200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000458	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000601	OMIM:244200	IEA				P		HPO:iea	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000767	OMIM:244200	TAS				P		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0000786	OMIM:244200	TAS				P		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0001250	OMIM:244200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0001763	OMIM:244200	TAS				P		HPO:skoehler	
OMIM	244200	HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3		HP:0003829	OMIM:244200	TAS				C		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000007	OMIM:244300	IEA				I		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000028	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000054	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000059	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000079	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000175	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000204	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000369	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000384	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000405	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000414	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000470	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000480	PMID:20358618	PCS				P		HPO:probinson	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000518	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000568	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000612	PMID:1776630	PCS				P		HPO:probinson	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0000954	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001250	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001302	OMIM:244300	IEA				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001511	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001629	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001631	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001643	OMIM:244300	IEA				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0001864	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0002019	OMIM:244300	IEA				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0002126	OMIM:244300	IEA				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0002162	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0002566	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0002650	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0006887	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0007598	OMIM:244300	TAS				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0009473	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0009765	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0009778	OMIM:244300	IEA				P		HPO:iea	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0010557	OMIM:244300	IEA				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0010864	OMIM:244300	TAS				P		HPO:skoehler	
OMIM	244300	KAPUR-TORIELLO SYNDROME		HP:0100490	OMIM:244300	TAS				P		HPO:skoehler	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000007	OMIM:244400	IEA				I		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000246	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000389	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000405	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000458	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0000481	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0001334	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0001425	OMIM:244400	TAS				I		HPO:skoehler	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0001696	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0001746	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0002090	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0002110	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0002257	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0002315	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0002688	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0003251	OMIM:244400	IEA				P		HPO:iea	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0005938	OMIM:244400	TAS				P		HPO:probinson	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0011109	OMIM:244400	TAS				P		HPO:skoehler	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0012263	OMIM:244400	TAS				P		HPO:probinson	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0012265	OMIM:244400	IEA				P		HPO:skoehler	
OMIM	244400	#244400 CILIARY DYSKINESIA, PRIMARY, 1; CILD1;;PCD;;CILIARY DYSKINESIA, PRIMARY, 1, WITH OR WITHOUT SITUS INVERSUS;;IMMOTILE CILIA SYNDROME; ICS;;POLYNESIAN BRONCHIECTASISKARTAGENER SYNDROME, INCLUDED;;DEXTROCARDIA, BRONCHIECTASIS, AND SINUSITIS, INCLUDED;;SIEWERT SYNDROME, INCLUDED		HP:0100582	OMIM:244400	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000007	PMID:23200864	PCS				I		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000160	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000218	PMID:23200864	PCS		HP:0040284		P		HPO:iea	1/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000219	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000219	OMIM:244450	TAS				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000248	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000252	PMID:23200864	PCS				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000275	OMIM:244450	IEA		HP:0040284		P		HPO:iea	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000276	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000286	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000316	PMID:23200864	PCS		HP:0040284		P		HP:probinson	3/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000319	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000347	PMID:23200864	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000369	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000377	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000384	OMIM:244450	IEA		HP:0040284		P		HPO:iea	1/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000463	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000482	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000483	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000486	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000506	PMID:23200864	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000508	PMID:23200864	PCS		HP:0040284		P		HPO:iea	3/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000535	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000543	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000545	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000581	PMID:23200864	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000582	PMID:23200864	PCS		HP:0040284		P		HPO:iea	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000639	OMIM:244450	IEA		HP:0040284		P		HPO:iea	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000670	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000699	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000954	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0000963	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001270	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001290	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001344	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001508	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001591	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001629	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001631	PMID:23200864	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001680	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0001840	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002019	PMID:23200864	PCS		HP:0040284		P		HPO:iea	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002079	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002119	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002566	OMIM:244450	IEA				P		HPO:skoehler	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002643	OMIM:244450	IEA		HP:0040284		P		HPO:iea	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0002719	PMID:23200864	PCS		HP:0040284		P		HP:probinson	3/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0003146	PMID:23200864	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0003196	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0003300	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0004209	PMID:23200864	PCS		HP:0040284		P		HPO:iea	2/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0004283	OMIM:244450	TAS				P		HPO:probinson	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0005280	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0006511	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0008070	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0008665	OMIM:244450	IEA				P		HPO:iea	
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0008872	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0008936	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0010864	PMID:23200864	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	244450	KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS		HP:0011302	OMIM:244450	TAS				P		HPO:probinson	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:244460	IEA				I		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000316	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000670	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000883	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000890	OMIM:244460	TAS				P		HPO:probinson	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:244460	IEA				P		HPO:skoehler	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001281	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001476	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001511	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001773	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001903	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0002718	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0002750	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0002901	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE	HP:0012825	HP:0002917	OMIM:244460	TAS				P		HPO:probinson	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0003100	OMIM:244460	TAS				P		HPO:probinson	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0003508	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0003561	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0004279	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0004331	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0005450	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0006645	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0008198	OMIM:244460	IEA				P		HPO:iea	
OMIM	244460	#244460 KENNY-CAFFEY SYNDROME, TYPE 1; KCS1;;KCS;;KENNY-CAFFEY SYNDROME, AUTOSOMAL RECESSIVE		HP:0200055	OMIM:244460	TAS				P		HPO:skoehler	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000007	OMIM:244600	IEA				I		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000010	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000076	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000175	OMIM:244600	TAS				P		HPO:skoehler	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000204	OMIM:244600	TAS				P		HPO:skoehler	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000316	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000465	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000470	OMIM:244600	TAS				P		HPO:skoehler	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0000563	OMIM:244600	IEA				P		HPO:skoehler	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0001156	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0001263	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0001510	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0004209	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0005640	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0005852	OMIM:244600	IEA				P		HPO:iea	
OMIM	244600	KERATOCONUS POSTICUS CIRCUMSCRIPTUS		HP:0008511	OMIM:244600	IEA				P		HPO:iea	
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0000007	OMIM:244850	IEA				I		HPO:iea	
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0000962	PMID:2935332	PCS				P		HPO:lccarmody	
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0000982	OMIM:244850	IEA				P		HPO:iea	
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0000982	PMID:2935332	TAS		HP:0040284		P		HPO:lccarmody	1/6
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0011370	PMID:2935332	PCS		HP:0040284		P		HPO:lccarmody	3/6
OMIM	244850	KERATODERMA, PALMOPLANTAR, NORRBOTTEN RECESSIVE TYPE		HP:0200034	PMID:2935332	PCS				P		HPO:lccarmody	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0000007	OMIM:245000	IEA				I		HPO:iea	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0000166	OMIM:245000	IEA	HP:0003593			P		HPO:iea	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0000972	OMIM:245000	IEA				P		HPO:iea	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0006308	OMIM:245000	IEA				P		HPO:iea	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0006480	OMIM:245000	IEA				P		HPO:iea	
OMIM	245000	PAPILLON-LEFEVRE SYNDROME		HP:0006960	OMIM:245000	IEA				P		HPO:skoehler	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0000007	OMIM:245010	IEA				I		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0000166	OMIM:245010	IEA	HP:0003593			P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0001166	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0001763	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0001805	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0005406	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0006224	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0007545	OMIM:245010	IEA				P		HPO:iea	
OMIM	245010	HAIM-MUNK SYNDROME		HP:0009771	OMIM:245010	IEA				P		HPO:iea	
OMIM	245050	SUCCINYL-COA:3-OXOACID COA TRANSFERASE DEFICIENCY		HP:0000007	OMIM:245050	IEA				I		HPO:iea	
OMIM	245050	SUCCINYL-COA:3-OXOACID COA TRANSFERASE DEFICIENCY		HP:0002013	OMIM:245050	IEA				P		HPO:iea	
OMIM	245050	SUCCINYL-COA:3-OXOACID COA TRANSFERASE DEFICIENCY		HP:0002789	OMIM:245050	IEA				P		HPO:iea	
OMIM	245050	SUCCINYL-COA:3-OXOACID COA TRANSFERASE DEFICIENCY		HP:0002919	OMIM:245050	IEA				P		HPO:iea	
OMIM	245050	SUCCINYL-COA:3-OXOACID COA TRANSFERASE DEFICIENCY	HP:0012828	HP:0005974	OMIM:245050	TAS				P		HPO:iea	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000007	OMIM:245100	IEA				I		HPO:iea	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000135	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000365	OMIM:245100	IEA				P		HPO:iea	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000407	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000486	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000639	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000718	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0000786	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001249	OMIM:245100	IEA				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001251	OMIM:245100	IEA				P		HPO:iea	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS	HP:0012828	HP:0001263	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001284	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001761	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001762	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0001763	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0002300	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0002919	OMIM:245100	TAS				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0003202	OMIM:245100	IEA				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0003593	OMIM:245100	TAS				C		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0003676	OMIM:245100	TAS				C		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0006827	OMIM:245100	IEA				P		HPO:skoehler	
OMIM	245100	RICHARDS-RUNDLE SYNDROME; RRNS		HP:0008187	OMIM:245100	IEA				P		HPO:iea	
OMIM	245130	KETOADIPICACIDURIA		HP:0000007	OMIM:245130	TAS				I		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0001249	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0001250	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0001252	OMIM:245130	IEA				P		HPO:iea	
OMIM	245130	KETOADIPICACIDURIA		HP:0001263	OMIM:245130	IEA				P		HPO:iea	
OMIM	245130	KETOADIPICACIDURIA		HP:0001270	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0001290	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0001552	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0003355	OMIM:245130	IEA				P		HPO:skoehler	
OMIM	245130	KETOADIPICACIDURIA		HP:0007479	OMIM:245130	TAS				P		HPO:probinson	
OMIM	245130	KETOADIPICACIDURIA		HP:0007514	OMIM:245130	TAS				P		HPO:probinson	
OMIM	245130	KETOADIPICACIDURIA		HP:0012098	OMIM:245130	TAS				P		HPO:probinson	
OMIM	245130	KETOADIPICACIDURIA		HP:0100759	OMIM:245130	TAS				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000007	OMIM:245150	IEA				I		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000246	OMIM:245150	IEA				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000272	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000276	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000365	OMIM:245150	TAS				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000400	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000403	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0000822	OMIM:245150	IEA				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001250	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001256	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001507	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001611	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001629	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0001642	OMIM:245150	TAS				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0002002	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0002097	OMIM:245150	IEA				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0002514	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0002837	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0004969	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0004971	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0005103	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0005268	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0005275	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0005280	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0006140	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0006536	OMIM:245150	IEA				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0006646	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0008747	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0009778	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0009882	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0010109	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0010655	OMIM:245150	IEA				P		HPO:iea	
OMIM	245150	KEUTEL SYNDROME; KTLS		HP:0011109	OMIM:245150	TAS				P		HPO:skoehler	
OMIM	245150	KEUTEL SYNDROME; KTLS	HP:0012825	HP:0011800	OMIM:245150	TAS				P		HPO:skoehler	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000160	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000205	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000218	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000470	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000508	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000768	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0000926	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0001083	OMIM:245160	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0001371	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0001387	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0002002	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0002947	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0002980	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0002982	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0003745	OMIM:245160	IEA				I		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0004322	OMIM:245160	IEA				P		HPO:iea	
OMIM	245160	245160 KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS;;BURTON SYNDROME		HP:0008820	OMIM:245160	IEA				P		HPO:iea	
OMIM	245180	KIFAFA SEIZURE DISORDER		HP:0000007	OMIM:245180	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	245180	KIFAFA SEIZURE DISORDER		HP:0001249	OMIM:245180	IEA				P		HPO:iea	
OMIM	245180	KIFAFA SEIZURE DISORDER		HP:0001250	OMIM:245180	IEA				P		HPO:iea	
OMIM	245180	KIFAFA SEIZURE DISORDER		HP:0006932	OMIM:245180	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000007	OMIM:245190	IEA				I		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000160	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000175	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000260	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000272	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000316	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000369	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000377	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000470	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000773	OMIM:245190	TAS				P		HPO:probinson	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000774	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000885	OMIM:245190	TAS				P		HPO:probinson	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000926	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000941	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000946	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000947	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0000969	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001156	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001538	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001561	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001622	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001623	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001631	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001643	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0001762	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0002652	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0003015	OMIM:245190	TAS				P		HPO:probinson	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0003025	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0003025	OMIM:245190	TAS				P		HPO:probinson	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0003417	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0004482	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0008479	OMIM:245190	IEA				P		HPO:skoehler	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0008905	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0008909	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0011675	OMIM:245190	IEA				P		HPO:iea	
OMIM	245190	KNIEST-LIKE DYSPLASIA, LETHAL		HP:0012368	OMIM:245190	TAS				P		HPO:skoehler	
OMIM	245200	KRABBE DISEASE		HP:0000007	OMIM:245200	IEA				I		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0000238	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0000365	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0000618	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0000639	OMIM:245200	TAS				P		HPO:skoehler	
OMIM	245200	KRABBE DISEASE		HP:0000648	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0000762	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0001250	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0001252	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0001276	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0001508	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0001954	OMIM:245200	TAS				P		HPO:skoehler	
OMIM	245200	KRABBE DISEASE		HP:0001973	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002013	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002180	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002191	OMIM:245200	TAS				P		HPO:skoehler	
OMIM	245200	KRABBE DISEASE		HP:0002333	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002353	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002376	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002506	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0002922	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0006801	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0007141	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0007305	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0007928	OMIM:245200	IEA				P		HPO:iea	
OMIM	245200	KRABBE DISEASE		HP:0011096	OMIM:245200	PCS				P		HPO:probinson	
OMIM	245200	KRABBE DISEASE		HP:0025013	OMIM:245200	TAS				P		HPO:skoehler	
OMIM	245300	KURU, SUSCEPTIBILITY TO		HP:0000496	OMIM:245300	IEA				P		HPO:iea	
OMIM	245300	KURU, SUSCEPTIBILITY TO		HP:0001251	OMIM:245300	IEA				P		HPO:iea	
OMIM	245300	KURU, SUSCEPTIBILITY TO		HP:0001268	OMIM:245300	IEA				P		HPO:iea	
OMIM	245300	KURU, SUSCEPTIBILITY TO		HP:0002180	OMIM:245300	TAS				P		HPO:probinson	
OMIM	245300	KURU, SUSCEPTIBILITY TO		HP:0002317	OMIM:245300	TAS				P		HPO:probinson	
OMIM	245340	#245340 ERYTHROCYTE LACTATE TRANSPORTER DEFECT;;LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO		HP:0000006	OMIM:245340	IEA				I		HPO:iea	
OMIM	245340	#245340 ERYTHROCYTE LACTATE TRANSPORTER DEFECT;;LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO		HP:0003236	OMIM:245340	IEA				P		HPO:iea	
OMIM	245340	#245340 ERYTHROCYTE LACTATE TRANSPORTER DEFECT;;LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO		HP:0003710	OMIM:245340	IEA				P		HPO:iea	
OMIM	245340	#245340 ERYTHROCYTE LACTATE TRANSPORTER DEFECT;;LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO		HP:0008967	OMIM:245340	IEA				P		HPO:iea	
OMIM	245340	#245340 ERYTHROCYTE LACTATE TRANSPORTER DEFECT;;LACTATE TRANSPORTER DEFECT, MYOPATHY DUE TO		HP:0009020	OMIM:245340	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0000007	OMIM:245348	IEA				I		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0000252	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0000508	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0000639	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0000657	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001251	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001256	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001263	OMIM:245348	TAS				P		HPO:skoehler	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001266	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001319	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0001347	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0002194	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0002268	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0002307	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0002465	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0002928	OMIM:245348	TAS				P		HPO:skoehler	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD	HP:0012825	HP:0003128	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0003593	OMIM:245348	IEA				C		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0006961	OMIM:245348	IEA				P		HPO:iea	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0025356	OMIM:245348	IEA				P		HPO:skoehler	
OMIM	245348	PYRUVATE DEHYDROGENASE E2 DEFICIENCY; PDHDD		HP:0040284	OMIM:245348	IEA						HPO:skoehler	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000007	OMIM:245349	IEA				I		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000218	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000243	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000252	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000286	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000316	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000496	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000648	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0000767	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001249	OMIM:245349	IEA				P		HPO:skoehler	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001250	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001251	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001258	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001263	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001319	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001332	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001338	OMIM:245349	TAS				P		HPO:probinson	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0001942	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0002317	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0002416	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0002510	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0002928	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0003128	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0003348	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0003542	OMIM:245349	IEA				P		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0003577	OMIM:245349	TAS				C		HPO:skoehler	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0003828	OMIM:245349	IEA				C		HPO:iea	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0007010	OMIM:245349	TAS				P		HPO:probinson	
OMIM	245349	PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY		HP:0007015	OMIM:245349	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0000007	OMIM:245400	TAS				I		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0000365	OMIM:245400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0000951	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0000975	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001249	OMIM:245400	IEA				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001250	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001251	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001252	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY	HP:0012828	HP:0001263	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001298	OMIM:245400	IEA				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001508	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001510	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0001943	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0002059	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0002148	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0002275	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0002317	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0002878	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0003128	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0003202	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0003593	OMIM:245400	TAS				C		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0005941	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0008335	OMIM:245400	IEA				P		HPO:iea	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0010864	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0011968	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245400	#245400 MITOCHONDRIAL DNA DEPLETION SYNDROME 9 (ENCEPHALOMYOPATHIC TYPE WITHMETHYLMALONIC ACIDURIA); MTDPS9;;LACTIC ACIDOSIS, FATAL INFANTILE, FORMERLY		HP:0012120	OMIM:245400	TAS				P		HPO:skoehler	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0000007	OMIM:245450	IEA				I		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0000023	OMIM:245450	IEA				P		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0000252	OMIM:245450	IEA				P		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0000494	OMIM:245450	IEA				P		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0000526	OMIM:245450	IEA				P		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0001249	OMIM:245450	IEA				P		HPO:iea	
OMIM	245450	LACTIC ACIDURIA DUE TO D-LACTIC ACID		HP:0003648	OMIM:245450	IEA				P		HPO:skoehler	
OMIM	245480	SPECIFIC GRANULE DEFICIENCY		HP:0000007	PMID:11313242	PCS				I		HPO:probinson	
OMIM	245480	SPECIFIC GRANULE DEFICIENCY		HP:0002718	PMID:11313242	PCS				P		HP:probinson	
OMIM	245480	SPECIFIC GRANULE DEFICIENCY		HP:0011447	OMIM:245480	TAS				P		HPO:probinson	
OMIM	245480	SPECIFIC GRANULE DEFICIENCY		HP:0011993	PMID:10359588	PCS				P		HP:probinson	
OMIM	245480	SPECIFIC GRANULE DEFICIENCY		HP:0012551	OMIM:245480	TAS				P		HPO:probinson	
OMIM	245550	LAMBERT SYNDROME		HP:0000007	OMIM:245550	IEA				I		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000023	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000047	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000154	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000272	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000384	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0000952	OMIM:245550	IEA				P		HPO:skoehler	
OMIM	245550	LAMBERT SYNDROME		HP:0001249	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0001762	OMIM:245550	IEA				P		HPO:iea	
OMIM	245550	LAMBERT SYNDROME		HP:0005248	OMIM:245550	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000007	OMIM:245552	IEA				I		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000160	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000252	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000278	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000316	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000400	OMIM:245552	TAS				P		HPO:skoehler	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000413	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000444	OMIM:245552	TAS				P		HPO:skoehler	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000486	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0000506	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0001511	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0001629	OMIM:245552	TAS				P		HPO:skoehler	
OMIM	245552	LAMBOTTE SYNDROME		HP:0001841	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0001841	OMIM:245552	TAS				P		HPO:probinson	
OMIM	245552	LAMBOTTE SYNDROME		HP:0002507	OMIM:245552	IEA				P		HPO:iea	
OMIM	245552	LAMBOTTE SYNDROME		HP:0007700	OMIM:245552	IEA				P		HPO:iea	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0000006	OMIM:245570	TAS				I		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0000708	OMIM:245570	IEA				P		HPO:iea	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0000750	OMIM:245570	TAS				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0001249	OMIM:245570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0001250	OMIM:245570	IEA				P		HPO:iea	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0001263	OMIM:245570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0002357	OMIM:245570	TAS				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0002381	OMIM:245570	IEA				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0003828	OMIM:245570	TAS				C		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0003829	OMIM:245570	TAS				C		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0007018	OMIM:245570	TAS				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0010524	OMIM:245570	IEA				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0011098	OMIM:245570	TAS				P		HPO:skoehler	
OMIM	245570	LANDAU-KLEFFNER SYNDROME		HP:0012557	OMIM:245570	TAS				P		HPO:probinson	
OMIM	245590	#245590 GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY;;LARON SYNDROME DUE TO POSTRECEPTOR DEFECT;;GROWTH HORMONE INSENSITIVITY DUE TO POSTRECEPTOR DEFECT		HP:0000824	OMIM:245590	IEA				P		HPO:skoehler	
OMIM	245590	#245590 GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY;;LARON SYNDROME DUE TO POSTRECEPTOR DEFECT;;GROWTH HORMONE INSENSITIVITY DUE TO POSTRECEPTOR DEFECT		HP:0002098	OMIM:245590	IEA				P		HPO:skoehler	
OMIM	245590	#245590 GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY;;LARON SYNDROME DUE TO POSTRECEPTOR DEFECT;;GROWTH HORMONE INSENSITIVITY DUE TO POSTRECEPTOR DEFECT		HP:0003510	OMIM:245590	IEA				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000007	OMIM:245600	IEA				I		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000023	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000160	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000175	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000238	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000248	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000274	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000308	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000316	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000369	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000465	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000470	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000494	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000540	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000565	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000574	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000592	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000646	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000691	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000768	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000774	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000776	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000878	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000938	OMIM:245600	TAS	HP:0011463			P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000939	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000973	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0000974	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001087	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001090	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001222	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001252	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001270	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001290	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001388	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001388	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001634	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001640	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001647	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001655	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001712	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001762	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001763	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001772	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001840	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0001852	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002007	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002162	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002616	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002650	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002750	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002757	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002827	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002857	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002974	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0002987	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0003051	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0003834	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0004298	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0004322	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0004976	OMIM:245600	IEA				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0005021	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0005280	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0005616	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0006099	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0008551	OMIM:245600	IEA				P		HPO:iea	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0008593	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0008905	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0009880	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0011220	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0011800	OMIM:245600	TAS				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0012095	OMIM:245600	IEA				P		HPO:skoehler	
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0012368	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245600	MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS		HP:0040160	OMIM:245600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0000007	OMIM:245650	IEA				I		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0001373	OMIM:245650	IEA				P		HPO:skoehler	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0001601	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0001939	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0002089	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0002093	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0002779	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0003811	OMIM:245650	IEA				M		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0008178	OMIM:245650	IEA				P		HPO:iea	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0010444	OMIM:245650	IEA				P		HPO:skoehler	
OMIM	245650	245650 LARSEN-LIKE SYNDROME, LETHAL TYPE		HP:0012095	OMIM:245650	TAS				P		HPO:skoehler	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0000007	OMIM:245660	IEA				I		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0000478	OMIM:245660	IEA				P		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0000705	OMIM:245660	IEA				P		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0001612	OMIM:245660	IEA				P		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0001615	OMIM:245660	IEA				P		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0003593	OMIM:245660	IEA				C		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0008390	OMIM:245660	IEA				P		HPO:iea	
OMIM	245660	LARYNGOONYCHOCUTANEOUS SYNDROME		HP:0200042	OMIM:245660	IEA				P		HPO:skoehler	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0000007	OMIM:245800	IEA				I		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0000046	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0000054	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0000580	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0000639	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0001155	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0001249	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0001251	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0001258	OMIM:245800	IEA				P		HPO:iea	
OMIM	245800	245800 LAURENCE-MOON SYNDROME		HP:0004322	OMIM:245800	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:245900	IEA				I		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0000083	OMIM:245900	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0000093	OMIM:245900	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0001878	OMIM:245900	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0001895	OMIM:245900	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0002155	OMIM:245900	IEA				P		HPO:iea	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0003233	OMIM:245900	TAS				P		HPO:probinson	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0003651	OMIM:245900	IEA				P		HPO:skoehler	
OMIM	245900	LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY		HP:0007759	OMIM:245900	IEA				P		HPO:iea	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0000007	PMID:5694533	PCS				I		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0000505	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0000519	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0001093	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0002023	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0002650	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0002655	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0006824	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0007834	PMID:5694533	PCS	HP:0003577			P		HPO:lccarmody	
OMIM	246000	LEG, ABSENCE DEFORMITY OF, WITH CONGENITAL CATARACT		HP:0009136	PMID:5694533	PCS				P		HPO:lccarmody	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000007	OMIM:246200	IEA				I		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000040	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000138	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000154	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000179	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000212	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000274	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000369	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000400	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000520	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000826	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000842	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000956	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000962	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0000998	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001034	OMIM:246200	IEA				P		HPO:skoehler	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001176	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001395	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001396	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001511	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001525	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0001833	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0002164	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0002719	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0002750	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0003074	OMIM:246200	IEA				P		HPO:skoehler	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0003162	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0003202	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0003270	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0004298	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0004405	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0004428	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0004510	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0008665	OMIM:246200	TAS				P		HPO:skoehler	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0008887	OMIM:246200	IEA				P		HPO:iea	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0008897	OMIM:246200	TAS				P		HPO:skoehler	
OMIM	246200	#246200 DONOHUE SYNDROME;;LEPRECHAUNISMINSULIN RECEPTOR, DEFECT IN, INCLUDED		HP:0011998	OMIM:246200	TAS				P		HPO:skoehler	
OMIM	246300	#246300 LEPROSY, SUSCEPTIBILITY TO, 3; LPRS3		HP:0000006	OMIM:246300	TAS				I		HPO:skoehler	
OMIM	246300	#246300 LEPROSY, SUSCEPTIBILITY TO, 3; LPRS3		HP:0000007	OMIM:246300	IEA				I		HPO:iea	
OMIM	246300	#246300 LEPROSY, SUSCEPTIBILITY TO, 3; LPRS3		HP:0002715	OMIM:246300	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0000007	OMIM:246400	IEA				I		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0000737	OMIM:246400	IEA				P		HPO:skoehler	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0000924	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0000952	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0000980	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001051	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001298	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001433	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001873	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001875	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001903	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0001945	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0002094	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0002113	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0003270	OMIM:246400	IEA				P		HPO:iea	
OMIM	246400	LETTERER-SIWE DISEASE		HP:0010280	OMIM:246400	IEA				P		HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0000007	OMIM:246450	IEA				I	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0000741	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001250	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001257	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001259	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001262	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001263	OMIM:246450	IEA		HP:0040284		P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	HP:0040284
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001336	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001903	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001942	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001943	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001945	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0001987	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD	HP:0031796	HP:0002013	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0002149	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0002240	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0002353	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0002500	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0003150	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0003234	OMIM:246450	TAS				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0003344	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0003819	OMIM:246450	IEA				M	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:iea	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0025356	OMIM:246450	IEA		HP:0040284		P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	HP:0040284
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0032198	OMIM:246450	IEA				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:skoehler	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0410051	PMID:23705938	PCS				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:NicoleVasilevsky	
OMIM	246450	3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD		HP:0410066	PMID:22626821	PCS				P	3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY; HMGCLD	HPO:NicoleVasilevsky	
OMIM	246470	LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER		HP:0000007	OMIM:246470	IEA				I		HPO:iea	
OMIM	246470	LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER		HP:0000119	OMIM:246470	IEA				P		HPO:iea	
OMIM	246470	LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER		HP:0003003	OMIM:246470	TAS				P		HPO:skoehler	
OMIM	246470	LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER		HP:0004808	OMIM:246470	IEA				P		HPO:iea	
OMIM	246470	LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER		HP:0005227	OMIM:246470	IEA				P		HPO:iea	
OMIM	246500	LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS		HP:0000007	OMIM:246500	IEA				I		HPO:iea	
OMIM	246500	LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS		HP:0000668	OMIM:246500	IEA				P		HPO:iea	
OMIM	246500	LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS		HP:0001006	OMIM:246500	IEA				P		HPO:iea	
OMIM	246500	LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS		HP:0001249	OMIM:246500	IEA				P		HPO:iea	
OMIM	246500	LEUKOMELANODERMA, INFANTILISM, MENTAL RETARDATION, HYPODONTIA, HYPOTRICHOSIS		HP:0001510	OMIM:246500	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000007	OMIM:246550	IEA				I		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000286	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000463	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000664	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000670	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME	HP:0012825	HP:0000767	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000939	OMIM:246550	IEA				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0000954	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0001761	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0001875	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0001999	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002086	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002205	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002423	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002659	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002714	OMIM:246550	TAS				P		HPO:probinson	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002719	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0002720	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0003320	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0006070	OMIM:246550	IEA				P		HPO:iea	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0006297	OMIM:246550	TAS				P		HPO:skoehler	
OMIM	246550	246550 LICHTENSTEIN SYNDROME		HP:0009465	OMIM:246550	IEA				P		HPO:iea	
OMIM	246555	LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY		HP:0000007	OMIM:246555	IEA				I		HPO:iea	
OMIM	246555	LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY		HP:0001171	OMIM:246555	IEA				P		HPO:iea	
OMIM	246555	LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY		HP:0001249	OMIM:246555	IEA				P		HPO:iea	
OMIM	246555	LIMB DEFECTS, DISTAL TRANSVERSE, WITH MENTAL RETARDATION AND SPASTICITY		HP:0001258	OMIM:246555	IEA				P		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000006	OMIM:246560	TAS				I		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000007	OMIM:246560	IEA				I		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000089	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000160	OMIM:246560	IEA				P		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000175	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000218	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000308	OMIM:246560	IEA				P		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000327	OMIM:246560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000377	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0000545	OMIM:246560	IEA				P		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0001171	OMIM:246560	IEA				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0001249	OMIM:246560	IEA				P		HPO:iea	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0001807	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0008404	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246560	#246560 SPLIT-HAND/FOOT MALFORMATION 3; SHFM3;;SHSF3;;LIMB DEFICIENCIES, DISTAL, WITH MICROGNATHIA;;CHROMOSOME 10Q24 DUPLICATION SYNDROME		HP:0012385	OMIM:246560	TAS				P		HPO:skoehler	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0000006	OMIM:246570	IEA				I		HPO:iea	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0001155	OMIM:246570	IEA				P		HPO:iea	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0001159	OMIM:246570	IEA				P		HPO:skoehler	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0001180	OMIM:246570	TAS				P		HPO:probinson	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0001849	OMIM:246570	TAS				P		HPO:probinson	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0002982	OMIM:246570	IEA				P		HPO:probinson	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0002990	OMIM:246570	TAS				P		HPO:skoehler	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0003745	OMIM:246570	TAS				I		HPO:skoehler	
OMIM	246570	FIBULAR APLASIA, TIBIAL CAMPOMELIA, AND OLIGOSYNDACTYLY SYNDROME		HP:0006436	OMIM:246570	TAS				P		HPO:probinson	
OMIM	246650	LIPASE DEFICIENCY, COMBINED		HP:0000007	OMIM:246650	IEA				I		HPO:iea	
OMIM	246650	LIPASE DEFICIENCY, COMBINED		HP:0001939	OMIM:246650	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0000007	OMIM:246700	IEA				I		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0000478	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0001249	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0001315	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0001508	OMIM:246700	IEA				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0001510	OMIM:246700	TAS				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0001871	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0002013	OMIM:246700	IEA				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0002014	OMIM:246700	IEA				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0002495	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0002570	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0003073	OMIM:246700	IEA				P		HPO:iea	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0003146	OMIM:246700	IEA				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0003563	OMIM:246700	IEA				P		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0003593	OMIM:246700	IEA				C		HPO:skoehler	
OMIM	246700	#246700 CHYLOMICRON RETENTION DISEASE; CMRD;;ANDERSON DISEASE; ANDD;;LIPID TRANSPORT DEFECT OF INTESTINE;;HYPOBETALIPOPROTEINEMIA WITH ACCUMULATION OF APOLIPOPROTEIN B-LIKEPROTEIN IN INTESTINAL CELLS		HP:0004395	OMIM:246700	IEA				P		HPO:iea	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:246900	TAS				I		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0000252	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001250	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001251	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001254	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001263	OMIM:246900	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY	HP:0025303	HP:0001298	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001332	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001410	OMIM:246900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001639	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001942	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0001943	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0002240	OMIM:246900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0002910	OMIM:246900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0003128	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0003828	OMIM:246900	TAS				C		HPO:skoehler	
OMIM	246900	DIHYDROLIPOAMIDE DEHYDROGENASE DEFICIENCY		HP:0011968	OMIM:246900	TAS				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0000007	OMIM:247100	IEA				I		HPO:iea	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0000718	OMIM:247100	TAS				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0000738	OMIM:247100	TAS				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0001072	OMIM:247100	IEA				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0001250	OMIM:247100	IEA				P		HPO:iea	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0001609	OMIM:247100	IEA				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0002232	OMIM:247100	TAS				P		HPO:skoehler	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0002354	OMIM:247100	IEA				P		HPO:iea	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0005671	OMIM:247100	IEA				P		HPO:iea	
OMIM	247100	LIPOID PROTEINOSIS OF URBACH AND WIETHE		HP:0011999	OMIM:247100	TAS				P		HPO:skoehler	
OMIM	247150	247150 LIP PRINTS		HP:0000007	OMIM:247150	TAS				I		HPO:skoehler	
OMIM	247150	247150 LIP PRINTS		HP:0000159	OMIM:247150	TAS				P		HPO:skoehler	
OMIM	247150	247150 LIP PRINTS		HP:0001426	OMIM:247150	TAS				I		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000006	OMIM:247200	TAS				I		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000023	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000028	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000125	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000175	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000215	PMID:1671808	PCS		HP:0040284		P		HPO:iea	25/25
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000219	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000252	PMID:1671808	PCS		HP:0040284		P		HPO:iea	17/25
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000286	PMID:1671808	PCS		HP:0040284		P		HPO:iea	8/22
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000347	PMID:1671808	PCS		HP:0040284		P		HPO:iea	26/27
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000358	PMID:12621583	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000369	PMID:1671808	PCS		HP:0040284		P		HPO:iea	14/27
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000431	PMID:1671808	PCS		HP:0040284		P		HPO:iea	24/25
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000463	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000518	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000582	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000684	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000954	PMID:1671808	PCS		HP:0040284		P		HPO:iea	5/24
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0000960	PMID:1671808	PCS		HP:0040284		P		HPO:iea	14/19
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001249	OMIM:247200	TAS		HP:0040280		P		HPO:iea	HP:0040280
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001270	OMIM:247200	TAS		HP:0040280		P		HPO:iea	HP:0040280
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001302	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001339	PMID:1671808	PCS		HP:0040284		P		HPO:iea	27/27
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001466	OMIM:247200	TAS				I		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001508	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001511	PMID:1671808	PCS		HP:0040284		P		HPO:iea	8/22
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001511	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001539	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001558	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001561	PMID:1671808	PCS		HP:0040284		P		HPO:iea	6/20
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001627	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0001939	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002007	PMID:12621583	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002079	PMID:1671808	PCS		HP:0040284		P		HPO:iea	17/23
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002100	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002247	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002282	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0002389	PMID:1671808	PCS		HP:0040284		P		HPO:iea	17/22
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0003196	PMID:1671808	PCS		HP:0040284		P		HPO:iea	26/26
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0004209	PMID:1671808	PCS		HP:0040284		P		HPO:iea	10/24
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0006191	PMID:1671808	PCS		HP:0040284		P		HPO:iea	14/21
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0007020	OMIM:247200	TAS				P		HPO:iea	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0007045	PMID:1671808	PCS		HP:0040284		P		HPO:iea	13/24
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0008947	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0009473	PMID:1671808	IEA		HP:0040284		P		HPO:iea	6/27
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0010442	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0012385	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0012469	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0025386	OMIM:247200	TAS				P		HPO:skoehler	
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0030680	PMID:1671808	PCS		HP:0040284		P		HPO:iea	6/27
OMIM	247200	MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS		HP:0031882	OMIM:247200	IEA				P		HPO:skoehler	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000007	OMIM:247410	IEA				I		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000083	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000112	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000431	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000506	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000508	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000518	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000829	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0000998	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0001004	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0001156	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0001634	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0002091	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0003102	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0004322	OMIM:247410	IEA				P		HPO:iea	
OMIM	247410	LYMPHEDEMA-HYPOPARATHYROIDISM SYNDROME		HP:0006521	OMIM:247410	IEA				P		HPO:iea	
OMIM	247420	LUTHERAN NULL		HP:0000007	OMIM:247420	IEA				I		HPO:iea	
OMIM	247420	LUTHERAN NULL		HP:0010971	OMIM:247420	IEA				P		HPO:iea	
OMIM	247430	LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF		HP:0000007	OMIM:247430	IEA				I		HPO:iea	
OMIM	247430	LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF		HP:0001939	OMIM:247430	IEA				P		HPO:iea	
OMIM	247430	LYMPHOBLASTIC TRANSFORMATION, INHIBITION OF		HP:0002728	OMIM:247430	IEA				P		HPO:iea	
OMIM	247450	LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN		HP:0000007	OMIM:247450	IEA				I		HPO:iea	
OMIM	247450	LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN		HP:0001939	OMIM:247450	IEA				P		HPO:iea	
OMIM	247450	LYMPHOBLASTIC TRANSFORMATION, INTRINSIC DEFECT IN		HP:0002728	OMIM:247450	IEA				P		HPO:iea	
OMIM	247610	LYMPHOID INTERSTITIAL PNEUMONIA		HP:0000007	OMIM:247610	IEA				I		HPO:iea	
OMIM	247610	LYMPHOID INTERSTITIAL PNEUMONIA		HP:0001217	OMIM:247610	IEA				P		HPO:iea	
OMIM	247610	LYMPHOID INTERSTITIAL PNEUMONIA		HP:0001648	OMIM:247610	IEA				P		HPO:iea	
OMIM	247610	LYMPHOID INTERSTITIAL PNEUMONIA		HP:0001650	OMIM:247610	IEA				P		HPO:iea	
OMIM	247610	LYMPHOID INTERSTITIAL PNEUMONIA		HP:0006527	OMIM:247610	IEA				P		HPO:iea	
OMIM	247630	247630 LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE		HP:0000007	OMIM:247630	IEA				I		HPO:iea	
OMIM	247630	247630 LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE		HP:0001888	OMIM:247630	IEA				P		HPO:iea	
OMIM	247630	247630 LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE		HP:0002843	OMIM:247630	IEA				P		HPO:iea	
OMIM	247630	247630 LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE		HP:0002850	OMIM:247630	TAS				P		HPO:skoehler	
OMIM	247630	247630 LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE		HP:0004315	OMIM:247630	IEA				P		HPO:iea	
OMIM	247640	LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES		HP:0000007	OMIM:247640	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	247640	LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES		HP:0002665	OMIM:247640	TAS				P		HPO:probinson	
OMIM	247640	LYMPHOBLASTIC LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES		HP:0006727	OMIM:247640	TAS				P		HPO:probinson	
OMIM	247650	LYMPHOKINE DEFICIENCY		HP:0000007	OMIM:247650	IEA				I		HPO:iea	
OMIM	247650	LYMPHOKINE DEFICIENCY		HP:0001939	OMIM:247650	IEA				P		HPO:iea	
OMIM	247650	LYMPHOKINE DEFICIENCY		HP:0002728	OMIM:247650	IEA				P		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0000007	OMIM:247800	IEA				I		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0000099	OMIM:247800	IEA				P		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0001888	OMIM:247800	IEA				P		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0001890	OMIM:247800	IEA				P		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0002090	OMIM:247800	IEA				P		HPO:skoehler	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0010702	OMIM:247800	IEA				P		HPO:iea	
OMIM	247800	%247800 LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS		HP:0030150	OMIM:247800	TAS				P		HPO:skoehler	
OMIM	247950	LYSINE MALABSORPTION SYNDROME		HP:0000007	OMIM:247950	IEA				I		HPO:iea	
OMIM	247950	LYSINE MALABSORPTION SYNDROME		HP:0001249	OMIM:247950	IEA				P		HPO:iea	
OMIM	247950	LYSINE MALABSORPTION SYNDROME		HP:0001510	OMIM:247950	IEA				P		HPO:iea	
OMIM	247950	LYSINE MALABSORPTION SYNDROME		HP:0003297	OMIM:247950	IEA				P		HPO:iea	
OMIM	247950	LYSINE MALABSORPTION SYNDROME		HP:0008272	OMIM:247950	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000007	OMIM:247990	IEA				I		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000050	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000126	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000252	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000294	OMIM:247990	TAS				P		HPO:skoehler	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000358	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0000400	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0001250	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0001263	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0001511	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0001522	OMIM:247990	IEA				M		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0002057	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0002119	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0002236	OMIM:247990	TAS				P		HPO:skoehler	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0002553	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0006610	OMIM:247990	IEA				P		HPO:iea	
OMIM	247990	MACDERMOT-WINTER SYNDROME		HP:0100490	OMIM:247990	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:248000	TAS				I		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000256	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000280	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000303	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000307	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000337	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000483	OMIM:248000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000545	OMIM:248000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000709	OMIM:248000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000716	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0000750	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0001355	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0003011	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0008239	OMIM:248000	IEA				P		HPO:iea	
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0010499	OMIM:248000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248000	MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE		HP:0030799	OMIM:248000	TAS				P		HPO:skoehler	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0000007	OMIM:248010	IEA				I		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0000939	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0001388	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0002208	OMIM:248010	IEA				P		HPO:skoehler	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0002656	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0002757	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0003037	OMIM:248010	TAS				P		HPO:skoehler	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0003199	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0003758	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0004322	OMIM:248010	IEA				P		HPO:iea	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0007495	OMIM:248010	TAS				P		HPO:probinson	
OMIM	248010	MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE		HP:0007602	OMIM:248010	IEA				P		HPO:iea	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0000007	OMIM:248100	IEA				I		HPO:iea	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0000924	OMIM:248100	IEA				P		HPO:iea	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0001513	OMIM:248100	IEA				P		HPO:skoehler	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0001520	OMIM:248100	TAS				P		HPO:skoehler	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0001880	OMIM:248100	IEA				P		HPO:iea	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0002591	OMIM:248100	IEA				P		HPO:iea	
OMIM	248100	248100 MACROSOMIA ADIPOSA CONGENITA		HP:0008256	OMIM:248100	IEA				P		HPO:iea	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0000007	OMIM:248110	IEA				I		HPO:iea	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0000568	OMIM:248110	IEA				P		HPO:iea	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0001507	OMIM:248110	IEA				P		HPO:iea	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0001520	OMIM:248110	TAS				P		HPO:skoehler	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0004880	OMIM:248110	IEA				P		HPO:iea	
OMIM	248110	248110 MACROSOMIA WITH MICROPHTHALMIA, LETHAL		HP:0009099	OMIM:248110	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000007	OMIM:248190	IEA				I		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000010	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000121	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000483	OMIM:248190	IEA				P		HPO:skoehler	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000486	OMIM:248190	IEA				P		HPO:skoehler	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000510	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000545	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000639	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000705	OMIM:248190	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0000787	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0001116	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0002150	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0002917	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0005567	OMIM:248190	IEA				P		HPO:iea	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0012608	OMIM:248190	TAS				P		HPO:skoehler	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0012622	OMIM:248190	TAS				P		HPO:probinson	
OMIM	248190	HYPOMAGNESEMIA 5, RENAL, WITH OR WITHOUT OCULAR INVOLVEMENT; HOMG5		HP:0012637	OMIM:248190	TAS				P		HPO:skoehler	
OMIM	248200	STARGARDT DISEASE 1		HP:0000007	OMIM:248200	TAS				I		HPO:probinson	
OMIM	248200	STARGARDT DISEASE 1		HP:0000608	OMIM:248200	TAS				P		HPO:probinson	
OMIM	248200	STARGARDT DISEASE 1		HP:0008035	OMIM:248200	TAS				P		HPO:probinson	
OMIM	248200	STARGARDT DISEASE 1		HP:0011504	OMIM:248200	TAS		HP:0040284		P		HPO:probinson	15/15
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000007	OMIM:248250	IEA				I		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000010	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000103	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000121	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000483	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000486	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000540	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000545	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000639	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000787	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0000790	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0001250	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0001281	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0001508	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0001947	OMIM:248250	IEA				P		HPO:skoehler	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0001959	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0002027	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0002149	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0002150	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0002917	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0003621	OMIM:248250	IEA				C		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0005567	OMIM:248250	TAS				P		HPO:probinson	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0008872	OMIM:248250	IEA				P		HPO:iea	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0012405	OMIM:248250	TAS				P		HPO:skoehler	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0012608	OMIM:248250	TAS				P		HPO:skoehler	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0012622	OMIM:248250	TAS				P		HPO:probinson	
OMIM	248250	#248250 HYPOMAGNESEMIA 3, RENAL; HOMG3;;HYPOMAGNESEMIA, PRIMARY, DUE TO DEFECT IN RENAL TUBULAR TRANSPORTOF MAGNESIUM;;HYPOMAGNESEMIA, ISOLATED RENAL;;HYPOMAGNESEMIA, FAMILIAL, WITH HYPERCALCIURIA AND NEPHROCALCINOSISHYPERCALCIURIA, CHILDHOOD, SELF-LIMITING, INCLUDED		HP:0012637	OMIM:248250	TAS				P		HPO:skoehler	
OMIM	248260	MAGNESIUM, ELEVATED RED CELL		HP:0000007	OMIM:248260	IEA				I		HPO:iea	
OMIM	248260	MAGNESIUM, ELEVATED RED CELL		HP:0001939	OMIM:248260	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0000007	OMIM:248300	IEA				I		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0000153	OMIM:248300	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0000975	OMIM:248300	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0001156	OMIM:248300	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0001808	OMIM:248300	TAS				P		HPO:probinson	
OMIM	248300	MAL DE MELEDA		HP:0003593	OMIM:248300	IEA				C		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0007553	OMIM:248300	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0008064	OMIM:248300	IEA				P		HPO:iea	
OMIM	248300	MAL DE MELEDA		HP:0010783	OMIM:248300	IEA				P		HPO:skoehler	
OMIM	248310	PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL		HP:0000007	OMIM:248310	IEA				I		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0000007	OMIM:248340	IEA				I		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0000048	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0000054	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0000175	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000204	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000316	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0000365	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000377	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000508	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000537	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000581	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0000808	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0001249	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0001510	OMIM:248340	IEA				P		HPO:iea	
OMIM	248340	3MC SYNDROME 3		HP:0002006	OMIM:248340	IEA				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0002553	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0004322	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0030084	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248340	3MC SYNDROME 3		HP:0100258	OMIM:248340	TAS				P		HPO:skoehler	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0000007	OMIM:248360	IEA				I		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001250	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001252	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001263	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001290	OMIM:248360	TAS				P		HPO:skoehler	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001302	OMIM:248360	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001639	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001942	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001943	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0001946	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0002013	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0002014	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0002019	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0002027	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0003128	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0004322	OMIM:248360	IEA				P		HPO:iea	
OMIM	248360	MALONYL-COA DECARBOXYLASE DEFICIENCY		HP:0012450	OMIM:248360	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000007	OMIM:248370	IEA				I		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000218	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000270	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000287	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000293	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000320	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000347	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000418	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000468	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000468	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000520	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000678	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000685	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000831	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000842	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000894	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0000905	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001070	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001371	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001387	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001425	OMIM:248370	TAS				I		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001596	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0001870	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0002209	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0002645	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003074	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003077	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003621	OMIM:248370	IEA				C		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003635	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003758	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0003761	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0004334	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0006480	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0008897	OMIM:248370	IEA				P		HPO:iea	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0009125	OMIM:248370	TAS				P		HPO:skoehler	
OMIM	248370	#248370 MANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY; MADA;;LIPODYSTROPHY, TYPE A, ASSOCIATED WITH MANDIBULOACRAL DYSPLASIA;;CRANIOMANDIBULAR DERMATODYSOSTOSISMANDIBULOACRAL DYSPLASIA WITH TYPE A LIPODYSTROPHY, ATYPICAL, INCLUDED		HP:0009839	OMIM:248370	IEA				P		HPO:iea	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000007	OMIM:248390	TAS				I		HPO:skoehler	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000175	OMIM:248390	TAS				P		HPO:skoehler	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000272	OMIM:248390	IEA				P		HPO:iea	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000347	OMIM:248390	TAS				P		HPO:skoehler	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000405	OMIM:248390	IEA				P		HPO:skoehler	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000494	OMIM:248390	IEA				P		HPO:iea	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000589	OMIM:248390	IEA				P		HPO:skoehler	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0000652	OMIM:248390	IEA				P		HPO:iea	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0005321	OMIM:248390	IEA				P		HPO:iea	
OMIM	248390	TREACHER COLLINS SYNDROME 3; TCS3		HP:0008551	OMIM:248390	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000154	OMIM:248400	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000218	OMIM:248400	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000272	OMIM:248400	IEA				P		HPO:iea	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000347	OMIM:248400	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000377	OMIM:248400	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000494	OMIM:248400	IEA				P		HPO:iea	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0000652	OMIM:248400	IEA				P		HPO:iea	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0001249	OMIM:248400	IEA				P		HPO:iea	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0002353	OMIM:248400	IEA				P		HPO:skoehler	
OMIM	248400	MANDIBULOFACIAL DYSOSTOSIS WITH MENTAL RETARDATION		HP:0005321	OMIM:248400	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0000007	OMIM:248450	IEA				I		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0000316	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0000528	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME	HP:0012828	HP:0000568	OMIM:248450	PCS				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0000579	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0000625	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0001539	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0001545	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0001595	OMIM:248450	IEA				P		HPO:iea	
OMIM	248450	MANITOBA OCULOTRICHOANAL SYNDROME		HP:0002025	OMIM:248450	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000007	OMIM:248500	IEA				I		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000023	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000158	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000212	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000256	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000272	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000280	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000286	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000294	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000303	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000337	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000400	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000407	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000457	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL	HP:0003676	HP:0000546	PMID:15534274	TAS	HP:0003581			P		HP:probinson	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000574	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000639	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000687	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000768	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000943	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0000998	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001249	OMIM:248500	IEA				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001252	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001257	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001260	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001263	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001272	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001290	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001347	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001510	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001547	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001744	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0001922	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002007	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002059	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002066	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002070	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002171	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002240	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002684	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002718	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0002980	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0003302	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0003487	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0004313	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0004570	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0005469	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0005619	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0007232	OMIM:248500	IEA				P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0007772	OMIM:248500	IEA	HP:0003581			P		HPO:iea	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0011800	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248500	MANNOSIDOSIS, ALPHA B, LYSOSOMAL		HP:0012448	OMIM:248500	TAS				P		HPO:skoehler	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0000007	OMIM:248510	TAS				I		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0000365	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0000503	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0000718	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0000752	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0001014	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0001249	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0001250	OMIM:248510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0001290	OMIM:248510	TAS				P		HPO:skoehler	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0001939	OMIM:248510	IEA				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL	HP:0012825	HP:0001999	OMIM:248510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0002167	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0002719	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0007108	OMIM:248510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	248510	MANNOSIDOSIS, BETA A, LYSOSOMAL		HP:0012066	OMIM:248510	TAS				P		HPO:probinson	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0000007	OMIM:248600	IEA				I		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0000738	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001249	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001250	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001251	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001252	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001254	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001259	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001276	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001290	OMIM:248600	TAS				P		HPO:skoehler	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001507	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001733	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001943	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0001946	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0002013	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0002181	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0003128	OMIM:248600	TAS				P		HPO:probinson	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0008344	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0008872	OMIM:248600	IEA				P		HPO:iea	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0031796	OMIM:248600	IEA				C		HPO:skoehler	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0410066	PMID:22626821	IEA				P		HPO:NicoleVasilevsky	
OMIM	248600	MAPLE SYRUP URINE DISEASE; MSUD		HP:0410066	PMID:19551947	PCS				P		HPO:NicoleVasilevsky	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000006	OMIM:248700	TAS				I		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000007	OMIM:248700	IEA				I		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000023	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000028	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000047	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000054	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000089	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000160	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000175	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000218	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000252	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000260	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000286	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000316	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000343	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000347	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000369	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000463	OMIM:248700	IEA				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000470	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000486	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000508	OMIM:248700	TAS				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000568	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000581	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0000766	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001166	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001249	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001250	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001252	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001274	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001290	OMIM:248700	TAS				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001305	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001321	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001511	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001651	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0001762	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002021	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002044	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002089	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002365	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002476	OMIM:248700	IEA				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002650	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002705	OMIM:248700	TAS				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002803	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002808	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0002974	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0003199	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0005329	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0007068	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0008897	OMIM:248700	TAS				P		HPO:skoehler	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0009473	OMIM:248700	IEA				P		HPO:iea	
OMIM	248700	MARDEN-WALKER SYNDROME		HP:0012385	OMIM:248700	TAS				P		HPO:skoehler	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000007	OMIM:248760	IEA				I		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000083	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000099	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000218	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000252	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0000303	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0001166	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0001249	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0001388	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0001519	OMIM:248760	IEA				P		HPO:iea	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0002705	OMIM:248760	TAS				P		HPO:skoehler	
OMIM	248760	248760 MARFANOID HABITUS WITH MICROCEPHALY AND GLOMERULONEPHRITIS		HP:0002808	OMIM:248760	IEA				P		HPO:skoehler	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0000007	OMIM:248770	IEA				I		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0000098	OMIM:248770	IEA				P		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0000272	OMIM:248770	IEA				P		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0001166	OMIM:248770	IEA				P		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0001249	OMIM:248770	IEA				P		HPO:skoehler	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0001252	OMIM:248770	TAS				P		HPO:skoehler	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0001263	OMIM:248770	IEA				P		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0003758	OMIM:248770	IEA				P		HPO:iea	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0012368	OMIM:248770	TAS				P		HPO:skoehler	
OMIM	248770	MARFANOID MENTAL RETARDATION SYNDROME, AUTOSOMAL		HP:0025356	OMIM:248770	IEA				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000007	OMIM:248800	IEA				I		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000252	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000486	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000519	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000639	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0000815	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001249	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001251	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001257	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001260	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001263	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001290	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001371	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001508	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0001763	OMIM:248800	TAS				P		HPO:probinson	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002066	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002070	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002650	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002673	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002808	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0002967	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003198	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003202	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003236	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003323	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003593	OMIM:248800	TAS				C		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003687	OMIM:248800	TAS				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0003805	OMIM:248800	IEA				P		HPO:skoehler	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0004322	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0008278	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0010049	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0010743	OMIM:248800	IEA				P		HPO:iea	
OMIM	248800	MARINESCO-SJOGREN SYNDROME; MSS		HP:0025356	OMIM:248800	IEA				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0000007	OMIM:248900	IEA				I		HPO:iea	
OMIM	248900	MAST SYNDROME		HP:0000726	OMIM:248900	IEA				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0001258	OMIM:248900	TAS				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0001260	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0001270	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0001288	OMIM:248900	TAS				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0001317	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0001347	OMIM:248900	TAS				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0002015	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0002186	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0002313	OMIM:248900	IEA				P		HPO:iea	
OMIM	248900	MAST SYNDROME		HP:0002476	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0003487	OMIM:248900	TAS				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0003674	OMIM:248900	IEA				C		HPO:iea	
OMIM	248900	MAST SYNDROME		HP:0003677	OMIM:248900	TAS				C		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0003828	OMIM:248900	TAS				C		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0007340	OMIM:248900	TAS				P		HPO:skoehler	
OMIM	248900	MAST SYNDROME		HP:0009830	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248900	MAST SYNDROME		HP:0012672	OMIM:248900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000007	OMIM:248910	IEA				I		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000218	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000252	OMIM:248910	IEA				P		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000347	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000405	OMIM:248910	IEA				P		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000430	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000431	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0000582	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0001000	OMIM:248910	IEA				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0001249	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0001290	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0001939	OMIM:248910	IEA				P		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0002650	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0004322	OMIM:248910	IEA				P		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0008551	OMIM:248910	IEA				P		HPO:iea	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0011968	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0011971	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248910	CUTANEOUS MASTOCYTOSIS, CONDUCTIVE HEARING LOSS AND MICROTIA		HP:0200151	OMIM:248910	TAS				P		HPO:skoehler	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000007	OMIM:248950	IEA				I		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000028	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000221	OMIM:248950	TAS				P		HPO:skoehler	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000303	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000316	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000322	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000347	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000448	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000486	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000508	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000582	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000664	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000689	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000767	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000768	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0000954	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001249	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001540	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001629	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001631	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001642	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001650	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001800	OMIM:248950	TAS				P		HPO:probinson	
OMIM	248950	MCDONOUGH SYNDROME		HP:0001999	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0002751	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0004322	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0008070	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0009466	OMIM:248950	IEA				P		HPO:iea	
OMIM	248950	MCDONOUGH SYNDROME		HP:0030084	OMIM:248950	TAS				P		HPO:skoehler	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000007	OMIM:249000	IEA				I		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000028	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000033	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000061	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000069	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000104	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000113	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000130	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000154	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000175	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000180	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000204	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000238	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000252	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000316	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000340	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000347	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000369	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000465	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000470	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000568	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000601	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000612	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000695	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0000835	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001159	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001162	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001195	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001274	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001305	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001321	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001341	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001408	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001511	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001539	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001562	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001600	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001623	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001643	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001671	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001680	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001744	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001746	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001747	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001829	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0001883	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002023	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002085	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002089	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002308	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002323	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002566	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0002617	OMIM:249000	IEA				P		HPO:skoehler	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0003241	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0004639	OMIM:249000	TAS				P		HPO:probinson	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0005343	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0006267	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0006487	OMIM:249000	IEA				P		HPO:skoehler	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0006872	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0009466	OMIM:249000	IEA				P		HPO:iea	
OMIM	249000	MECKEL SYNDROME, TYPE 1; MKS1		HP:0030084	OMIM:249000	TAS				P		HPO:skoehler	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0000007	OMIM:249100	IEA				I		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0000083	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0000100	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001287	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001369	OMIM:249100	TAS				P		HPO:skoehler	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001701	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001744	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001917	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001954	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0001974	OMIM:249100	TAS				P		HPO:skoehler	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0002027	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0002102	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0002240	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0002586	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0002829	OMIM:249100	IEA				P		HPO:iea	
OMIM	249100	FAMILIAL MEDITERRANEAN FEVER		HP:0003565	OMIM:249100	IEA				P		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0000007	OMIM:249230	IEA				I		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0000175	OMIM:249230	IEA				P		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0000286	OMIM:249230	IEA				P		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0000924	OMIM:249230	IEA				P		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0001999	OMIM:249230	IEA				P		HPO:iea	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0003510	OMIM:249230	IEA				P		HPO:skoehler	
OMIM	249230	MEGAEPIPHYSEAL DWARFISM		HP:0008494	OMIM:249230	IEA				P		HPO:iea	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0000007	OMIM:249240	PCS				I		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0001250	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0001251	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0001257	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0001355	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0002500	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0007266	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249240	MEGALENCEPHALY WITH DYSMYELINATION		HP:0010852	OMIM:249240	PCS				P		HPO:probinson	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000007	OMIM:249270	IEA				I		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000028	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000407	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000546	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000548	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000572	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000639	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000648	OMIM:249270	IEA				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000819	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0000951	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001250	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001251	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001263	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001297	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001609	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001629	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001631	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001638	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001696	OMIM:249270	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001873	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0001924	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0002020	OMIM:249270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0003355	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0004322	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0004860	OMIM:249270	IEA				P		HPO:iea	
OMIM	249270	#249270 THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME; TRMA;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 1 (MEGALOBLASTIC ANEMIA,DIABETES MELLITUS, AND DEAFNESS TYPE); THMD1;;MEGALOBLASTIC ANEMIA, THIAMINE-RESPONSIVE, WITH DIABETES MELLITUSAND SENSORINEURAL DEAFNESS;;ROGERS SYNDROME;;THIAMINE-RESPONSIVE ANEMIA SYNDROME;;THIAMINE-RESPONSIVE MYELODYSPLASIA		HP:0011675	OMIM:249270	TAS				P		HPO:skoehler	
OMIM	249300	249300 MEGALOCORNEA		HP:0000007	OMIM:249300	TAS		HP:0040283		I		HPO:skoehler	HP:0040283
OMIM	249300	249300 MEGALOCORNEA		HP:0000485	OMIM:249300	TAS				P		HPO:skoehler	
OMIM	249300	249300 MEGALOCORNEA		HP:0001417	OMIM:249300	TAS		HP:0040282		I		HPO:skoehler	HP:0040282
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:249310	IEA				I		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000193	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000218	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000252	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000256	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000294	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000311	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000343	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000347	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000378	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000431	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000485	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000494	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000545	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000832	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0000938	OMIM:249310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001166	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001250	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001251	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001252	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001290	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0001763	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002007	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002015	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002120	OMIM:249310	IEA				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002188	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002265	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002370	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002816	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0002857	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0003124	OMIM:249310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0004322	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0005280	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0007676	OMIM:249310	IEA				P		HPO:iea	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0008081	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249310	MEGALOCORNEA-MENTAL RETARDATION SYNDROME		HP:0100693	OMIM:249310	TAS				P		HPO:skoehler	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0000238	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0001250	OMIM:249400	IEA				P		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0001263	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0001268	OMIM:249400	IEA				P		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0001305	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0001522	OMIM:249400	IEA				M		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0002858	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0002861	OMIM:249400	IEA				P		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0003396	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0003745	OMIM:249400	IEA				I		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0005603	OMIM:249400	TAS				P		HPO:skoehler	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0006824	OMIM:249400	IEA				P		HPO:iea	
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0100702	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249400	#249400 MELANOSIS, NEUROCUTANEOUS; NCMS;;NEUROMELANOSIS		HP:0200022	OMIM:249400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000007	OMIM:249420	TAS				I		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000154	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000212	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000218	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000260	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000270	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000280	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000293	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000316	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000347	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000369	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000411	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000455	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000494	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000501	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000520	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000557	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000689	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000767	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000916	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000938	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0000939	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001061	OMIM:249420	IEA				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001090	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001270	OMIM:249420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001385	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001510	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001627	OMIM:249420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001634	PMID:24105366	PCS				P		HPO:probinson	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001762	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0001840	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0002645	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0003015	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0003026	OMIM:249420	TAS				P		HPO:probinson	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0004611	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0005469	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0005731	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0006487	OMIM:249420	TAS				P		HPO:probinson	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0009803	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0011220	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0030680	OMIM:249420	IEA				P		HPO:iea	
OMIM	249420	FRANK-TER HAAR SYNDROME; FTHS		HP:0040016	OMIM:249420	TAS				P		HPO:skoehler	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0000007	OMIM:249500	IEA				I		HPO:iea	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0000486	OMIM:249500	IEA				P		HPO:iea	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0000639	OMIM:249500	IEA				P		HPO:iea	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0001249	OMIM:249500	IEA				P		HPO:iea	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0003487	OMIM:249500	TAS				P		HPO:probinson	
OMIM	249500	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1		HP:0006801	OMIM:249500	TAS				P		HPO:probinson	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000007	OMIM:249599	IEA				I		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000276	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000303	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000445	OMIM:249599	IEA				P		HPO:skoehler	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000490	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000589	OMIM:249599	IEA				P		HPO:skoehler	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000815	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0000819	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0001250	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0002342	OMIM:249599	IEA				P		HPO:iea	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0003191	OMIM:249599	TAS				P		HPO:probinson	
OMIM	249599	MENTAL RETARDATION SYNDROME, BELGIAN TYPE		HP:0003782	OMIM:249599	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0000007	OMIM:249600	IEA				I		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0000460	OMIM:249600	TAS				P		HPO:probinson	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0000486	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0000639	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0001249	OMIM:249600	TAS				P		HPO:skoehler	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0001256	OMIM:249600	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0001763	OMIM:249600	IEA				P		HPO:skoehler	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0002987	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0003083	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0005093	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0008850	OMIM:249600	IEA				P		HPO:iea	
OMIM	249600	MENTAL RETARDATION SYNDROME, MIETENS-WEBER TYPE		HP:0009821	OMIM:249600	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000006	OMIM:249620	IEA				I		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000028	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000046	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000093	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000160	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000233	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000286	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000319	OMIM:249620	TAS				P		HPO:probinson	
OMIM	249620	OHDO SYNDROME		HP:0000343	OMIM:249620	TAS				P		HPO:probinson	
OMIM	249620	OHDO SYNDROME		HP:0000347	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000365	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000402	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000431	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000463	OMIM:249620	TAS				P		HPO:probinson	
OMIM	249620	OHDO SYNDROME		HP:0000508	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000535	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000581	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0000685	OMIM:249620	IEA				P		HPO:skoehler	
OMIM	249620	OHDO SYNDROME		HP:0000687	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0001249	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0001250	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0001252	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0001290	OMIM:249620	TAS				P		HPO:skoehler	
OMIM	249620	OHDO SYNDROME		HP:0001388	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0001760	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0003196	OMIM:249620	TAS				P		HPO:probinson	
OMIM	249620	OHDO SYNDROME		HP:0004209	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0004322	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0005280	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0008551	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0008872	OMIM:249620	IEA				P		HPO:iea	
OMIM	249620	OHDO SYNDROME		HP:0030680	OMIM:249620	TAS				P		HPO:probinson	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000007	OMIM:249630	IEA				I		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000047	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000154	OMIM:249630	PCS				P		HPO:probinson	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000218	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000219	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000219	OMIM:249630	TAS				P		HPO:skoehler	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000238	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000252	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000303	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000316	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000348	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000369	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000411	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000431	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000448	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000486	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000494	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000508	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000527	OMIM:249630	PCS				P		HPO:probinson	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000545	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000635	OMIM:249630	IEA				P		HPO:skoehler	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000670	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000689	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000767	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0000768	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0001249	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0001338	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0001508	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0001631	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0001763	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0002064	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0002286	OMIM:249630	PCS				P		HPO:probinson	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0004209	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0005248	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0007665	OMIM:249630	PCS				P		HPO:probinson	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0008407	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0008425	OMIM:249630	IEA				P		HPO:iea	
OMIM	249630	MENTAL RETARDATION, BUENOS AIRES TYPE		HP:0008872	OMIM:249630	IEA				P		HPO:iea	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0000007	OMIM:249650	IEA				I		HPO:iea	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0000218	OMIM:249650	IEA				P		HPO:iea	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0001249	OMIM:249650	IEA				P		HPO:iea	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0002069	OMIM:249650	TAS				P		HPO:skoehler	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0002375	OMIM:249650	TAS				P		HPO:probinson	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0002705	OMIM:249650	TAS				P		HPO:skoehler	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0003355	OMIM:249650	IEA				P		HPO:iea	
OMIM	249650	%249650 MERCAPTOLACTATE-CYSTEINE DISULFIDURIA; MCDU;;DISULFIDURIA, MIXED		HP:0005280	OMIM:249650	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0000007	OMIM:249660	IEA				I		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0000083	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0000100	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0000639	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0000648	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0001249	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0001967	OMIM:249660	IEA				P		HPO:iea	
OMIM	249660	MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES		HP:0008043	OMIM:249660	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0000007	OMIM:249670	IEA				I		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0000232	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0000473	OMIM:249670	IEA				P		HPO:skoehler	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001161	OMIM:249670	IEA				P		HPO:skoehler	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001256	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001629	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001631	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001642	OMIM:249670	TAS				P		HPO:skoehler	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0001643	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0003241	OMIM:249670	IEA				P		HPO:iea	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0004150	OMIM:249670	IEA				P		HPO:skoehler	
OMIM	249670	MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION		HP:0004322	OMIM:249670	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0000007	OMIM:249700	IEA				I		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0000347	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0002938	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0002984	OMIM:249700	IEA				P		HPO:skoehler	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0002986	OMIM:249700	TAS				P		HPO:probinson	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0003022	OMIM:249700	TAS				P		HPO:probinson	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0003027	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0003067	OMIM:249700	TAS				P		HPO:probinson	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0003993	OMIM:249700	TAS				P		HPO:skoehler	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0006381	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0006436	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0008845	OMIM:249700	IEA				P		HPO:iea	
OMIM	249700	#249700 LANGER MESOMELIC DYSPLASIA; LMD;;DYSCHONDROSTEOSIS, HOMOZYGOUS;;MESOMELIC DWARFISM OF THE HYPOPLASTIC ULNA, FIBULA, AND MANDIBLE TYPE		HP:0100864	OMIM:249700	IEA				P		HPO:iea	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0000007	OMIM:249710	IEA				I		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0000175	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0000278	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0000347	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0002979	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0004987	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0005011	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0006488	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249710	MESOMELIC LIMB SHORTENING AND BOWING		HP:0100490	OMIM:249710	IEA				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0000007	OMIM:249900	IEA				I		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0000020	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0000762	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001250	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001252	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001260	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001263	OMIM:249900	PCS				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001265	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001268	OMIM:249900	TAS				P		HPO:skoehler	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001271	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001285	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001290	OMIM:249900	TAS				P		HPO:skoehler	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001324	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001324	OMIM:249900	TAS				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0001347	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0002015	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0002066	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0002371	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0002376	OMIM:249900	PCS				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0002518	OMIM:249900	PCS				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0003487	OMIM:249900	IEA				P		HPO:iea	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0003828	OMIM:249900	TAS				C		HPO:skoehler	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0007305	OMIM:249900	PCS				P		HPO:probinson	
OMIM	249900	METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY		HP:0011096	OMIM:249900	TAS				P		HPO:skoehler	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000007	OMIM:250100	IEA				I		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000020	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000648	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000712	OMIM:250100	PCS				P		HPO:probinson	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000738	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000746	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0000762	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001082	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001249	OMIM:250100	TAS				P		HPO:skoehler	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001250	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001251	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001252	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001260	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001265	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001268	OMIM:250100	PCS				P		HPO:probinson	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001283	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001288	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001290	OMIM:250100	TAS				P		HPO:skoehler	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001332	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0001347	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002072	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002371	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002445	OMIM:250100	TAS				P		HPO:skoehler	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002500	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002510	OMIM:250100	PCS				P		HPO:probinson	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0002922	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0003445	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0003487	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0005609	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0007133	OMIM:250100	IEA				P		HPO:iea	
OMIM	250100	METACHROMATIC LEUKODYSTROPHY		HP:0011096	OMIM:250100	PCS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000007	OMIM:250215	IEA				I		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000272	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000286	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000431	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000463	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000506	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0000926	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0001156	OMIM:250215	IEA				P		HPO:skoehler	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0001249	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0001363	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0001831	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002007	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002650	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002673	OMIM:250215	IEA				P		HPO:skoehler	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002684	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002970	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002982	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0002983	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0003016	OMIM:250215	TAS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0003021	OMIM:250215	TAS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0003275	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0003311	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0003510	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0004279	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0004586	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0005616	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA	HP:0012825	HP:0005792	OMIM:250215	TAS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0006059	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0006205	OMIM:250215	TAS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA	HP:0012828	HP:0009381	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0009803	OMIM:250215	TAS				P		HPO:probinson	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0010049	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0010230	OMIM:250215	IEA				P		HPO:iea	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0011220	OMIM:250215	TAS				P		HPO:skoehler	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0011800	OMIM:250215	TAS				P		HPO:skoehler	
OMIM	250215	METAPHYSEAL ACROSCYPHODYSPLASIA		HP:0012368	OMIM:250215	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000007	OMIM:250220	TAS				I		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000262	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000358	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000470	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000773	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000774	OMIM:250220	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000878	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000887	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0000926	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001156	OMIM:250220	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001290	OMIM:250220	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001582	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001631	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001762	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0001831	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0002132	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0002657	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0002663	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0002869	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003021	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003025	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003026	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003085	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003180	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0003375	OMIM:250220	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0004491	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0004688	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0005280	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0006059	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0007187	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0008786	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0008798	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0008905	OMIM:250220	TAS				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0009381	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0009803	OMIM:250220	IEA				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0010049	OMIM:250220	IEA				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0010230	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0011675	OMIM:250220	TAS				P		HPO:probinson	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0012819	OMIM:250220	IEA				P		HPO:skoehler	
OMIM	250220	SPONDYLOMETAPHYSEAL DYSPLASIA, SEDAGHATIAN TYPE; SMDS		HP:0031233	PMID:24706940	PCS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0000007	OMIM:250230	IEA				I		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0000189	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0000444	OMIM:250230	IEA				P		HPO:skoehler	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0000774	OMIM:250230	TAS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0000946	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001270	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001377	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001799	OMIM:250230	TAS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001821	OMIM:250230	IEA				P		HPO:skoehler	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001821	OMIM:250230	TAS				P		HPO:skoehler	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0001831	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0002086	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0002944	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0002983	OMIM:250230	TAS				P		HPO:skoehler	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0003016	OMIM:250230	TAS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0003025	OMIM:250230	TAS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0003037	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0003411	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0005871	OMIM:250230	TAS				P		HPO:probinson	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0006094	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0008828	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0008873	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0009803	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0009826	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0010049	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0010230	OMIM:250230	IEA				P		HPO:iea	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0010743	OMIM:250230	TAS				P		HPO:skoehler	
OMIM	250230	250230 METAPHYSEAL CHONDRODYSPLASIA, KAITILA TYPE		HP:0100255	OMIM:250230	IEA				P		HPO:skoehler	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0000007	OMIM:250250	TAS				I		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0000248	OMIM:250250	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0000535	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0000653	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0001377	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0001382	OMIM:250250	TAS				P		HPO:skoehler	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0001875	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0001888	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0001972	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002024	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002032	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002213	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002251	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002286	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002644	OMIM:250250	IEA				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH	HP:0012825	HP:0002650	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002665	PMID:11124791	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002938	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0002980	OMIM:250250	TAS				P		HPO:skoehler	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0003016	PMID:10494084	PCS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0003021	PMID:10494084	PCS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0003311	OMIM:250250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0003347	OMIM:250250	PCS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0004279	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0004810	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0005360	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0005374	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0006589	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0007464	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0008069	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0008450	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0008921	OMIM:250250	IEA				P		HPO:probinson	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0031087	OMIM:250250	IEA				P		HPO:skoehler	
OMIM	250250	CARTILAGE-HAIR HYPOPLASIA; CHH		HP:0100255	OMIM:250250	TAS				P		HPO:probinson	
OMIM	250300	METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE		HP:0000007	OMIM:250300	IEA				I		HPO:iea	
OMIM	250300	METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE		HP:0001939	OMIM:250300	IEA				P		HPO:iea	
OMIM	250300	METAPHYSEAL CHONDRODYSPLASIA, PENA TYPE		HP:0005871	OMIM:250300	TAS				P		HPO:probinson	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0000007	OMIM:250400	IEA				I		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0000234	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0001270	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0002515	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0002857	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0003016	OMIM:250400	TAS				P		HPO:probinson	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0003498	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0004979	OMIM:250400	TAS				P		HPO:probinson	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0005871	OMIM:250400	TAS				P		HPO:probinson	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0006385	OMIM:250400	IEA				P		HPO:iea	
OMIM	250400	METAPHYSEAL CHONDRODYSPLASIA, SPAHR TYPE		HP:0006409	OMIM:250400	IEA				P		HPO:iea	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000007	OMIM:250410	IEA				I		HPO:iea	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000085	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000107	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000256	OMIM:250410	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000347	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000369	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000400	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000430	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000494	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000510	OMIM:250410	IEA				P		HPO:iea	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0000750	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001156	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001249	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001263	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001363	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001629	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0001792	OMIM:250410	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0002007	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0004322	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0005871	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0009882	OMIM:250410	IEA				P		HPO:iea	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0010049	OMIM:250410	TAS				P		HPO:iea	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0011968	OMIM:250410	TAS				P		HPO:skoehler	
OMIM	250410	RETINITIS PIGMENTOSA WITH OR WITHOUT SKELETAL ANOMALIES; RPSKA		HP:0025356	OMIM:250410	IEA				P		HPO:skoehler	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000007	OMIM:250420	IEA				I		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000403	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000405	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000486	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000540	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000773	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000887	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0000911	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001134	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001156	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001169	OMIM:250420	TAS				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001256	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001388	OMIM:250420	IEA				P		HPO:skoehler	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001498	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001513	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001597	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001769	OMIM:250420	IEA				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0001773	OMIM:250420	IEA				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002650	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002812	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002857	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002868	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002938	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0002970	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0003016	OMIM:250420	TAS				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0003021	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0003025	OMIM:250420	TAS				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0003026	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0003796	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0004279	OMIM:250420	TAS				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0005899	OMIM:250420	TAS				P		HPO:probinson	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0006009	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0006606	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0008873	OMIM:250420	IEA				P		HPO:iea	
OMIM	250420	METAPHYSEAL DYSOSTOSIS, MENTAL RETARDATION, AND CONDUCTIVE DEAFNESS		HP:0100255	OMIM:250420	IEA				P		HPO:iea	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0000007	OMIM:250450	IEA				I		HPO:iea	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0000648	OMIM:250450	IEA				P		HPO:iea	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0001293	OMIM:250450	IEA				P		HPO:iea	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0004334	OMIM:250450	IEA				P		HPO:skoehler	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0007401	OMIM:250450	IEA				P		HPO:skoehler	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0032026	OMIM:250450	IEA				P		HPO:skoehler	
OMIM	250450	METAPHYSEAL DYSPLASIA, ANETODERMA, AND OPTIC ATROPHY		HP:0100255	OMIM:250450	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0000007	OMIM:250460	IEA				I		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0000925	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0001388	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0001595	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0002644	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0002715	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0002970	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0002983	OMIM:250460	TAS				P		HPO:skoehler	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0003025	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0003026	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0003510	OMIM:250460	IEA				P		HPO:skoehler	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0006028	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0010049	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0010230	OMIM:250460	IEA				P		HPO:iea	
OMIM	250460	#250460 METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS;;CARTILAGE-HAIR HYPOPLASIA-LIKE SKELETAL DYSPLASIA WITHOUT HYPOTRICHOSISOR IMMUNODEFICIENCY;;CARTILAGE-HAIR HYPOPLASIA VARIANT, SKELETAL MANIFESTATIONS ONLY; CHHV		HP:0100255	OMIM:250460	IEA				P		HPO:iea	
OMIM	250500	METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA		HP:0000007	OMIM:250500	IEA				I		HPO:iea	
OMIM	250500	METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA		HP:0000951	OMIM:250500	IEA				P		HPO:iea	
OMIM	250500	METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA		HP:0001258	OMIM:250500	IEA				P		HPO:iea	
OMIM	250500	METAPHYSEAL MODELING ABNORMALITY, SKIN LESIONS, AND SPASTIC PARAPLEGIA		HP:0011001	OMIM:250500	IEA				P		HPO:iea	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0000007	OMIM:250620	IEA				I		HPO:iea	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0000286	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0000486	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0000639	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0000925	OMIM:250620	IEA				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001250	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001263	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001274	OMIM:250620	IEA				P		HPO:iea	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001290	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001310	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001332	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001336	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001636	OMIM:250620	IEA				P		HPO:iea	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0001999	OMIM:250620	IEA				P		HPO:iea	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0002376	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0003355	OMIM:250620	IEA				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0003468	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0003593	OMIM:250620	TAS				C		HPO:skoehler	
OMIM	250620	3-HYDROXYISOBUTYRYL-COA HYDROLASE DEFICIENCY		HP:0011968	OMIM:250620	TAS				P		HPO:skoehler	
OMIM	250650	METHANE PRODUCTION		HP:0000007	OMIM:250650	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	250650	METHANE PRODUCTION		HP:0001438	OMIM:250650	IEA				P		HPO:iea	
OMIM	250650	METHANE PRODUCTION		HP:0003003	OMIM:250650	IEA				P		HPO:skoehler	
OMIM	250700	250700 METHEMOGLOBIN REDUCTASE DEFICIENCY;;NADPH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY;;TPNH-METHEMOGLOBIN REDUCTASE DEFICIENCY		HP:0000007	OMIM:250700	IEA				I		HPO:probinson	
OMIM	250700	250700 METHEMOGLOBIN REDUCTASE DEFICIENCY;;NADPH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY;;TPNH-METHEMOGLOBIN REDUCTASE DEFICIENCY		HP:0001877	OMIM:250700	TAS				P		HPO:probinson	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000007	OMIM:250790	IEA				I		HPO:iea	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000037	OMIM:250790	TAS				P		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000047	OMIM:250790	IEA				P		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000048	OMIM:250790	IEA				P		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000054	OMIM:250790	IEA				P		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000062	OMIM:250790	IEA				P		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0000961	OMIM:250790	IEA				P		HPO:iea	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0001939	OMIM:250790	IEA				P		HPO:iea	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0003593	OMIM:250790	TAS				C		HPO:skoehler	
OMIM	250790	METHEMOGLOBINEMIA AND AMBIGUOUS GENITALIA; METAG		HP:0012119	OMIM:250790	TAS				P		HPO:skoehler	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0000007	OMIM:250800	IEA				I		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0000252	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0000486	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0000961	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0001249	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0001263	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0001276	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0001510	OMIM:250800	IEA				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0001901	OMIM:250800	TAS				P		HPO:iea	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0002179	OMIM:250800	TAS				P		HPO:skoehler	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0002315	OMIM:250800	IEA				P		HPO:probinson	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0002875	OMIM:250800	TAS				P		HPO:probinson	
OMIM	250800	METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE		HP:0012119	OMIM:250800	TAS				P		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0000006	OMIM:250850	PCS				I		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0000007	OMIM:250850	PCS				I		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0001249	OMIM:250850	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0001332	OMIM:250850	PCS				P		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0001347	OMIM:250850	PCS				P		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0003235	OMIM:250850	PCS				P		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0007305	OMIM:250850	PCS				P		HPO:probinson	
OMIM	250850	#250850 METHIONINE ADENOSYLTRANSFERASE DEFICIENCY;;MAT DEFICIENCY;;MAT I/III DEFICIENCY;;HYPERMETHIONINEMIA, ISOLATED PERSISTENT		HP:0011096	OMIM:250850	TAS				P		HPO:skoehler	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0000007	OMIM:250900	IEA				I		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0000635	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0001249	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0001250	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0002014	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0002789	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0003355	OMIM:250900	IEA				P		HPO:skoehler	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0003612	OMIM:250900	IEA				P		HPO:iea	
OMIM	250900	%250900 METHIONINE MALABSORPTION SYNDROME;;SMITH-STRANG DISEASE;;OASTHOUSE URINE DISEASE		HP:0011364	OMIM:250900	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0000007	OMIM:250940	IEA				I		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0000618	OMIM:250940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0000639	OMIM:250940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001249	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001250	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001263	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001288	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001290	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001508	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0001889	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0002059	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0002156	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0002160	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0002370	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0003223	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0003524	OMIM:250940	TAS				P		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0003593	OMIM:250940	TAS				C		HPO:skoehler	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0003658	OMIM:250940	IEA				P		HPO:iea	
OMIM	250940	HOMOCYSTINURIA-MEGALOBLASTIC ANEMIA, CBLG COMPLEMENTATION TYPE		HP:0008872	OMIM:250940	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0000007	OMIM:250950	IEA				I		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0000020	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0000648	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0000736	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0000750	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001251	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001260	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001263	OMIM:250950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001270	OMIM:250950	IEA				P		HPO:skoehler	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001332	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001347	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001508	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0001942	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0002059	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0002305	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0002352	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0002373	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0002510	OMIM:250950	IEA				P		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0003535	OMIM:250950	IEA				P		HPO:skoehler	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0003593	OMIM:250950	IEA				C		HPO:iea	
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0025356	OMIM:250950	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	250950	3-METHYLGLUTACONIC ACIDURIA, TYPE I; MGCA1		HP:0100543	OMIM:250950	TAS				P		HPO:skoehler	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0000007	OMIM:250951	IEA				I		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0000023	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0000028	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0000954	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0001263	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0001284	OMIM:250951	TAS				P		HPO:probinson	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0001319	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0001682	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0002643	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0003344	OMIM:250951	IEA				P		HPO:iea	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0007033	OMIM:250951	TAS				P		HPO:probinson	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0011344	OMIM:250951	TAS				P		HPO:skoehler	
OMIM	250951	3-@METHYLGLUTACONIC ACIDURIA, TYPE IV		HP:0200128	OMIM:250951	TAS				P		HPO:skoehler	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0000007	OMIM:251000	IEA				I		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001252	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001254	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001259	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001263	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001290	OMIM:251000	TAS				P		HPO:skoehler	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001508	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001638	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001733	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001873	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001882	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001944	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001970	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0001987	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002013	OMIM:251000	IEA				P		HPO:skoehler	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002154	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002188	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002240	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002453	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0002912	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0003774	OMIM:251000	IEA				P		HPO:iea	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0005979	OMIM:251000	TAS				P		HPO:probinson	
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0011695	OMIM:251000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251000	METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-COA MUTASE DEFICIENCY		HP:0012120	OMIM:251000	TAS				P		HPO:skoehler	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0000007	OMIM:251100	IEA				I		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001250	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001252	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001254	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001259	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001263	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001290	OMIM:251100	TAS				P		HPO:skoehler	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001337	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001508	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001873	OMIM:251100	TAS				P		HPO:skoehler	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001875	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001876	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001903	OMIM:251100	TAS				P		HPO:skoehler	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001942	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001944	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001946	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0001987	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002013	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002098	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002154	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002240	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002912	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0002919	OMIM:251100	IEA				P		HPO:skoehler	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0003145	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0003210	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0003593	OMIM:251100	IEA				C		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0008872	OMIM:251100	IEA				P		HPO:iea	
OMIM	251100	METHYLMALONIC ACIDURIA, CBLA TYPE		HP:0012120	OMIM:251100	TAS				P		HPO:skoehler	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0000007	OMIM:251110	IEA				I		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001252	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001254	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001259	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001263	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001290	OMIM:251110	TAS				P		HPO:skoehler	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001508	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001873	OMIM:251110	TAS				P		HPO:skoehler	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001875	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001876	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001903	OMIM:251110	TAS				P		HPO:skoehler	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001942	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001944	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001946	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0001987	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002013	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002098	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002154	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002240	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002912	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0002919	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0003145	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0003210	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0003623	OMIM:251110	IEA				C		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0008872	OMIM:251110	IEA				P		HPO:iea	
OMIM	251110	METHYLMALONIC ACIDURIA, CBLB TYPE		HP:0012120	OMIM:251110	TAS				P		HPO:skoehler	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0000007	OMIM:251120	IEA				I	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0001508	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0001942	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0001944	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0002020	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0002912	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED		HP:0002919	OMIM:251120	IEA				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:iea	
OMIM	251120	#251120 METHYLMALONYL-CoA EPIMERASE DEFICIENCY;;METHYLMALONYL-CoA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-CoA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HP:0012825	HP:0012120	OMIM:251120	TAS				P	#251120 METHYLMALONYL-COA EPIMERASE DEFICIENCY;;METHYLMALONYL-COA RACEMASE DEFICIENCY;;METHYLMALONIC ACIDURIA III, FORMERLYMETHYLMALONYL-COA EPIMERASE DEFICIENCY WITH SEPIAPTERIN REDUCTASEDEFICIENCY, INCLUDED	HPO:skoehler	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0000007	OMIM:251190	IEA				I		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0000252	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE	HP:0012825	HP:0000347	OMIM:251190	TAS				P		HPO:probinson	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0000494	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0000518	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0001249	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0001511	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0001773	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0001875	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0002205	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0002750	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0002850	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0003510	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0003795	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0004279	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0004315	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0005819	OMIM:251190	TAS				P		HPO:probinson	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0006297	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0009466	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0009638	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0010107	OMIM:251190	IEA				P		HPO:iea	
OMIM	251190	251190 MICROCEPHALIC PRIMORDIAL DWARFISM, TORIELLO TYPE		HP:0030084	OMIM:251190	TAS				P		HPO:skoehler	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0000007	OMIM:251200	IEA				I		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0000252	OMIM:251200	IEA				P		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0001249	OMIM:251200	IEA				P		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0001250	OMIM:251200	IEA				P		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0002472	OMIM:251200	IEA				P		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0003451	OMIM:251200	IEA				P		HPO:iea	
OMIM	251200	MICROCEPHALY, PRIMARY AUTOSOMAL RECESSIVE, 1		HP:0004322	OMIM:251200	TAS	HP:0003593	HP:0040283		P		HPO:iea	HP:0040283
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0000007	OMIM:251220	IEA				I		HPO:iea	
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0000252	OMIM:251220	IEA				P		HPO:iea	
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001249	OMIM:251220	IEA				P		HPO:iea	
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001644	OMIM:251220	IEA				P		HPO:iea	
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0001852	OMIM:251220	IEA				P		HPO:iea	
OMIM	251220	MICROCEPHALY-CARDIOMYOPATHY		HP:0004209	OMIM:251220	IEA				P		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000007	OMIM:251230	IEA				I		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000160	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000175	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000252	OMIM:251230	IEA				P		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000444	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000445	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000476	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0000568	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0001155	OMIM:251230	TAS				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0001511	OMIM:251230	IEA				P		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0001562	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0001762	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0002983	OMIM:251230	IEA				P		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0003041	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0003974	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0005736	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0007370	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0009821	OMIM:251230	IEA				P		HPO:iea	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0009879	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0012165	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251230	MICROCEPHALY-MICROMELIA SYNDROME; MIMIS		HP:0012745	OMIM:251230	IEA				P		HPO:skoehler	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000007	OMIM:251240	IEA				I		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000135	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000252	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000340	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000347	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000400	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000411	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0000444	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0001371	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0002650	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0002719	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0003065	OMIM:251240	IEA				P		HPO:iea	
OMIM	251240	MICROCEPHALY WITH CHEMOTACTIC DEFECT AND TRANSIENT HYPOGAMMAGLOBULINEMIA		HP:0005432	OMIM:251240	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0000007	OMIM:251250	IEA				I		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0000252	OMIM:251250	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0001249	OMIM:251250	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0002176	OMIM:251250	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0002948	OMIM:251250	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0004322	OMIM:251250	IEA				P		HPO:iea	
OMIM	251250	MICROCEPHALY WITH CERVICAL SPINE FUSION ANOMALIES		HP:0005881	OMIM:251250	IEA				P		HPO:iea	
OMIM	251255	Jawad syndrome		HP:0000007	PMID:21998596	PCS				I	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0000278	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:skoehler	
OMIM	251255	Jawad syndrome		HP:0000448	PMID:21998596	PCS				P	JAWAD SYNDROME	HPO:skoehler	
OMIM	251255	Jawad syndrome		HP:0000718	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:skoehler	
OMIM	251255	Jawad syndrome		HP:0001249	PMID:21998596	PCS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0001263	PMID:21998596	PCS				P	JAWAD SYNDROME	HP:probinson	
OMIM	251255	Jawad syndrome		HP:0001822	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0002943	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:skoehler	
OMIM	251255	Jawad syndrome		HP:0004220	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0004692	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0005780	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0006216	OMIM:251255	TAS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251255	Jawad syndrome		HP:0011451	PMID:21998596	PCS				P	JAWAD SYNDROME	HPO:probinson	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000007	OMIM:251260	IEA				I		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000010	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000126	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000175	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000204	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000246	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000252	OMIM:251260	TAS				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000265	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000340	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000347	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000388	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000400	OMIM:251260	TAS				P		HPO:probinson	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000453	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000582	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000752	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0000957	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0001249	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0001511	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0001873	OMIM:251260	IEA				P		HPO:skoehler	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0001890	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002014	OMIM:251260	TAS				P		HPO:skoehler	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002023	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002025	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002110	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002180	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002665	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002837	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002859	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002885	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0002961	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0003189	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0004322	OMIM:251260	TAS				P		HPO:skoehler	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0004798	OMIM:251260	TAS				P		HPO:skoehler	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0005403	OMIM:251260	TAS				P		HPO:skoehler	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0005602	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0006532	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0008209	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0009733	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0010620	OMIM:251260	IEA				P		HPO:iea	
OMIM	251260	NIJMEGEN BREAKAGE SYNDROME		HP:0010976	OMIM:251260	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000007	OMIM:251270	IEA				I		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000252	OMIM:251270	IEA				P		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000340	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000505	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000518	OMIM:251270	IEA				P		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000541	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000543	OMIM:251270	IEA				P		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000556	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000568	OMIM:251270	IEA				P		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0000639	OMIM:251270	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001000	OMIM:251270	IEA				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001249	OMIM:251270	IEA				P		HPO:iea	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001250	OMIM:251270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001263	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001302	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0001321	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0002059	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0003577	OMIM:251270	TAS				C		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0004322	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0007703	OMIM:251270	TAS				P		HPO:probinson	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0007731	PMID:11146476	PCS				P		HPO:probinson	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0008052	OMIM:251270	TAS				P		HPO:probinson	
OMIM	251270	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 1; MCCRP1		HP:0009879	OMIM:251270	TAS				P		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0000007	OMIM:251280	IEA				I		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0000252	OMIM:251280	IEA				P		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0001263	OMIM:251280	IEA				P		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0001332	OMIM:251280	IEA				P		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0001347	OMIM:251280	IEA				P		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0002123	OMIM:251280	IEA	HP:0003593			P		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0002187	OMIM:251280	IEA				P		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0002510	OMIM:251280	IEA				P		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0003593	OMIM:251280	IEA				C		HPO:iea	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0003593	OMIM:251280	TAS				C		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0005484	OMIM:251280	TAS				P		HPO:skoehler	
OMIM	251280	MICROCEPHALY, SEIZURES, SPASTICITY, AND BRAIN CALCIFICATIONS; MISSBC		HP:0008936	OMIM:251280	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000007	OMIM:251290	IEA				I		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000083	OMIM:251290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000218	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000252	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000308	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000340	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000343	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000369	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000463	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000518	OMIM:251290	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000639	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000952	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0000967	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001250	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001257	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME	HP:0012829	HP:0001263	OMIM:251290	TAS				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001302	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001321	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001410	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001508	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001744	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0001873	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002119	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002126	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002187	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002240	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002514	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002910	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0002922	OMIM:251290	TAS				P		HPO:skoehler	
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0007759	OMIM:251290	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251290	#251290 BAND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA;BLCPMG;;PSEUDO-TORCH SYNDROME		HP:0008936	OMIM:251290	IEA				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000007	PMID:26123727	PCS				I		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000083	OMIM:251300	IEA				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000093	PMID:26123727	PCS		HP:0040284		P		HPO:iea	6/12
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000097	PMID:26123727	PCS				P		HPO:probinson	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000100	PMID:26123727	PCS				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000154	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000218	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000252	PMID:26123727	PCS		HP:0040284		P		HPO:iea	13/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000286	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000316	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000340	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000347	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000369	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000400	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000418	OMIM:251300	IEA				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000448	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000486	PMID:26123727	PCS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000508	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000518	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000568	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000639	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000648	PMID:26123727	PCS		HP:0040284		P		HPO:iea	13/14
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0000750	OMIM:251300	PCS		HP:0040284		P		HPO:probinson	11/12
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001010	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001188	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001238	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001249	PMID:26123727	PCS		HP:0040284		P		HPO:skoehler	15/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001250	PMID:26123727	PCS		HP:0040284		P		HPO:skoehler	7/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001251	OMIM:251300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001252	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001257	PMID:26123727	PCS		HP:0040284		P		HPO:probinson	9/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001263	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001272	PMID:26123727	PCS		HP:0040284		P		HPO:skoehler	12/12
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001302	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001305	OMIM:251300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001332	PMID:26123727	PCS		HP:0040284		P		HPO:skoehler	8/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001347	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001511	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001518	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001562	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001761	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001762	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001792	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0001967	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002036	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002059	PMID:26123727	PCS		HP:0040284		P		HPO:skoehler	8/12
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002079	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002360	PMID:26123727	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002365	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002465	OMIM:251300	IEA				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0002510	OMIM:251300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0003073	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0003593	OMIM:251300	IEA				C		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0004322	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0005469	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0005484	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0007676	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0007759	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0008936	PMID:26123727	PCS		HP:0040284		P		HPO:probinson	11/15
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0009473	OMIM:251300	IEA				P		HPO:iea	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0011800	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0011968	OMIM:251300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251300	GALLOWAY-MOWAT SYNDROME 1; GAMOS1		HP:0012385	OMIM:251300	TAS				P		HPO:skoehler	
OMIM	251400	MICROCOLON		HP:0000007	OMIM:251400	IEA				I		HPO:iea	
OMIM	251400	MICROCOLON		HP:0001425	OMIM:251400	IEA				I		HPO:iea	
OMIM	251400	MICROCOLON		HP:0004388	OMIM:251400	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000007	OMIM:251450	IEA				I		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000160	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000272	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000308	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000311	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000470	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000520	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000545	OMIM:251450	TAS	HP:0003584			P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000774	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000926	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0000939	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001087	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001156	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001249	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001252	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001270	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001290	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001388	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001513	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001762	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001763	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0001852	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002515	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002650	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002673	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002758	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002808	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002812	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0002970	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003016	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003071	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003180	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003196	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003307	OMIM:251450	IEA				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003510	OMIM:251450	TAS	HP:0003577			P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0003828	OMIM:251450	TAS				C		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0004233	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0005067	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0005280	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0006243	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0006429	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0006439	OMIM:251450	TAS				P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0008082	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0008108	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0008873	OMIM:251450	TAS	HP:0003577			P		HPO:probinson	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0009611	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0010034	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0010068	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0010097	OMIM:251450	IEA				P		HPO:iea	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0010743	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0011800	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251450	DESBUQUOIS DYSPLASIA 1		HP:0100864	OMIM:251450	TAS				P		HPO:skoehler	
OMIM	251505	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4		HP:0000007	OMIM:251505	IEA				I		HPO:iea	
OMIM	251505	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4		HP:0000482	PMID:1621783	PCS		HP:0040284		P		HPO:lccarmody	155/196
OMIM	251505	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4		HP:0000568	OMIM:251505	IEA		HP:0040284		P		HPO:iea	11/196
OMIM	251505	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4		HP:0000589	OMIM:251505	IEA		HP:0040284		P		HPO:skoehler	185/196
OMIM	251505	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 4		HP:0001144	PMID:1621783	PCS		HP:0040284		P		HPO:lccarmody	11/196
OMIM	251600	MICROPHTHALMIA, ISOLATED 1		HP:0000007	OMIM:251600	IEA				I		HPO:iea	
OMIM	251600	MICROPHTHALMIA, ISOLATED 1		HP:0000501	OMIM:251600	IEA				P		HPO:iea	
OMIM	251600	MICROPHTHALMIA, ISOLATED 1		HP:0000528	OMIM:251600	TAS				P		HPO:probinson	
OMIM	251600	MICROPHTHALMIA, ISOLATED 1		HP:0000568	OMIM:251600	IEA				P		HPO:iea	
OMIM	251600	MICROPHTHALMIA, ISOLATED 1		HP:0008499	OMIM:251600	TAS				P		HPO:probinson	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0000007	OMIM:251700	IEA				I		HPO:iea	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0000164	OMIM:251700	IEA				P		HPO:iea	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0000501	OMIM:251700	IEA				P		HPO:iea	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0000546	OMIM:251700	IEA				P		HPO:iea	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0000568	OMIM:251700	IEA				P		HPO:iea	
OMIM	251700	MICROPHTHALMIA WITH HYPEROPIA, RETINAL DEGENERATION, MACROPHAKIA,AND DENTAL ANOMALIES		HP:0008499	OMIM:251700	IEA				P		HPO:iea	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000007	OMIM:251750	IEA				I		HPO:iea	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000218	OMIM:251750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000485	OMIM:251750	TAS				P		HPO:skoehler	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000501	OMIM:251750	IEA				P		HPO:skoehler	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000540	OMIM:251750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000545	OMIM:251750	IEA				P		HPO:skoehler	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0000767	OMIM:251750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0001083	OMIM:251750	TAS				P		HPO:skoehler	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0007765	OMIM:251750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0030961	OMIM:251750	TAS				P		HPO:skoehler	
OMIM	251750	MICROSPHEROPHAKIA AND/OR MEGALOCORNEA, WITH ECTOPIA LENTIS AND WITH OR WITHOUT SECONDARY GLAUCOMA; MSPKA		HP:0100693	OMIM:251750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0000007	OMIM:251800	IEA				I		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0000154	OMIM:251800	IEA				P		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0000324	OMIM:251800	IEA				P		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0000405	OMIM:251800	IEA				P		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0008551	OMIM:251800	IEA				P		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0008773	OMIM:251800	IEA				P		HPO:iea	
OMIM	251800	MICROTIA WITH MEATAL ATRESIA AND CONDUCTIVE DEAFNESS		HP:0009892	OMIM:251800	IEA				P		HPO:skoehler	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0000007	OMIM:251850	TAS				I		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0001510	OMIM:251850	TAS				P		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0001522	OMIM:251850	TAS				M		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0001944	OMIM:251850	TAS				P		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0004385	OMIM:251850	TAS				P		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0004395	OMIM:251850	TAS				P		HPO:probinson	
OMIM	251850	DIARRHEA 2, WITH MICROVILLOUS ATROPHY		HP:0011473	OMIM:251850	TAS				P		HPO:probinson	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0000007	OMIM:251880	IEA				I		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0000252	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0000549	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0000639	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0000952	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001250	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001252	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001271	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001290	OMIM:251880	TAS				P		HPO:skoehler	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001298	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001347	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001397	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001399	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001404	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001405	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001409	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001413	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001508	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001510	OMIM:251880	TAS				P		HPO:skoehler	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001541	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001744	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001873	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0001943	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002013	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002045	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002059	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002240	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002904	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002909	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0002910	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0003073	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0003128	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0006581	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0008872	OMIM:251880	IEA				P		HPO:iea	
OMIM	251880	MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)		HP:0008972	OMIM:251880	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0000006	OMIM:251900	TAS				I		HPO:nvasilevsky	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0000007	OMIM:251900	TAS				I		HPO:nvasilevsky	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0000158	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001252	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001265	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001270	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001290	OMIM:251900	TAS				P		HPO:skoehler	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001324	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001427	OMIM:251900	TAS				I		HPO:nvasilevsky	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0001939	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0002240	OMIM:251900	IEA				P		HPO:iea	
OMIM	251900	MITOCHONDRIAL MYOPATHY		HP:0003737	OMIM:251900	IEA				P		HPO:iea	
OMIM	251945	MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT		HP:0000007	OMIM:251945	IEA				I		HPO:iea	
OMIM	251945	MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT		HP:0001324	OMIM:251945	IEA				P		HPO:iea	
OMIM	251945	MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT		HP:0001939	OMIM:251945	IEA				P		HPO:iea	
OMIM	251945	MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT		HP:0003546	OMIM:251945	IEA				P		HPO:iea	
OMIM	251945	MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT		HP:0003737	OMIM:251945	IEA				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0000007	OMIM:251950	IEA				I		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001250	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001257	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001260	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001269	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001290	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001310	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001324	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0001332	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0002151	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0002384	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0002572	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003128	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003348	OMIM:251950	PCS				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003391	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003542	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003593	OMIM:251950	TAS				C		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003676	OMIM:251950	TAS				C		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0003737	OMIM:251950	IEA				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0008504	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0008897	OMIM:251950	IEA				P		HPO:iea	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0012378	OMIM:251950	IEA				P		HPO:skoehler	
OMIM	251950	MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDOSIS; MMLA		HP:0040083	OMIM:251950	TAS				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000007	OMIM:252010	IEA				I		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000407	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000486	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000508	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000543	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000618	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000639	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0000817	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001138	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001250	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001251	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001252	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001254	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001257	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001259	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001263	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001265	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001272	OMIM:252010	TAS				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001290	OMIM:252010	TAS				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001347	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001399	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001423	OMIM:252010	IEA				I		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001427	OMIM:252010	IEA				I		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001508	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001510	OMIM:252010	TAS				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001639	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0001943	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002013	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002093	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002181	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002352	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002376	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002415	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002421	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002490	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0002878	OMIM:252010	TAS				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0003128	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0003202	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0003487	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0003546	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0003593	OMIM:252010	IEA				C		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0004481	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0006965	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0008316	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0008872	OMIM:252010	IEA				P		HPO:iea	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0008972	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252010	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1		HP:0100660	OMIM:252010	IEA				P		HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000007	OMIM:252011	IEA				I	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000505	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000508	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000580	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000602	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000639	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0000648	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001250	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001251	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001257	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001319	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001324	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001332	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001336	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001347	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001371	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001639	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0001644	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY	HP:0012825	HP:0002151	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:probinson	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0002376	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0003200	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0003487	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0003546	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0003593	OMIM:252011	IEA				C	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0004322	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0004897	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0006980	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0008314	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:iea	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0008316	OMIM:252011	IEA				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0012240	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:probinson	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0030682	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252011	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE CoQ REDUCTASE DEFICIENCY		HP:0100543	OMIM:252011	TAS				P	#252011 MITOCHONDRIAL COMPLEX II DEFICIENCY;;SUCCINATE COQ REDUCTASE DEFICIENCY	HPO:skoehler	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000007	ISBN-13:978-0721606156	PCS				I		HPO:iea	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000161	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000175	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000180	ISBN-13:978-0721606156;OMIM:252100	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000191	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000199	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000218	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000238	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000272	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000316	OMIM:252100	TAS				P		HPO:skoehler	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000327	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000347	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000405	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000455	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000456	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000506	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0000767	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001156	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001159	OMIM:252100	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001162	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001177	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001830	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0001841	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0002132	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0002645	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0002650	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0003015	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0003025	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0004209	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=ofd1;ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0004279	OMIM:252100	TAS				P		HPO:skoehler	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0004322	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0005280	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0006136	OMIM:252100	TAS				P		HPO:skoehler	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0006289	ISBN-13:978-0721606156	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0010101	OMIM:252100	TAS				P		HPO:skoehler	
OMIM	252100	%252100 MOHR SYNDROME;;OROFACIODIGITAL SYNDROME II; OFD2;;OFDS II;;ORAL-FACIAL-DIGITAL SYNDROME, TYPE II		HP:0010297	ISBN-13:978-0721606156	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000007	OMIM:252150	IEA				I		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000252	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000256	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000276	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000293	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000316	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000343	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000639	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0000804	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0001249	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0001250	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0001285	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0001510	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002007	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002059	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002079	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002119	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002171	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002179	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002510	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0002932	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003166	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003196	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003359	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003447	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003534	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003537	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003570	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003606	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003643	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003676	OMIM:252150	TAS				C		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0003739	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0008872	OMIM:252150	IEA				P		HPO:iea	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0010934	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0011096	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0011814	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0011935	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0011942	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0011943	OMIM:252150	TAS				P		HPO:probinson	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0012019	OMIM:252150	IEA				P		HPO:skoehler	
OMIM	252150	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP A; MOCODA		HP:0012471	OMIM:252150	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000007	OMIM:252160	TAS				I		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000252	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000256	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000276	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000293	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000316	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000343	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000639	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0000804	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0001083	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0001250	OMIM:252160	IEA				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0001510	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002007	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002059	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002079	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002119	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002171	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002179	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0002510	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003166	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003196	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003447	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003537	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003570	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003676	OMIM:252160	TAS				C		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0003739	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0010934	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0011096	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0011814	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0011968	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0012019	OMIM:252160	IEA				P		HPO:skoehler	
OMIM	252160	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP B; MOCODB		HP:0012471	OMIM:252160	TAS				P		HPO:skoehler	
OMIM	252250	MONOCYTE CHEMOTACTIC DISORDER		HP:0000007	OMIM:252250	IEA				I		HPO:iea	
OMIM	252250	MONOCYTE CHEMOTACTIC DISORDER		HP:0002728	OMIM:252250	IEA				P		HPO:iea	
OMIM	252250	MONOCYTE CHEMOTACTIC DISORDER		HP:0002965	OMIM:252250	IEA				P		HPO:iea	
OMIM	252270	MONOSOMY 7 OF BONE MARROW		HP:0000007	OMIM:252270	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	252270	MONOSOMY 7 OF BONE MARROW		HP:0001873	OMIM:252270	IEA				P		HPO:iea	
OMIM	252270	MONOSOMY 7 OF BONE MARROW		HP:0002863	OMIM:252270	IEA				P		HPO:skoehler	
OMIM	252270	MONOSOMY 7 OF BONE MARROW		HP:0004808	OMIM:252270	IEA				P		HPO:skoehler	
OMIM	252270	MONOSOMY 7 OF BONE MARROW		HP:0005518	OMIM:252270	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0000007	OMIM:252300	IEA				I		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0000926	OMIM:252300	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0001249	OMIM:252300	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0002655	OMIM:252300	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0003510	OMIM:252300	IEA				P		HPO:skoehler	
OMIM	252300	MORQUIO SYNDROME C		HP:0003610	OMIM:252300	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0005723	OMIM:252300	IEA				P		HPO:iea	
OMIM	252300	MORQUIO SYNDROME C		HP:0007957	OMIM:252300	IEA				P		HPO:iea	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0000007	OMIM:252320	PCS				I		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0000762	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0000961	OMIM:252320	IEA				P		HPO:skoehler	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0000975	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0001278	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0002571	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0003202	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0003323	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0009830	OMIM:252320	IEA				P		HPO:skoehler	
OMIM	252320	MOTOR NEUROPATHY, PERIPHERAL, WITH DYSAUTONOMIA		HP:0011096	OMIM:252320	PCS				P		HPO:probinson	
OMIM	252350	MOYAMOYA DISEASE 1; MYMY1		HP:0000007	OMIM:252350	IEA				I		HPO:iea	
OMIM	252350	MOYAMOYA DISEASE 1; MYMY1		HP:0001009	OMIM:252350	IEA				P		HPO:skoehler	
OMIM	252350	MOYAMOYA DISEASE 1; MYMY1		HP:0005291	OMIM:252350	IEA				P		HPO:iea	
OMIM	252350	MOYAMOYA DISEASE 1; MYMY1		HP:0012474	OMIM:252350	IEA				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000007	OMIM:252500	IEA				I		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000023	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000158	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000280	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000286	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000341	OMIM:252500	TAS				P		HPO:probinson	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000343	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000348	OMIM:252500	TAS				P		HPO:probinson	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000403	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000463	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000485	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000535	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000882	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0000938	OMIM:252500	IEA				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001048	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001171	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001263	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001319	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001498	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001508	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001537	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001538	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001540	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001547	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001609	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001635	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001639	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001640	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001659	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001744	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0001762	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002196	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002240	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002684	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002690	OMIM:252500	IEA				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002756	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002827	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002837	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0002869	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003016	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003026	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003180	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003264	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003300	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003311	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003333	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003414	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003423	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003538	OMIM:252500	IEA				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0003819	OMIM:252500	IEA				M		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0004562	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0005280	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0006362	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0006532	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0006610	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0007759	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0008155	OMIM:252500	IEA				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0008470	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0008850	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0009092	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0009769	OMIM:252500	IEA				P		HPO:iea	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0011344	OMIM:252500	TAS				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0030148	OMIM:252500	TAS				P		HPO:skoehler	
OMIM	252500	#252500 MUCOLIPIDOSIS II ALPHA/BETA;;MUCOLIPIDOSIS II; ML II;;ML II ALPHA/BETA;;I-CELL DISEASE; ICD		HP:0100540	OMIM:252500	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000007	OMIM:252600	IEA				I		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000280	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000303	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000484	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000488	OMIM:252600	IEA				P		HPO:skoehler	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000546	PMID:20301730	TAS				P		HPO:skoehler	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA	HP:0012825	HP:0000773	OMIM:252600	TAS				P		HPO:probinson	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000885	OMIM:252600	TAS				P		HPO:probinson	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0000943	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001072	OMIM:252600	TAS				P		HPO:probinson	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001171	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001249	OMIM:252600	TAS				P		HPO:skoehler	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001328	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001363	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001498	OMIM:252600	TAS				P		HPO:probinson	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0001659	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0002650	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0002680	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0003026	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0003182	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0003264	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0003333	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0003538	OMIM:252600	IEA				P		HPO:skoehler	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0004236	OMIM:252600	TAS				P		HPO:probinson	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0004322	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0006162	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0007759	OMIM:252600	IEA				P		HPO:iea	
OMIM	252600	MUCOLIPIDOSIS III ALPHA/BETA		HP:0012185	OMIM:252600	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000007	OMIM:252605	IEA				I		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000280	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000470	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000545	OMIM:252605	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000768	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0000943	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0001155	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0001256	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA	HP:0003676	HP:0001387	OMIM:252605	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0001547	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0001650	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0001659	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0002650	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0002808	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0002829	OMIM:252605	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0002857	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0002869	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0003307	OMIM:252605	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0003333	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0003370	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0003538	OMIM:252605	TAS				P		HPO:skoehler	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0004322	OMIM:252605	IEA				P		HPO:iea	
OMIM	252605	MUCOLIPIDOSIS III GAMMA		HP:0007759	OMIM:252605	IEA				P		HPO:skoehler	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000007	PMID:10973263	PCS				I		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000252	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000486	PMID:21763169	PCS				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000505	PMID:21763169	PCS				P		HP:probinson	
OMIM	252650	MUCOLIPIDOSIS IV	HP:0003676	HP:0000546	PMID:11786056	PCS	HP:0003593			P		HP:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000613	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000648	PMID:21763169	PCS				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0000654	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001249	PMID:21763169	PCS				P		HPO:skoehler	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001252	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001263	PMID:21763169	PCS				P		HPO:skoehler	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001272	PMID:21763169	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001290	OMIM:252650	TAS				P		HPO:skoehler	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001332	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001344	OMIM:252650	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001347	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0001438	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0002344	OMIM:252650	IEA				P		HPO:skoehler	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0002510	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0003487	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0003593	OMIM:252650	PCS				C		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0004345	OMIM:252650	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0006989	PMID:21763169	PCS				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0007266	OMIM:252650	IEA				P		HPO:iea	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0007281	OMIM:252650	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0007759	OMIM:252650	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0011020	OMIM:252650	PCS				P		HPO:probinson	
OMIM	252650	MUCOLIPIDOSIS IV		HP:0500167	PMID:21763169	PCS				P		HP:probinson	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0000007	OMIM:252700	IEA				I		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0000280	OMIM:252700	IEA				P		HPO:skoehler	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0001507	OMIM:252700	IEA				P		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0001654	OMIM:252700	IEA				P		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0003610	OMIM:252700	IEA				P		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0005187	OMIM:252700	IEA				P		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0007759	OMIM:252700	IEA				P		HPO:skoehler	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0008155	OMIM:252700	IEA				P		HPO:iea	
OMIM	252700	MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES		HP:0025131	OMIM:252700	IEA				P		HPO:skoehler	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000007	OMIM:252900	IEA				I		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000250	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000280	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000365	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000664	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000752	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000900	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0000943	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001007	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001249	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001250	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA	HP:0012825	HP:0001387	OMIM:252900	TAS				P		HPO:probinson	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001507	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001670	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0001744	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002014	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002159	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002208	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002240	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002360	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0002788	OMIM:252900	IEA				P		HPO:iea	
OMIM	252900	MUCOPOLYSACCHARIDOSIS TYPE IIIA		HP:0003309	OMIM:252900	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000007	OMIM:252920	IEA				I		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000250	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000280	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000365	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000664	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000718	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000752	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000900	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0000943	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001007	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001249	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001250	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB	HP:0012825	HP:0001387	OMIM:252920	TAS				P		HPO:probinson	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001640	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001670	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0001744	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002014	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002159	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002208	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002240	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002344	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002360	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0002788	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0003309	OMIM:252920	IEA				P		HPO:iea	
OMIM	252920	MUCOPOLYSACCHARIDOSIS TYPE IIIB		HP:0003621	OMIM:252920	IEA				C		HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:252930	IEA				I	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000232	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000250	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000268	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000280	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000365	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000510	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000664	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000752	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000900	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0000943	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001007	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001249	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001250	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001270	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HP:0012825	HP:0001387	OMIM:252930	TAS				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:probinson	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001507	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001670	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0001744	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002014	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002015	OMIM:252930	TAS				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002159	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002208	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002240	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002333	OMIM:252930	TAS				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002360	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002371	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002751	OMIM:252930	TAS				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0002788	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0003309	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0003653	OMIM:252930	IEA				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:iea	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0003828	OMIM:252930	IEA				C	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252930	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-CoA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY		HP:0100790	OMIM:252930	TAS				P	#252930 MUCOPOLYSACCHARIDOSIS TYPE IIIC;;MPS IIIC; MPS3C;;SANFILIPPO SYNDROME C;;ACETYL-COA:ALPHA-GLUCOSAMINIDE N-ACETYLTRANSFERASE DEFICIENCY	HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000007	OMIM:252940	IEA				I		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000154	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000179	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000280	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000365	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000369	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000463	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000470	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000574	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000664	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000752	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000900	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0000943	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001007	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001249	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001250	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001260	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001344	OMIM:252940	TAS				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001371	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY	HP:0012825	HP:0001387	OMIM:252940	TAS				P		HPO:probinson	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001507	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001670	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0001744	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002007	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002014	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002015	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002159	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002208	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002240	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002307	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002360	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0002788	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0003309	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0003653	OMIM:252940	IEA				P		HPO:iea	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0003676	OMIM:252940	IEA				C		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0005280	OMIM:252940	IEA				P		HPO:skoehler	
OMIM	252940	#252940 MUCOPOLYSACCHARIDOSIS, TYPE IIID; MPS3D;;MPS IIID;;SANFILIPPO SYNDROME D;;N-ACETYLGLUCOSAMINE-6-SULFATASE DEFICIENCY		HP:0011220	OMIM:252940	TAS				P		HPO:skoehler	
OMIM	253000	MORQUIO SYNDROME A		HP:0000007	OMIM:253000	TAS				I		HPO:probinson	
OMIM	253000	MORQUIO SYNDROME A		HP:0000023	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000154	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000280	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000303	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000365	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000670	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000683	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000687	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000884	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000904	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000926	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0000939	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0001223	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0001388	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0001654	OMIM:253000	TAS				P		HPO:probinson	
OMIM	253000	MORQUIO SYNDROME A		HP:0002091	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002240	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002318	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002650	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002673	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002788	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002808	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0002857	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003016	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003049	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003053	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003277	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003300	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003307	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003308	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003311	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003521	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0003621	OMIM:253000	IEA				C		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0007759	OMIM:253000	IEA				P		HPO:iea	
OMIM	253000	MORQUIO SYNDROME A		HP:0012069	OMIM:253000	TAS				P		HPO:probinson	
OMIM	253000	MORQUIO SYNDROME A		HP:0012070	OMIM:253000	TAS				P		HPO:probinson	
OMIM	253000	MORQUIO SYNDROME A		HP:0030865	PMID:24602160	PCS				P		HPO:probinson	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000007	OMIM:253010	IEA				I		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000023	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000154	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000280	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000303	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000365	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000670	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000683	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000687	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000884	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000904	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000926	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0000939	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0001223	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0001388	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0001650	OMIM:253010	IEA				P		HPO:skoehler	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002091	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002240	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002318	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002650	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002673	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002788	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002808	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0002857	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003016	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003049	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003053	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003277	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003300	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003307	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003308	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003311	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003521	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0003621	OMIM:253010	IEA				C		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0005292	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0007759	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0008166	OMIM:253010	IEA				P		HPO:iea	
OMIM	253010	#253010 MUCOPOLYSACCHARIDOSIS TYPE IVB;;MORQUIO SYNDROME B;;MPS IVB; MPS4B		HP:0012069	OMIM:253010	TAS				P		HPO:probinson	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000007	OMIM:253200	IEA				I		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000023	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000158	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000238	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000256	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000268	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000280	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000365	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000501	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000884	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000885	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0000943	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001007	OMIM:253200	IEA				P		HPO:skoehler	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001171	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001385	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001387	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001537	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001638	OMIM:253200	IEA				P		HPO:skoehler	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001654	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0001744	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002240	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002318	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002656	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002788	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002857	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002866	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002869	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0002938	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003016	OMIM:253200	TAS				P		HPO:probinson	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003025	OMIM:253200	TAS				P		HPO:probinson	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003274	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003300	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003311	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0003521	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0005280	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0007759	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0008301	OMIM:253200	IEA				P		HPO:iea	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0008432	OMIM:253200	TAS				P		HPO:probinson	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0010885	OMIM:253200	IEA				P		HPO:skoehler	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0011941	OMIM:253200	TAS				P		HPO:probinson	
OMIM	253200	MUCOPOLYSACCHARIDOSIS, TYPE VI; MPS6		HP:0012185	OMIM:253200	TAS				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000007	OMIM:253220	IEA				I		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000023	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000212	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000238	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000256	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000280	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000365	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000470	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000574	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000687	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000768	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000926	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0000943	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001007	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001249	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001371	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001537	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001638	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001654	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001744	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001762	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001789	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0001840	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002159	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002180	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002240	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002465	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002650	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002680	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002788	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0002857	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0003311	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0003375	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0004322	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0004607	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0005619	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0005952	OMIM:253220	IEA				P		HPO:skoehler	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0006119	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0007957	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0008301	OMIM:253220	TAS				P		HPO:probinson	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0008430	OMIM:253220	TAS				P		HPO:probinson	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0008807	OMIM:253220	IEA				P		HPO:iea	
OMIM	253220	MUCOPOLYSACCHARIDOSIS, TYPE VII; MPS7		HP:0008897	OMIM:253220	TAS				P		HPO:skoehler	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0000007	OMIM:253240	IEA				I		HPO:iea	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0000246	OMIM:253240	TAS				P		HPO:skoehler	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0001939	OMIM:253240	IEA				P		HPO:iea	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0002110	OMIM:253240	TAS				P		HPO:skoehler	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0002205	OMIM:253240	TAS				P		HPO:skoehler	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0006541	OMIM:253240	IEA				P		HPO:iea	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0100750	OMIM:253240	TAS				P		HPO:skoehler	
OMIM	253240	%253240 MUCUS INSPISSATION OF RESPIRATORY TRACT		HP:0100759	OMIM:253240	TAS				P		HPO:skoehler	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000007	OMIM:253250	IEA				I		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000171	OMIM:253250	IEA				P		HPO:skoehler	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000268	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000316	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000325	OMIM:253250	IEA				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000431	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000483	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000486	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000580	PMID:7726235	PCS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000668	OMIM:253250	IEA				P		HPO:skoehler	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0000678	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001252	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001260	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001620	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001621	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001635	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0001685	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002007	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002119	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002240	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002667	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002680	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002688	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0002738	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0003764	OMIM:253250	IEA				P		HPO:skoehler	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0004322	OMIM:253250	IEA				P		HPO:skoehler	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0005132	OMIM:253250	IEA				P		HPO:iea	
OMIM	253250	#253250 MULIBREY NANISM;;MUSCLE-LIVER-BRAIN-EYE NANISM;;PERICARDIAL CONSTRICTION AND GROWTH FAILURE;;PERHEENTUPA SYNDROME		HP:0005280	OMIM:253250	TAS				P		HPO:probinson	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000007	OMIM:253260	IEA				I		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000407	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000509	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000572	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000648	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0000988	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001051	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001250	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001251	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001252	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001254	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001263	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001290	OMIM:253260	TAS				P		HPO:skoehler	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001581	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001596	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001744	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001987	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0001992	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002013	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002014	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002104	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002240	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002506	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0002789	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0005979	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0008872	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0100275	OMIM:253260	IEA				P		HPO:iea	
OMIM	253260	BIOTINIDASE DEFICIENCYMULTIPLE CARBOXYLASE DEFICIENCY, LATE-ONSET		HP:0410145	PMID:3930842	PCS				P		HPO:nvasilevsky	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0000007	OMIM:253270	IEA				I		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0000737	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0000988	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001250	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001252	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001254	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001259	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001263	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001276	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001290	OMIM:253270	TAS				P		HPO:skoehler	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001596	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001873	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001942	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001987	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0001992	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0002013	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0002789	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0002883	OMIM:253270	IEA				P		HPO:iea	
OMIM	253270	HOLOCARBOXYLASE SYNTHETASE DEFICIENCY		HP:0008872	OMIM:253270	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000007	OMIM:253280	IEA				I		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000232	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000238	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000252	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000272	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3	HP:0012825	HP:0000347	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000485	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000486	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000501	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000518	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3	HP:0012828	HP:0000545	PMID:15236414	PCS	HP:0003577			P		HP:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000546	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000550	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000557	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000568	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000589	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000639	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000648	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000654	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0000980	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001105	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001250	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001257	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001290	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001302	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001321	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001324	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001336	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0001425	OMIM:253280	TAS				I		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002119	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002126	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002187	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002350	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002353	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0002365	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0003194	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0003236	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0003324	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0003560	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0003577	OMIM:253280	IEA				C		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0006829	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007033	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007260	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007370	OMIM:253280	IEA				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007738	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007759	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007770	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0007973	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0008045	OMIM:253280	IEA				P		HPO:iea	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0010864	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0011344	OMIM:253280	PCS				P		HPO:probinson	
OMIM	253280	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 3; MDDGA3		HP:0011800	OMIM:253280	TAS				P		HPO:skoehler	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000007	OMIM:253290	TAS				I		HPO:skoehler	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000175	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000286	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000316	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000347	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000369	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000457	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000476	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000883	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0000969	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001040	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001371	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001373	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001511	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001561	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001961	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001989	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0001999	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0002047	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0002089	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0002304	OMIM:253290	IEA				P		HPO:skoehler	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0002659	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0002948	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0003634	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE		HP:0005905	OMIM:253290	IEA				P		HPO:iea	
OMIM	253290	#253290 MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS;;PTERYGIUM SYNDROME, MULTIPLE, LETHAL TYPE	HP:0012828	HP:0009381	OMIM:253290	IEA				P		HPO:probinson	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0000007	OMIM:253300	IEA				I		HPO:iea	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001284	OMIM:253300	IEA				P		HPO:iea	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001308	OMIM:253300	TAS				P		HPO:probinson	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001558	OMIM:253300	IEA				P		HPO:iea	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001629	OMIM:253300	IEA				P		HPO:skoehler	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001631	OMIM:253300	IEA				P		HPO:skoehler	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0001631	OMIM:253300	TAS				P		HPO:probinson	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0002093	OMIM:253300	IEA				P		HPO:iea	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0002205	OMIM:253300	IEA				P		HPO:skoehler	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0002878	OMIM:253300	TAS				P		HPO:skoehler	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0003445	OMIM:253300	IEA				P		HPO:iea	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0007126	OMIM:253300	TAS				P		HPO:probinson	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0007269	OMIM:253300	IEA				P		HPO:skoehler	
OMIM	253300	#253300 SPINAL MUSCULAR ATROPHY, TYPE I; SMA1;;SMA I;;SMA, INFANTILE ACUTE FORM;;MUSCULAR ATROPHY, INFANTILE;;WERDNIG-HOFFMANN DISEASE		HP:0008994	OMIM:253300	TAS				P		HPO:probinson	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0000007	OMIM:253310	IEA				I		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0000347	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0000765	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0000969	OMIM:253310	IEA				P		HPO:skoehler	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0001560	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0002089	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0002804	OMIM:253310	TAS				P		HPO:skoehler	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0003202	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0003811	OMIM:253310	IEA				M		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0004571	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0007277	OMIM:253310	IEA				P		HPO:iea	
OMIM	253310	#253310 LETHAL CONGENITAL CONTRACTURE SYNDROME 1; LCCS1;;LCCS;;MULTIPLE CONTRACTURE SYNDROME, FINNISH TYPE		HP:0009004	OMIM:253310	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0000007	OMIM:253320	IEA				I		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0000044	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0000508	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0001939	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0002938	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0003198	OMIM:253320	IEA				P		HPO:skoehler	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0004322	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0006887	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0010628	OMIM:253320	IEA				P		HPO:iea	
OMIM	253320	253320 MULTICORE MYOPATHY WITH MENTAL RETARDATION, SHORT STATURE, AND HYPOGONADOTROPICHYPOGONADISM;;CHUDLEY SYNDROME		HP:0010864	OMIM:253320	TAS				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0000007	OMIM:253400	IEA				I		HPO:iea	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0001265	OMIM:253400	TAS				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0001308	OMIM:253400	IEA				P		HPO:iea	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0002378	OMIM:253400	IEA				P		HPO:iea	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0002398	OMIM:253400	IEA				P		HPO:iea	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0002522	OMIM:253400	TAS				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0003394	OMIM:253400	TAS				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0003457	OMIM:253400	IEA				P		HPO:iea	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0003676	OMIM:253400	TAS				C		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0003701	OMIM:253400	IEA				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0007269	OMIM:253400	IEA				P		HPO:skoehler	
OMIM	253400	SPINAL MUSCULAR ATROPHY, TYPE III; SMA3		HP:0007289	OMIM:253400	IEA				P		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0000007	OMIM:253550	IEA				I		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0001308	OMIM:253550	IEA				P		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0001324	OMIM:253550	IEA				P		HPO:skoehler	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0002205	OMIM:253550	IEA				P		HPO:skoehler	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0002378	OMIM:253550	IEA				P		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0002398	OMIM:253550	IEA				P		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0003457	OMIM:253550	IEA				P		HPO:iea	
OMIM	253550	SPINAL MUSCULAR ATROPHY, TYPE II		HP:0007269	OMIM:253550	IEA				P		HPO:skoehler	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0000007	OMIM:253590	IEA				I		HPO:iea	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0001250	OMIM:253590	IEA				P		HPO:iea	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0001324	OMIM:253590	IEA				P		HPO:skoehler	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0002066	OMIM:253590	IEA				P		HPO:skoehler	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0002352	OMIM:253590	IEA				P		HPO:skoehler	
OMIM	253590	MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY		HP:0003560	OMIM:253590	IEA				P		HPO:skoehler	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0000007	OMIM:253600	IEA				I		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0001371	OMIM:253600	IEA				P		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0001880	OMIM:253600	IEA				P		HPO:skoehler	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0002312	OMIM:253600	IEA				P		HPO:skoehler	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0002355	OMIM:253600	IEA				P		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0003236	OMIM:253600	IEA				P		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0003560	OMIM:253600	IEA				P		HPO:skoehler	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0003691	OMIM:253600	IEA				P		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0007126	OMIM:253600	IEA				P		HPO:iea	
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0010628	OMIM:253600	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	253600	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A		HP:0100614	OMIM:253600	IEA				P		HPO:skoehler	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0000007	OMIM:253601	IEA				I		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003236	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003458	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003551	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003555	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003557	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003560	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003677	OMIM:253601	IEA				C		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0003701	OMIM:253601	IEA				P		HPO:iea	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0009025	OMIM:253601	IEA				P		HPO:skoehler	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0009046	OMIM:253601	TAS				P		HPO:skoehler	
OMIM	253601	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B		HP:0012378	OMIM:253601	IEA				P		HPO:skoehler	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0000007	OMIM:253700	IEA				I		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0001371	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0001667	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0002090	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0002091	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0002650	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003202	OMIM:253700	TAS				P		HPO:skoehler	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003236	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003307	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003391	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003560	OMIM:253700	IEA				P		HPO:skoehler	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003678	OMIM:253700	IEA				C		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003707	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0003713	OMIM:253700	IEA				P		HPO:iea	
OMIM	253700	#253700 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C;;MUSCULAR DYSTROPHY, DUCHENNE-LIKE;;DUCHENNE-LIKE MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE, TYPE 1; DMDA1;;DMDA;;ADHALIN DEFICIENCY, SECONDARY;;SARCOGLYCAN, GAMMA, DEFICIENCY OF;;SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, NORTH AFRICANTYPE; SCARMD;;MAGHREBIAN MYOPATHY		HP:0005133	OMIM:253700	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000007	OMIM:253800	IEA				I		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000238	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000486	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000518	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000540	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000541	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000545	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000568	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0000648	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001249	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001250	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001252	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001274	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001284	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001290	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001302	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001321	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001324	OMIM:253800	IEA				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001360	OMIM:253800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4	HP:0003676	HP:0001371	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001631	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001642	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001644	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001669	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0001685	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002084	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002093	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002126	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002267	OMIM:253800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002350	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002365	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0002650	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0003202	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0003236	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0003306	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0003593	OMIM:253800	TAS				C		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0003741	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0007260	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0007348	OMIM:253800	IEA				P		HPO:iea	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0007973	OMIM:253800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0008981	OMIM:253800	TAS				P		HPO:skoehler	
OMIM	253800	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4; MDDGA4		HP:0031882	OMIM:253800	IEA				P		HPO:skoehler	
OMIM	253900	MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS		HP:0000007	OMIM:253900	IEA				I		HPO:iea	
OMIM	253900	MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS		HP:0001939	OMIM:253900	IEA				P		HPO:iea	
OMIM	253900	MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS		HP:0002804	OMIM:253900	IEA				P		HPO:skoehler	
OMIM	253900	MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS		HP:0003198	OMIM:253900	IEA				P		HPO:iea	
OMIM	253900	MUSCULAR DYSTROPHY, CONGENITAL, PRODUCING ARTHROGRYPOSIS		HP:0003741	OMIM:253900	IEA				P		HPO:skoehler	
OMIM	254000	MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM		HP:0000007	OMIM:254000	IEA				I		HPO:iea	
OMIM	254000	MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM		HP:0000135	OMIM:254000	IEA				P		HPO:iea	
OMIM	254000	MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM		HP:0000518	OMIM:254000	IEA				P		HPO:skoehler	
OMIM	254000	MUSCULAR DYSTROPHY, CONGENITAL, WITH INFANTILE CATARACT AND HYPOGONADISM		HP:0003741	OMIM:254000	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000006	OMIM:254090	IEA				I		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000007	OMIM:254090	IEA				I		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000218	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000311	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000411	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000473	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0000975	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001270	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001319	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001371	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001388	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001508	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001533	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0001762	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002650	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002747	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002783	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002808	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002827	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0002877	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003306	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003557	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003593	OMIM:254090	IEA				C		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003676	OMIM:254090	IEA				C		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003700	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003701	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003713	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003741	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003803	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0003828	OMIM:254090	IEA				C		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0005072	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0006149	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0006460	OMIM:254090	IEA				P		HPO:iea	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0007502	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0008180	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0008872	OMIM:254090	IEA				P		HPO:skoehler	
OMIM	254090	#254090 ULLRICH CONGENITAL MUSCULAR DYSTROPHY; UCMD;;MUSCULAR DYSTROPHY, SCLEROATONIC;;ULLRICH DISEASE;;ULLRICH SCLEROATONIC MUSCULAR DYSTROPHY		HP:0010628	OMIM:254090	IEA				P		HPO:iea	
OMIM	254100	MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION		HP:0000007	OMIM:254100	IEA				I		HPO:iea	
OMIM	254100	MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION		HP:0001324	OMIM:254100	IEA				P		HPO:skoehler	
OMIM	254100	MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION		HP:0003678	OMIM:254100	IEA				C		HPO:iea	
OMIM	254100	MUSCULAR DYSTROPHY, CONGENITAL, WITH RAPID PROGRESSION		HP:0003741	OMIM:254100	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0000007	OMIM:254110	IEA				I		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0001265	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0001284	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0002515	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003236	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003391	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003458	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003547	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003557	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003560	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003677	OMIM:254110	IEA				C		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003687	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003707	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003722	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003724	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003731	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003738	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0003749	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0008988	OMIM:254110	IEA				P		HPO:iea	
OMIM	254110	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2H		HP:0010628	OMIM:254110	IEA				P		HPO:iea	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0000007	OMIM:254120	IEA				I		HPO:iea	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0001276	OMIM:254120	IEA				P		HPO:skoehler	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0001537	OMIM:254120	IEA				P		HPO:iea	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0001558	OMIM:254120	TAS				P		HPO:skoehler	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0001626	OMIM:254120	IEA				P		HPO:iea	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0002090	OMIM:254120	IEA				P		HPO:iea	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0002375	OMIM:254120	IEA				P		HPO:skoehler	
OMIM	254120	MUSCULAR HYPERTONIA, LETHAL		HP:0100660	OMIM:254120	IEA				P		HPO:skoehler	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0000007	OMIM:254130	TAS				I		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0001425	OMIM:254130	TAS				I		HPO:skoehler	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0002460	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003236	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003551	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003560	OMIM:254130	IEA				P		HPO:iea	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003581	OMIM:254130	TAS		HP:0040282		C		HPO:probinson	HP:0040282
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003693	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0003791	OMIM:254130	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0007340	OMIM:254130	TAS				P		HPO:skoehler	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0009072	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0010546	OMIM:254130	TAS				P		HPO:probinson	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0040083	OMIM:254130	IEA				P		HPO:skoehler	
OMIM	254130	MIYOSHI MUSCULAR DYSTROPHY 1; MMD1		HP:0200101	OMIM:254130	TAS				P		HPO:skoehler	
OMIM	254150	MUSK, INABILITY TO SMELL		HP:0000007	OMIM:254150	IEA				I		HPO:iea	
OMIM	254150	MUSK, INABILITY TO SMELL		HP:0000458	OMIM:254150	IEA				P		HPO:skoehler	
OMIM	254150	MUSK, INABILITY TO SMELL		HP:0000618	OMIM:254150	IEA				P		HPO:skoehler	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0000007	OMIM:254190	IEA				I		HPO:iea	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0000544	OMIM:254190	IEA				P		HPO:iea	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0001939	OMIM:254190	IEA				P		HPO:iea	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0003473	OMIM:254190	TAS				P		HPO:skoehler	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0003701	OMIM:254190	IEA				P		HPO:skoehler	
OMIM	254190	MYASTHENIA, CONGENITAL, REFRACTORY TO ACETYLCHOLINESTERASE INHIBITORS		HP:0007970	OMIM:254190	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0000508	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0000651	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0000818	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0001260	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0001426	OMIM:254200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0001611	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0002015	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0002715	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0002960	OMIM:254200	TAS				P		HPO:skoehler	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0003473	OMIM:254200	TAS				P		HPO:skoehler	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0003690	OMIM:254200	IEA				P		HPO:skoehler	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0003701	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0005216	OMIM:254200	IEA				P		HPO:skoehler	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0010628	OMIM:254200	IEA				P		HPO:iea	
OMIM	254200	MYASTHENIA GRAVIS; MG		HP:0100522	OMIM:254200	TAS				P		HPO:skoehler	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0000007	OMIM:254210	IEA				I		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0000486	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0000508	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0000597	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0001283	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0001425	OMIM:254210	TAS				I		HPO:skoehler	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0001612	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002015	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002033	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002098	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002715	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002747	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002804	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002872	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0002882	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003397	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003402	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003403	OMIM:254210	IEA				P		HPO:skoehler	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003473	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003554	OMIM:254210	IEA				P		HPO:iea	
OMIM	254210	MYASTHENIC SYNDROME, CONGENITAL, 6, PRESYNAPTIC; CMS6		HP:0003577	OMIM:254210	IEA				C		HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0000007	OMIM:254300	IEA				I	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0000508	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0000597	OMIM:254300	IEA		HP:0040283		P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	HP:0040283
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0001283	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0001558	OMIM:254300	IEA		HP:0040283		P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	HP:0040283
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0002515	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0002715	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0002747	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003388	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003391	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003394	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003473	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003621	OMIM:254300	IEA				C	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0003693	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0007126	OMIM:254300	TAS				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0008180	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:iea	
OMIM	254300	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE Ib; CMS1B;;CMS Ib;;MYASTHENIC MYOPATHY, FORMERLY		HP:0010628	OMIM:254300	IEA				P	#254300 MYASTHENIA, LIMB-GIRDLE, FAMILIAL;;LGM;;CONGENITAL MYASTHENIC SYNDROME TYPE IB; CMS1B;;CMS IB;;MYASTHENIC MYOPATHY, FORMERLY	HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0000964	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0000989	OMIM:254400	IEA				P		HPO:iea	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0002665	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0002716	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0003765	OMIM:254400	TAS				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0008069	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0010783	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254400	MYCOSIS FUNGOIDES		HP:0200035	OMIM:254400	IEA				P		HPO:skoehler	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0000006	OMIM:254450	IEA				I		HPO:iea	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0000979	PMID:9766805	PCS				P		HPO:lccarmody	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0000980	PMID:9766805	PCS				P		HPO:lccarmody	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0001428	OMIM:254450	TAS				I		HPO:skoehler	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0001744	PMID:9766805	PCS				P		HPO:lccarmody	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0001945	PMID:9766805	PCS				P		HPO:lccarmody	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0005547	PMID:7436463	PCS				P		HPO:probinson	
OMIM	254450	MYELOFIBROSISMYELOFIBROSIS WITH MYELOID METAPLASIA, INCLUDED		HP:0011974	PMID:9766805	PCS				P		HPO:probinson	
OMIM	254500	MYELOMA, MULTIPLE		HP:0000007	OMIM:254500	IEA				I		HPO:iea	
OMIM	254500	MYELOMA, MULTIPLE		HP:0001428	OMIM:254500	TAS				I		HPO:skoehler	
OMIM	254500	MYELOMA, MULTIPLE		HP:0001871	OMIM:254500	IEA				P		HPO:iea	
OMIM	254500	MYELOMA, MULTIPLE		HP:0006775	OMIM:254500	TAS				P		HPO:skoehler	
OMIM	254500	MYELOMA, MULTIPLE		HP:0011034	OMIM:254500	IEA				P		HPO:skoehler	
OMIM	254500	MYELOMA, MULTIPLE		HP:0031047	OMIM:254500	TAS				P		HPO:skoehler	
OMIM	254600	MYELOPEROXIDASE DEFICIENCY		HP:0000007	OMIM:254600	IEA				I		HPO:iea	
OMIM	254600	MYELOPEROXIDASE DEFICIENCY		HP:0001871	OMIM:254600	IEA				P		HPO:iea	
OMIM	254600	MYELOPEROXIDASE DEFICIENCY		HP:0001939	OMIM:254600	IEA				P		HPO:iea	
OMIM	254600	MYELOPEROXIDASE DEFICIENCY		HP:0002715	OMIM:254600	IEA				P		HPO:iea	
OMIM	254700	MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:254700	IEA				I		HPO:iea	
OMIM	254700	MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE		HP:0004852	OMIM:254700	IEA				P		HPO:iea	
OMIM	254700	MYELOPROLIFERATIVE DISEASE, AUTOSOMAL RECESSIVE		HP:0005547	OMIM:254700	IEA				P		HPO:iea	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0000006	OMIM:254770	TAS				I		HPO:skoehler	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0000007	OMIM:254770	TAS				I		HPO:probinson	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0002069	OMIM:254770	TAS				P		HPO:probinson	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0002121	OMIM:254770	TAS				P		HPO:probinson	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0002133	OMIM:254770	TAS				P		HPO:probinson	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0007000	OMIM:254770	TAS				P		HPO:probinson	
OMIM	254770	#254770 EPILEPSY, MYOCLONIC JUVENILE; EJM;;MYOCLONIC EPILEPSY, JUVENILE; JME;;PETIT MAL, IMPULSIVE;;JANZ SYNDROMEMYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 1, INCLUDED; EJM1,INCLUDED		HP:0012001	OMIM:254770	TAS				P		HPO:probinson	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0000007	OMIM:254780	IEA				I		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0000572	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0000709	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0000726	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0000992	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0001288	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0001336	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0001399	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0001425	OMIM:254780	IEA				I		HPO:skoehler	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0001939	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0002121	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0002123	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0002186	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0002344	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0002367	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0003678	OMIM:254780	TAS				C		HPO:skoehler	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0007334	OMIM:254780	IEA				P		HPO:skoehler	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0011165	OMIM:254780	IEA				P		HPO:iea	
OMIM	254780	MYOCLONIC EPILEPSY OF LAFORA		HP:0025121	OMIM:254780	TAS				P		HPO:skoehler	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0000007	OMIM:254800	IEA				I		HPO:iea	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0001251	OMIM:254800	IEA				P		HPO:iea	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0001260	OMIM:254800	IEA				P		HPO:iea	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0001268	OMIM:254800	IEA				P		HPO:iea	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0001336	OMIM:254800	IEA				P		HPO:skoehler	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0002069	OMIM:254800	IEA				P		HPO:iea	
OMIM	254800	MYOCLONIC EPILEPSY OF UNVERRICHT AND LUNDBORG		HP:0002121	OMIM:254800	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000007	OMIM:254900	IEA				I		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000083	OMIM:254900	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000093	OMIM:254900	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000097	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000100	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0000112	OMIM:254900	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0001260	OMIM:254900	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0001272	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0001336	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0001873	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0002015	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0002066	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0002080	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0002174	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0002197	OMIM:254900	IEA				P		HPO:iea	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0003678	OMIM:254900	TAS				C		HPO:skoehler	
OMIM	254900	EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE; EPM4		HP:0100820	OMIM:254900	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000007	OMIM:254940	IEA				I		HPO:iea	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000162	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000171	OMIM:254940	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000175	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000201	OMIM:254940	IEA				P		HPO:iea	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000211	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000252	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000256	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000278	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000286	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000347	OMIM:254940	IEA				P		HPO:iea	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000455	OMIM:254940	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000463	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000494	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000501	OMIM:254940	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000508	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000518	OMIM:254940	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0000602	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001182	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001249	OMIM:254940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001263	OMIM:254940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001270	OMIM:254940	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001290	OMIM:254940	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001357	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001371	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001508	OMIM:254940	IEA				P		HPO:iea	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001510	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001558	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001671	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0001762	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0002015	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0002020	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0002093	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0002119	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0002365	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0003198	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0003202	OMIM:254940	IEA				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0003593	OMIM:254940	IEA				C		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0003677	OMIM:254940	IEA				C		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0005280	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0006829	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0010628	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0011968	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254940	CAREY-FINEMAN-ZITER SYNDROME; CFZS		HP:0012246	OMIM:254940	TAS				P		HPO:skoehler	
OMIM	254950	MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA		HP:0000007	OMIM:254950	IEA				I		HPO:iea	
OMIM	254950	MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA		HP:0001324	OMIM:254950	IEA				P		HPO:iea	
OMIM	254950	MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA		HP:0001939	OMIM:254950	IEA				P		HPO:iea	
OMIM	254950	MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA		HP:0002486	OMIM:254950	IEA				P		HPO:skoehler	
OMIM	254950	MYOPATHY, GRANULOVACUOLAR LOBULAR, WITH ELECTRICAL MYOTONIA		HP:0003202	OMIM:254950	IEA				P		HPO:skoehler	
OMIM	254960	MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT		HP:0000007	OMIM:254960	IEA				I		HPO:iea	
OMIM	254960	MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT		HP:0003198	OMIM:254960	IEA				P		HPO:iea	
OMIM	254960	MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT		HP:0003236	OMIM:254960	IEA				P		HPO:iea	
OMIM	254960	MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT		HP:0003738	OMIM:254960	IEA				P		HPO:iea	
OMIM	254960	MYOPATHY DUE TO MALATE-ASPARTATE SHUTTLE DEFECT		HP:0040318	OMIM:254960	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0000007	OMIM:255100	TAS				I		HPO:iea	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0001290	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0001638	OMIM:255100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0001992	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0002015	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0002093	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0002650	OMIM:255100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0003198	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0003236	OMIM:255100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0003546	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0003701	OMIM:255100	TAS				P		HPO:probinson	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0004755	OMIM:255100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0011968	OMIM:255100	TAS				P		HPO:skoehler	
OMIM	255100	LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY		HP:0012548	OMIM:255100	TAS				P		HPO:probinson	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0000006	OMIM:255110	TAS				I		HPO:skoehler	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0000007	OMIM:255110	IEA				I		HPO:iea	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0000083	OMIM:255110	IEA				P		HPO:iea	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0001324	OMIM:255110	IEA				P		HPO:skoehler	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0002913	OMIM:255110	IEA				P		HPO:skoehler	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0003201	OMIM:255110	IEA				P		HPO:iea	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0003326	OMIM:255110	IEA				P		HPO:iea	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0003394	OMIM:255110	IEA				P		HPO:iea	
OMIM	255110	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED		HP:0003552	OMIM:255110	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0000007	OMIM:255120	IEA				I		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001250	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001252	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001254	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001259	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001290	OMIM:255120	TAS				P		HPO:skoehler	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001397	OMIM:255120	IEA				P		HPO:skoehler	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001640	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001947	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001985	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0001987	OMIM:255120	IEA				P		HPO:skoehler	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0002014	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0002240	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0002686	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0002910	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0003236	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0007335	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0008279	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0008872	OMIM:255120	IEA				P		HPO:iea	
OMIM	255120	CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY		HP:0011675	OMIM:255120	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0000007	OMIM:255125	IEA				I		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0001324	OMIM:255125	IEA				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0001924	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0001962	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0002094	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0002151	OMIM:255125	IEA				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0002913	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003128	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003198	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003201	OMIM:255125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003236	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003394	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003546	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003548	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003621	OMIM:255125	IEA				C		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0003737	OMIM:255125	IEA				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0008306	OMIM:255125	IEA				P		HPO:iea	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0008314	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0011923	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0011924	OMIM:255125	TAS				P		HPO:skoehler	
OMIM	255125	MYOPATHY WITH EXERCISE INTOLERANCE, SWEDISH TYPE		HP:0012240	OMIM:255125	IEA				P		HPO:probinson	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0000007	OMIM:255140	IEA				I		HPO:iea	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0001252	OMIM:255140	IEA				P		HPO:iea	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0001290	OMIM:255140	TAS				P		HPO:skoehler	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0001510	OMIM:255140	IEA				P		HPO:iea	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0001939	OMIM:255140	IEA				P		HPO:iea	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0003198	OMIM:255140	IEA				P		HPO:skoehler	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0003701	OMIM:255140	IEA				P		HPO:iea	
OMIM	255140	MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA		HP:0003797	OMIM:255140	TAS				P		HPO:skoehler	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:255160	IEA				I		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0000218	OMIM:255160	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0001635	OMIM:255160	TAS				P		HPO:skoehler	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0001639	OMIM:255160	TAS				P		HPO:skoehler	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0001644	OMIM:255160	TAS				P		HPO:skoehler	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0002058	OMIM:255160	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0002093	OMIM:255160	TAS				P		HPO:skoehler	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0002650	OMIM:255160	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003236	OMIM:255160	IEA				P		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003458	OMIM:255160	IEA				P		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003677	OMIM:255160	IEA				C		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003687	OMIM:255160	IEA				P		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003697	OMIM:255160	IEA				P		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003704	OMIM:255160	IEA				P		HPO:iea	
OMIM	255160	#255160 MYOPATHY, MYOSIN STORAGE, AUTOSOMAL RECESSIVE; MSMB;;MYOPATHY, HYALINE BODY, AUTOSOMAL RECESSIVE		HP:0003803	OMIM:255160	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:255200	IEA				I		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0000218	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0000276	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0000508	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0000602	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001256	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001270	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001284	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001319	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001371	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001618	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001761	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0001762	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0002460	OMIM:255200	IEA				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0002515	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0002650	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0002747	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0002808	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003307	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003327	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003391	OMIM:255200	TAS				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003458	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003674	OMIM:255200	IEA				C		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003687	OMIM:255200	IEA				P		HPO:skoehler	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003691	OMIM:255200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003700	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0003701	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0008872	OMIM:255200	IEA				P		HPO:iea	
OMIM	255200	#255200 MYOPATHY, CENTRONUCLEAR, 2; CNM2;;MYOPATHY, CENTRONUCLEAR, AUTOSOMAL RECESSIVE;;MYOTUBULAR MYOPATHY, AUTOSOMAL RECESSIVE		HP:0010628	OMIM:255200	IEA				P		HPO:iea	
OMIM	255300	MYOPATHY, CONGENITAL		HP:0000007	OMIM:255300	IEA				I		HPO:iea	
OMIM	255300	MYOPATHY, CONGENITAL		HP:0000707	OMIM:255300	IEA				P		HPO:iea	
OMIM	255300	MYOPATHY, CONGENITAL		HP:0003198	OMIM:255300	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000006	OMIM:255310	IEA				I		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000007	OMIM:255310	TAS				I		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000218	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000275	OMIM:255310	TAS				P		HPO:probinson	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000276	OMIM:255310	TAS				P		HPO:probinson	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000508	OMIM:255310	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0000602	OMIM:255310	TAS		HP:0040284		P		HPO:probinson	20%
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001283	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001319	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001374	OMIM:255310	IEA		HP:0040284		P		HPO:probinson	13%
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001425	OMIM:255310	IEA				I		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001508	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001558	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001612	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0001644	OMIM:255310	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0002015	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0002093	OMIM:255310	TAS				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0002650	OMIM:255310	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0002747	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0002938	OMIM:255310	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003121	OMIM:255310	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003324	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003577	OMIM:255310	IEA				C		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003687	OMIM:255310	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003701	OMIM:255310	IEA				P		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003755	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0003828	OMIM:255310	TAS				C		HPO:skoehler	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0010628	OMIM:255310	IEA				P		HPO:iea	
OMIM	255310	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION		HP:0011968	OMIM:255310	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000007	OMIM:255320	IEA				I		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000218	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000508	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000544	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001252	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001270	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001284	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001319	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001388	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001558	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001561	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001789	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002058	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002089	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002093	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002205	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002650	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003202	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003324	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003327	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003557	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003560	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003623	OMIM:255320	TAS				C		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003701	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003738	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003787	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003798	OMIM:255320	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0008872	OMIM:255320	IEA				P		HPO:iea	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0009025	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0009046	OMIM:255320	TAS				P		HPO:skoehler	
OMIM	255320	#255320 MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MINICORE MYOPATHY;;MULTICORE MYOPATHY;;MULTIMINICORE MYOPATHY MULTICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA;;MULTIMINICORE DISEASE WITH EXTERNAL OPHTHALMOPLEGIA		HP:0010628	OMIM:255320	IEA				P		HPO:iea	
OMIM	255500	MYOPIA, INFANTILE SEVERE		HP:0000007	OMIM:255500	IEA				I		HPO:iea	
OMIM	255500	MYOPIA, INFANTILE SEVERE		HP:0000545	OMIM:255500	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0000007	OMIM:255600	IEA				I		HPO:iea	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0001771	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0002460	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0002938	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0002944	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003202	OMIM:255600	TAS				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003236	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003306	OMIM:255600	TAS				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003621	OMIM:255600	IEA				C		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003676	OMIM:255600	IEA				C		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0003701	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0004322	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0005952	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0005997	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0009025	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255600	#255600 MYOSCLEROSIS, AUTOSOMAL RECESSIVE;;MYOPATHY, MYOSCLEROTIC;;MYOSCLEROSIS, CONGENITAL, OF LOWENTHAL		HP:0010628	OMIM:255600	IEA				P		HPO:skoehler	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:255700	TAS				I		HPO:iea	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0001324	OMIM:255700	IEA		HP:0040284		P		HPO:skoehler	75%
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0002015	OMIM:255700	TAS				P		HPO:probinson	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0003326	OMIM:255700	PCS		HP:0040284		P		HPO:probinson	11/27
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0003552	PMID:18337100	PCS		HP:0040284		P		HPO:probinson	25/27
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0003712	OMIM:255700	PCS		HP:0040284		P		HPO:probinson	15/27
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0003730	OMIM:255700	IEA				P		HPO:iea	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0003740	OMIM:255700	PCS		HP:0040284		P		HPO:probinson	27/27
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0008968	OMIM:255700	TAS				P		HPO:skoehler	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0010548	PMID:18337100	PCS		HP:0040284		P		HPO:probinson	26/27
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0011463	OMIM:255700	PCS				C		HPO:probinson	
OMIM	255700	MYOTONIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0025605	OMIM:255700	IEA				P		HPO:skoehler	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0000007	OMIM:255710	IEA				I		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0000768	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0001256	OMIM:255710	IEA				P		HPO:skoehler	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0001591	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0002486	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0002751	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0002857	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0003712	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0003725	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0004322	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0006361	OMIM:255710	IEA				P		HPO:iea	
OMIM	255710	MYOTONIA WITH SKELETAL ABNORMALITIES AND MENTAL RETARDATION		HP:0008422	OMIM:255710	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000007	OMIM:255800	IEA				I		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000023	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000160	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000205	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000272	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000293	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000347	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000369	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000396	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000470	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000482	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000508	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000518	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000545	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000581	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000768	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000926	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0000939	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001239	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001249	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001265	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001324	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001374	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001537	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001620	OMIM:255800	TAS				P		HPO:probinson	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001621	OMIM:255800	TAS				P		HPO:probinson	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001762	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0001763	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002047	OMIM:255800	IEA				P		HPO:skoehler	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002230	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002486	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002673	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002750	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002751	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002812	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0002938	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003016	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003044	OMIM:255800	IEA				P		HPO:skoehler	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003202	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003273	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003417	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0003712	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0004322	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0005830	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0006473	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0006499	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0007740	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0008734	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0009473	OMIM:255800	IEA				P		HPO:iea	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0012368	OMIM:255800	TAS				P		HPO:skoehler	
OMIM	255800	SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1		HP:0045025	OMIM:255800	IEA				P		HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0000007	OMIM:255900	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0000821	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0000853	OMIM:255900	IEA				P		HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0000958	OMIM:255900	IEA				P		HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0000966	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0001254	OMIM:255900	TAS				P		HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0001324	OMIM:255900	TAS				P		HPO:skoehler	
OMIM	255900	MYXEDEMA		HP:0001609	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0002019	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0002354	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0002925	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0003388	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0003394	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0003401	OMIM:255900	IEA				P		HPO:iea	
OMIM	255900	MYXEDEMA		HP:0012378	OMIM:255900	TAS				P		HPO:skoehler	
OMIM	255960	MYXOMA, INTRACARDIAC		HP:0000006	OMIM:255960	TAS				I		HPO:skoehler	
OMIM	255960	MYXOMA, INTRACARDIAC		HP:0000007	OMIM:255960	IEA				I		HPO:iea	
OMIM	255960	MYXOMA, INTRACARDIAC		HP:0006689	OMIM:255960	IEA				P		HPO:iea	
OMIM	255960	MYXOMA, INTRACARDIAC		HP:0006691	OMIM:255960	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000006	OMIM:255980	IEA				I		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000189	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000215	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000218	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000286	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000316	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0000407	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0001597	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0001609	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0001642	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0001831	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0002007	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0002263	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0004322	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0005280	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0006026	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0009765	OMIM:255980	TAS				P		HPO:skoehler	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0009803	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0009836	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0010041	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0010055	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0010580	OMIM:255980	IEA				P		HPO:iea	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0011220	OMIM:255980	TAS				P		HPO:skoehler	
OMIM	255980	NASODIGITOACOUSTIC SYNDROME		HP:0011304	OMIM:255980	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0000007	OMIM:255990	IEA				I		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0000119	OMIM:255990	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0000365	OMIM:255990	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0000518	OMIM:255990	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0001510	OMIM:255990	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0003115	OMIM:255990	IEA				P		HPO:iea	
OMIM	255990	NATHALIE SYNDROME		HP:0003202	OMIM:255990	IEA				P		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000007	OMIM:255995	IEA				I		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000028	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000175	OMIM:255995	IEA				P		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000218	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000248	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000252	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000347	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000369	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000405	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000494	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000506	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000508	OMIM:255995	IEA				P		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0000581	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001249	OMIM:255995	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001265	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001270	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001324	OMIM:255995	TAS	HP:0003577			P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001371	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0001883	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002047	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002058	OMIM:255995	IEA				P		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002111	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002119	OMIM:255995	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002714	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0002751	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0003202	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0004322	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0005775	OMIM:255995	IEA				P		HPO:iea	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0011800	OMIM:255995	IEA				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0011968	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	255995	MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB		HP:0012745	OMIM:255995	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000007	OMIM:256000	IEA				I		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000407	PMID:22114105	PCS				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000486	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000508	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000580	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000602	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000639	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000648	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000712	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0000998	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001249	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001250	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001251	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001252	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001257	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001260	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001263	OMIM:256000	PCS				P		HPO:probinson	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001290	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001332	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001347	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001404	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001425	OMIM:256000	TAS				I		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001427	OMIM:256000	IEA				I		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0001508	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002093	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002151	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002171	OMIM:256000	PCS				P		HPO:probinson	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002171	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002490	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002793	OMIM:256000	IEA				P		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0002878	OMIM:256000	TAS				P		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0003128	OMIM:256000	PCS				P		HPO:probinson	
OMIM	256000	LEIGH SYNDROME; LS		HP:0003593	OMIM:256000	IEA				C		HPO:iea	
OMIM	256000	LEIGH SYNDROME; LS		HP:0003676	OMIM:256000	TAS				C		HPO:skoehler	
OMIM	256000	LEIGH SYNDROME; LS		HP:0007305	OMIM:256000	PCS				P		HPO:probinson	
OMIM	256000	LEIGH SYNDROME; LS		HP:0025356	OMIM:256000	IEA				P		HPO:skoehler	
OMIM	256020	256020 NAIL-PATELLA-LIKE RENAL DISEASE;;GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE		HP:0000007	OMIM:256020	IEA				I		HPO:iea	
OMIM	256020	256020 NAIL-PATELLA-LIKE RENAL DISEASE;;GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE		HP:0000083	OMIM:256020	IEA				P		HPO:iea	
OMIM	256020	256020 NAIL-PATELLA-LIKE RENAL DISEASE;;GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE		HP:0000093	OMIM:256020	IEA				P		HPO:iea	
OMIM	256020	256020 NAIL-PATELLA-LIKE RENAL DISEASE;;GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE		HP:0000112	OMIM:256020	IEA				P		HPO:iea	
OMIM	256020	256020 NAIL-PATELLA-LIKE RENAL DISEASE;;GLOMERULAR BASEMENT MEMBRANE DISEASE, NAIL-PATELLA SYNDROME TYPE		HP:0000924	OMIM:256020	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000007	OMIM:256030	IEA				I		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000175	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000218	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000343	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000369	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0000478	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001265	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001270	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001283	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001284	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001319	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001371	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001425	OMIM:256030	TAS				I		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001533	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001547	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001558	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0001561	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002015	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002058	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2	HP:0012828	HP:0002104	OMIM:256030	TAS				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002359	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002515	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002540	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002650	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0002747	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2	HP:0012828	HP:0002804	OMIM:256030	TAS				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003306	OMIM:256030	TAS				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003307	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003324	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003445	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003458	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003593	OMIM:256030	IEA				C		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003690	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003701	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003722	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003798	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003803	OMIM:256030	IEA				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0003810	OMIM:256030	TAS				P		HPO:iea	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0008180	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0010628	OMIM:256030	TAS				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0011968	OMIM:256030	TAS				P		HPO:skoehler	
OMIM	256030	NEMALINE MYOPATHY 2; NEM2		HP:0030059	OMIM:256030	IEA				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000007	OMIM:256040	IEA				I		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000158	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000179	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000400	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000448	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000509	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000938	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0000953	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001090	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001250	OMIM:256040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001256	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001324	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001507	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001508	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001635	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001640	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001744	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001873	OMIM:256040	IEA				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001903	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0001935	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002135	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002155	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002240	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002653	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002716	OMIM:256040	IEA				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002829	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002910	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0002987	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0003202	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0003565	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0004322	OMIM:256040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1	HP:0012828	HP:0005830	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0008887	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0009125	OMIM:256040	TAS	HP:0011463			P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0010702	OMIM:256040	IEA				P		HPO:iea	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0010783	OMIM:256040	IEA				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0011675	OMIM:256040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0012490	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0025131	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0030053	OMIM:256040	IEA				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1	HP:0012828	HP:0100490	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0100534	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0100759	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256040	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 1; PRAAS1		HP:0100807	OMIM:256040	TAS				P		HPO:skoehler	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000007	OMIM:256050	IEA				I		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000175	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000272	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000347	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000470	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0000926	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0001762	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0001852	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0001939	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002089	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002093	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002650	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002938	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002947	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0002983	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0003180	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0003185	OMIM:256050	TAS				P		HPO:skoehler	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0003417	OMIM:256050	IEA				P		HPO:skoehler	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0003440	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0003826	OMIM:256050	IEA				M		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0005257	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0005280	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0005819	OMIM:256050	TAS				P		HPO:skoehler	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0006375	OMIM:256050	IEA				P		HPO:iea	
OMIM	256050	#256050 ATELOSTEOGENESIS, TYPE II; AOII;;AO2;;NEONATAL OSSEOUS DYSPLASIA IDE LA CHAPELLE DYSPLASIA, INCLUDED; DLCD, INCLUDED		HP:0011800	OMIM:256050	TAS				P		HPO:skoehler	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000007	OMIM:256100	IEA				I		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000090	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000092	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000103	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000108	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0000822	OMIM:256100	IEA				P		HPO:skoehler	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0001510	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0001903	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0001959	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0003158	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0003774	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0005576	OMIM:256100	IEA				P		HPO:iea	
OMIM	256100	NEPHRONOPHTHISIS 1		HP:0005583	OMIM:256100	IEA				P		HPO:iea	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0000007	OMIM:256120	TAS				I		HPO:skoehler	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0000083	OMIM:256120	TAS				P		HPO:skoehler	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0000112	OMIM:256120	TAS				P		HPO:skoehler	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0000407	OMIM:256120	TAS				P		HPO:skoehler	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0000843	OMIM:256120	TAS				P		HPO:skoehler	
OMIM	256120	256120 NEPHROPATHY, DEAFNESS, AND HYPERPARATHYROIDISM		HP:0008208	OMIM:256120	TAS				P		HPO:skoehler	
OMIM	256150	NEPHROSIALIDOSIS		HP:0000007	OMIM:256150	IEA				I		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0000083	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0000100	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0000112	OMIM:256150	IEA				P		HPO:skoehler	
OMIM	256150	NEPHROSIALIDOSIS		HP:0000924	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0001541	OMIM:256150	IEA				P		HPO:skoehler	
OMIM	256150	NEPHROSIALIDOSIS		HP:0001698	OMIM:256150	IEA				P		HPO:skoehler	
OMIM	256150	NEPHROSIALIDOSIS		HP:0001939	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0001999	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0003593	OMIM:256150	TAS				C		HPO:skoehler	
OMIM	256150	NEPHROSIALIDOSIS		HP:0003819	OMIM:256150	IEA				M		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0004333	OMIM:256150	IEA				P		HPO:iea	
OMIM	256150	NEPHROSIALIDOSIS		HP:0010864	OMIM:256150	IEA				P		HPO:iea	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0000007	OMIM:256200	TAS				I		HPO:nvasilevsky	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0000100	OMIM:256200	IEA				P		HPO:iea	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0000193	OMIM:256200	IEA				P		HPO:iea	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0000365	OMIM:256200	IEA				P		HPO:skoehler	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0001423	OMIM:256200	TAS				I		HPO:nvasilevsky	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0009611	OMIM:256200	TAS				P		HPO:probinson	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0009650	OMIM:256200	TAS				P		HPO:probinson	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0010097	OMIM:256200	TAS				P		HPO:probinson	
OMIM	256200	NEPHROSIS WITH DEAFNESS AND URINARY TRACT AND DIGITAL MALFORMATIONS		HP:0010103	OMIM:256200	TAS				P		HPO:probinson	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000007	OMIM:256300	IEA				I		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000083	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000092	OMIM:256300	TAS				P		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000093	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000096	OMIM:256300	IEA				P		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000821	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0000969	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0001510	OMIM:256300	TAS				P		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0001518	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0001967	OMIM:256300	TAS				P		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0002020	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0002021	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0002643	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0002719	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003073	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003075	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003077	OMIM:256300	TAS				P		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003270	OMIM:256300	IEA				P		HPO:iea	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003577	OMIM:256300	TAS				C		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0003678	OMIM:256300	TAS				C		HPO:skoehler	
OMIM	256300	NEPHROTIC SYNDROME, TYPE 1; NPHS1		HP:0008677	OMIM:256300	IEA				P		HPO:iea	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0000006	OMIM:256370	TAS				I		HPO:skoehler	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0000007	OMIM:256370	IEA				I		HPO:iea	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0000083	OMIM:256370	IEA				P		HPO:iea	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0000097	OMIM:256370	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0000100	OMIM:256370	IEA				P		HPO:iea	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0001967	OMIM:256370	IEA				P		HPO:iea	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0002667	OMIM:256370	IEA				P		HPO:skoehler	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0003676	OMIM:256370	TAS				C		HPO:skoehler	
OMIM	256370	NEPHROTIC SYNDROME, TYPE 4		HP:0011463	OMIM:256370	TAS				C		HPO:probinson	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0000006	OMIM:256450	IEA				I		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0000007	OMIM:256450	IEA				I		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0000825	OMIM:256450	IEA				P		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0001249	OMIM:256450	IEA				P		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0001325	OMIM:256450	TAS				P		HPO:probinson	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0001425	OMIM:256450	TAS				I		HPO:skoehler	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0001520	OMIM:256450	IEA				P		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0002173	OMIM:256450	IEA				P		HPO:iea	
OMIM	256450	#256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1;;PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY; PHHI;;HYPOGLYCEMIA, HYPERINSULINEMIC, OF INFANCY;;HYPERINSULINEMIC HYPOGLYCEMIA DUE TO FOCAL ADENOMATOUS HYPERPLASIA;;NESIDIOBLASTOSIS OF PANCREAS;;HYPERINSULINISM, FAMILIAL, WITH PANCREATIC NESIDIOBLASTOSIS;;HYPERINSULINISM, CONGENITAL		HP:0004510	OMIM:256450	IEA				P		HPO:iea	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0000007	OMIM:256500	IEA				I		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0000535	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0001019	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0001025	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0001263	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0001508	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0002099	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0002209	OMIM:256500	TAS				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0002299	OMIM:256500	TAS				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0002719	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0003011	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0003193	OMIM:256500	TAS				P		HPO:skoehler	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0003212	OMIM:256500	TAS				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0004779	OMIM:256500	IEA				P		HPO:skoehler	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0004906	OMIM:256500	IEA				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0007479	OMIM:256500	TAS				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0011473	OMIM:256500	TAS				P		HPO:probinson	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0100665	OMIM:256500	TAS				P		HPO:skoehler	
OMIM	256500	NETHERTON SYNDROME; NETH		HP:0500093	OMIM:256500	IEA				P		HPO:skoehler	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000007	OMIM:256520	IEA				I		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000028	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000104	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000136	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000175	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000179	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000204	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000252	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000316	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000340	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000347	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000400	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000470	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000518	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000520	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000561	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0000568	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001059	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001196	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001274	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001305	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001321	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001339	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001511	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001558	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001561	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001629	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001643	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001655	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001669	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001770	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001838	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0001848	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0002089	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0002190	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0002324	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0002414	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0002983	OMIM:256520	TAS				P		HPO:skoehler	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0003826	OMIM:256520	IEA				M		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0006101	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0006266	OMIM:256520	TAS				P		HPO:skoehler	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0007430	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0007525	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0009466	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0009473	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0009826	OMIM:256520	IEA				P		HPO:iea	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0011224	OMIM:256520	TAS				P		HPO:skoehler	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0012385	OMIM:256520	TAS				P		HPO:skoehler	
OMIM	256520	#256520 NEU-LAXOVA SYNDROME; NLS		HP:0030084	OMIM:256520	TAS				P		HPO:skoehler	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0000007	PMID:8725271	PCS				I		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0000280	PMID:23915561	PCS	HP:0003593			P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0000365	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0000524	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0000943	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0001028	OMIM:256540	IEA				P		HPO:skoehler	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0001249	PMID:23915561	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0001250	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0001433	OMIM:256540	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0001790	PMID:19466716	PCS	HP:0030674			P		HP:probinson	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0003271	PMID:23915561	PCS	HP:0003593			P		HP:probinson	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0003510	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0007759	OMIM:256540	IEA				P		HPO:iea	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0008166	OMIM:256540	TAS				P		HPO:probinson	
OMIM	256540	NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY		HP:0010729	PMID:23915561	PCS	HP:0003593			P		HPO:skoehler	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000007	OMIM:256550	TAS				I		HPO:probinson	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000023	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000093	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000280	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000282	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000407	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000518	OMIM:256550	IEA				P		HPO:skoehler	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000529	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000639	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0000943	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001249	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001250	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001252	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001290	OMIM:256550	TAS				P		HPO:skoehler	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001310	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001324	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001336	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001347	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001350	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001541	OMIM:256550	TAS				P		HPO:probinson	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001638	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001640	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001744	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001789	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0001922	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0002240	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0003202	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0003461	OMIM:256550	TAS				P		HPO:probinson	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0004322	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0004333	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0010655	OMIM:256550	IEA				P		HPO:iea	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0010729	OMIM:256550	IEA				P		HPO:skoehler	
OMIM	256550	NEURAMINIDASE DEFICIENCY		HP:0012061	OMIM:256550	TAS				P		HPO:probinson	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000007	OMIM:256600	IEA				I		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000347	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000365	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000486	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000572	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000639	OMIM:256600	IEA				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000648	OMIM:256600	IEA				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000649	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0000762	OMIM:256600	IEA		HP:0040284		P		HPO:skoehler	30%
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001249	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001250	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001251	OMIM:256600	IEA				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001252	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001263	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001272	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001284	OMIM:256600	IEA		HP:0040284		P		HPO:skoehler	30%
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001290	OMIM:256600	TAS				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001347	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0001939	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002007	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002059	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002062	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002171	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002180	OMIM:256600	IEA				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002317	OMIM:256600	IEA				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002376	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002510	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0002529	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0003196	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0003324	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0003444	OMIM:256600	IEA				P		HPO:iea	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0003593	OMIM:256600	TAS		HP:0040282		C		HPO:iea	HP:0040282
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0007256	OMIM:256600	TAS				P		HPO:skoehler	
OMIM	256600	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A		HP:0011220	OMIM:256600	TAS				P		HPO:skoehler	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0000007	OMIM:256690	IEA				I		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0000122	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0001199	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0001249	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0001939	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0002007	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0002353	OMIM:256690	IEA				P		HPO:skoehler	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0004122	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0004322	OMIM:256690	IEA				P		HPO:iea	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0011220	OMIM:256690	TAS				P		HPO:skoehler	
OMIM	256690	256690 NEUROFACIODIGITORENAL SYNDROME;;NFDR SYNDROME		HP:0011803	OMIM:256690	TAS				P		HPO:skoehler	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0000006	OMIM:256700	IEA				I		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0000765	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0000822	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001251	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001336	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001425	OMIM:256700	IEA				I		HPO:skoehler	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001508	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001824	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001903	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0001945	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0002014	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0002027	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0002176	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0002277	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0002653	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0003005	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0003006	OMIM:256700	TAS				P		HPO:probinson	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0003745	OMIM:256700	IEA				I		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0003829	OMIM:256700	IEA				C		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0006747	OMIM:256700	IEA				P		HPO:iea	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0010543	OMIM:256700	IEA				P		HPO:skoehler	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0011977	OMIM:256700	TAS				P		HPO:probinson	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0011978	OMIM:256700	TAS				P		HPO:probinson	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0011979	OMIM:256700	TAS				P		HPO:probinson	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0031500	OMIM:256700	IEA				P		HPO:skoehler	
OMIM	256700	NEUROBLASTOMA, SUSCEPTIBILITY TO		HP:0200036	OMIM:256700	IEA				P		HPO:skoehler	
OMIM	256710	ELEJALDE DISEASE		HP:0000007	OMIM:256710	IEA				I		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0000577	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0000639	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001008	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001010	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001249	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001250	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001251	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001252	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001257	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001263	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0001290	OMIM:256710	TAS				P		HPO:skoehler	
OMIM	256710	ELEJALDE DISEASE		HP:0002218	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0002220	OMIM:256710	IEA				P		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0003593	OMIM:256710	IEA				C		HPO:iea	
OMIM	256710	ELEJALDE DISEASE		HP:0003819	OMIM:256710	IEA				M		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0000007	OMIM:256720	IEA				I		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0000939	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0001271	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0001939	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0002445	OMIM:256720	IEA				P		HPO:skoehler	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0002757	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0002827	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0003202	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0006887	OMIM:256720	IEA				P		HPO:iea	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0010864	OMIM:256720	TAS				P		HPO:skoehler	
OMIM	256720	256720 NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY		HP:0030043	OMIM:256720	TAS				P		HPO:skoehler	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000007	OMIM:256730	IEA				I		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000253	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000529	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000550	OMIM:256730	IEA				P		HPO:skoehler	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000608	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000618	OMIM:256730	TAS	HP:0011463			P		HPO:probinson	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000648	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000654	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000716	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000737	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0000738	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001249	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001250	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001251	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001252	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001257	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001263	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001290	OMIM:256730	TAS				P		HPO:skoehler	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001336	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001371	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0001939	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002059	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002074	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002353	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002360	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002361	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0002371	OMIM:256730	IEA				P		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0003674	OMIM:256730	IEA				C		HPO:iea	
OMIM	256730	CEROID LIPOFUSCINOSIS, NEURONAL, 1		HP:0005484	OMIM:256730	TAS				P		HPO:probinson	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0000007	OMIM:256731	IEA				I	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0000529	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0000546	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0000639	OMIM:256731	TAS		HP:0040283		P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:skoehler	HP:0040283
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001249	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001250	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001251	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001260	OMIM:256731	TAS		HP:0040283		P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:skoehler	HP:0040283
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001272	OMIM:256731	TAS		HP:0040283		P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:skoehler	HP:0040283
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001310	OMIM:256731	TAS		HP:0040283		P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:skoehler	HP:0040283
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001311	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0001336	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0002074	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0002075	OMIM:256731	TAS		HP:0040283		P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:skoehler	HP:0040283
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0002312	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0002333	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0002376	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0003205	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0003208	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256731	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH vLINCL, INCLUDED		HP:0003226	OMIM:256731	IEA				P	#256731 CEROID LIPOFUSCINOSIS, NEURONAL, 5; CLN5;;CEROID LIPOFUSCINOSIS, NEURONAL, 5, VARIABLE AGE AT ONSETNEURONAL CEROID LIPOFUSCINOSIS, LATE INFANTILE, FINNISH VARIANT, INCLUDED;;FINNISH VLINCL, INCLUDED	HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000007	OMIM:256800	IEA				I		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000491	OMIM:256800	IEA				P		HPO:skoehler	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000495	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000559	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000712	OMIM:256800	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000742	OMIM:256800	IEA				P		HPO:skoehler	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000752	OMIM:256800	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0000970	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0001058	OMIM:256800	TAS				P		HP:probinson	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0001249	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0001263	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA	HP:0012828	HP:0001954	OMIM:256800	TAS				P		HPO:probinson	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0002164	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0002754	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0002821	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0003593	OMIM:256800	IEA				C		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0004782	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0005307	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0006121	OMIM:256800	IEA				P		HP:probinson	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0007021	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0007249	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0007460	OMIM:256800	TAS				P		HP:probinson	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0007759	OMIM:256800	IEA				P		HPO:iea	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0008404	OMIM:256800	TAS				P		HPO:skoehler	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0012804	OMIM:256800	TAS				P		HPO:skoehler	
OMIM	256800	INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA		HP:0100725	OMIM:256800	IEA				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0000007	OMIM:256810	IEA				I		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0000495	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0000639	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001251	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001263	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001265	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001284	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001290	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001332	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001394	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001403	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001414	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001508	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0001943	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002013	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002014	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002240	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002460	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002659	OMIM:256810	TAS				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002661	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002715	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0002910	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0003128	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0003380	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0003593	OMIM:256810	IEA				C		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0003676	OMIM:256810	TAS				C		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0004322	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0005010	OMIM:256810	TAS				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0006121	OMIM:256810	TAS				P		HP:probinson	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0006554	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0006579	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0006582	OMIM:256810	IEA				P		HPO:iea	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0007021	OMIM:256810	TAS				P		HPO:skoehler	
OMIM	256810	NAVAJO NEUROHEPATOPATHY		HP:0007141	OMIM:256810	IEA				P		HPO:skoehler	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:256840	IEA				I		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:256840	IEA				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0001760	OMIM:256840	IEA				P		HPO:skoehler	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0002064	OMIM:256840	IEA				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0002169	OMIM:256840	IEA				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0002936	OMIM:256840	TAS				P		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003146	OMIM:256840	TAS				P		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003431	OMIM:256840	TAS				P		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003477	OMIM:256840	TAS				P		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:256840	IEA				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003563	OMIM:256840	TAS				P		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:256840	TAS				C		HPO:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003621	OMIM:256840	IEA				C		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0003693	OMIM:256840	TAS				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0006121	OMIM:256840	TAS				P		HP:probinson	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0006827	OMIM:256840	IEA				P		HPO:iea	
OMIM	256840	NEUROPATHY, HEREDITARY SENSORY, WITH SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE		HP:0006984	OMIM:256840	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0000007	OMIM:256850	IEA				I		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0000639	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001155	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001249	OMIM:256850	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001258	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001260	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001317	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001347	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001761	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001762	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0001763	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002062	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002212	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002460	OMIM:256850	TAS				P		HPO:probinson	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002522	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002600	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002650	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0002936	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003376	OMIM:256850	IEA				P		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003380	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003390	OMIM:256850	IEA				P		HPO:probinson	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003621	OMIM:256850	TAS				C		HPO:probinson	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003677	OMIM:256850	IEA				C		HPO:iea	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003693	OMIM:256850	TAS				P		HPO:probinson	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0003701	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0007002	OMIM:256850	IEA				P		HPO:probinson	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0007256	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256850	#256850 GIANT AXONAL NEUROPATHY 1, AUTOSOMAL RECESSIVE; GAN1;;GAN		HP:0010628	OMIM:256850	TAS				P		HPO:skoehler	
OMIM	256860	NEUROPATHY, HEREDITARY SENSORY, ATYPICAL		HP:0000007	OMIM:256860	TAS				I		HPO:skoehler	
OMIM	256860	NEUROPATHY, HEREDITARY SENSORY, ATYPICAL		HP:0000763	OMIM:256860	TAS				P		HPO:skoehler	
OMIM	256860	NEUROPATHY, HEREDITARY SENSORY, ATYPICAL		HP:0001251	OMIM:256860	IEA				P		HPO:skoehler	
OMIM	256860	NEUROPATHY, HEREDITARY SENSORY, ATYPICAL		HP:0003487	OMIM:256860	TAS				P		HPO:skoehler	
OMIM	256860	NEUROPATHY, HEREDITARY SENSORY, ATYPICAL		HP:0010871	OMIM:256860	TAS				P		HPO:probinson	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0000007	OMIM:256870	TAS				I		HPO:iea	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0001945	OMIM:256870	IEA				P		HPO:skoehler	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0003202	OMIM:256870	TAS				P		HPO:iea	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0003593	OMIM:256870	TAS				C		HPO:iea	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0007340	OMIM:256870	TAS				P		HPO:skoehler	
OMIM	256870	NEUROPATHY, PAINFUL		HP:0009830	OMIM:256870	TAS				P		HPO:skoehler	
OMIM	257000	NEUROVISCERAL STORAGE DISEASE WITH CURVILINEAR BODIES		HP:0000007	OMIM:257000	IEA				I		HPO:iea	
OMIM	257000	NEUROVISCERAL STORAGE DISEASE WITH CURVILINEAR BODIES		HP:0000707	OMIM:257000	IEA				P		HPO:iea	
OMIM	257000	NEUROVISCERAL STORAGE DISEASE WITH CURVILINEAR BODIES		HP:0001939	OMIM:257000	IEA				P		HPO:iea	
OMIM	257100	NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA		HP:0000007	OMIM:257100	TAS				I		HPO:probinson	
OMIM	257100	NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA		HP:0001875	OMIM:257100	TAS				P		HPO:probinson	
OMIM	257100	NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA		HP:0001880	OMIM:257100	TAS				P		HPO:probinson	
OMIM	257100	NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA		HP:0003811	OMIM:257100	TAS				M		HPO:probinson	
OMIM	257150	NEUTROPHIL ACTIN DYSFUNCTION		HP:0000007	OMIM:257150	IEA				I		HPO:iea	
OMIM	257150	NEUTROPHIL ACTIN DYSFUNCTION		HP:0001939	OMIM:257150	IEA				P		HPO:iea	
OMIM	257150	NEUTROPHIL ACTIN DYSFUNCTION		HP:0002718	OMIM:257150	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0000007	OMIM:257200	IEA				I		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0000939	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0000991	OMIM:257200	TAS				P		HPO:probinson	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001249	OMIM:257200	IEA				P		HPO:skoehler	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001252	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001257	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001263	OMIM:257200	TAS				P		HPO:skoehler	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001265	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001290	OMIM:257200	TAS				P		HPO:skoehler	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001324	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001508	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001538	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001744	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001935	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0001982	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002013	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002019	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002063	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002205	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002207	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002240	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002305	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0002716	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0003593	OMIM:257200	IEA				C		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0003609	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0004322	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0004333	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0006579	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0006579	OMIM:257200	TAS				P		HPO:probinson	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0008872	OMIM:257200	IEA				P		HPO:iea	
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0010729	OMIM:257200	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	257200	NIEMANN-PICK DISEASE, TYPE A		HP:0025356	OMIM:257200	IEA				P		HPO:skoehler	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0000007	PMID:11182931	PCS				I		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0000511	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0000709	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0000726	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001249	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001250	PMID:11182931	PCS		HP:0040284		P		HPO:iea	12/14
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001251	PMID:11182931	PCS				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001252	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001257	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001260	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001263	PMID:11182931	PCS				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001290	OMIM:257220	TAS				P		HPO:skoehler	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001332	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001425	OMIM:257220	TAS				I		HPO:skoehler	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001744	PMID:11182931	PCS		HP:0040284		P		HPO:iea	4/13
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001791	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0001982	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002015	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002185	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002240	PMID:11182931	PCS		HP:0040284		P		HPO:iea	7/13
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002371	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002524	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0002529	OMIM:257220	IEA				P		HPO:skoehler	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0003349	PMID:3378364	PCS				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0003640	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0003674	OMIM:257220	IEA				C		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0004333	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0006579	OMIM:257220	IEA				P		HPO:iea	
OMIM	257220	NIEMANN-PICK DISEASE, TYPE C1		HP:0006583	OMIM:257220	IEA				P		HPO:iea	
OMIM	257270	#257270 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B;;NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:257270	IEA				I		HPO:iea	
OMIM	257270	#257270 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B;;NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000545	OMIM:257270	IEA				P		HPO:iea	
OMIM	257270	#257270 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B;;NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0007642	OMIM:257270	IEA				P		HPO:skoehler	
OMIM	257270	#257270 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B;;NIGHT BLINDNESS, CONGENITAL STATIONARY, COMPLETE, AUTOSOMAL RECESSIVE;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0012047	OMIM:257270	TAS				P		HPO:skoehler	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000007	OMIM:257300	IEA				I		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000028	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000047	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000048	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000054	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000062	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000107	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000175	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000207	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000238	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000248	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME	HP:0012828	HP:0000252	OMIM:257300	TAS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000272	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000286	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000316	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000343	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000347	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000348	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000358	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000369	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000445	OMIM:257300	TAS				P		HPO:skoehler	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000463	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000470	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000518	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000582	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000639	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0000879	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001274	OMIM:257300	TAS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001290	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001305	OMIM:257300	TAS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001321	OMIM:257300	TAS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001511	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001518	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001562	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0001909	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002069	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002119	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002123	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002187	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002667	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0002859	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0003196	OMIM:257300	TAS				P		HPO:skoehler	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0004322	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0005280	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0005387	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0006849	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0006872	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0008872	OMIM:257300	IEA				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0008897	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0011344	OMIM:257300	PCS				P		HPO:probinson	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0011800	OMIM:257300	TAS				P		HPO:skoehler	
OMIM	257300	#257300 MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1; MVA1;;MVA SYNDROME		HP:0200024	OMIM:257300	TAS				P		HPO:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0000007	PMID:10973257	PCS				I		HPO:iea	
OMIM	257320	LISSENCEPHALY 2		HP:0000252	PMID:10973257	PCS				P		HPO:iea	
OMIM	257320	LISSENCEPHALY 2		HP:0000340	PMID:10973257	PCS				P		HPO:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0000426	OMIM:257320	TAS				P		HPO:iea	
OMIM	257320	LISSENCEPHALY 2		HP:0001004	PMID:10973257	PCS	HP:0003577			P		HP:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0001252	PMID:10973257	PCS	HP:0003577	HP:0040284		P		HP:probinson	6/6
OMIM	257320	LISSENCEPHALY 2		HP:0001263	PMID:10973257	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	257320	LISSENCEPHALY 2		HP:0001321	PMID:10973257	PCS				P		HP:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0002197	PMID:10973257	PCS				P		HP:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0006818	PMID:6476009	PCS				P		HP:probinson	
OMIM	257320	LISSENCEPHALY 2		HP:0012110	PMID:10973257	PCS				P		HP:probinson	
OMIM	257350	NUCHAL BLEB, FAMILIAL		HP:0000007	OMIM:257350	TAS				I		HPO:skoehler	
OMIM	257350	NUCHAL BLEB, FAMILIAL		HP:0001789	OMIM:257350	TAS				P		HPO:skoehler	
OMIM	257350	NUCHAL BLEB, FAMILIAL		HP:0003826	OMIM:257350	TAS				M		HPO:probinson	
OMIM	257350	NUCHAL BLEB, FAMILIAL		HP:0010878	OMIM:257350	TAS				P		HPO:skoehler	
OMIM	257400	NYSTAGMUS, CONGENITAL MOTOR, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:257400	IEA				I		HPO:iea	
OMIM	257400	NYSTAGMUS, CONGENITAL MOTOR, AUTOSOMAL RECESSIVE		HP:0006934	OMIM:257400	TAS				P		HPO:skoehler	
OMIM	257500	OBESITY-HYPOVENTILATION SYNDROME		HP:0000007	OMIM:257500	IEA				I		HPO:iea	
OMIM	257500	OBESITY-HYPOVENTILATION SYNDROME		HP:0000961	OMIM:257500	IEA				P		HPO:iea	
OMIM	257500	OBESITY-HYPOVENTILATION SYNDROME		HP:0001262	OMIM:257500	IEA				P		HPO:iea	
OMIM	257500	OBESITY-HYPOVENTILATION SYNDROME		HP:0001513	OMIM:257500	IEA				P		HPO:iea	
OMIM	257500	OBESITY-HYPOVENTILATION SYNDROME		HP:0002791	OMIM:257500	IEA				P		HPO:skoehler	
OMIM	257550	OCULAR MOTOR APRAXIA		HP:0000007	OMIM:257550	IEA				I		HPO:iea	
OMIM	257550	OCULAR MOTOR APRAXIA		HP:0000090	OMIM:257550	TAS				P		HPO:skoehler	
OMIM	257550	OCULAR MOTOR APRAXIA		HP:0000657	OMIM:257550	IEA				P		HPO:iea	
OMIM	257550	OCULAR MOTOR APRAXIA		HP:0006961	OMIM:257550	IEA				P		HPO:iea	
OMIM	257550	OCULAR MOTOR APRAXIA		HP:0008026	OMIM:257550	IEA				P		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0000007	OMIM:257600	IEA				I		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0001939	OMIM:257600	IEA				P		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0003198	OMIM:257600	IEA				P		HPO:skoehler	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0003621	OMIM:257600	IEA				C		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0003690	OMIM:257600	IEA				P		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0008507	OMIM:257600	IEA				P		HPO:iea	
OMIM	257600	%257600 OCULAR MYOPATHY WITH CURARE SENSITIVITY		HP:0011463	OMIM:257600	TAS				C		HPO:skoehler	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000007	OMIM:257790	IEA				I		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000218	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000268	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000518	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000687	OMIM:257790	TAS				P		HPO:probinson	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0000691	OMIM:257790	TAS				P		HPO:probinson	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0001263	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0001510	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0001931	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0002705	OMIM:257790	TAS				P		HPO:skoehler	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0007513	OMIM:257790	IEA				P		HPO:iea	
OMIM	257790	OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS		HP:0025356	OMIM:257790	IEA				P		HPO:skoehler	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0000007	OMIM:257800	IEA				I		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0000478	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0001010	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0001249	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0001257	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0001305	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0001510	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0002218	OMIM:257800	IEA				P		HPO:iea	
OMIM	257800	OCULOCEREBRAL SYNDROME WITH HYPOPIGMENTATION		HP:0002305	OMIM:257800	IEA				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:257850	TAS				I		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000160	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000233	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000239	OMIM:257850	IEA				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000248	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000286	OMIM:257850	TAS				P		HPO:probinson	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000327	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000343	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000347	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000369	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000430	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000460	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000482	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000494	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000506	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000545	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000568	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000653	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000675	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000678	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000682	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000684	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000685	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0000689	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0001508	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0001773	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0002007	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0002750	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0003189	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0005622	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0005768	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0005769	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0009748	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0009917	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0010705	OMIM:257850	TAS				P		HPO:iea	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0011342	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0012745	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257850	OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE		HP:0200055	OMIM:257850	TAS				P		HPO:skoehler	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0000007	OMIM:257910	IEA				I		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0000175	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0000252	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0000555	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0000568	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0001249	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0001257	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0004322	OMIM:257910	IEA				P		HPO:iea	
OMIM	257910	OCULOPALATOCEREBRAL SYNDROME		HP:0007968	OMIM:257910	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000007	OMIM:257920	IEA				I		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000126	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000175	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000204	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000252	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000260	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000316	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000405	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000496	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000501	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000508	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000524	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000537	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000581	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000593	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000678	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0000960	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0001256	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0001510	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0001539	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0001629	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0001631	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0001643	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0001769	OMIM:257920	TAS				P		HPO:probinson	
OMIM	257920	3MC SYNDROME 1		HP:0001773	OMIM:257920	TAS				P		HPO:probinson	
OMIM	257920	3MC SYNDROME 1		HP:0002553	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0002558	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0002678	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0002825	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0002974	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0003298	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0004209	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0004440	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0004443	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0006216	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0008897	OMIM:257920	TAS				P		HPO:skoehler	
OMIM	257920	3MC SYNDROME 1		HP:0009237	OMIM:257920	IEA				P		HPO:iea	
OMIM	257920	3MC SYNDROME 1		HP:0009891	OMIM:257920	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0000007	OMIM:257960	IEA				I		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0000510	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0000653	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0000670	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0000958	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0001808	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0001939	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0002164	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0002209	OMIM:257960	PCS				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0002215	OMIM:257960	PCS				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0002225	OMIM:257960	PCS				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0002552	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0004528	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0005338	OMIM:257960	PCS				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0006313	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0006347	OMIM:257960	IEA				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0006349	OMIM:257960	PCS				P		HPO:iea	
OMIM	257960	257960 OCULOTRICHODYSPLASIA; OTD		HP:0040189	OMIM:257960	TAS				P		HPO:skoehler	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0000007	OMIM:257970	IEA				I		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0000096	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0000112	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0000546	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0001249	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0001264	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0001266	OMIM:257970	IEA				P		HPO:iea	
OMIM	257970	OCULORENOCEREBELLAR SYNDROME		HP:0001939	OMIM:257970	IEA				P		HPO:iea	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000007	PMID:19559398	PCS				I		HPO:iea	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000535	PMID:19559398	PCS		HP:0040284		P		HPO:iea	7/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000613	PMID:19559398	PCS		HP:0040284		P		HPO:iea	3/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000668	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000958	PMID:19559398	PCS		HP:0040284		P		HPO:iea	6/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000966	PMID:19559398	PCS		HP:0040284		P		HPO:iea	3/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0000975	PMID:19559398	PCS		HP:0040284		P		HPO:iea	2/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0001798	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0001810	PMID:19559398	PCS		HP:0040284		P		HPO:iea	7/11
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0002164	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0002209	PMID:19559398	PCS		HP:0040284		P		HPO:iea	6/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0002213	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0002231	PMID:19559398	PCS		HP:0040284		P		HPO:iea	5/8
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0006349	PMID:19559398	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0006481	PMID:19559398	PCS		HP:0040284		P		HPO:iea	5/11
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0007410	OMIM:257980	TAS				P		HPO:probinson	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0007556	PMID:19559398	PCS		HP:0040284		P		HPO:iea	3/10
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0008070	OMIM:257980	IEA				P		HPO:iea	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0008391	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0010298	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0010783	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0011359	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0025092	OMIM:257980	TAS				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0025114	OMIM:257980	IEA				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0032152	OMIM:257980	IEA				P		HPO:skoehler	
OMIM	257980	ODONTOONYCHODERMAL DYSPLASIA; OODD		HP:0040162	OMIM:257980	IEA				P		HPO:skoehler	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000028	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000033	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000039	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000054	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000061	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000066	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000072	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000081	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000104	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000125	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000126	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000136	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000143	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000238	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0000878	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0001374	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0001539	OMIM:258040	TAS				P		HPO:probinson	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0001545	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0001586	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0001762	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002023	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002144	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002308	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002475	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002566	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002836	OMIM:258040	IEA				P		HPO:skoehler	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0002937	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0003745	OMIM:258040	IEA				I		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0005223	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0008490	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0008707	OMIM:258040	IEA				P		HPO:iea	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0010305	OMIM:258040	TAS				P		HPO:skoehler	
OMIM	258040	258040 OEIS COMPLEX;;OMPHALOCELE-EXSTROPHY-IMPERFORATE ANUS-SPINAL DEFECTS		HP:0010475	OMIM:258040	TAS				P		HPO:skoehler	
OMIM	258100	#258100 OGUCHI DISEASE 1;;NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 1; CSNBO1		HP:0000007	OMIM:258100	IEA				I		HPO:iea	
OMIM	258100	#258100 OGUCHI DISEASE 1;;NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 1; CSNBO1		HP:0007642	OMIM:258100	TAS				P		HPO:skoehler	
OMIM	258100	#258100 OGUCHI DISEASE 1;;NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 1; CSNBO1		HP:0012047	OMIM:258100	TAS				P		HPO:probinson	
OMIM	258150	SPERMATOGENIC FAILURE 1; SPGF1		HP:0000007	OMIM:258150	IEA				I		HPO:iea	
OMIM	258150	SPERMATOGENIC FAILURE 1; SPGF1		HP:0000027	OMIM:258150	IEA				P		HPO:skoehler	
OMIM	258150	SPERMATOGENIC FAILURE 1; SPGF1		HP:0000789	OMIM:258150	IEA				P		HPO:iea	
OMIM	258150	SPERMATOGENIC FAILURE 1; SPGF1		HP:0001939	OMIM:258150	IEA				P		HPO:iea	
OMIM	258200	OLIVER SYNDROME		HP:0000007	OMIM:258200	IEA				I		HPO:iea	
OMIM	258200	OLIVER SYNDROME		HP:0001162	OMIM:258200	IEA				P		HPO:iea	
OMIM	258200	OLIVER SYNDROME		HP:0001249	OMIM:258200	IEA				P		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:258300	IEA				I		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0001022	OMIM:258300	IEA				P		HPO:skoehler	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0001251	OMIM:258300	IEA				P		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:258300	IEA				P		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0002168	OMIM:258300	IEA				P		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0002346	OMIM:258300	IEA				P		HPO:iea	
OMIM	258300	OLIVOPONTOCEREBELLAR ATROPHY II, AUTOSOMAL RECESSIVE		HP:0002542	OMIM:258300	TAS				P		HPO:skoehler	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000007	OMIM:258315	IEA				I		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000028	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000272	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000286	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000343	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000347	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000431	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000470	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0000581	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0001028	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0001060	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0001537	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0001629	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0001631	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0002007	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0003038	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0003196	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0004415	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005025	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005050	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005060	OMIM:258315	TAS				P		HPO:skoehler	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005085	OMIM:258315	TAS				P		HPO:skoehler	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005280	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005736	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0005792	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0008800	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0008873	OMIM:258315	TAS				P		HPO:probinson	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0008905	OMIM:258315	IEA				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0009756	OMIM:258315	TAS				P		HPO:iea	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0012107	OMIM:258315	TAS				P		HPO:skoehler	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0012368	OMIM:258315	TAS				P		HPO:skoehler	
OMIM	258315	OMODYSPLASIA 1; OMOD1		HP:0045025	OMIM:258315	IEA				P		HPO:skoehler	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0000007	OMIM:258320	IEA				I		HPO:iea	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0000175	OMIM:258320	TAS				P		HPO:probinson	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0000193	OMIM:258320	IEA				P		HPO:iea	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0000238	OMIM:258320	IEA				P		HPO:iea	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0000813	OMIM:258320	IEA				P		HPO:iea	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0001522	OMIM:258320	IEA				M		HPO:iea	
OMIM	258320	OMPHALOCELE-CLEFT PALATE SYNDROME, LETHAL		HP:0001539	OMIM:258320	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0000007	OMIM:258360	IEA				I		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0001256	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0001598	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0001804	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0001875	OMIM:258360	TAS				P		HPO:probinson	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0002212	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0002225	OMIM:258360	IEA				P		HPO:skoehler	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0002719	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0007665	OMIM:258360	TAS				P		HPO:probinson	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0007717	OMIM:258360	IEA				P		HPO:iea	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0009886	OMIM:258360	TAS				P		HPO:probinson	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0010764	OMIM:258360	TAS				P		HPO:probinson	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0100827	OMIM:258360	TAS				P		HPO:skoehler	
OMIM	258360	ONYCHOTRICHODYSPLASIA AND NEUTROPENIA		HP:0410252	OMIM:258360	IEA				P		HPO:skoehler	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000007	OMIM:258400	IEA				I		HPO:iea	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000486	OMIM:258400	IEA				P		HPO:iea	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000508	OMIM:258400	IEA				P		HPO:iea	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000602	OMIM:258400	IEA				P		HPO:iea	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000616	OMIM:258400	IEA				P		HPO:iea	
OMIM	258400	OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS		HP:0000646	OMIM:258400	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:258450	IEA				I		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000505	OMIM:258450	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000508	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000590	OMIM:258450	IEA				P		HPO:skoehler	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:258450	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000712	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0000716	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001265	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001284	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001300	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001618	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001634	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001638	OMIM:258450	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001653	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0001761	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002015	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002063	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002066	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002067	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002070	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002403	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002460	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002747	OMIM:258450	TAS				P		HPO:skoehler	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0002922	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003200	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003376	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003390	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003434	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003458	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003546	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003548	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003557	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003581	OMIM:258450	TAS		HP:0040282		C		HPO:iea	HP:0040282
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003688	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003689	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003700	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003701	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0003713	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE	HP:0012828	HP:0003737	OMIM:258450	TAS				P		HPO:probinson	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0006858	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0006886	OMIM:258450	IEA				P		HPO:iea	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0007641	OMIM:258450	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0008180	OMIM:258450	TAS				P		HPO:skoehler	
OMIM	258450	#258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL RECESSIVE; PEOB;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL RECESSIVE		HP:0010628	OMIM:258450	IEA				P		HPO:iea	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0000007	OMIM:258470	TAS				I		HPO:nvasilevsky	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0000508	OMIM:258470	IEA				P		HPO:iea	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0000508	OMIM:258470	TAS				P		HPO:nvasilevsky	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0000602	OMIM:258470	IEA				P		HPO:iea	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0001291	OMIM:258470	IEA				P		HPO:iea	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0001324	OMIM:258470	IEA				P		HPO:iea	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0001427	OMIM:258470	TAS				I		HPO:nvasilevsky	
OMIM	258470	OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA		HP:0008316	OMIM:258470	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000007	OMIM:258480	IEA				I		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000117	OMIM:258480	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258480	OPSISMODYSPLASIA		HP:0000239	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000256	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000316	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000343	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000463	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000470	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000774	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0000907	OMIM:258480	TAS				P		HPO:probinson	
OMIM	258480	OPSISMODYSPLASIA		HP:0000922	OMIM:258480	TAS				P		HPO:probinson	
OMIM	258480	OPSISMODYSPLASIA		HP:0000969	OMIM:258480	IEA				P		HPO:skoehler	
OMIM	258480	OPSISMODYSPLASIA		HP:0001252	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0001290	OMIM:258480	TAS				P		HPO:skoehler	
OMIM	258480	OPSISMODYSPLASIA		HP:0001538	OMIM:258480	TAS				P		HPO:probinson	
OMIM	258480	OPSISMODYSPLASIA		HP:0001561	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0001591	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0001773	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0002007	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0002148	OMIM:258480	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258480	OPSISMODYSPLASIA		HP:0002205	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003021	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003026	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003173	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003175	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003177	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003180	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0003196	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0004279	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0004565	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0005280	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0008479	OMIM:258480	IEA				P		HPO:iea	
OMIM	258480	OPSISMODYSPLASIA		HP:0008873	OMIM:258480	TAS				P		HPO:probinson	
OMIM	258480	OPSISMODYSPLASIA		HP:0008905	OMIM:258480	IEA				P		HPO:iea	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:258500	TAS				I		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0000505	OMIM:258500	TAS				P		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0000613	OMIM:258500	TAS				P		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0000642	OMIM:258500	TAS				P		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:258500	TAS				P		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:258500	TAS				C		HPO:skoehler	
OMIM	258500	%258500 OPTIC ATROPHY 6; OPA6;;OPTIC ATROPHY, CONGENITAL OR EARLY INFANTILE, AUTOSOMAL RECESSIVE		HP:0003677	OMIM:258500	TAS				C		HPO:skoehler	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:258501	IEA				I		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0000505	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0001251	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0001257	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0002071	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0002072	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:258501	IEA				P		HPO:iea	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0003535	OMIM:258501	IEA				P		HPO:skoehler	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0007663	OMIM:258501	TAS				P		HPO:skoehler	
OMIM	258501	#258501 3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3;;MGA, TYPE III; MGA3;;OPTIC ATROPHY PLUS SYNDROME;;OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA;;IRAQI-JEWISH 'OPTIC ATROPHY PLUS';;COSTEFF SYNDROME;;OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE;;OPA3, AUTOSOMAL RECESSIVE		HP:0100543	OMIM:258501	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0000007	OMIM:258650	IEA				I		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0000408	OMIM:258650	IEA	HP:0003621			P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0000505	OMIM:258650	IEA	HP:0003621			P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0000648	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0000767	OMIM:258650	TAS				P		HPO:probinson	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0001284	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002066	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002136	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002403	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002460	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002936	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0002943	OMIM:258650	TAS				P		HPO:probinson	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0003828	OMIM:258650	IEA				C		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0007149	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0009473	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0009487	OMIM:258650	TAS				P		HPO:probinson	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0009778	OMIM:258650	IEA				P		HPO:iea	
OMIM	258650	258650 OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE		HP:0011096	OMIM:258650	IEA				P		HPO:iea	
OMIM	258660	NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO		HP:0000007	OMIM:258660	IEA				I		HPO:iea	
OMIM	258660	NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO		HP:0007634	OMIM:258660	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0000007	OMIM:258700	IEA				I		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0000365	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0000572	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0000648	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0001268	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0001344	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0002510	OMIM:258700	IEA				P		HPO:iea	
OMIM	258700	OPTICOCOCHLEODENTATE DEGENERATION		HP:0005102	OMIM:258700	IEA				P		HPO:iea	
OMIM	258800	ORAL SENSIBILITY, DISTURBANCE OF		HP:0000007	OMIM:258800	TAS				I		HPO:probinson	
OMIM	258800	ORAL SENSIBILITY, DISTURBANCE OF		HP:0002307	OMIM:258800	TAS				P		HPO:probinson	
OMIM	258800	ORAL SENSIBILITY, DISTURBANCE OF		HP:0002311	OMIM:258800	TAS				P		HPO:probinson	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0000007	OMIM:258840	IEA				I		HPO:iea	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0000160	OMIM:258840	IEA				P		HPO:iea	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0000219	OMIM:258840	IEA				P		HPO:iea	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0000219	OMIM:258840	TAS				P		HPO:skoehler	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0001032	OMIM:258840	IEA				P		HPO:iea	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0001182	OMIM:258840	IEA				P		HPO:iea	
OMIM	258840	258840 ORAL AND DIGITAL ANOMALIES WITH ICHTHYOSIS		HP:0007395	OMIM:258840	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000007	OMIM:258850	IEA				I		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000193	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000199	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000316	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000369	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000414	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000691	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000767	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0000879	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0001162	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0001249	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0001336	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0001795	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0001830	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0002808	OMIM:258850	IEA				P		HPO:iea	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0010297	OMIM:258850	TAS				P		HPO:skoehler	
OMIM	258850	OROFACIODIGITAL SYNDROME III		HP:0011069	OMIM:258850	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000007	OMIM:258860	TAS				I		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000175	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000180	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000191	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000199	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000218	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000286	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000316	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000347	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000369	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0000767	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0001156	OMIM:258860	TAS				P		HPO:skoehler	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0001161	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0001770	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0001829	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0002059	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0002132	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0004322	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0005736	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0009381	OMIM:258860	TAS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0011802	PMID:22883145	PCS				P		HPO:probinson	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0030084	OMIM:258860	TAS				P		HPO:skoehler	
OMIM	258860	OROFACIODIGITAL SYNDROME IV; OFD4		HP:0100259	OMIM:258860	IEA				P		HPO:skoehler	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000161	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000164	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000175	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000191	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000218	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000316	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000455	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000456	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000480	OMIM:258865	IEA				P		HPO:skoehler	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000486	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0000506	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0001056	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0001161	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0001263	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0001419	OMIM:258865	IEA				I		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0001770	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0002100	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0004322	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0005349	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0005736	OMIM:258865	IEA				P		HPO:iea	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0010566	OMIM:258865	IEA				P		HPO:skoehler	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0012385	OMIM:258865	IEA				P		HPO:skoehler	
OMIM	258865	OROFACIODIGITAL SYNDROME IX; OFD9		HP:0012444	OMIM:258865	IEA				P		HPO:skoehler	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0000007	OMIM:258870	IEA				I		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0000533	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0000545	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0000618	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0000662	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0001939	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0003457	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0003701	OMIM:258870	IEA				P		HPO:iea	
OMIM	258870	ORNITHINE AMINOTRANSFERASE DEFICIENCY		HP:0007787	OMIM:258870	IEA				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0000007	OMIM:258900	IEA				I		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0000790	OMIM:258900	TAS				P		HPO:skoehler	
OMIM	258900	OROTIC ACIDURIA		HP:0001263	OMIM:258900	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	258900	OROTIC ACIDURIA		HP:0001508	OMIM:258900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258900	OROTIC ACIDURIA		HP:0001629	OMIM:258900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258900	OROTIC ACIDURIA		HP:0001631	OMIM:258900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	258900	OROTIC ACIDURIA		HP:0003218	OMIM:258900	TAS				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0003267	OMIM:258900	IEA				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0003339	OMIM:258900	TAS				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0003526	OMIM:258900	TAS				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0004447	OMIM:258900	TAS				P		HPO:skoehler	
OMIM	258900	OROTIC ACIDURIA		HP:0004826	OMIM:258900	IEA				P		HPO:iea	
OMIM	258900	OROTIC ACIDURIA		HP:0005435	OMIM:258900	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	258900	OROTIC ACIDURIA		HP:0011273	OMIM:258900	TAS				P		HPO:skoehler	
OMIM	258900	OROTIC ACIDURIA		HP:0032231	OMIM:258900	IEA				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000006	OMIM:259050	TAS				I		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000160	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000179	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000248	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000256	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000272	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000327	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000337	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000365	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000400	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000490	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000494	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000508	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000664	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000711	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000717	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000718	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000767	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000771	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000774	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000815	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000819	OMIM:259050	IEA				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000851	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0000939	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001115	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001249	OMIM:259050	TAS				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001290	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001761	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001840	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0001956	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002079	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002180	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002209	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002221	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002514	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002550	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002714	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002808	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002857	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0002868	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0003273	OMIM:259050	TAS				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0003301	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0003693	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0003745	OMIM:259050	IEA				I		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0004322	OMIM:259050	TAS				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0005103	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0005121	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0005758	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0006380	OMIM:259050	TAS				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0008541	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0008689	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0009882	OMIM:259050	IEA				P		HPO:probinson	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0011800	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0040160	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0040309	OMIM:259050	TAS				P		HPO:skoehler	
OMIM	259050	PRIMROSE SYNDROME; PRIMS		HP:0100716	OMIM:259050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000007	OMIM:259100	IEA				I		HPO:iea	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000218	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000239	OMIM:259100	IEA				P		HPO:iea	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000280	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000508	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000767	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000890	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000938	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000939	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000972	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000975	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0000976	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001051	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001217	OMIM:259100	IEA				P		HPO:iea	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001369	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001376	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001519	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001582	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0001643	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0002645	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0002684	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0002829	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0003040	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0003577	OMIM:259100	IEA				C		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0009771	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0010783	OMIM:259100	TAS				P		HPO:skoehler	
OMIM	259100	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1; PHOAR1		HP:0031284	OMIM:259100	IEA				P		HPO:skoehler	
OMIM	259200	BLOUNT DISEASE, ADOLESCENT		HP:0000007	OMIM:259200	TAS				I		HPO:nvasilevsky	
OMIM	259200	BLOUNT DISEASE, ADOLESCENT		HP:0001426	OMIM:259200	TAS				I		HPO:nvasilevsky	
OMIM	259200	BLOUNT DISEASE, ADOLESCENT		HP:0002970	OMIM:259200	TAS				P		HPO:iea	
OMIM	259200	BLOUNT DISEASE, ADOLESCENT		HP:0010886	OMIM:259200	TAS				P		HPO:probinson	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0000007	OMIM:259270	IEA				I		HPO:iea	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0001510	OMIM:259270	IEA				P		HPO:iea	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0001831	OMIM:259270	PCS				P		HPO:probinson	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0002205	OMIM:259270	PCS				P		HPO:probinson	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0002644	OMIM:259270	PCS				P		HPO:probinson	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0009381	OMIM:259270	PCS				P		HPO:probinson	
OMIM	259270	OSTEODYSPLASTY, PRECOCIOUS, OF DANKS, MAYNE, AND KOZLOWSKI		HP:0011314	OMIM:259270	PCS				P		HPO:probinson	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000007	OMIM:259410	IEA				I		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000252	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000519	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000592	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000767	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000768	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0000963	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0002645	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0002691	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0003023	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0003826	OMIM:259410	TAS				M		HPO:skoehler	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0005474	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0005855	OMIM:259410	IEA				P		HPO:iea	
OMIM	259410	OSTEOGENESIS IMPERFECTA CONGENITA, MICROCEPHALY, AND CATARACTS		HP:0008873	OMIM:259410	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000006	OMIM:259420	IEA				I		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000007	OMIM:259420	IEA				I		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000260	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000325	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000347	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000365	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000592	OMIM:259420	TAS	HP:0003577			P		HPO:probinson	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000703	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000707	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0000765	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002007	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002092	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002645	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002650	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002691	OMIM:259420	TAS				P		HPO:probinson	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002757	OMIM:259420	TAS				P		HPO:probinson	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002808	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0002982	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0003023	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0003100	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0003179	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0004586	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0005474	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0005758	OMIM:259420	TAS				P		HPO:skoehler	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0005855	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0005897	OMIM:259420	IEA				P		HPO:iea	
OMIM	259420	#259420 OSTEOGENESIS IMPERFECTA, TYPE III;;OI, TYPE III;;OI3;;OSTEOGENESIS IMPERFECTA, PROGRESSIVELY DEFORMING, WITH NORMAL SCLERAE		HP:0008921	OMIM:259420	TAS				P		HPO:probinson	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000007	PMID:21282188	PCS				I	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000592	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000703	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000767	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000768	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000923	PMID:21282188	PCS	HP:0003577			P	OSTEOGENESIS IMPERFECTA, TYPE IX	HP:probinson	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0000926	PMID:21282188	PCS	HP:0030674			P	OSTEOGENESIS IMPERFECTA, TYPE IX	HP:probinson	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0002645	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0002650	PMID:21282188	PCS				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0002757	OMIM:259440	TAS				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0002808	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0003023	PMID:21282188	PCS				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0005474	PMID:21282188	PCS				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HP:probinson	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0005855	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0006385	PMID:21282188	PCS	HP:0003577			P	OSTEOGENESIS IMPERFECTA, TYPE IX	HP:probinson	
OMIM	259440	Osteogenesis imperfecta, type IX		HP:0008873	OMIM:259440	IEA				P	OSTEOGENESIS IMPERFECTA, TYPE IX	HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0000007	OMIM:259450	TAS				I		HPO:probinson	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0000768	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0000926	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0000939	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0001059	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0001388	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0001762	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0002650	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0002659	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0002808	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0002812	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0002987	OMIM:259450	TAS	HP:0003577			P		HPO:probinson	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0003179	OMIM:259450	IEA				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0003273	OMIM:259450	TAS	HP:0003577			P		HPO:probinson	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0004322	OMIM:259450	TAS				P		HPO:iea	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0006380	OMIM:259450	TAS	HP:0003577			P		HPO:probinson	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0006466	OMIM:259450	TAS	HP:0003577			P		HPO:probinson	
OMIM	259450	#259450 BRUCK SYNDROME 1; BRKS1		HP:0008422	OMIM:259450	TAS				P		HPO:skoehler	
OMIM	259500	OSTEOGENIC SARCOMA		HP:0000007	OMIM:259500	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	259500	OSTEOGENIC SARCOMA		HP:0001939	OMIM:259500	IEA				P		HPO:iea	
OMIM	259500	OSTEOGENIC SARCOMA		HP:0002669	OMIM:259500	IEA				P		HPO:iea	
OMIM	259500	OSTEOGENIC SARCOMA		HP:0009919	OMIM:259500	IEA				P		HPO:skoehler	
OMIM	259550	OSTEOID OSTEOMA		HP:0000007	OMIM:259550	TAS				I		HPO:nvasilevsky	
OMIM	259550	OSTEOID OSTEOMA		HP:0030433	OMIM:259550	TAS				P		HPO:skoehler	
OMIM	259550	OSTEOID OSTEOMA		HP:0100246	OMIM:259550	IEA				P		HPO:skoehler	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000007	OMIM:259600	IEA				I		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000212	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000248	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000280	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000316	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000327	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000347	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000414	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000446	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000520	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000598	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000684	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000765	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000938	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0000939	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001007	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001034	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001072	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001171	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001220	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001239	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001288	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001473	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001476	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001482	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001495	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001504	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001761	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001763	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001783	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0001836	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0002007	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0002751	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0002829	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0002953	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003016	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003179	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003273	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003320	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003493	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003593	OMIM:259600	IEA				C		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0003621	OMIM:259600	IEA				C		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0004322	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0005441	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0006012	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0006086	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0006234	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0006252	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0006466	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0008011	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0008078	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0008090	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0008133	OMIM:259600	IEA				P		HPO:iea	
OMIM	259600	MULTICENTRIC OSTEOLYSIS, NODULOSIS, AND ARTHROPATHY; MONA		HP:0025131	OMIM:259600	IEA				P		HPO:skoehler	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0000007	OMIM:259610	IEA				I		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0000327	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0000455	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0000520	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0001249	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0001504	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0001760	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0002987	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0003621	OMIM:259610	IEA				C		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0004322	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0006380	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0006449	OMIM:259610	IEA				P		HPO:iea	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0009839	OMIM:259610	TAS				P		HPO:probinson	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0009847	OMIM:259610	TAS				P		HPO:probinson	
OMIM	259610	259610 OSTEOLYSIS SYNDROME, RECESSIVE;;OSTEOLYSIS, DISTAL, WITH SHORT STATURE, MENTAL RETARDATION, AND CHARACTERISTICFACIAL APPEARANCE		HP:0009855	OMIM:259610	TAS				P		HPO:probinson	
OMIM	259650	OSTEOMA OF MIDDLE EAR		HP:0000007	OMIM:259650	IEA				I		HPO:iea	
OMIM	259650	OSTEOMA OF MIDDLE EAR		HP:0000598	OMIM:259650	IEA				P		HPO:iea	
OMIM	259650	OSTEOMA OF MIDDLE EAR		HP:0100246	OMIM:259650	IEA				P		HPO:skoehler	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0000007	OMIM:259660	IEA				I		HPO:iea	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0002749	OMIM:259660	TAS				P		HPO:skoehler	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0005789	OMIM:259660	TAS				P		HPO:skoehler	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0005849	OMIM:259660	IEA				P		HPO:iea	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0006647	OMIM:259660	IEA				P		HPO:iea	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0008497	OMIM:259660	IEA				P		HPO:iea	
OMIM	259660	259660 OSTEOMALACIA, SCLEROSING, WITH CEREBRAL CALCIFICATION		HP:0011001	OMIM:259660	IEA				P		HPO:iea	
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0000007	OMIM:259680	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0001945	PMID:30532310	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0002653	PMID:30532310	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0002754	PMID:30532310	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0003565	PMID:30532310	PCS		HP:0040284		P		HP:probinson	5/6
OMIM	259680	CHRONIC RECURRENT MULTIFOCAL OSTEOMYELITIS		HP:0100847	PMID:30532310	PCS				P		HP:probinson	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0000007	OMIM:259690	IEA				I		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0000271	OMIM:259690	IEA				P		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0000938	OMIM:259690	IEA				P		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0001249	OMIM:259690	IEA				P		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0001252	OMIM:259690	IEA				P		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0001290	OMIM:259690	TAS				P		HPO:skoehler	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0001388	OMIM:259690	IEA				P		HPO:iea	
OMIM	259690	OSTEOPENIA AND SPARSE HAIR		HP:0008070	OMIM:259690	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000007	OMIM:259700	IEA				I		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000238	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000256	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000365	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000597	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000618	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000639	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000648	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0000670	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001250	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001281	OMIM:259700	IEA				P		HPO:skoehler	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001425	OMIM:259700	TAS				I		HPO:skoehler	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001508	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001744	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001876	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0001903	OMIM:259700	TAS				P		HPO:skoehler	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0002007	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0002240	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0002754	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0002756	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0002812	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0003015	OMIM:259700	IEA				P		HPO:skoehler	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0003155	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0004618	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0007209	OMIM:259700	TAS				P		HPO:skoehler	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0010628	OMIM:259700	IEA				P		HPO:iea	
OMIM	259700	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1		HP:0011002	OMIM:259700	IEA				P		HPO:skoehler	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0000007	OMIM:259710	TAS				I		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0000303	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0000618	OMIM:259710	TAS				P		HPO:skoehler	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0000648	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0000670	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0001433	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0001873	OMIM:259710	TAS				P		HPO:skoehler	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0001876	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0001903	OMIM:259710	TAS				P		HPO:skoehler	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0001978	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0002757	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0002857	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0003034	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0004437	OMIM:259710	IEA				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0004499	OMIM:259710	IEA				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0006335	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0007209	OMIM:259710	TAS				P		HPO:iea	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0007626	OMIM:259710	TAS				P		HPO:skoehler	
OMIM	259710	#259710 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2;;OSTEOPETROSIS, OSTEOCLAST-POOR;;OSTEOPETROSIS, MILD AUTOSOMAL RECESSIVE FORM		HP:0011002	OMIM:259710	TAS				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000007	OMIM:259720	TAS				I		HPO:probinson	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000238	OMIM:259720	TAS				P		HPO:probinson	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000252	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000347	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000505	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000543	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0000648	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001290	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001399	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001541	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001873	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001876	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001903	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0001978	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002059	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002169	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002197	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002240	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002510	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002901	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0002904	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0003015	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0003256	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0003826	OMIM:259720	TAS				M		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0005564	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0008936	OMIM:259720	IEA				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5	HP:0012828	HP:0011002	OMIM:259720	TAS				P		HPO:skoehler	
OMIM	259720	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 5; OPTB5		HP:0030328	OMIM:259720	TAS				P		HPO:probinson	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0000007	OMIM:259730	IEA				I		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0000505	OMIM:259730	IEA				P		HPO:skoehler	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0000572	OMIM:259730	TAS				P		HPO:skoehler	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0000689	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0001249	OMIM:259730	IEA				P		HPO:skoehler	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0001433	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0001903	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0001978	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0002135	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0003034	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0003148	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0004322	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0004437	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0007807	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0008153	OMIM:259730	TAS				P		HPO:skoehler	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0008341	OMIM:259730	IEA				P		HPO:iea	
OMIM	259730	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 3; OPTB3		HP:0011002	OMIM:259730	IEA				P		HPO:skoehler	
OMIM	259750	OSTEOPOROSIS, JUVENILE		HP:0000007	OMIM:259750	TAS				I		HPO:probinson	
OMIM	259750	OSTEOPOROSIS, JUVENILE		HP:0000939	OMIM:259750	TAS				P		HPO:iea	
OMIM	259750	OSTEOPOROSIS, JUVENILE		HP:0012052	OMIM:259750	TAS				P		HPO:probinson	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000007	OMIM:259770	IEA				I		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000252	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000518	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000568	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000618	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000667	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000926	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0000939	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001089	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001252	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001256	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001290	OMIM:259770	TAS				P		HPO:skoehler	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001382	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001552	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0001629	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0002659	OMIM:259770	TAS				P		HPO:skoehler	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0002751	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0002756	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0003016	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0004322	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0007773	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0008037	OMIM:259770	IEA				P		HPO:iea	
OMIM	259770	OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME		HP:0009733	OMIM:259770	IEA				P		HPO:skoehler	
OMIM	259775	RAINE SYNDROME		HP:0000007	OMIM:259775	TAS				I		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000072	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000126	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000154	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000160	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000175	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000212	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000218	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000238	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000239	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000244	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000252	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000272	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000303	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000316	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000347	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000358	OMIM:259775	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000369	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000410	OMIM:259775	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000411	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000452	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000453	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000470	OMIM:259775	TAS				P		HPO:skoehler	
OMIM	259775	RAINE SYNDROME		HP:0000494	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000520	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0000691	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000695	OMIM:259775	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0000767	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0001156	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0001263	OMIM:259775	TAS				P		HPO:skoehler	
OMIM	259775	RAINE SYNDROME		HP:0001357	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0001847	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0002089	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0002148	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0002514	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0002553	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0002804	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0002983	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0003155	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0003196	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0003811	OMIM:259775	IEA				M		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0004322	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0005257	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0005280	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0006297	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0006487	OMIM:259775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259775	RAINE SYNDROME		HP:0010808	OMIM:259775	TAS				P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0011001	OMIM:259775	TAS	HP:0003623			P		HPO:probinson	
OMIM	259775	RAINE SYNDROME		HP:0011800	OMIM:259775	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000007	OMIM:259780	IEA				I		HPO:iea	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000047	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000268	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000358	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000369	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000400	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0000598	OMIM:259780	IEA				P		HPO:iea	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0001270	OMIM:259780	IEA				P		HPO:iea	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0001597	OMIM:259780	IEA				P		HPO:iea	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0003273	OMIM:259780	TAS				P		HPO:probinson	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0006380	OMIM:259780	TAS				P		HPO:probinson	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0006466	OMIM:259780	TAS				P		HPO:probinson	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0006492	OMIM:259780	TAS				P		HPO:probinson	
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0006587	OMIM:259780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	259780	OTOONYCHOPERONEAL SYNDROME		HP:0011247	OMIM:259780	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000007	OMIM:259900	IEA				I		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000083	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000121	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000488	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000648	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000790	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0000965	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0001063	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0001138	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0001678	OMIM:259900	TAS				P		HPO:probinson	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0001942	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0002653	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0002756	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0003159	OMIM:259900	TAS				P		HPO:probinson	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0004417	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0004950	OMIM:259900	IEA				P		HPO:iea	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0008672	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0009830	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0011001	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0011506	OMIM:259900	IEA				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0025324	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0025520	OMIM:259900	IEA				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0030507	PMID:23666469	PCS				P		HPO:probinson	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0030880	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	259900	HYPEROXALURIA, PRIMARY, TYPE I; HP1		HP:0100758	OMIM:259900	TAS				P		HPO:skoehler	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0000007	OMIM:260000	IEA				I		HPO:iea	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0000083	OMIM:260000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0000121	OMIM:260000	TAS				P		HPO:skoehler	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0000790	OMIM:260000	TAS				P		HPO:skoehler	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0003159	OMIM:260000	IEA				P		HPO:iea	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0003355	OMIM:260000	IEA				P		HPO:skoehler	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0003828	OMIM:260000	TAS				C		HPO:skoehler	
OMIM	260000	HYPEROXALURIA, PRIMARY, TYPE II; HP2		HP:0008672	OMIM:260000	IEA				P		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0000006	OMIM:260005	TAS				I		HPO:skoehler	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0000007	OMIM:260005	IEA				I		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0002013	OMIM:260005	IEA				P		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0002014	OMIM:260005	IEA				P		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0002027	OMIM:260005	IEA				P		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0003137	OMIM:260005	TAS				P		HPO:skoehler	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0004387	OMIM:260005	IEA				P		HPO:iea	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0008672	OMIM:260005	TAS				P		HPO:skoehler	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0040142	OMIM:260005	TAS				P		HPO:skoehler	
OMIM	260005	5-@OXOPROLINASE DEFICIENCY; OPLAHD		HP:0410132	PMID:10094443	PCS				P		HPO:NicoleVasilevsky	
OMIM	260100	PA POLYMORPHISM OF ALPHA-2-GLOBULIN		HP:0000007	OMIM:260100	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	260100	PA POLYMORPHISM OF ALPHA-2-GLOBULIN		HP:0010701	OMIM:260100	IEA				P		HPO:skoehler	
OMIM	260130	260130 PACHYONYCHIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:260130	IEA				I		HPO:iea	
OMIM	260130	260130 PACHYONYCHIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0001805	OMIM:260130	TAS				P		HPO:skoehler	
OMIM	260130	260130 PACHYONYCHIA CONGENITA, AUTOSOMAL RECESSIVE		HP:0008392	OMIM:260130	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0000007	OMIM:260150	IEA				I		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0000175	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0000414	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0000582	OMIM:260150	TAS				P		HPO:probinson	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0001270	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0002263	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0004322	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0006887	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0009185	OMIM:260150	TAS				P		HPO:probinson	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0009276	OMIM:260150	IEA				P		HPO:iea	
OMIM	260150	260150 PALANT CLEFT PALATE SYNDROME		HP:0010864	OMIM:260150	TAS				P		HPO:skoehler	
OMIM	260200	PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA		HP:0000510	OMIM:260200	TAS	HP:0003593			P		HPO:probinson	
OMIM	260200	PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA		HP:0000618	OMIM:260200	TAS				P		HPO:probinson	
OMIM	260200	PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA		HP:0001260	OMIM:260200	TAS				P		HPO:probinson	
OMIM	260200	PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA		HP:0007132	OMIM:260200	TAS				P		HPO:probinson	
OMIM	260200	PALLIDAL DEGENERATION, PROGRESSIVE, WITH RETINITIS PIGMENTOSA		HP:0007158	OMIM:260200	TAS				P		HPO:probinson	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000007	OMIM:260300	IEA				I		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000338	OMIM:260300	TAS				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000514	OMIM:260300	IEA				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001260	OMIM:260300	IEA				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001332	OMIM:260300	IEA				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001337	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001347	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001762	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002061	OMIM:260300	TAS				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002063	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002067	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002071	OMIM:260300	TAS				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002172	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002548	OMIM:260300	IEA				P		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003487	OMIM:260300	IEA				P		HPO:iea	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003677	OMIM:260300	IEA				C		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0011462	OMIM:260300	TAS				C		HPO:skoehler	
OMIM	260300	PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0012407	OMIM:260300	TAS				P		HPO:skoehler	
OMIM	260350	PANCREATIC CANCER		HP:0000006	OMIM:260350	TAS				I		HPO:skoehler	
OMIM	260350	PANCREATIC CANCER		HP:0001428	OMIM:260350	TAS				I		HPO:skoehler	
OMIM	260350	PANCREATIC CANCER		HP:0002894	OMIM:260350	IEA				P		HPO:skoehler	
OMIM	260350	PANCREATIC CANCER		HP:0410067	PMID:2311216	PCS				P		HPO:NicoleVasilevsky	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0000007	OMIM:260370	IEA				I		HPO:iea	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0000819	OMIM:260370	IEA	HP:0003593			P		HPO:iea	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0000857	OMIM:260370	TAS				P		HPO:skoehler	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0001508	OMIM:260370	TAS				P		HPO:skoehler	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0001511	OMIM:260370	IEA				P		HPO:iea	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0001738	OMIM:260370	IEA				P		HPO:iea	
OMIM	260370	#260370 PANCREATIC AGENESIS, CONGENITAL; PAGEN;;PANCREATIC HYPOPLASIA, CONGENITAL		HP:0002594	OMIM:260370	IEA				P		HPO:iea	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0000007	OMIM:260400	TAS				I		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0000121	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0000774	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0000907	PMID:25416932	PCS	HP:0003593	HP:0040284		P		HPO:probinson	6/6
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0000920	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001256	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001263	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001328	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001508	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001518	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001700	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001738	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001873	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001875	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001876	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0001903	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002240	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002570	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002643	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002719	OMIM:260400	TAS				P		HPO:skoehler	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002750	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002812	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002863	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0002910	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0003016	PMID:25416932	PCS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0003300	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0003411	PMID:25416932	PCS	HP:0003593	HP:0040284		P		HPO:probinson	6/6
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0004322	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0004808	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0004979	PMID:25416932	PCS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0005871	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0006461	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0006598	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0008803	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260400	SHWACHMAN-DIAMOND SYNDROME		HP:0011904	OMIM:260400	TAS				P		HPO:probinson	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0000007	OMIM:260450	IEA				I		HPO:iea	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0001635	OMIM:260450	IEA				P		HPO:iea	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0001738	OMIM:260450	IEA				P		HPO:iea	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0002023	OMIM:260450	IEA				P		HPO:iea	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0003075	OMIM:260450	IEA				P		HPO:iea	
OMIM	260450	PANCREATIC INSUFFICIENCY, COMBINED EXOCRINE		HP:0012050	OMIM:260450	TAS				P		HPO:probinson	
OMIM	260470	PANENCEPHALITIS, SUBACUTE SCLEROSING		HP:0000007	OMIM:260470	IEA				I		HPO:iea	
OMIM	260470	PANENCEPHALITIS, SUBACUTE SCLEROSING		HP:0002383	OMIM:260470	IEA				P		HPO:skoehler	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000007	OMIM:260480	IEA				I		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000217	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000505	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000952	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000989	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0000992	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0001097	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0001733	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0002240	OMIM:260480	IEA				P		HPO:iea	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0007663	OMIM:260480	TAS				P		HPO:skoehler	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0012378	OMIM:260480	IEA				P		HPO:skoehler	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0030318	OMIM:260480	TAS				P		HPO:skoehler	
OMIM	260480	PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX		HP:0030991	OMIM:260480	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0000006	OMIM:260500	TAS				I		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0000007	OMIM:260500	IEA				I		HPO:iea	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0000238	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0001085	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0001250	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0002013	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0002018	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0002315	OMIM:260500	TAS				P		HPO:skoehler	
OMIM	260500	PAPILLOMA OF CHOROID PLEXUS		HP:0200022	OMIM:260500	IEA				P		HPO:skoehler	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0000007	OMIM:260530	IEA				I		HPO:iea	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0000951	OMIM:260530	IEA				P		HPO:iea	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0001438	OMIM:260530	IEA				P		HPO:iea	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0002093	OMIM:260530	IEA				P		HPO:iea	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0006596	OMIM:260530	IEA				P		HPO:iea	
OMIM	260530	PARANA HARD-SKIN SYNDROME		HP:0008850	OMIM:260530	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0000006	OMIM:260540	TAS				I		HPO:nvasilevsky	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0000007	OMIM:260540	TAS				I		HPO:nvasilevsky	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0000597	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0000726	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0001300	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0001337	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0002062	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0002063	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0002751	OMIM:260540	IEA				P		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0003581	OMIM:260540	IEA				C		HPO:iea	
OMIM	260540	PARKINSON-DEMENTIA SYNDROMESUPRANUCLEAR PALSY, PROGRESSIVE ATYPICAL, INCLUDED		HP:0007256	OMIM:260540	TAS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000007	PMID:8301648	PCS				I		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000194	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000253	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000278	PMID:070547	IEA				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000286	PMID:28335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000293	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000341	PMID:28335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0000648	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001182	PMID:2070547	PCS				P		HPO:lccarmody	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001250	PMID:8723564	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001263	PMID:8460530	PCS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001272	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001290	OMIM:260565	IEA				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001302	OMIM:260565	TAS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001336	OMIM:260565	TAS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0001347	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0002079	OMIM:260565	TAS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0002126	OMIM:260565	TAS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0002187	PMID:8301648	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0002521	PMID:28335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0002529	PMID:28335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0003196	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0003469	PMID:8335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0006829	PMID:28335020	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0007105	PMID:2070547	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0007281	PMID:8301648	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0007514	PMID:8723564	PCS				P		HPO:lccarmody	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0007965	PMID:8301648	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0008872	PMID:8301648	PCS				P		HPO:probinson	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0010804	PMID:8460530	PCS				P		HPO:skoehler	
OMIM	260565	PEHO SYNDROME; PEHO		HP:0012098	PMID:8723564	PCS				P		HPO:lccarmody	
OMIM	260570	260570 PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN		HP:0000007	OMIM:260570	IEA				I		HPO:iea	
OMIM	260570	260570 PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN		HP:0001871	OMIM:260570	IEA				P		HPO:iea	
OMIM	260570	260570 PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN		HP:0001945	OMIM:260570	IEA				P		HPO:skoehler	
OMIM	260570	260570 PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN		HP:0001954	OMIM:260570	TAS				P		HPO:skoehler	
OMIM	260570	260570 PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN		HP:0002027	OMIM:260570	IEA				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0000007	OMIM:260600	TAS				I		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0000252	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0000280	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0000505	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0000639	OMIM:260600	IEA				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0001250	OMIM:260600	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3	HP:0012828	HP:0001263	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0001508	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0001522	OMIM:260600	IEA				M		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0001622	OMIM:260600	IEA				P		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002283	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002313	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002353	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002415	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002587	OMIM:260600	IEA				P		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002751	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0002804	OMIM:260600	IEA				P		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0003269	OMIM:260600	IEA				P		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0003676	OMIM:260600	TAS				C		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0005876	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0006918	OMIM:260600	IEA				P		HPO:iea	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0007256	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0007371	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260600	LEUKODYSTROPHY, HYPOMYELINATING, 3; HLD3		HP:0008936	OMIM:260600	TAS				P		HPO:skoehler	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0000007	OMIM:260650	IEA				I		HPO:iea	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0000518	OMIM:260650	TAS				P		HPO:probinson	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0000651	OMIM:260650	IEA				P		HPO:iea	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0000988	OMIM:260650	TAS				P		HPO:probinson	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0001251	OMIM:260650	IEA				P		HPO:iea	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0001260	OMIM:260650	IEA				P		HPO:iea	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0001263	OMIM:260650	IEA				P		HPO:iea	
OMIM	260650	PELLAGRA-LIKE SYNDROME		HP:0001289	OMIM:260650	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000007	OMIM:260660	IEA				I		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000033	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000061	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000126	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000171	OMIM:260660	TAS				P		HPO:probinson	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000175	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000238	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000347	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000482	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000568	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000581	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000882	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0000890	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0001239	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0001591	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0001762	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0001770	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0001999	OMIM:260660	IEA				P		HPO:skoehler	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0002324	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0002866	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0002990	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0003027	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0003083	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0003173	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0003175	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0004209	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0004691	OMIM:260660	TAS				P		HPO:probinson	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0004692	OMIM:260660	TAS				P		HPO:probinson	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0006077	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0008472	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0008488	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0008905	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0009085	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0009473	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0009937	OMIM:260660	IEA				P		HPO:skoehler	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0011266	OMIM:260660	IEA				P		HPO:iea	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0012385	OMIM:260660	TAS				P		HPO:skoehler	
OMIM	260660	#260660 COUSIN SYNDROME;;CRANIOFACIAL DYSMORPHISM, HYPOPLASIA OF SCAPULA AND PELVIS, AND SHORTSTATURE;;PELVISCAPULAR DYSPLASIA		HP:0012745	OMIM:260660	TAS				P		HPO:skoehler	
OMIM	260800	PENTOSURIA		HP:0000007	OMIM:260800	IEA				I		HPO:iea	
OMIM	260800	PENTOSURIA		HP:0003110	OMIM:260800	IEA				P		HPO:skoehler	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC		HP:0000007	OMIM:260900	IEA				I		HPO:iea	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC		HP:0001136	OMIM:260900	IEA				P		HPO:iea	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC		HP:0001698	OMIM:260900	TAS				P		HPO:probinson	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC	HP:0012825	HP:0001901	OMIM:260900	IEA				P		HPO:skoehler	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC		HP:0002563	OMIM:260900	TAS				P		HPO:probinson	
OMIM	260900	PERICARDIAL EFFUSION, CHRONIC		HP:0031284	OMIM:260900	IEA				P		HPO:skoehler	
OMIM	260910	PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL		HP:0002293	OMIM:260910	IEA				P		HPO:skoehler	
OMIM	260910	PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL		HP:0003745	OMIM:260910	TAS				I		HPO:iea	
OMIM	260910	PERIFOLLICULITIS CAPITIS ABSCEDENS ET SUFFODIENS, FAMILIAL		HP:0012322	OMIM:260910	IEA				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0000007	OMIM:260920	IEA				I		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0000510	OMIM:260920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	260920	HYPER-IGD SYNDROME		HP:0000543	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0000662	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0000988	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0001034	OMIM:260920	IEA				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0001369	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0001744	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0001974	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002013	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002014	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002027	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002315	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002321	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002716	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0002829	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0003261	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0003565	OMIM:260920	IEA				P		HPO:iea	
OMIM	260920	HYPER-IGD SYNDROME		HP:0011897	OMIM:260920	TAS				P		HPO:skoehler	
OMIM	260950	PERIODONTITIS, CHRONIC		HP:0000007	OMIM:260950	IEA				I		HPO:iea	
OMIM	260950	PERIODONTITIS, CHRONIC		HP:0000230	OMIM:260950	TAS				P		HPO:skoehler	
OMIM	260950	PERIODONTITIS, CHRONIC		HP:0000704	OMIM:260950	IEA				P		HPO:iea	
OMIM	260950	PERIODONTITIS, CHRONIC		HP:0003674	OMIM:260950	IEA				C		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0000007	OMIM:260970	IEA				I		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0001251	OMIM:260970	IEA				P		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0001271	OMIM:260970	IEA				P		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0006976	OMIM:260970	IEA				P		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0007267	OMIM:260970	TAS				P		HPO:iea	
OMIM	260970	PERIPHERAL NEUROPATHY, ATAXIA, FOCAL NECROTIZING ENCEPHALOPATHY, AND		HP:0007313	OMIM:260970	TAS				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0000007	OMIM:261000	IEA				I		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0001889	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0001939	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0002024	OMIM:261000	IEA				P		HPO:skoehler	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0002715	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0003401	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0003474	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0003621	OMIM:261000	IEA				C		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0005219	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0005518	OMIM:261000	IEA				P		HPO:iea	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0200118	OMIM:261000	TAS				P		HPO:skoehler	
OMIM	261000	#261000 INTRINSIC FACTOR DEFICIENCY; IFD;;PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR		HP:0200143	OMIM:261000	TAS				P		HPO:skoehler	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0000007	OMIM:261100	IEA				I		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0000093	PMID:17285242	PCS				P		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0000726	OMIM:261100	IEA				P		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0001289	OMIM:261100	IEA				P		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0001889	PMID:17285242	PCS				P		HPO:probinson	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0003401	OMIM:261100	IEA				P		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0003474	OMIM:261100	IEA				P		HPO:iea	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0011463	OMIM:261100	TAS				C		HPO:probinson	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0100502	PMID:17285242	PCS				P		HP:probinson	
OMIM	261100	MEGALOBLASTIC ANEMIA 1		HP:0200118	PMID:17285242	PCS				P		HPO:skoehler	
OMIM	261400	PERONEUS TERTIUS MUSCLE, ABSENCE OF		HP:0000007	OMIM:261400	TAS				I		HPO:probinson	
OMIM	261400	PERONEUS TERTIUS MUSCLE, ABSENCE OF		HP:0003011	OMIM:261400	IEA				P		HPO:iea	
OMIM	261400	PERONEUS TERTIUS MUSCLE, ABSENCE OF		HP:0009027	OMIM:261400	TAS				P		HPO:probinson	
OMIM	261500	EOSINOPHIL PEROXIDASE DEFICIENCY; EPXD		HP:0000007	OMIM:261500	TAS				I		HPO:iea	
OMIM	261500	EOSINOPHIL PEROXIDASE DEFICIENCY; EPXD		HP:0001879	OMIM:261500	TAS				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000007	OMIM:261515	IEA				I		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000107	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000218	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000239	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000256	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000268	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000270	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000278	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000286	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000316	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000343	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000347	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000348	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000369	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000486	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000505	OMIM:261515	TAS				P		HPO:skoehler	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000550	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000572	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000582	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000639	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000762	OMIM:261515	TAS		HP:0040284		P		HPO:probinson	67%
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000767	OMIM:261515	TAS				P		HPO:probinson	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0000938	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001171	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001250	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001263	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001319	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001396	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001397	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001408	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001508	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001561	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001762	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001765	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001791	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0001999	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002007	OMIM:261515	TAS				P		HPO:skoehler	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002079	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002119	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002126	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002171	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002240	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002539	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002750	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002832	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0002910	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0003199	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0003593	OMIM:261515	IEA				C		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0005257	OMIM:261515	IEA				P		HPO:skoehler	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0005280	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0006872	OMIM:261515	TAS		HP:0040284		P		HPO:probinson	45%
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0007058	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0007266	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0007360	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0007371	OMIM:261515	IEA				P		HPO:skoehler	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0008207	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0008872	OMIM:261515	IEA				P		HPO:iea	
OMIM	261515	D-BIFUNCTIONAL PROTEIN DEFICIENCY		HP:0030799	OMIM:261515	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000007	OMIM:261540	IEA				I		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000013	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000028	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000047	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000059	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000060	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000073	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000089	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000126	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000175	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000200	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000204	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000219	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000233	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000238	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000252	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000256	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000260	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000276	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000311	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000316	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000327	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000343	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000347	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000365	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000369	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000402	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000411	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000465	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000475	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000480	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000501	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000508	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000518	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000545	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000582	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000612	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000639	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000659	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000690	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000767	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0000954	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001080	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001156	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001159	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001169	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001250	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001263	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001274	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001363	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001388	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001511	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001537	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001540	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001545	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001561	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001629	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001631	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001642	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001761	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001769	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001773	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0001831	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002007	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002059	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002119	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002219	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002263	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002644	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002650	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002937	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0002996	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0003278	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0003561	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0004209	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0004279	OMIM:261540	IEA				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0004325	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0004467	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0005608	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0006610	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0006887	OMIM:261540	IEA		HP:0040284		P		HPO:skoehler	20%
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0008569	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0008726	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0008872	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0008897	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0008905	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0009623	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0010049	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0010743	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0011065	OMIM:261540	IEA				P		HPO:iea	
OMIM	261540	PETERS-PLUS SYNDROME; PTRPLS		HP:0011220	OMIM:261540	TAS				P		HPO:skoehler	
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0000007	PMID:8162013	PCS				I		HPO:iea	
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0000022	PMID:4144375	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0000023	PMID:9302384	PCS		HP:0040284		P		HPO:iea	80%
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0003117	PMID:8162013;PMID:8872466	PCS		HP:0040284		P		HPO:iea	50%
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0003251	PMID:11760020	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	261550	PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II		HP:0008689	PMID:11760020;PMID:9302384	PCS		HP:0040284		P		HPO:iea	20%
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0000007	OMIM:261560	IEA				I		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0000286	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0000378	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0000581	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0001387	OMIM:261560	IEA				P		HPO:skoehler	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0001620	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0001650	OMIM:261560	IEA				P		HPO:skoehler	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0004322	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0006297	OMIM:261560	IEA				P		HPO:iea	
OMIM	261560	PFEIFFER-PALM-TELLER SYNDROME		HP:0045025	OMIM:261560	IEA				P		HPO:skoehler	
OMIM	261590	PHENFORMIN 4-HYDROXYLATION		HP:0000007	OMIM:261590	IEA				I		HPO:iea	
OMIM	261590	PHENFORMIN 4-HYDROXYLATION		HP:0003128	OMIM:261590	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000007	OMIM:261600	IEA				I		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000252	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000518	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000635	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000709	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000716	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000718	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000722	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000737	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000739	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000742	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0000958	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0000964	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0001249	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0001250	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0001347	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0002286	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0002514	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0002686	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0004920	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0004923	OMIM:261600	PCS				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0005982	OMIM:261600	PCS				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0007018	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0007513	OMIM:261600	IEA				P		HPO:iea	
OMIM	261600	PHENYLKETONURIA		HP:0100324	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0100610	OMIM:261600	TAS				P		HPO:skoehler	
OMIM	261600	PHENYLKETONURIA		HP:0410066	PMID:22626821,PMID:19551947	PCS				P		HPO:NicoleVasilevsky	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0000007	OMIM:261630	IEA				I		HPO:iea	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0000252	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0000737	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001249	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001250	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001252	OMIM:261630	IEA				P		HPO:iea	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001263	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001266	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001276	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001332	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001336	OMIM:261630	IEA				P		HPO:iea	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001337	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0001954	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0002015	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0002344	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0002514	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0003593	OMIM:261630	IEA				C		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0003781	OMIM:261630	TAS				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0003828	OMIM:261630	IEA				C		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0004923	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261630	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C		HP:0025356	OMIM:261630	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0000007	OMIM:261640	IEA				I		HPO:iea	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0000252	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0000737	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001250	OMIM:261640	IEA				P		HPO:iea	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001251	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001262	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001263	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001266	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001276	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001300	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001332	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001337	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001347	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001518	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0001954	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0002015	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0002033	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0002063	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0002067	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0002344	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0003593	OMIM:261640	TAS				C		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0003781	OMIM:261640	TAS				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0004923	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0006887	OMIM:261640	IEA				P		HPO:iea	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0008936	OMIM:261640	TAS				P		HPO:probinson	
OMIM	261640	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A; HPABH4A		HP:0025356	OMIM:261640	IEA				P		HPO:skoehler	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0000007	OMIM:261650	IEA				I		HPO:iea	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0000799	OMIM:261650	IEA				P		HPO:iea	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0001397	OMIM:261650	IEA				P		HPO:iea	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0001399	OMIM:261650	IEA				P		HPO:iea	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0001943	OMIM:261650	IEA				P		HPO:iea	
OMIM	261650	PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL		HP:0005959	OMIM:261650	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0000007	OMIM:261670	IEA				I		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0000083	OMIM:261670	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0002913	OMIM:261670	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003198	OMIM:261670	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003201	OMIM:261670	IEA				P		HPO:skoehler	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003236	OMIM:261670	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003546	OMIM:261670	IEA				P		HPO:skoehler	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003710	OMIM:261670	IEA				P		HPO:iea	
OMIM	261670	PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF		HP:0003738	OMIM:261670	IEA				P		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0000007	OMIM:261680	IEA				I		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0000648	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0000799	OMIM:261680	IEA				P		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0000961	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0001250	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC	HP:0012828	HP:0001263	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0001397	OMIM:261680	IEA				P		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0001399	OMIM:261680	IEA				P		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0001943	OMIM:261680	IEA				P		HPO:iea	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0002059	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC	HP:0025303	HP:0002104	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0002240	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0002353	OMIM:261680	TAS				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0002480	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0002919	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0003128	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0003162	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0003572	OMIM:261680	IEA				P		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0003593	OMIM:261680	TAS				C		HPO:skoehler	
OMIM	261680	PHOSPHOENOLPYRUVATE CARBOXYKINASE DEFICIENCY, CYTOSOLIC; PCKDC		HP:0005959	OMIM:261680	IEA				P		HPO:iea	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0000006	OMIM:261740	TAS				I		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0000007	OMIM:261740	IEA				I		HPO:iea	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0000158	OMIM:261740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0000961	OMIM:261740	IEA				P		HPO:iea	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001250	OMIM:261740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001541	OMIM:261740	TAS				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001635	OMIM:261740	IEA				P		HPO:iea	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001638	OMIM:261740	IEA				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001640	OMIM:261740	TAS				P		HPO:probinson	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001662	OMIM:261740	IEA				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001998	OMIM:261740	IEA				P		HPO:iea	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0001999	OMIM:261740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0002615	OMIM:261740	TAS				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0003198	OMIM:261740	IEA				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0005165	OMIM:261740	TAS				P		HPO:probinson	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0100598	OMIM:261740	TAS				P		HPO:skoehler	
OMIM	261740	GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL		HP:0200128	OMIM:261740	TAS				P		HPO:skoehler	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0000007	OMIM:261750	TAS				I		HPO:probinson	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0001290	OMIM:261750	TAS				P		HPO:skoehler	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB	HP:0012825	HP:0001324	OMIM:261750	TAS				P		HPO:probinson	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0002014	OMIM:261750	TAS				P		HPO:probinson	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0002240	OMIM:261750	TAS				P		HPO:probinson	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0004322	OMIM:261750	TAS				P		HPO:skoehler	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0006568	OMIM:261750	TAS				P		HPO:probinson	
OMIM	261750	GLYCOGEN STORAGE DISEASE IXB		HP:0009051	OMIM:261750	TAS				P		HPO:probinson	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0000007	OMIM:261800	IEA				I		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0000162	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0000175	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0000201	OMIM:261800	TAS				P		HPO:skoehler	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0000347	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0001648	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0002643	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0002781	OMIM:261800	IEA				P		HPO:iea	
OMIM	261800	PIERRE ROBIN SYNDROME		HP:0008872	OMIM:261800	IEA				P		HPO:skoehler	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0000006	OMIM:261900	TAS				I		HPO:skoehler	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0000007	OMIM:261900	IEA				I		HPO:iea	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0002208	OMIM:261900	IEA				P		HPO:iea	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0002299	OMIM:261900	TAS				P		HPO:skoehler	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0003329	OMIM:261900	IEA				P		HPO:iea	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0003745	OMIM:261900	TAS				I		HPO:skoehler	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0003777	OMIM:261900	IEA				P		HPO:iea	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0006297	OMIM:261900	IEA				P		HPO:iea	
OMIM	261900	PILI TORTI, EARLY-ONSET		HP:0011359	OMIM:261900	TAS				P		HPO:skoehler	
OMIM	261990	PILI TORTI - DEVELOPMENTAL DELAY - NEUROLOGICAL ABNORMALITIES		HP:0001263	OMIM:261990	IEA				P		HPO:skoehler	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0000007	OMIM:262000	TAS				I		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0000135	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0000407	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0000970	OMIM:262000	TAS				P		HPO:skoehler	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0001249	OMIM:262000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0001596	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0002208	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0002299	PMID:15345881	PCS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0003329	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0003777	OMIM:262000	TAS				P		HPO:skoehler	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0003828	OMIM:262000	TAS				C		HPO:skoehler	
OMIM	262000	#262000 BJORNSTAD SYNDROME; BJS;;PILI TORTI AND NERVE DEAFNESS;;PTD		HP:0011359	OMIM:262000	TAS				P		HPO:probinson	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0000007	OMIM:262020	IEA				I		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0000431	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0000540	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0000668	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0000968	OMIM:262020	TAS				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0001597	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0002209	OMIM:262020	PCS				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0002299	OMIM:262020	PCS				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0004779	OMIM:262020	IEA				P		HPO:skoehler	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0007502	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0007588	OMIM:262020	IEA				P		HPO:iea	
OMIM	262020	PILODENTAL DYSPLASIA WITH REFRACTIVE ERRORS		HP:0011065	OMIM:262020	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000007	OMIM:262190	IEA				I		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000040	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000218	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000280	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000303	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000826	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000831	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000842	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000956	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000958	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0000998	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0001263	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0001518	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0001943	OMIM:262190	IEA				P		HPO:skoehler	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0001953	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0003074	OMIM:262190	IEA				P		HPO:skoehler	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0003162	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0004322	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0006288	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0008665	OMIM:262190	IEA				P		HPO:iea	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0011998	OMIM:262190	TAS				P		HPO:skoehler	
OMIM	262190	PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES		HP:0012542	OMIM:262190	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0000007	OMIM:262300	TAS				I		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0000518	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0000613	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0001141	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0007641	OMIM:262300	TAS				P		HPO:skoehler	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0007803	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0007811	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0011003	OMIM:262300	TAS				P		HPO:probinson	
OMIM	262300	#262300 ACHROMATOPSIA 3; ACHM3;;PINGELAPESE BLINDNESS;;TOTAL COLORBLINDNESS WITH MYOPIA;;ACHROMATOPSIA WITH MYOPIA;;ACHM1, FORMERLY;;ROD MONOCHROMATISM 1, FORMERLY;;ROD MONOCHROMACY 1, FORMERLY; RMCH1, FORMERLY		HP:0011516	OMIM:262300	IEA				P		HPO:skoehler	
OMIM	262400	PITUITARY DWARFISM I		HP:0000007	OMIM:262400	IEA				I		HPO:iea	
OMIM	262400	PITUITARY DWARFISM I		HP:0000271	OMIM:262400	IEA				P		HPO:iea	
OMIM	262400	PITUITARY DWARFISM I		HP:0000839	OMIM:262400	IEA				P		HPO:skoehler	
OMIM	262400	PITUITARY DWARFISM I		HP:0001943	OMIM:262400	IEA				P		HPO:iea	
OMIM	262400	PITUITARY DWARFISM I		HP:0002715	OMIM:262400	IEA				P		HPO:iea	
OMIM	262400	PITUITARY DWARFISM I		HP:0003510	OMIM:262400	IEA				P		HPO:skoehler	
OMIM	262500	LARON SYNDROME		HP:0000007	OMIM:262500	TAS				I		HPO:probinson	
OMIM	262500	LARON SYNDROME		HP:0000274	OMIM:262500	IEA				P		HPO:iea	
OMIM	262500	LARON SYNDROME		HP:0000592	OMIM:262500	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	262500	LARON SYNDROME		HP:0001367	OMIM:262500	IEA				P		HPO:iea	
OMIM	262500	LARON SYNDROME		HP:0001620	OMIM:262500	IEA				P		HPO:iea	
OMIM	262500	LARON SYNDROME		HP:0001939	OMIM:262500	IEA				P		HPO:iea	
OMIM	262500	LARON SYNDROME		HP:0002750	OMIM:262500	TAS				P		HPO:probinson	
OMIM	262500	LARON SYNDROME		HP:0003026	OMIM:262500	TAS	HP:0003593			P		HPO:probinson	
OMIM	262500	LARON SYNDROME		HP:0003510	OMIM:262500	TAS				P		HPO:skoehler	
OMIM	262500	LARON SYNDROME		HP:0009826	OMIM:262500	IEA				P		HPO:skoehler	
OMIM	262500	LARON SYNDROME		HP:0012569	OMIM:262500	TAS				P		HPO:probinson	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0000007	OMIM:262600	IEA				I		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0000135	OMIM:262600	IEA				P		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0000821	OMIM:262600	IEA				P		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0000846	OMIM:262600	IEA				P		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0000871	OMIM:262600	IEA				P		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0001250	OMIM:262600	IEA				P		HPO:skoehler	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0001998	OMIM:262600	IEA				P		HPO:iea	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0002173	OMIM:262600	TAS				P		HPO:skoehler	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0004322	OMIM:262600	IEA				P		HPO:skoehler	
OMIM	262600	#262600 PITUITARY HORMONE DEFICIENCY, COMBINED, 2; CPHD2;;PANHYPOPITUITARISM;;ATELIOTIC DWARFISM WITH HYPOGONADISM;;PITUITARY DWARFISM III;;HANHART DWARFISM		HP:0008202	OMIM:262600	TAS				P		HPO:skoehler	
OMIM	262650	PITUITARY DWARFISM IV		HP:0000007	OMIM:262650	IEA				I		HPO:iea	
OMIM	262650	PITUITARY DWARFISM IV		HP:0000839	OMIM:262650	IEA				P		HPO:iea	
OMIM	262650	PITUITARY DWARFISM IV		HP:0001939	OMIM:262650	IEA				P		HPO:iea	
OMIM	262650	PITUITARY DWARFISM IV		HP:0002750	OMIM:262650	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0000006	OMIM:262700	IEA				I		HPO:skoehler	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0000007	OMIM:262700	IEA				I		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0000821	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0000839	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0000846	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0001943	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0003799	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0008850	OMIM:262700	IEA				P		HPO:iea	
OMIM	262700	PITUITARY DWARFISM WITH SMALL SELLA TURCICA		HP:0010538	OMIM:262700	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	262710	PITUITARY DWARFISM WITH LARGE SELLA TURCICA		HP:0000007	OMIM:262710	IEA				I		HPO:iea	
OMIM	262710	PITUITARY DWARFISM WITH LARGE SELLA TURCICA		HP:0000821	OMIM:262710	IEA				P		HPO:iea	
OMIM	262710	PITUITARY DWARFISM WITH LARGE SELLA TURCICA		HP:0000824	OMIM:262710	TAS				P		HPO:iea	
OMIM	262710	PITUITARY DWARFISM WITH LARGE SELLA TURCICA		HP:0000839	OMIM:262710	IEA				P		HPO:iea	
OMIM	262710	PITUITARY DWARFISM WITH LARGE SELLA TURCICA		HP:0002690	OMIM:262710	IEA				P		HPO:iea	
OMIM	262800	PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF		HP:0000007	OMIM:262800	IEA				I		HPO:iea	
OMIM	262800	PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF		HP:0000978	OMIM:262800	TAS				P		HPO:skoehler	
OMIM	262800	PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF		HP:0001058	OMIM:262800	IEA				P		HPO:iea	
OMIM	262800	PLASMA CLOT RETRACTION FACTOR, DEFICIENCY OF		HP:0002239	OMIM:262800	IEA				P		HPO:iea	
OMIM	262850	PLASMIN INHIBITOR DEFICIENCY		HP:0000007	OMIM:262850	TAS				I		HPO:probinson	
OMIM	262850	PLASMIN INHIBITOR DEFICIENCY		HP:0000978	OMIM:262850	TAS				P		HPO:probinson	
OMIM	262850	PLASMIN INHIBITOR DEFICIENCY		HP:0001934	OMIM:262850	TAS				P		HPO:probinson	
OMIM	262850	PLASMIN INHIBITOR DEFICIENCY		HP:0005261	OMIM:262850	TAS				P		HPO:probinson	
OMIM	262850	PLASMIN INHIBITOR DEFICIENCY		HP:0012151	OMIM:262850	TAS				P		HPO:probinson	
OMIM	262875	PLATELET PROSTACYCLIN RECEPTOR DEFECT		HP:0000007	OMIM:262875	IEA				I		HPO:iea	
OMIM	262875	PLATELET PROSTACYCLIN RECEPTOR DEFECT		HP:0001939	OMIM:262875	IEA				P		HPO:iea	
OMIM	262875	PLATELET PROSTACYCLIN RECEPTOR DEFECT		HP:0004417	OMIM:262875	IEA				P		HPO:iea	
OMIM	262890	#262890 SCOTT SYNDROME; SCTS;;BLEEDING DISORDER, PLATELET-TYPE, 7; BDPLT7;;BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTORX;;PROTHROMBIN CONVERSION DEFECT, FAMILIAL;;PROTHROMBIN CONSUMPTION DEFICIENCY;;PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL		HP:0000007	OMIM:262890	TAS				I		HPO:probinson	
OMIM	262890	#262890 SCOTT SYNDROME; SCTS;;BLEEDING DISORDER, PLATELET-TYPE, 7; BDPLT7;;BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTORX;;PROTHROMBIN CONVERSION DEFECT, FAMILIAL;;PROTHROMBIN CONSUMPTION DEFICIENCY;;PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL		HP:0001892	OMIM:262890	TAS				P		HPO:skoehler	
OMIM	262890	#262890 SCOTT SYNDROME; SCTS;;BLEEDING DISORDER, PLATELET-TYPE, 7; BDPLT7;;BLEEDING ABNORMALITY DUE TO DEFICIENCY OF PLATELET BINDING OF FACTORX;;PROTHROMBIN CONVERSION DEFECT, FAMILIAL;;PROTHROMBIN CONSUMPTION DEFICIENCY;;PROTHROMBIN CONSUMPTION INHIBITOR, FAMILIAL		HP:0008354	OMIM:262890	TAS				P		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0000007	OMIM:262900	TAS				I		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0001270	OMIM:262900	TAS				P		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0001319	OMIM:262900	TAS				P		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0003198	OMIM:262900	IEA				P		HPO:skoehler	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0003470	OMIM:262900	IEA				P		HPO:skoehler	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0003701	OMIM:262900	TAS				P		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0007126	OMIM:262900	TAS				P		HPO:probinson	
OMIM	262900	PLEOCONIAL MYOPATHY WITH SALT CRAVING		HP:0030083	OMIM:262900	TAS				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0000007	OMIM:263000	IEA				I		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0000961	OMIM:263000	IEA				P		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0001508	OMIM:263000	IEA				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0001648	OMIM:263000	IEA				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0001939	OMIM:263000	IEA				P		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0002098	OMIM:263000	IEA				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0002788	OMIM:263000	IEA				P		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0002789	OMIM:263000	IEA				P		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0002878	OMIM:263000	TAS	HP:0003593			P		HPO:probinson	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0003593	OMIM:263000	TAS				C		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0005576	OMIM:263000	IEA				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0005942	OMIM:263000	IEA				P		HPO:iea	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0006515	OMIM:263000	TAS				P		HPO:skoehler	
OMIM	263000	INTERSTITIAL PNEUMONITIS, DESQUAMATIVE, FAMILIAL; DIP		HP:0012735	OMIM:263000	TAS				P		HPO:skoehler	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0000007	OMIM:263100	IEA				I		HPO:iea	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0000113	OMIM:263100	IEA				P		HPO:iea	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0000518	OMIM:263100	TAS				P		HPO:probinson	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0000556	OMIM:263100	IEA				P		HPO:iea	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0007770	OMIM:263100	IEA				P		HPO:iea	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0007875	OMIM:263100	IEA				P		HPO:skoehler	
OMIM	263100	POLYCYSTIC KIDNEY, CATARACT, AND CONGENITAL BLINDNESS		HP:0025492	OMIM:263100	TAS				P		HPO:skoehler	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:263200	IEA				I		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0000083	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0000105	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0000107	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0000113	OMIM:263200	TAS				P		HPO:probinson	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001405	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001407	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001409	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001562	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001737	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001744	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0001944	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0002009	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0002040	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0002089	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0002240	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0003811	OMIM:263200	TAS		HP:0040283		M		HPO:probinson	HP:0040283
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0005564	OMIM:263200	IEA				P		HPO:iea	
OMIM	263200	POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE		HP:0005576	OMIM:263200	IEA				P		HPO:iea	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000007	PMID:25966638	PCS				I		HPO:iea	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000113	PMID:25966638	PCS		HP:0040284		P		HPO:iea	9/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000248	OMIM:263210	TAS				P		HPO:probinson	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000252	PMID:25966638	PCS		HP:0040284		P		HPO:probinson	9/11
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000260	PMID:25966638	PCS		HP:0040284		P		HP:probinson	4/6
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000278	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000286	PMID:25966638	PCS		HP:0040284		P		HP:probinson	3/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000316	PMID:25966638	PCS		HP:0040284		P		HPO:iea	6/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000319	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000347	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000358	PMID:25966638	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000369	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000430	OMIM:263210	TAS				P		HPO:skoehler	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000430	PMID:25966638	PCS		HP:0040284		P		HP:probinson	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000444	OMIM:263210	TAS				P		HPO:skoehler	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000444	PMID:25966638	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000470	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000474	PMID:25966638	PCS		HP:0040284		P		HP:probinson	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000506	PMID:25966638	PCS		HP:0040284		P		HPO:iea	6/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000520	PMID:25966638	PCS		HP:0040284		P		HP:probinson	8/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000776	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	1/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0000813	PMID:25966638	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001371	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	1/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001405	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	6/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001539	PMID:25966638	PCS		HP:0040284		P		HP:probinson	2/5
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001561	PMID:25966638	PCS		HP:0040284		P		HP:probinson	1/5
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001562	PMID:25966638	PCS		HP:0040284		P		HP:probinson	1/5
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0001627	PMID:25966638	PCS	HP:0003577	HP:0040284		P		HP:probinson	6/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0002089	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0002101	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0002265	PMID:25966638	PCS		HP:0040284		P		HPO:iea	5/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0002652	OMIM:263210	TAS				P		HPO:skoehler	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0003016	PMID:25966638	PCS		HP:0040284		P		HP:probinson	8/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0003026	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0003375	PMID:25966638	PCS		HP:0040284		P		HP:probinson	8/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0003577	PMID:25966638	PCS				C		HPO:skoehler	
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0004331	PMID:25966638	PCS		HP:0040284		P		HP:probinson	7/8
OMIM	263210	GILLESSEN-KAESBACH-NISHIMURA SYNDROME		HP:0009487	PMID:25966638	PCS		HP:0040284		P		HPO:skoehler	8/8
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0000006	OMIM:263300	IEA				I		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001342	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001428	OMIM:263300	IEA				I		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001744	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001873	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001894	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001898	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001899	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001900	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001907	OMIM:263300	TAS				P		HPO:skoehler	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001974	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0001977	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0002239	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0002637	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0002639	OMIM:263300	IEA				P		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0003745	OMIM:263300	IEA				I		HPO:iea	
OMIM	263300	#263300 POLYCYTHEMIA VERA;;PV;;POLYCYTHEMIA RUBRA VERA; PRV		HP:0005513	OMIM:263300	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0000007	OMIM:263400	IEA				I		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001028	OMIM:263400	IEA				P		HPO:skoehler	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001050	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001297	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001342	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001898	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001899	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0001900	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0002315	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0002615	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0002619	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0002641	OMIM:263400	IEA				P		HPO:iea	
OMIM	263400	#263400 ERYTHROCYTOSIS, FAMILIAL, 2; ECYT2;;ERYTHROCYTOSIS, AUTOSOMAL RECESSIVE BENIGN;;POLYCYTHEMIA, VHL-DEPENDENT;;POLYCYTHEMIA, CHUVASH TYPE		HP:0012378	OMIM:263400	TAS				P		HPO:skoehler	
OMIM	263450	%263450 POLYDACTYLY, POSTAXIAL, TYPE A5; PAPA5		HP:0000007	OMIM:263450	IEA				I		HPO:iea	
OMIM	263450	%263450 POLYDACTYLY, POSTAXIAL, TYPE A5; PAPA5		HP:0001159	OMIM:263450	IEA				P		HPO:skoehler	
OMIM	263450	%263450 POLYDACTYLY, POSTAXIAL, TYPE A5; PAPA5		HP:0001162	OMIM:263450	IEA				P		HPO:iea	
OMIM	263450	%263450 POLYDACTYLY, POSTAXIAL, TYPE A5; PAPA5		HP:0009701	OMIM:263450	IEA				P		HPO:skoehler	
OMIM	263450	%263450 POLYDACTYLY, POSTAXIAL, TYPE A5; PAPA5		HP:0010554	OMIM:263450	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000007	OMIM:263520	TAS				I		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000054	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000062	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000113	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000161	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000171	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000175	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000248	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000540	OMIM:263520	IEA				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000556	OMIM:263520	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000750	OMIM:263520	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000768	OMIM:263520	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000773	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000774	OMIM:263520	TAS				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000888	OMIM:263520	TAS				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001156	OMIM:263520	IEA				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001162	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001177	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001270	OMIM:263520	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001302	OMIM:263520	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001320	OMIM:263520	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001395	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001629	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001631	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0001789	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0002089	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0002566	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0003027	OMIM:263520	IEA				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0005180	OMIM:263520	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0005349	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0005766	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0005817	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0005873	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0006644	OMIM:263520	IEA				P		HPO:skoehler	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0006956	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0010984	OMIM:263520	TAS				I		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0011802	OMIM:263520	TAS				P		HPO:probinson	
OMIM	263520	SHORT-RIB THORACIC DYSPLASIA 6 WITH OR WITHOUT POLYDACTYLY; SRTD6		HP:0100732	OMIM:263520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000007	OMIM:263540	IEA				I		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000193	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000286	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000303	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000369	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000465	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000668	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000767	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000768	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0000774	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001156	OMIM:263540	TAS				P		HPO:skoehler	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001162	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001572	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001770	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001830	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0001837	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0002162	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0002751	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0002937	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0002948	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0003416	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0004209	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0004691	OMIM:263540	TAS				P		HPO:probinson	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0005819	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0006045	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0006297	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0008368	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0008479	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0008577	OMIM:263540	IEA				P		HPO:iea	
OMIM	263540	263540 POLYDACTYLY, POSTAXIAL, WITH DENTAL AND VERTEBRAL ANOMALIES		HP:0011088	OMIM:263540	TAS				P		HPO:skoehler	
OMIM	263550	POLYMYOCLONUS, INFANTILE		HP:0000007	OMIM:263550	IEA				I		HPO:iea	
OMIM	263550	POLYMYOCLONUS, INFANTILE		HP:0000737	OMIM:263550	IEA				P		HPO:iea	
OMIM	263550	POLYMYOCLONUS, INFANTILE		HP:0001251	OMIM:263550	IEA				P		HPO:iea	
OMIM	263550	POLYMYOCLONUS, INFANTILE		HP:0001336	OMIM:263550	IEA				P		HPO:skoehler	
OMIM	263550	POLYMYOCLONUS, INFANTILE		HP:0007295	OMIM:263550	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0000007	OMIM:263570	IEA				I		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0000011	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0000011	OMIM:263570	TAS				P		HPO:probinson	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0001258	OMIM:263570	TAS				P		HPO:skoehler	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0001278	OMIM:263570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0001288	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0001939	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0002127	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0002273	OMIM:263570	TAS				P		HPO:skoehler	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0002500	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0002936	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0003401	OMIM:263570	IEA				P		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0003477	OMIM:263570	TAS				P		HPO:skoehler	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0003581	OMIM:263570	TAS				C		HPO:skoehler	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0003677	OMIM:263570	IEA				C		HPO:iea	
OMIM	263570	POLYGLUCOSAN BODY NEUROPATHY, ADULT FORM		HP:0100543	OMIM:263570	IEA				P		HPO:iea	
OMIM	263600	POLYSACCHARIDE, STORAGE OF UNUSUAL		HP:0000007	OMIM:263600	TAS				I		HPO:probinson	
OMIM	263600	POLYSACCHARIDE, STORAGE OF UNUSUAL		HP:0011012	OMIM:263600	TAS				P		HPO:probinson	
OMIM	263610	POLYHYDRAMNIOS, CHRONIC IDIOPATHIC		HP:0000007	OMIM:263610	TAS				I		HPO:probinson	
OMIM	263610	POLYHYDRAMNIOS, CHRONIC IDIOPATHIC		HP:0001561	OMIM:263610	TAS				P		HPO:probinson	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0000007	OMIM:263630	IEA				I		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0000107	OMIM:263630	IEA				P		HPO:skoehler	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0000316	OMIM:263630	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0000463	OMIM:263630	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001159	OMIM:263630	IEA				P		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001177	OMIM:263630	IEA				P		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001407	OMIM:263630	IEA				P		HPO:skoehler	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001561	OMIM:263630	IEA				P		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001629	OMIM:263630	IEA				P		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001631	OMIM:263630	IEA				P		HPO:iea	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001792	OMIM:263630	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0001999	OMIM:263630	IEA				P		HPO:skoehler	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0003826	OMIM:263630	TAS				M		HPO:skoehler	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0003826	OMIM:263630	IEA				M		HPO:skoehler	
OMIM	263630	%263630 POLYSYNDACTYLY WITH CARDIAC MALFORMATION;;BONNEAU SYNDROME		HP:0010066	OMIM:263630	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000007	OMIM:263650	IEA				I		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000050	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000059	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000062	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000175	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000204	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000316	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000327	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000347	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000369	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000378	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000561	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000568	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0000882	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0001060	OMIM:263650	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0001159	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0001511	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0001792	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0001798	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0002006	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0002025	OMIM:263650	TAS				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0002223	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0003196	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0006610	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0007418	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0007759	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0008689	OMIM:263650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0009755	OMIM:263650	IEA				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0009756	OMIM:263650	IEA				P		HPO:skoehler	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0009777	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0009803	OMIM:263650	IEA				P		HPO:iea	
OMIM	263650	BARTSOCAS-PAPAS SYNDROME; BPS		HP:0010609	OMIM:263650	IEA				P		HPO:skoehler	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000007	OMIM:263700	IEA				I		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000153	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000509	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000559	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000938	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000953	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000987	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000992	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0000998	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001010	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001081	OMIM:263700	IEA				P		HPO:skoehler	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001596	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001744	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001873	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0001878	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0002223	OMIM:263700	TAS				P		HPO:skoehler	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0002756	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0002797	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0002953	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0003577	OMIM:263700	IEA				C		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0004322	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0009473	OMIM:263700	IEA				P		HPO:iea	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0011457	OMIM:263700	TAS				P		HPO:skoehler	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0032001	OMIM:263700	IEA				P		HPO:skoehler	
OMIM	263700	PORPHYRIA, CONGENITAL ERYTHROPOIETIC		HP:0100324	OMIM:263700	TAS				P		HPO:skoehler	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000007	OMIM:263750	IEA				I		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000028	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000054	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000077	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000175	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000204	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000272	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000347	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000369	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000378	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000405	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000453	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000494	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000625	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000656	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000698	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0000767	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0001159	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0001374	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0001510	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0001760	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0002021	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0002558	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0002946	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0002974	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0002984	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0003022	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0005211	OMIM:263750	IEA				P		HPO:iea	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0008897	OMIM:263750	TAS				P		HPO:skoehler	
OMIM	263750	#263750 POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS;;MILLER SYNDROME;;GENEE-WIEDEMANN SYNDROME		HP:0009778	OMIM:263750	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0000007	PMID:22009145	PCS				I		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0000017	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0000103	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0000128	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0000622	PMID:22009145	PCS		HP:0040284		P		HP:probinson	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0000805	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0000823	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0000848	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0000934	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001250	PMID:22009145	PCS		HP:0040284		P		HP:probinson	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0001251	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001281	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001324	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001508	PMID:28003083	PCS		HP:0040284		P		HP:probinson	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0001657	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001949	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0001954	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0001959	PMID:28003083	PCS				P		HPO:skoehler	
OMIM	263800	GITELMAN SYNDROME		HP:0001962	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002013	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002019	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002027	PMID:22009145	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	263800	GITELMAN SYNDROME		HP:0002321	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002615	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002829	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0002900	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0002917	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0003127	OMIM:263800	IEA				P		HPO:skoehler	
OMIM	263800	GITELMAN SYNDROME		HP:0003201	PMID:22009145	PCS		HP:0040284		P		HP:probinson	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0003324	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0003394	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0003401	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0003470	PMID:28003083	PCS		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0003621	OMIM:263800	IEA				C		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0004756	PMID:22009145	PCS		HP:0040284		P		HP:probinson	HP:0040284
OMIM	263800	GITELMAN SYNDROME		HP:0005567	OMIM:263800	IEA				P		HPO:iea	
OMIM	263800	GITELMAN SYNDROME		HP:0012378	PMID:28003083	PCS				P		HP:probinson	
OMIM	263800	GITELMAN SYNDROME		HP:0030083	PMID:28003083	PCS				P		HP:probinson	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0000007	OMIM:264010	IEA				I		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0000078	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0000938	OMIM:264010	TAS				P		HPO:skoehler	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0000939	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0001249	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0001513	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0004322	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0009473	OMIM:264010	IEA				P		HPO:iea	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0010580	OMIM:264010	TAS				P		HPO:skoehler	
OMIM	264010	264010 PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY;;URBAN-ROGERS-MEYER SYNDROME		HP:0012385	OMIM:264010	TAS				P		HPO:skoehler	
OMIM	264050	PRENATAL BOWING		HP:0000007	OMIM:264050	IEA				I		HPO:iea	
OMIM	264050	PRENATAL BOWING		HP:0000951	OMIM:264050	IEA				P		HPO:iea	
OMIM	264050	PRENATAL BOWING		HP:0006487	OMIM:264050	IEA				P		HPO:skoehler	
OMIM	264060	PREPAPILLARY VASCULAR LOOPS		HP:0000007	OMIM:264060	IEA				I		HPO:iea	
OMIM	264060	PREPAPILLARY VASCULAR LOOPS		HP:0000478	OMIM:264060	IEA				P		HPO:iea	
OMIM	264060	PREPAPILLARY VASCULAR LOOPS		HP:0001626	OMIM:264060	IEA				P		HPO:iea	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0000007	OMIM:264070	IEA				I		HPO:iea	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0001252	OMIM:264070	IEA				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0001270	OMIM:264070	IEA				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0001276	OMIM:264070	IEA				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0001290	OMIM:264070	TAS				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0001337	OMIM:264070	IEA				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0004923	OMIM:264070	TAS				P		HPO:skoehler	
OMIM	264070	HYPERPHENYLALANINEMIA, BH4-DEFICIENT, D		HP:0008297	OMIM:264070	IEA				P		HPO:iea	
OMIM	264080	PROGESTERONE RESISTANCE		HP:0000007	OMIM:264080	IEA				I		HPO:iea	
OMIM	264080	PROGESTERONE RESISTANCE		HP:0001939	OMIM:264080	IEA				P		HPO:iea	
OMIM	264080	PROGESTERONE RESISTANCE		HP:0008222	OMIM:264080	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000007	OMIM:264090	IEA				I		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000028	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000040	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000047	OMIM:264090	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000160	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000242	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000256	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000272	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000316	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000325	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000347	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000369	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000387	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000418	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000535	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000582	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000592	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000621	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000639	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000653	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000656	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000695	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000771	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000883	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000946	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0000963	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001006	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001043	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001176	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001249	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001263	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001290	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001371	OMIM:264090	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001476	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001508	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001511	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001792	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0001833	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002015	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002078	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002080	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002155	OMIM:264090	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002205	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0002209	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0003097	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0003269	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0003577	OMIM:264090	TAS				C		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0003758	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0004322	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0004492	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0005792	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0007485	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0010511	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0011968	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0030088	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0030680	OMIM:264090	IEA				P		HPO:iea	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0100578	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0100678	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264090	PROGEROID SYNDROME, NEONATAL		HP:0100807	OMIM:264090	TAS				P		HPO:skoehler	
OMIM	264110	PROLACTIN DEFICIENCY, ISOLATED		HP:0000007	OMIM:264110	TAS				I		HPO:probinson	
OMIM	264110	PROLACTIN DEFICIENCY, ISOLATED		HP:0000789	OMIM:264110	TAS				P		HPO:skoehler	
OMIM	264110	PROLACTIN DEFICIENCY, ISOLATED		HP:0000858	OMIM:264110	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	264110	PROLACTIN DEFICIENCY, ISOLATED		HP:0008202	OMIM:264110	TAS				P		HPO:probinson	
OMIM	264120	PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES		HP:0000007	OMIM:264120	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	264120	PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES		HP:0000053	OMIM:264120	TAS				P		HPO:probinson	
OMIM	264120	PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES		HP:0001513	OMIM:264120	TAS				P		HPO:probinson	
OMIM	264120	PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES		HP:0006889	OMIM:264120	TAS				P		HPO:probinson	
OMIM	264120	PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES		HP:0008202	OMIM:264120	TAS				P		HPO:probinson	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0000007	OMIM:264140	TAS				I		HPO:nvasilevsky	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0000072	OMIM:264140	TAS				P		HPO:probinson	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0000126	OMIM:264140	IEA				P		HPO:iea	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0000407	OMIM:264140	IEA				P		HPO:iea	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0001249	OMIM:264140	IEA				P		HPO:iea	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0001417	PMID:157583	TAS				I		HPO:nvasilevsky	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0001642	OMIM:264140	IEA				P		HPO:iea	
OMIM	264140	PRUNE BELLY SYNDROME WITH PULMONIC STENOSIS, MENTAL RETARDATION, ANDDEAFNESS		HP:0004392	OMIM:264140	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000007	OMIM:264180	IEA				I		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000248	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000272	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000319	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000347	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000463	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000465	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000470	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000592	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0000926	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0001508	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0001762	OMIM:264180	IEA				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0001945	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0002007	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0002650	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0002719	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0002938	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0003042	OMIM:264180	TAS				P		HPO:probinson	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0003311	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0003510	PMID:7923357	PCS				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0005680	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0006243	OMIM:264180	TAS				P		HPO:probinson	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0008905	OMIM:264180	IEA				P		HPO:iea	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0011800	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264180	PSEUDODIASTROPHIC DYSPLASIA		HP:0012385	OMIM:264180	TAS				P		HPO:skoehler	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0000007	OMIM:264270	IEA				I		HPO:iea	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0000062	OMIM:264270	IEA				P		HPO:iea	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0000327	OMIM:264270	IEA				P		HPO:iea	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0000786	OMIM:264270	IEA				P		HPO:iea	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0005790	OMIM:264270	IEA				P		HPO:iea	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0005856	OMIM:264270	TAS				P		HPO:probinson	
OMIM	264270	PSEUDOHERMAPHRODITISM, FEMALE, WITH SKELETAL ANOMALIES		HP:0008665	OMIM:264270	IEA				P		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0000007	OMIM:264300	IEA				I		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0000037	OMIM:264300	IEA				P		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0000771	OMIM:264300	IEA				P		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0000789	OMIM:264300	IEA				P		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0000821	OMIM:264300	IEA				P		HPO:iea	
OMIM	264300	17-@BETA HYDROXYSTEROID DEHYDROGENASE III DEFICIENCY		HP:0001939	OMIM:264300	IEA				P		HPO:iea	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:264350	TAS				I		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0000127	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0000841	OMIM:264350	TAS				P		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0000859	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0001508	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0001942	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0001944	OMIM:264350	TAS				P		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002013	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002014	OMIM:264350	TAS				P		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002153	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002205	OMIM:264350	TAS				P		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002615	OMIM:264350	TAS				P		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0002902	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:264350	TAS				C		HPO:skoehler	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0008242	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264350	#264350 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1B;;PHA I, AUTOSOMAL RECESSIVE		HP:0008872	OMIM:264350	TAS				P		HPO:probinson	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0000007	OMIM:264420	IEA				I		HPO:iea	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0000529	OMIM:264420	TAS				P		HPO:probinson	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0000545	OMIM:264420	IEA				P		HPO:iea	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0000573	OMIM:264420	IEA				P		HPO:iea	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0007641	OMIM:264420	IEA				P		HPO:iea	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0007769	OMIM:264420	IEA				P		HPO:iea	
OMIM	264420	FUNDUS DYSTROPHY, PSEUDOINFLAMMATORY, RECESSIVE FORM		HP:0007822	OMIM:264420	IEA				P		HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000007	OMIM:264470	IEA				I	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000248	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HP:0012825	HP:0000316	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000369	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000431	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000486	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000510	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000580	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000639	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000648	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000654	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0000737	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0001250	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0001276	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0001319	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0001332	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0002007	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0002015	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HP:0012825	HP:0002240	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0002376	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0002415	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0002910	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0003186	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0003487	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0003593	OMIM:264470	PCS				C	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0005280	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0006555	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0006887	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0007305	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0008619	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0008763	OMIM:264470	IEA				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:iea	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0010864	OMIM:264470	TAS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:skoehler	
OMIM	264470	#264470 PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-CoA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY		HP:0011344	OMIM:264470	PCS				P	#264470 PEROXISOMAL ACYL-COA OXIDASE DEFICIENCY;;STRAIGHT-CHAIN ACYL-COA OXIDASE DEFICIENCY;;PSEUDONEONATAL ADRENOLEUKODYSTROPHY	HPO:probinson	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000007	OMIM:264475	IEA				I		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000189	OMIM:264475	TAS				P		HPO:skoehler	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000218	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000286	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000347	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000365	OMIM:264475	IEA				P		HPO:skoehler	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000369	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000413	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000494	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000538	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000581	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000601	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000674	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000684	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000689	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000767	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0000824	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0001054	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0001438	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0001508	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0001773	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0001852	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0002750	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0002751	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0004322	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0006101	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0009803	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0010049	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0011069	OMIM:264475	IEA				P		HPO:iea	
OMIM	264475	264475 PSEUDOPAPILLEDEMA, OCULAR HYPOTELORISM, BLEPHAROPHIMOSIS, AND HANDANOMALIES;;ACROOTOOCULAR SYNDROME;;AOO SYNDROME		HP:0012810	OMIM:264475	TAS				P		HPO:skoehler	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000007	OMIM:264480	IEA				I		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000028	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000054	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000089	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000104	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000238	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000252	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000358	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000369	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000568	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000582	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000601	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000813	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000835	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0000878	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001162	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001252	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001274	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001290	OMIM:264480	TAS				P		HPO:skoehler	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001321	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001360	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001539	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001629	OMIM:264480	TAS				P		HPO:skoehler	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001631	OMIM:264480	TAS				P		HPO:skoehler	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001651	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001674	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001680	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0001830	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0002023	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0002084	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0002086	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0002126	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0002937	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0004691	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0008501	OMIM:264480	IEA				P		HPO:iea	
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0009914	OMIM:264480	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	264480	PSEUDOTRISOMY 13 SYNDROME		HP:0011662	OMIM:264480	TAS				P		HPO:skoehler	
OMIM	264500	PSEUDOURIDINURIA AND MENTAL DEFECT		HP:0000007	OMIM:264500	IEA				I		HPO:iea	
OMIM	264500	PSEUDOURIDINURIA AND MENTAL DEFECT		HP:0001249	OMIM:264500	IEA				P		HPO:iea	
OMIM	264500	PSEUDOURIDINURIA AND MENTAL DEFECT		HP:0001939	OMIM:264500	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000007	OMIM:264600	IEA				I		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000028	OMIM:264600	IEA				P		HPO:skoehler	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000033	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000048	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000051	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000054	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0000818	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0001595	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0001608	OMIM:264600	IEA				P		HPO:iea	
OMIM	264600	PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH		HP:0001939	OMIM:264600	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000007	OMIM:264700	IEA				I		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000684	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000737	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000867	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000886	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000893	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0000920	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001252	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001270	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001290	OMIM:264700	TAS				P		HPO:skoehler	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001508	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001510	OMIM:264700	TAS				P		HPO:skoehler	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0001538	OMIM:264700	TAS				P		HPO:probinson	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002007	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002148	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002199	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002355	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002653	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002663	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002748	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002752	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002753	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002757	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002909	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002979	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002980	OMIM:264700	TAS				P		HPO:probinson	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0002982	OMIM:264700	TAS				P		HPO:probinson	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003013	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003020	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003025	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003029	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003106	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003155	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003165	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0003698	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0004492	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0005469	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0006297	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0009023	OMIM:264700	IEA				P		HPO:iea	
OMIM	264700	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A		HP:0010502	OMIM:264700	TAS				P		HPO:probinson	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000007	OMIM:264800	IEA				I		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000083	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000153	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000573	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000608	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0000822	OMIM:264800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001034	OMIM:264800	IEA				P		HPO:skoehler	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001102	PMID:26903188	PCS				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001297	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001634	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001635	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001681	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001718	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0001723	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0002239	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0004417	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0004943	OMIM:264800	IEA				P		HPO:iea	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0007663	OMIM:264800	TAS				P		HPO:probinson	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0011506	OMIM:264800	IEA				P		HPO:skoehler	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0011510	OMIM:264800	IEA				P		HPO:skoehler	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0025115	OMIM:264800	TAS				P		HPO:skoehler	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0025533	OMIM:264800	IEA				P		HPO:skoehler	
OMIM	264800	PSEUDOXANTHOMA ELASTICUM; PXE		HP:0100817	OMIM:264800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000007	OMIM:265000	IEA				I		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000023	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000028	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000047	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000160	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000175	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000218	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000276	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000286	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000316	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000343	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000347	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000369	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000405	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000464	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000494	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000508	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000776	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000890	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0000902	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001060	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001159	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001166	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001537	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001558	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001762	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001836	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001838	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0001884	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002089	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002557	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002643	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002650	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002714	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002804	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002808	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002827	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0002949	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0003083	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0004322	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0004459	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0005617	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0006443	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0006446	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0008729	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009110	OMIM:265000	TAS				P		HPO:probinson	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009756	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009757	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009759	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009760	OMIM:265000	IEA				P		HPO:iea	
OMIM	265000	#265000 MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS;;ESCOBAR SYNDROME;;MULTIPLE PTERYGIUM SYNDROME, NONLETHAL TYPE;;PTERYGIUM SYNDROME;;MULTIPLE PTERYGIUM SYNDROME;;PTERYGIUM COLLI SYNDROME;;PTERYGIUM UNIVERSALE		HP:0009761	OMIM:265000	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000007	OMIM:265050	IEA				I		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000028	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000047	OMIM:265050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265050	3MC SYNDROME 2		HP:0000085	OMIM:265050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265050	3MC SYNDROME 2		HP:0000175	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000204	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000289	OMIM:265050	TAS				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000316	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000337	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000365	OMIM:265050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265050	3MC SYNDROME 2		HP:0000426	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000431	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000437	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000473	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000486	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000494	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0000508	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000537	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000581	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0000925	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0001249	OMIM:265050	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265050	3MC SYNDROME 2		HP:0001263	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0001363	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0001382	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0001540	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0002553	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0002714	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0002825	OMIM:265050	TAS				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0002827	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0002974	OMIM:265050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265050	3MC SYNDROME 2		HP:0002996	OMIM:265050	TAS				P		HPO:probinson	
OMIM	265050	3MC SYNDROME 2		HP:0002996	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0003468	OMIM:265050	TAS				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0005243	OMIM:265050	IEA				P		HPO:iea	
OMIM	265050	3MC SYNDROME 2		HP:0008897	OMIM:265050	TAS				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0009004	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265050	3MC SYNDROME 2		HP:0010759	OMIM:265050	IEA				P		HPO:skoehler	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0000007	OMIM:265100	IEA				I		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0002111	OMIM:265100	IEA				P		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0003674	OMIM:265100	IEA				C		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0003677	OMIM:265100	IEA				C		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0006514	OMIM:265100	IEA				P		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0006520	OMIM:265100	IEA				P		HPO:iea	
OMIM	265100	PULMONARY ALVEOLAR MICROLITHIASIS		HP:0020034	OMIM:265100	TAS				C		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0000007	OMIM:265120	IEA				I		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0000961	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0001217	OMIM:265120	TAS				P		HPO:probinson	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0001425	OMIM:265120	TAS				I		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0001508	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0001939	OMIM:265120	IEA				P		HPO:iea	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002092	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002094	OMIM:265120	TAS				P		HPO:probinson	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002098	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002104	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002789	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0002878	OMIM:265120	TAS	HP:0003623			P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0003593	OMIM:265120	TAS				C		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0003678	OMIM:265120	IEA				C		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0005942	OMIM:265120	IEA				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0006517	OMIM:265120	TAS				P		HPO:skoehler	
OMIM	265120	SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 1; SMDP1		HP:0006530	OMIM:265120	TAS				P		HPO:probinson	
OMIM	265140	PULMONARY ARTERIOVENOUS FISTULAS		HP:0000961	OMIM:265140	IEA				P		HPO:iea	
OMIM	265140	PULMONARY ARTERIOVENOUS FISTULAS		HP:0004952	OMIM:265140	IEA				P		HPO:iea	
OMIM	265140	PULMONARY ARTERIOVENOUS FISTULAS		HP:0100759	OMIM:265140	TAS				P		HPO:probinson	
OMIM	265140	PULMONARY ARTERIOVENOUS FISTULAS		HP:0100760	OMIM:265140	TAS				P		HPO:probinson	
OMIM	265150	265150 PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM		HP:0000007	OMIM:265150	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	265150	265150 PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM		HP:0004935	OMIM:265150	IEA				P		HPO:iea	
OMIM	265150	265150 PULMONARY ATRESIA WITH INTACT VENTRICULAR SEPTUM		HP:0010954	OMIM:265150	TAS				P		HPO:skoehler	
OMIM	265200	PULMONARY BULLAE CAUSING PNEUMOTHORAX		HP:0000007	OMIM:265200	IEA				I		HPO:iea	
OMIM	265200	PULMONARY BULLAE CAUSING PNEUMOTHORAX		HP:0006522	OMIM:265200	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000007	OMIM:265300	IEA				I		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000272	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000282	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000316	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000431	OMIM:265300	TAS				P		HPO:probinson	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0000767	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0001530	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0001561	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0001790	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0002202	OMIM:265300	TAS				P		HPO:probinson	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0002205	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0003828	OMIM:265300	TAS				C		HPO:skoehler	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0005280	OMIM:265300	TAS				P		HPO:probinson	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0006521	OMIM:265300	TAS	HP:0003577			P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0006533	OMIM:265300	IEA				P		HPO:iea	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0010310	OMIM:265300	IEA				P		HPO:skoehler	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0010741	OMIM:265300	IEA				P		HPO:skoehler	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0012281	OMIM:265300	TAS				P		HPO:skoehler	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0012368	OMIM:265300	TAS				P		HPO:skoehler	
OMIM	265300	%265300 LYMPHANGIECTASIA, PULMONARY, CONGENITAL; CPL;;LYMPHANGIOMATOSIS, PULMONARY;;PULMONARY CYSTIC LYMPHANGIECTASIS		HP:0100540	OMIM:265300	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0000006	OMIM:265380	TAS				I		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0000007	OMIM:265380	IEA				I		HPO:probinson	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0000072	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0000126	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0000822	OMIM:265380	IEA				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0001561	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0001631	OMIM:265380	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0001643	OMIM:265380	IEA				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0001694	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0001734	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0002092	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0002101	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0002245	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0002247	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0002566	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0003811	OMIM:265380	IEA				M		HPO:probinson	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0010444	OMIM:265380	TAS				P		HPO:skoehler	
OMIM	265380	ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS; ACDMPV		HP:0011718	OMIM:265380	IEA				P		HPO:probinson	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:265400	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001279	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001324	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001667	OMIM:265400	TAS				P		HPO:probinson	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001681	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001708	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002092	OMIM:265400	TAS				P		HPO:skoehler	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002875	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003388	OMIM:265400	IEA				P		HPO:iea	
OMIM	265400	265400 PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE		HP:0012378	OMIM:265400	TAS				P		HPO:skoehler	
OMIM	265430	PULMONARY HYPOPLASIA, PRIMARY		HP:0000007	OMIM:265430	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	265430	PULMONARY HYPOPLASIA, PRIMARY	HP:0012832	HP:0002089	OMIM:265430	TAS				P		HPO:probinson	
OMIM	265430	PULMONARY HYPOPLASIA, PRIMARY		HP:0003811	OMIM:265430	IEA				M		HPO:iea	
OMIM	265450	PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT		HP:0000006	OMIM:265450	TAS				I		HPO:skoehler	
OMIM	265450	PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT		HP:0002092	OMIM:265450	TAS				P		HPO:skoehler	
OMIM	265450	PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT		HP:0006518	OMIM:265450	IEA				P		HPO:iea	
OMIM	265450	PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT		HP:0030848	OMIM:265450	TAS				P		HPO:skoehler	
OMIM	265500	PULMONIC STENOSIS		HP:0000007	OMIM:265500	TAS				I		HPO:nvasilevsky	
OMIM	265500	PULMONIC STENOSIS		HP:0001426	PMID:12987021	TAS				I		HPO:nvasilevsky	
OMIM	265500	PULMONIC STENOSIS		HP:0001642	OMIM:265500	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000007	OMIM:265800	IEA				I		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000189	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000269	OMIM:265800	TAS				P		HPO:probinson	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000347	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000448	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000668	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000670	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000680	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000696	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0000765	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0001156	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0001807	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0002007	OMIM:265800	TAS				P		HPO:probinson	
OMIM	265800	PYCNODYSOSTOSIS		HP:0002644	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0002645	OMIM:265800	TAS				P		HPO:probinson	
OMIM	265800	PYCNODYSOSTOSIS		HP:0002650	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0002688	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0003302	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0003304	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0004322	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0004474	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0006335	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0009839	OMIM:265800	IEA				P		HPO:iea	
OMIM	265800	PYCNODYSOSTOSIS		HP:0011001	OMIM:265800	IEA				P		HPO:iea	
OMIM	265850	PYGMY		HP:0000007	OMIM:265850	IEA				I		HPO:iea	
OMIM	265850	PYGMY		HP:0000818	OMIM:265850	IEA				P		HPO:iea	
OMIM	265850	PYGMY		HP:0001426	OMIM:265850	IEA				I		HPO:iea	
OMIM	265850	PYGMY		HP:0001939	OMIM:265850	IEA				P		HPO:iea	
OMIM	265850	PYGMY		HP:0004322	OMIM:265850	TAS	HP:0003593			P		HPO:skoehler	
OMIM	265880	PYKNOACHONDROGENESIS		HP:0000007	OMIM:265880	IEA				I		HPO:iea	
OMIM	265880	PYKNOACHONDROGENESIS		HP:0003826	OMIM:265880	TAS				M		HPO:skoehler	
OMIM	265880	PYKNOACHONDROGENESIS	HP:0012828	HP:0011001	OMIM:265880	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0000007	OMIM:265900	IEA				I		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0000303	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0000670	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0000684	OMIM:265900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	265900	PYLE DISEASE; PYL		HP:0000765	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0000926	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0001324	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0001377	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0002650	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0002684	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0002689	OMIM:265900	TAS				P		HPO:skoehler	
OMIM	265900	PYLE DISEASE; PYL		HP:0002738	OMIM:265900	TAS				P		HPO:skoehler	
OMIM	265900	PYLE DISEASE; PYL		HP:0002829	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0002857	OMIM:265900	IEA				P		HPO:iea	
OMIM	265900	PYLE DISEASE; PYL		HP:0003016	OMIM:265900	IEA				P		HPO:skoehler	
OMIM	265900	PYLE DISEASE; PYL		HP:0004349	OMIM:265900	TAS				P		HPO:skoehler	
OMIM	265900	PYLE DISEASE; PYL		HP:0100255	OMIM:265900	TAS				P		HPO:probinson	
OMIM	265950	PYLORIC ATRESIA		HP:0000007	OMIM:265950	IEA				I		HPO:iea	
OMIM	265950	PYLORIC ATRESIA		HP:0001561	OMIM:265950	IEA				P		HPO:iea	
OMIM	265950	PYLORIC ATRESIA		HP:0004399	OMIM:265950	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0000007	OMIM:266100	IEA				I		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0000750	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001249	OMIM:266100	TAS				P		HPO:skoehler	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001252	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001263	OMIM:266100	TAS				P		HPO:skoehler	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001290	OMIM:266100	TAS				P		HPO:skoehler	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001557	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0001939	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0002069	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0002098	OMIM:266100	TAS	HP:0003623			P		HPO:skoehler	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0002123	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0002133	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0002643	OMIM:266100	IEA				P		HPO:iea	
OMIM	266100	EPILEPSY, PYRIDOXINE-DEPENDENT		HP:0025116	OMIM:266100	TAS				P		HPO:skoehler	
OMIM	266120	URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIADUE TO		HP:0000007	OMIM:266120	IEA				I		HPO:iea	
OMIM	266120	URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIADUE TO		HP:0001878	OMIM:266120	IEA				P		HPO:iea	
OMIM	266120	URIDINE 5-PRIME MONOPHOSPHATE HYDROLASE DEFICIENCY, HEMOLYTIC ANEMIADUE TO		HP:0003641	OMIM:266120	IEA				P		HPO:iea	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0000007	OMIM:266130	TAS				I		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0000580	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001249	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001250	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001251	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001260	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001285	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001345	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY	HP:0025303	HP:0001875	OMIM:266130	TAS				P		HPO:skoehler	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY	HP:0012825	HP:0001878	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0001996	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0002080	OMIM:266130	TAS				P		HPO:probinson	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0003343	OMIM:266130	TAS				P		HPO:skoehler	
OMIM	266130	GLUTATHIONE SYNTHETASE DEFICIENCY		HP:0410132	PMID:4557757	PCS				P		HPO:NicoleVasilevsky	
OMIM	266140	PYROPOIKILOCYTOSIS, HEREDITARY		HP:0000007	OMIM:266140	IEA				I		HPO:iea	
OMIM	266140	PYROPOIKILOCYTOSIS, HEREDITARY		HP:0001878	OMIM:266140	IEA				P		HPO:iea	
OMIM	266140	PYROPOIKILOCYTOSIS, HEREDITARY		HP:0004445	OMIM:266140	IEA				P		HPO:iea	
OMIM	266140	PYROPOIKILOCYTOSIS, HEREDITARY		HP:0004835	OMIM:266140	IEA				P		HPO:iea	
OMIM	266140	PYROPOIKILOCYTOSIS, HEREDITARY		HP:0004839	OMIM:266140	TAS				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0000007	OMIM:266150	IEA				I		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001249	OMIM:266150	IEA				P		HPO:skoehler	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001250	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001252	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001263	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001290	OMIM:266150	TAS				P		HPO:skoehler	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0001943	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0002049	OMIM:266150	TAS				P		HPO:probinson	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0002151	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0002169	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0002240	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0002415	OMIM:266150	IEA				P		HPO:skoehler	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0003128	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0003348	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0003542	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0003577	OMIM:266150	TAS				C		HPO:skoehler	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0006970	OMIM:266150	IEA				P		HPO:iea	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0007190	OMIM:266150	TAS				P		HPO:skoehler	
OMIM	266150	PYRUVATE CARBOXYLASE DEFICIENCY		HP:0025356	OMIM:266150	IEA				P		HPO:skoehler	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0000007	OMIM:266200	IEA				I		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0000952	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001081	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001082	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001511	OMIM:266200	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001560	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001744	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001790	OMIM:266200	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0001923	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0004870	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0005502	OMIM:266200	IEA				P		HPO:iea	
OMIM	266200	PYRUVATE KINASE DEFICIENCY OF RED CELLS		HP:0008282	OMIM:266200	TAS				P		HPO:probinson	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0000007	OMIM:266250	IEA				I		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0001284	OMIM:266250	IEA				P		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0001319	OMIM:266250	IEA				P		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0001561	OMIM:266250	IEA				P		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0002028	OMIM:266250	IEA				P		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0002460	OMIM:266250	IEA				P		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0003819	OMIM:266250	IEA				M		HPO:iea	
OMIM	266250	RADICULONEUROPATHY, FATAL NEONATAL		HP:0009113	OMIM:266250	TAS				P		HPO:skoehler	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000007	OMIM:266255	IEA				I		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000256	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000268	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000275	OMIM:266255	TAS				P		HPO:probinson	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000276	OMIM:266255	TAS				P		HPO:probinson	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0000448	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0001263	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0001290	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0002974	OMIM:266255	IEA				P		HPO:iea	
OMIM	266255	RADIOULNAR SYNOSTOSIS, UNILATERAL, WITH DEVELOPMENTAL RETARDATIONAND HYPOTONIA		HP:0003083	OMIM:266255	IEA	HP:0003577			P		HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000007	OMIM:266265	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000252	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000280	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000349	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000403	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000414	PMID:24403049	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000704	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000717	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000722	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0000739	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001156	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001252	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001263	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001290	OMIM:266265	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:skoehler	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001574	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001773	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0001939	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0002090	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0002120	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0002373	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0004322	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	2/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0005400	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:iea	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0006887	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0010529	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0010864	OMIM:266265	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:skoehler	
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0011950	PMID:24403049	PCS		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:lccarmody	1/2
OMIM	266265	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc; CDG2C		HP:0100658	OMIM:266265	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIC; CDG2C	HPO:skoehler	
OMIM	266270	RAMON SYNDROME		HP:0000007	OMIM:266270	IEA				I		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000169	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000189	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000365	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000543	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000580	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000684	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0000962	OMIM:266270	IEA				P		HPO:skoehler	
OMIM	266270	RAMON SYNDROME		HP:0000998	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0001009	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0001014	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0001249	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0001250	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0001492	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0002650	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0002808	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0004322	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0004325	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0005681	OMIM:266270	IEA				P		HPO:iea	
OMIM	266270	RAMON SYNDROME		HP:0008683	OMIM:266270	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000007	OMIM:266280	IEA				I		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000175	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000218	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000276	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000331	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000365	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0000417	OMIM:266280	IEA				P		HPO:skoehler	
OMIM	266280	RAPADILINO SYNDROME		HP:0000581	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0001070	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0001373	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0002014	OMIM:266280	IEA				P		HPO:skoehler	
OMIM	266280	RAPADILINO SYNDROME		HP:0002705	OMIM:266280	TAS				P		HPO:skoehler	
OMIM	266280	RAPADILINO SYNDROME		HP:0004322	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0005198	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0006498	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0006501	OMIM:266280	TAS				P		HPO:probinson	
OMIM	266280	RAPADILINO SYNDROME		HP:0009777	OMIM:266280	IEA				P		HPO:iea	
OMIM	266280	RAPADILINO SYNDROME		HP:0045025	OMIM:266280	IEA				P		HPO:skoehler	
OMIM	266300	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2		HP:0000007	OMIM:266300	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	266300	SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2		HP:0002297	OMIM:266300	IEA				P		HPO:iea	
OMIM	266350	RED SKIN PIGMENT ANOMALY OF NEW GUINEA		HP:0000007	OMIM:266350	IEA				I		HPO:iea	
OMIM	266350	RED SKIN PIGMENT ANOMALY OF NEW GUINEA		HP:0000613	OMIM:266350	IEA				P		HPO:iea	
OMIM	266350	RED SKIN PIGMENT ANOMALY OF NEW GUINEA		HP:0000639	OMIM:266350	IEA				P		HPO:iea	
OMIM	266350	RED SKIN PIGMENT ANOMALY OF NEW GUINEA		HP:0001595	OMIM:266350	IEA				P		HPO:iea	
OMIM	266400	REESE RETINAL DYSPLASIA		HP:0000007	OMIM:266400	TAS				I		HPO:iea	
OMIM	266400	REESE RETINAL DYSPLASIA		HP:0007968	OMIM:266400	TAS				P		HPO:probinson	
OMIM	266400	REESE RETINAL DYSPLASIA		HP:0007973	OMIM:266400	TAS				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0000007	OMIM:266500	IEA				I		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000407	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000458	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000508	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000510	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000518	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0000546	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0000616	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0000639	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0000662	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0001251	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0001265	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0001635	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0001638	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0001640	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0001761	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0002654	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0002922	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0003474	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0003690	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0004689	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0007141	OMIM:266500	IEA				P		HPO:skoehler	
OMIM	266500	REFSUM DISEASE		HP:0008064	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0010571	OMIM:266500	TAS				P		HPO:probinson	
OMIM	266500	REFSUM DISEASE		HP:0011675	OMIM:266500	IEA				P		HPO:iea	
OMIM	266500	REFSUM DISEASE		HP:0012211	OMIM:266500	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000007	OMIM:266510	IEA				I		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000272	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000407	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000457	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000510	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000512	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000939	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0000954	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001249	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001252	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001263	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001265	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001271	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001290	OMIM:266510	TAS				P		HPO:skoehler	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001508	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0001892	OMIM:266510	IEA				P		HPO:skoehler	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0002240	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0002570	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0003146	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0003577	OMIM:266510	IEA				C		HPO:skoehler	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0008167	OMIM:266510	IEA				P		HPO:iea	
OMIM	266510	PEROXISOME BIOGENESIS DISORDER 3B		HP:0012368	OMIM:266510	TAS				P		HPO:skoehler	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0001425	OMIM:266600	IEA				I		HPO:iea	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0001426	OMIM:266600	IEA				I		HPO:iea	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0001510	OMIM:266600	IEA				P		HPO:skoehler	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0001824	OMIM:266600	IEA				P		HPO:iea	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0002014	OMIM:266600	IEA				P		HPO:iea	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0002027	OMIM:266600	IEA				P		HPO:iea	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0005214	OMIM:266600	TAS				P		HPO:skoehler	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0011107	OMIM:266600	IEA				P		HPO:skoehler	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0011107	OMIM:266600	TAS				P		HPO:skoehler	
OMIM	266600	#266600 INFLAMMATORY BOWEL DISEASE 1; IBD1REGIONAL ENTERITIS, INCLUDED;;CROHN DISEASE, INCLUDED;;ULCERATIVE COLITIS, INCLUDED;;CROHN DISEASE-ASSOCIATED GROWTH FAILURE, SUSCEPTIBILITY TO, INCLUDED		HP:0100279	OMIM:266600	IEA				P		HPO:skoehler	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000007	OMIM:266810	IEA				I		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000034	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000085	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000089	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000151	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000316	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA	HP:0012825	HP:0000347	OMIM:266810	TAS				P		HPO:probinson	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0000486	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0002007	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0003196	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0006887	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0008648	OMIM:266810	IEA				P		HPO:iea	
OMIM	266810	RENAL AND MULLERIAN DUCT HYPOPLASIA		HP:0008850	OMIM:266810	IEA				P		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0000007	OMIM:266900	IEA				I		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0000090	OMIM:266900	TAS	HP:0003621			P		HPO:probinson	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0000103	OMIM:266900	IEA				P		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0000510	OMIM:266900	IEA				P		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0001425	OMIM:266900	IEA				I		HPO:skoehler	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0001903	OMIM:266900	IEA				P		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0001959	OMIM:266900	IEA				P		HPO:iea	
OMIM	266900	SENIOR-LOKEN SYNDROME 1		HP:0003774	OMIM:266900	IEA				P		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000007	OMIM:266910	IEA				I		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000028	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000089	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000110	OMIM:266910	IEA				P		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000160	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000218	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000233	OMIM:266910	TAS				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000269	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000347	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000369	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000377	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000444	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000470	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000773	OMIM:266910	IEA				P		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000879	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0000883	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0001195	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0001511	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0001562	OMIM:266910	IEA				P		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0001762	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002089	OMIM:266910	IEA				P		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002098	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002107	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002878	OMIM:266910	TAS				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002984	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0002990	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0003811	OMIM:266910	IEA				M		HPO:iea	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0003982	OMIM:266910	TAS				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0005280	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0008665	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0009800	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0009829	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266910	266910 RENAL DYSPLASIA-LIMB DEFECTS SYNDROME;;RL SYNDROME		HP:0010049	OMIM:266910	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000007	OMIM:266920	IEA				I		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000090	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000107	OMIM:266920	TAS				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000110	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000112	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000154	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000158	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000193	OMIM:266920	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000218	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000243	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000252	OMIM:266920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000341	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000510	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000572	OMIM:266920	TAS				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000639	OMIM:266920	TAS				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000687	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000691	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0000773	OMIM:266920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0001251	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0001363	OMIM:266920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0001395	OMIM:266920	IEA				P		HPO:iea	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0001396	OMIM:266920	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0001903	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0002007	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0002240	OMIM:266920	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0003090	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0003593	OMIM:266920	TAS				C		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0003774	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0004322	OMIM:266920	TAS				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0009803	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0010579	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0011220	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0030799	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0100543	OMIM:266920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	266920	SHORT-RIB THORACIC DYSPLASIA 9 WITH OR WITHOUT POLYDACTYLY; SRTD9		HP:0100864	OMIM:266920	IEA				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000007	OMIM:267000	IEA				I		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000028	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000194	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000347	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000369	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000431	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000776	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0000969	OMIM:267000	IEA				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001263	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001274	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001507	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001520	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001541	OMIM:267000	IEA				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001561	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001626	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0001999	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0002580	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0002667	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0003271	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0004510	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0005247	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0005280	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0008643	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0008696	OMIM:267000	IEA				P		HPO:iea	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0010804	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0011341	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0011611	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0100880	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267000	#267000 PERLMAN SYNDROME; PRLMNS;;RENAL HAMARTOMAS, NEPHROBLASTOMATOSIS, AND FETAL GIGANTISM;;NEPHROBLASTOMATOSIS, FETAL ASCITES, MACROSOMIA, AND WILMS TUMOR		HP:0200116	OMIM:267000	TAS				P		HPO:skoehler	
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0000003	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0000007	PMID:18371931	PCS				I		HPO:skoehler	
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0000023	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0000239	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/5
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0000348	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001276	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001305	PMID:18371931	PCS		HP:0040284		P		HPO:skoehler	1/5
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001396	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001408	PMID:15666242	PCS				P		HPO:skoehler	
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001409	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001433	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001562	PMID:18371931	PCS	HP:0030674	HP:0040284		P		HPO:probinson	3/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001631	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001643	PMID:18371931	PCS	HP:0030674	HP:0040284		P		HPO:probinson	2/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001650	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001667	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001696	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001737	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/5
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0001830	PMID:18371931	PCS	HP:0003577	HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0002190	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0002613	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0003774	PMID:18371931	PCS	HP:0003593	HP:0040284		P		HPO:probinson	2/7
OMIM	267010	#267010 MECKEL SYNDROME, TYPE 7; MKS7;;RENAL-HEPATIC-PANCREATIC DYSPLASIA WITH DANDY-WALKER CYST;;GOLDSTON SYNDROME		HP:0100611	PMID:18371931	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0000007	OMIM:267200	IEA				I		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0000121	OMIM:267200	IEA				P		HPO:skoehler	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0000787	OMIM:267200	IEA				P		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0002748	OMIM:267200	IEA				P		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0002749	OMIM:267200	IEA				P		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0002900	OMIM:267200	IEA				P		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0003768	OMIM:267200	IEA				P		HPO:iea	
OMIM	267200	RENAL TUBULAR ACIDOSIS III		HP:0004910	OMIM:267200	IEA				P		HPO:iea	
OMIM	267300	RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE NERVE DEAFNESS		HP:0000007	OMIM:267300	IEA				I		HPO:iea	
OMIM	267300	RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE NERVE DEAFNESS		HP:0000407	OMIM:267300	IEA				P		HPO:iea	
OMIM	267300	RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE NERVE DEAFNESS		HP:0000787	OMIM:267300	IEA				P		HPO:iea	
OMIM	267300	RENAL TUBULAR ACIDOSIS, DISTAL, WITH PROGRESSIVE NERVE DEAFNESS		HP:0001947	OMIM:267300	IEA				P		HPO:iea	
OMIM	267400	RENAL, GENITAL, AND MIDDLE EAR ANOMALIES		HP:0000007	OMIM:267400	IEA				I		HPO:iea	
OMIM	267400	RENAL, GENITAL, AND MIDDLE EAR ANOMALIES		HP:0000148	OMIM:267400	IEA				P		HPO:iea	
OMIM	267400	RENAL, GENITAL, AND MIDDLE EAR ANOMALIES		HP:0000365	OMIM:267400	IEA				P		HPO:iea	
OMIM	267400	RENAL, GENITAL, AND MIDDLE EAR ANOMALIES		HP:0004452	OMIM:267400	IEA				P		HPO:iea	
OMIM	267400	RENAL, GENITAL, AND MIDDLE EAR ANOMALIES		HP:0008678	OMIM:267400	IEA				P		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0000007	OMIM:267430	IEA				I		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0000079	OMIM:267430	IEA				P		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0000252	OMIM:267430	IEA				P		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0001562	OMIM:267430	IEA				P		HPO:skoehler	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0002009	OMIM:267430	IEA				P		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0002089	OMIM:267430	IEA				P		HPO:skoehler	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0002093	OMIM:267430	IEA				P		HPO:skoehler	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0002615	OMIM:267430	IEA				P		HPO:skoehler	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0004492	OMIM:267430	IEA				P		HPO:iea	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0008660	OMIM:267430	TAS				P		HPO:skoehler	
OMIM	267430	#267430 RENAL TUBULAR DYSGENESIS; RTD;;PRIMITIVE RENAL TUBULE SYNDROMERENAL TUBULAR DYSGENESIS WITH CHOANAL ATRESIA AND ATHELIA, INCLUDED		HP:0100519	OMIM:267430	TAS				P		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0001426	OMIM:267450	IEA				I		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0001622	OMIM:267450	IEA				P		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0002098	OMIM:267450	IEA				P		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0002643	OMIM:267450	IEA				P		HPO:iea	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0002789	OMIM:267450	IEA				P		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0003577	OMIM:267450	IEA				C		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0003745	OMIM:267450	IEA				I		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0005521	OMIM:267450	IEA				P		HPO:iea	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0100598	OMIM:267450	IEA				P		HPO:skoehler	
OMIM	267450	#267450 RESPIRATORY DISTRESS SYNDROME IN PREMATURE INFANTS;;RDS OF PREMATURITY;;HYALINE MEMBRANE DISEASE, FORMERLY		HP:0100750	OMIM:267450	TAS				P		HPO:skoehler	
OMIM	267480	267480 RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA		HP:0000007	OMIM:267480	IEA				I		HPO:iea	
OMIM	267480	267480 RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA		HP:0002093	OMIM:267480	IEA				P		HPO:iea	
OMIM	267480	267480 RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA		HP:0002878	OMIM:267480	TAS				P		HPO:skoehler	
OMIM	267480	267480 RESPIRATORY UNDERRESPONSIVENESS TO HYPOXIA AND HYPERCAPNIA		HP:0012416	OMIM:267480	IEA				P		HPO:skoehler	
OMIM	267500	RETICULAR DYSGENESIA		HP:0000007	OMIM:267500	IEA				I		HPO:iea	
OMIM	267500	RETICULAR DYSGENESIA		HP:0000778	PMID:19043417	PCS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0001888	PMID:19043417	PCS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0005354	OMIM:267500	TAS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0005387	PMID:19043417	PCS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0005435	OMIM:267500	TAS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0005541	PMID:19043417	PCS				P		HPO:probinson	
OMIM	267500	RETICULAR DYSGENESIA		HP:0100806	PMID:19043417	PCS				P		HPO:probinson	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0000007	OMIM:267700	IEA				I		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0000737	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0000952	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001250	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001251	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001252	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001259	OMIM:267700	TAS				P		HPO:skoehler	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001263	OMIM:267700	TAS				P		HPO:skoehler	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001276	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001287	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001290	OMIM:267700	TAS				P		HPO:skoehler	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001508	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001744	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001873	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001882	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0001903	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002155	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002240	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002301	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002383	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002445	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002516	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002716	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002902	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0002922	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003073	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003075	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003141	OMIM:267700	TAS				P		HPO:probinson	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003233	OMIM:267700	TAS				P		HPO:probinson	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003281	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003362	OMIM:267700	TAS				P		HPO:probinson	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003573	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0003645	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0007430	OMIM:267700	IEA				P		HPO:iea	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0008151	OMIM:267700	TAS				P		HPO:skoehler	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0011900	OMIM:267700	TAS				P		HPO:skoehler	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0012156	OMIM:267700	TAS				P		HPO:probinson	
OMIM	267700	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1		HP:0012229	OMIM:267700	TAS				P		HPO:probinson	
OMIM	267730	RETICULUM CELL SARCOMA		HP:0000007	OMIM:267730	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	267730	RETICULUM CELL SARCOMA		HP:0100242	OMIM:267730	IEA				P		HPO:skoehler	
OMIM	267740	RETINAL DEGENERATION AND EPILEPSY		HP:0000007	OMIM:267740	IEA				I		HPO:iea	
OMIM	267740	RETINAL DEGENERATION AND EPILEPSY		HP:0000546	OMIM:267740	IEA				P		HPO:iea	
OMIM	267740	RETINAL DEGENERATION AND EPILEPSY		HP:0001250	OMIM:267740	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000007	OMIM:267750	IEA				I		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000519	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000541	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000572	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000585	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000639	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0000667	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0001104	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0001250	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0001251	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0001268	OMIM:267750	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0001272	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0002059	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0002085	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0002119	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0002126	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0007773	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0011003	OMIM:267750	IEA				P		HPO:iea	
OMIM	267750	KNOBLOCH SYNDROME 1; KNO1		HP:0500087	OMIM:267750	IEA				P		HPO:skoehler	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000007	OMIM:267760	IEA				I		HPO:iea	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000501	OMIM:267760	IEA				P		HPO:iea	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000540	PMID:3827713	PCS				P		HP:probinson	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000568	PMID:3827713	PCS				P		HPO:skoehler	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000594	PMID:3827713	PCS	HP:0011463			P		HP:probinson	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0000662	PMID:3827713	PCS				P		HPO:skoehler	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0001133	PMID:3827713	PCS				P		HP:probinson	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0007401	PMID:3827713	PCS	HP:0003581			P		HPO:skoehler	
OMIM	267760	RETINAL DEGENERATION WITH NANOPHTHALMOS, CYSTIC MACULAR DEGENERATION,AND ANGLE CLOSURE GLAUCOMA		HP:0008028	OMIM:267760	IEA				P		HPO:iea	
OMIM	267800	267800 RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE		HP:0000007	OMIM:267800	TAS				I		HPO:iea	
OMIM	267800	267800 RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE		HP:0000556	OMIM:267800	TAS				P		HPO:iea	
OMIM	267800	267800 RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE		HP:0007937	OMIM:267800	TAS				P		HPO:iea	
OMIM	267800	267800 RETINAL DYSTROPHY, RETICULAR PIGMENTARY, OF POSTERIOR POLE		HP:0011510	OMIM:267800	TAS				P		HPO:skoehler	
OMIM	267900	RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA		HP:0000007	OMIM:267900	IEA				I		HPO:iea	
OMIM	267900	RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA		HP:0002972	OMIM:267900	IEA				P		HPO:iea	
OMIM	267900	RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA		HP:0004315	OMIM:267900	IEA				P		HPO:iea	
OMIM	267900	RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA		HP:0007763	OMIM:267900	IEA				P		HPO:iea	
OMIM	268000	RETINITIS PIGMENTOSA		HP:0000006	OMIM:268000	TAS		HP:0040284		I		HPO:nvasilevsky	30-40%
OMIM	268000	RETINITIS PIGMENTOSA		HP:0000007	OMIM:268000	TAS		HP:0040284		I		HPO:nvasilevsky	50-60%
OMIM	268000	RETINITIS PIGMENTOSA		HP:0000510	OMIM:268000	IEA				P		HPO:iea	
OMIM	268000	RETINITIS PIGMENTOSA		HP:0000510	OMIM:268000	TAS				P		HPO:nvasilevsky	
OMIM	268000	RETINITIS PIGMENTOSA		HP:0000662	OMIM:268000	IEA				P		HPO:iea	
OMIM	268000	RETINITIS PIGMENTOSA		HP:0001133	OMIM:268000	IEA				P		HPO:iea	
OMIM	268000	RETINITIS PIGMENTOSA		HP:0001419	OMIM:268000	TAS		HP:0040284		I		HPO:nvasilevsky	5-15%
OMIM	268000	RETINITIS PIGMENTOSA		HP:0031605	OMIM:268000	TAS				P		HPO:nvasilevsky	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0000007	PMID:5571218	PCS				I		HPO:iea	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0000407	PMID:5571218	PCS				P		HPO:iea	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0000510	OMIM:268010	IEA				P		HPO:skoehler	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0000618	OMIM:268010	IEA				P		HPO:skoehler	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0003241	PMID:5571218	PCS				P		HPO:iea	
OMIM	268010	RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS		HP:0008035	PMID:5571218	PCS				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000007	OMIM:268020	IEA				I		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000147	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000280	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000510	OMIM:268020	TAS				P		HPO:skoehler	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000523	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000580	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000598	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000639	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000771	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000815	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000831	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000869	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000956	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0000958	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0001169	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0001249	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0001272	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0001769	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0002059	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM	HP:0012825	HP:0002910	OMIM:268020	PCS				P		HPO:probinson	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0004322	OMIM:268020	IEA				P		HPO:iea	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0004322	OMIM:268020	PCS				P		HPO:probinson	
OMIM	268020	RETINITIS PIGMENTOSA, DEAFNESS, MENTAL RETARDATION, AND HYPOGONADISM		HP:0008070	OMIM:268020	IEA				P		HPO:iea	
OMIM	268025	RETINITIS PIGMENTOSA, LATE-ADULT ONSET		HP:0000007	OMIM:268025	IEA				I		HPO:iea	
OMIM	268025	RETINITIS PIGMENTOSA, LATE-ADULT ONSET		HP:0000510	OMIM:268025	IEA	HP:0003584			P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0000007	OMIM:268040	IEA				I		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0000543	OMIM:268040	TAS				P		HPO:skoehler	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0000789	OMIM:268040	IEA				P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0000821	OMIM:268040	IEA				P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0000980	OMIM:268040	IEA				P		HPO:skoehler	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0001000	OMIM:268040	IEA				P		HPO:skoehler	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0003236	OMIM:268040	IEA				P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0004904	OMIM:268040	IEA				P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0005237	OMIM:268040	IEA				P		HPO:iea	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0007803	OMIM:268040	TAS				P		HPO:skoehler	
OMIM	268040	268040 RETINOHEPATOENDOCRINOLOGIC SYNDROME;;RHE SYNDROME		HP:0008020	OMIM:268040	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000007	OMIM:268050	IEA				I		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000135	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000252	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000518	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000545	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0000580	OMIM:268050	TAS				P		HPO:probinson	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0001166	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0001382	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0001956	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0002650	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0004283	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0006887	OMIM:268050	IEA				P		HPO:iea	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0007663	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0008848	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268050	RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION		HP:0010864	OMIM:268050	TAS				P		HPO:skoehler	
OMIM	268060	RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:268060	TAS				I		HPO:probinson	
OMIM	268060	RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE		HP:0000483	OMIM:268060	TAS				P		HPO:probinson	
OMIM	268060	RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE		HP:0000486	OMIM:268060	TAS				P		HPO:probinson	
OMIM	268060	RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE		HP:0000540	OMIM:268060	TAS				P		HPO:probinson	
OMIM	268060	RETINOPATHY, PERICENTRAL PIGMENTARY, AUTOSOMAL RECESSIVE		HP:0000580	OMIM:268060	TAS				P		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0000007	OMIM:268080	TAS				I		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0000510	OMIM:268080	TAS				P		HPO:skoehler	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0000512	OMIM:268080	TAS				P		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0000540	OMIM:268080	TAS				P		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA	HP:0012825	HP:0000572	OMIM:268080	TAS				P		HPO:skoehler	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0000662	OMIM:268080	TAS				P		HPO:skoehler	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0007754	OMIM:268080	TAS				P		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0012152	OMIM:268080	TAS				P		HPO:probinson	
OMIM	268080	RETINOSCHISIS OF FOVEA		HP:0032037	OMIM:268080	IEA				P		HPO:skoehler	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000007	OMIM:268100	IEA				I		HPO:iea	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000518	OMIM:268100	IEA				P		HPO:iea	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000550	OMIM:268100	IEA				P		HPO:iea	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000580	OMIM:268100	TAS				P		HPO:probinson	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000662	OMIM:268100	IEA				P		HPO:iea	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0000969	OMIM:268100	IEA				P		HPO:skoehler	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0007773	OMIM:268100	IEA				P		HPO:iea	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0012047	OMIM:268100	TAS				P		HPO:skoehler	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0030502	OMIM:268100	TAS				P		HPO:skoehler	
OMIM	268100	ENHANCED S-CONE SYNDROME		HP:0040049	OMIM:268100	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0000006	OMIM:268130	TAS				I		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0000485	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0000555	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0000639	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001251	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001263	OMIM:268130	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0001276	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001321	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001511	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001803	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001915	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0001939	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0002213	OMIM:268130	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0002344	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0002514	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0002745	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0003745	OMIM:268130	IEA				I		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0005528	OMIM:268130	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0007617	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0007898	OMIM:268130	IEA				P		HPO:iea	
OMIM	268130	REVESZ SYNDROME		HP:0008070	OMIM:268130	IEA				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0008402	OMIM:268130	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0008404	OMIM:268130	TAS				P		HPO:skoehler	
OMIM	268130	REVESZ SYNDROME		HP:0025356	OMIM:268130	IEA				P		HPO:skoehler	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0000007	OMIM:268150	IEA				I		HPO:iea	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0000952	OMIM:268150	IEA				P		HPO:iea	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0001878	OMIM:268150	IEA				P		HPO:iea	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0004446	OMIM:268150	IEA				P		HPO:iea	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0005502	OMIM:268150	IEA				P		HPO:iea	
OMIM	268150	RH-NULL, REGULATOR TYPE		HP:0008282	OMIM:268150	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0000007	OMIM:268200	IEA				I		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0001265	OMIM:268200	IEA				P		HPO:skoehler	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0001284	OMIM:268200	IEA				P		HPO:skoehler	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0001324	OMIM:268200	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0001919	OMIM:268200	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0001945	OMIM:268200	IEA				P		HPO:skoehler	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0002153	OMIM:268200	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0002913	OMIM:268200	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0003236	OMIM:268200	IEA				P		HPO:skoehler	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0003326	OMIM:268200	IEA				P		HPO:iea	
OMIM	268200	RHABDOMYOLYSIS, ACUTE RECURRENT		HP:0008942	OMIM:268200	IEA				P		HPO:skoehler	
OMIM	268210	RHABDOMYOSARCOMA 1		HP:0000007	OMIM:268210	IEA				I		HPO:iea	
OMIM	268210	RHABDOMYOSARCOMA 1		HP:0006743	OMIM:268210	IEA				P		HPO:iea	
OMIM	268220	RHABDOMYOSARCOMA 2		HP:0000007	OMIM:268220	IEA				I		HPO:iea	
OMIM	268220	RHABDOMYOSARCOMA 2		HP:0006779	OMIM:268220	IEA				P		HPO:iea	
OMIM	268240	RHEUMATIC FEVER-RELATED ANTIGENRHEUMATIC FEVER, ACUTE, SUSCEPTIBILITY TO, INCLUDED		HP:0000007	OMIM:268240	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	268240	RHEUMATIC FEVER-RELATED ANTIGENRHEUMATIC FEVER, ACUTE, SUSCEPTIBILITY TO, INCLUDED		HP:0001945	OMIM:268240	IEA				P		HPO:skoehler	
OMIM	268240	RHEUMATIC FEVER-RELATED ANTIGENRHEUMATIC FEVER, ACUTE, SUSCEPTIBILITY TO, INCLUDED		HP:0002715	OMIM:268240	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0000007	OMIM:268250	IEA				I		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0000252	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0000260	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0000347	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0001642	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0002827	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0008905	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0009611	OMIM:268250	IEA				P		HPO:iea	
OMIM	268250	RHIZOMELIC SYNDROME		HP:0009943	OMIM:268250	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000007	OMIM:268300	IEA				I		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000028	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000040	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000047	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000085	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000113	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000175	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000204	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000218	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000238	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000248	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000252	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000272	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000316	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000347	OMIM:268300	TAS				P		HPO:probinson	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000358	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000369	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000387	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000430	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000431	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000470	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000476	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000494	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000518	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000520	OMIM:268300	TAS				P		HPO:probinson	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000568	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000586	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000589	OMIM:268300	IEA				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000592	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000625	OMIM:268300	TAS				P		HPO:probinson	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000813	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0000957	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001080	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001156	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001159	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001163	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001180	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001239	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001249	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001363	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001561	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001629	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001631	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001643	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001747	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0001772	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0002987	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0003616	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0003826	OMIM:268300	TAS		HP:0040283		M		HPO:probinson	HP:0040283
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0006380	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0006466	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0006824	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0007330	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0007452	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0007759	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0008070	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0008665	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0008683	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0008846	OMIM:268300	TAS				P		HPO:probinson	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0008897	OMIM:268300	TAS				P		HPO:probinson	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0009466	OMIM:268300	IEA				P		HPO:iea	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0009933	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0030084	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268300	ROBERTS SYNDROME; RBS		HP:0030721	OMIM:268300	TAS				P		HPO:skoehler	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000007	OMIM:268305	IEA				I		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000160	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000193	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000201	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000218	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000308	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000369	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000411	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0000448	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0001263	OMIM:268305	TAS				P		HPO:skoehler	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0001608	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0001762	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0002827	OMIM:268305	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0002984	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0003027	OMIM:268305	IEA				P		HPO:skoehler	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0003038	OMIM:268305	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0004209	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0004322	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0005736	OMIM:268305	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0006355	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0008744	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0008753	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0008807	OMIM:268305	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0009094	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0009486	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0009623	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0009778	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0009803	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0010049	OMIM:268305	IEA				P		HPO:iea	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0010752	OMIM:268305	IEA				P		HPO:skoehler	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0011968	OMIM:268305	TAS				P		HPO:skoehler	
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0030043	OMIM:268305	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	268305	ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES		HP:0100499	OMIM:268305	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000007	OMIM:268310	IEA				I		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000023	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000028	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000054	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000059	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000060	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000075	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000126	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000158	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000207	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000212	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000219	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	29%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000219	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000256	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000260	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000270	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000272	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000278	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	37%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000316	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000343	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000347	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000358	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000369	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	45%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000431	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000463	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000463	OMIM:268310	IEA		HP:0040284		P		HPO:probinson	95%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000470	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	31%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000494	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000520	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000527	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	59%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000637	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000678	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000696	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000767	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000902	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0000921	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001052	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001156	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001249	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001263	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001537	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001705	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001837	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0001853	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002007	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002164	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	35%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002650	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002750	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002944	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0002948	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0003027	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0003196	OMIM:268310	IEA		HP:0040284		P		HPO:probinson	95%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0004220	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0004279	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0004322	OMIM:268310	TAS	HP:0003593	HP:0040284		P		HPO:probinson	97%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0004590	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0005280	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	49%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0005914	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0008467	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0009466	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0009883	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0010292	OMIM:268310	IEA				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0010297	OMIM:268310	IEA		HP:0040284		P		HPO:skoehler	59%
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0011304	OMIM:268310	IEA				P		HPO:iea	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0011800	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0012368	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0030084	OMIM:268310	TAS				P		HPO:skoehler	
OMIM	268310	#268310 ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS;;COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY;;COVESDEM SYNDROME, FORMERLYROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OFPHALANGES AND METACARPALS/METATARSALS, INCLUDED;;ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY,INCLUDED		HP:0200055	OMIM:268310	TAS		HP:0040284		P		HPO:skoehler	84%
OMIM	268320	RODRIGUES BLINDNESS		HP:0000007	OMIM:268320	IEA				I		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000411	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000446	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000482	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000568	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000618	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000647	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000692	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0000968	OMIM:268320	IEA				P		HPO:skoehler	
OMIM	268320	RODRIGUES BLINDNESS		HP:0001249	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0001999	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0002213	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0004322	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0008070	OMIM:268320	IEA				P		HPO:iea	
OMIM	268320	RODRIGUES BLINDNESS		HP:0030863	OMIM:268320	IEA				P		HPO:skoehler	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000007	PMID:10319867	PCS				I	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000028	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000135	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000303	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000482	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000486	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000501	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000568	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000684	PMID:20113479	PCS		HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	41/41
OMIM	268400	Rothmund-Thomson syndrome		HP:0000691	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000939	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0000992	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001009	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001029	PMID:11471165	PCS	HP:0003593	HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	41/41
OMIM	268400	Rothmund-Thomson syndrome		HP:0001249	PMID:20113479	PCS		HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	13/41
OMIM	268400	Rothmund-Thomson syndrome		HP:0001374	PMID:20113479	PCS	HP:0003577			P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001518	PMID:20113479	PCS		HP:0040282		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	HP:0040282
OMIM	268400	Rothmund-Thomson syndrome		HP:0001545	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001596	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001734	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001762	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0001773	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0002007	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0002216	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0002669	PMID:11471165	PCS	HP:0011463	HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	13/41
OMIM	268400	Rothmund-Thomson syndrome		HP:0002671	PMID:20113479	PCS	HP:0003581			P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0002751	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0002860	PMID:20113479	PCS	HP:0003581			P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0003196	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0004279	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0004322	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0004334	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0006349	PMID:20113479	PCS		HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	2/41
OMIM	268400	Rothmund-Thomson syndrome		HP:0006368	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0008070	PMID:20113479	PCS		HP:0040284		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	50%
OMIM	268400	Rothmund-Thomson syndrome		HP:0008404	PMID:20113479	PCS		HP:0040282		P	ROTHMUND-THOMSON SYNDROME	HP:probinson	HP:0040282
OMIM	268400	Rothmund-Thomson syndrome		HP:0009778	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0010920	PMID:20113479	PCS	HP:0003621			P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0011069	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268400	Rothmund-Thomson syndrome		HP:0200055	PMID:20113479	PCS				P	ROTHMUND-THOMSON SYNDROME	HP:probinson	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0000007	OMIM:268500	IEA				I		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0000822	OMIM:268500	IEA				P		HPO:skoehler	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0001510	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0001648	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0001667	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0002092	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0003011	OMIM:268500	TAS				P		HPO:probinson	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0003355	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0003758	OMIM:268500	IEA				P		HPO:iea	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0006532	OMIM:268500	TAS				P		HPO:probinson	
OMIM	268500	ROWLEY-ROSENBERG SYNDROME		HP:0100750	OMIM:268500	TAS				P		HPO:skoehler	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000007	OMIM:268650	IEA				I		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000023	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000054	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000138	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000280	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000813	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0000954	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0001042	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0001371	OMIM:268650	IEA				P		HPO:skoehler	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0001522	OMIM:268650	IEA				M		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0001609	OMIM:268650	IEA				P		HPO:skoehler	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0001804	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0002007	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0005280	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0008714	OMIM:268650	IEA				P		HPO:iea	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0011220	OMIM:268650	TAS				P		HPO:skoehler	
OMIM	268650	268650 RUDIGER SYNDROME		HP:0011927	OMIM:268650	TAS				P		HPO:probinson	
OMIM	268700	SACCHAROPINURIA		HP:0000007	OMIM:268700	IEA				I		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0001249	OMIM:268700	IEA				P		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0001264	OMIM:268700	IEA				P		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0002353	OMIM:268700	IEA				P		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0002927	OMIM:268700	IEA				P		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0003297	OMIM:268700	IEA				P		HPO:iea	
OMIM	268700	SACCHAROPINURIA		HP:0004322	OMIM:268700	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000007	OMIM:268800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0000020	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000158	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000256	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000280	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000618	PMID:23785136	PCS	HP:0003593			P		HPO:probinson	
OMIM	268800	SANDHOFF DISEASE		HP:0000802	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0000966	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0000975	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0001251	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0001260	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0001278	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0001324	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0001347	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0001433	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0001640	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0002028	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0002380	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0002493	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0002574	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0003202	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0004343	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268800	SANDHOFF DISEASE		HP:0006901	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0007272	OMIM:268800	IEA				P		HPO:iea	
OMIM	268800	SANDHOFF DISEASE		HP:0010729	OMIM:268800	IEA				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000007	OMIM:268850	IEA				I		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000175	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000204	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000248	OMIM:268850	TAS				P		HPO:probinson	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000252	OMIM:268850	TAS				P		HPO:probinson	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000272	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000275	OMIM:268850	TAS				P		HPO:probinson	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000276	OMIM:268850	TAS				P		HPO:probinson	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000303	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000336	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000341	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000365	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000486	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000490	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000494	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000508	OMIM:268850	TAS				P		HPO:probinson	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000565	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000601	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000612	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000625	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000639	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000717	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0000767	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0001249	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0001290	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0002066	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0003298	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0004322	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0007517	OMIM:268850	IEA				P		HPO:iea	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0009891	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268850	RICHIERI-COSTA/GUION-ALMEIDA SYNDROME		HP:0011297	OMIM:268850	TAS				P		HPO:skoehler	
OMIM	268900	SARCOSINEMIA		HP:0000007	OMIM:268900	IEA				I		HPO:iea	
OMIM	268900	SARCOSINEMIA		HP:0010896	OMIM:268900	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000007	OMIM:269000	IEA				I		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000204	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000252	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000347	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000358	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000430	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0000592	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0001250	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0001263	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0001511	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0001650	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0002286	OMIM:269000	IEA				P		HPO:skoehler	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0002645	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0003273	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0003616	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0003974	OMIM:269000	TAS				P		HPO:probinson	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0003982	OMIM:269000	TAS				P		HPO:probinson	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0004322	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0006380	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0007452	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0008070	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0009466	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0009778	OMIM:269000	IEA				P		HPO:iea	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0009829	OMIM:269000	IEA				P		HPO:skoehler	
OMIM	269000	#269000 SC PHOCOMELIA SYNDROME;;SC PSEUDOTHALIDOMIDE SYNDROME		HP:0030084	OMIM:269000	TAS				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000006	OMIM:269150	IEA				I		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000046	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000047	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000054	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000059	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000064	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000071	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000072	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000126	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000158	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000272	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000280	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000316	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000329	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000340	OMIM:269150	TAS				P		HPO:probinson	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000348	OMIM:269150	TAS				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000369	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000452	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000463	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000470	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000586	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000813	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000879	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000885	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000890	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000935	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000954	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0000998	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001162	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001249	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001250	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001508	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001631	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001739	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001762	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0001795	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002059	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002079	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002119	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002179	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002521	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002557	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002645	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002694	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002884	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0002982	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0003196	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0004492	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0005280	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0005495	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0006387	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0006392	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0006657	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0008897	OMIM:269150	TAS				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0009104	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0009792	OMIM:269150	IEA				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0009882	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0010034	OMIM:269150	IEA				P		HPO:iea	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0011220	OMIM:269150	TAS				P		HPO:probinson	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0011800	OMIM:269150	TAS				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0030736	OMIM:269150	TAS				P		HPO:skoehler	
OMIM	269150	SCHINZEL-GIEDION MIDFACE-RETRACTION SYNDROME		HP:0032075	PMID:18398855	PCS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	269160	SCHIZENCEPHALY		HP:0001274	PMID:26576802	PCS				P		HPO:lccarmody	
OMIM	269160	SCHIZENCEPHALY		HP:0002120	PMID:26576802	PCS				P		HPO:lccarmody	
OMIM	269160	SCHIZENCEPHALY		HP:0010636	OMIM:269160	IEA				P		HPO:skoehler	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000006	OMIM:269200	TAS				I		HPO:nvasilevsky	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000007	OMIM:269200	TAS				I		HPO:nvasilevsky	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000518	OMIM:269200	IEA				P		HPO:skoehler	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000585	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000821	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0000836	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001096	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001250	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001281	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001394	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001426	OMIM:269200	TAS				I		HPO:nvasilevsky	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001596	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001738	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001746	OMIM:269200	TAS				P		HPO:probinson	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0001891	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0002086	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0002570	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0002728	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0005978	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0008207	OMIM:269200	IEA				P		HPO:iea	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0100522	OMIM:269200	TAS				P		HPO:skoehler	
OMIM	269200	AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE II		HP:0200123	OMIM:269200	TAS				P		HPO:skoehler	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000007	OMIM:269250	TAS				I		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000175	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000256	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000272	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000470	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000773	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000774	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000882	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000895	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000907	OMIM:269250	TAS				P		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0000947	OMIM:269250	IEA				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0001156	OMIM:269250	IEA				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0001561	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0003025	OMIM:269250	IEA				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0003180	OMIM:269250	IEA				P		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0003300	OMIM:269250	TAS				P		HPO:probinson	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0003826	OMIM:269250	TAS				M		HPO:skoehler	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0003826	OMIM:269250	IEA				M		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0004233	OMIM:269250	IEA				P		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0008108	OMIM:269250	IEA				P		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0008873	OMIM:269250	TAS				P		HPO:iea	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0011800	OMIM:269250	TAS				P		HPO:skoehler	
OMIM	269250	SCHNECKENBECKEN DYSPLASIA		HP:0031026	OMIM:269250	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000007	OMIM:269300	TAS				I		HPO:iea	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000218	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000256	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000260	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000272	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD	HP:0012825	HP:0000303	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000369	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000494	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000670	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000678	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000691	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000695	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000885	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0000938	OMIM:269300	IEA				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0001090	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0001355	OMIM:269300	IEA				P		HPO:iea	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002645	OMIM:269300	IEA				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002650	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002673	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002689	OMIM:269300	IEA				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002694	OMIM:269300	IEA				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002857	OMIM:269300	TAS				P		HPO:probinson	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002967	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0002970	OMIM:269300	TAS				P		HPO:probinson	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0003015	OMIM:269300	TAS				P		HPO:probinson	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0003155	OMIM:269300	IEA				P		HPO:iea	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0004322	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0005622	OMIM:269300	IEA				P		HPO:iea	
OMIM	269300	CRANIOMETADIAPHYSEAL DYSPLASIA; CRMDD		HP:0011220	OMIM:269300	TAS				P		HPO:skoehler	
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000007	OMIM:269400	IEA				I		HPO:iea	
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000356	OMIM:269400	IEA				P		HPO:iea	
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000482	OMIM:269400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000518	OMIM:269400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000557	OMIM:269400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000568	OMIM:269400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0000647	OMIM:269400	IEA				P		HPO:iea	
OMIM	269400	#269400 CORNEAL OPACIFICATION WITH OTHER OCULAR ANOMALIES; COPOA;;SCLEROCORNEA WITH OTHER OCULAR ANOMALIES		HP:0007906	OMIM:269400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000007	OMIM:269500	IEA				I		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000272	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000303	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000316	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000365	OMIM:269500	TAS				P		HPO:probinson	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000431	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000520	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000565	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000572	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000639	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000648	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000689	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000885	OMIM:269500	TAS				P		HPO:probinson	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0000916	OMIM:269500	TAS				P		HPO:probinson	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0001133	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0001233	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0001474	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0001548	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0001699	OMIM:269500	TAS				M		HPO:probinson	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0002007	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0002164	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0002315	OMIM:269500	IEA				P		HPO:skoehler	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0002516	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0002644	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0004097	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0004576	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0005280	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0006415	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0007285	OMIM:269500	IEA				P		HPO:iea	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0010628	OMIM:269500	IEA				P		HPO:skoehler	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0011800	OMIM:269500	TAS				P		HPO:skoehler	
OMIM	269500	SCLEROSTEOSIS 1; SOST1		HP:0100543	OMIM:269500	IEA				P		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0000007	OMIM:269600	IEA				I		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0000478	OMIM:269600	IEA				P		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0001394	OMIM:269600	IEA				P		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0001744	OMIM:269600	IEA				P		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0001873	OMIM:269600	IEA				P		HPO:iea	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0001982	OMIM:269600	TAS				P		HPO:skoehler	
OMIM	269600	SEA-BLUE HISTIOCYTE DISEASE		HP:0002221	OMIM:269600	IEA				P		HPO:iea	
OMIM	269630	SECOND METATARSAL-METACARPAL SYNDROME		HP:0000007	OMIM:269630	IEA				I		HPO:iea	
OMIM	269630	SECOND METATARSAL-METACARPAL SYNDROME		HP:0000926	OMIM:269630	IEA				P		HPO:iea	
OMIM	269630	SECOND METATARSAL-METACARPAL SYNDROME		HP:0005916	OMIM:269630	IEA				P		HPO:iea	
OMIM	269630	SECOND METATARSAL-METACARPAL SYNDROME		HP:0100266	OMIM:269630	IEA				P		HPO:iea	
OMIM	269650	SECRETORY COMPONENT DEFICIENCY		HP:0000007	OMIM:269650	IEA				I		HPO:iea	
OMIM	269650	SECRETORY COMPONENT DEFICIENCY		HP:0002254	OMIM:269650	TAS				P		HPO:probinson	
OMIM	269650	SECRETORY COMPONENT DEFICIENCY		HP:0004433	OMIM:269650	IEA				P		HPO:iea	
OMIM	269650	SECRETORY COMPONENT DEFICIENCY		HP:0005411	OMIM:269650	IEA				P		HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000007	OMIM:269700	IEA				I	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000065	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000098	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000144	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000147	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000303	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000325	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000400	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000787	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000842	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000868	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000877	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0000956	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001007	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001176	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001256	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001394	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001397	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001425	OMIM:269700	TAS				I	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001537	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001544	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001620	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001639	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001735	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001744	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0001833	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0002155	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0002240	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0002591	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0002833	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0002910	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0003292	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0003577	OMIM:269700	IEA				C	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0003716	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0003758	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HP:probinson	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0003809	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0005144	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:lccarmody	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0005616	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0008665	OMIM:269700	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:iea	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0009125	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HPO:skoehler	
OMIM	269700	Lipodystrophy, congenital generalized, type 2		HP:0025128	OMIM:269700	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2	HP:probinson	
OMIM	269720	269720 SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;BFNS, AUTOSOMAL RECESSIVE;;CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:269720	IEA				I		HPO:iea	
OMIM	269720	269720 SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;BFNS, AUTOSOMAL RECESSIVE;;CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE		HP:0001276	OMIM:269720	TAS				P		HPO:probinson	
OMIM	269720	269720 SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;BFNS, AUTOSOMAL RECESSIVE;;CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE		HP:0002069	OMIM:269720	IEA	HP:0003623			P		HPO:iea	
OMIM	269720	269720 SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;BFNS, AUTOSOMAL RECESSIVE;;CONVULSIONS, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE;;EPILEPSY, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE		HP:0002372	OMIM:269720	TAS				P		HPO:iea	
OMIM	269800	269800 SENILE PLAQUE FORMATION		HP:0000007	OMIM:269800	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	269800	269800 SENILE PLAQUE FORMATION		HP:0000707	OMIM:269800	IEA				P		HPO:iea	
OMIM	269800	269800 SENILE PLAQUE FORMATION		HP:0100256	OMIM:269800	TAS				P		HPO:skoehler	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0000007	OMIM:269840	IEA				I		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0000976	OMIM:269840	TAS				P		HPO:skoehler	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0001508	OMIM:269840	IEA				P		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0001744	OMIM:269840	IEA				P		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0002014	OMIM:269840	IEA				P		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0002090	OMIM:269840	TAS				P		HPO:skoehler	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0002240	OMIM:269840	IEA				P		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0003139	OMIM:269840	IEA				P		HPO:iea	
OMIM	269840	#269840 SELECTIVE T-CELL DEFECT; STCD		HP:0005401	OMIM:269840	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000007	OMIM:269860	TAS				I		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000023	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000062	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000089	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000180	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000238	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000256	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000286	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000316	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000348	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000358	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000369	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000377	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000470	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000695	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000773	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000774	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000800	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000882	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000888	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0000969	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001156	OMIM:269860	IEA				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001169	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001360	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001405	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001511	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001538	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001539	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001541	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001561	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001629	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001643	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001655	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001744	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001769	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001773	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0001831	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002089	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002093	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002240	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002323	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002557	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002566	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0002979	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0003026	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0003811	OMIM:269860	TAS				M		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0004279	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0006488	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0006610	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0006644	OMIM:269860	IEA				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0008501	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0009381	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0009826	OMIM:269860	TAS				P		HPO:probinson	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0010306	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0011802	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0012368	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269860	SHORT-RIB THORACIC DYSPLASIA 12; SRTD12		HP:0100750	OMIM:269860	TAS				P		HPO:skoehler	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000007	OMIM:269870	IEA				I		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000340	OMIM:269870	IEA				P		HPO:probinson	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000341	OMIM:269870	IEA				P		HPO:probinson	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000347	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000426	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0000460	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0001156	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0001513	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0002983	OMIM:269870	TAS				P		HPO:skoehler	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0004209	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0004322	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0008551	OMIM:269870	IEA				P		HPO:iea	
OMIM	269870	269870 SHORT STATURE-OBESITY SYNDROME; SSOS		HP:0009826	OMIM:269870	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000006	OMIM:269880	IEA				I		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000023	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000325	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000347	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000400	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000407	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000430	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000431	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000485	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000490	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000501	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000506	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000518	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000545	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000558	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000668	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000684	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000689	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000750	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000831	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000951	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0000963	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0001388	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0001511	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0001518	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0002007	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0002714	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0002715	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0002750	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0003074	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0003561	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0009125	OMIM:269880	IEA				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0009466	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0010580	OMIM:269880	IEA				P		HPO:iea	
OMIM	269880	SHORT SYNDROME		HP:0010751	OMIM:269880	IEA				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0011220	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0011800	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0030084	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0100578	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269880	SHORT SYNDROME		HP:0100678	OMIM:269880	TAS				P		HPO:skoehler	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000007	OMIM:269920	IEA				I		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000100	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000212	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000218	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000238	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000280	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000286	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000463	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000508	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000639	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000765	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0000938	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001010	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001250	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001252	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001263	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001290	OMIM:269920	TAS				P		HPO:skoehler	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001508	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001541	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001622	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001635	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001640	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001744	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001760	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001789	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0001922	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0002059	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0002240	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0002286	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0002680	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0002908	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0003025	OMIM:269920	IEA				P		HPO:iea	
OMIM	269920	INFANTILE SIALIC ACID STORAGE DISEASE		HP:0003819	OMIM:269920	IEA				M		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000006	OMIM:269921	IEA				I		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000023	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000218	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000219	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000219	OMIM:269921	TAS				P		HPO:skoehler	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000280	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000286	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000316	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000319	OMIM:269921	TAS				P		HPO:probinson	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000343	OMIM:269921	TAS				P		HPO:probinson	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000369	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000431	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000629	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0000664	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001250	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001263	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001538	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001744	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001847	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0001939	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002007	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002162	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002230	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002240	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002557	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0002650	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0004691	OMIM:269921	TAS				P		HPO:probinson	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0005257	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0007018	OMIM:269921	IEA				P		HPO:iea	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0010535	OMIM:269921	IEA				P		HPO:skoehler	
OMIM	269921	#269921 SIALURIA;;SIALURIA, FRENCH TYPE		HP:0011220	OMIM:269921	TAS				P		HPO:skoehler	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0000006	OMIM:270100	TAS				I		HPO:skoehler	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0000007	OMIM:270100	IEA				I		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0001511	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0001629	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0001631	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0001651	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0001669	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0002086	OMIM:270100	IEA				P		HPO:iea	
OMIM	270100	#270100 HETEROTAXY, VISCERAL, 5, AUTOSOMAL; HTX5;;SITUS INVERSUS VISCERUM; SIV		HP:0003363	OMIM:270100	IEA				P		HPO:iea	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0000007	OMIM:270150	IEA				I		HPO:iea	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0000217	OMIM:270150	IEA				P		HPO:iea	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0001097	OMIM:270150	TAS				P		HPO:skoehler	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0001370	OMIM:270150	IEA				P		HPO:iea	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0001939	OMIM:270150	IEA				P		HPO:iea	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0001970	OMIM:270150	TAS				P		HPO:skoehler	
OMIM	270150	%270150 SJOGREN SYNDROME;;SICCA SYNDROME		HP:0002960	OMIM:270150	IEA				P		HPO:iea	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0000007	OMIM:270200	TAS				I		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0000608	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0000613	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0001249	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0001250	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0001257	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0002942	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0004322	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0006297	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0007305	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0007722	OMIM:270200	IEA				P		HPO:skoehler	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0007727	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0008064	OMIM:270200	TAS				P		HPO:probinson	
OMIM	270200	SJOGREN-LARSSON SYNDROME; SLS		HP:0030329	OMIM:270200	IEA				P		HPO:skoehler	
OMIM	270220	SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT		HP:0000007	OMIM:270220	IEA				I		HPO:iea	
OMIM	270220	SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT		HP:0000962	OMIM:270220	IEA				P		HPO:iea	
OMIM	270220	SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT		HP:0007431	OMIM:270220	IEA				P		HPO:iea	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0000007	OMIM:270300	IEA				I		HPO:iea	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0000989	OMIM:270300	TAS				P		HPO:probinson	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0001806	OMIM:270300	TAS				P		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0001939	OMIM:270300	IEA				P		HPO:iea	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0002099	OMIM:270300	TAS				P		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0002299	OMIM:270300	TAS				P		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0003212	OMIM:270300	TAS				P		HPO:probinson	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0003577	OMIM:270300	TAS				C		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0004322	OMIM:270300	TAS				P		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0010719	OMIM:270300	IEA				P		HPO:iea	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0010783	OMIM:270300	IEA				P		HPO:skoehler	
OMIM	270300	#270300 PEELING SKIN SYNDROME 1; PSS1;;PSS;;SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED;;KERATOLYSIS EXFOLIATIVA CONGENITA;;DECIDUOUS SKIN		HP:0040189	OMIM:270300	IEA				P		HPO:skoehler	
OMIM	270350	SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL		HP:0000007	OMIM:270350	IEA				I		HPO:iea	
OMIM	270350	SKUNK N-BUTYLMERCAPTAN, INABILITY TO SMELL		HP:0000458	OMIM:270350	TAS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000007	OMIM:270400	TAS				I		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000028	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000046	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000047	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000048	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000054	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000062	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000074	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000089	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000104	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000107	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000122	OMIM:270400	IEA				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000126	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000171	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000175	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000187	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000238	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000252	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000286	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000316	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000341	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000343	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000347	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000358	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000365	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000369	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000403	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000431	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000463	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000486	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000508	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000518	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000639	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000678	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000717	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000718	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000742	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000752	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000813	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000826	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000964	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0000996	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001153	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001162	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001249	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001276	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS	HP:0011463			P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS	HP:0003593			P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001305	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001360	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001508	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001511	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001558	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001622	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001623	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001629	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001631	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001643	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001680	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001765	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001830	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001831	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001840	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001845	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0001884	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002013	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002019	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002020	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002021	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002033	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002079	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002089	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002101	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002251	PMID:9024558	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002566	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002579	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002611	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002827	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0002983	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0003146	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0004322	PMID:10807690	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0004691	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0005280	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0005280	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0006979	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0007165	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0007333	ISBN-13:978-0721606156	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0007537	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0009623	PMID:9678700	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0009778	PMID:9678700	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0010569	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0010569	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=slo	PCS				P		HPO:probinson	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0010655	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270400	SMITH-LEMLI-OPITZ SYNDROME; SLOS		HP:0030043	OMIM:270400	TAS				P		HPO:skoehler	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000007	OMIM:270420	IEA				I		HPO:iea	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000073	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000143	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000256	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000316	OMIM:270420	IEA				P		HPO:skoehler	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000369	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000453	OMIM:270420	IEA				P		HPO:skoehler	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000588	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0000973	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0001561	OMIM:270420	IEA				P		HPO:iea	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0001939	OMIM:270420	IEA				P		HPO:iea	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0002023	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0002566	OMIM:270420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0003270	OMIM:270420	IEA				P		HPO:iea	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0005208	OMIM:270420	IEA				P		HPO:iea	
OMIM	270420	DIARRHEA 3, SECRETORY SODIUM, CONGENITAL, WITH OR WITHOUT OTHER CONGENITAL ANOMALIES		HP:0200020	OMIM:270420	TAS				P		HPO:skoehler	
OMIM	270425	SODIUM-POTASSIUM-ATPASE ACTIVITY OF RED CELL		HP:0000007	OMIM:270425	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	270425	SODIUM-POTASSIUM-ATPASE ACTIVITY OF RED CELL		HP:0001939	OMIM:270425	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000006	OMIM:270450	IEA				I		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000007	OMIM:270450	IEA				I		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000160	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000218	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000219	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000219	OMIM:270450	TAS				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000252	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000278	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000319	OMIM:270450	TAS				P		HPO:probinson	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000325	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000343	OMIM:270450	TAS				P		HPO:probinson	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000347	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000431	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000486	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000490	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000558	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000582	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000664	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000713	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000739	OMIM:270450	TAS				P		HPO:probinson	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000750	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000767	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0000819	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001249	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001263	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001270	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001511	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001547	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001629	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001655	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001773	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001852	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0001956	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0002079	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0002553	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0002750	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0003577	OMIM:270450	IEA				C		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0003758	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0004322	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0004325	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0009125	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0009466	OMIM:270450	IEA				P		HPO:iea	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0030084	OMIM:270450	TAS				P		HPO:skoehler	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0030269	OMIM:270450	TAS				P		HPO:probinson	
OMIM	270450	INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TO; IGF1RES		HP:0200055	OMIM:270450	IEA				P		HPO:skoehler	
OMIM	270460	SONODA SYNDROME		HP:0000007	OMIM:270460	IEA				I		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0000160	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0000311	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0001042	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0001249	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0001629	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0004322	OMIM:270460	IEA				P		HPO:iea	
OMIM	270460	SONODA SYNDROME		HP:0005280	OMIM:270460	IEA				P		HPO:iea	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0000007	OMIM:270500	IEA				I		HPO:iea	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0000407	OMIM:270500	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0000639	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0000648	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001249	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001257	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001260	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001263	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001310	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001317	OMIM:270500	IEA				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0001337	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0002136	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0002312	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0002370	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0002497	OMIM:270500	IEA				P		HPO:iea	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0002650	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0003487	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0003621	OMIM:270500	IEA				C		HPO:iea	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0003676	OMIM:270500	TAS				C		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0007663	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0009830	OMIM:270500	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	270500	ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION		HP:0011448	OMIM:270500	TAS				P		HPO:skoehler	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0000007	OMIM:270550	IEA				I		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0000012	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0000639	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001249	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001257	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001260	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001310	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001347	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001761	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0001765	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002166	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002168	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002460	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002497	OMIM:270550	TAS				P		HPO:probinson	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002527	OMIM:270550	IEA				P		HPO:skoehler	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0002936	OMIM:270550	TAS				P		HPO:probinson	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003387	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003431	OMIM:270550	TAS				P		HPO:skoehler	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003438	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003448	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003487	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0003593	OMIM:270550	IEA				C		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE	HP:0012828	HP:0003693	OMIM:270550	TAS				P		HPO:probinson	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0006150	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0006855	OMIM:270550	TAS				P		HPO:probinson	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007001	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007221	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007240	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007772	OMIM:270550	IEA				P		HPO:skoehler	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007922	OMIM:270550	IEA				P		HPO:iea	
OMIM	270550	SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE		HP:0007922	OMIM:270550	TAS				P		HPO:probinson	
OMIM	270600	SPASTIC DIPLEGIA, INFANTILE TYPE		HP:0000007	OMIM:270600	IEA				I		HPO:iea	
OMIM	270600	SPASTIC DIPLEGIA, INFANTILE TYPE		HP:0001249	OMIM:270600	IEA				P		HPO:iea	
OMIM	270600	SPASTIC DIPLEGIA, INFANTILE TYPE		HP:0001264	OMIM:270600	IEA				P		HPO:iea	
OMIM	270600	SPASTIC DIPLEGIA, INFANTILE TYPE		HP:0003593	OMIM:270600	IEA				C		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0000006	OMIM:270685	IEA				I		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0001258	OMIM:270685	TAS				P		HPO:skoehler	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0001347	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0001761	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0002061	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0002064	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0002166	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003392	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003393	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003426	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003427	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003487	OMIM:270685	IEA				P		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0003677	OMIM:270685	IEA				C		HPO:iea	
OMIM	270685	#270685 SPASTIC PARAPLEGIA 17; SPG17;;SPASTIC PARAPLEGIA WITH AMYOTROPHY OF HANDS AND FEET;;SILVER SYNDROME;;SILVER SPASTIC PARAPLEGIA SYNDROME		HP:0007340	OMIM:270685	TAS				P		HPO:skoehler	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000007	OMIM:270700	IEA				I		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000012	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000020	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000505	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000608	OMIM:270700	PCS				P		HPO:probinson	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000639	PMID:19805727	PCS		HP:0040284		P		HPO:probinson	4/10
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000709	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0000720	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001249	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001251	OMIM:270700	TAS				P		HPO:skoehler	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001258	OMIM:270700	PCS				P		HPO:probinson	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001260	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001317	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0001761	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002061	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002064	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002079	OMIM:270700	PCS				P		HPO:probinson	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002169	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002607	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0002839	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0003477	PMID:19805727	PCS		HP:0040284		P		HPO:probinson	5/9
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0003487	OMIM:270700	IEA				P		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0003676	OMIM:270700	IEA				C		HPO:iea	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0003693	OMIM:270700	PCS				P		HPO:probinson	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0007340	OMIM:270700	TAS				P		HPO:skoehler	
OMIM	270700	#270700 SPASTIC PARAPLEGIA 15, AUTOSOMAL RECESSIVE; SPG15;;SPASTIC PARAPLEGIA AND RETINAL DEGENERATION;;KJELLIN SYNDROME		HP:0007663	OMIM:270700	TAS				P		HPO:skoehler	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0000007	OMIM:270750	IEA				I		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0000252	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0000275	OMIM:270750	TAS				P		HPO:skoehler	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0000278	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0000347	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0001045	OMIM:270750	IEA				P		HPO:skoehler	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME	HP:0012828	HP:0001258	OMIM:270750	IEA				P		HPO:probinson	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0001347	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0003487	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0004771	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0005586	OMIM:270750	IEA				P		HPO:iea	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0007340	OMIM:270750	TAS				P		HPO:skoehler	
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0009830	OMIM:270750	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	270750	%270750 SPASTIC PARAPLEGIA 23; SPG23;;SPASTIC PARAPLEGIA WITH PIGMENTARY ABNORMALITIES;;SPASTIC PARAPARESIS, VITILIGO, PREMATURE GRAYING, CHARACTERISTIC FACIES;;LISON SYNDROME		HP:0100543	OMIM:270750	IEA				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000007	PMID:19439420	PCS				I		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000020	PMID:19439420	PCS				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000407	OMIM:270800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000518	OMIM:270800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000639	OMIM:270800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0000648	OMIM:270800	IEA				P		HPO:skoehler	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0001258	OMIM:270800	TAS				P		HPO:probinson	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0001260	OMIM:270800	IEA				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0001317	OMIM:270800	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0001347	OMIM:270800	IEA				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0001761	OMIM:270800	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0002061	PMID:19439420	PCS				P		HPO:probinson	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0002064	OMIM:270800	IEA				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0002166	PMID:19439420	PCS				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0002406	PMID:19439420	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0003487	PMID:19439420	PCS				P		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0003676	OMIM:270800	IEA				C		HPO:iea	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0006858	OMIM:270800	TAS				P		HPO:probinson	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0007340	OMIM:270800	TAS				P		HPO:skoehler	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0010550	OMIM:270800	IEA				P		HPO:skoehler	
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0030890	PMID:19439420	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	270800	SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE; SPG5A		HP:0100543	OMIM:270800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	270850	SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION		HP:0000007	OMIM:270850	IEA				I		HPO:iea	
OMIM	270850	SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION		HP:0000501	OMIM:270850	IEA				P		HPO:iea	
OMIM	270850	SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION		HP:0001249	OMIM:270850	IEA				P		HPO:iea	
OMIM	270850	SPASTIC PARESIS, GLAUCOMA, AND MENTAL RETARDATION		HP:0001258	OMIM:270850	IEA				P		HPO:iea	
OMIM	270900	SPASTIC PSEUDOSCLEROSIS		HP:0000007	OMIM:270900	IEA				I		HPO:iea	
OMIM	270900	SPASTIC PSEUDOSCLEROSIS		HP:0000707	OMIM:270900	IEA				P		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0000007	OMIM:270950	IEA				I		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0000365	OMIM:270950	IEA				P		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0000510	OMIM:270950	IEA				P		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0000572	OMIM:270950	IEA				P		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0001249	OMIM:270950	IEA				P		HPO:iea	
OMIM	270950	SPASTIC QUADRIPLEGIA, RETINITIS PIGMENTOSA, AND MENTAL RETARDATION		HP:0002510	OMIM:270950	IEA				P		HPO:iea	
OMIM	270960	#270960 SPERMATOGENIC FAILURE 4; SPGF4;;AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS;;AZOOSPERMIA WITH MATURATION ARREST;;SPERMATOGENESIS ARRESTPREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 4; RPRGL4		HP:0000006	OMIM:270960	TAS				I		HPO:skoehler	
OMIM	270960	#270960 SPERMATOGENIC FAILURE 4; SPGF4;;AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS;;AZOOSPERMIA WITH MATURATION ARREST;;SPERMATOGENESIS ARRESTPREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 4; RPRGL4		HP:0000007	OMIM:270960	IEA				I		HPO:iea	
OMIM	270960	#270960 SPERMATOGENIC FAILURE 4; SPGF4;;AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS;;AZOOSPERMIA WITH MATURATION ARREST;;SPERMATOGENESIS ARRESTPREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 4; RPRGL4		HP:0000027	OMIM:270960	IEA				P		HPO:iea	
OMIM	270960	#270960 SPERMATOGENIC FAILURE 4; SPGF4;;AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS;;AZOOSPERMIA WITH MATURATION ARREST;;SPERMATOGENESIS ARRESTPREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 4; RPRGL4		HP:0001939	OMIM:270960	IEA				P		HPO:iea	
OMIM	270960	#270960 SPERMATOGENIC FAILURE 4; SPGF4;;AZOOSPERMIA DUE TO PERTURBATIONS OF MEIOSIS;;AZOOSPERMIA WITH MATURATION ARREST;;SPERMATOGENESIS ARRESTPREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 4; RPRGL4		HP:0200067	OMIM:270960	TAS				P		HPO:skoehler	
OMIM	270970	SPHEROCYTOSIS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:270970	TAS				I		HPO:probinson	
OMIM	270970	SPHEROCYTOSIS, AUTOSOMAL RECESSIVE	HP:0012828	HP:0001878	OMIM:270970	TAS				P		HPO:probinson	
OMIM	270970	SPHEROCYTOSIS, AUTOSOMAL RECESSIVE		HP:0004444	OMIM:270970	TAS				P		HPO:probinson	
OMIM	271109	SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION		HP:0000007	OMIM:271109	IEA				I		HPO:iea	
OMIM	271109	SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION		HP:0000252	OMIM:271109	IEA				P		HPO:iea	
OMIM	271109	SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION		HP:0001159	OMIM:271109	IEA				P		HPO:skoehler	
OMIM	271109	SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION		HP:0001249	OMIM:271109	IEA				P		HPO:iea	
OMIM	271109	SPINAL MUSCULAR ATROPHY WITH MENTAL RETARDATION		HP:0007269	OMIM:271109	IEA				P		HPO:iea	
OMIM	271110	SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY		HP:0000007	OMIM:271110	IEA				I		HPO:iea	
OMIM	271110	SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY		HP:0000252	OMIM:271110	IEA				P		HPO:iea	
OMIM	271110	SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY		HP:0001249	OMIM:271110	IEA				P		HPO:iea	
OMIM	271110	SPINAL MUSCULAR ATROPHY WITH MICROCEPHALY AND MENTAL SUBNORMALITY		HP:0006959	OMIM:271110	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0000007	OMIM:271150	IEA				I		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0001308	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0002378	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0002398	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0002522	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0003445	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0003581	OMIM:271150	TAS				C		HPO:probinson	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0003677	OMIM:271150	IEA				C		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0003701	OMIM:271150	TAS				P		HPO:skoehler	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0007126	OMIM:271150	IEA				P		HPO:iea	
OMIM	271150	SPINAL MUSCULAR ATROPHY, TYPE IV		HP:0007269	OMIM:271150	TAS				P		HPO:skoehler	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0000007	OMIM:271200	IEA				I		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0001761	OMIM:271200	IEA				P		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0002380	OMIM:271200	IEA				P		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0002751	OMIM:271200	IEA				P		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0003593	OMIM:271200	IEA				C		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0007126	OMIM:271200	IEA				P		HPO:iea	
OMIM	271200	SPINAL MUSCULAR ATROPHY, RYUKYUAN TYPE		HP:0007269	OMIM:271200	IEA				P		HPO:iea	
OMIM	271220	SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL		HP:0000007	OMIM:271220	IEA				I		HPO:iea	
OMIM	271220	SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL		HP:0007269	OMIM:271220	IEA				P		HPO:iea	
OMIM	271220	SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL		HP:0009049	OMIM:271220	IEA				P		HPO:iea	
OMIM	271220	SPINAL MUSCULAR ATROPHY, SCAPULOPERONEAL		HP:0009060	OMIM:271220	IEA				P		HPO:iea	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000007	OMIM:271225	IEA				I		HPO:iea	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000218	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000721	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000767	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000938	PMID:10528250,PMID:12503654	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0000998	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0001166	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0001290	PMID:10528250	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0001371	PMID:10528250	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0001374	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0001838	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0002098	PMID:12503654	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0002398	PMID:12503654	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0003199	PMID:12503654	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0003700	PMID:12503654	PCS				P		HPO:lccarmody	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0005855	OMIM:271225	IEA				P		HPO:iea	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0007280	OMIM:271225	IEA				P		HPO:iea	
OMIM	271225	SPINAL MUSCULAR ATROPHY, TYPE I, WITH CONGENITAL BONE FRACTURES		HP:0007430	PMID:12503655	PCS				P		HPO:lccarmody	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000007	OMIM:271245	IEA				I		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000365	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000602	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000639	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000648	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000709	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000815	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0000817	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001249	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001251	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001252	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001262	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001272	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001284	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001290	OMIM:271245	TAS				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001298	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001324	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0001328	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002076	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002120	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002133	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002305	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002312	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0002910	OMIM:271245	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0003390	OMIM:271245	IEA				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0003676	OMIM:271245	IEA				C		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0006957	OMIM:271245	IEA				P		HPO:iea	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0007366	OMIM:271245	TAS				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0012847	OMIM:271245	TAS				P		HPO:skoehler	
OMIM	271245	MITOCHONDRIAL DNA DEPLETION SYNDROME 7 (HEPATOCEREBRAL TYPE)		HP:0200134	OMIM:271245	TAS				P		HPO:skoehler	
OMIM	271250	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3		HP:0000007	OMIM:271250	IEA				I		HPO:iea	
OMIM	271250	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3		HP:0000365	OMIM:271250	IEA				P		HPO:iea	
OMIM	271250	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3		HP:0000618	OMIM:271250	IEA				P		HPO:iea	
OMIM	271250	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3		HP:0001251	OMIM:271250	IEA				P		HPO:iea	
OMIM	271250	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 3		HP:0005102	OMIM:271250	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000007	OMIM:271270	IEA				I		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000179	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000280	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000337	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000463	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0000508	OMIM:271270	IEA				P		HPO:skoehler	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001251	OMIM:271270	TAS				P		HPO:skoehler	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001252	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001260	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001263	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001265	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001272	OMIM:271270	TAS				P		HPO:skoehler	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001290	OMIM:271270	TAS				P		HPO:skoehler	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0001760	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0002208	OMIM:271270	TAS				P		HPO:probinson	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0002650	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0002714	OMIM:271270	TAS				P		HPO:skoehler	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0003196	OMIM:271270	IEA				P		HPO:iea	
OMIM	271270	SPINOCEREBELLAR ATAXIA WITH DYSMORPHISM		HP:0003487	OMIM:271270	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0000007	OMIM:271310	IEA				I		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0001131	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0001141	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0001249	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0001251	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0001939	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0002503	OMIM:271310	IEA				P		HPO:iea	
OMIM	271310	SPINOCEREBELLAR DEGENERATION AND CORNEAL DYSTROPHY		HP:0007759	OMIM:271310	IEA				P		HPO:iea	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0000007	OMIM:271320	IEA				I		HPO:iea	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0000519	OMIM:271320	IEA				P		HPO:iea	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0000545	OMIM:271320	IEA				P		HPO:skoehler	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0001131	OMIM:271320	IEA				P		HPO:skoehler	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0002497	OMIM:271320	IEA				P		HPO:iea	
OMIM	271320	SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITALCATARACTS, AND MYOPIA		HP:0002503	OMIM:271320	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0000007	OMIM:271322	IEA				I		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0000478	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0000514	OMIM:271322	TAS				P		HPO:skoehler	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0000924	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0001271	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0001288	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0001939	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0002071	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0002503	OMIM:271322	IEA				P		HPO:iea	
OMIM	271322	271322 SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS; SDSEM		HP:0100543	OMIM:271322	IEA				P		HPO:skoehler	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0000006	OMIM:271400	TAS				I		HPO:skoehler	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0000007	OMIM:271400	IEA				I		HPO:iea	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0001438	OMIM:271400	IEA				P		HPO:iea	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0001746	OMIM:271400	TAS				P		HPO:skoehler	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0001894	OMIM:271400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0001939	OMIM:271400	IEA				P		HPO:iea	
OMIM	271400	#271400 ASPLENIA, ISOLATED CONGENITAL; ICAS;;HYPOSPLENIA, ISOLATED CONGENITAL;;SPLENIC HYPOPLASIA;;ASPLENIA, FAMILIAL		HP:0003593	OMIM:271400	TAS				C		HPO:skoehler	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0000007	OMIM:271500	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES	HP:0012825	HP:0000819	OMIM:271500	IEA				P		HPO:probinson	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0001394	OMIM:271500	IEA				P		HPO:skoehler	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0001395	OMIM:271500	IEA				P		HPO:iea	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0001541	OMIM:271500	IEA				P		HPO:iea	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0001744	OMIM:271500	IEA				P		HPO:iea	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0001987	OMIM:271500	IEA				P		HPO:iea	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0005201	OMIM:271500	IEA				P		HPO:iea	
OMIM	271500	SPLENOPORTAL VASCULAR ANOMALIES		HP:0007111	OMIM:271500	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000007	OMIM:271510	IEA				I		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000164	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000272	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000316	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000463	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000926	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0000938	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0001216	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0001249	OMIM:271510	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0001377	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0001607	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002007	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002651	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002750	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002751	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002812	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002938	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0002942	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0003025	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0003027	OMIM:271510	IEA				P		HPO:skoehler	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0003196	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0003370	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0004315	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0004482	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0004586	OMIM:271510	TAS				P		HPO:probinson	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0005280	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0006336	OMIM:271510	TAS				P		HPO:skoehler	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0006887	OMIM:271510	IEA				P		HPO:skoehler	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0007787	OMIM:271510	IEA				P		HPO:skoehler	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0008486	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0008755	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0008873	OMIM:271510	IEA				P		HPO:iea	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0011800	OMIM:271510	TAS				P		HPO:skoehler	
OMIM	271510	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE		HP:0031367	OMIM:271510	IEA				P		HPO:skoehler	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000007	OMIM:271520	IEA				I		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000023	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000042	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000068	OMIM:271520	TAS				P		HPO:probinson	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000126	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000151	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000268	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000316	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000470	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000773	OMIM:271520	TAS				P		HPO:probinson	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000883	OMIM:271520	TAS				P		HPO:probinson	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000902	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0000921	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0001195	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0001562	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0002023	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0002089	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0002650	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0002937	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0002946	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0003250	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0003270	OMIM:271520	IEA				P		HPO:iea	
OMIM	271520	SPONDYLOCOSTAL DYSOSTOSIS WITH ANAL ATRESIA AND UROGENITAL ANOMALIES		HP:0003305	OMIM:271520	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0000007	OMIM:271530	IEA				I		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0000470	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0000478	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0000768	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA	HP:0012825	HP:0000938	OMIM:271530	TAS				P		HPO:probinson	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0002650	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0002808	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0002945	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA	HP:0012825	HP:0003026	OMIM:271530	IEA				P		HPO:probinson	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0003180	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0003418	OMIM:271530	IEA				P		HPO:skoehler	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0003521	OMIM:271530	TAS				P		HPO:probinson	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0003952	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0005004	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0008418	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0100864	OMIM:271530	IEA				P		HPO:iea	
OMIM	271530	%271530 BRACHYOLMIA TYPE 1, HOBAEK TYPE;;BRACHYOLMIA, RECESSIVE TYPE OF HOBAEK;;SPONDYLODYSPLASIA WITH PURE BRACHYOLMIA		HP:0100866	OMIM:271530	TAS				P		HPO:skoehler	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:271600	TAS				I		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0000926	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0002655	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0005194	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE	HP:0012828	HP:0008843	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271600	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE		HP:0011909	OMIM:271600	TAS				P		HPO:probinson	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0000007	OMIM:271620	IEA				I		HPO:iea	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0000926	OMIM:271620	IEA				P		HPO:iea	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0001249	OMIM:271620	IEA				P		HPO:iea	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0002655	OMIM:271620	IEA				P		HPO:skoehler	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0002673	OMIM:271620	IEA				P		HPO:skoehler	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0003185	OMIM:271620	TAS				P		HPO:iea	
OMIM	271620	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH MENTAL RETARDATION		HP:0008430	OMIM:271620	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0000007	OMIM:271630	IEA				I		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0000470	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0001288	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0002751	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0002945	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0003301	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0003418	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0003521	OMIM:271630	TAS				P		HPO:skoehler	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0006413	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0006607	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0007759	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0008418	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0008922	OMIM:271630	IEA				P		HPO:iea	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0012066	OMIM:271630	TAS				P		HPO:probinson	
OMIM	271630	%271630 BRACHYOLMIA TYPE 1, TOLEDO TYPE;;SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, TOLEDO TYPE;;SED, CHONDROITIN SULFATE TYPE;;PAPS-CHONDROITIN SULFATE SULFOTRANSFERASE DEFICIENCY		HP:0100864	OMIM:271630	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000007	OMIM:271640	TAS				I		HPO:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000175	OMIM:271640	TAS		HP:0040284		P		HPO:iea	31%
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000218	OMIM:271640	TAS		HP:0040284		P		HPO:iea	12%
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000272	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000300	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000343	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000347	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000470	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000520	PMID:23664117	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000545	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1	HP:0012825	HP:0000545	PMID:23664118	PCS				P		HP:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000592	PMID:23664117	PCS		HP:0040284		P		HPO:iea	4/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000878	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000887	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000904	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000926	OMIM:271640	IEA	HP:0011463			P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000926	PMID:23664117	PCS		HP:0040284		P		HPO:skoehler	7/7
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0000939	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1	HP:0012825	HP:0000974	OMIM:271640	TAS				P		HPO:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001027	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001030	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001083	OMIM:271640	TAS				P		HPO:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001252	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001290	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001371	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001388	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001629	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001631	OMIM:271640	IEA		HP:0040284		P		HPO:iea	5/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001647	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001653	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001762	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001763	OMIM:271640	IEA		HP:0040284		P		HPO:iea	3/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001799	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001822	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0001840	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002176	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002209	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002651	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002656	OMIM:271640	IEA				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002673	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002751	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002756	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002827	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002857	OMIM:271640	TAS		HP:0040284		P		HPO:probinson	80%
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002869	OMIM:271640	TAS				P		HPO:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0002986	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003015	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003016	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003026	OMIM:271640	TAS				P		HPO:probinson	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003048	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003083	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003100	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003300	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003301	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0003510	PMID:23664117	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0004233	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0004325	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0008818	OMIM:271640	IEA		HP:0040284		P		HPO:iea	5/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0008824	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0008828	OMIM:271640	TAS				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0009702	OMIM:271640	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0009836	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0010049	OMIM:271640	IEA				P		HPO:iea	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0010550	OMIM:271640	IEA				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0011220	PMID:23664117	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0011341	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0011800	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0012368	PMID:23664117	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0030043	OMIM:271640	TAS				P		HPO:skoehler	
OMIM	271640	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 1, WITH OR WITHOUT FRACTURES; SEMDJL1		HP:0100864	OMIM:271640	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0000007	OMIM:271650	IEA				I		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0000768	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0000920	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0000926	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0001169	OMIM:271650	TAS				P		HPO:probinson	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0001241	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0001377	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0001769	OMIM:271650	IEA				P		HPO:skoehler	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002515	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002651	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002758	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002812	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002829	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002857	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0002938	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0003521	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0004279	OMIM:271650	TAS				P		HPO:probinson	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0004590	OMIM:271650	TAS				P		HPO:skoehler	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0006429	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0009824	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0010049	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0010743	OMIM:271650	IEA				P		HPO:iea	
OMIM	271650	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, IRAPA TYPE		HP:0100255	OMIM:271650	IEA				P		HPO:iea	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000007	OMIM:271665	TAS				I		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000218	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000272	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000316	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000347	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000464	OMIM:271665	IEA				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000520	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000767	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000773	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000907	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000922	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0000926	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0001230	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0001263	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0001290	OMIM:271665	TAS				P		HPO:skoehler	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0001591	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0001840	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002007	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002091	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002176	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002650	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002651	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002787	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002869	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002979	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002983	OMIM:271665	TAS				P		HPO:skoehler	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0002987	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003015	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003026	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003085	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003196	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003311	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003320	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003396	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0003467	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0005257	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0005280	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0005462	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0006009	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0006380	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0006532	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0006600	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0008873	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0009164	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0009803	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0009875	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0010049	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0010655	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0011800	OMIM:271665	TAS				P		HPO:skoehler	
OMIM	271665	SPONDYLOMETAEPIPHYSEAL DYSPLASIA, SHORT LIMB-HAND TYPE		HP:0030043	OMIM:271665	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000006	OMIM:271700	IEA				I		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000272	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000339	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000407	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000768	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0000926	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001156	OMIM:271700	IEA				P		HPO:skoehler	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001169	OMIM:271700	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001377	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001552	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001773	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0001831	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0002655	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0002808	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0003022	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0003180	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0003370	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0004180	OMIM:271700	TAS				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0004227	OMIM:271700	TAS				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0004322	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0005068	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0006110	OMIM:271700	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0006144	OMIM:271700	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0009290	OMIM:271700	TAS				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0009566	OMIM:271700	TAS				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0009778	OMIM:271700	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0009882	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0010049	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0010230	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0010454	OMIM:271700	IEA				P		HPO:skoehler	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0010743	OMIM:271700	IEA				P		HPO:iea	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0011304	OMIM:271700	TAS				P		HPO:probinson	
OMIM	271700	SPONDYLOPERIPHERAL DYSPLASIA		HP:0011800	OMIM:271700	TAS				P		HPO:skoehler	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000007	OMIM:264470	PCS				I		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000256	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000365	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000618	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000639	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0000648	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0001252	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0001476	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0002179	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0002197	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0002376	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0002977	OMIM:271900	TAS				P		HPO:skoehler	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0007305	OMIM:264470	PCS				P		HPO:probinson	
OMIM	271900	#271900 CANAVAN DISEASE;;CANAVAN-VAN BOGAERT-BERTRAND DISEASE;;SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM;;ASPARTOACYLASE DEFICIENCY;;ASPA DEFICIENCY;;ASP DEFICIENCY;;AMINOACYLASE 2 DEFICIENCY;;ACY2 DEFICIENCY		HP:0012444	OMIM:271900	TAS				P		HPO:skoehler	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0000007	OMIM:271930	IEA				I		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0000648	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0001249	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0001257	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0001266	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0001332	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0001508	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0002015	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0002376	OMIM:271930	TAS				P		HPO:skoehler	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0007281	OMIM:271930	IEA				P		HPO:iea	
OMIM	271930	#271930 STRIATONIGRAL DEGENERATION, INFANTILE; SNDI;;INFANTILE BILATERAL STRIATAL NECROSIS; IBSN;;BILATERAL STRIATAL NECROSIS, INFANTILE;;STRIATAL DEGENERATION, FAMILIAL		HP:0012043	OMIM:271930	TAS				P		HPO:skoehler	
OMIM	271950	271950 SUBAORTIC STENOSIS, MEMBRANOUS		HP:0000007	OMIM:271950	TAS				I		HPO:skoehler	
OMIM	271950	271950 SUBAORTIC STENOSIS, MEMBRANOUS		HP:0001682	OMIM:271950	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000007	OMIM:271960	IEA				I		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000160	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000188	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000272	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000286	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000311	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000327	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000369	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000431	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000463	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000470	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000482	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000486	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000501	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000568	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000699	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000767	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0000914	OMIM:271960	TAS				P		HPO:skoehler	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001249	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001500	OMIM:271960	TAS				P		HPO:probinson	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001510	OMIM:271960	IEA				P		HPO:skoehler	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001552	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001682	OMIM:271960	TAS				P		HPO:probinson	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001773	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001831	OMIM:271960	TAS				P		HPO:probinson	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0001837	OMIM:271960	TAS				P		HPO:probinson	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0003196	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0004279	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0005174	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0006610	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0007759	OMIM:271960	IEA				P		HPO:iea	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0009803	OMIM:271960	TAS				P		HPO:probinson	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0011800	OMIM:271960	TAS				P		HPO:skoehler	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0012368	OMIM:271960	TAS				P		HPO:skoehler	
OMIM	271960	271960 SUBAORTIC STENOSIS--SHORT STATURE SYNDROME;;ONAT SYNDROME		HP:0200055	OMIM:271960	TAS				P		HPO:skoehler	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000007	OMIM:271980	IEA				I		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000496	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000709	OMIM:271980	TAS				P		HPO:probinson	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD	HP:0012825	HP:0000717	OMIM:271980	TAS				P		HPO:probinson	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000718	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000738	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000739	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000750	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0000752	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001249	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001251	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001252	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001263	OMIM:271980	TAS				P		HPO:skoehler	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001265	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001270	OMIM:271980	IEA				P		HPO:skoehler	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001290	OMIM:271980	TAS				P		HPO:skoehler	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0001939	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002069	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002121	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002123	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002133	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002353	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0002487	OMIM:271980	IEA				P		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0003593	OMIM:271980	IEA				C		HPO:iea	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0025356	OMIM:271980	IEA				P		HPO:skoehler	
OMIM	271980	SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD		HP:0100716	OMIM:271980	TAS				P		HPO:skoehler	
OMIM	272000	SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION		HP:0000007	OMIM:272000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	272000	SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION		HP:0001249	OMIM:272000	IEA				P		HPO:iea	
OMIM	272000	SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION		HP:0001939	OMIM:272000	IEA				P		HPO:iea	
OMIM	272000	SUCROSURIA, HIATUS HERNIA AND MENTAL RETARDATION		HP:0002036	OMIM:272000	IEA				P		HPO:iea	
OMIM	272100	SUDANOPHILIC CEREBRAL SCLEROSIS		HP:0000007	OMIM:272100	TAS				I		HPO:probinson	
OMIM	272100	SUDANOPHILIC CEREBRAL SCLEROSIS		HP:0006918	OMIM:272100	TAS				P		HPO:probinson	
OMIM	272100	SUDANOPHILIC CEREBRAL SCLEROSIS		HP:0100704	OMIM:272100	TAS				P		HPO:probinson	
OMIM	272120	SUDDEN INFANT DEATH SYNDROME		HP:0000007	OMIM:272120	TAS				I		HPO:nvasilevsky	
OMIM	272120	SUDDEN INFANT DEATH SYNDROME		HP:0001426	OMIM:272120	TAS				I		HPO:nvasilevsky	
OMIM	272120	SUDDEN INFANT DEATH SYNDROME		HP:0001699	OMIM:272120	TAS				M		HPO:skoehler	
OMIM	272120	SUDDEN INFANT DEATH SYNDROME		HP:0002047	OMIM:272120	IEA				P		HPO:skoehler	
OMIM	272120	SUDDEN INFANT DEATH SYNDROME		HP:0005949	OMIM:272120	TAS				P		HPO:skoehler	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0000007	OMIM:272150	IEA				I		HPO:iea	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0001156	OMIM:272150	TAS				P		HPO:skoehler	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0005894	OMIM:272150	IEA				P		HPO:iea	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0009857	OMIM:272150	TAS				P		HPO:probinson	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0010241	OMIM:272150	TAS				P		HPO:probinson	
OMIM	272150	272150 SUGARMAN BRACHYDACTYLY;;BRACHYDACTYLY WITH MAJOR PROXIMAL PHALANGEAL SHORTENING		HP:0011926	OMIM:272150	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000007	OMIM:272200	IEA				I		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000238	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000280	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000365	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000463	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000546	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0000943	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001249	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001251	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001257	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001263	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001272	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001319	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0001744	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002003	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002059	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002119	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002240	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002395	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002518	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0002922	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0004322	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0007305	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0007307	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0007957	OMIM:272200	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0008064	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0008155	OMIM:272200	TAS				P		HPO:probinson	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0008479	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0010055	OMIM:272200	IEA				P		HPO:iea	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0011096	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0011220	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0011304	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0012368	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272200	#272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;MUCOSULFATIDOSIS;;SULFATIDOSIS, JUVENILE, AUSTIN TYPE		HP:0100539	OMIM:272200	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0000007	OMIM:272300	IEA				I		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0000684	OMIM:272300	TAS				P		HPO:probinson	
OMIM	272300	SULFOCYSTEINURIA		HP:0000713	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0000964	OMIM:272300	IEA				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0001083	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001250	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001251	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001263	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001266	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001276	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0001290	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0001522	OMIM:272300	TAS				M		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0002213	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0002301	OMIM:272300	IEA				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0003359	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0003643	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0007325	OMIM:272300	IEA				P		HPO:iea	
OMIM	272300	SULFOCYSTEINURIA		HP:0008947	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272300	SULFOCYSTEINURIA		HP:0011942	OMIM:272300	TAS				P		HPO:skoehler	
OMIM	272350	SUMMITT SYNDROME		HP:0000007	OMIM:272350	IEA				I		HPO:iea	
OMIM	272350	SUMMITT SYNDROME		HP:0000263	OMIM:272350	TAS				P		HPO:skoehler	
OMIM	272350	SUMMITT SYNDROME		HP:0001159	OMIM:272350	IEA				P		HPO:iea	
OMIM	272350	SUMMITT SYNDROME		HP:0001363	OMIM:272350	IEA				P		HPO:iea	
OMIM	272350	SUMMITT SYNDROME		HP:0001513	OMIM:272350	IEA				P		HPO:iea	
OMIM	272370	SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS		HP:0000007	OMIM:272370	IEA				I		HPO:iea	
OMIM	272370	SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS		HP:0002715	OMIM:272370	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000007	OMIM:272430	IEA				I		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000160	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000211	OMIM:272430	IEA				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000218	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000278	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000293	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000343	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000347	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000369	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000445	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000463	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000470	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000491	OMIM:272430	IEA				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1	HP:0012828	HP:0000670	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0000975	OMIM:272430	IEA				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001181	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001182	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001249	OMIM:272430	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001250	OMIM:272430	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001377	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001611	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001762	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001763	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0001954	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0002094	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0002179	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0002751	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0002987	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0004279	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0005280	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0008872	OMIM:272430	IEA				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0009466	OMIM:272430	IEA				P		HPO:iea	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0010628	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0012385	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272430	CRISPONI/COLD-INDUCED SWEATING SYNDROME 1; CISS1		HP:0100729	OMIM:272430	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000007	OMIM:272440	IEA				I		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000028	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000062	OMIM:272440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000233	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000252	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000322	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000337	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000430	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000431	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000505	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000520	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000648	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000668	OMIM:272440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000691	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000954	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0000998	OMIM:272440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001249	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001250	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001272	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001332	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001511	OMIM:272440	PCS				P		HPO:probinson	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0001629	OMIM:272440	IEA				P		HPO:iea	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0004325	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0008070	OMIM:272440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0008897	OMIM:272440	PCS				P		HPO:probinson	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0009765	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0010714	OMIM:272440	PCS				P		HPO:probinson	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0011335	OMIM:272440	TAS				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0012725	OMIM:272440	IEA				P		HPO:skoehler	
OMIM	272440	FILIPPI SYNDROME; FLPIS		HP:0040019	OMIM:272440	IEA				P		HPO:skoehler	
OMIM	272450	SYNDESMODYSPLASIC DWARFISM		HP:0000007	OMIM:272450	IEA				I		HPO:iea	
OMIM	272450	SYNDESMODYSPLASIC DWARFISM		HP:0001387	OMIM:272450	IEA				P		HPO:skoehler	
OMIM	272450	SYNDESMODYSPLASIC DWARFISM		HP:0003510	OMIM:272450	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000007	PMID:14991055	PCS				I		HPO:probinson	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000107	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000175	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000283	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000316	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000384	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000407	OMIM:272460	TAS				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000410	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000455	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000470	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0000518	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0001156	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0001241	PMID:14991055	PCS				P		HPO:probinson	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0001762	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0001763	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0002091	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0002644	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0002650	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0002656	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0002750	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003196	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003305	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003307	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003311	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003521	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0003865	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0004209	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0006297	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0007703	PMID:14991055	PCS		HP:0040284		P		HPO:probinson	HP:0040284
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0008368	OMIM:272460	IEA				P		HPO:skoehler	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0008456	OMIM:272460	IEA				P		HPO:iea	
OMIM	272460	SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME; SCT		HP:0009702	OMIM:272460	IEA				P		HPO:iea	
OMIM	272600	272600 TAPETORETINAL DEGENERATION WITH ATAXIA		HP:0000007	OMIM:272600	TAS				I		HPO:skoehler	
OMIM	272600	272600 TAPETORETINAL DEGENERATION WITH ATAXIA		HP:0000510	OMIM:272600	IEA				P		HPO:iea	
OMIM	272600	272600 TAPETORETINAL DEGENERATION WITH ATAXIA		HP:0001251	OMIM:272600	IEA				P		HPO:iea	
OMIM	272600	272600 TAPETORETINAL DEGENERATION WITH ATAXIA		HP:0001425	OMIM:272600	IEA				I		HPO:iea	
OMIM	272620	TARDIVE DYSKINESIA		HP:0000007	OMIM:272620	IEA				I		HPO:iea	
OMIM	272620	TARDIVE DYSKINESIA		HP:0031943	OMIM:272620	IEA				P		HPO:skoehler	
OMIM	272620	TARDIVE DYSKINESIA		HP:0040141	OMIM:272620	TAS				P		HPO:skoehler	
OMIM	272650	TATSUMI FACTOR DEFICIENCY		HP:0000007	OMIM:272650	IEA				I		HPO:iea	
OMIM	272650	TATSUMI FACTOR DEFICIENCY		HP:0003010	OMIM:272650	IEA				P		HPO:iea	
OMIM	272650	TATSUMI FACTOR DEFICIENCY		HP:0003337	OMIM:272650	IEA				P		HPO:iea	
OMIM	272700	TAURODONTISM		HP:0000007	OMIM:272700	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	272700	TAURODONTISM		HP:0000679	OMIM:272700	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0000007	OMIM:272750	IEA				I		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0000618	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0000726	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0000741	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001250	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001252	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001263	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001276	OMIM:272750	IEA				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001285	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001290	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001332	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0001347	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002059	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002072	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002180	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002267	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002371	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002421	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002476	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0002835	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0003470	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0003495	OMIM:272750	IEA				P		HPO:iea	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0003828	OMIM:272750	TAS				C		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0007256	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0008936	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272750	GM2-GANGLIOSIDOSIS, AB VARIANT		HP:0010780	OMIM:272750	TAS				P		HPO:skoehler	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0000007	OMIM:272800	TAS				I		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0000618	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0000726	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0000741	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0000980	OMIM:272800	IEA				P		HPO:skoehler	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0001250	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0001276	OMIM:272800	IEA				P		HPO:skoehler	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0001290	OMIM:272800	TAS				P		HPO:skoehler	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0002267	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0002361	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0002421	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0002835	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0003495	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0003593	OMIM:272800	TAS				C		HPO:probinson	
OMIM	272800	TAY-SACHS DISEASE; TSD		HP:0010729	OMIM:272800	TAS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000007	PMID:23918592	PCS				I		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000071	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000085	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000126	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000154	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000160	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000175	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000252	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000262	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000294	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000316	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000319	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000341	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000369	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000385	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000430	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000431	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000455	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000506	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000508	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000568	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000677	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000767	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000768	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0000954	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001159	OMIM:272950	IEA				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001629	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001650	OMIM:272950	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001762	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001838	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0001840	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0002217	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0002553	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0002705	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0002825	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0004322	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0006610	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0008070	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0008589	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0009487	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0010291	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0011220	OMIM:272950	TAS				P		HPO:skoehler	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0012385	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272950	TEEBI-SHALTOUT SYNDROME; TBSH		HP:0030799	PMID:23918592	PCS				P		HPO:probinson	
OMIM	272980	TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR		HP:0000007	OMIM:272980	IEA				I		HPO:iea	
OMIM	272980	TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR		HP:0000677	OMIM:272980	IEA				P		HPO:iea	
OMIM	272980	TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR		HP:0000679	OMIM:272980	IEA				P		HPO:iea	
OMIM	272980	TEETH, CONGENITAL ABSENCE OF, WITH TAURODONTIA AND SPARSE HAIR		HP:0008070	OMIM:272980	IEA				P		HPO:iea	
OMIM	273000	TEETH, FUSED		HP:0000007	OMIM:273000	IEA				I		HPO:iea	
OMIM	273000	TEETH, FUSED		HP:0000164	OMIM:273000	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0000007	OMIM:273050	IEA				I		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0000358	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0000369	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0000680	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0000706	OMIM:273050	TAS				P		HPO:skoehler	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0002857	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0005439	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0006321	OMIM:273050	IEA				P		HPO:iea	
OMIM	273050	TEETH, NONERUPTION OF, WITH MAXILLARY HYPOPLASIA AND GENU VALGUM		HP:0006329	OMIM:273050	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0000007	OMIM:273120	IEA				I		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0000103	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0000639	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0000651	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0001269	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0001438	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0001959	OMIM:273120	IEA				P		HPO:iea	
OMIM	273120	TERATOMA, PINEAL		HP:0002514	OMIM:273120	IEA				P		HPO:skoehler	
OMIM	273120	TERATOMA, PINEAL		HP:0009792	OMIM:273120	IEA				P		HPO:skoehler	
OMIM	273150	TESTES, RUDIMENTARY		HP:0000007	OMIM:273150	IEA				I		HPO:iea	
OMIM	273150	TESTES, RUDIMENTARY		HP:0000815	OMIM:273150	IEA				P		HPO:iea	
OMIM	273150	TESTES, RUDIMENTARY		HP:0008734	OMIM:273150	IEA				P		HPO:iea	
OMIM	273250	TESTICULAR REGRESSION SYNDROME		HP:0000007	OMIM:273250	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	273250	TESTICULAR REGRESSION SYNDROME		HP:0000812	OMIM:273250	IEA				P		HPO:skoehler	
OMIM	273250	TESTICULAR REGRESSION SYNDROME		HP:0012870	OMIM:273250	TAS				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0000027	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0000028	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0000133	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0001428	OMIM:273300	TAS				I		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0001939	OMIM:273300	IEA				P		HPO:iea	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0003745	OMIM:273300	IEA				I		HPO:iea	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0009792	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0030731	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273300	TESTICULAR GERM CELL TUMOR; TGCT		HP:0100768	OMIM:273300	IEA				P		HPO:skoehler	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000007	OMIM:273390	IEA				I		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000028	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000154	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000414	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000582	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000960	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0000968	OMIM:273390	IEA				P		HPO:skoehler	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0001006	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0001092	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0001249	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0001537	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0001939	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0002019	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0002705	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0002714	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0003057	OMIM:273390	IEA				P		HPO:skoehler	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0004467	OMIM:273390	IEA				P		HPO:iea	
OMIM	273390	TETRA-AMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES		HP:0007900	OMIM:273390	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:273395	IEA				I		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000042	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000068	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000104	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000148	OMIM:273395	TAS				P		HPO:probinson	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000175	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000204	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000238	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000347	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000369	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000453	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000568	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0000775	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0001195	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0001425	OMIM:273395	IEA				I		HPO:skoehler	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0001543	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0001746	OMIM:273395	TAS				P		HPO:probinson	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0002023	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0002089	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0003057	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0005316	OMIM:273395	IEA				P		HPO:iea	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0008697	OMIM:273395	TAS				P		HPO:skoehler	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0008839	OMIM:273395	TAS				P		HPO:probinson	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0009932	OMIM:273395	TAS				P		HPO:probinson	
OMIM	273395	#273395 TETRAAMELIA, AUTOSOMAL RECESSIVE		HP:0011743	OMIM:273395	TAS				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000007	OMIM:273400	IEA				I		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000135	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000164	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000204	OMIM:273400	IEA				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000377	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000464	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000579	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0000968	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0001006	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0001249	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0001792	OMIM:273400	IEA				P		HPO:iea	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0002353	OMIM:273400	IEA				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0002557	OMIM:273400	TAS				P		HPO:probinson	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0003057	OMIM:273400	IEA				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0003355	OMIM:273400	IEA				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0011675	OMIM:273400	IEA				P		HPO:skoehler	
OMIM	273400	TETRAMELIC DEFICIENCIES, ECTODERMAL DYSPLASIA, DEFORMED EARS, ANDOTHER ABNORMALITIES		HP:0100853	OMIM:273400	TAS				P		HPO:probinson	
OMIM	273600	THALIDOMIDE SUSCEPTIBILITY		HP:0000924	OMIM:273600	IEA				P		HPO:iea	
OMIM	273600	THALIDOMIDE SUSCEPTIBILITY		HP:0009830	OMIM:273600	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0000007	OMIM:273680	IEA				I		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0000518	OMIM:273680	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0001433	OMIM:273680	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0001903	OMIM:273680	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0001939	OMIM:273680	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0002983	OMIM:273680	IEA				P		HPO:iea	
OMIM	273680	THANATOPHORIC DYSPLASIA, GLASGOW VARIANT		HP:0003811	OMIM:273680	IEA				M		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0000007	OMIM:273730	IEA				I		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0000773	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0000774	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0001263	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0001334	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0002093	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0002878	OMIM:273730	TAS				P		HPO:skoehler	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME		HP:0006644	OMIM:273730	IEA				P		HPO:iea	
OMIM	273730	273730 THORACIC DYSPLASIA-HYDROCEPHALUS SYNDROME	HP:0012825	HP:0009826	OMIM:273730	IEA				P		HPO:iea	
OMIM	273740	THORACOMELIC DYSPLASIA		HP:0000007	OMIM:273740	IEA				I		HPO:iea	
OMIM	273740	THORACOMELIC DYSPLASIA		HP:0000773	OMIM:273740	IEA				P		HPO:iea	
OMIM	273740	THORACOMELIC DYSPLASIA		HP:0001591	OMIM:273740	IEA				P		HPO:iea	
OMIM	273740	THORACOMELIC DYSPLASIA		HP:0008873	OMIM:273740	IEA				P		HPO:iea	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000007	OMIM:273750	TAS				I		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000047	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000179	OMIM:273750	IEA				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000268	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000272	OMIM:273750	TAS				P		HPO:skoehler	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000303	OMIM:273750	TAS				P		HPO:skoehler	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000307	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000325	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000343	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000463	OMIM:273750	TAS				P		HPO:skoehler	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000470	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000574	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000767	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0000773	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0001382	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0001511	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0001518	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0001763	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0002007	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0002643	OMIM:273750	TAS				P		HPO:skoehler	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0002750	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0002827	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0003100	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0003298	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0003307	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0003691	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0004209	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0004322	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0004570	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0005280	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0008734	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0008839	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0008897	OMIM:273750	TAS				P		HPO:skoehler	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0009237	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273750	#273750 THREE M SYNDROME 1; 3M1;;3@M SYNDROME;;LE MERRER SYNDROME;;DOLICHOSPONDYLIC DYSPLASIA;;GLOOMY FACE SYNDROMEYAKUT SHORT STATURE SYNDROME, INCLUDED		HP:0010306	OMIM:273750	TAS				P		HPO:probinson	
OMIM	273770	THREONINEMIA		HP:0000007	OMIM:273770	IEA				I		HPO:iea	
OMIM	273770	THREONINEMIA		HP:0001250	OMIM:273770	IEA				P		HPO:iea	
OMIM	273770	THREONINEMIA		HP:0001510	OMIM:273770	IEA				P		HPO:iea	
OMIM	273770	THREONINEMIA		HP:0003296	OMIM:273770	IEA				P		HPO:iea	
OMIM	273770	THREONINEMIA		HP:0003354	OMIM:273770	IEA				P		HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0000007	OMIM:273800	TAS				I	GLANZMANN THROMBASTHENIA	HPO:probinson	
OMIM	273800	Glanzmann thrombasthenia		HP:0000132	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0000225	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0000421	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0000978	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0000979	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0001975	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0002170	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0002239	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0003010	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0003540	OMIM:273800	IEA				P	GLANZMANN THROMBASTHENIA	HPO:iea	
OMIM	273800	Glanzmann thrombasthenia		HP:0031126	PMID:2867408	PCS				P	GLANZMANN THROMBASTHENIA	HP:probinson	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0000007	OMIM:273900	IEA				I		HPO:iea	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0000421	OMIM:273900	TAS				P		HPO:skoehler	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0000924	OMIM:273900	IEA				P		HPO:iea	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0001873	OMIM:273900	IEA				P		HPO:iea	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0001892	OMIM:273900	IEA				P		HPO:iea	
OMIM	273900	THROMBOCYTOPENIA 3		HP:0005537	OMIM:273900	TAS				P		HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000007	OMIM:274000	TAS				I	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000085	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000151	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000248	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000272	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000347	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000463	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000486	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000508	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000891	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0000895	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001051	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001181	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001249	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001250	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001263	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001270	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001321	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001433	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001498	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001522	OMIM:274000;ISBN-13:978-3-7945-2657-4	TAS		HP:0040284		M	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	40%
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001629	PMID:17236129	PCS		HP:0040284		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	2/26
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001631	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001636	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001680	OMIM:274000	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001737	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001762	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001873	PMID:17236129	PCS		HP:0040284		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	29/29
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001880	ISBN-13:978-3-7945-2657-4	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0001903	ISBN-13:978-3-7945-2657-4	TAS	HP:0003593	HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002188	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002245	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002389	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002414	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002673	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002827	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002949	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002970	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002990	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0002999	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0003043	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0004209	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0004313	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0004322	ISBN-13:978-3-7945-2657-4	TAS		HP:0040284		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	7%
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0004717	OMIM:274000	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0004977	PMID:17236129	PCS		HP:0040284		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	29/29
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0006101	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0006443	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0006495	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040281		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040281
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0006507	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040284		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	50%
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0007413	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0007514	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0008952	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0009702	OMIM:274000	TAS				P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:skoehler	
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0009803	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0009829	ISBN-13:978-3-7945-2657-4;http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0011304	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0012098	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0100327	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=tar	TAS		HP:0040282		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040282
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0100694	ISBN-13:978-3-7945-2657-4	TAS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274000	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KB		HP:0100694	ISBN-13:978-0-12-383834-6	PCS		HP:0040283		P	#274000 THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME; TAR;;TAR SYNDROME;;CHROMOSOME 1Q21.1 DELETION SYNDROME, 200-KB	HPO:iea	HP:0040283
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0000007	OMIM:274150	IEA				I		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0000093	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0000952	OMIM:274150	IEA				P		HPO:skoehler	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001289	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001337	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001425	OMIM:274150	IEA				I		HPO:skoehler	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001873	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001923	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001937	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001945	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0001981	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0002098	OMIM:274150	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0002151	OMIM:274150	IEA				P		HPO:skoehler	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0002907	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0003138	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0003259	OMIM:274150	IEA				P		HPO:iea	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0005575	OMIM:274150	IEA				P		HPO:skoehler	
OMIM	274150	#274150 THROMBOTIC THROMBOCYTOPENIC PURPURA, CONGENITAL; TTP;;MICROANGIOPATHIC HEMOLYTIC ANEMIA;;THROMBOTIC MICROANGIOPATHY, FAMILIAL;;UPSHAW-SCHULMAN SYNDROME; USS;;SCHULMAN-UPSHAW SYNDROME;;UPSHAW FACTOR, DEFICIENCY OF;;MICROANGIOPATHIC HEMOLYTIC ANEMIA, CONGENITAL;;THROMBOTIC THROMBOCYTOPENIC PURPURA, FAMILIAL		HP:0006579	OMIM:274150	TAS				P		HPO:skoehler	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0000007	OMIM:274190	IEA				I		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0000458	OMIM:274190	IEA				P		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0000823	OMIM:274190	IEA				P		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0001574	OMIM:274190	IEA				P		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0001671	OMIM:274190	TAS				P		HPO:probinson	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0004322	OMIM:274190	IEA				P		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0004430	OMIM:274190	IEA				P		HPO:iea	
OMIM	274190	THUMB AGENESIS, SHORT STATURE, AND IMMUNODEFICIENCY		HP:0009777	OMIM:274190	IEA				P		HPO:iea	
OMIM	274200	THUMB, DISTAL HYPEREXTENSIBILITY OF		HP:0000007	OMIM:274200	IEA				I		HPO:iea	
OMIM	274200	THUMB, DISTAL HYPEREXTENSIBILITY OF		HP:0005722	OMIM:274200	IEA				P		HPO:iea	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0000007	OMIM:274205	TAS				I		HPO:iea	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0000028	OMIM:274205	TAS				P		HPO:iea	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0000365	OMIM:274205	TAS				P		HPO:skoehler	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0000518	OMIM:274205	TAS				P		HPO:iea	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0000567	OMIM:274205	TAS				P		HPO:probinson	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0001263	OMIM:274205	TAS				P		HPO:iea	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0009738	OMIM:274205	TAS				P		HPO:skoehler	
OMIM	274205	THUMB, HYPOPLASTIC, WITH CHOROID COLOBOMA, POORLY DEVELOPED ANTIHELIX,AND DEAFNESS		HP:0009778	OMIM:274205	TAS				P		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0000007	OMIM:274210	IEA				I		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0000104	OMIM:274210	IEA				P		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0000818	OMIM:274210	IEA				P		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0001507	OMIM:274210	IEA				P		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0001660	OMIM:274210	IEA				P		HPO:skoehler	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0002089	OMIM:274210	IEA				P		HPO:iea	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0003826	OMIM:274210	TAS				M		HPO:skoehler	
OMIM	274210	274210 THYMIC APLASIA WITH FETAL DEATH		HP:0012300	OMIM:274210	TAS				P		HPO:skoehler	
OMIM	274230	THYMOMA, FAMILIAL		HP:0000007	OMIM:274230	IEA				I		HPO:iea	
OMIM	274230	THYMOMA, FAMILIAL		HP:0001428	OMIM:274230	TAS				I		HPO:skoehler	
OMIM	274230	THYMOMA, FAMILIAL		HP:0002093	OMIM:274230	IEA				P		HPO:iea	
OMIM	274230	THYMOMA, FAMILIAL		HP:0002664	OMIM:274230	IEA				P		HPO:iea	
OMIM	274230	THYMOMA, FAMILIAL		HP:0100522	OMIM:274230	TAS				P		HPO:skoehler	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0000007	OMIM:274240	IEA				I		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0000123	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0000407	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0000853	OMIM:274240	IEA				P		HPO:skoehler	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0001250	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0001251	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0001336	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0001350	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0001873	OMIM:274240	IEA				P		HPO:iea	
OMIM	274240	THYROCEREBRORETINAL SYNDROME		HP:0003202	OMIM:274240	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0000007	OMIM:274265	IEA				I		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0000104	OMIM:274265	TAS				P		HPO:probinson	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0000818	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0001511	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0001562	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0001939	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0002023	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0002086	OMIM:274265	IEA				P		HPO:iea	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0008631	OMIM:274265	TAS				P		HPO:probinson	
OMIM	274265	THYMIC-RENAL-ANAL-LUNG DYSPLASIA		HP:0012300	OMIM:274265	TAS				P		HPO:probinson	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:274270	IEA				I		HPO:iea	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000252	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000568	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000589	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000639	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000648	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000717	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000750	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0000752	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001249	OMIM:274270	TAS				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001250	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001252	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001254	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001270	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001274	OMIM:274270	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001276	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:274270	TAS				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001508	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0001510	OMIM:274270	TAS				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0002059	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0002445	OMIM:274270	IEA				P		HPO:skoehler	
OMIM	274270	DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY		HP:0003654	OMIM:274270	IEA				P		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:274300	IEA				I		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0000365	OMIM:274300	IEA				P		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0000520	OMIM:274300	IEA				P		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0000853	OMIM:274300	IEA				P		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0001518	OMIM:274300	IEA				P		HPO:skoehler	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0002930	OMIM:274300	IEA				P		HPO:iea	
OMIM	274300	THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE		HP:0010655	OMIM:274300	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0000007	OMIM:274400	IEA				I		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0000158	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0000821	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0000853	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0000958	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0001249	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0001254	OMIM:274400	IEA				P		HPO:skoehler	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0001510	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0001537	OMIM:274400	IEA				P		HPO:iea	
OMIM	274400	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 1		HP:0002019	OMIM:274400	IEA				P		HPO:iea	
OMIM	274500	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A		HP:0000007	OMIM:274500	IEA				I		HPO:iea	
OMIM	274500	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A		HP:0000821	OMIM:274500	IEA				P		HPO:iea	
OMIM	274500	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A		HP:0000853	OMIM:274500	IEA				P		HPO:iea	
OMIM	274500	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A		HP:0001939	OMIM:274500	IEA				P		HPO:iea	
OMIM	274500	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2A		HP:0008263	OMIM:274500	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0000007	OMIM:274600	IEA				I		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0000853	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0001249	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0001751	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0001939	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0002890	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0008223	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0008527	OMIM:274600	IEA				P		HPO:iea	
OMIM	274600	PENDRED SYNDROME		HP:0008554	OMIM:274600	IEA				P		HPO:iea	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0000007	OMIM:274700	TAS				I		HPO:skoehler	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0000853	OMIM:274700	TAS				P		HPO:skoehler	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0001249	OMIM:274700	TAS				P		HPO:skoehler	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0002890	OMIM:274700	TAS				P		HPO:skoehler	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0008223	OMIM:274700	TAS				P		HPO:skoehler	
OMIM	274700	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 3		HP:0012559	OMIM:274700	TAS				P		HPO:probinson	
OMIM	274800	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4		HP:0000007	OMIM:274800	IEA				I		HPO:iea	
OMIM	274800	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4		HP:0000821	OMIM:274800	IEA				P		HPO:iea	
OMIM	274800	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4		HP:0000853	OMIM:274800	IEA				P		HPO:iea	
OMIM	274800	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4		HP:0001249	OMIM:274800	IEA				P		HPO:iea	
OMIM	274800	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 4		HP:0001510	OMIM:274800	IEA				P		HPO:iea	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0000007	OMIM:274900	IEA				I		HPO:skoehler	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0000821	OMIM:274900	IEA				P		HPO:iea	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0000853	OMIM:274900	IEA				P		HPO:iea	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0001249	OMIM:274900	IEA				P		HPO:iea	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0001510	OMIM:274900	IEA				P		HPO:iea	
OMIM	274900	THYROID HORMONOGENESIS, GENETIC DEFECT IN, 5		HP:0001939	OMIM:274900	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000007	OMIM:275000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000520	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000737	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000752	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000853	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0000975	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001324	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001347	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001438	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001635	OMIM:275000	IEA				P		HPO:skoehler	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001806	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001824	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0001939	OMIM:275000	IEA				P		HPO:iea	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0002591	OMIM:275000	TAS				P		HPO:skoehler	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0100647	OMIM:275000	IEA				P		HPO:skoehler	
OMIM	275000	%275000 GRAVES DISEASE;;GRD;;THYROTOXICOSIS;;HYPERTHYROIDISM, AUTOIMMUNEGRAVES DISEASE, SUSCEPTIBILITY TO, 1, INCLUDED; GRD1, INCLUDED		HP:0200028	OMIM:275000	IEA				P		HPO:skoehler	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0000007	OMIM:275100	IEA				I		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0000158	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0000260	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0000851	OMIM:275100	TAS				P		HPO:skoehler	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001252	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001290	OMIM:275100	TAS				P		HPO:skoehler	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001537	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001539	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001615	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0001939	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0005280	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0006887	OMIM:275100	IEA				P		HPO:iea	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0008850	OMIM:275100	TAS				P		HPO:skoehler	
OMIM	275100	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 4		HP:0010864	OMIM:275100	TAS				P		HPO:skoehler	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0000007	OMIM:275120	TAS				I		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0000958	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0001249	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0001324	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0001609	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0002019	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0002750	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0004322	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275120	THYROTROPIN-RELEASING HORMONE DEFICIENCY		HP:0008237	OMIM:275120	TAS				P		HPO:probinson	
OMIM	275190	TIGLIC ACIDEMIA		HP:0000007	OMIM:275190	IEA				I		HPO:iea	
OMIM	275190	TIGLIC ACIDEMIA		HP:0001941	OMIM:275190	IEA				P		HPO:iea	
OMIM	275190	TIGLIC ACIDEMIA		HP:0001946	OMIM:275190	IEA				P		HPO:skoehler	
OMIM	275190	TIGLIC ACIDEMIA		HP:0002574	OMIM:275190	IEA				P		HPO:iea	
OMIM	275190	TIGLIC ACIDEMIA		HP:0003355	OMIM:275190	IEA				P		HPO:skoehler	
OMIM	275200	#275200 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1;;THYROTROPIN RESISTANCE;;THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH;;TSH RESISTANCE;;HYPOTHYROIDISM, NONAUTOIMMUNE;;HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE;;HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN		HP:0000007	OMIM:275200	IEA				I		HPO:iea	
OMIM	275200	#275200 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1;;THYROTROPIN RESISTANCE;;THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH;;TSH RESISTANCE;;HYPOTHYROIDISM, NONAUTOIMMUNE;;HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE;;HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN		HP:0000851	OMIM:275200	IEA				P		HPO:skoehler	
OMIM	275200	#275200 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1;;THYROTROPIN RESISTANCE;;THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH;;TSH RESISTANCE;;HYPOTHYROIDISM, NONAUTOIMMUNE;;HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE;;HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN		HP:0002925	OMIM:275200	TAS				P		HPO:probinson	
OMIM	275200	#275200 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1;;THYROTROPIN RESISTANCE;;THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH;;TSH RESISTANCE;;HYPOTHYROIDISM, NONAUTOIMMUNE;;HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE;;HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN		HP:0003593	OMIM:275200	IEA				C		HPO:iea	
OMIM	275200	#275200 HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 1; CHNG1;;THYROTROPIN RESISTANCE;;THYROID-STIMULATING HORMONE, RESISTANCE TO; RTSH;;TSH RESISTANCE;;HYPOTHYROIDISM, NONAUTOIMMUNE;;HYPOTHYROIDISM, CONGENITAL, DUE TO TSH RESISTANCE;;HYPOTHYROIDISM DUE TO UNRESPONSIVENESS TO THYROTROPIN		HP:0005990	OMIM:275200	IEA				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000007	OMIM:275210	IEA				I		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000047	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000073	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000160	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000176	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000239	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000316	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000347	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000369	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000377	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000418	OMIM:275210	IEA				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000453	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000561	OMIM:275210	IEA				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000581	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000621	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000653	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000695	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0000835	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001196	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001371	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001425	OMIM:275210	IEA				I		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001511	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001558	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001561	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001622	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001631	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001643	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001788	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001799	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0001838	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0002089	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0002751	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0003826	OMIM:275210	IEA				M		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0005253	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0005474	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0006391	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0006585	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0006645	OMIM:275210	TAS				P		HPO:probinson	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0007394	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0007543	OMIM:275210	IEA				P		HPO:iea	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0011414	OMIM:275210	TAS				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0012478	OMIM:275210	IEA				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0012745	OMIM:275210	TAS				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0031013	OMIM:275210	IEA				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0100840	OMIM:275210	TAS				P		HPO:skoehler	
OMIM	275210	RESTRICTIVE DERMOPATHY, LETHAL		HP:0200041	OMIM:275210	IEA				P		HPO:skoehler	
OMIM	275220	275220 TIBIAL HEMIMELIA;;THM;;TIBIA, ABSENCE OF		HP:0000007	OMIM:275220	IEA				I		HPO:iea	
OMIM	275220	275220 TIBIAL HEMIMELIA;;THM;;TIBIA, ABSENCE OF		HP:0000924	OMIM:275220	IEA				P		HPO:iea	
OMIM	275220	275220 TIBIAL HEMIMELIA;;THM;;TIBIA, ABSENCE OF		HP:0009556	OMIM:275220	TAS				P		HPO:skoehler	
OMIM	275230	275230 TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS		HP:0000007	OMIM:275230	IEA				I		HPO:iea	
OMIM	275230	275230 TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS		HP:0000365	OMIM:275230	IEA				P		HPO:iea	
OMIM	275230	275230 TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS		HP:0000924	OMIM:275230	IEA				P		HPO:iea	
OMIM	275230	275230 TIBIA, ABSENCE OF, WITH CONGENITAL DEAFNESS		HP:0009556	OMIM:275230	TAS				P		HPO:skoehler	
OMIM	275240	TINEA IMBRICATA, SUSCEPTIBILITY TO		HP:0000007	OMIM:275240	IEA				I		HPO:iea	
OMIM	275240	TINEA IMBRICATA, SUSCEPTIBILITY TO		HP:0000951	OMIM:275240	IEA				P		HPO:iea	
OMIM	275240	TINEA IMBRICATA, SUSCEPTIBILITY TO		HP:0001939	OMIM:275240	IEA				P		HPO:iea	
OMIM	275250	TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF		HP:0000007	OMIM:275250	IEA				I		HPO:iea	
OMIM	275250	TONGUE, PIGMENTED FUNGIFORM PAPILLAE OF		HP:0000157	OMIM:275250	IEA				P		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0000007	OMIM:275300	IEA				I		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0000924	OMIM:275300	IEA				P		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0001522	OMIM:275300	IEA				M		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0002110	OMIM:275300	IEA				P		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0006509	OMIM:275300	IEA				P		HPO:iea	
OMIM	275300	TRACHEOBRONCHOMEGALY		HP:0006538	OMIM:275300	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0000007	OMIM:275350	IEA				I		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0000153	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0000737	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001249	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001251	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001254	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001324	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001508	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001875	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001876	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001896	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001972	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0001980	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0002013	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0002014	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0002720	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0002850	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0004315	OMIM:275350	IEA				P		HPO:iea	
OMIM	275350	#275350 TRANSCOBALAMIN II DEFICIENCY;;TC II DEFICIENCY;;TCN2 DEFICIENCY		HP:0012120	OMIM:275350	TAS				P		HPO:skoehler	
OMIM	275355	SQUAMOUS CELL CARCINOMA, HEAD AND NECK		HP:0000007	OMIM:275355	TAS				I		HPO:skoehler	
OMIM	275355	SQUAMOUS CELL CARCINOMA, HEAD AND NECK		HP:0002860	OMIM:275355	TAS				P		HPO:skoehler	
OMIM	275370	TRICARBOXYLIC ACID CYCLE, DEFECT OF		HP:0000007	OMIM:275370	IEA				I		HPO:iea	
OMIM	275370	TRICARBOXYLIC ACID CYCLE, DEFECT OF		HP:0000707	OMIM:275370	IEA				P		HPO:iea	
OMIM	275370	TRICARBOXYLIC ACID CYCLE, DEFECT OF		HP:0002928	OMIM:275370	IEA				P		HPO:iea	
OMIM	275370	TRICARBOXYLIC ACID CYCLE, DEFECT OF		HP:0004898	OMIM:275370	IEA				P		HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000007	PMID:25480986	PCS				I	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000028	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000044	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000527	PMID:16152639	PCS		HP:0040284		P	OLIVER-MCFARLANE SYNDROME	HPO:iea	2/2
OMIM	275400	Oliver-McFarlane syndrome		HP:0000546	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:skoehler	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000580	PMID:2816997	PCS				P	OLIVER-MCFARLANE SYNDROME	HPO:probinson	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000580	PMID:16152639	PCS		HP:0040284		P	OLIVER-MCFARLANE SYNDROME	HP:probinson	2/2
OMIM	275400	Oliver-McFarlane syndrome		HP:0000639	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000823	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0000824	PMID:25480986	PCS		HP:0040284		P	OLIVER-MCFARLANE SYNDROME	HPO:iea	6/6
OMIM	275400	Oliver-McFarlane syndrome		HP:0001249	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0001518	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0001596	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:skoehler	
OMIM	275400	Oliver-McFarlane syndrome		HP:0002460	OMIM:275400	TAS				P	OLIVER-MCFARLANE SYNDROME	HPO:skoehler	
OMIM	275400	Oliver-McFarlane syndrome		HP:0003477	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0003510	OMIM:275400	TAS				P	OLIVER-MCFARLANE SYNDROME	HPO:skoehler	
OMIM	275400	Oliver-McFarlane syndrome		HP:0003693	OMIM:275400	TAS				P	OLIVER-MCFARLANE SYNDROME	HPO:probinson	
OMIM	275400	Oliver-McFarlane syndrome		HP:0004523	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0007818	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275400	Oliver-McFarlane syndrome		HP:0008070	PMID:16152639	PCS		HP:0040284		P	OLIVER-MCFARLANE SYNDROME	HP:probinson	2/2
OMIM	275400	Oliver-McFarlane syndrome		HP:0008736	OMIM:275400	IEA				P	OLIVER-MCFARLANE SYNDROME	HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0000007	OMIM:275450	IEA				I		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0000674	OMIM:275450	IEA				P		HPO:skoehler	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0000968	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0000995	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0001006	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0002164	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0002558	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0006297	OMIM:275450	IEA				P		HPO:iea	
OMIM	275450	275450 TRICHOODONTOONYCHIAL DYSPLASIA WITH BONE DEFICIENCY		HP:0008404	OMIM:275450	TAS				P		HPO:skoehler	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000007	OMIM:275595	IEA				I		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000243	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000248	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000341	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000347	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000414	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0000456	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0001263	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0001783	OMIM:275595	TAS				P		HPO:probinson	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0005487	OMIM:275595	IEA				P		HPO:iea	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0006009	OMIM:275595	TAS				P		HPO:probinson	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0011344	OMIM:275595	TAS				P		HPO:skoehler	
OMIM	275595	275595 TRIGONOBRACHYCEPHALY, BULBOUS BIFID NOSE, MICROGNATHIA, AND ABNORMALITIESOF THE HANDS AND FEET		HP:0011803	OMIM:275595	IEA				P		HPO:skoehler	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000007	OMIM:275630	IEA				I		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000232	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000407	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000486	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000523	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000639	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0000656	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001249	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001251	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001324	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001397	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001596	OMIM:275630	IEA				P		HPO:skoehler	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0001871	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0002240	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0003198	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0007479	OMIM:275630	IEA				P		HPO:iea	
OMIM	275630	CHANARIN-DORFMAN SYNDROME		HP:0008551	OMIM:275630	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0000007	OMIM:275900	IEA				I		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0000316	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0000712	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001156	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001256	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001258	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001260	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001263	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001270	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001272	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001310	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001317	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001347	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001371	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001761	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001765	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0001773	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0002064	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0002307	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0002313	OMIM:275900	IEA				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0002355	OMIM:275900	TAS				P		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0002751	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0003487	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0003693	OMIM:275900	TAS				P		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0004322	OMIM:275900	TAS				P		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0005639	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0006986	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0007340	OMIM:275900	IEA				P		HPO:iea	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0011448	OMIM:275900	TAS				P		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0011449	OMIM:275900	TAS				P		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0011463	OMIM:275900	TAS				C		HPO:probinson	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0012371	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0012385	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	275900	#275900 SPASTIC PARAPLEGIA 20, AUTOSOMAL RECESSIVE; SPG20;;TROYER SYNDROME;;SPASTIC PARAPARESIS, CHILDHOOD-ONSET, WITH DISTAL MUSCLE WASTING;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, TROYER TYPE		HP:0030084	OMIM:275900	TAS				P		HPO:skoehler	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0000007	OMIM:276100	IEA				I		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0000524	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0000992	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0001249	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0001251	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0001288	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0003361	OMIM:276100	IEA				P		HPO:iea	
OMIM	276100	TRYPTOPHANURIA WITH DWARFISM		HP:0003510	OMIM:276100	IEA				P		HPO:iea	
OMIM	276200	T-SUBSTANCE ANOMALY		HP:0000007	OMIM:276200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	276200	T-SUBSTANCE ANOMALY		HP:0001249	OMIM:276200	IEA				P		HPO:iea	
OMIM	276200	T-SUBSTANCE ANOMALY		HP:0001510	OMIM:276200	IEA				P		HPO:iea	
OMIM	276200	T-SUBSTANCE ANOMALY		HP:0001939	OMIM:276200	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0000007	OMIM:276300	IEA				I		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0000957	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0000997	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0001034	OMIM:276300	TAS				P		HPO:skoehler	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0001274	OMIM:276300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0001438	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0001909	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0002665	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0002671	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0002859	OMIM:276300	IEA				P		HPO:skoehler	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0002885	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0002888	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0003006	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0009592	OMIM:276300	IEA				P		HPO:iea	
OMIM	276300	#276300 MISMATCH REPAIR CANCER SYNDROME; MMRCS;;MISMATCH REPAIR DEFICIENCY;;MMR DEFICIENCY;;CHILDHOOD CANCER SYNDROME;;BRAIN TUMOR-POLYPOSIS SYNDROME 1; BTPS1;;BTP1 SYNDROME;;TURCOT SYNDROME;;CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY SYNDROME; CMMRDS		HP:0012174	OMIM:276300	TAS				P		HPO:skoehler	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0000007	OMIM:276600	IEA				I		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0000951	OMIM:276600	IEA				P		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0001249	OMIM:276600	IEA				P		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0001510	OMIM:276600	IEA				P		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0003161	OMIM:276600	IEA				P		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0003231	OMIM:276600	IEA				P		HPO:iea	
OMIM	276600	TYROSINE TRANSAMINASE DEFICIENCY		HP:0007812	OMIM:276600	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0000007	OMIM:276700	IEA				I		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0000083	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0000096	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0000105	OMIM:276700	TAS				P		HPO:skoehler	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0000121	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001394	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001402	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001508	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001541	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001639	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001744	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001892	OMIM:276700	IEA				P		HPO:skoehler	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001928	OMIM:276700	TAS				P		HPO:skoehler	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001943	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0001994	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0002239	OMIM:276700	TAS				P		HPO:probinson	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0002240	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0002590	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0002910	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0003163	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0003231	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0003235	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0003768	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0004298	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0004510	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0004912	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0006254	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0006554	OMIM:276700	IEA				P		HPO:iea	
OMIM	276700	TYROSINEMIA, TYPE I; TYRSN1		HP:0006949	OMIM:276700	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0000007	OMIM:276710	IEA				I		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0001250	OMIM:276710	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0001256	OMIM:276710	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0001392	OMIM:276710	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0003161	OMIM:276710	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0003231	OMIM:276710	IEA				P		HPO:iea	
OMIM	276710	#276710 TYROSINEMIA, TYPE III; TYRSN3;;4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY;;4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY		HP:0003607	OMIM:276710	IEA				P		HPO:iea	
OMIM	276800	TYROSINOSIS		HP:0000007	OMIM:276800	IEA				I		HPO:iea	
OMIM	276800	TYROSINOSIS		HP:0003231	OMIM:276800	IEA				P		HPO:iea	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000007	OMIM:276820	IEA				I		HPO:iea	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000028	PMID:3066902	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000046	PMID:3066902	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000047	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000151	OMIM:276820	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000189	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000218	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000276	PMID:3066902	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000286	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000369	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000431	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000470	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000475	PMID:3066902	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000768	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000884	PMID:3066902	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000885	PMID:3066902	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0000916	PMID:3066902	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001171	OMIM:276820	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001180	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001552	PMID:3066902	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001773	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001798	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001849	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0001964	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002436	OMIM:276820	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002557	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002827	PMID:16826533	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002937	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002980	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002984	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002986	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002987	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0002990	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0003041	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0003070	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0003252	PMID:3066902	PCS		HP:0040284		P		HPO:iea	4/5
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0003498	OMIM:276820	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0003982	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0004231	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0005474	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0005613	PMID:16826533	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0005914	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0006502	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0006585	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0008363	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0008817	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0009104	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0009767	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0009829	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0010173	PMID:16826533	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0010769	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276820	#276820 ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY;;LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS;;AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS;;SCHINZEL PHOCOMELIA SYNDROME		HP:0400004	OMIM:276820	TAS				P		HPO:skoehler	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0000007	OMIM:276821	IEA				I		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0001762	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0001802	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0001817	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0002187	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0002996	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0005648	OMIM:276821	IEA				P		HPO:iea	
OMIM	276821	ULNAR HYPOPLASIA WITH MENTAL RETARDATION		HP:0010501	OMIM:276821	IEA				P		HPO:iea	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0000007	OMIM:276822	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0001180	OMIM:276822	IEA				P		HPO:iea	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0001706	OMIM:276822	IEA				P		HPO:iea	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0001789	OMIM:276822	IEA				P		HPO:iea	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0003811	OMIM:276822	IEA				M		HPO:iea	
OMIM	276822	ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS		HP:0003982	OMIM:276822	TAS				P		HPO:probinson	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0000007	OMIM:276880	IEA				I		HPO:iea	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0000635	OMIM:276880	IEA				P		HPO:iea	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0000639	OMIM:276880	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0000718	OMIM:276880	TAS				P		HPO:probinson	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0001251	OMIM:276880	TAS				P		HPO:skoehler	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0001337	OMIM:276880	TAS				P		HPO:skoehler	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0002286	OMIM:276880	IEA				P		HPO:iea	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0004322	OMIM:276880	IEA				P		HPO:iea	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0006887	OMIM:276880	IEA				P		HPO:iea	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0010864	OMIM:276880	TAS				P		HPO:skoehler	
OMIM	276880	#276880 UROCANASE DEFICIENCY		HP:0012237	OMIM:276880	TAS				P		HPO:probinson	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0000007	OMIM:276900	TAS				I		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0000407	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0000510	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0000550	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0000572	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0001270	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0001425	OMIM:276900	TAS				I		HPO:skoehler	
OMIM	276900	#276900 USHER SYNDROME, TYPE I; USH1;;US1;;RETINITIS PIGMENTOSA AND CONGENITAL DEAFNESSUSHER SYNDROME, TYPE IB, INCLUDED; USH1B, INCLUDED;;USHER SYNDROME, TYPE IA, FORMERLY, INCLUDED; USH1A, FORMERLY, INCLUDED;;USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY, INCLUDED		HP:0008555	OMIM:276900	TAS				P		HPO:skoehler	
OMIM	276901	USHER SYNDROME, TYPE IIA		HP:0000007	OMIM:276901	IEA				I		HPO:iea	
OMIM	276901	USHER SYNDROME, TYPE IIA		HP:0000510	OMIM:276901	IEA				P		HPO:iea	
OMIM	276901	USHER SYNDROME, TYPE IIA		HP:0008527	OMIM:276901	IEA				P		HPO:iea	
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0000007	OMIM:276902	TAS				I		HPO:probinson	
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0000407	OMIM:276902	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0000510	OMIM:276902	TAS				P		HPO:probinson	
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0000662	OMIM:276902	TAS				P		HPO:probinson	
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0001123	OMIM:276902	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0001751	OMIM:276902	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	276902	USHER SYNDROME, TYPE IIIA		HP:0007663	OMIM:276902	TAS				P		HPO:probinson	
OMIM	276904	USHER SYNDROME, TYPE IC		HP:0000007	OMIM:276904	IEA				I		HPO:iea	
OMIM	276904	USHER SYNDROME, TYPE IC		HP:0000510	OMIM:276904	IEA				P		HPO:iea	
OMIM	276904	USHER SYNDROME, TYPE IC		HP:0001756	OMIM:276904	IEA				P		HPO:iea	
OMIM	276904	USHER SYNDROME, TYPE IC	HP:0012829	HP:0008527	OMIM:276904	TAS				P		HPO:probinson	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0000007	OMIM:276950	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0000089	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0000238	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0000925	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0001627	OMIM:276950	TAS				P		HPO:skoehler	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0002023	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0002093	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0002410	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0002878	OMIM:276950	TAS				P		HPO:skoehler	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0003468	OMIM:276950	TAS				P		HPO:skoehler	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0003826	OMIM:276950	TAS				M		HPO:probinson	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0004059	OMIM:276950	TAS				P		HPO:skoehler	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0009777	OMIM:276950	IEA				P		HPO:iea	
OMIM	276950	VACTERL ASSOCIATION WITH HYDROCEPHALUS		HP:0030680	OMIM:276950	IEA				P		HPO:iea	
OMIM	277000	%277000 MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME;;MRKH SYNDROME;;MULLERIAN APLASIA/DYSGENESIS;;VON MAYER-ROKITANSKY-KUSTER ANOMALY;;MRKH ANOMALY;;MRK ANOMALY;;UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA;;CONGENITAL ABSENCE OF UTERUS AND VAGINA; CAUVUROGENITAL ADYSPLASIA, INCLUDED		HP:0000006	OMIM:277000	IEA				I		HPO:iea	
OMIM	277000	%277000 MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME;;MRKH SYNDROME;;MULLERIAN APLASIA/DYSGENESIS;;VON MAYER-ROKITANSKY-KUSTER ANOMALY;;MRKH ANOMALY;;MRK ANOMALY;;UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA;;CONGENITAL ABSENCE OF UTERUS AND VAGINA; CAUVUROGENITAL ADYSPLASIA, INCLUDED		HP:0000007	OMIM:277000	IEA				I		HPO:iea	
OMIM	277000	%277000 MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME;;MRKH SYNDROME;;MULLERIAN APLASIA/DYSGENESIS;;VON MAYER-ROKITANSKY-KUSTER ANOMALY;;MRKH ANOMALY;;MRK ANOMALY;;UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA;;CONGENITAL ABSENCE OF UTERUS AND VAGINA; CAUVUROGENITAL ADYSPLASIA, INCLUDED		HP:0000013	OMIM:277000	IEA				P		HPO:iea	
OMIM	277000	%277000 MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME;;MRKH SYNDROME;;MULLERIAN APLASIA/DYSGENESIS;;VON MAYER-ROKITANSKY-KUSTER ANOMALY;;MRKH ANOMALY;;MRK ANOMALY;;UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA;;CONGENITAL ABSENCE OF UTERUS AND VAGINA; CAUVUROGENITAL ADYSPLASIA, INCLUDED		HP:0000141	OMIM:277000	IEA				P		HPO:skoehler	
OMIM	277000	%277000 MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROME;;MRKH SYNDROME;;MULLERIAN APLASIA/DYSGENESIS;;VON MAYER-ROKITANSKY-KUSTER ANOMALY;;MRKH ANOMALY;;MRK ANOMALY;;UTERUS BIPARTITUS SOLIDUS RUDIMENTARIUS CUM VAGINA SOLIDA;;CONGENITAL ABSENCE OF UTERUS AND VAGINA; CAUVUROGENITAL ADYSPLASIA, INCLUDED		HP:0003250	OMIM:277000	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0000007	OMIM:277100	IEA				I		HPO:iea	
OMIM	277100	VALINEMIA		HP:0001324	OMIM:277100	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0001508	OMIM:277100	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0002013	OMIM:277100	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0002329	OMIM:277100	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0002487	OMIM:277100	IEA				P		HPO:iea	
OMIM	277100	VALINEMIA		HP:0010910	OMIM:277100	TAS				P		HPO:probinson	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000007	OMIM:277150	IEA				I		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000347	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000377	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000483	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000545	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0000692	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0001256	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0001595	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0005033	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0005280	OMIM:277150	IEA				P		HPO:iea	
OMIM	277150	VAN BOGAERT-HOZAY SYNDROME		HP:0009771	OMIM:277150	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000007	OMIM:277170	IEA				I		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000104	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000110	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000175	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000191	OMIM:277170	IEA				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000199	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000204	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000218	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000286	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000316	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000347	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000358	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000369	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000405	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000455	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000565	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0000639	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001156	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001177	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001249	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001252	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001263	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001290	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001320	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001508	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001770	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0001841	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0002419	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0002444	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0004322	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0006145	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0006159	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0009466	OMIM:277170	IEA				P		HPO:iea	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0030084	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277170	OROFACIODIGITAL SYNDROME VI		HP:0100259	OMIM:277170	TAS				P		HPO:skoehler	
OMIM	277175	VASCULAR HYALINOSIS		HP:0000007	OMIM:277175	IEA				I		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0001029	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002024	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002138	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002216	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002243	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002514	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002573	OMIM:277175	IEA				P		HPO:iea	
OMIM	277175	VASCULAR HYALINOSIS		HP:0002617	OMIM:277175	IEA				P		HPO:skoehler	
OMIM	277175	VASCULAR HYALINOSIS		HP:0007777	OMIM:277175	IEA				P		HPO:iea	
OMIM	277180	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF		HP:0000007	OMIM:277180	IEA				I		HPO:iea	
OMIM	277180	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF		HP:0000027	OMIM:277180	IEA				P		HPO:iea	
OMIM	277180	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF		HP:0001425	OMIM:277180	IEA				I		HPO:iea	
OMIM	277200	RIGHT VENTRICULAR HYPOPLASIA, ISOLATED		HP:0000007	OMIM:277200	IEA				I		HPO:iea	
OMIM	277200	RIGHT VENTRICULAR HYPOPLASIA, ISOLATED		HP:0004762	OMIM:277200	IEA				P		HPO:iea	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0000007	PMID:12746394	PCS				I		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0000470	PMID:10742114	PCS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0000902	OMIM:277300	TAS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0001522	OMIM:277300	TAS				M		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0002205	OMIM:277300	TAS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0002751	PMID:12746394	PCS				P		HP:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0002937	OMIM:277300	TAS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003270	PMID:10742114	PCS				P		HP:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003305	OMIM:277300	TAS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003310	OMIM:277300	TAS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003418	PMID:29765785	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003422	PMID:12746394	PCS				P		HP:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003510	PMID:10742114	PCS				P		HPO:probinson	
OMIM	277300	SPONDYLOCOSTAL DYSOSTOSIS, AUTOSOMAL RECESSIVE 1		HP:0003521	PMID:12746394	PCS				P		HPO:probinson	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000007	OMIM:277320	IEA				I		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000508	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000544	OMIM:277320	TAS				P		HPO:skoehler	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0000602	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0001939	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002027	OMIM:277320	IEA				P		HPO:skoehler	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002578	OMIM:277320	TAS				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0002617	OMIM:277320	IEA				P		HPO:skoehler	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0003270	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0004395	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0005203	OMIM:277320	IEA				P		HPO:iea	
OMIM	277320	VISCERAL MYOPATHY, FAMILIAL, WITH EXTERNAL OPHTHALMOPLEGIA		HP:0009830	OMIM:277320	IEA				P		HPO:skoehler	
OMIM	277350	VITAMIN A METABOLIC DEFECT		HP:0000007	OMIM:277350	IEA				I		HPO:iea	
OMIM	277350	VITAMIN A METABOLIC DEFECT		HP:0000662	OMIM:277350	IEA				P		HPO:iea	
OMIM	277350	VITAMIN A METABOLIC DEFECT		HP:0004905	OMIM:277350	IEA				P		HPO:iea	
OMIM	277350	VITAMIN A METABOLIC DEFECT		HP:0007462	OMIM:277350	IEA				P		HPO:iea	
OMIM	277350	VITAMIN A METABOLIC DEFECT		HP:0007502	OMIM:277350	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000007	OMIM:277380	IEA				I		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000206	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000218	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000219	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000219	OMIM:277380	TAS				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000286	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000369	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0000988	OMIM:277380	TAS				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001252	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001254	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001263	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001290	OMIM:277380	TAS				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001508	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001873	OMIM:277380	TAS				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001875	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001876	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0001889	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0002156	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0002160	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0002311	OMIM:277380	TAS				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0002912	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003145	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003153	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003223	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003286	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003524	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0003593	OMIM:277380	IEA				C		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0008551	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0008872	OMIM:277380	IEA				P		HPO:iea	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0010280	OMIM:277380	IEA				P		HPO:skoehler	
OMIM	277380	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLF TYPE		HP:0012120	OMIM:277380	IEA				P		HPO:skoehler	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000007	OMIM:277400	IEA				I	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000083	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000093	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000112	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:skoehler	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000238	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000252	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000276	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000319	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000348	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000369	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000400	OMIM:277400	TAS				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000505	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000580	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000639	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000726	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0000790	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001249	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001250	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001252	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001254	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001263	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001290	OMIM:277400	TAS				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:skoehler	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001337	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001508	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001873	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001875	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001889	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001907	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0001942	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0002071	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0002120	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0002156	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0002160	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0002912	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003145	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003153	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003210	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003223	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003286	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003524	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003593	OMIM:277400	TAS		HP:0040282		C	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:probinson	HP:0040282
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0003658	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0005575	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0007663	OMIM:277400	TAS				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:skoehler	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0008872	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:iea	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0012120	OMIM:277400	TAS				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:skoehler	
OMIM	277400	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE; MAHCC		HP:0031258	OMIM:277400	IEA				P	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLC TYPE; MAHCC	HPO:skoehler	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0000007	OMIM:277410	IEA				I		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0000639	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001249	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001250	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001252	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001254	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001263	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001290	OMIM:277410	TAS				P		HPO:skoehler	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001332	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0001889	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0002120	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0002156	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0002160	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0002497	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0002912	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003145	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003210	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003223	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003524	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003593	OMIM:277410	IEA				C		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0003658	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0005518	OMIM:277410	IEA				P		HPO:iea	
OMIM	277410	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLD TYPE		HP:0012120	OMIM:277410	TAS				P		HPO:skoehler	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000007	OMIM:277440	IEA				I		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000670	OMIM:277440	TAS				P		HPO:probinson	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000684	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000737	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000867	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000886	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000893	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0000951	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001252	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001270	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001290	OMIM:277440	TAS				P		HPO:skoehler	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001508	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001510	OMIM:277440	TAS				P		HPO:skoehler	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0001538	OMIM:277440	TAS				P		HPO:probinson	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002007	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002148	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002199	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002289	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002355	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002653	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002663	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002748	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002752	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002753	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002757	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002979	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002980	OMIM:277440	TAS				P		HPO:probinson	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0002982	OMIM:277440	TAS				P		HPO:probinson	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003013	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003020	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003025	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003029	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003106	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003152	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003155	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003165	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003593	OMIM:277440	IEA				C		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0003698	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0004492	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0005469	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0006297	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0009023	OMIM:277440	IEA				P		HPO:iea	
OMIM	277440	VITAMIN D-DEPENDENT RICKETS, TYPE 2A		HP:0010502	OMIM:277440	TAS				P		HPO:probinson	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0000007	OMIM:277450	IEA				I		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0000421	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0000978	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0001892	OMIM:277450	TAS	HP:0003623			P		HPO:probinson	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0003196	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0003645	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0005261	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0009882	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0010655	OMIM:277450	IEA				P		HPO:iea	
OMIM	277450	VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1; VKCFD1		HP:0031364	OMIM:277450	IEA				P		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0000007	OMIM:277460	TAS				I		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0001114	OMIM:277460	TAS				P		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0001251	OMIM:277460	TAS				P		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0001284	OMIM:277460	TAS				P		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0002155	OMIM:277460	TAS				P		HPO:probinson	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0003124	OMIM:277460	TAS				P		HPO:probinson	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0003141	OMIM:277460	TAS				P		HPO:probinson	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0010874	OMIM:277460	TAS				P		HPO:skoehler	
OMIM	277460	VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF		HP:0100513	OMIM:277460	TAS				P		HPO:probinson	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0000007	OMIM:277465	IEA				I		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0000444	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0001249	OMIM:277465	IEA				P		HPO:skoehler	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0001263	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0001510	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0001939	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0002705	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0003621	OMIM:277465	IEA				C		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0005602	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0008706	OMIM:277465	IEA				P		HPO:iea	
OMIM	277465	277465 VITILIGO, PROGRESSIVE, WITH MENTAL RETARDATION AND URETHRAL DUPLICATION		HP:0011463	OMIM:277465	TAS				C		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0000007	OMIM:277470	IEA				I		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0000252	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0000253	OMIM:277470	TAS				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0000505	OMIM:277470	IEA				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0000711	OMIM:277470	TAS	HP:0003577			P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0001250	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0001321	OMIM:277470	IEA				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0001321	OMIM:277470	TAS				P		HPO:probinson	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0002033	OMIM:277470	TAS				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0002120	OMIM:277470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0002171	OMIM:277470	TAS				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0002179	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0002518	OMIM:277470	TAS				P		HPO:skoehler	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0003577	OMIM:277470	IEA				C		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0003819	OMIM:277470	TAS		HP:0040283		M		HPO:skoehler	HP:0040283
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0007308	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0007772	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0008872	OMIM:277470	IEA				P		HPO:iea	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0011344	OMIM:277470	TAS				P		HPO:probinson	
OMIM	277470	PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A		HP:0012110	OMIM:277470	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0000007	OMIM:277480	TAS				I		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0000132	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0000421	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0000978	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0001873	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0001934	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0003010	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0003125	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0003540	OMIM:277480	IEA				P		HPO:probinson	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0004846	OMIM:277480	IEA				P		HPO:skoehler	
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0005261	OMIM:277480	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	277480	VON WILLEBRAND DISEASE, TYPE 3; VWD3		HP:0008330	OMIM:277480	TAS				P		HPO:probinson	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0000006	OMIM:277580	IEA				I		HPO:skoehler	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0000007	OMIM:277580	IEA				I		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0000407	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0000635	OMIM:277580	IEA				P		HPO:skoehler	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0000639	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001053	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001100	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001251	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001252	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001263	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001271	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0001425	OMIM:277580	IEA				I		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002211	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002216	OMIM:277580	IEA				P		HPO:skoehler	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002226	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002227	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002251	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002313	OMIM:277580	IEA				P		HPO:iea	
OMIM	277580	WAARDENBURG-SHAH SYNDROME		HP:0002415	OMIM:277580	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000006	OMIM:277590	IEA				I		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000023	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000028	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000034	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000256	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000278	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000286	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000303	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0000311	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0000316	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000343	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000400	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000486	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000494	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000708	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0000750	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000773	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0000973	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001176	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001212	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001249	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0001250	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001252	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001257	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0001260	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001263	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0001276	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001290	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0001331	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001350	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001377	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001537	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001540	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001761	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001762	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001814	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001816	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0001840	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001845	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0001848	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0002213	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0002650	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0002673	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0002808	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0002834	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0002866	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0003066	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0003186	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0003911	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0004689	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0005280	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0005616	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0006956	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0008070	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0009466	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0009473	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0010300	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0010751	OMIM:277590	TAS				P		HPO:probinson	
OMIM	277590	WEAVER SYNDROME		HP:0011304	OMIM:277590	IEA				P		HPO:iea	
OMIM	277590	WEAVER SYNDROME		HP:0012385	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0030084	OMIM:277590	TAS				P		HPO:skoehler	
OMIM	277590	WEAVER SYNDROME		HP:0200000	OMIM:277590	IEA				P		HPO:skoehler	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000007	PMID:15368195	PCS				I		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000189	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000248	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000327	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000501	PMID:15368195	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000586	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000594	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000618	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000692	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0000885	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001083	PMID:15368195	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001156	PMID:15368195	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001169	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001230	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001256	OMIM:277600	IEA		HP:0040284		P		HPO:skoehler	11%
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001387	PMID:15368195	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001629	OMIM:277600	IEA				P		HPO:skoehler	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001642	PMID:15368195	PCS		HP:0040284		P		HPO:skoehler	2/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001643	OMIM:277600	IEA				P		HPO:skoehler	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001650	PMID:15368195	PCS		HP:0040284		P		HPO:skoehler	2/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001653	OMIM:277600	IEA				P		HPO:skoehler	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0001783	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0002650	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0002682	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0002753	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0002938	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0003416	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0003508	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0004322	PMID:15368195	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0005280	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0006482	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0009768	OMIM:277600	IEA				P		HPO:iea	
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0011003	PMID:15368195	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	277600	WEILL-MARCHESANI SYNDROME, AUTOSOMAL RECESSIVE		HP:0030961	PMID:15368195	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	277700	WERNER SYNDROME; WRN		HP:0000007	OMIM:277700	IEA				I		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000135	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000444	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000518	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000546	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000819	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0000939	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0001595	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0002669	OMIM:277700	TAS				P		HPO:probinson	
OMIM	277700	WERNER SYNDROME; WRN		HP:0002858	OMIM:277700	TAS				P		HPO:skoehler	
OMIM	277700	WERNER SYNDROME; WRN		HP:0004322	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0005177	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0005328	OMIM:277700	TAS				P		HPO:skoehler	
OMIM	277700	WERNER SYNDROME; WRN		HP:0007618	OMIM:277700	IEA				P		HPO:iea	
OMIM	277700	WERNER SYNDROME; WRN		HP:0100324	OMIM:277700	IEA				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000007	OMIM:277720	IEA				I		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000023	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000160	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000171	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000211	OMIM:277720	TAS				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000218	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000272	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000286	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000316	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000343	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000346	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000347	OMIM:277720	TAS				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000426	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000430	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000470	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000506	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000508	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0000581	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0001762	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0002751	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0002987	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0003044	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0006380	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0009465	OMIM:277720	IEA				P		HPO:iea	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0010751	OMIM:277720	IEA				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0011800	OMIM:277720	TAS				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0012385	OMIM:277720	TAS				P		HPO:skoehler	
OMIM	277720	WHISTLING FACE SYNDROME, RECESSIVE FORM		HP:0012745	OMIM:277720	TAS				P		HPO:skoehler	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0000007	OMIM:277730	IEA				I		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0000508	OMIM:277730	IEA				P		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0000602	OMIM:277730	IEA				P		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0000666	OMIM:277730	IEA				P		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0000709	OMIM:277730	TAS				P		HPO:skoehler	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0001251	OMIM:277730	IEA				P		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0001259	OMIM:277730	TAS				P		HPO:skoehler	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0001271	OMIM:277730	IEA				P		HPO:iea	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0002354	OMIM:277730	TAS				P		HPO:skoehler	
OMIM	277730	WERNICKE-KORSAKOFF SYNDROME		HP:0031258	OMIM:277730	IEA				P		HPO:skoehler	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0000007	OMIM:277740	IEA				I		HPO:iea	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0000316	OMIM:277740	IEA				P		HPO:iea	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0001631	OMIM:277740	IEA				P		HPO:iea	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0002211	OMIM:277740	IEA				P		HPO:iea	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0002290	OMIM:277740	IEA				P		HPO:skoehler	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0002780	OMIM:277740	TAS				P		HPO:skoehler	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0007457	OMIM:277740	IEA				P		HPO:iea	
OMIM	277740	WHITE FORELOCK WITH MALFORMATIONS		HP:0010185	OMIM:277740	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000007	OMIM:277900	IEA				I		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000093	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000124	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000726	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000751	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000787	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000829	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000934	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0000939	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001259	OMIM:277900	IEA				P		HPO:skoehler	
OMIM	277900	WILSON DISEASE		HP:0001260	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001271	OMIM:277900	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	277900	WILSON DISEASE		HP:0001332	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001337	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001382	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001394	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001399	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0001402	OMIM:277900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	277900	WILSON DISEASE		HP:0001878	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002015	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002040	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002150	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002240	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002275	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002307	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002749	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0002758	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0003076	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0003109	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0003355	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0007327	OMIM:277900	IEA				P		HPO:iea	
OMIM	277900	WILSON DISEASE		HP:0010838	OMIM:277900	TAS				P		HPO:skoehler	
OMIM	277900	WILSON DISEASE		HP:0200032	OMIM:277900	IEA		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	277900	WILSON DISEASE		HP:0200122	OMIM:277900	TAS				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0000212	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0000280	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0003040	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0007957	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0009134	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0040160	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277950	#277950 WINCHESTER SYNDROME; WNCHRS		HP:0045039	OMIM:277950	IEA				P		HPO:skoehler	
OMIM	277990	INTELLECTUAL DISABILITY, WOLFF TYPE		HP:0001249	OMIM:277990	IEA				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0000007	OMIM:278000	IEA				I		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001394	OMIM:278000	TAS				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001395	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001397	OMIM:278000	TAS				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001433	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001508	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001522	OMIM:278000	IEA				M		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001538	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001744	OMIM:278000	TAS				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0001922	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002013	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002014	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002040	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002092	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002155	OMIM:278000	TAS				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002240	OMIM:278000	TAS				P		HPO:skoehler	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0002570	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0003124	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0004333	OMIM:278000	IEA				P		HPO:iea	
OMIM	278000	LYSOSOMAL ACID LIPASE DEFICIENCY		HP:0010512	OMIM:278000	IEA				P		HPO:skoehler	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0000007	OMIM:278100	IEA				I		HPO:iea	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0001510	OMIM:278100	IEA				P		HPO:iea	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0001927	OMIM:278100	PCS				P		HPO:probinson	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0002013	OMIM:278100	IEA				P		HPO:iea	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0002630	OMIM:278100	PCS				P		HPO:probinson	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0010512	OMIM:278100	PCS				P		HPO:probinson	
OMIM	278100	WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS		HP:0010981	OMIM:278100	PCS				P		HPO:probinson	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0000006	OMIM:278150	IEA				I		HPO:iea	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0000007	OMIM:278150	IEA				I		HPO:skoehler	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0000535	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0000653	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0001006	OMIM:278150	IEA				P		HPO:skoehler	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0001803	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0001807	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0002208	OMIM:278150	IEA				P		HPO:skoehler	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0002209	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0002215	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0002224	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0002286	OMIM:278150	IEA				P		HPO:iea	
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0011359	OMIM:278150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278150	HYPOTRICHOSIS 8; HYPT8		HP:0025249	OMIM:278150	IEA				P		HPO:skoehler	
OMIM	278200	WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS		HP:0000007	OMIM:278200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	278200	WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS		HP:0000232	OMIM:278200	TAS				P		HPO:skoehler	
OMIM	278200	WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS		HP:0000411	OMIM:278200	TAS				P		HPO:skoehler	
OMIM	278200	WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS		HP:0001006	OMIM:278200	TAS				P		HPO:skoehler	
OMIM	278200	WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS		HP:0002224	OMIM:278200	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000007	OMIM:278250	IEA				I		HPO:iea	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000023	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000028	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000218	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000252	OMIM:278250	IEA				P		HPO:iea	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000253	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000260	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000270	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000286	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000316	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000319	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000343	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000369	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000431	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000494	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000670	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000684	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000691	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000750	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000767	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0000938	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001249	OMIM:278250	IEA				P		HPO:iea	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001252	OMIM:278250	TAS				P		HPO:probinson	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001374	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001382	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001508	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001537	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001611	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001762	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001763	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001788	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001799	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001808	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0001869	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0002645	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0002650	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0002808	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0002812	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0003100	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0003160	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0003691	OMIM:278250	TAS				P		HPO:probinson	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0004322	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0006191	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0007414	OMIM:278250	IEA				P		HPO:iea	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0007517	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0008070	OMIM:278250	TAS				P		HPO:skoehler	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0009004	OMIM:278250	IEA				P		HPO:iea	
OMIM	278250	#278250 WRINKLY SKIN SYNDROME; WSS		HP:0011995	OMIM:278250	TAS				P		HPO:probinson	
OMIM	278300	XANTHINURIA, TYPE I		HP:0000007	OMIM:278300	IEA				I		HPO:iea	
OMIM	278300	XANTHINURIA, TYPE I		HP:0000126	OMIM:278300	IEA				P		HPO:iea	
OMIM	278300	XANTHINURIA, TYPE I		HP:0000804	OMIM:278300	IEA				P		HPO:iea	
OMIM	278300	XANTHINURIA, TYPE I		HP:0001939	OMIM:278300	IEA				P		HPO:iea	
OMIM	278300	XANTHINURIA, TYPE I		HP:0003198	OMIM:278300	IEA				P		HPO:iea	
OMIM	278300	XANTHINURIA, TYPE I		HP:0003534	OMIM:278300	TAS				P		HPO:skoehler	
OMIM	278300	XANTHINURIA, TYPE I		HP:0010933	PMID:9153281	PCS				P		HP:probinson	
OMIM	278300	XANTHINURIA, TYPE I		HP:0010934	OMIM:278300	TAS				P		HPO:skoehler	
OMIM	278300	XANTHINURIA, TYPE I		HP:0012330	OMIM:278300	TAS				P		HPO:skoehler	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000007	OMIM:278700	IEA				I		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000252	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000407	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000491	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000509	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000613	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000621	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000656	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0000992	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001009	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001029	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001249	OMIM:278700	PCS				P		HPO:probinson	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001251	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001257	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001265	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001266	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0001268	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0002861	OMIM:278700	IEA				P		HPO:skoehler	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0003079	OMIM:278700	IEA				P		HPO:iea	
OMIM	278700	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP A; XPA		HP:0004334	OMIM:278700	IEA				P		HPO:iea	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000007	OMIM:278720	TAS				I		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000491	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000509	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000613	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000621	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000656	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0000992	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0001009	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0001010	OMIM:278720	TAS				P		HPO:skoehler	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0001029	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0002671	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0003079	OMIM:278720	IEA				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0004334	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0006739	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0011463	OMIM:278720	TAS				C		HPO:probinson	
OMIM	278720	#278720 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC;;XPCC;;XP, GROUP C;;XERODERMA PIGMENTOSUM III; XP3		HP:0012056	OMIM:278720	TAS				P		HPO:probinson	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000007	OMIM:278730	IEA				I		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000252	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000407	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000491	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000509	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000518	OMIM:278730	IEA				P		HPO:skoehler	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000568	OMIM:278730	TAS				P		HPO:skoehler	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000613	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000621	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000656	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0000992	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001009	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001029	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001097	OMIM:278730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001249	OMIM:278730	PCS				P		HPO:probinson	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001251	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001257	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001265	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001266	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0001268	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0002861	OMIM:278730	IEA				P		HPO:skoehler	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0003079	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0004334	OMIM:278730	IEA				P		HPO:iea	
OMIM	278730	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD		HP:0011496	OMIM:278730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000007	OMIM:278740	IEA				I		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000491	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000509	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000613	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000621	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000656	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0000992	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0001009	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0001029	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0002671	OMIM:278740	TAS				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0002861	OMIM:278740	TAS				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0003079	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0004334	OMIM:278740	IEA				P		HPO:probinson	
OMIM	278740	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP E		HP:0006739	OMIM:278740	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000007	OMIM:278750	TAS				I		HPO:skoehler	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000491	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000509	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000613	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000621	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000656	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0000992	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0001009	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0001029	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0002671	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0002860	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0004334	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278750	#278750 XERODERMA PIGMENTOSUM, VARIANT TYPE; XPV;;XERODERMA PIGMENTOSUM WITH NORMAL DNA REPAIR RATES;;PHOTOSENSITIVITY WITH DEFECTIVE DNA SYNTHESIS		HP:0012056	OMIM:278750	TAS				P		HPO:probinson	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000007	OMIM:278760	IEA				I		HPO:iea	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000252	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000365	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000483	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000490	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000639	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000726	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0000992	OMIM:278760	IEA				P		HPO:skoehler	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0001249	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0001251	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0001337	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0001371	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0002011	OMIM:278760	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0002650	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0003079	OMIM:278760	TAS				P		HPO:skoehler	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0004322	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0004325	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0007587	OMIM:278760	IEA				P		HPO:skoehler	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0012444	OMIM:278760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0031287	OMIM:278760	IEA				P		HPO:skoehler	
OMIM	278760	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF		HP:0200034	OMIM:278760	IEA				P		HPO:skoehler	
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0000007	OMIM:278780	TAS				I		HPO:iea	
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0000252	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0000518	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0000568	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0000992	OMIM:278780	TAS				P		HPO:skoehler	
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0001251	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0001257	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0001337	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0001510	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0001761	OMIM:278780	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0003079	OMIM:278780	TAS				P		HPO:iea	
OMIM	278780	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG		HP:0003828	OMIM:278780	TAS				C		HPO:skoehler	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000007	OMIM:278800	IEA				I		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000252	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000407	OMIM:278800	TAS				P		HPO:probinson	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000491	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000509	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000613	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000621	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000656	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0000992	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001009	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001029	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001249	OMIM:278800	TAS				P		HPO:probinson	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001251	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001257	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001265	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001266	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001268	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001272	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0001284	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0002542	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0002861	OMIM:278800	IEA				P		HPO:skoehler	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0003079	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0003510	OMIM:278800	TAS				P		HPO:probinson	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0004334	OMIM:278800	IEA				P		HPO:iea	
OMIM	278800	DE SANCTIS-CACCHIONE SYNDROME		HP:0008639	OMIM:278800	IEA				P		HPO:iea	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000006	OMIM:278850	TAS				I		HPO:iea	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000013	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000027	OMIM:278850	TAS				P		HPO:iea	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000046	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000048	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000051	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0000054	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0008726	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0010459	OMIM:278850	TAS				P		HPO:iea	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0012245	OMIM:278850	IEA				P		HPO:skoehler	
OMIM	278850	46,XX SEX REVERSAL 2		HP:0012861	OMIM:278850	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	278850	46,XX SEX REVERSAL 2		HP:0040171	OMIM:278850	TAS				P		HPO:skoehler	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0000007	OMIM:278900	IEA				I		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0000252	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0000365	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0000618	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0001250	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0001252	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0001266	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0001290	OMIM:278900	TAS				P		HPO:skoehler	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0001939	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0002119	OMIM:278900	IEA				P		HPO:iea	
OMIM	278900	XYLOSIDASE DEFICIENCY		HP:0002521	OMIM:278900	IEA				P		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0000007	OMIM:279000	IEA				I		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0000027	OMIM:279000	IEA				P		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0002110	OMIM:279000	IEA				P		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0002837	OMIM:279000	IEA				P		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0005425	OMIM:279000	IEA				P		HPO:iea	
OMIM	279000	YOUNG SYNDROME		HP:0010959	OMIM:279000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000007	OMIM:280000	IEA				I		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000074	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000081	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000126	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000154	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000175	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000179	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000248	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000286	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000316	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000322	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000396	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000405	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000431	OMIM:280000	TAS				P		HPO:probinson	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000465	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000480	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000687	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0000972	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001176	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001249	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001250	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001252	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001290	OMIM:280000	TAS				P		HPO:skoehler	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001357	OMIM:280000	TAS				P		HPO:nvasilevsky	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001507	PMID:22444671	TAS				P		HPO:nvasilevsky	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001520	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001629	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001636	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001669	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0001833	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002007	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002059	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002136	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002213	OMIM:280000	IEA				P		HPO:skoehler	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002557	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0002562	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0004209	OMIM:280000	TAS				P		HPO:probinson	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0004969	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0005280	OMIM:280000	TAS				P		HPO:probinson	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0006721	OMIM:280000	IEA		HP:0040284		P		HPO:iea	1/7
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0008070	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0008760	OMIM:280000	IEA				P		HPO:iea	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0009185	OMIM:280000	TAS				P		HPO:nvasilevsky	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0009473	OMIM:280000	IEA				P		HPO:skoehler	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0011220	OMIM:280000	TAS				P		HPO:skoehler	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0012385	OMIM:280000	IEA				P		HPO:skoehler	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0012471	OMIM:280000	TAS				P		HPO:nvasilevsky	
OMIM	280000	ZUNICH NEUROECTODERMAL SYNDROME		HP:0100040	PMID:8893234	TAS				P		HPO:nvasilevsky	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000028	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000047	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000175	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000204	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000218	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000219	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000219	OMIM:300000	TAS				P		HPO:skoehler	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000316	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000319	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000349	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000431	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000463	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0000506	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001263	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001274	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001419	OMIM:300000	IEA				I		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001425	OMIM:300000	TAS				I		HPO:skoehler	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001627	OMIM:300000	TAS				P		HPO:skoehler	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0001739	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0002007	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0002015	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0002020	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0002023	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0002835	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0006783	OMIM:300000	IEA				P		HPO:iea	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0011220	OMIM:300000	TAS				P		HPO:skoehler	
OMIM	300000	OPITZ GBBB SYNDROME, TYPE I; GBBB1		HP:0030680	OMIM:300000	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000028	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000047	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000110	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000187	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000218	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000252	OMIM:300004	TAS				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000280	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000294	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000336	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000411	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000486	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000505	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000639	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000648	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0000664	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001007	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001090	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001182	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001250	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001263	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001274	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001274	OMIM:300004	TAS				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001319	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001417	OMIM:300004	IEA				I		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001795	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0001845	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0002445	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0002510	OMIM:300004	TAS				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0002650	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0003121	OMIM:300004	IEA				P		HPO:iea	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0004322	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0006887	OMIM:300004	IEA				P		HPO:skoehler	
OMIM	300004	#300004 CORPUS CALLOSUM, AGENESIS OF, WITH ABNORMAL GENITALIA;;ACC WITH ABNORMAL GENITALIA;;PROUD SYNDROME		HP:0010864	OMIM:300004	TAS				P		HPO:skoehler	
OMIM	300009	DENT DISEASE 1		HP:0000114	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0000117	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0000121	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0000787	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0001419	OMIM:300009	IEA				I		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002148	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002150	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002653	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002663	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002748	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002749	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002752	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002753	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002757	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002907	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002979	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0002980	OMIM:300009	TAS				P		HPO:probinson	
OMIM	300009	DENT DISEASE 1		HP:0002982	OMIM:300009	TAS				P		HPO:probinson	
OMIM	300009	DENT DISEASE 1		HP:0003013	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003020	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003025	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003029	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003076	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003109	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003126	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0003152	OMIM:300009	IEA				P		HPO:skoehler	
OMIM	300009	DENT DISEASE 1		HP:0003355	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0004322	OMIM:300009	IEA				P		HPO:iea	
OMIM	300009	DENT DISEASE 1		HP:0010502	OMIM:300009	TAS				P		HPO:probinson	
OMIM	300009	DENT DISEASE 1		HP:0012622	OMIM:300009	TAS				P		HPO:probinson	
OMIM	300018	DOSAGE-SENSITIVE SEX REVERSAL		HP:0001417	OMIM:300018	TAS				I		HPO:probinson	
OMIM	300018	DOSAGE-SENSITIVE SEX REVERSAL		HP:0012245	OMIM:300018	TAS				P		HPO:probinson	
OMIM	300029	#300029 RETINITIS PIGMENTOSA 3; RP3;;RETINITIS PIGMENTOSA 15; RP15;;CONE-ROD DEGENERATION, X-LINKED;;CHOROIDORETINAL DEGENERATION WITH RETINAL REFLEX IN HETEROZYGOUS WOMEN		HP:0000510	OMIM:300029	IEA				P		HPO:skoehler	
OMIM	300029	#300029 RETINITIS PIGMENTOSA 3; RP3;;RETINITIS PIGMENTOSA 15; RP15;;CONE-ROD DEGENERATION, X-LINKED;;CHOROIDORETINAL DEGENERATION WITH RETINAL REFLEX IN HETEROZYGOUS WOMEN		HP:0000548	OMIM:300029	IEA				P		HPO:skoehler	
OMIM	300029	#300029 RETINITIS PIGMENTOSA 3; RP3;;RETINITIS PIGMENTOSA 15; RP15;;CONE-ROD DEGENERATION, X-LINKED;;CHOROIDORETINAL DEGENERATION WITH RETINAL REFLEX IN HETEROZYGOUS WOMEN		HP:0001417	OMIM:300029	IEA				I		HPO:skoehler	
OMIM	300030	DEAFNESS, X-LINKED 3	HP:0012828	HP:0001419	OMIM:300030	TAS				I		HPO:probinson	
OMIM	300030	DEAFNESS, X-LINKED 3	HP:0012828	HP:0008527	OMIM:300030	TAS				P		HPO:probinson	
OMIM	300042	ALOPECIA, CONGENITAL		HP:0001006	OMIM:300042	TAS				P		HPO:probinson	
OMIM	300042	ALOPECIA, CONGENITAL		HP:0001417	OMIM:300042	TAS				I		HPO:probinson	
OMIM	300042	ALOPECIA, CONGENITAL		HP:0001596	OMIM:300042	TAS				P		HPO:probinson	
OMIM	300046	MENTAL RETARDATION, X-LINKED 23		HP:0001249	OMIM:300046	TAS				P		HPO:probinson	
OMIM	300046	MENTAL RETARDATION, X-LINKED 23		HP:0001419	OMIM:300046	TAS				I		HPO:probinson	
OMIM	300047	MENTAL RETARDATION, X-LINKED 20		HP:0001249	OMIM:300047	IEA				P		HPO:iea	
OMIM	300047	MENTAL RETARDATION, X-LINKED 20		HP:0001417	OMIM:300047	IEA				I		HPO:iea	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0000126	OMIM:300048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0000316	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0000319	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0000369	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0000494	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0001250	OMIM:300048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0001264	OMIM:300048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0001419	OMIM:300048	PCS				I		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0001643	OMIM:300048	TAS				P		HPO:skoehler	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0001873	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED	HP:0012825	HP:0001999	OMIM:300048	TAS				P		HPO:skoehler	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0002013	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0002021	OMIM:300048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0002566	OMIM:300048	TAS				P		HPO:skoehler	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0003270	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0003593	OMIM:300048	PCS				C		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0004389	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0008872	OMIM:300048	PCS				P		HPO:probinson	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0011877	OMIM:300048	TAS				P		HPO:skoehler	
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0030889	OMIM:300048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300048	INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED		HP:0040309	OMIM:300048	TAS				P		HPO:skoehler	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001250	OMIM:300049	TAS				P		HPO:skoehler	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001256	OMIM:300049	IEA				P		HPO:iea	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001297	OMIM:300049	TAS				P		HPO:skoehler	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001423	OMIM:300049	IEA				I		HPO:iea	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001643	OMIM:300049	IEA				P		HPO:iea	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0001647	OMIM:300049	TAS				P		HPO:skoehler	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0002269	OMIM:300049	IEA				P		HPO:iea	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0002282	OMIM:300049	TAS				P		HPO:skoehler	
OMIM	300049	#300049 HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT;;HETEROTOPIA, FAMILIAL NODULAR;;PERIVENTRICULAR NODULAR HETEROTOPIA 1; PVNH1;;NODULAR HETEROTOPIA, BILATERAL PERIVENTRICULAR; NHBP; BPNHHETEROTOPIA, PERIVENTRICULAR NODULAR, WITH FRONTOMETAPHYSEAL DYSPLASIA,INCLUDED		HP:0003256	OMIM:300049	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000053	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000164	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000218	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000252	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000297	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000347	OMIM:300055	TAS				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000400	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000470	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000709	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0000750	OMIM:300055	TAS				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001250	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001251	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001256	OMIM:300055	IEA				P		HPO:skoehler	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001263	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001266	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001300	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001337	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001347	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001419	OMIM:300055	IEA				I		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0001761	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0002064	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0002307	OMIM:300055	IEA				P		HPO:skoehler	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0002353	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0002362	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0003487	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0003677	OMIM:300055	IEA				C		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0003763	OMIM:300055	IEA				P		HPO:iea	
OMIM	300055	MENTAL RETARDATION, X-LINKED, SYNDROMIC 13		HP:0003781	OMIM:300055	TAS				P		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0000053	OMIM:300062	IEA				P		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0001250	OMIM:300062	IEA				P		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0001417	OMIM:300062	IEA				I		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0001999	OMIM:300062	IEA				P		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0002342	OMIM:300062	IEA				P		HPO:iea	
OMIM	300062	MENTAL RETARDATION, X-LINKED 14		HP:0002465	OMIM:300062	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0000248	OMIM:300064	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0000280	OMIM:300064	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0001357	OMIM:300064	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0001417	OMIM:300064	IEA				I		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0002007	OMIM:300064	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0002342	OMIM:300064	IEA				P		HPO:iea	
OMIM	300064	300064 MENTAL RETARDATION, X-LINKED, WITH CRANIOFACIAL DYSMORPHISM;;MENTAL RETARDATION, X-LINKED, HYDE-FORSTER TYPE		HP:0011220	OMIM:300064	TAS				P		HPO:skoehler	
OMIM	300066	DEAFNESS, X-LINKED 4		HP:0000407	OMIM:300066	TAS				P		HPO:probinson	
OMIM	300066	DEAFNESS, X-LINKED 4		HP:0001423	OMIM:300066	TAS				I		HPO:probinson	
OMIM	300066	DEAFNESS, X-LINKED 4		HP:0005101	OMIM:300066	TAS				P		HPO:probinson	
OMIM	300066	DEAFNESS, X-LINKED 4		HP:0011463	OMIM:300066	TAS				C		HPO:probinson	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0000054	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0000639	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001249	OMIM:300067	PCS				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001250	OMIM:300067	PCS				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001251	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001257	OMIM:300067	IEA				P		HPO:skoehler	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001260	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001270	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001274	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001302	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001417	OMIM:300067	IEA				I		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0001522	OMIM:300067	IEA				M		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0002282	OMIM:300067	IEA				P		HPO:skoehler	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0003593	OMIM:300067	TAS				C		HPO:skoehler	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0003829	OMIM:300067	IEA				C		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0008897	OMIM:300067	PCS				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0008936	OMIM:300067	IEA				P		HPO:iea	
OMIM	300067	LISSENCEPHALY, X-LINKED, 1; LISX1		HP:0031882	OMIM:300067	IEA				P		HPO:skoehler	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0000023	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0000066	OMIM:300068	TAS				P		HPO:skoehler	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0000771	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0000786	OMIM:300068	TAS				P		HPO:skoehler	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0001419	OMIM:300068	IEA				I		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0001507	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0002215	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0002225	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0002550	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0002664	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0008232	OMIM:300068	TAS				P		HPO:probinson	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0008730	OMIM:300068	IEA				P		HPO:iea	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0011969	OMIM:300068	TAS				P		HPO:probinson	
OMIM	300068	ANDROGEN INSENSITIVITY SYNDROME		HP:0040314	OMIM:300068	TAS				P		HPO:skoehler	
OMIM	300071	#300071 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A;;CSNB, INCOMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2		HP:0000505	OMIM:300071	IEA				P		HPO:iea	
OMIM	300071	#300071 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A;;CSNB, INCOMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2		HP:0001417	OMIM:300071	TAS				I		HPO:skoehler	
OMIM	300071	#300071 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A;;CSNB, INCOMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2		HP:0001425	OMIM:300071	IEA				I		HPO:iea	
OMIM	300071	#300071 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A;;CSNB, INCOMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2		HP:0007642	OMIM:300071	IEA				P		HPO:iea	
OMIM	300071	#300071 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A;;CSNB, INCOMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2; CSNB2		HP:0007663	OMIM:300071	TAS				P		HPO:skoehler	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0000506	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0000581	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0001274	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0001417	OMIM:300073	IEA				I		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0001561	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0001989	OMIM:300073	TAS				P		HPO:probinson	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0002139	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0002375	OMIM:300073	IEA				P		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0003826	OMIM:300073	IEA				M		HPO:iea	
OMIM	300073	FETAL AKINESIA SYNDROME, X-LINKED		HP:0045025	OMIM:300073	IEA				P		HPO:skoehler	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0000009	OMIM:300076	IEA				P		HPO:iea	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0000662	PMID:7783167	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0001258	OMIM:300076	IEA				P		HPO:skoehler	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED	HP:0012828	HP:0001319	PMID:7783167	PCS				P		HP:probinson	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0001348	PMID:7783167	PCS				P		HPO:iea	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0001423	PMID:7783167	PCS				I		HPO:iea	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0001518	OMIM:300076	IEA				P		HPO:iea	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0003811	PMID:7783167	PCS				M		HPO:probinson	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0008348	PMID:7783167	PCS				P		HPO:probinson	
OMIM	300076	IMMUNONEUROLOGIC DISORDER, X-LINKED		HP:0009073	PMID:7783167	PCS				P		HPO:iea	
OMIM	300082	COGNITIVE FUNCTION 1, SOCIAL		HP:0000707	OMIM:300082	IEA				P		HPO:iea	
OMIM	300085	CONE-ROD DYSTROPHY, X-LINKED, 2		HP:0001417	OMIM:300085	TAS				I		HPO:probinson	
OMIM	300085	CONE-ROD DYSTROPHY, X-LINKED, 2		HP:0008020	OMIM:300085	TAS				P		HPO:probinson	
OMIM	300087	#300087 X INACTIVATION, FAMILIAL SKEWED, 1; SXI1		HP:0005268	OMIM:300087	IEA				P		HPO:skoehler	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0000709	OMIM:300088	IEA				P		HPO:iea	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0000718	OMIM:300088	IEA				P		HPO:iea	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0001249	OMIM:300088	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0001263	OMIM:300088	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0001417	OMIM:300088	IEA				I		HPO:iea	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0002069	OMIM:300088	TAS				P		HPO:probinson	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0002121	OMIM:300088	TAS				P		HPO:probinson	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0002123	OMIM:300088	TAS				P		HPO:probinson	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0002133	OMIM:300088	IEA				P		HPO:iea	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0002376	OMIM:300088	IEA				P		HPO:skoehler	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0003593	OMIM:300088	IEA				C		HPO:iea	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0007359	OMIM:300088	TAS				P		HPO:probinson	
OMIM	300088	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 9; EIEE9		HP:0010819	OMIM:300088	TAS				P		HPO:probinson	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000020	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000135	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000365	OMIM:300100	IEA				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000572	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000618	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000709	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000726	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000802	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000924	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0000953	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001250	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001258	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001271	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001283	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001350	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001417	OMIM:300100	IEA				I		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0001419	OMIM:300100	TAS				I		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002070	OMIM:300100	TAS				P		HPO:probinson	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002078	OMIM:300100	TAS				P		HPO:probinson	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY	HP:0003676	HP:0002180	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002311	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002371	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002385	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002500	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002607	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0002839	OMIM:300100	IEA				P		HPO:iea	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0003455	OMIM:300100	TAS				P		HPO:probinson	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0003676	OMIM:300100	TAS				C		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0007018	OMIM:300100	TAS				P		HPO:skoehler	
OMIM	300100	#300100 ADRENOLEUKODYSTROPHY; ALD;;ADDISON DISEASE AND CEREBRAL SCLEROSIS;;ADRENOMYELONEUROPATHY; AMN;;SIEMERLING-CREUTZFELDT DISEASE;;BRONZE SCHILDER DISEASE;;MELANODERMIC LEUKODYSTROPHY		HP:0008207	OMIM:300100	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX	HP:0012825	HP:0000327	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0000768	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0000894	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0000922	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0000926	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001156	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001216	OMIM:300106	TAS				P		HPO:skoehler	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001230	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001377	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001419	OMIM:300106	IEA				I		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0001773	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0002651	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0002673	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0002808	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0002869	OMIM:300106	TAS				P		HPO:skoehler	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0002938	OMIM:300106	TAS				P		HPO:skoehler	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003025	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003026	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003085	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003180	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003275	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX	HP:0012825	HP:0003311	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003521	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0003988	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0004000	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0004279	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0004573	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0004981	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0005066	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0006009	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0006059	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0006371	OMIM:300106	TAS				P		HPO:skoehler	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0009486	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0009803	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0010049	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0010230	OMIM:300106	IEA				P		HPO:iea	
OMIM	300106	300106 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED;;SEMD, X-LINKED; SEMDX		HP:0011940	OMIM:300106	TAS				P		HPO:probinson	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000276	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000280	OMIM:300114	TAS				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000303	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000486	OMIM:300114	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000494	OMIM:300114	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000708	OMIM:300114	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000716	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000718	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000722	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000729	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0000739	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001250	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001256	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001263	OMIM:300114	TAS				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001290	OMIM:300114	TAS				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001344	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001417	OMIM:300114	IEA				I		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0001419	OMIM:300114	TAS				I		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0002061	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0002073	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0002120	OMIM:300114	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0002650	OMIM:300114	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0007302	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0011800	OMIM:300114	IEA				P		HPO:skoehler	
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0100704	OMIM:300114	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300114	RAYNAUD-CLAES SYNDROME; MRXSRC		HP:0200134	OMIM:300114	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300115	%300115 MENTAL RETARDATION, X-LINKED 50; MRX50		HP:0001256	OMIM:300115	IEA				P		HPO:skoehler	
OMIM	300115	%300115 MENTAL RETARDATION, X-LINKED 50; MRX50		HP:0001417	OMIM:300115	IEA				I		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0000821	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0000824	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0000871	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0001256	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0001263	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0001417	OMIM:300123	IEA				I		HPO:skoehler	
OMIM	300123	#300123 MENTAL RETARDATION, X-LINKED, WITH PANHYPOPITUITARISMMENTAL RETARDATION, X-LINKED, WITH ISOLATED GROWTH HORMONE DEFICIENCY,INCLUDED; MRGH, INCLUDED		HP:0004322	OMIM:300123	IEA				P		HPO:skoehler	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0000613	OMIM:300125	IEA				P		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0001417	OMIM:300125	IEA				I		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0002013	OMIM:300125	IEA				P		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0002018	OMIM:300125	IEA				P		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0002077	OMIM:300125	IEA				P		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0002083	OMIM:300125	IEA				P		HPO:iea	
OMIM	300125	MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2		HP:0002183	OMIM:300125	IEA				P		HPO:iea	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000194	OMIM:300143	TAS				P		HPO:skoehler	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000303	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000316	OMIM:300143	TAS				P		HPO:skoehler	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000582	OMIM:300143	TAS				P		HPO:skoehler	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000664	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000678	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000717	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0000752	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0001250	OMIM:300143	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0001382	OMIM:300143	TAS				P		HPO:skoehler	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0001419	OMIM:300143	TAS				I		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0002342	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0003196	OMIM:300143	TAS				P		HPO:skoehler	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0009909	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300143	#300143 MENTAL RETARDATION, X-LINKED 21; MRX21;;MENTAL RETARDATION, X-LINKED 34; MRX34		HP:0010804	OMIM:300143	TAS				P		HPO:probinson	
OMIM	300147	%300147 PROSTATE CANCER, HEREDITARY, X-LINKED 1; HPCX1;;PROSTATE CANCER SUSCEPTIBILITY, X-LINKED; PCSX		HP:0001417	OMIM:300147	IEA				I		HPO:skoehler	
OMIM	300147	%300147 PROSTATE CANCER, HEREDITARY, X-LINKED 1; HPCX1;;PROSTATE CANCER SUSCEPTIBILITY, X-LINKED; PCSX		HP:0012125	OMIM:300147	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000026	PMID:28055140	PCS		HP:0040284		P		HP:probinson	9/11
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000054	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000175	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000194	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000252	PMID:28055140	PCS		HP:0040284		P		HP:probinson	9/9
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000276	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000343	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000437	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000455	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000486	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000545	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000718	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000750	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000823	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0000824	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001249	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001250	PMID:28055140	PCS		HP:0040284		P		HP:probinson	7/12
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001257	PMID:28055140	PCS		HP:0040284		P		HP:probinson	3/8
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001263	PMID:28055140	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001285	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001290	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001347	PMID:28055140	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001419	PMID:28055140	PCS				I		HP:probinson	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001513	PMID:28055140	PCS	HP:0003593	HP:0040284		P		HP:probinson	8/10
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001518	PMID:28055140	PCS		HP:0040284		P		HP:probinson	6/9
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0001943	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002066	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002079	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002119	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002307	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002355	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002465	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0002540	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0003487	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0003561	PMID:28055140	PCS		HP:0040284		P		HP:probinson	5/7
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0003828	OMIM:300148	IEA				C		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0008936	PMID:28055140	PCS		HP:0040284		P		HP:probinson	3/7
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0400000	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300148	MEHMO SYNDROME; MEHMO		HP:0410030	OMIM:300148	IEA				P		HPO:skoehler	
OMIM	300155	%300155 RETINITIS PIGMENTOSA 24; RP24		HP:0000510	OMIM:300155	IEA	HP:0003621			P		HPO:skoehler	
OMIM	300155	%300155 RETINITIS PIGMENTOSA 24; RP24		HP:0001417	OMIM:300155	IEA				I		HPO:skoehler	
OMIM	300155	%300155 RETINITIS PIGMENTOSA 24; RP24		HP:0008020	OMIM:300155	IEA				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0001288	OMIM:300158	TAS				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0001419	OMIM:300158	TAS				I		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0001763	OMIM:300158	TAS				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0002804	OMIM:300158	IEA				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0003273	OMIM:300158	TAS				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0003680	OMIM:300158	TAS				C		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0006380	OMIM:300158	TAS				P		HPO:skoehler	
OMIM	300158	%300158 ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED; ACLLX;;ARTHROGRYPOSIS, X-LINKED, TYPE V, FORMERLY; AMCX5, FORMERLY		HP:0006466	OMIM:300158	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000028	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000047	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000176	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000193	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000252	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000275	OMIM:300166	TAS				P		HPO:probinson	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000276	OMIM:300166	TAS				P		HPO:probinson	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000343	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000358	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000407	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000426	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000455	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000456	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000482	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000501	OMIM:300166	IEA				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000508	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000519	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000528	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000541	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000568	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000572	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000574	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000577	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000581	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000667	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000677	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000684	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000689	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000821	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0000846	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001153	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001188	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001250	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001256	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001270	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001371	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001423	OMIM:300166	IEA				I		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001537	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001629	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001631	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001634	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001642	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001643	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001650	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001651	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001719	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001762	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0001765	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0002079	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0002313	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0002650	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0002974	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0004322	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0004325	OMIM:300166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0004691	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0006335	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0007733	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0007968	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0010722	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0011069	OMIM:300166	IEA				P		HPO:iea	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0011090	OMIM:300166	TAS				P		HPO:skoehler	
OMIM	300166	MICROPHTHALMIA, SYNDROMIC 2; MCOPS2		HP:0040080	OMIM:300166	IEA				P		HPO:skoehler	
OMIM	300194	ALPORT SYNDROME - INTELLECTUAL DISABILITY - MIDFACE HYPOPLASIA - ELLIPTOCYTOSIS		HP:0001249	OMIM:300194	TAS				P		HPO:skoehler	
OMIM	300194	ALPORT SYNDROME - INTELLECTUAL DISABILITY - MIDFACE HYPOPLASIA - ELLIPTOCYTOSIS		HP:0001466	OMIM:300194	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	300194	ALPORT SYNDROME - INTELLECTUAL DISABILITY - MIDFACE HYPOPLASIA - ELLIPTOCYTOSIS		HP:0004445	OMIM:300194	TAS				P		HPO:skoehler	
OMIM	300194	ALPORT SYNDROME - INTELLECTUAL DISABILITY - MIDFACE HYPOPLASIA - ELLIPTOCYTOSIS		HP:0011800	OMIM:300194	TAS				P		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000007	OMIM:300200	TAS				I		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000027	OMIM:300200	TAS				P		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000028	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000044	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000127	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000798	OMIM:300200	TAS				P		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000823	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000826	OMIM:300200	TAS				P		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000835	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0000953	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0001419	OMIM:300200	IEA				I		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0001508	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0001944	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0002902	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0003560	OMIM:300200	IEA				P		HPO:skoehler	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0004319	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0008163	OMIM:300200	IEA				P		HPO:iea	
OMIM	300200	ADRENAL HYPOPLASIA, CONGENITAL		HP:0008197	OMIM:300200	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000003	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000023	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000054	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000154	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000175	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000218	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000219	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000219	OMIM:300209	TAS				P		HPO:skoehler	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000256	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000268	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000280	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000286	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000316	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000358	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000369	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000445	OMIM:300209	TAS				P		HPO:probinson	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000463	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000470	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000474	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000954	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0000996	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001169	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001182	OMIM:300209	TAS				P		HPO:probinson	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001252	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001290	OMIM:300209	TAS				P		HPO:skoehler	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001374	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001419	OMIM:300209	IEA				I		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001547	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001762	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0001792	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0002002	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0002090	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0002788	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0003196	OMIM:300209	TAS				P		HPO:probinson	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0006610	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0006801	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0006887	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0009381	OMIM:300209	TAS				P		HPO:probinson	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0009466	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0010806	OMIM:300209	IEA				P		HPO:iea	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0010864	OMIM:300209	TAS				P		HPO:skoehler	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0030084	OMIM:300209	TAS				P		HPO:skoehler	
OMIM	300209	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2		HP:0030799	OMIM:300209	TAS				P		HPO:skoehler	
OMIM	300210	MENTAL RETARDATION, X-LINKED 58		HP:0001256	OMIM:300210	IEA				P		HPO:skoehler	
OMIM	300210	MENTAL RETARDATION, X-LINKED 58		HP:0001417	OMIM:300210	IEA				I		HPO:skoehler	
OMIM	300210	MENTAL RETARDATION, X-LINKED 58		HP:0001419	OMIM:300210	TAS				I		HPO:skoehler	
OMIM	300211	%300211 EPISODIC MUSCLE WEAKNESS, X-LINKED; EMWX		HP:0001324	OMIM:300211	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300211	%300211 EPISODIC MUSCLE WEAKNESS, X-LINKED; EMWX		HP:0001417	OMIM:300211	IEA				I		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000054	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000062	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000218	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000219	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000219	OMIM:300215	TAS				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000260	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000343	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000347	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000348	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000369	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000426	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0000431	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001250	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001252	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001257	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001274	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001290	OMIM:300215	TAS				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001302	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001328	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001347	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0001417	OMIM:300215	IEA				I		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0002014	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0002119	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0002171	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0008734	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0008872	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0009921	OMIM:300215	IEA				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0011341	OMIM:300215	TAS				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0011344	OMIM:300215	TAS				P		HPO:skoehler	
OMIM	300215	LISSENCEPHALY, X-LINKED, 2		HP:0012736	OMIM:300215	TAS				P		HPO:skoehler	
OMIM	300216	Coats disease	HP:0012833	HP:0000555	PMID:29567893	PCS				P	COATS DISEASE	HP:probinson	
OMIM	300216	Coats disease		HP:0001428	PMID:10484772	PCS				I	COATS DISEASE	HP:probinson	
OMIM	300216	Coats disease	HP:0012833	HP:0007763	PMID:10484772	PCS				P	COATS DISEASE	HP:probinson	
OMIM	300216	Coats disease	HP:0012833	HP:0012231	PMID:10484772	PCS				P	COATS DISEASE	HP:probinson	
OMIM	300218	SYNDROMIC X-LINKED INTELLECTUAL DISABILITY 7		HP:0001249	OMIM:300218	IEA				P		HPO:skoehler	
OMIM	300228	%300228 TESTICULAR GERM CELL TUMOR 1; TGCT1		HP:0001417	OMIM:300228	IEA				I		HPO:skoehler	
OMIM	300228	%300228 TESTICULAR GERM CELL TUMOR 1; TGCT1		HP:0100728	OMIM:300228	IEA				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000218	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000272	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000280	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000294	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000316	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000369	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000455	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000470	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000543	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000574	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000883	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000884	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000907	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0000926	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001156	OMIM:300232	TAS				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001169	OMIM:300232	IEA				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001250	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001371	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001419	OMIM:300232	IEA				I		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0001769	OMIM:300232	IEA				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002079	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002188	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002645	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002651	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002750	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002812	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002869	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0002942	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0003016	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0003071	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0003071	OMIM:300232	TAS				P		HPO:probinson	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0003311	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0004322	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0005280	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0006028	OMIM:300232	TAS				P		HPO:probinson	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0006423	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0006887	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0008789	OMIM:300232	IEA				P		HPO:iea	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0009381	OMIM:300232	TAS				P		HPO:probinson	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0010585	OMIM:300232	TAS				P		HPO:probinson	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0011800	OMIM:300232	TAS				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0012704	OMIM:300232	TAS				P		HPO:skoehler	
OMIM	300232	300232 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, X-LINKED, WITH MENTAL DETERIORATION;;SEMD, X-LINKED, WITH MENTAL DETERIORATION		HP:0100864	OMIM:300232	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000053	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000179	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000280	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000336	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000400	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000414	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000581	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0000629	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0001328	OMIM:300238	IEA				P		HPO:skoehler	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0001419	OMIM:300238	IEA				I		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0001513	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0002342	OMIM:300238	IEA				P		HPO:iea	
OMIM	300238	MENTAL RETARDATION, X-LINKED, SYNDROMIC 11; MRXS11		HP:0045025	OMIM:300238	IEA				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000020	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000194	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000252	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000275	OMIM:300243	TAS				P		HPO:probinson	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000276	OMIM:300243	TAS				P		HPO:probinson	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000303	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000400	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000486	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000574	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000602	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0000774	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001181	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001238	OMIM:300243	IEA				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001263	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001272	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001290	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001344	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001371	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001423	OMIM:300243	IEA				I		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0001760	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002015	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002078	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002300	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002307	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002360	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002487	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002529	OMIM:300243	IEA				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0002607	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0003189	OMIM:300243	TAS				P		HPO:probinson	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0003202	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0004325	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0006794	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0006887	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0007207	OMIM:300243	IEA				P		HPO:iea	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0010864	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300243	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE		HP:0040082	OMIM:300243	TAS				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000175	OMIM:300244	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000190	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000272	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000286	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000316	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000369	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000506	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000508	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0000612	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001000	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001156	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001159	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001831	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001836	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0001863	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0002828	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0004987	OMIM:300244	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0005011	OMIM:300244	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0010614	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0010660	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0010675	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0011355	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300244	TERMINAL OSSEOUS DYSPLASIA; TOD		HP:0100490	OMIM:300244	IEA				P		HPO:skoehler	
OMIM	300245	%300245 PTOSIS, HEREDITARY CONGENITAL 2;;PTOS2;;PTOSIS, X-LINKED; PTOSX		HP:0000508	OMIM:300245	IEA				P		HPO:skoehler	
OMIM	300245	%300245 PTOSIS, HEREDITARY CONGENITAL 2;;PTOS2;;PTOSIS, X-LINKED; PTOSX		HP:0001423	OMIM:300245	TAS				I		HPO:skoehler	
OMIM	300245	%300245 PTOSIS, HEREDITARY CONGENITAL 2;;PTOS2;;PTOSIS, X-LINKED; PTOSX		HP:0001477	OMIM:300245	IEA				P		HPO:skoehler	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0000505	OMIM:300257	TAS				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:skoehler	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001249	OMIM:300257	TAS		HP:0040284		P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:skoehler	70%
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001263	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001423	OMIM:300257	IEA				I	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001639	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001640	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001644	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001685	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001700	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001716	OMIM:300257	TAS				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:skoehler	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0001761	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0002375	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003236	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003458	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003546	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003700	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003701	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0003710	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:iea	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY		HP:0011675	OMIM:300257	IEA				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:skoehler	
OMIM	300257	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIb; GSD2B, FORMERLY;;GSD IIb, FORMERLY	HP:0012825	HP:0100543	OMIM:300257	TAS				P	#300257 DANON DISEASE;;VACUOLAR CARDIOMYOPATHY AND MYOPATHY, X-LINKED;;PSEUDOGLYCOGENOSIS II;;ANTOPOL DISEASE;;LYSOSOMAL GLYCOGEN STORAGE DISEASE WITHOUT ACID MALTASE DEFICIENCY,FORMERLY;;GLYCOGEN STORAGE DISEASE IIB; GSD2B, FORMERLY;;GSD IIB, FORMERLY	HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000028	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000160	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000164	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000248	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000252	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000256	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000272	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000297	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000369	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000400	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000716	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000739	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0000817	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001249	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001250	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001251	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001344	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001419	OMIM:300260	IEA				I		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0001939	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002015	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002019	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002020	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002063	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002072	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002191	OMIM:300260	TAS				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002205	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0002307	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0003676	OMIM:300260	IEA				C		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0003763	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0005280	OMIM:300260	IEA				P		HPO:iea	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0008947	OMIM:300260	TAS				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0010804	OMIM:300260	TAS				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0011344	OMIM:300260	TAS				P		HPO:probinson	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0011800	OMIM:300260	TAS				P		HPO:skoehler	
OMIM	300260	LUBS X-LINKED MENTAL RETARDATION SYNDROME; MRXSL		HP:0031473	OMIM:300260	IEA				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0000175	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0000272	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0000486	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0000501	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0000518	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0001249	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0001250	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0001419	OMIM:300261	TAS				I		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0001773	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0004322	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0005922	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0011220	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0011800	OMIM:300261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300261	%300261 ARMFIELD X-LINKED MENTAL RETARDATION SYNDROME; MRXSA;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARMFIELD TYPE		HP:0200055	OMIM:300261	TAS				P		HPO:skoehler	
OMIM	300262	X-LINKED INTELLECTUAL DISABILITY, ABIDI TYPE		HP:0001249	OMIM:300262	IEA				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000175	OMIM:300263	IEA				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000276	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000336	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000340	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000455	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000582	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000664	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0000750	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0001176	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0001249	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0001419	OMIM:300263	TAS				I		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0001611	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0001763	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0002162	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0002942	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0010511	OMIM:300263	TAS				P		HPO:skoehler	
OMIM	300263	SIDERIUS X-LINKED MENTAL RETARDATION SYNDROME; MRXSSD		HP:0410030	OMIM:300263	IEA				P		HPO:skoehler	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000012	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000020	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000297	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000327	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000486	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000505	OMIM:300266	TAS				P		HPO:probinson	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000711	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000720	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0000744	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0001249	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0001258	OMIM:300266	IEA				P		HPO:skoehler	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0001347	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0001419	OMIM:300266	TAS				I		HPO:probinson	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0002362	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0002427	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0002445	OMIM:300266	IEA				P		HPO:skoehler	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0002445	OMIM:300266	TAS				P		HPO:probinson	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0002839	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0003487	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0003621	OMIM:300266	IEA				C		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0007210	OMIM:300266	IEA				P		HPO:iea	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0007340	OMIM:300266	TAS				P		HPO:skoehler	
OMIM	300266	SPASTIC PARAPLEGIA 16, X-LINKED		HP:0009882	OMIM:300266	TAS				P		HPO:probinson	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0000119	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0000485	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0001263	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0001397	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0001417	OMIM:300270	IEA				I		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0002019	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0003198	OMIM:300270	IEA				P		HPO:skoehler	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0008207	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0008291	OMIM:300270	IEA				P		HPO:iea	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0011344	OMIM:300270	TAS				P		HPO:skoehler	
OMIM	300270	300270 ADRENOMYODYSTROPHY		HP:0012450	OMIM:300270	TAS				P		HPO:skoehler	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0000256	OMIM:300271	IEA				P		HPO:skoehler	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0000268	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0000276	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0000733	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0000752	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0001249	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0001250	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0001263	OMIM:300271	IEA				P		HPO:iea	
OMIM	300271	MENTAL RETARDATION, X-LINKED 72		HP:0001419	OMIM:300271	IEA				I		HPO:iea	
OMIM	300273	GOITER, MULTINODULAR 2		HP:0000866	OMIM:300273	IEA				P		HPO:iea	
OMIM	300273	GOITER, MULTINODULAR 2		HP:0001423	OMIM:300273	IEA				I		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000232	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000244	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000278	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000336	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000339	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000358	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000369	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000445	OMIM:300280	IEA				P		HPO:skoehler	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000448	OMIM:300280	IEA				P		HPO:skoehler	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000494	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0000664	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001169	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001374	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001419	OMIM:300280	IEA				I		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001608	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001638	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001653	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001714	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001821	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001822	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0001836	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0002355	OMIM:300280	IEA				P		HPO:skoehler	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0002650	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0002808	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0002996	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0003236	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0008075	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0008141	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0009042	OMIM:300280	IEA				P		HPO:iea	
OMIM	300280	URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME; FCMSU		HP:0009473	OMIM:300280	IEA				P		HPO:iea	
OMIM	300291	#300291 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY;;HED-IDECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY, INCLUDED;;EDA-ID, INCLUDED;;HYPER-IGM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMALDYSPLASIA, INCLUDED;;XHM-ED, INCLUDED		HP:0000968	OMIM:300291	IEA				P		HPO:skoehler	
OMIM	300291	#300291 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY;;HED-IDECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY, INCLUDED;;EDA-ID, INCLUDED;;HYPER-IGM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMALDYSPLASIA, INCLUDED;;XHM-ED, INCLUDED		HP:0001419	OMIM:300291	IEA				I		HPO:skoehler	
OMIM	300291	#300291 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY;;HED-IDECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY, INCLUDED;;EDA-ID, INCLUDED;;HYPER-IGM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMALDYSPLASIA, INCLUDED;;XHM-ED, INCLUDED		HP:0002719	OMIM:300291	IEA				P		HPO:skoehler	
OMIM	300291	#300291 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY;;HED-IDECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY, INCLUDED;;EDA-ID, INCLUDED;;HYPER-IGM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMALDYSPLASIA, INCLUDED;;XHM-ED, INCLUDED		HP:0002721	OMIM:300291	TAS				P		HPO:skoehler	
OMIM	300291	#300291 ECTODERMAL DYSPLASIA, HYPOHIDROTIC, WITH IMMUNE DEFICIENCY;;HED-IDECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNE DEFICIENCY, INCLUDED;;EDA-ID, INCLUDED;;HYPER-IGM IMMUNODEFICIENCY, X-LINKED, WITH HYPOHIDROTIC ECTODERMALDYSPLASIA, INCLUDED;;XHM-ED, INCLUDED		HP:0002961	OMIM:300291	IEA				P		HPO:skoehler	
OMIM	300299	#300299 NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX;;XLN		HP:0000951	OMIM:300299	IEA				P		HPO:iea	
OMIM	300299	#300299 NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX;;XLN		HP:0001419	OMIM:300299	IEA				I		HPO:iea	
OMIM	300299	#300299 NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX;;XLN		HP:0001875	OMIM:300299	IEA				P		HPO:iea	
OMIM	300299	#300299 NEUTROPENIA, SEVERE CONGENITAL, X-LINKED; SCNX;;XLN		HP:0002718	OMIM:300299	IEA				P		HPO:iea	
OMIM	300301	#300301 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS,AND LYMPHEDEMA; OLEDAID		HP:0000968	OMIM:300301	IEA				P		HPO:skoehler	
OMIM	300301	#300301 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS,AND LYMPHEDEMA; OLEDAID		HP:0001004	OMIM:300301	IEA				P		HPO:skoehler	
OMIM	300301	#300301 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS,AND LYMPHEDEMA; OLEDAID		HP:0002719	OMIM:300301	IEA				P		HPO:skoehler	
OMIM	300301	#300301 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS,AND LYMPHEDEMA; OLEDAID		HP:0002721	OMIM:300301	IEA				P		HPO:skoehler	
OMIM	300301	#300301 ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH IMMUNODEFICIENCY, OSTEOPETROSIS,AND LYMPHEDEMA; OLEDAID		HP:0011002	OMIM:300301	IEA				P		HPO:skoehler	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0001369	OMIM:300310	IEA				P		HPO:skoehler	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0001417	OMIM:300310	TAS				I		HPO:probinson	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0001954	OMIM:300310	TAS				P		HPO:skoehler	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0002024	OMIM:300310	TAS				P		HPO:probinson	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0002718	OMIM:300310	TAS				P		HPO:probinson	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0003003	OMIM:300310	TAS				P		HPO:probinson	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0004432	OMIM:300310	TAS				P		HPO:probinson	
OMIM	300310	AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2		HP:0005215	OMIM:300310	TAS				P		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0000411	OMIM:300321	IEA				P		HPO:skoehler	
OMIM	300321	FG SYNDROME 2; FGS2	HP:0012825	HP:0000750	PMID:17632775	PCS				P		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0001319	PMID:17632775	TAS				P		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0001417	PMID:17632775	PCS				I		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0002003	PMID:17632775	PCS				P		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0002019	PMID:17632775	PCS				P		HPO:probinson	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0011220	OMIM:300321	IEA				P		HPO:skoehler	
OMIM	300321	FG SYNDROME 2; FGS2		HP:0011246	PMID:17632775	PCS				P		HPO:probinson	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0000029	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0000787	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001249	OMIM:300322	IEA				P		HPO:skoehler	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001252	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001257	OMIM:300322	TAS				P		HPO:probinson	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001260	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001266	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001270	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001290	OMIM:300322	TAS				P		HPO:skoehler	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001332	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001347	OMIM:300322	TAS				P		HPO:probinson	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001419	OMIM:300322	IEA				I		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001854	OMIM:300322	TAS				P		HPO:probinson	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0001889	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0002013	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0002015	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0002071	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0002149	OMIM:300322	IEA				P		HPO:skoehler	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0002179	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0003149	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0004322	OMIM:300322	IEA				P		HPO:iea	
OMIM	300322	LESCH-NYHAN SYNDROME; LNS		HP:0100716	OMIM:300322	IEA				P		HPO:skoehler	
OMIM	300323	GOUT, HPRT-RELATED		HP:0000083	OMIM:300323	TAS				P		HPO:probinson	
OMIM	300323	GOUT, HPRT-RELATED		HP:0000787	OMIM:300323	TAS				P		HPO:probinson	
OMIM	300323	GOUT, HPRT-RELATED		HP:0001419	OMIM:300323	TAS				I		HPO:probinson	
OMIM	300323	GOUT, HPRT-RELATED		HP:0001854	OMIM:300323	TAS				P		HPO:probinson	
OMIM	300323	GOUT, HPRT-RELATED		HP:0002149	OMIM:300323	TAS				P		HPO:probinson	
OMIM	300323	GOUT, HPRT-RELATED		HP:0003149	OMIM:300323	TAS				P		HPO:probinson	
OMIM	300324	MENTAL RETARDATION, X-LINKED 53		HP:0001249	OMIM:300324	TAS				P		HPO:skoehler	
OMIM	300324	MENTAL RETARDATION, X-LINKED 53		HP:0001419	OMIM:300324	TAS				I		HPO:skoehler	
OMIM	300331	THROMBOCYTOSIS, FAMILIAL X-LINKED		HP:0001419	OMIM:300331	IEA				I		HPO:iea	
OMIM	300331	THROMBOCYTOSIS, FAMILIAL X-LINKED		HP:0001744	OMIM:300331	IEA				P		HPO:iea	
OMIM	300331	THROMBOCYTOSIS, FAMILIAL X-LINKED		HP:0001894	OMIM:300331	IEA				P		HPO:iea	
OMIM	300331	THROMBOCYTOSIS, FAMILIAL X-LINKED		HP:0002240	OMIM:300331	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000179	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000252	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000256	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000280	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000286	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000316	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000486	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000518	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0000612	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001159	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001161	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001249	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001250	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001425	OMIM:300337	IEA				I		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001442	OMIM:300337	IEA				I		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001596	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0001939	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0002059	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0002282	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0002650	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0002808	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0005593	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0006316	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0009466	OMIM:300337	IEA				P		HPO:iea	
OMIM	300337	#300337 HYPOMELANOSIS OF ITO; HMI;;INCONTINENTIA PIGMENTI ACHROMIANS; IPA;;ITO HYPOMELANOSIS; ITO;;INCONTINENTIA PIGMENTI, TYPE I, FORMERLY; IP1, FORMERLY		HP:0030084	OMIM:300337	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000098	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000252	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000272	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000275	OMIM:300352	TAS				P		HPO:probinson	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000276	OMIM:300352	TAS				P		HPO:probinson	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000303	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000337	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000508	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000540	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000577	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000718	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000733	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000735	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0000750	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001249	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001250	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001257	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001263	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001270	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001288	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001290	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001319	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001332	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001382	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001419	OMIM:300352	IEA				I		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001508	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001761	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0001939	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002013	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002019	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002058	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002079	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002251	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0002595	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0003593	OMIM:300352	IEA				C		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0004322	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0007018	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0007057	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0008583	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0008872	OMIM:300352	IEA				P		HPO:iea	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0011800	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0012448	OMIM:300352	TAS				P		HPO:skoehler	
OMIM	300352	CREATINE DEFICIENCY SYNDROME, X-LINKED		HP:0025051	PMID:11326334	PCS				P		HP:probinson	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000028	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000047	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000054	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000135	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000154	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000158	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000179	PMID:17236139	PCS		HP:0040284		P		HPO:iea	6/17
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000280	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000303	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000348	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000377	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000414	OMIM:300354	IEA				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000718	PMID:17236139	PCS		HP:0040284		P		HPO:probinson	12/15
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000720	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000750	PMID:17236139	PCS		HP:0040284		P		HPO:probinson	18/18
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000752	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000771	PMID:17236139	PCS		HP:0040284		P		HPO:iea	7/10
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0000823	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001065	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001156	PMID:17273978	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001249	PMID:17236139	PCS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001250	PMID:17236139	PCS	HP:0003593	HP:0040284		P		HPO:probinson	8/11
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001270	PMID:17236139	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001290	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001337	OMIM:300354	PCS		HP:0040284		P		HPO:iea	11/15
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001344	OMIM:300354	IEA				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001388	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001419	PMID:17236139	PCS				I		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001761	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001763	PMID:17236139	PCS		HP:0040284		P		HPO:skoehler	7/8
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001773	PMID:17236139	PCS		HP:0040284		P		HPO:iea	7/14
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0001852	OMIM:300354	IEA				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002066	PMID:17236139	PCS		HP:0040284		P		HPO:iea	6/12
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002079	OMIM:300354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002119	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002126	OMIM:300354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002539	OMIM:300354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0002808	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0003011	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0004322	OMIM:300354	IEA				P		HPO:iea	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0004482	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0005280	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0006855	OMIM:300354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0008734	PMID:17236139	PCS		HP:0040284		P		HPO:iea	10/15
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0008944	PMID:17236139	PCS		HP:0040284		P		HPO:probinson	7/12
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0009879	OMIM:300354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0012743	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	15/19
OMIM	300354	MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC		HP:0200055	OMIM:300354	TAS				P		HPO:skoehler	
OMIM	300355	MENTAL RETARDATION, X-LINKED 73		HP:0000664	OMIM:300355	TAS				P		HPO:skoehler	
OMIM	300355	MENTAL RETARDATION, X-LINKED 73		HP:0001256	OMIM:300355	IEA				P		HPO:skoehler	
OMIM	300355	MENTAL RETARDATION, X-LINKED 73		HP:0001417	OMIM:300355	IEA				I		HPO:skoehler	
OMIM	300355	MENTAL RETARDATION, X-LINKED 73		HP:0001419	OMIM:300355	TAS				I		HPO:skoehler	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0000421	OMIM:300367	IEA				P		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0000967	OMIM:300367	IEA				P		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0000978	OMIM:300367	IEA				P		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0001419	OMIM:300367	IEA				I		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0001905	OMIM:300367	IEA				P		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0001927	OMIM:300367	IEA				P		HPO:skoehler	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0001934	OMIM:300367	TAS				P		HPO:iea	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0003593	OMIM:300367	TAS				C		HPO:skoehler	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0003828	OMIM:300367	TAS				C		HPO:skoehler	
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0004447	OMIM:300367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300367	#300367 THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA;XLTDA		HP:0010972	OMIM:300367	IEA				P		HPO:iea	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000003	OMIM:300373	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000175	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000179	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000193	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000201	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000204	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000218	OMIM:300373	TAS		HP:0040284		P		HPO:skoehler	15%
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000238	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000239	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000256	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000286	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000316	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000341	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000347	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000358	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000369	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000396	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000405	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000431	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000465	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000678	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000689	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000695	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000750	OMIM:300373	IEA		HP:0040284		P		HPO:skoehler	10%
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000767	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0000885	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001166	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001250	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001256	OMIM:300373	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001290	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001338	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001423	PMID:22043478	PCS				I		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001476	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001508	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001539	OMIM:300373	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001561	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001562	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001611	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001629	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001631	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001643	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0001762	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002007	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002020	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002023	OMIM:300373	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002025	OMIM:300373	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002104	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002315	OMIM:300373	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002566	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002650	OMIM:300373	TAS		HP:0040284		P		HPO:skoehler	23%
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002684	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002694	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002779	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0002990	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0003038	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0003298	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0004209	OMIM:300373	TAS				P		HPO:probinson	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0004322	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0005464	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0005619	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0005830	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0005950	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0006587	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0006610	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0006784	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0008551	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0009473	OMIM:300373	IEA				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0010628	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0010740	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300373	OSTEOPATHIA STRIATA WITH CRANIAL SCLEROSIS		HP:0012385	OMIM:300373	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0001265	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0001324	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0001419	OMIM:300376	TAS				I		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0001638	OMIM:300376	TAS	HP:0003584			P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003115	OMIM:300376	IEA				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003236	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003326	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003560	OMIM:300376	IEA				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003581	OMIM:300376	TAS				C		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0003707	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300376	MUSCULAR DYSTROPHY, BECKER TYPE; BMD		HP:0011675	OMIM:300376	TAS				P		HPO:skoehler	
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0000252	OMIM:300387	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0000739	OMIM:300387	TAS				P		HPO:skoehler	
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0001249	OMIM:300387	TAS				P		HPO:probinson	
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0001347	OMIM:300387	TAS				P		HPO:skoehler	
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0001423	OMIM:300387	TAS				I		HPO:skoehler	
OMIM	300387	MENTAL RETARDATION, X-LINKED 63		HP:0002463	OMIM:300387	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0000750	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0001423	OMIM:300388	TAS				I		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0002069	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0002126	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0007024	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0007270	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0010522	OMIM:300388	TAS				P		HPO:skoehler	
OMIM	300388	POLYMICROGYRIA, BILATERAL PERISYLVIAN		HP:0100543	OMIM:300388	TAS				P		HPO:probinson	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0000778	OMIM:300400	TAS				P		HPO:probinson	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0000988	OMIM:300400	IEA				P		HPO:skoehler	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0001419	OMIM:300400	IEA				I		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0001508	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0002028	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0002090	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0002240	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0002841	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0004430	OMIM:300400	TAS				P		HPO:skoehler	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0004432	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0007274	OMIM:300400	IEA				P		HPO:iea	
OMIM	300400	SEVERE COMBINED IMMUNODEFICIENCY, X-LINKED		HP:0009098	OMIM:300400	TAS				P		HPO:probinson	
OMIM	300419	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED		HP:0000629	OMIM:300419	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300419	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED		HP:0000637	OMIM:300419	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300419	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED		HP:0001249	OMIM:300419	TAS				P		HPO:probinson	
OMIM	300419	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED		HP:0001250	OMIM:300419	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300419	MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT SEIZURES, ARX-RELATED		HP:0001419	OMIM:300419	TAS				I		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0000316	PMID:19200522	PCS				P		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0000407	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	4/6
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0000431	PMID:19200522	PCS				P		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0001249	PMID:19200522	PCS				P		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0001250	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0001263	PMID:19200522	PCS				P		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0001319	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0001417	PMID:19200522	PCS				I		HPO:probinson	
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0002650	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0008872	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	300422	#300422 FG SYNDROME 4; FGS4MENTAL RETARDATION, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED		HP:0011220	PMID:19200522	PCS		HP:0040284		P		HPO:probinson	3/8
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0000338	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0000750	OMIM:300423	IEA				P		HPO:iea	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001249	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001265	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001270	OMIM:300423	IEA				P		HPO:iea	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001272	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001288	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001300	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0001419	OMIM:300423	IEA				I		HPO:iea	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002059	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002067	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002069	OMIM:300423	IEA				P		HPO:iea	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002079	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002186	OMIM:300423	IEA				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0002345	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0003487	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0003593	OMIM:300423	IEA				C		HPO:iea	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0003828	OMIM:300423	TAS				C		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0010527	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300423	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH		HP:0011812	OMIM:300423	TAS				P		HPO:skoehler	
OMIM	300424	#300424 RETINITIS PIGMENTOSA 23; RP23		HP:0000510	OMIM:300424	IEA				P		HPO:skoehler	
OMIM	300424	#300424 RETINITIS PIGMENTOSA 23; RP23		HP:0000551	OMIM:300424	TAS				P		HPO:skoehler	
OMIM	300424	#300424 RETINITIS PIGMENTOSA 23; RP23		HP:0001419	OMIM:300424	TAS				I		HPO:skoehler	
OMIM	300424	#300424 RETINITIS PIGMENTOSA 23; RP23		HP:0007787	OMIM:300424	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000717	OMIM:300425	TAS				P		HPO:probinson	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000721	OMIM:300425	IEA				P		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000723	OMIM:300425	TAS				P		HPO:skoehler	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000732	OMIM:300425	IEA				P		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000733	OMIM:300425	TAS				P		HPO:probinson	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000750	OMIM:300425	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0000758	OMIM:300425	IEA				P		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0001249	OMIM:300425	IEA				P		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0001250	OMIM:300425	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0001417	OMIM:300425	IEA				I		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0001425	OMIM:300425	TAS				I		HPO:skoehler	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0001426	OMIM:300425	IEA				I		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0002332	OMIM:300425	IEA				P		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0002353	OMIM:300425	TAS		HP:0040284		P		HPO:probinson	20%
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0003144	OMIM:300425	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0003745	OMIM:300425	IEA				I		HPO:iea	
OMIM	300425	AUTISM, SUSCEPTIBILITY TO, X-LINKED 1; AUTSX1		HP:0011463	OMIM:300425	IEA				C		HPO:iea	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0000053	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0000218	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0000321	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0001249	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0001417	OMIM:300428	TAS				I		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0004322	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0004482	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300428	MENTAL RETARDATION, X-LINKED 2		HP:0007010	OMIM:300428	TAS				P		HPO:skoehler	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000053	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000098	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000179	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000256	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000280	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000316	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000455	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0000494	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001169	OMIM:300431	TAS				P		HPO:probinson	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001182	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001250	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001256	OMIM:300431	TAS				P		HPO:skoehler	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001388	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001423	OMIM:300431	IEA				I		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001513	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001566	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0001593	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002007	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002054	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002650	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002708	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002711	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002808	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002816	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0002857	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0004279	OMIM:300431	TAS				P		HPO:probinson	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0004322	OMIM:300431	IEA				P		HPO:iea	
OMIM	300431	ATKIN-FLAITZ SYNDROME		HP:0011220	OMIM:300431	TAS				P		HPO:skoehler	
OMIM	300433	MENTAL RETARDATION, X-LINKED 81		HP:0001249	OMIM:300433	TAS				P		HPO:skoehler	
OMIM	300433	MENTAL RETARDATION, X-LINKED 81		HP:0001419	OMIM:300433	TAS				I		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0000252	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0000286	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0000316	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0000486	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0000752	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001007	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001250	OMIM:300434	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001263	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001344	OMIM:300434	IEA				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001417	OMIM:300434	TAS				I		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001762	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0001773	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0002020	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0002187	OMIM:300434	IEA				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0002650	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0002808	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0002827	OMIM:300434	IEA				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0003763	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0004322	OMIM:300434	IEA				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0005280	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300434	STOCCO DOS SANTOS X-LINKED MENTAL RETARDATION SYNDROME; SDSX		HP:0200055	OMIM:300434	TAS				P		HPO:skoehler	
OMIM	300436	MENTAL RETARDATION, X-LINKED 46		HP:0000407	OMIM:300436	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300436	MENTAL RETARDATION, X-LINKED 46		HP:0001249	OMIM:300436	TAS				P		HPO:probinson	
OMIM	300436	MENTAL RETARDATION, X-LINKED 46		HP:0001419	OMIM:300436	TAS				I		HPO:probinson	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000407	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000546	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000572	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000639	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000648	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000711	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000713	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000718	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0000750	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001249	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001250	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001252	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001260	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001263	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001266	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001290	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001423	OMIM:300438	IEA				I		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001639	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001942	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0001943	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0002120	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0002344	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0002376	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0002510	OMIM:300438	TAS				P		HPO:skoehler	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0003128	OMIM:300438	IEA				P		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0003593	OMIM:300438	IEA				C		HPO:iea	
OMIM	300438	HSD10 MITOCHONDRIAL DISEASE; HSD10MD		HP:0008322	OMIM:300438	IEA				P		HPO:skoehler	
OMIM	300448	#300448 ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS;;HEMOGLOBIN H DISEASE, ACQUIRED		HP:0002863	PMID:12858175	PCS				P		HPO:probinson	
OMIM	300448	#300448 ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS;;HEMOGLOBIN H DISEASE, ACQUIRED		HP:0004840	PMID:15358626	PCS				P		HPO:probinson	
OMIM	300448	#300448 ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS;;HEMOGLOBIN H DISEASE, ACQUIRED		HP:0011903	PMID:15358626	PCS				P		HPO:probinson	
OMIM	300448	#300448 ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME; ATMDS;;HEMOGLOBIN H DISEASE, ACQUIRED		HP:0011907	PMID:12858175	PCS				P		HPO:probinson	
OMIM	300454	MENTAL RETARDATION, X-LINKED 77		HP:0000752	OMIM:300454	TAS				P		HPO:skoehler	
OMIM	300454	MENTAL RETARDATION, X-LINKED 77		HP:0001249	OMIM:300454	TAS				P		HPO:skoehler	
OMIM	300454	MENTAL RETARDATION, X-LINKED 77		HP:0001419	OMIM:300454	TAS				I		HPO:skoehler	
OMIM	300454	MENTAL RETARDATION, X-LINKED 77		HP:0002373	OMIM:300454	TAS				P		HPO:skoehler	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0000388	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0000510	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0001419	PMID:16055928	PCS				I		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0002837	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0005101	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0005376	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0011109	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300455	#300455 RETINITIS PIGMENTOSA, X-LINKED, AND SINORESPIRATORY INFECTIONS, WITHOR WITHOUT DEAFNESS		HP:0100750	PMID:16055928	PCS				P		HPO:probinson	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0000252	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0000322	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0000490	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0000494	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0000995	OMIM:300471	TAS				P		HPO:probinson	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0001250	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0001419	OMIM:300471	IEA				I		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0001956	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0001999	OMIM:300471	IEA				P		HPO:skoehler	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0002342	OMIM:300471	IEA				P		HPO:iea	
OMIM	300471	CUBITUS VALGUS WITH MENTAL RETARDATION AND UNUSUAL FACIES		HP:0002967	OMIM:300471	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000218	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000256	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000278	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000348	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000369	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000378	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000407	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000470	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000475	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000494	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000505	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000588	OMIM:300472	TAS				P		HPO:probinson	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000612	OMIM:300472	TAS				P		HPO:probinson	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0000767	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0001249	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0001274	OMIM:300472	TAS				P		HPO:probinson	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0001419	OMIM:300472	IEA				I		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0002650	OMIM:300472	IEA				P		HPO:iea	
OMIM	300472	CORPUS CALLOSUM, AGENESIS OF, WITH MENTAL RETARDATION, OCULAR COLOBOMA,AND MICROGNATHIA		HP:0004322	OMIM:300472	IEA				P		HPO:iea	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0000252	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0000407	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0000486	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0000648	OMIM:300475	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001250	OMIM:300475	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001263	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001272	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001332	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001419	OMIM:300475	TAS				I		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001508	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0001999	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0002059	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0002445	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0006808	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0007256	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300475	DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH		HP:0010864	OMIM:300475	TAS				P		HPO:skoehler	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000483	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000541	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000543	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000545	PMID:12807962	PCS				P		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000548	OMIM:300476	IEA				P		HPO:skoehler	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000551	PMID:16505158	PCS				P		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000603	PMID:12807962	PCS				P		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000613	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0000639	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0001419	PMID:16505158	PCS				I		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0007663	OMIM:300476	TAS				P		HPO:skoehler	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0008002	PMID:12807962	PCS				P		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0008323	PMID:16505158	PCS				P		HPO:probinson	
OMIM	300476	CONE-ROD DYSTROPHY, X-LINKED, 3		HP:0030825	OMIM:300476	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000161	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000175	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000218	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000316	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000455	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000456	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000486	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0000506	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0001056	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0001159	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0001263	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0001419	OMIM:300484	TAS				I		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0002100	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0004322	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0005349	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0005736	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0010442	OMIM:300484	TAS				P		HPO:skoehler	
OMIM	300484	OROFACIODIGITAL SYNDROME VIII; OFD8		HP:0010566	OMIM:300484	IEA				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000028	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000046	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000054	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000219	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000219	OMIM:300486	TAS				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000256	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000276	PMID:29960046	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000303	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000322	OMIM:300486	PCS				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000336	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000400	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000486	PMID:29960046	PCS				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000490	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000601	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000639	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000750	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0000752	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001249	OMIM:300486	TAS				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001250	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001252	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001257	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001263	PMID:29960046	PCS				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001290	OMIM:300486	TAS				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001321	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0001419	OMIM:300486	PCS				I		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0002007	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0002066	PMID:29960046	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0002280	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0003189	OMIM:300486	TAS				P		HPO:probinson	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0003593	OMIM:300486	IEA				C		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0006951	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0007065	OMIM:300486	IEA				P		HPO:iea	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0011220	OMIM:300486	TAS				P		HPO:skoehler	
OMIM	300486	MENTAL RETARDATION, X-LINKED, WITH CEREBELLAR HYPOPLASIA AND DISTINCTIVE FACIAL APPEARANCE		HP:0030260	OMIM:300486	TAS				P		HPO:skoehler	
OMIM	300488	MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1		HP:0000818	OMIM:300488	IEA				P		HPO:iea	
OMIM	300488	MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 1		HP:0001423	OMIM:300488	IEA				I		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0000759	OMIM:300489	TAS				P		HPO:skoehler	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0001265	OMIM:300489	IEA				P		HPO:skoehler	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0001419	OMIM:300489	IEA				I		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0001761	OMIM:300489	IEA				P		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0002317	OMIM:300489	IEA				P		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0002460	OMIM:300489	IEA				P		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0002936	OMIM:300489	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0003445	OMIM:300489	IEA				P		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0003621	OMIM:300489	IEA				C		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0003677	OMIM:300489	IEA				C		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0003693	OMIM:300489	IEA				P		HPO:iea	
OMIM	300489	SPINAL MUSCULAR ATROPHY, DISTAL, X-LINKED 3		HP:0007269	OMIM:300489	TAS				P		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0000256	OMIM:300491	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0000718	OMIM:300491	TAS				P		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0000729	OMIM:300491	TAS				P		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0001328	OMIM:300491	IEA				P		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0001419	OMIM:300491	TAS				I		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0001423	OMIM:300491	TAS				I		HPO:skoehler	
OMIM	300491	#300491 EPILEPSY, X-LINKED, WITH VARIABLE LEARNING DISABILITIES AND BEHAVIORDISORDERS		HP:0007359	OMIM:300491	TAS				P		HPO:probinson	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000717	OMIM:300494	IEA				P		HPO:skoehler	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000721	OMIM:300494	IEA				P		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000723	OMIM:300494	TAS				P		HPO:skoehler	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000728	OMIM:300494	IEA				P		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000732	OMIM:300494	IEA				P		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000733	OMIM:300494	TAS				P		HPO:skoehler	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0000758	OMIM:300494	TAS				P		HPO:probinson	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0001417	OMIM:300494	IEA				I		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0001425	OMIM:300494	TAS				I		HPO:skoehler	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0001426	OMIM:300494	IEA				I		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0003621	OMIM:300494	IEA				C		HPO:iea	
OMIM	300494	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 1; ASPGX1		HP:0003745	OMIM:300494	IEA				I		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000717	OMIM:300495	TAS				P		HPO:skoehler	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000721	OMIM:300495	IEA				P		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000723	OMIM:300495	TAS				P		HPO:skoehler	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000732	OMIM:300495	IEA				P		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000733	OMIM:300495	TAS				P		HPO:skoehler	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000750	OMIM:300495	IEA				P		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0000758	OMIM:300495	TAS				P		HPO:skoehler	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0001249	OMIM:300495	IEA				P		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0001250	OMIM:300495	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0001417	OMIM:300495	IEA				I		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0001425	OMIM:300495	TAS				I		HPO:skoehler	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0001426	OMIM:300495	IEA				I		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0002332	OMIM:300495	IEA				P		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0002353	OMIM:300495	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0003144	OMIM:300495	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0003745	OMIM:300495	IEA				I		HPO:iea	
OMIM	300495	AUTISM, SUSCEPTIBILITY TO, X-LINKED 2; AUTSX2		HP:0011463	OMIM:300495	IEA				C		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000717	OMIM:300496	TAS				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000721	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000723	OMIM:300496	TAS				P		HPO:skoehler	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000732	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000733	OMIM:300496	TAS				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000750	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0000758	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0001249	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0001250	OMIM:300496	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0001417	OMIM:300496	IEA				I		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0001425	OMIM:300496	TAS				I		HPO:skoehler	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0001426	OMIM:300496	IEA				I		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0002332	OMIM:300496	IEA				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0002353	OMIM:300496	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0003144	OMIM:300496	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0003745	OMIM:300496	IEA				I		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0005324	OMIM:300496	TAS				P		HPO:iea	
OMIM	300496	AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3		HP:0011463	OMIM:300496	IEA				C		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000717	OMIM:300497	IEA				P		HPO:skoehler	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000721	OMIM:300497	IEA				P		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000723	OMIM:300497	TAS				P		HPO:skoehler	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000728	OMIM:300497	IEA				P		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000732	OMIM:300497	IEA				P		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000733	OMIM:300497	TAS				P		HPO:skoehler	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0000758	OMIM:300497	IEA				P		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0001417	OMIM:300497	IEA				I		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0001425	OMIM:300497	TAS				I		HPO:skoehler	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0001426	OMIM:300497	IEA				I		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0003621	OMIM:300497	IEA				C		HPO:iea	
OMIM	300497	ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2; ASPGX2		HP:0003745	OMIM:300497	TAS				I		HPO:skoehler	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0000218	OMIM:300498	TAS				P		HPO:skoehler	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0000400	PMID:15121780	TAS				P		HPO:probinson	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0000411	OMIM:300498	TAS				P		HPO:skoehler	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0000426	OMIM:300498	TAS				P		HPO:skoehler	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0001249	PMID:15121780	TAS				P		HPO:probinson	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0001419	PMID:15121780	TAS				I		HPO:probinson	
OMIM	300498	MENTAL RETARDATION, X-LINKED 45		HP:0004322	OMIM:300498	TAS				P		HPO:skoehler	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0000505	OMIM:300500	IEA				P		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0000613	OMIM:300500	IEA				P		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0001107	OMIM:300500	TAS				P		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0001361	OMIM:300500	IEA				P		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0001417	OMIM:300500	IEA				I		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0005592	OMIM:300500	IEA				P		HPO:probinson	
OMIM	300500	ALBINISM, OCULAR, TYPE I		HP:0007680	OMIM:300500	IEA				P		HPO:probinson	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0000368	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0000494	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0001249	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0001250	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0001419	OMIM:300504	TAS				I		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0002650	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0003307	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0004209	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300504	MENTAL RETARDATION, X-LINKED 52		HP:0011800	OMIM:300504	TAS				P		HPO:skoehler	
OMIM	300505	MENTAL RETARDATION, X-LINKED 84		HP:0000337	OMIM:300505	TAS				P		HPO:skoehler	
OMIM	300505	MENTAL RETARDATION, X-LINKED 84		HP:0001249	OMIM:300505	TAS				P		HPO:skoehler	
OMIM	300505	MENTAL RETARDATION, X-LINKED 84		HP:0001419	OMIM:300505	TAS				I		HPO:skoehler	
OMIM	300505	MENTAL RETARDATION, X-LINKED 84		HP:0004322	OMIM:300505	TAS				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000006	OMIM:300510	TAS				I		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000013	OMIM:300510	TAS				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000130	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000786	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000815	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000823	OMIM:300510	TAS				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0000869	OMIM:300510	TAS				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0001007	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0008209	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0008209	OMIM:300510	TAS				P		HPO:skoehler	
OMIM	300510	OVARIAN DYSGENESIS 2		HP:0008639	OMIM:300510	IEA				P		HPO:skoehler	
OMIM	300511	PREMATURE OVARIAN FAILURE 2A		HP:0000869	OMIM:300511	TAS				P		HPO:skoehler	
OMIM	300511	PREMATURE OVARIAN FAILURE 2A		HP:0001423	OMIM:300511	TAS				I		HPO:skoehler	
OMIM	300511	PREMATURE OVARIAN FAILURE 2A		HP:0008209	OMIM:300511	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0000104	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0000369	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0001419	PMID:21910217	PCS				I		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0001510	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0001873	OMIM:300514	IEA				P		HPO:skoehler	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0001903	OMIM:300514	TAS				P		HPO:skoehler	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0002101	PMID:21910217	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0002119	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0002575	PMID:21910217	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0003220	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0003468	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0003974	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300514	FANCONI ANEMIA, COMPLEMENTATION GROUP B; FANCB		HP:0009777	PMID:21910217	PCS				P		HPO:probinson	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0000729	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0001249	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0001250	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0001419	OMIM:300518	TAS				I		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0002353	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0002650	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300518	MENTAL RETARDATION, X-LINKED 82		HP:0002808	OMIM:300518	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000028	OMIM:300519	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000048	OMIM:300519	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000054	OMIM:300519	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000083	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000089	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000093	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000154	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000179	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000252	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000272	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000286	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000316	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000347	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000369	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000407	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000431	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000506	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000545	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000689	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0000821	OMIM:300519	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0001009	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0001249	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0001419	OMIM:300519	TAS				I		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0001537	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0001876	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0002557	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0004322	OMIM:300519	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300519	MENTAL RETARDATION, X-LINKED, SYNDROMIC, MARTIN-PROBST TYPE		HP:0006610	OMIM:300519	TAS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000252	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000341	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000395	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000400	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000549	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000737	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000767	PMID:15488219	PCS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0000821	OMIM:300523	IEA				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001251	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001258	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001260	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001319	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001347	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001371	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001423	PMID:15488219	PCS				I		HPO:probinson	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001583	OMIM:300523	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001763	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0001822	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002169	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002188	OMIM:300523	TAS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002305	PMID:15488219	PCS				P		HPO:probinson	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002307	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002415	OMIM:300523	IEA				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002510	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002540	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0002650	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME	HP:0012825	HP:0002925	OMIM:300523	TAS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0003487	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0003577	OMIM:300523	TAS				C		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0003700	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0006887	OMIM:300523	IEA				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0008583	PMID:15488219	PCS				P		HPO:probinson	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0008872	OMIM:300523	TAS				P		HPO:iea	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0010864	OMIM:300523	TAS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0011344	OMIM:300523	TAS				P		HPO:skoehler	
OMIM	300523	ALLAN-HERNDON-DUDLEY SYNDROME		HP:0100015	OMIM:300523	IEA				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000028	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000054	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000218	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000219	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000219	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000221	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000252	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000256	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000297	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000303	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000319	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000327	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000347	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000350	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000400	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000486	OMIM:300534	TAS		HP:0040284		P		HPO:probinson	2/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000490	OMIM:300534	IEA				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000540	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000545	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000582	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000699	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000711	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000718	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000744	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0000767	OMIM:300534	TAS				P		HPO:probinson	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001156	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001176	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001250	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001419	OMIM:300534	IEA				I		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001762	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0001773	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0002229	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0002362	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0002395	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0002705	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0003487	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0004322	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	5/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0006887	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0006895	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0007020	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0008124	OMIM:300534	IEA				P		HPO:iea	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0008734	PMID:18697827	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0008944	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0009882	OMIM:300534	TAS				P		HPO:probinson	
OMIM	300534	#300534 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, JARID1C-RELATED; MRXSJ		HP:0010864	OMIM:300534	TAS				P		HPO:skoehler	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0000737	OMIM:300539	IEA				P		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0001250	OMIM:300539	IEA				P		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0001419	OMIM:300539	IEA				I		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0002902	OMIM:300539	IEA				P		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0003351	OMIM:300539	IEA				P		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0004421	OMIM:300539	IEA				P		HPO:iea	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0012101	OMIM:300539	IEA				P		HPO:skoehler	
OMIM	300539	NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NSIAD		HP:0012605	OMIM:300539	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0000114	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0000117	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0000121	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0000787	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0001419	OMIM:300554	IEA				I		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002148	OMIM:300554	IEA				P		HPO:skoehler	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002150	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002653	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002663	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002748	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002749	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002752	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002753	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002757	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002979	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002980	OMIM:300554	TAS				P		HPO:probinson	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0002982	OMIM:300554	TAS				P		HPO:probinson	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003013	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003020	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003025	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003029	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003126	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0003152	OMIM:300554	IEA				P		HPO:skoehler	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0004322	OMIM:300554	IEA				P		HPO:iea	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0004912	OMIM:300554	TAS				P		HPO:probinson	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0010502	OMIM:300554	TAS				P		HPO:probinson	
OMIM	300554	HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE		HP:0012622	OMIM:300554	TAS				P		HPO:probinson	
OMIM	300555	#300555 DENT DISEASE 2		HP:0000114	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0000121	OMIM:300555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300555	#300555 DENT DISEASE 2		HP:0001263	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0001419	OMIM:300555	TAS				I		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0001537	OMIM:300555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300555	#300555 DENT DISEASE 2		HP:0002150	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0003126	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0003236	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0003355	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0004322	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0011463	OMIM:300555	TAS				C		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0012622	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300555	#300555 DENT DISEASE 2		HP:0100543	OMIM:300555	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000194	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000218	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000219	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000219	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000252	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000400	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000463	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000709	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000711	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000713	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000718	OMIM:300558	PCS				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000736	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000739	OMIM:300558	PCS				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000750	OMIM:300558	PCS				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0000752	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0001249	OMIM:300558	PCS				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0001250	OMIM:300558	IEA				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0001419	OMIM:300558	IEA				I		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0002194	OMIM:300558	PCS				P		HPO:iea	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0002307	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0003196	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0003828	OMIM:300558	TAS				C		HPO:skoehler	
OMIM	300558	#300558 MENTAL RETARDATION, X-LINKED 30; MRX30;;MENTAL RETARDATION, X-LINKED 47; MRX47		HP:0012368	OMIM:300558	TAS				P		HPO:skoehler	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0001324	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0001419	OMIM:300559	IEA				I		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0003202	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0003236	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0003546	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0003738	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0008305	OMIM:300559	IEA				P		HPO:iea	
OMIM	300559	MUSCLE GLYCOGENOSIS, X-LINKED		HP:0008967	OMIM:300559	IEA				P		HPO:iea	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0000218	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0000286	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001250	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001256	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001263	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001344	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001417	OMIM:300577	IEA				I		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001423	OMIM:300577	TAS				I		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001513	OMIM:300577	IEA	HP:0003593			P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001572	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001773	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0001999	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0002162	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0002967	OMIM:300577	TAS				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0003196	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0006829	OMIM:300577	IEA	HP:0003593			P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0009237	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0025356	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0030084	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300577	MENTAL RETARDATION, X-LINKED 91; MRX91		HP:0200055	OMIM:300577	IEA				P		HPO:skoehler	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0000252	OMIM:300578	IEA				P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0000505	OMIM:300578	TAS				P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:probinson	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0000510	OMIM:300578	IEA	HP:0003593			P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0000618	OMIM:300578	IEA				P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:skoehler	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0000662	OMIM:300578	IEA		HP:0040283		P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	HP:0040283
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0001249	OMIM:300578	IEA				P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0001419	OMIM:300578	IEA				I	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	
OMIM	300578	CHROMOSOME Xp11.3 DELETION SYNDROME		HP:0004322	OMIM:300578	IEA				P	CHROMOSOME XP11.3 DELETION SYNDROME	HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0000347	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0000508	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0001423	OMIM:300580	IEA				I		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0001425	OMIM:300580	TAS				I		HPO:skoehler	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0001561	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0001612	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0001644	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0002033	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0002098	OMIM:300580	TAS				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0002747	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0003198	OMIM:300580	TAS				P		HPO:probinson	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0003755	OMIM:300580	TAS				P		HPO:probinson	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0004322	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0004325	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0004661	OMIM:300580	IEA				P		HPO:iea	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0008935	OMIM:300580	TAS				P		HPO:probinson	
OMIM	300580	MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED; CFTDX		HP:0010628	OMIM:300580	TAS				P		HPO:skoehler	
OMIM	300582	#300582 SHORT STATURE, IDIOPATHIC, X-LINKED; ISS		HP:0001417	PMID:19578035	PCS				I		HPO:probinson	
OMIM	300582	#300582 SHORT STATURE, IDIOPATHIC, X-LINKED; ISS		HP:0004322	PMID:19578035	PCS				P		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0001419	PMID:16532398	PCS				I		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0002720	PMID:16532398	PCS				P		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0002721	OMIM:300584	IEA				P		HPO:skoehler	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0002847	PMID:16532398	PCS				P		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0003496	PMID:16532398	PCS				P		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0004315	PMID:16532398	PCS				P		HPO:probinson	
OMIM	300584	#300584 IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA;;IMMUNODEFICIENCY, ISOLATED;;IMMUNODEFICIENCY, PURE		HP:0011275	PMID:16532398	PCS				P		HPO:probinson	
OMIM	300589	%300589 NYSTAGMUS 5, CONGENITAL, X-LINKED; NYS5		HP:0000484	OMIM:300589	TAS				P		HPO:skoehler	
OMIM	300589	%300589 NYSTAGMUS 5, CONGENITAL, X-LINKED; NYS5		HP:0000486	OMIM:300589	TAS				P		HPO:skoehler	
OMIM	300589	%300589 NYSTAGMUS 5, CONGENITAL, X-LINKED; NYS5		HP:0000639	OMIM:300589	TAS	HP:0003593			P		HPO:skoehler	
OMIM	300589	%300589 NYSTAGMUS 5, CONGENITAL, X-LINKED; NYS5		HP:0001423	OMIM:300589	TAS				I		HPO:skoehler	
OMIM	300589	%300589 NYSTAGMUS 5, CONGENITAL, X-LINKED; NYS5		HP:0011515	OMIM:300589	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000218	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000219	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000248	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000252	PMID:20358602	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000294	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000319	PMID:22106055	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000341	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000347	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000426	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000463	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000470	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000494	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000508	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000527	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000574	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000664	PMID:22106055	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0000965	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001007	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001156	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001249	PMID:20358602	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001250	OMIM:300590	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001263	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001419	PMID:20358602	PCS				I		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001423	OMIM:300590	TAS				I		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001511	PMID:20358602	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001639	OMIM:300590	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0001773	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002020	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002119	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002465	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002553	PMID:22106055	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002714	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0002996	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0004322	PMID:20358602	PCS				P		HPO:probinson	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0009623	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0030084	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0100543	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300590	CORNELIA DE LANGE SYNDROME 2		HP:0200055	OMIM:300590	TAS				P		HPO:skoehler	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0000483	OMIM:300600	IEA				P		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0000545	OMIM:300600	IEA				P		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0000639	OMIM:300600	IEA				P		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0001022	OMIM:300600	IEA				P		HPO:skoehler	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0001141	OMIM:300600	IEA				P		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0001417	OMIM:300600	IEA				I		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0001939	OMIM:300600	IEA				P		HPO:iea	
OMIM	300600	ALAND ISLAND EYE DISEASE		HP:0007750	OMIM:300600	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000053	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000098	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000179	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000256	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000280	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000455	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0000494	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001169	OMIM:300602	TAS				P		HPO:probinson	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001182	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001249	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001250	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001388	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001417	OMIM:300602	IEA				I		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001513	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001566	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0001593	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002007	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002054	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002650	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002708	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002711	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002808	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002816	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0002857	OMIM:300602	IEA				P		HPO:iea	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0004279	OMIM:300602	TAS				P		HPO:probinson	
OMIM	300602	CLARK-BARAITSER SYNDROME		HP:0011220	OMIM:300602	TAS				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0000098	OMIM:300604	IEA				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0000164	OMIM:300604	IEA				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0000786	OMIM:300604	IEA				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0000823	OMIM:300604	TAS				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0000939	OMIM:300604	IEA				P		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0001419	OMIM:300604	TAS				I		HPO:skoehler	
OMIM	300604	PREMATURE OVARIAN FAILURE 2B		HP:0008209	OMIM:300604	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0001250	OMIM:300607	IEA				P		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0001276	OMIM:300607	IEA				P		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0001419	OMIM:300607	TAS				I		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0002267	OMIM:300607	IEA				P		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0003577	OMIM:300607	IEA				C		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0006887	OMIM:300607	IEA				P		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0010864	OMIM:300607	TAS				P		HPO:skoehler	
OMIM	300607	#300607 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8; EIEE8;;HYPEREKPLEXIA AND EPILEPSY		HP:0200134	OMIM:300607	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000160	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000219	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000219	OMIM:300612	TAS				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000252	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000325	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000358	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000369	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000378	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000411	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000414	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000490	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000537	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000545	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000565	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000581	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000639	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000648	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000750	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000752	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0000767	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001182	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001250	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001264	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001274	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001347	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001371	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001419	OMIM:300612	TAS				I		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0001518	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002059	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002151	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002162	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002353	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002370	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0002376	OMIM:300612	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0003199	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0004322	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0005280	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0006887	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0008850	OMIM:300612	IEA				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0010864	OMIM:300612	TAS				P		HPO:skoehler	
OMIM	300612	%300612 BROOKS-WISNIEWSKI-BROWN SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, BROOKS-WISNIEWSKI-BROWN TYPE;MRXSBWB		HP:0012745	OMIM:300612	TAS				P		HPO:skoehler	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0000360	OMIM:300614	TAS				P		HPO:skoehler	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0000365	OMIM:300614	TAS				P		HPO:probinson	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0001284	OMIM:300614	IEA				P		HPO:skoehler	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0001419	OMIM:300614	TAS				I		HPO:probinson	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0001963	OMIM:300614	TAS				P		HPO:probinson	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0002317	OMIM:300614	TAS				P		HPO:skoehler	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0002936	OMIM:300614	TAS				P		HPO:probinson	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0003390	OMIM:300614	TAS				P		HPO:probinson	
OMIM	300614	DEAFNESS, X-LINKED 5; DFNX5		HP:0004454	OMIM:300614	TAS				P		HPO:probinson	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0000717	PMID:24169519	PCS				P		HPO:skoehler	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0000718	PMID:24169519	PCS				P		HPO:probinson	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0000744	PMID:24169519	PCS				P		HPO:probinson	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0001249	PMID:24169519	PCS				P		HPO:probinson	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0001270	PMID:24169519	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0001419	PMID:24169519	PCS				I		HPO:skoehler	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0002315	OMIM:300615	IEA				P		HPO:skoehler	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0030186	OMIM:300615	IEA				P		HPO:skoehler	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0100710	OMIM:300615	IEA				P		HPO:skoehler	
OMIM	300615	BRUNNER SYNDROME; BRNRS		HP:0100716	PMID:24169519	PCS				P		HPO:probinson	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001249	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001251	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001252	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001260	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001290	OMIM:300619	TAS				P		HPO:skoehler	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001324	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0001419	OMIM:300619	IEA				I		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0002174	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0004322	OMIM:300619	IEA				P		HPO:iea	
OMIM	300619	CATARACT, ATAXIA, SHORT STATURE, AND MENTAL RETARDATION		HP:0007787	OMIM:300619	IEA				P		HPO:iea	
OMIM	300622	#300622 TN POLYAGGLUTINATION SYNDROME; TNPS;;GALACTOSYLTRANSFERASE DEFICIENCY		HP:0001428	OMIM:300622	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	300622	#300622 TN POLYAGGLUTINATION SYNDROME; TNPS;;GALACTOSYLTRANSFERASE DEFICIENCY		HP:0001877	OMIM:300622	IEA				P		HPO:skoehler	
OMIM	300622	#300622 TN POLYAGGLUTINATION SYNDROME; TNPS;;GALACTOSYLTRANSFERASE DEFICIENCY		HP:0002960	OMIM:300622	IEA				P		HPO:skoehler	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000020	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000298	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000365	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000639	OMIM:300623	TAS				P		HPO:skoehler	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000716	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000726	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000734	OMIM:300623	TAS				P		HPO:skoehler	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000739	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000802	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0000821	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001152	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001260	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001265	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001272	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001300	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001310	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0001423	OMIM:309550	TAS				I		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002066	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002067	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002075	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002080	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002174	OMIM:300623	TAS				P		HPO:skoehler	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002322	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002354	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002506	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0002607	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0003326	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0003581	OMIM:309550	TAS				C		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0006886	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0007010	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0008209	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0008770	OMIM:309550	TAS				P		HPO:probinson	
OMIM	300623	FRAGILE X TREMOR/ATAXIA SYNDROME; FXTAS		HP:0031629	OMIM:300623	IEA				P		HPO:skoehler	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000256	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000276	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000280	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000303	OMIM:300624	TAS				P		HPO:probinson	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000400	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000717	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000752	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000767	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0000817	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0001250	OMIM:300624	TAS				P		HPO:skoehler	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0001388	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0001423	OMIM:300624	IEA				I		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0001634	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0001763	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0002003	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0002050	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0002342	OMIM:300624	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0002457	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0002650	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0003564	OMIM:300624	IEA				P		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0003829	OMIM:300624	IEA				C		HPO:iea	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0007165	OMIM:300624	TAS				P		HPO:probinson	
OMIM	300624	FRAGILE X MENTAL RETARDATION SYNDROME		HP:0008640	OMIM:300624	IEA				P		HPO:iea	
OMIM	300633	#300633 HYPOSPADIAS 1, X-LINKED; HYSP1		HP:0000051	OMIM:300633	TAS				P		HPO:skoehler	
OMIM	300633	#300633 HYPOSPADIAS 1, X-LINKED; HYSP1		HP:0001419	OMIM:300633	TAS				I		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001061	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001417	PMID:20489057	PCS				I		HPO:probinson	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001581	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001744	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	9/10
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001915	OMIM:300635	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0001945	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	9/10
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0002155	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0002583	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0002719	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0002721	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0003281	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0004313	PMID:20489057	PCS				P		HPO:probinson	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0011900	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0012115	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	8/9
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0012156	PMID:20489057	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0012219	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300635	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2		HP:0025084	OMIM:300635	IEA				P		HPO:skoehler	
OMIM	300636	IMMUNODEFICIENCY 33		HP:0000684	OMIM:300636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300636	IMMUNODEFICIENCY 33		HP:0000698	OMIM:300636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300636	IMMUNODEFICIENCY 33		HP:0001419	OMIM:300636	TAS				I		HPO:skoehler	
OMIM	300636	IMMUNODEFICIENCY 33		HP:0002718	OMIM:300636	IEA				P		HPO:skoehler	
OMIM	300636	IMMUNODEFICIENCY 33		HP:0002721	OMIM:300636	IEA				P		HPO:skoehler	
OMIM	300640	#300640 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2; IPD2		HP:0000668	PMID:16950813	PCS				P		HPO:probinson	
OMIM	300640	#300640 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2; IPD2		HP:0000958	PMID:16950813	PCS				P		HPO:probinson	
OMIM	300640	#300640 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2; IPD2		HP:0002007	PMID:16950813	PCS				P		HPO:probinson	
OMIM	300640	#300640 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2; IPD2		HP:0005366	PMID:16950813	PCS				P		HPO:probinson	
OMIM	300640	#300640 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 2; IPD2		HP:0011065	PMID:16950813	PCS				P		HPO:probinson	
OMIM	300643	#300643 ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED;RESDX		HP:0000006	OMIM:300643	IEA				I		HPO:skoehler	
OMIM	300643	#300643 ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED;RESDX		HP:0001256	OMIM:300643	IEA				P		HPO:skoehler	
OMIM	300643	#300643 ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED;RESDX		HP:0007095	OMIM:300643	IEA				P		HPO:skoehler	
OMIM	300643	#300643 ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED;RESDX		HP:0007359	OMIM:300643	IEA				P		HPO:skoehler	
OMIM	300643	#300643 ROLANDIC EPILEPSY, MENTAL RETARDATION, AND SPEECH DYSPRAXIA, X-LINKED;RESDX		HP:0011098	OMIM:300643	IEA				P		HPO:skoehler	
OMIM	300645	#300645 ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 2; AMCBX2;;ATYPICAL MYCOBACTERIAL INFECTION, DISSEMINATED, X-LINKED 2;;ATYPICAL MYCOBACTERIAL INFECTION, FAMILIAL DISSEMINATED, X-LINKED2;;MYCOBACTERIAL DISEASE, SUSCEPTIBILITY TO, X-LINKED 2;;MYCOBACTERIAL DISEASE, MENDELIAN SUSCEPTIBILITY TO, X-LINKED RECESSIVE2; XRMSMD2		HP:0001419	OMIM:300645	TAS				I		HPO:skoehler	
OMIM	300645	#300645 ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 2; AMCBX2;;ATYPICAL MYCOBACTERIAL INFECTION, DISSEMINATED, X-LINKED 2;;ATYPICAL MYCOBACTERIAL INFECTION, FAMILIAL DISSEMINATED, X-LINKED2;;MYCOBACTERIAL DISEASE, SUSCEPTIBILITY TO, X-LINKED 2;;MYCOBACTERIAL DISEASE, MENDELIAN SUSCEPTIBILITY TO, X-LINKED RECESSIVE2; XRMSMD2		HP:0005428	OMIM:300645	TAS				P		HPO:skoehler	
OMIM	300645	#300645 ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 2; AMCBX2;;ATYPICAL MYCOBACTERIAL INFECTION, DISSEMINATED, X-LINKED 2;;ATYPICAL MYCOBACTERIAL INFECTION, FAMILIAL DISSEMINATED, X-LINKED2;;MYCOBACTERIAL DISEASE, SUSCEPTIBILITY TO, X-LINKED 2;;MYCOBACTERIAL DISEASE, MENDELIAN SUSCEPTIBILITY TO, X-LINKED RECESSIVE2; XRMSMD2		HP:0011274	OMIM:300645	TAS				P		HPO:skoehler	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0000505	OMIM:300650	IEA				P		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0000613	OMIM:300650	IEA				P		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0001022	OMIM:300650	TAS				P		HPO:probinson	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0001361	OMIM:300650	IEA				P		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0001417	OMIM:300650	IEA				I		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0005592	OMIM:300650	IEA				P		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0007680	OMIM:300650	IEA				P		HPO:iea	
OMIM	300650	ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS		HP:0008615	OMIM:300650	IEA	HP:0003584			P		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0000962	OMIM:300652	IEA				P		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0000962	OMIM:300652	TAS				P		HPO:probinson	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0001423	OMIM:300652	IEA				I		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0002213	OMIM:300652	PCS				P		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0003577	OMIM:300652	IEA				C		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0003677	OMIM:300652	IEA				C		HPO:iea	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0008070	OMIM:300652	TAS				P		HPO:probinson	
OMIM	300652	ANGIOMA SERPIGINOSUM, X-LINKED		HP:0008404	OMIM:300652	TAS				P		HPO:probinson	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0000083	OMIM:300653	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0000556	OMIM:300653	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0000572	OMIM:300653	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0000712	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0000750	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001249	OMIM:300653	TAS				P		HPO:skoehler	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001250	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001251	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001263	OMIM:300653	TAS		HP:0040284		P		HPO:iea	50%
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001419	OMIM:300653	IEA				I		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001878	OMIM:300653	TAS		HP:0040284		P		HPO:probinson	60%
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0001923	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0002076	OMIM:300653	IEA				P		HPO:skoehler	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0003198	OMIM:300653	TAS		HP:0040284		P		HPO:probinson	45%
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0003201	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0003546	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0003710	OMIM:300653	IEA				P		HPO:iea	
OMIM	300653	#300653 PHOSPHOGLYCERATE KINASE 1 DEFICIENCY;;PGK1 DEFICIENCY		HP:0008305	OMIM:300653	TAS				P		HPO:probinson	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000028	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000256	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000276	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000378	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000400	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0000750	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0001252	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0001256	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0001290	OMIM:300659	TAS				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0001419	OMIM:300659	TAS				I		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0001763	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0002007	OMIM:300659	IEA				P		HPO:skoehler	
OMIM	300659	MENTAL RETARDATION, X-LINKED 93		HP:0011220	OMIM:300659	TAS				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0000272	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0000463	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0000572	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0000666	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001249	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001258	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001288	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001337	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001347	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0001419	OMIM:300660	TAS				I		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0002352	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0002500	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0002506	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0003487	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0003621	OMIM:300660	IEA				C		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0003677	OMIM:300660	IEA				C		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0005280	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300660	%300660 LEUKOENCEPHALOPATHY WITH METAPHYSEAL CHONDRODYSPLASIA; LKMCD		HP:0005871	OMIM:300660	IEA				P		HPO:skoehler	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0000083	OMIM:300661	IEA				P		HPO:skoehler	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0000407	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0000791	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001249	OMIM:300661	IEA				P		HPO:skoehler	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001251	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001252	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001270	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001290	OMIM:300661	TAS				P		HPO:skoehler	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001419	OMIM:300661	IEA				I		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0001997	PMID:8253776	PCS				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0002149	PMID:8253776	PCS				P		HPO:probinson	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0003149	OMIM:300661	IEA				P		HPO:iea	
OMIM	300661	PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE SUPERACTIVITY		HP:0003240	PMID:8253776	PCS				P		HPO:probinson	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000179	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000253	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000337	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000463	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000490	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000733	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0000817	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001182	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001250	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001252	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001263	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001290	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001336	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001423	OMIM:300672	TAS				I		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0001773	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002019	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002020	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002123	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002187	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002376	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002521	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002540	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002650	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0002883	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0003593	OMIM:300672	IEA				C		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0004279	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0010845	PMID:22264704	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0011220	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0012469	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0031165	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0100704	PMID:22264704	PCS				P		HP:probinson	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0200055	OMIM:300672	TAS				P		HPO:skoehler	
OMIM	300672	#300672 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 2; EIEE2;;INFANTILE SPASM SYNDROME, X-LINKED 2; ISSX2		HP:0200134	OMIM:300672	IEA				P		HPO:skoehler	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0000253	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001250	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001263	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001298	OMIM:300673	TAS				P		HPO:probinson	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001336	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001347	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001419	OMIM:300673	IEA				I		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0001508	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002020	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002063	OMIM:300673	IEA				P		HPO:skoehler	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002093	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002104	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002126	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0002353	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0003577	OMIM:300673	IEA				C		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0006887	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0007110	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0008872	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0008936	OMIM:300673	IEA				P		HPO:iea	
OMIM	300673	#300673 ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS		HP:0010864	OMIM:300673	TAS				P		HPO:skoehler	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000218	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000256	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000275	OMIM:300676	TAS				P		HPO:probinson	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000276	OMIM:300676	TAS				P		HPO:probinson	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000303	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000327	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000426	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000767	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000768	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0000774	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001166	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001249	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001419	OMIM:300676	IEA				I		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001507	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001611	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0001833	OMIM:300676	TAS				P		HPO:skoehler	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0002007	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0002650	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0002808	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0003011	OMIM:300676	IEA				P		HPO:iea	
OMIM	300676	#300676 MENTAL RETARDATION, X-LINKED, SYNDROMIC 14; MRXS14		HP:0011220	OMIM:300676	TAS				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0001265	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0001371	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0001423	OMIM:300695	TAS				I		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0002515	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003198	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED	HP:0003676	HP:0003202	OMIM:300695	TAS				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003236	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003376	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003581	OMIM:300695	IEA				C		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003691	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003701	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0003715	OMIM:300695	TAS				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0007340	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0009027	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0009054	OMIM:300695	TAS				P		HPO:skoehler	
OMIM	300695	#300695 SCAPULOPERONEAL MYOPATHY, X-LINKED DOMINANT; SPM;;SCAPULOPERONEAL MYOPATHY, FHL1-RELATED		HP:0011675	OMIM:300695	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0000470	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0001371	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0001419	OMIM:300696	TAS				I		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0001639	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0002093	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003236	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003306	OMIM:300696	TAS				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003418	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003676	OMIM:300696	IEA				C		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003691	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003701	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003704	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0003805	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300696	#300696 MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY; XMPMAEMERY-DREIFUSS MUSCULAR DYSTROPHY 6, X-LINKED, INCLUDED; EDMD6, INCLUDED		HP:0011675	OMIM:300696	IEA				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000248	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000256	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000336	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000490	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000717	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0000718	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001249	PMID:17989220	PCS				P		HPO:probinson	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001250	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001265	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001336	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001419	PMID:17989220	PCS				I		HPO:probinson	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0001533	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0002460	PMID:17989220	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0004322	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300699	MENTAL RETARDATION, X-LINKED, SYNDROMIC, WU TYPE; MRXSW		HP:0010864	OMIM:300699	TAS				P		HPO:skoehler	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0000478	OMIM:300700	IEA				P		HPO:iea	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0001022	OMIM:300700	IEA				P		HPO:skoehler	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0001417	OMIM:300700	IEA				I		HPO:iea	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0007443	OMIM:300700	TAS				P		HPO:probinson	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0007509	OMIM:300700	IEA				P		HPO:iea	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0007544	OMIM:300700	IEA				P		HPO:iea	
OMIM	300700	%300700 ALBINISM-DEAFNESS SYNDROME; ADFN;;ALDS		HP:0008527	OMIM:300700	IEA				P		HPO:iea	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0000639	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0001251	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0001260	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0001270	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0001319	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0001419	OMIM:300703	TAS				I		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0002345	OMIM:300703	IEA				P		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0003593	OMIM:300703	IEA				C		HPO:skoehler	
OMIM	300703	%300703 SPINOCEREBELLAR ATAXIA, X-LINKED 5; SCAX5		HP:0003680	OMIM:300703	IEA				C		HPO:skoehler	
OMIM	300705	#300705 MENTAL RETARDATION, X-LINKED 17; MRX17;;MENTAL RETARDATION, X-LINKED 31; MRX31		HP:0000750	OMIM:300705	TAS				P		HPO:probinson	
OMIM	300705	#300705 MENTAL RETARDATION, X-LINKED 17; MRX17;;MENTAL RETARDATION, X-LINKED 31; MRX31		HP:0001249	OMIM:300705	TAS				P		HPO:probinson	
OMIM	300705	#300705 MENTAL RETARDATION, X-LINKED 17; MRX17;;MENTAL RETARDATION, X-LINKED 31; MRX31		HP:0001417	OMIM:300705	TAS				I		HPO:probinson	
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0000053	OMIM:300706	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0000256	OMIM:300706	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0001182	OMIM:300706	IEA				P		HPO:skoehler	
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0001249	OMIM:300706	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0001360	OMIM:300706	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0001377	OMIM:300706	IEA				P		HPO:skoehler	
OMIM	300706	#300706 MENTAL RETARDATION, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST;;MENTAL RETARDATION AND MACROCEPHALY SYNDROME		HP:0001417	OMIM:300706	IEA				I		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000066	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000076	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000125	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000143	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000219	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000369	OMIM:300707	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000377	OMIM:300707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000455	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000460	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000506	OMIM:300707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0000813	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001363	OMIM:300707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001423	OMIM:300707	TAS				I		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001511	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001518	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001647	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0001770	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0002025	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0003298	OMIM:300707	IEA				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0004209	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0004322	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0004969	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0008665	OMIM:300707	TAS				P		HPO:skoehler	
OMIM	300707	TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS; STAR		HP:0009921	OMIM:300707	IEA				P		HPO:skoehler	
OMIM	300709	X-LINKED INTELLECTUAL DISABILITY, SHRIMPTON TYPE		HP:0001249	OMIM:300709	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000028	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000047	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000126	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000126	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000175	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000219	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000219	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000239	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000252	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000322	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000325	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000347	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000358	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000453	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000453	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000494	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000581	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0000914	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001156	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001263	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001321	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001419	OMIM:300712	TAS				I		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001423	OMIM:300712	TAS				I		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001511	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001552	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001629	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001631	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001643	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001763	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0001773	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0002738	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0002777	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0002868	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0002901	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0004209	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0004279	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0004322	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0006610	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0008551	OMIM:300712	IEA				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0011467	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0011611	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0012745	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300712	%300712 CRANIOFACIOSKELETAL SYNDROME		HP:0200055	OMIM:300712	TAS				P		HPO:skoehler	
OMIM	300716	MENTAL RETARDATION, X-LINKED 95		HP:0000750	PMID:18455129	PCS				P		HPO:probinson	
OMIM	300716	MENTAL RETARDATION, X-LINKED 95		HP:0001249	PMID:18455129	PCS				P		HPO:probinson	
OMIM	300716	MENTAL RETARDATION, X-LINKED 95		HP:0001417	PMID:18455129	PCS				I		HPO:probinson	
OMIM	300716	MENTAL RETARDATION, X-LINKED 95		HP:0001423	OMIM:300716	TAS				I		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0001265	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0001284	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0001371	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0001423	OMIM:300717	TAS				I		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0002747	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0003236	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0003557	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0003678	OMIM:300717	IEA				C		HPO:skoehler	
OMIM	300717	#300717 MYOPATHY, REDUCING BODY, X-LINKED, EARLY-ONSET, SEVERE		HP:0003701	OMIM:300717	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0000470	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0001265	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0001371	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0001417	OMIM:300718	IEA				I		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0001644	OMIM:300718	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0002359	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0002650	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0002747	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0002808	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003236	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003306	OMIM:300718	TAS				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003307	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003557	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003678	OMIM:300718	IEA				C		HPO:skoehler	
OMIM	300718	#300718 MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET		HP:0003701	OMIM:300718	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0000365	OMIM:300719	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0000510	OMIM:300719	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0000518	OMIM:300719	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0000789	OMIM:300719	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0001000	OMIM:300719	IEA				P		HPO:skoehler	
OMIM	300719	%300719 DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES		HP:0001419	OMIM:300719	TAS				I		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000218	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000253	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000286	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000300	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000316	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000343	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000347	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000400	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000407	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000426	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000431	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000455	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000486	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000543	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000609	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000639	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0000966	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001090	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001250	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001257	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001263	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001290	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001321	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001324	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001344	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001347	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0001423	OMIM:300749	TAS				I		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0002198	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0002342	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0002650	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0003196	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0004322	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0004325	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0007227	OMIM:300749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0008897	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300749	MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH		HP:0008936	OMIM:300749	TAS				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0001258	OMIM:300750	IEA				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0001419	OMIM:300750	TAS				I		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0002064	OMIM:300750	IEA				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0002169	OMIM:300750	IEA				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0002495	OMIM:300750	IEA				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0003487	OMIM:300750	IEA				P		HPO:skoehler	
OMIM	300750	%300750 SPASTIC PARAPLEGIA 34, X-LINKED; SPG34		HP:0003677	OMIM:300750	IEA				C		HPO:skoehler	
OMIM	300751	#300751 ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA;;ANEMIA, HYPOCHROMIC; ANH1;;ANEMIA, HEREDITARY SIDEROBLASTIC;;HEREDITARY IRON-LOADING ANEMIA		HP:0001419	OMIM:300751	TAS				I		HPO:skoehler	
OMIM	300751	#300751 ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA;;ANEMIA, HYPOCHROMIC; ANH1;;ANEMIA, HEREDITARY SIDEROBLASTIC;;HEREDITARY IRON-LOADING ANEMIA		HP:0001924	OMIM:300751	IEA				P		HPO:skoehler	
OMIM	300751	#300751 ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA;;ANEMIA, HYPOCHROMIC; ANH1;;ANEMIA, HEREDITARY SIDEROBLASTIC;;HEREDITARY IRON-LOADING ANEMIA		HP:0001972	OMIM:300751	IEA				P		HPO:skoehler	
OMIM	300751	#300751 ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA;;ANEMIA, HYPOCHROMIC; ANH1;;ANEMIA, HEREDITARY SIDEROBLASTIC;;HEREDITARY IRON-LOADING ANEMIA		HP:0003828	OMIM:300751	IEA				C		HPO:skoehler	
OMIM	300751	#300751 ANEMIA, SIDEROBLASTIC, X-LINKED; XLSA;;ANEMIA, HYPOCHROMIC; ANH1;;ANEMIA, HEREDITARY SIDEROBLASTIC;;HEREDITARY IRON-LOADING ANEMIA		HP:0004840	OMIM:300751	IEA				P		HPO:skoehler	
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0000992	PMID:18760763	PCS				P		HPO:probinson	
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0001081	OMIM:300752	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0001423	PMID:18760763	PCS				I		HPO:probinson	
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0001891	OMIM:300752	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0002910	OMIM:300752	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0011463	OMIM:300752	TAS				C		HPO:probinson	
OMIM	300752	#300752 PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED; XLEPP;;PROTOPORPHYRIA, ERYTHROPOIETIC, X-LINKED DOMINANT; XLDPP;;ERYTHROHEPATIC PROTOPORPHYRIA, X-LINKED;		HP:0012187	PMID:18760763	PCS				P		HPO:probinson	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000010	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000024	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000031	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000246	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000365	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000388	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000509	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000750	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0000999	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0001287	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0001412	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0001419	OMIM:300755	TAS				I		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0001648	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0002014	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0002090	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0002383	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0002664	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0002732	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0003095	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0003729	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300755	#300755 AGAMMAGLOBULINEMIA, X-LINKED; XLA;;BRUTON-TYPE AGAMMAGLOBULINEMIA;;AGAMMAGLOBULINEMIA, X-LINKED, TYPE 1; AGMX1;;IMMUNODEFICIENCY 1; IMD1HYPOGAMMAGLOBULINEMIA, X-LINKED, INCLUDED		HP:0004432	OMIM:300755	IEA				P		HPO:skoehler	
OMIM	300758	#300758 HYPOSPADIAS 2, X-LINKED; HYSP2		HP:0000808	OMIM:300758	TAS				P		HPO:skoehler	
OMIM	300758	#300758 HYPOSPADIAS 2, X-LINKED; HYSP2		HP:0001419	OMIM:300758	TAS				I		HPO:skoehler	
OMIM	300770	#300770 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4; SMDP4;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 4;;PAP DUE TO CSF2RA DEFICIENCY;;CSF2RA DEFICIENCY		HP:0001417	PMID:18955570	PCS				I		HPO:probinson	
OMIM	300770	#300770 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4; SMDP4;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 4;;PAP DUE TO CSF2RA DEFICIENCY;;CSF2RA DEFICIENCY	HP:0012828	HP:0002091	PMID:18955570	PCS				P		HPO:probinson	
OMIM	300770	#300770 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4; SMDP4;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 4;;PAP DUE TO CSF2RA DEFICIENCY;;CSF2RA DEFICIENCY		HP:0002789	PMID:18955570	PCS				P		HPO:probinson	
OMIM	300770	#300770 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 4; SMDP4;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 4;;PAP DUE TO CSF2RA DEFICIENCY;;CSF2RA DEFICIENCY		HP:0006517	OMIM:300770	IEA				P		HPO:skoehler	
OMIM	300778	%300778 CORNEAL DYSTROPHY, LISCH EPITHELIAL; LECD;;LISCH EPITHELIAL CORNEAL DYSTROPHY;;BAND-SHAPED AND WHORLED MICROCYSTIC CORNEAL EPITHELIAL DYSTROPHY		HP:0001131	OMIM:300778	IEA				P		HPO:skoehler	
OMIM	300778	%300778 CORNEAL DYSTROPHY, LISCH EPITHELIAL; LECD;;LISCH EPITHELIAL CORNEAL DYSTROPHY;;BAND-SHAPED AND WHORLED MICROCYSTIC CORNEAL EPITHELIAL DYSTROPHY		HP:0001423	OMIM:300778	TAS				I		HPO:skoehler	
OMIM	300779	CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED; XECD		HP:0000585	OMIM:300779	IEA				P		HPO:skoehler	
OMIM	300779	CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED; XECD		HP:0001131	OMIM:300779	IEA				P		HPO:skoehler	
OMIM	300779	CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED; XECD		HP:0001423	OMIM:300779	TAS				I		HPO:skoehler	
OMIM	300779	CORNEAL DYSTROPHY, ENDOTHELIAL, X-LINKED; XECD		HP:0007957	OMIM:300779	TAS	HP:0003577			P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0000411	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0000486	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0000708	OMIM:300799	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0000768	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0001166	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0001249	OMIM:300799	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0001417	OMIM:300799	IEA				I		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0001519	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0001763	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300799	#300799 MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR		HP:0009183	OMIM:300799	IEA				P		HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001159	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001423	OMIM:300801	TAS				I	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001609	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001611	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001761	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0001763	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0002121	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0002353	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0002465	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0006889	OMIM:300801	IEA				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300801	#300801 CHROMOSOME Xp11.23-p11.22 DUPLICATION SYNDROME		HP:0100962	OMIM:300801	TAS				P	#300801 CHROMOSOME XP11.23-P11.22 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300802	#300802 MENTAL RETARDATION, X-LINKED 96; MRX96		HP:0001249	OMIM:300802	TAS				P		HPO:skoehler	
OMIM	300802	#300802 MENTAL RETARDATION, X-LINKED 96; MRX96		HP:0001250	OMIM:300802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300802	#300802 MENTAL RETARDATION, X-LINKED 96; MRX96		HP:0001423	OMIM:300802	TAS				I		HPO:skoehler	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0000276	OMIM:300803	IEA				P		HPO:skoehler	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0000283	OMIM:300803	IEA				P		HPO:skoehler	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0000750	OMIM:300803	IEA				P		HPO:skoehler	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0001249	PMID:19377476	PCS				P		HPO:probinson	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0001270	OMIM:300803	IEA				P		HPO:skoehler	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0001417	PMID:19377476	PCS				I		HPO:probinson	
OMIM	300803	MENTAL RETARDATION, X-LINKED 97; MRX97		HP:0002342	OMIM:300803	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000256	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000286	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000369	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000431	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000494	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0000510	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001007	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001249	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001263	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001320	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001419	PMID:19800048	PCS				I		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0001510	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002002	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002007	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002187	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002280	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002419	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0002719	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0008872	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300804	JOUBERT SYNDROME 10		HP:0012471	OMIM:300804	TAS				P		HPO:skoehler	
OMIM	300804	JOUBERT SYNDROME 10		HP:0100259	PMID:19800048	PCS				P		HPO:probinson	
OMIM	300807	#300807 THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT; THPH8DEEP VENOUS THROMBOSIS, PROTECTION AGAINST, INCLUDED		HP:0001417	OMIM:300807	IEA				I		HPO:skoehler	
OMIM	300807	#300807 THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT; THPH8DEEP VENOUS THROMBOSIS, PROTECTION AGAINST, INCLUDED		HP:0002625	OMIM:300807	IEA				P		HPO:skoehler	
OMIM	300807	#300807 THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT; THPH8DEEP VENOUS THROMBOSIS, PROTECTION AGAINST, INCLUDED		HP:0010989	OMIM:300807	IEA				P		HPO:skoehler	
OMIM	300807	#300807 THROMBOPHILIA, X-LINKED, DUE TO FACTOR IX DEFECT; THPH8DEEP VENOUS THROMBOSIS, PROTECTION AGAINST, INCLUDED		HP:0100724	OMIM:300807	IEA				P		HPO:skoehler	
OMIM	300813	SARCOMA, SYNOVIAL		HP:0001428	OMIM:300813	IEA				I		HPO:probinson	
OMIM	300813	SARCOMA, SYNOVIAL		HP:0012570	OMIM:300813	IEA				P		HPO:probinson	
OMIM	300814	#300814 NYSTAGMUS 6, CONGENITAL, X-LINKED; NYS6		HP:0000484	OMIM:300814	TAS				P		HPO:probinson	
OMIM	300814	#300814 NYSTAGMUS 6, CONGENITAL, X-LINKED; NYS6		HP:0000646	OMIM:300814	TAS				P		HPO:probinson	
OMIM	300814	#300814 NYSTAGMUS 6, CONGENITAL, X-LINKED; NYS6		HP:0000666	OMIM:300814	TAS				P		HPO:probinson	
OMIM	300814	#300814 NYSTAGMUS 6, CONGENITAL, X-LINKED; NYS6		HP:0001417	OMIM:300814	TAS				I		HPO:probinson	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001250	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001263	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001265	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001271	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001290	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0001419	OMIM:300816	TAS				I		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002134	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002151	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002375	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002376	OMIM:300816	TAS	HP:0003593			P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002380	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002445	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002490	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0002747	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0003200	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0003202	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0003542	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0003593	OMIM:300816	TAS				C		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0003676	OMIM:300816	TAS				C		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0009025	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0011398	OMIM:300816	TAS				P		HPO:skoehler	
OMIM	300816	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6		HP:0025356	OMIM:300816	IEA				P		HPO:skoehler	
OMIM	300818	#300818 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PNH		HP:0001428	OMIM:300818	TAS				I		HPO:skoehler	
OMIM	300818	#300818 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA; PNH		HP:0004818	OMIM:300818	TAS				P		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0000717	OMIM:300830	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0000718	OMIM:300830	TAS				P		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0001249	OMIM:300830	TAS				P		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0001290	OMIM:300830	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0001419	OMIM:300830	TAS				I		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0003593	OMIM:300830	TAS				C		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0003828	OMIM:300830	TAS				C		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0007018	OMIM:300830	TAS				P		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0100034	OMIM:300830	TAS				P		HPO:skoehler	
OMIM	300830	AUTISM, SUSCEPTIBILITY TO, X-LINKED 4		HP:0100710	OMIM:300830	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000218	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000252	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000272	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000275	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000276	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000278	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000286	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000347	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000358	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000426	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000486	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000582	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000678	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000718	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000737	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000750	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0000752	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001249	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001250	OMIM:300831	TAS	HP:0003593			P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001263	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001290	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001302	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001382	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001419	OMIM:300831	TAS				I		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0001533	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0002126	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0002360	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0002650	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0002808	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0003103	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0003307	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0007874	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300831	#300831 CK SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH THIN BODY HABITUS AND CORTICALMALFORMATION		HP:0011297	OMIM:300831	TAS				P		HPO:skoehler	
OMIM	300833	#300833 46,XX SEX REVERSAL 3; SRXX3;;CHROMOSOME Xq26 DUPLICATION SYNDROME;;46,XX SEX REVERSAL, SOX3-RELATEDCHROMOSOME Xq26 DELETION SYNDROME, INCLUDED		HP:0001423	OMIM:300833	TAS				I	#300833 46,XX SEX REVERSAL 3; SRXX3;;CHROMOSOME XQ26 DUPLICATION SYNDROME;;46,XX SEX REVERSAL, SOX3-RELATEDCHROMOSOME XQ26 DELETION SYNDROME, INCLUDED	HPO:skoehler	
OMIM	300833	#300833 46,XX SEX REVERSAL 3; SRXX3;;CHROMOSOME Xq26 DUPLICATION SYNDROME;;46,XX SEX REVERSAL, SOX3-RELATEDCHROMOSOME Xq26 DELETION SYNDROME, INCLUDED		HP:0012245	OMIM:300833	TAS				P	#300833 46,XX SEX REVERSAL 3; SRXX3;;CHROMOSOME XQ26 DUPLICATION SYNDROME;;46,XX SEX REVERSAL, SOX3-RELATEDCHROMOSOME XQ26 DELETION SYNDROME, INCLUDED	HPO:probinson	
OMIM	300834	#300834 MACULAR DEGENERATION, X-LINKED ATROPHIC		HP:0000608	PMID:12160730	PCS				P		HPO:probinson	
OMIM	300834	#300834 MACULAR DEGENERATION, X-LINKED ATROPHIC		HP:0001419	PMID:12160730	PCS				I		HPO:probinson	
OMIM	300834	#300834 MACULAR DEGENERATION, X-LINKED ATROPHIC		HP:0007663	PMID:12160730	PCS				P		HPO:probinson	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0001419	OMIM:300835	TAS				I		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0001873	OMIM:300835	TAS	HP:0003584	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0001875	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0001900	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0001972	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0003540	OMIM:300835	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0003593	OMIM:300835	TAS				C		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0003828	OMIM:300835	TAS				C		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0004312	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0004445	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0011273	OMIM:300835	TAS				P		HPO:skoehler	
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0011875	OMIM:300835	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300835	#300835 ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES;XLANP		HP:0012135	OMIM:300835	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0000716	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0000722	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0000739	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001260	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001284	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001324	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001417	OMIM:300842	TAS				I		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001433	OMIM:300842	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001638	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001644	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0001927	OMIM:300842	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0002197	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0003198	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0003201	OMIM:300842	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0003236	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0005110	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0007002	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0012075	OMIM:300842	TAS				P		HPO:skoehler	
OMIM	300842	MCLEOD SYNDROME; MCLDS		HP:0100660	OMIM:300842	IEA				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0000483	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0000609	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0000646	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0000654	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0001419	OMIM:300843	TAS				I		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0007703	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0011003	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0011521	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300843	%300843 BORNHOLM EYE DISEASE; BED;;MYOPIA, HIGH, WITH NONPROGRESSIVE CONE DYSFUNCTION		HP:0011522	OMIM:300843	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0000179	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0000455	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0000678	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0000750	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001249	OMIM:300844	TAS				P		HPO:probinson	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001270	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001290	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001423	OMIM:300844	TAS				I		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001518	OMIM:300844	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0001833	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0002751	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300844	MENTAL RETARDATION, X-LINKED 19		HP:0011220	OMIM:300844	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000027	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000278	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000316	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000343	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000369	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000445	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000490	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000508	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000518	OMIM:300845	TAS	HP:0011463	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000815	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0000824	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001250	OMIM:300845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001263	OMIM:300845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001342	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001419	OMIM:300845	TAS				I		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001500	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001644	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001711	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0001999	OMIM:300845	IEA				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0002216	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0002401	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0004322	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0005288	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0005922	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0008734	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0009803	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0011834	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300845	#300845 MOYAMOYA DISEASE 4 WITH SHORT STATURE, HYPERGONADOTROPIC HYPOGONADISM,AND FACIAL DYSMORPHISM; MYMY4;;CHROMOSOME XQ28 DELETION SYNDROME, 3.4-KB;;SYNDROMIC MOYAMOYA DISEASE		HP:0200055	OMIM:300845	TAS				P		HPO:skoehler	
OMIM	300848	#300848 MENTAL RETARDATION, X-LINKED 89; MRX89		HP:0000750	OMIM:300848	TAS				P		HPO:skoehler	
OMIM	300848	#300848 MENTAL RETARDATION, X-LINKED 89; MRX89		HP:0001249	OMIM:300848	IEA				P		HPO:skoehler	
OMIM	300848	#300848 MENTAL RETARDATION, X-LINKED 89; MRX89		HP:0001263	OMIM:300848	TAS				P		HPO:skoehler	
OMIM	300848	#300848 MENTAL RETARDATION, X-LINKED 89; MRX89		HP:0001423	OMIM:300848	TAS				I		HPO:skoehler	
OMIM	300848	#300848 MENTAL RETARDATION, X-LINKED 89; MRX89		HP:0002123	OMIM:300848	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0001249	PMID:22002931	PCS				P		HPO:probinson	
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0001263	OMIM:300849	TAS				P		HPO:skoehler	
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0001290	OMIM:300849	TAS				P		HPO:skoehler	
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0001417	PMID:22002931	PCS				I		HPO:probinson	
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0001423	OMIM:300849	TAS				I		HPO:skoehler	
OMIM	300849	MENTAL RETARDATION, X-LINKED 41		HP:0002121	OMIM:300849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000218	OMIM:300850	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000486	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000582	OMIM:300850	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000708	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000750	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000774	OMIM:300850	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0000805	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001249	PMID:15185169	PCS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001250	OMIM:300850	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001263	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001290	OMIM:300850	TAS				P		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001417	PMID:15185169	PCS				I		HPO:skoehler	
OMIM	300850	MENTAL RETARDATION, X-LINKED 90		HP:0001419	OMIM:300850	TAS				I		HPO:skoehler	
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0000581	PMID:16385466	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0001249	PMID:16385466	PCS				P		HPO:probinson	
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0001417	PMID:16385466	PCS				I		HPO:probinson	
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0001419	OMIM:300851	TAS				I		HPO:skoehler	
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0004322	PMID:16385466	PCS		HP:0040284		P		HPO:probinson	3/8
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0008734	PMID:16385466	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300851	MENTAL RETARDATION, X-LINKED 92		HP:0011003	PMID:16385466	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300852	MENTAL RETARDATION, X-LINKED 88		HP:0000717	OMIM:300852	TAS		HP:0040284		P		HPO:probinson	2/9
OMIM	300852	MENTAL RETARDATION, X-LINKED 88		HP:0001249	OMIM:300852	TAS				P		HPO:probinson	
OMIM	300852	MENTAL RETARDATION, X-LINKED 88		HP:0001250	OMIM:300852	TAS		HP:0040284		P		HPO:probinson	5/9
OMIM	300852	MENTAL RETARDATION, X-LINKED 88		HP:0001263	OMIM:300852	TAS				P		HPO:skoehler	
OMIM	300852	MENTAL RETARDATION, X-LINKED 88		HP:0001417	OMIM:300852	TAS				I		HPO:probinson	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0001417	PMID:21796205	PCS				I		HPO:probinson	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0002665	PMID:21796205	PCS				P		HPO:probinson	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0002721	OMIM:300853	IEA				P		HPO:skoehler	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0004429	PMID:21796205	PCS				P		HPO:probinson	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0005407	PMID:21796205	PCS				P		HPO:probinson	
OMIM	300853	#300853 IMMUNODEFICIENCY, X-LINKED, WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUSINFECTION, AND NEOPLASIA; XMEN		HP:0005419	PMID:21796205	PCS				P		HPO:probinson	
OMIM	300854	#300854 RENAL CELL CARCINOMA, Xp11-ASSOCIATED; RCCX1		HP:0001428	OMIM:300854	TAS				I	#300854 RENAL CELL CARCINOMA, XP11-ASSOCIATED; RCCX1	HPO:probinson	
OMIM	300854	#300854 RENAL CELL CARCINOMA, Xp11-ASSOCIATED; RCCX1		HP:0005584	OMIM:300854	TAS				P	#300854 RENAL CELL CARCINOMA, XP11-ASSOCIATED; RCCX1	HPO:probinson	
OMIM	300855	OGDEN SYNDROME		HP:0000023	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000028	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000164	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000215	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000218	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000219	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000252	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000270	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000280	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000286	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000308	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000369	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000400	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000430	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000431	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000494	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000520	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000527	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000535	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0000733	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME	HP:0012828	HP:0001263	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001276	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001419	OMIM:300855	TAS				I		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001423	OMIM:300855	TAS				I		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001582	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001629	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001631	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0001664	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0002000	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0002002	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0002059	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0002213	OMIM:300855	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300855	OGDEN SYNDROME		HP:0002650	OMIM:300855	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300855	OGDEN SYNDROME		HP:0002719	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0003577	OMIM:300855	TAS				C		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0003717	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0003828	OMIM:300855	TAS				C		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0004322	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0004415	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0004755	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0004756	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0005280	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0005288	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0006682	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0008897	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0009762	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0010055	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0010803	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300855	OGDEN SYNDROME		HP:0011220	OMIM:300855	TAS				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0001260	OMIM:300857	TAS				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0001332	OMIM:300857	TAS				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0001423	OMIM:300857	TAS				I		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0002015	OMIM:300857	TAS				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0002145	OMIM:300857	IEA				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0002171	OMIM:300857	IEA				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0002305	OMIM:300857	TAS				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0003447	OMIM:300857	IEA				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0003470	OMIM:300857	IEA				P		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0003581	OMIM:300857	IEA				C		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0003676	OMIM:300857	TAS				C		HPO:skoehler	
OMIM	300857	AMYOTROPHIC LATERAL SCLEROSIS 15 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS15		HP:0007354	OMIM:300857	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0000522	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0001249	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0001263	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0001270	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0001344	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0001419	OMIM:300858	TAS				I		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0002015	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0002571	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300858	%300858 MENTAL RETARDATION, X-LINKED, SYNDROMIC 17; MRXS17;;MENTAL RETARDATION, X-LINKED, WITH ALACRIMA AND ACHALASIA		HP:0009916	OMIM:300858	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000054	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000154	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000233	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000256	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000272	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000283	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000336	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000470	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000475	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000490	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000582	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000664	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000718	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0000958	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001007	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001249	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001250	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001419	OMIM:300860	TAS				I		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001763	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0001773	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0002162	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0002164	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0002465	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0002714	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0004324	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0005280	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0005590	OMIM:300860	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0006610	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0007103	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0007874	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0008404	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0010055	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0010529	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0010721	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0011356	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300860	#300860 MENTAL RETARDATION, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 30; MRXS30		HP:0011800	OMIM:300860	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0000303	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0000316	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0000411	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0000664	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0000954	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001007	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001250	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001251	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001263	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001272	OMIM:300861	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0001419	OMIM:300861	TAS				I		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002057	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002317	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002342	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002465	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002650	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002720	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002808	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0002850	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0004315	OMIM:300861	TAS				P		HPO:skoehler	
OMIM	300861	%300861 MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE; MRXSCS;;MENTAL RETARDATION, X-LINKED, WITH SEIZURES, HYPOGAMMAGLOBULINEMIA,AND GAIT DISTURBANCE		HP:0009830	OMIM:300861	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000238	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000256	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000369	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000457	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000568	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000878	OMIM:300863	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0000883	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA	HP:0012828	HP:0000926	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0001256	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0001423	OMIM:300863	TAS				I		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0001511	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0002007	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0002866	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0003196	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0004331	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0006028	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0006208	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0006402	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0008905	OMIM:300863	TAS				P		HPO:skoehler	
OMIM	300863	CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA		HP:0012789	OMIM:300863	TAS				P		HPO:probinson	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000238	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000256	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000358	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000369	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000567	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000772	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0000932	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0001250	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0001263	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0001274	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0001290	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0001419	OMIM:300864	TAS				I		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0002104	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0002245	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0006817	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0006956	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300864	CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED		HP:0011398	OMIM:300864	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000175	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000196	PMID:23913813	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000218	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	3/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000252	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	2/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000286	PMID:23913813	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000347	PMID:23913813,PMID:23076834,PMID:27302555	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000365	PMID:23076834	PCS		HP:0040284		P		HP:probinson	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000369	PMID:23354975	PCS		HP:0040284		P		HPO:probinson	1/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000378	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000400	PMID:27302555	PCS		HP:0040284		P		HP:probinson	10/11
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000403	PMID:23913813	PCS		HP:0040284		P		HP:probinson	2/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000411	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	2/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000437	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	3/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000455	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000486	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000527	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000527	OMIM:300867	PCS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000592	PMID:27302555	PCS		HP:0040284		P		HP:probinson	6/11
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000637	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000668	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	2/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000689	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000695	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000708	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0000769	OMIM:300867	TAS	HP:0003593			P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001007	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001156	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001212	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001249	PMID:23913813	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001250	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001252	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001263	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001290	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001388	PMID:23913813	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001423	OMIM:300867	TAS				I		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001511	PMID:23913813	PCS	HP:0030674	HP:0040284		P		HP:probinson	2/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001631	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001642	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001680	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001998	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0001998	PMID:27302555	PCS	HP:0003623	HP:0040284		P		HP:probinson	5/10
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0002000	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0002553	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0002827	PMID:23913813	PCS		HP:0040284		P		HP:probinson	2/3
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0004322	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	5/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0004325	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0005338	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0006695	OMIM:300867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0007655	PMID:23913813	PCS		HP:0040284		P		HPO:skoehler	4/5
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0008872	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0008897	PMID:23913813	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0009237	PMID:23913813	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	300867	#300867 KABUKI SYNDROME 2; KABUK2		HP:0011398	OMIM:300867	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000054	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000076	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000081	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000160	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000207	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000212	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000218	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000239	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000256	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000269	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000272	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000280	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000316	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000347	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000365	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000396	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000463	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000470	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000582	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000687	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0000691	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001000	OMIM:300868	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001051	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001257	OMIM:300868	IEA				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2	HP:0012828	HP:0001263	PMID:9307258	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001321	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001331	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001341	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001344	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001347	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001371	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001394	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001419	OMIM:300868	TAS				I		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001520	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001522	OMIM:300868	TAS				M		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001548	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001561	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001631	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	Occasional
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001789	PMID:8599356	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0001792	PMID:22305531	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002061	OMIM:300868	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002079	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002120	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002123	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002171	OMIM:300868	IEA				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002240	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002521	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002529	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0002714	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0003155	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0003517	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0003828	OMIM:300868	TAS				C		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0005280	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0005484	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0006986	OMIM:300868	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0007361	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0008064	OMIM:300868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0008936	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0011398	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0012448	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0012465	PMID:24259288	TAS				P		HPO:nvasilevsky	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0100704	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300868	#300868 MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 2; MCAHS2		HP:0200134	OMIM:300868	TAS				P		HPO:skoehler	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000028	PMID:19844254	PCS	HP:0003577	HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000135	OMIM:300869	IEA				P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000233	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000414	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000490	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000771	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	1/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0000837	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001256	OMIM:300869	IEA				P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001263	OMIM:300869	IEA				P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME	HP:0012825	HP:0001328	PMID:19844254	PCS	HP:0011463	HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001419	PMID:19844254	PCS				I	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001511	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001518	OMIM:300869	IEA				P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0001773	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0002231	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0004322	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0008734	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0012743	PMID:19844254	PCS				P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0040171	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300869	CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME		HP:0200055	PMID:19844254	PCS		HP:0040284		P	CHROMOSOME XQ27.3-Q28 DUPLICATION SYNDROME	HP:probinson	3/3
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0000717	OMIM:300872	IEA				P		HPO:skoehler	
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0000750	OMIM:300872	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0001249	OMIM:300872	IEA				P		HPO:skoehler	
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0001250	OMIM:300872	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0001419	OMIM:300872	TAS				I		HPO:skoehler	
OMIM	300872	AUTISM, SUSCEPTIBILITY TO, X-LINKED 6		HP:0002376	OMIM:300872	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000023	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000175	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000193	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000252	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000272	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000286	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000389	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000405	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000483	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000664	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000668	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000678	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000750	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000768	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0000926	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001156	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001263	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001388	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001419	OMIM:300881	TAS				I		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001620	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0001956	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0002162	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0002938	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0002970	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0003048	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0003180	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0003502	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0003561	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0005257	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0005280	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0008905	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0010049	OMIM:300881	IEA				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0010535	OMIM:300881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0010554	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0011800	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300881	BARATELA-SCOTT SYNDROME		HP:0100864	OMIM:300881	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000028	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000054	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000135	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000175	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000218	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	3/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000233	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000248	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	3/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000252	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000278	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000294	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000316	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000343	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000347	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000365	OMIM:300882	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000426	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000455	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000463	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	2/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000470	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000490	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000506	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000508	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	2/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000527	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000545	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000664	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000687	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0000965	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	2/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001007	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001249	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001250	PMID:22885700	IEA				P		HPO:probinson	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001263	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001290	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001377	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001417	PMID:22885700	IEA				I		HPO:probinson	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001423	OMIM:300882	TAS				I		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001770	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001773	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	3/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0001956	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0002020	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0002119	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	3/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0002553	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0002714	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	4/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0003764	OMIM:300882	IEA				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0003828	OMIM:300882	TAS				C		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0004209	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0004322	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0005280	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0008734	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0008872	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	2/4
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0008897	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0009623	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0040082	OMIM:300882	TAS				P		HPO:skoehler	
OMIM	300882	CORNELIA DE LANGE SYNDROME 5; CDLS5		HP:0200055	PMID:22885700	IEA		HP:0040284		P		HPO:probinson	2/5
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000238	OMIM:300884	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000252	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000316	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000369	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000463	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000648	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000666	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0000817	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36	HP:0031375	HP:0001250	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001263	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001290	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001371	OMIM:300884	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001419	OMIM:300884	TAS				I		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001423	OMIM:300884	TAS				I		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0001999	OMIM:300884	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0002059	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0002071	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0002240	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0002521	OMIM:300884	IEA				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0002719	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0003593	OMIM:300884	TAS				C		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0003642	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0007256	OMIM:300884	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0010864	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300884	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 36; EIEE36		HP:0012448	OMIM:300884	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0000053	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0000238	OMIM:300886	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0000400	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001250	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001257	OMIM:300886	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001263	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001344	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001419	OMIM:300886	TAS				I		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001635	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0001640	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0002187	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0002751	OMIM:300886	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0004749	OMIM:300886	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300886	#300886 MENTAL RETARDATION, X-LINKED, SYNDROMIC 32; MRXS32		HP:0005781	OMIM:300886	TAS				P		HPO:skoehler	
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000252	OMIM:300887	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000316	OMIM:300887	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000331	OMIM:300887	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000343	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000348	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000358	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000505	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000543	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0000545	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001057	OMIM:300887	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001263	OMIM:300887	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001423	OMIM:300887	TAS				I		HPO:skoehler	
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001631	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001636	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001714	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001852	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0001999	OMIM:300887	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0002079	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0002092	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0002553	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0003196	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0004322	OMIM:300887	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0006610	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0012448	OMIM:300887	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300887	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2; LSDMCA2		HP:0025356	OMIM:300887	IEA				P		HPO:skoehler	
OMIM	300888	HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT		HP:0000821	OMIM:300888	IEA				P		HPO:skoehler	
OMIM	300888	HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT		HP:0001419	OMIM:300888	TAS				I		HPO:skoehler	
OMIM	300888	HYPOTHYROIDISM, CENTRAL, AND TESTICULAR ENLARGEMENT		HP:0025502	OMIM:300888	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0000496	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0000718	OMIM:300894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0000726	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0000743	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001249	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001250	OMIM:300894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001263	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001272	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001300	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001332	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001337	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001344	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0001423	OMIM:300894	TAS				I		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002059	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002063	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002067	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002180	OMIM:300894	IEA				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002313	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0002465	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300894	#300894 NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5;;BETA-PROPELLER PROTEIN-ASSOCIATED NEURODEGENERATION; BPAN;;STATIC ENCEPHALOPATHY OF CHILDHOOD WITH NEURODEGENERATION IN ADULTHOOD;SENDA		HP:0012332	OMIM:300894	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000028	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000046	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000160	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000233	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000280	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000319	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000343	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000347	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000365	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000414	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000431	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000448	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000508	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000581	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0000957	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0001249	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0001263	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0001382	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0001419	OMIM:300895	TAS				I		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0004325	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0005280	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0011968	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300895	#300895 OHDO SYNDROME, X-LINKED; OHDOX;;BLEPHAROPHIMOSIS-MENTAL RETARDATION SYNDROME, MAAT-KIEVIT-BRUNNERTYPE		HP:0030084	OMIM:300895	TAS				P		HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000194	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000252	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000280	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000431	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000510	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000574	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0000639	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001250	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001263	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001290	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001321	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001423	OMIM:300896	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0001442	OMIM:300896	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0002020	OMIM:300896	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	HP:0040283
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0002059	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0002079	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0002521	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0002719	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0003593	OMIM:300896	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0012448	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0012471	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0031931	OMIM:300896	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300896	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm; CDG2M		HP:0200134	OMIM:300896	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIM; CDG2M	HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0000407	OMIM:300905	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0001265	OMIM:300905	IEA				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0001271	OMIM:300905	IEA				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0001423	OMIM:300905	TAS				I		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0001761	OMIM:300905	TAS				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0002378	OMIM:300905	TAS				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0003376	OMIM:300905	TAS				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0003474	OMIM:300905	IEA				P		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0003677	OMIM:300905	TAS				C		HPO:skoehler	
OMIM	300905	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 6; CMTX6		HP:0030237	OMIM:300905	TAS				P		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0000980	OMIM:300908	IEA				P		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0001419	OMIM:300908	TAS				I		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0001923	OMIM:30908	TAS				P		HPO:probinson	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0001974	OMIM:300908	IEA				P		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0003641	OMIM:300908	IEA				P		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0004447	OMIM:300908	IEA				P		HPO:skoehler	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0004814	OMIM:30908	TAS				P		HPO:probinson	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0006579	OMIM:30908	TAS				P		HPO:probinson	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0008282	OMIM:30908	TAS				P		HPO:probinson	
OMIM	300908	ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY		HP:0011273	OMIM:300908	IEA				P		HPO:skoehler	
OMIM	300909	ACQUIRED ANGIOEDEMA		HP:0100665	OMIM:300909	IEA				P		HPO:skoehler	
OMIM	300910	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18		HP:0000938	OMIM:300910	TAS				P		HPO:skoehler	
OMIM	300910	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18		HP:0000939	OMIM:300910	TAS				P		HPO:skoehler	
OMIM	300910	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18		HP:0001423	OMIM:300910	TAS				I		HPO:skoehler	
OMIM	300910	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18		HP:0002953	OMIM:300910	TAS				P		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0000007	OMIM:300911	TAS				I		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0001257	OMIM:300911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0001300	OMIM:300911	TAS				P		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0001347	OMIM:300911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0001419	OMIM:300911	TAS				I		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0002067	OMIM:300911	TAS				P		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0002322	OMIM:300911	TAS				P		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0002396	OMIM:300911	TAS				P		HPO:skoehler	
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0003487	OMIM:300911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300911	PARKINSONISM WITH SPASTICITY, X-LINKED		HP:0003677	OMIM:300911	TAS				C		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000020	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000311	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000322	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000341	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000426	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000430	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000463	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000565	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000733	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000752	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0000817	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001249	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001250	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001251	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001257	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98	HP:0012828	HP:0001263	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001344	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001419	OMIM:300912	TAS				I		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001508	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0001510	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0002020	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0002121	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0002123	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0002133	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0002521	OMIM:300912	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0003196	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0003577	OMIM:300912	TAS				C		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0003829	OMIM:300912	IEA				C		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0005484	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0008936	OMIM:300912	TAS				P		HPO:skoehler	
OMIM	300912	MENTAL RETARDATION, X-LINKED 98; MRX98		HP:0011968	OMIM:300912	IEA				P		HPO:skoehler	
OMIM	300914	#300914 DEAFNESS, X-LINKED 6; DFNX6		HP:0000365	OMIM:300914	IEA				P		HPO:skoehler	
OMIM	300914	#300914 DEAFNESS, X-LINKED 6; DFNX6		HP:0001419	OMIM:300914	TAS				I		HPO:skoehler	
OMIM	300914	#300914 DEAFNESS, X-LINKED 6; DFNX6		HP:0008554	OMIM:300914	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000252	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000377	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000482	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000508	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000565	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000568	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0000589	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0001249	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0001263	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0001417	OMIM:300915	TAS				I		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0002751	OMIM:300915	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0004322	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0012043	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300915	#300915 MICROPHTHALMIA, SYNDROMIC 13; MCOPS13;;MAINE MICROPHTHALMOS;;COLOBOMATOUS MICROPHTHALMIA WITH MICROCEPHALY, SHORT STATURE, ANDPSYCHOMOTOR RETARDATION		HP:0040080	OMIM:300915	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED	HP:0012828	HP:0000972	OMIM:300918	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0000982	OMIM:300918	IEA				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0001036	OMIM:300918	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0001419	OMIM:300918	TAS				I		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0007418	OMIM:300918	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0008392	OMIM:300918	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0025092	OMIM:300918	TAS				P		HPO:skoehler	
OMIM	300918	PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED		HP:0025610	OMIM:300918	IEA				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0000718	OMIM:300919	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0001249	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0001263	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0001290	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0001419	OMIM:300919	TAS				I		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0004322	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0011220	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300919	MENTAL RETARDATION, X-LINKED 99		HP:0011304	OMIM:300919	TAS				P		HPO:skoehler	
OMIM	300923	MENTAL RETARDATION, X-LINKED 100		HP:0001249	OMIM:300923	TAS				P		HPO:skoehler	
OMIM	300923	MENTAL RETARDATION, X-LINKED 100		HP:0001250	OMIM:300923	TAS				P		HPO:skoehler	
OMIM	300923	MENTAL RETARDATION, X-LINKED 100		HP:0001419	OMIM:300923	TAS				I		HPO:skoehler	
OMIM	300923	MENTAL RETARDATION, X-LINKED 100		HP:0001999	OMIM:300923	TAS				P		HPO:skoehler	
OMIM	300923	MENTAL RETARDATION, X-LINKED 100		HP:0002465	OMIM:300923	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0000276	OMIM:300928	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0000400	OMIM:300928	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0000486	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0000752	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0001249	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0001250	OMIM:300928	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0001263	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0001344	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0001419	OMIM:300928	TAS				I		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0002465	OMIM:300928	TAS				P		HPO:skoehler	
OMIM	300928	MENTAL RETARDATION, X-LINKED 101; MRX101		HP:0003577	OMIM:300928	TAS				C		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY	HP:0012825	HP:0000047	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000154	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000252	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000347	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000400	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000486	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000490	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0000687	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001249	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY	HP:0012825	HP:0001250	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001263	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001290	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001373	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001419	OMIM:300934	TAS				I		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001508	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0001928	OMIM:300934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0002079	OMIM:300934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0002650	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0003577	OMIM:300934	TAS				C		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0003642	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0011968	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300934	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IY		HP:0030084	OMIM:300934	TAS				P		HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0000098	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0000280	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0000845	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0000956	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0001176	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0001423	OMIM:300942	TAS				I	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0001714	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0001833	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0002591	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0002893	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0005616	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0010535	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0025267	OMIM:300942	TAS				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300942	CHROMOSOME Xq26.3 DUPLICATION SYNDROME		HP:0500001	OMIM:300942	IEA				P	CHROMOSOME XQ26.3 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	300943	#300943 PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 2; PAGH2;;ACROMEGALY DUE TO PITUITARY ADENOMA 2;;ACROMEGALY, X-LINKED		HP:0000845	PMID:25806920	PCS	HP:0003581			P		HPO:skoehler	
OMIM	300943	#300943 PITUITARY ADENOMA, GROWTH HORMONE-SECRETING, 2; PAGH2;;ACROMEGALY DUE TO PITUITARY ADENOMA 2;;ACROMEGALY, X-LINKED		HP:0002893	PMID:25470569	PCS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0000347	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0000405	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0000494	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0000653	OMIM:300946	IEA				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0001419	OMIM:300946	TAS				I		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0001972	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0008551	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300946	DIAMOND-BLACKFAN ANEMIA 14 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA14		HP:0011800	OMIM:300946	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0000486	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0000545	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0000564	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0000639	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001250	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001274	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001423	OMIM:300952	TAS				I		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001508	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001644	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001663	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0001695	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0004756	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0006956	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0007572	OMIM:300952	IEA				P		HPO:skoehler	
OMIM	300952	LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3		HP:0008936	OMIM:300952	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000054	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000154	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000253	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000303	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000348	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000556	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000609	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000965	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0000992	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0001305	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0001321	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0001423	OMIM:300953	TAS				I		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0001511	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002028	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002136	OMIM:300953	IEA				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002187	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002217	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002283	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002299	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0002719	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0004313	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0004322	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0005328	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0006313	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300953	TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5		HP:0008070	OMIM:300953	TAS				P		HPO:skoehler	
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0000252	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001249	OMIM:300957	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001288	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001290	OMIM:300957	TAS				P		HPO:skoehler	
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001321	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001337	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001419	OMIM:300957	TAS				I		HPO:skoehler	
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0001956	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0002171	OMIM:300957	TAS				P		HPO:skoehler	
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0004322	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0030260	OMIM:300957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300957	MENTAL RETARDATION, X-LINKED 12; MRX12		HP:0031418	OMIM:300957	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000175	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000204	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000252	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000365	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000718	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000752	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0000826	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001249	OMIM:300958	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001250	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001257	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001290	OMIM:300958	TAS				P		HPO:skoehler	
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001419	OMIM:300958	TAS				I		HPO:skoehler	
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001423	OMIM:300958	TAS				I		HPO:skoehler	
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0001999	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0002079	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0002119	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0002136	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0002650	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0003593	OMIM:300958	TAS				C		HPO:skoehler	
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0004325	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300958	MENTAL RETARDATION, X-LINKED 102		HP:0100660	OMIM:300958	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300960	MEND SYNDROME; MEND		HP:0000028	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000218	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000238	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000308	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000369	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000426	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000518	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0000752	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001249	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001250	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001263	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001276	OMIM:300960	IEA				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001290	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001305	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001419	OMIM:300960	TAS				I		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001650	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0001845	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0004322	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0004691	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0008064	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0010442	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0010557	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0011800	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300960	MEND SYNDROME; MEND		HP:0100807	OMIM:300960	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000028	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000256	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000316	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000322	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000337	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000475	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0000582	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001159	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001263	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001290	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001305	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001321	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001419	OMIM:300963	TAS				I		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001629	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001631	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001643	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0001845	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0002162	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0002465	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0002650	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0009882	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0010055	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0010808	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0012385	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300963	RITSCHER-SCHINZEL SYNDROME 2		HP:0030084	OMIM:300963	TAS				P		HPO:skoehler	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000219	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000252	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000276	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000307	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000308	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000316	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000336	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000343	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000365	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000369	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	9/12
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000389	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	6/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000391	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000400	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000411	OMIM:300966	TAS				P		HPO:skoehler	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000414	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000437	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000455	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000470	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000486	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	8/12
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000490	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/14
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000494	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000496	PMID:26637982	IEA		HP:0040284		P		HPO:probinson	3/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000520	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000545	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000579	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000639	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000664	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000729	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	7/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000739	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000750	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	8/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000767	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000938	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000960	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0000964	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001007	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/12
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001057	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001249	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	10/11
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001250	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001251	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001263	OMIM:300966	TAS				P		HPO:skoehler	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001264	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001272	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001290	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	9/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001315	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001320	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001321	OMIM:300966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001332	OMIM:300966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001337	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001382	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	6/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001385	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001419	PMID:26637982	PCS				I		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0001511	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002019	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	6/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002020	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002079	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33	HP:0012825	HP:0002119	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002141	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002194	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	10/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002650	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002705	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	8/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0002808	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0003577	OMIM:300966	TAS				C		HPO:skoehler	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0004696	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0005469	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0006979	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0007018	PMID:26637982	IEA		HP:0040284		P		HPO:probinson	2/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0007375	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/8
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0008070	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0008472	OMIM:300966	TAS				P		HPO:skoehler	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0008897	PMID:26637982	IEA		HP:0040284		P		HPO:probinson	8/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0009894	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0011220	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0011410	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	6/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0011822	PMID:26637982	PCS				P		HPO:probinson	
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0011927	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	3/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0040016	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	9/10
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0100797	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	300966	MENTAL RETARDATION, X-LINKED, SYNDROMIC 33		HP:0200136	PMID:26637982	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000028	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000154	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000160	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000194	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000256	OMIM:300967	IEA				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000272	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000276	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000448	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000486	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000545	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000582	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000678	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000687	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000718	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0000823	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001249	PMID:27550220	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001250	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001251	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001270	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001290	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001319	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001321	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001337	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001388	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001419	PMID:27550220	PCS				I		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001533	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001611	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001629	PMID:27550220	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001643	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001655	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001667	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001763	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0001822	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002007	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002020	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002650	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002684	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002705	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0002808	OMIM:300967	TAS				P		HPO:skoehler	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0004411	OMIM:300967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0011342	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0030223	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0030682	PMID:27550220	PCS				P		HPO:probinson	
OMIM	300967	MENTAL RETARDATION, X-LINKED, SYNDROMIC 34; MRXS34		HP:0040194	PMID:27329731	PCS				P		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000110	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000126	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000164	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000175	PMID:26833328	PCS				P		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000193	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000248	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000319	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000324	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000341	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000343	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000358	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000365	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	11/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000369	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000414	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000431	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000448	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000453	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	6/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000483	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000486	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000518	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000540	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000545	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000601	PMID:26833328	PCS				P		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000750	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000960	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0000998	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001182	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001249	PMID:26833328	PCS				P		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001250	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	4/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001263	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	17/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001290	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	8/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001305	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/13
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001321	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	6/11
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001385	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	8/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001388	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001423	PMID:26833328	PCS				I		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001631	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001643	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001761	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0001773	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002023	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	9/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002079	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	8/13
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002098	OMIM:300968	TAS	HP:0003623			P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002205	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	9/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002536	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/10
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002650	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	11/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002827	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0002926	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	6/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0004322	PMID:26833328	PCS				P		HPO:probinson	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0005280	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0011220	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0011968	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0012745	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0012813	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	5/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0100259	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	9/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0100559	PMID:26833328	PCS		HP:0040284		P		HPO:probinson	7/17
OMIM	300968	MENTAL RETARDATION, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED		HP:0200055	OMIM:300968	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0000103	PMID:27120771	PCS				P		HPO:probinson	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0000848	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0001419	PMID:27120771	PCS				I		HPO:probinson	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0001561	PMID:27120771	PCS				P		HPO:probinson	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0001563	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0001622	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0002150	PMID:27120771	PCS				P		HPO:probinson	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0002900	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0002902	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0003113	OMIM:300971	TAS				P		HPO:skoehler	
OMIM	300971	BARTTER SYNDROME, TYPE 5, ANTENATAL, TRANSIENT		HP:0012408	PMID:27120771	PCS				P		HPO:probinson	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0000407	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0000540	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001249	OMIM:300972	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001250	OMIM:300972	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001394	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001397	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001419	OMIM:300972	TAS				I		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001744	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0001882	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0002240	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0002718	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0002910	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0003828	OMIM:300972	TAS				C		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0004313	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300972	IMMUNODEFICIENCY 47		HP:0006579	OMIM:300972	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000054	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000232	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000268	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000286	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000348	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000455	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000456	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0000582	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0001272	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0001290	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0001419	OMIM:300977	TAS				I		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0001773	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0002751	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0003065	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0003758	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0007256	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0008734	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0010864	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0031878	OMIM:300977	IEA				P		HPO:skoehler	
OMIM	300977	SCHOLTE SYNDROME; SHLTS		HP:0200055	OMIM:300977	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000028	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000047	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000054	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000160	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000220	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000252	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000272	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000316	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000337	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000347	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000426	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000431	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000448	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000494	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000601	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000708	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000718	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000739	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0000750	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001156	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001249	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001257	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001263	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001337	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001347	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001419	OMIM:300978	TAS				I		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001510	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0001792	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0002015	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0002136	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0002213	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0002465	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0002714	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0008734	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0011304	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0011968	OMIM:300978	TAS				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0100716	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300978	TONNE-KALSCHEUER SYNDROME; TOKAS		HP:0100962	OMIM:300978	IEA				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000272	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000286	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000297	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000303	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000574	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000739	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000750	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0000752	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001249	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001250	OMIM:300979	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001263	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001290	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001321	OMIM:300979	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0001417	OMIM:300979	TAS				I		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0002079	OMIM:300979	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0002360	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0002553	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0004322	OMIM:300979	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0012471	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300979	XQ25 DUPLICATION SYNDROME		HP:0045075	OMIM:300979	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0000028	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0000054	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0000154	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0000280	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0000463	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0001249	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0001250	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0001263	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0001344	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0001419	OMIM:300982	TAS				I		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0002119	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300982	MENTAL RETARDATION, X-LINKED 103		HP:0002126	OMIM:300982	TAS				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000278	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000348	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000486	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000639	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000648	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000718	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000752	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0000817	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001249	OMIM:300983	TAS				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001250	OMIM:300983	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001251	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001257	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001263	OMIM:300983	TAS				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001337	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001344	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001347	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0001419	OMIM:300983	TAS				I		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0002079	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0002120	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0003593	OMIM:300983	IEA				C		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0012448	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300983	MENTAL RETARDATION, X-LINKED 104; MRX104		HP:0031936	OMIM:300983	IEA				P		HPO:skoehler	
OMIM	300984	MENTAL RETARDATION, X-LINKED 105; MRX105		HP:0000708	OMIM:300984	TAS				P		HPO:skoehler	
OMIM	300984	MENTAL RETARDATION, X-LINKED 105; MRX105		HP:0001249	OMIM:300984	TAS				P		HPO:skoehler	
OMIM	300984	MENTAL RETARDATION, X-LINKED 105; MRX105		HP:0001344	OMIM:300984	IEA				P		HPO:skoehler	
OMIM	300984	MENTAL RETARDATION, X-LINKED 105; MRX105		HP:0001419	OMIM:300984	TAS				I		HPO:skoehler	
OMIM	300985	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED		HP:0000027	OMIM:300985	TAS				P		HPO:skoehler	
OMIM	300985	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED		HP:0001417	OMIM:300985	TAS				I		HPO:skoehler	
OMIM	300985	VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED		HP:0012873	OMIM:300985	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000154	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000218	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000286	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000316	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000322	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000347	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000430	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000601	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000718	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000722	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000729	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0000739	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001249	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001250	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001251	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001263	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001276	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001288	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001290	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001317	OMIM:300986	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001344	OMIM:300986	IEA				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001388	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001423	OMIM:300986	TAS				I		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001508	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0001763	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0002019	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0002020	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0002376	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0002650	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0003307	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0004322	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0005484	OMIM:300986	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0011968	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0012471	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300986	MENTAL RETARDATION, X-LINKED, SYNDROMIC, BAIN TYPE; MRXSB		HP:0012745	OMIM:300986	TAS				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0000010	OMIM:300988	TAS				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0000964	OMIM:300988	TAS				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0001419	OMIM:300988	TAS				I		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0001875	OMIM:300988	IEA				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0001888	OMIM:300988	TAS				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0002205	OMIM:300988	TAS				P		HPO:skoehler	
OMIM	300988	IMMUNODEFICIENCY 50; IMD50		HP:0004313	OMIM:300988	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0000193	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0000272	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0000316	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0000494	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0000520	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0001373	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0001382	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0001417	OMIM:300989	TAS				I		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0001653	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0001763	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0002007	OMIM:300989	TAS				P		HPO:skoehler	
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0002119	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0002647	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0004482	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0004937	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0004944	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0010646	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300989	MEESTER-LOEYS SYNDROME		HP:0012385	OMIM:300989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000110	OMIM:300990	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000121	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000160	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000175	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000193	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000219	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000337	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000347	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000407	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000410	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000494	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000518	OMIM:300990	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000565	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000678	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0000684	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN	HP:0012825	HP:0001249	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0001419	PMID:27811305	PCS				I		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0001763	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0001883	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0001903	OMIM:300990	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0002003	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0002150	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0003593	OMIM:300990	IEA				C		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0004209	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0004445	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0009836	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0011800	OMIM:300990	IEA				P		HPO:skoehler	
OMIM	300990	MIDFACE HYPOPLASIA, HEARING IMPAIRMENT, ELLIPTOCYTOSIS, AND NEPHROCALCINOSIS; MFHIEN		HP:0012368	PMID:27811305	PCS				P		HPO:probinson	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0000789	OMIM:300991	TAS				P		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0001419	OMIM:300991	TAS				I		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0001696	OMIM:300991	TAS				P		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0002110	OMIM:300991	TAS				P		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0002643	OMIM:300991	TAS				P		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0011108	OMIM:300991	TAS				P		HPO:skoehler	
OMIM	300991	CILIARY DYSKINESIA, PRIMARY, 36, X-LINKED; CILD36		HP:0012735	OMIM:300991	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0000047	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0000194	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0000316	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0000639	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0000646	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0001249	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0001263	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0008499	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300997	MENTAL RETARDATION, X-LINKED 106; MRX106		HP:0008734	OMIM:300997	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000028	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000047	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000160	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000219	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000286	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000303	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000308	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000319	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000343	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000365	OMIM:300998	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000411	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000545	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000750	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0000954	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001156	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001182	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001249	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001250	OMIM:300998	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001251	OMIM:300998	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001263	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001321	OMIM:300998	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0001511	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0002650	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0002655	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0008734	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0012385	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	300998	MENTAL RETARDATION, X-LINKED, SYNDROMIC, 35; MRXS35		HP:0030084	OMIM:300998	IEA				P		HPO:skoehler	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000112	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000225	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000246	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000388	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000421	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000964	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0000967	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001287	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001419	OMIM:301000	IEA				I		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001873	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001878	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001888	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001891	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0001983	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002037	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002090	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002248	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002249	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002783	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002788	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002848	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002850	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002963	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0002971	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0003010	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0003212	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0003261	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0005310	OMIM:301000	TAS				P		HPO:probinson	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0005537	OMIM:301000	IEA				P		HPO:iea	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0011944	OMIM:301000	TAS				P		HPO:probinson	
OMIM	301000	#301000 WISKOTT-ALDRICH SYNDROME; WAS;;WISKOTT-ALDRICH SYNDROME 1; WAS1;;ALDRICH SYNDROME;;ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME;;IMMUNODEFICIENCY 2; IMD2		HP:0040184	OMIM:301000	TAS				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000096	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000100	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000341	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000347	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000565	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000639	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0000750	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001249	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001250	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001257	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001263	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001272	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0001310	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0002059	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0002126	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0003774	OMIM:301006	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	301006	GALLOWAY-MOWAT SYNDROME 2, X-LINKED; GAMOS2		HP:0012579	OMIM:301006	IEA				P		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0001250	OMIM:301008	IEA				P		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0001263	OMIM:301008	IEA				P		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0001344	OMIM:301008	IEA				P		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0003828	OMIM:301008	IEA				C		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0007018	OMIM:301008	IEA				P		HPO:skoehler	
OMIM	301008	MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE; MRXSHG		HP:0100710	OMIM:301008	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000275	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000276	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000303	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000319	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000400	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000729	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0000752	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0001249	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301013	MENTAL RETARDATION, X-LINKED 107; MRX107		HP:0001263	OMIM:301013	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0000767	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0000768	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0000938	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0002650	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0002757	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0004586	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0008422	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301014	OSTEOGENESIS IMPERFECTA, TYPE XIX; OI19		HP:0008905	OMIM:301014	IEA				P		HPO:skoehler	
OMIM	301015	HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED		HP:0001878	OMIM:301015	IEA				P		HPO:skoehler	
OMIM	301015	HEMOLYTIC ANEMIA, CONGENITAL, X-LINKED		HP:0003577	OMIM:301015	IEA				C		HPO:skoehler	
OMIM	301018	DEAFNESS, X-LINKED 7; DFNX7		HP:0000365	OMIM:301018	IEA				P		HPO:skoehler	
OMIM	301018	DEAFNESS, X-LINKED 7; DFNX7		HP:0000506	OMIM:301018	IEA				P		HPO:skoehler	
OMIM	301018	DEAFNESS, X-LINKED 7; DFNX7		HP:0000508	OMIM:301018	IEA				P		HPO:skoehler	
OMIM	301018	DEAFNESS, X-LINKED 7; DFNX7		HP:0000574	OMIM:301018	IEA				P		HPO:skoehler	
OMIM	301018	DEAFNESS, X-LINKED 7; DFNX7		HP:0003577	OMIM:301018	IEA				C		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0001263	OMIM:301020	IEA				P		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0001266	OMIM:301020	IEA				P		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0001272	OMIM:301020	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0002071	OMIM:301020	IEA				P		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0002123	OMIM:301020	IEA				P		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0002151	OMIM:301020	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0003828	OMIM:301020	IEA				C		HPO:skoehler	
OMIM	301020	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12; MC1DN12		HP:0031936	OMIM:301020	IEA				P		HPO:skoehler	
OMIM	301021	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30; MC1DN30		HP:0003577	OMIM:301021	IEA				C		HPO:skoehler	
OMIM	301021	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30; MC1DN30		HP:0003811	OMIM:301021	IEA				M		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000028	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000047	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000049	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000054	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000104	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000126	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000158	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000179	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000252	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000272	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000286	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000316	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000358	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000369	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000407	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0000463	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001182	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001249	OMIM:301040	IEA				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001250	OMIM:301040	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001257	OMIM:301040	IEA				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001263	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001423	OMIM:301040	IEA				I		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001510	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001537	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001566	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001629	OMIM:301040	IEA				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001762	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0001939	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002019	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002020	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002059	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002673	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002688	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002751	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0002937	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0003196	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX	HP:0012825	HP:0004840	OMIM:301040	TAS				P		HPO:probinson	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0005280	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0008551	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0008897	OMIM:301040	TAS				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0008947	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0009466	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0010806	OMIM:301040	IEA				P		HPO:iea	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0010808	OMIM:301040	TAS				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0011682	OMIM:301040	TAS				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0011903	OMIM:301040	IEA				P		HPO:skoehler	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0011907	OMIM:301040	TAS				P		HPO:probinson	
OMIM	301040	ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX		HP:0030084	OMIM:301040	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000083	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000093	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000100	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000123	OMIM:301050	IEA				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000407	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000519	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000545	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000822	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0000829	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0001142	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0001417	OMIM:301050	IEA				I		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0001423	OMIM:301050	TAS				I		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0001425	OMIM:301050	TAS				I		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0001873	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0002907	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0003676	OMIM:301050	TAS				C		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0003774	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0004722	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0006756	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0008064	OMIM:301050	IEA				P		HPO:iea	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0011501	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0030034	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301050	ALPORT SYNDROME, X-LINKED; ATS		HP:0200020	OMIM:301050	TAS				P		HPO:skoehler	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0000691	OMIM:301200	IEA				P		HPO:iea	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0000705	OMIM:301200	IEA				P		HPO:iea	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0001423	OMIM:301200	IEA				I		HPO:iea	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0001939	OMIM:301200	IEA				P		HPO:iea	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0006297	OMIM:301200	TAS				P		HPO:skoehler	
OMIM	301200	#301200 AMELOGENESIS IMPERFECTA, TYPE IE; AI1E;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1;;AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, WITH SNOW-CAPPED TEETH;;AMELOGENESIS IMPERFECTA, X-LINKED 1; AIH1;;ENAMEL HYPOPLASIA, X-LINKED		HP:0200095	OMIM:301200	TAS				P		HPO:skoehler	
OMIM	301201	AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2		HP:0000705	OMIM:301201	IEA				P		HPO:skoehler	
OMIM	301201	AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 2		HP:0001417	OMIM:301201	IEA				I		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000023	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000505	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000559	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000572	OMIM:301220	IEA				P		HPO:probinson	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000613	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000962	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0000966	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001249	OMIM:301220	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001250	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001263	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001417	OMIM:301220	IEA				I		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001419	OMIM:301220	TAS				I		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001531	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0001939	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0002014	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0002301	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0002583	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0004798	OMIM:301220	IEA				P		HPO:probinson	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0006532	OMIM:301220	PCS				P		HPO:probinson	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0007599	OMIM:301220	IEA				P		HPO:probinson	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0007759	OMIM:301220	IEA				P		HPO:iea	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0011034	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0011229	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301220	PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS, X-LINKED		HP:0012227	OMIM:301220	TAS				P		HPO:skoehler	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0001260	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0001310	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0001419	OMIM:301310	IEA				I		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0001924	OMIM:301310	TAS				P		HPO:skoehler	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0001939	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0002075	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0002080	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0002169	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0002470	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0003487	OMIM:301310	IEA				P		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0003621	OMIM:301310	IEA				C		HPO:iea	
OMIM	301310	ANEMIA, SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA		HP:0004840	OMIM:301310	IEA				P		HPO:iea	
OMIM	301410	301410 NEURAL TUBE DEFECTS, X-LINKEDSPINA BIFIDA, X-LINKED, INCLUDED		HP:0001417	OMIM:301410	TAS				I		HPO:skoehler	
OMIM	301410	301410 NEURAL TUBE DEFECTS, X-LINKEDSPINA BIFIDA, X-LINKED, INCLUDED		HP:0002323	OMIM:301410	IEA				P		HPO:skoehler	
OMIM	301410	301410 NEURAL TUBE DEFECTS, X-LINKEDSPINA BIFIDA, X-LINKED, INCLUDED		HP:0002414	OMIM:301410	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0000083	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0000093	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0000822	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0000823	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0000966	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001004	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001014	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001131	OMIM:301500	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001155	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001250	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001419	OMIM:301500	IEA				I		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001635	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001658	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001681	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001712	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0001903	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002013	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002014	OMIM:301500	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002018	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002027	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002326	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0002380	OMIM:301500	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0003394	OMIM:301500	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0003401	OMIM:301500	IEA				P		HPO:skoehler	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0003621	OMIM:301500	IEA				C		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0005144	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED	HP:0012825	HP:0006536	OMIM:301500	IEA				P		HPO:probinson	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0011675	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0012332	OMIM:301500	IEA				P		HPO:iea	
OMIM	301500	#301500 FABRY DISEASE;;ANGIOKERATOMA CORPORIS DIFFUSUM;;ANDERSON-FABRY DISEASE;;HEREDITARY DYSTOPIC LIPIDOSIS;;ALPHA-GALACTOSIDASE A DEFICIENCY;;GLA DEFICIENCY;;CERAMIDE TRIHEXOSIDASE DEFICIENCYFABRY DISEASE, CARDIAC VARIANT, INCLUDED		HP:0012702	OMIM:301500	TAS				P		HPO:skoehler	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0000175	OMIM:301590	IEA				P		HPO:iea	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0000384	OMIM:301590	IEA				P		HPO:iea	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0000528	OMIM:301590	TAS				P		HPO:skoehler	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0000568	OMIM:301590	IEA				P		HPO:skoehler	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0000924	OMIM:301590	IEA				P		HPO:iea	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0001249	OMIM:301590	IEA				P		HPO:iea	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0001417	OMIM:301590	IEA				I		HPO:iea	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0001419	OMIM:301590	TAS				I		HPO:skoehler	
OMIM	301590	MICROPHTHALMIA, SYNDROMIC 4		HP:0009755	OMIM:301590	IEA				P		HPO:skoehler	
OMIM	301700	ANOSMIA		HP:0000458	OMIM:301700	IEA				P		HPO:iea	
OMIM	301700	ANOSMIA		HP:0001417	OMIM:301700	IEA				I		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0000407	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0000543	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0000565	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0000648	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0000726	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001250	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001252	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001254	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001257	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001263	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001265	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001272	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001284	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001290	OMIM:301790	TAS				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001310	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001324	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001419	OMIM:301790	IEA				I		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0001522	OMIM:301790	IEA				M		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002013	OMIM:301790	IEA				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002015	OMIM:301790	IEA				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002020	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002080	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002171	OMIM:301790	IEA				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002205	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002311	OMIM:301790	TAS				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002529	OMIM:301790	IEA				P		HPO:skoehler	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0002599	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0003593	OMIM:301790	IEA				C		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0004881	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0004885	OMIM:301790	IEA				P		HPO:iea	
OMIM	301790	SPINOCEREBELLAR ATAXIA, X-LINKED 3		HP:0008757	OMIM:301790	IEA				P		HPO:iea	
OMIM	301800	ANUS, IMPERFORATE		HP:0000047	OMIM:301800	IEA				P		HPO:iea	
OMIM	301800	ANUS, IMPERFORATE		HP:0000365	OMIM:301800	IEA				P		HPO:iea	
OMIM	301800	ANUS, IMPERFORATE		HP:0001417	OMIM:301800	IEA				I		HPO:iea	
OMIM	301800	ANUS, IMPERFORATE		HP:0002023	OMIM:301800	IEA				P		HPO:iea	
OMIM	301800	ANUS, IMPERFORATE		HP:0004397	OMIM:301800	IEA				P		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0000202	OMIM:301815	IEA				P		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0000968	OMIM:301815	IEA				P		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:301815	IEA				P		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0001417	OMIM:301815	IEA				I		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0001510	OMIM:301815	IEA				P		HPO:iea	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0002803	OMIM:301815	IEA				P		HPO:skoehler	
OMIM	301815	ARTHROGRYPOSIS, ECTODERMAL DYSPLASIA, CLEFT LIP/PALATE, AND DEVELOPMENTAL DELAY		HP:0025356	OMIM:301815	IEA				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000023	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000028	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000047	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000054	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000347	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0000508	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001252	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001284	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001308	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001419	OMIM:301830	TAS				I		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001558	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0001939	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002058	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002093	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002398	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002650	OMIM:301830	IEA				P		HPO:iea	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002747	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002804	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0002828	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0003198	OMIM:301830	IEA				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0006829	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0007269	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301830	#301830 SPINAL MUSCULAR ATROPHY, X-LINKED 2; SMAX2;;SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE;;SPINAL MUSCULAR ATROPHY, INFANTILE X-LINKED; XLSMA;;ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, X-LINKED;;AMC, DISTAL, X-LINKED;;ARTHROGRYPOSIS, X-LINKED, TYPE I; AMCX1		HP:0010628	OMIM:301830	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0000365	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0000572	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0000639	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0000648	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001249	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001250	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001251	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001263	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001284	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001319	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001344	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001347	OMIM:301835	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001419	OMIM:301835	IEA				I		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001510	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0001522	OMIM:301835	IEA				M		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002015	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002307	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002445	OMIM:301835	IEA				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002719	PMID:8498830	PCS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002721	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0002788	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0003323	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18		HP:0008311	OMIM:301835	IEA				P		HPO:iea	
OMIM	301835	#301835 ARTS SYNDROME; ARTS;;MENTAL RETARDATION, X-LINKED, SYNDROMIC, ARTS TYPE; MRXSARTS;;ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 18; MRXS18	HP:0003676	HP:0009830	OMIM:301835	TAS				P		HPO:skoehler	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0000726	OMIM:301840	IEA				P		HPO:skoehler	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0001251	OMIM:301840	IEA				P		HPO:iea	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0001337	OMIM:301840	IEA				P		HPO:iea	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0001417	OMIM:301840	IEA				I		HPO:iea	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0002062	OMIM:301840	IEA				P		HPO:iea	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0007256	OMIM:301840	TAS				P		HPO:skoehler	
OMIM	301840	SPINOCEREBELLAR ATAXIA, X-LINKED 4		HP:0031936	OMIM:301840	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000153	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000418	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000430	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000953	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000964	OMIM:301845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	301845	BAZEX SYNDROME; BZX		HP:0000966	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0001006	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0001047	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0001056	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0001382	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0001423	OMIM:301845	IEA				I		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0002208	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0002671	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0003593	OMIM:301845	IEA				C		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0003764	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0003777	OMIM:301845	IEA				P		HPO:iea	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0009765	OMIM:301845	TAS				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0009886	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0025367	OMIM:301845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	301845	BAZEX SYNDROME; BZX		HP:0032152	OMIM:301845	IEA				P		HPO:skoehler	
OMIM	301845	BAZEX SYNDROME; BZX		HP:0040154	OMIM:301845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000028	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000054	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000252	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000280	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000336	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000400	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000490	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000505	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000508	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000581	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000639	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000771	OMIM:301900	IEA				P		HPO:skoehler	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0000823	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001182	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001250	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001252	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001290	OMIM:301900	TAS				P		HPO:skoehler	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001419	OMIM:301900	IEA				I		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001513	OMIM:301900	IEA				P		HPO:skoehler	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0001831	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0002353	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0002650	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0002684	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0002808	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0004322	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0006110	OMIM:301900	TAS				P		HPO:probinson	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0006118	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0008094	OMIM:301900	TAS				P		HPO:probinson	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0008445	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0008478	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0008687	OMIM:301900	IEA				P		HPO:iea	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0010864	OMIM:301900	IEA				P		HPO:probinson	
OMIM	301900	BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS		HP:0045025	OMIM:301900	IEA				P		HPO:skoehler	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0001423	OMIM:301940	IEA				I		HPO:iea	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0003502	OMIM:301940	IEA				P		HPO:iea	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0005067	OMIM:301940	IEA				P		HPO:iea	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0005802	OMIM:301940	TAS				P		HPO:skoehler	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0005807	OMIM:301940	IEA				P		HPO:skoehler	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0009565	OMIM:301940	TAS				P		HPO:probinson	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0010034	OMIM:301940	TAS				P		HPO:probinson	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0010105	OMIM:301940	TAS				P		HPO:probinson	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0010432	OMIM:301940	TAS				P		HPO:probinson	
OMIM	301940	BRACHYDACTYLY, MONONEN TYPE		HP:0100266	OMIM:301940	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000028	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000218	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000252	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000365	OMIM:301950	IEA				P		HPO:skoehler	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000369	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000411	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000465	OMIM:301950	IEA				P		HPO:skoehler	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0000494	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0001328	OMIM:301950	IEA				P		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0001417	OMIM:301950	IEA				I		HPO:iea	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0001642	OMIM:301950	IEA				P		HPO:skoehler	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0002705	OMIM:301950	TAS				P		HPO:skoehler	
OMIM	301950	301950 BRANCHIAL ARCH SYNDROME, X-LINKED;;MANDIBULOFACIAL DYSOSTOSIS, TORIELLO TYPE		HP:0004322	OMIM:301950	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0000252	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0000953	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0001063	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0001182	OMIM:302000	TAS				P		HPO:probinson	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0001249	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0001417	OMIM:302000	IEA				I		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0001597	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0003510	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0003819	OMIM:302000	IEA				M		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0007418	OMIM:302000	IEA				P		HPO:iea	
OMIM	302000	BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE		HP:0009381	OMIM:302000	TAS				P		HPO:probinson	
OMIM	302030	CALVARIAL HYPEROSTOSIS		HP:0000348	OMIM:302030	IEA				P		HPO:skoehler	
OMIM	302030	CALVARIAL HYPEROSTOSIS		HP:0001417	OMIM:302030	IEA				I		HPO:iea	
OMIM	302030	CALVARIAL HYPEROSTOSIS		HP:0001939	OMIM:302030	IEA				P		HPO:iea	
OMIM	302030	CALVARIAL HYPEROSTOSIS		HP:0004490	OMIM:302030	IEA				P		HPO:iea	
OMIM	302030	CALVARIAL HYPEROSTOSIS		HP:0005280	OMIM:302030	IEA				P		HPO:skoehler	
OMIM	302045	CARDIOMYOPATHY, DILATED, 3B		HP:0001417	OMIM:302045	IEA				I		HPO:iea	
OMIM	302045	CARDIOMYOPATHY, DILATED, 3B		HP:0001644	OMIM:302045	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000293	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000303	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000311	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000337	OMIM:302060	IEA				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000400	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0000490	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001270	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001288	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001419	OMIM:302060	IEA				I		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001508	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001510	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001635	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001639	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001644	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001706	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001762	OMIM:302060	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001875	OMIM:302060	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001913	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0001992	OMIM:302060	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302060	BARTH SYNDROME; BTHS		HP:0002058	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0003535	OMIM:302060	IEA				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0003546	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0003756	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0004913	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0005437	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0008322	OMIM:302060	IEA				P		HPO:iea	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0011675	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302060	BARTH SYNDROME; BTHS		HP:0012378	OMIM:302060	TAS				P		HPO:skoehler	
OMIM	302200	CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES		HP:0001141	OMIM:302200	TAS				P		HPO:probinson	
OMIM	302200	CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES		HP:0001417	PMID:19414485	PCS				I		HPO:probinson	
OMIM	302200	CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES		HP:0010695	OMIM:302200	TAS				P		HPO:probinson	
OMIM	302200	CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES		HP:0100018	OMIM:302200	TAS	HP:0003577			P		HPO:probinson	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000275	OMIM:302350	TAS				P		HPO:probinson	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000276	OMIM:302350	TAS				P		HPO:probinson	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000400	OMIM:302350	TAS				P		HPO:probinson	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000426	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000448	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000482	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000501	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000519	OMIM:302350	TAS				P		HPO:skoehler	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000568	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000572	OMIM:302350	IEA				P		HPO:skoehler	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000639	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000699	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0000717	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0001423	OMIM:302350	IEA				I		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0001500	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0002342	OMIM:302350	IEA		HP:0040284		P		HPO:skoehler	80%
OMIM	302350	NANCE-HORAN SYNDROME		HP:0006332	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0006346	PMID:29042737	PCS		HP:0040284		P		HPO:iea	1/1
OMIM	302350	NANCE-HORAN SYNDROME		HP:0008031	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0009803	OMIM:302350	IEA				P		HPO:iea	
OMIM	302350	NANCE-HORAN SYNDROME		HP:0011092	PMID:29042737	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	302400	CENTRAL INCISORS, ABSENCE OF		HP:0001417	OMIM:302400	IEA				I		HPO:iea	
OMIM	302400	CENTRAL INCISORS, ABSENCE OF		HP:0006289	OMIM:302400	IEA				P		HPO:iea	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0000486	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0000514	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0000639	OMIM:302500	IEA				P		HPO:iea	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001251	OMIM:302500	IEA				P		HPO:iea	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001260	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001270	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001272	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001319	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001417	OMIM:302500	IEA				I		HPO:iea	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0001419	OMIM:302500	TAS				I		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0002080	OMIM:302500	TAS				P		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0003577	OMIM:302500	TAS				C		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0003621	OMIM:302500	IEA				C		HPO:iea	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0003680	OMIM:302500	TAS				C		HPO:skoehler	
OMIM	302500	SPINOCEREBELLAR ATAXIA, X-LINKED 1; SCAX1		HP:0003698	OMIM:302500	IEA				P		HPO:skoehler	
OMIM	302600	SPINOCEREBELLAR ATAXIA, X-LINKED 2		HP:0001251	OMIM:302600	IEA				P		HPO:iea	
OMIM	302600	SPINOCEREBELLAR ATAXIA, X-LINKED 2		HP:0001417	OMIM:302600	IEA				I		HPO:iea	
OMIM	302600	SPINOCEREBELLAR ATAXIA, X-LINKED 2		HP:0002071	OMIM:302600	IEA				P		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0000365	OMIM:302700	IEA				P		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0000618	OMIM:302700	IEA				P		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0000726	OMIM:302700	IEA				P		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0001258	OMIM:302700	IEA				P		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0001417	OMIM:302700	IEA				I		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0003621	OMIM:302700	IEA				C		HPO:iea	
OMIM	302700	CEREBRAL SCLEROSIS, DIFFUSE, SCHOLZ TYPE		HP:0007340	OMIM:302700	IEA				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0000407	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0000639	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0000763	OMIM:302800	IEA				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0000764	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001260	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001265	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001270	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001272	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001310	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001337	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001419	OMIM:302800	TAS				I		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001423	OMIM:302800	IEA				I		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001761	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0001771	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002015	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002311	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002355	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002385	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002395	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002427	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002460	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002460	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002500	OMIM:302800	IEA				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0002936	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003380	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003383	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003431	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003487	OMIM:302800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003677	OMIM:302800	TAS				C		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003693	OMIM:302800	IEA				P		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0003829	OMIM:302800	IEA				C		HPO:iea	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0009830	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0040078	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302800	#302800 CHARCOT-MARIE-TOOTH DISEASE, X-LINKED DOMINANT, 1; CMTX1;;CMTX;;CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED;;HEREDITARY MOTOR AND SENSORY NEUROPATHY, X-LINKED;;HMSN, X-LINKED;;CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED, 1;;CMT2, FORMERLY		HP:0040083	OMIM:302800	TAS				P		HPO:skoehler	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0001249	OMIM:302901	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0001284	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0001419	OMIM:302801	IEA				I		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0001761	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0002460	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2	HP:0012825	HP:0002936	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003376	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003431	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003482	OMIM:302801	IEA				P		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003484	OMIM:302901	IEA				P		HPO:probinson	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003593	OMIM:302801	IEA				C		HPO:iea	
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0003693	OMIM:302901	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	302801	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2		HP:0009027	OMIM:302801	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0000762	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0001284	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0001419	OMIM:302802	IEA				I		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0001761	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0002385	OMIM:302802	IEA				P		HPO:skoehler	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0002460	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0002936	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0003376	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0003482	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0003484	OMIM:302802	IEA				P		HPO:probinson	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0003693	OMIM:302802	IEA				P		HPO:iea	
OMIM	302802	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 3; CMTX3		HP:0009027	OMIM:302802	IEA				P		HPO:iea	
OMIM	302803	CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA		HP:0001362	OMIM:302803	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	302803	CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA		HP:0001419	OMIM:302803	TAS				I		HPO:probinson	
OMIM	302803	CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA		HP:0003390	OMIM:302803	TAS				P		HPO:probinson	
OMIM	302803	CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA		HP:0007002	OMIM:302803	TAS				P		HPO:probinson	
OMIM	302803	CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA		HP:0007385	OMIM:302803	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0000639	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0000819	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001251	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001260	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001284	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001417	OMIM:302900	IEA				I		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001635	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001691	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001761	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001765	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0001953	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0002062	OMIM:302900	PCS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0002495	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0002650	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0002936	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003115	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003116	OMIM:302900	TAS				P		HPO:skoehler	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003133	OMIM:302900	PCS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003134	OMIM:302900	PCS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003209	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003232	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003376	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003487	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0003621	OMIM:302900	IEA				C		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0005157	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0008954	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0008963	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0009005	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0009027	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0010831	OMIM:302900	TAS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0011397	OMIM:302900	PCS				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0011399	OMIM:302900	IEA				P		HPO:probinson	
OMIM	302900	302900 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED		HP:0011441	OMIM:302900	PCS				P		HPO:probinson	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000047	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000175	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000365	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000400	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000411	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0000589	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0001417	OMIM:302905	IEA				I		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0002974	OMIM:302905	IEA				P		HPO:iea	
OMIM	302905	CHARGE-LIKE SYNDROME, X-LINKED		HP:0004322	OMIM:302905	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000135	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000252	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000365	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000420	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000458	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000518	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0000925	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0001263	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0001419	OMIM:302950	IEA				I		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0003196	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0004322	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0005280	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0008064	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0009882	OMIM:302950	IEA				P		HPO:iea	
OMIM	302950	CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE		HP:0010655	OMIM:302950	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000126	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000272	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000365	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000377	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000470	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000494	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000501	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000518	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000535	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000568	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000639	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000653	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000765	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0000969	OMIM:302960	IEA				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001019	OMIM:302960	IEA				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001305	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001423	OMIM:302960	IEA				I		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001508	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001561	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001596	OMIM:302960	IEA				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0001776	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002007	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002342	OMIM:302960	IEA				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002644	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002650	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002777	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002787	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002937	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0002999	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0003462	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0003465	OMIM:302960	IEA				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0003577	OMIM:302960	IEA				C		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0003828	OMIM:302960	IEA				C		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0004241	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0007431	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0008131	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0008420	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0008897	OMIM:302960	IEA				P		HPO:iea	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0010442	OMIM:302960	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0010655	OMIM:302960	TAS				P		HPO:probinson	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0011120	OMIM:302960	TAS				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0012368	OMIM:302960	TAS				P		HPO:skoehler	
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0100259	OMIM:302960	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	302960	#302960 CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT; CDPX2;;CDPXD; CPXD;;CONRADI-HUNERMANN SYNDROME;;HAPPLE SYNDROME;;CONRADI-HUNERMANN-HAPPLE SYNDROME		HP:0100556	OMIM:302960	IEA				P		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0000529	OMIM:303100	IEA				P		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0000533	OMIM:303100	TAS				P		HPO:probinson	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0000662	OMIM:303100	IEA				P		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0001133	OMIM:303100	IEA				P		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0001139	OMIM:303100	IEA				P		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0001417	OMIM:303100	IEA				I		HPO:iea	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0001423	OMIM:303100	TAS				I		HPO:skoehler	
OMIM	303100	#303100 CHOROIDEREMIA; CHM;;TAPETOCHOROIDAL DYSTROPHY, PROGRESSIVE; TCDCHOROIDAL SCLEROSIS, INCLUDED		HP:0200065	OMIM:303100	IEA				P		HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000365	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000405	OMIM:303110	TAS				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000408	OMIM:303110	TAS				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000529	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000533	OMIM:303110	TAS				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:probinson	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0000662	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001133	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001139	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001249	OMIM:303110	TAS				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001263	OMIM:303110	TAS				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001417	OMIM:303110	IEA				I	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001419	OMIM:303110	TAS				I	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001466	OMIM:303110	TAS				I	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:skoehler	
OMIM	303110	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME Xq21 DELETION SYNDROME		HP:0001513	OMIM:303110	IEA				P	#303110 CHOROIDEREMIA, DEAFNESS, AND MENTAL RETARDATION;;CHROMOSOME XQ21 DELETION SYNDROME	HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0000238	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0000252	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0000256	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0000486	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001181	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001249	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001258	OMIM:303350	IEA				P		HPO:skoehler	
OMIM	303350	MASA SYNDROME		HP:0001274	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001419	OMIM:303350	IEA				I		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001761	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0001762	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0002119	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0002362	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0002381	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0002808	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0003307	OMIM:303350	IEA				P		HPO:iea	
OMIM	303350	MASA SYNDROME		HP:0004322	OMIM:303350	IEA				P		HPO:iea	
OMIM	303400	CLEFT PALATE, X-LINKED		HP:0000175	OMIM:303400	IEA				P		HPO:skoehler	
OMIM	303400	CLEFT PALATE, X-LINKED		HP:0000193	OMIM:303400	IEA				P		HPO:skoehler	
OMIM	303400	CLEFT PALATE, X-LINKED		HP:0001417	OMIM:303400	IEA				I		HPO:iea	
OMIM	303400	CLEFT PALATE, X-LINKED		HP:0010296	OMIM:303400	IEA				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000023	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000139	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000189	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000194	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000218	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000232	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000252	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000280	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000303	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000316	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000336	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000407	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000411	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000429	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000445	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000463	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000494	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000506	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000574	OMIM:303600	PCS				P		HPO:probinson	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000668	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000687	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000689	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000767	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000768	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000954	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000965	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0000973	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001063	OMIM:303600	IEA				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001169	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001182	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001187	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001249	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001250	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001252	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001290	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001423	OMIM:303600	IEA				I		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001476	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001595	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001653	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001763	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0001812	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002035	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002119	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002208	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002553	OMIM:303600	PCS				P		HPO:probinson	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002650	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002673	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002684	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002750	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002808	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0002868	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0003745	OMIM:303600	TAS				I		HPO:skoehler	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0004322	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0004325	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0006129	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0008454	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0009746	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0010049	OMIM:303600	IEA				P		HPO:iea	
OMIM	303600	COFFIN-LOWRY SYNDROME; CLS		HP:0010309	OMIM:303600	TAS				P		HPO:skoehler	
OMIM	303650	COLONIC ATRESIA		HP:0001417	OMIM:303650	TAS				I		HPO:skoehler	
OMIM	303650	COLONIC ATRESIA		HP:0003270	OMIM:303650	IEA				P		HPO:skoehler	
OMIM	303650	COLONIC ATRESIA		HP:0010448	OMIM:303650	IEA				P		HPO:skoehler	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0000505	OMIM:303700	PCS				P		HPO:probinson	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0000545	OMIM:303700	PCS				P		HPO:probinson	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0000613	OMIM:303700	PCS				P		HPO:probinson	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0000639	OMIM:303700	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0001419	OMIM:303700	PCS				I		HPO:probinson	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0007663	OMIM:303700	TAS				P		HPO:skoehler	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0007939	OMIM:303700	PCS				P		HPO:probinson	
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0008002	OMIM:303700	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	303700	BLUE CONE MONOCHROMACY; BCM		HP:0012043	OMIM:303700	TAS				P		HPO:skoehler	
OMIM	303800	COLORBLINDNESS, PARTIAL, DEUTAN SERIES		HP:0001419	OMIM:303800	PCS				I		HPO:probinson	
OMIM	303800	COLORBLINDNESS, PARTIAL, DEUTAN SERIES		HP:0011520	OMIM:303800	PCS				P		HPO:probinson	
OMIM	303900	COLORBLINDNESS, PARTIAL, PROTAN SERIES		HP:0001419	OMIM:303900	PCS				I		HPO:probinson	
OMIM	303900	COLORBLINDNESS, PARTIAL, PROTAN SERIES		HP:0200018	OMIM:303900	PCS				P		HPO:probinson	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0000505	OMIM:304020	IEA				P		HPO:iea	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0000545	OMIM:304020	IEA				P		HPO:iea	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0000548	OMIM:304020	IEA				P		HPO:skoehler	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0000613	OMIM:304020	IEA				P		HPO:iea	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0000639	OMIM:304020	IEA				P		HPO:skoehler	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0001939	OMIM:304020	IEA				P		HPO:iea	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0007663	OMIM:304020	TAS				P		HPO:skoehler	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0030637	OMIM:304020	TAS				P		HPO:skoehler	
OMIM	304020	CONE-ROD DYSTROPHY, X-LINKED, 1		HP:0200056	OMIM:304020	IEA				P		HPO:iea	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0000541	OMIM:304030	IEA				P		HPO:iea	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0000548	OMIM:304030	TAS				P		HPO:skoehler	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0000572	OMIM:304030	IEA				P		HPO:skoehler	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0001939	OMIM:304030	IEA				P		HPO:iea	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0003581	OMIM:304030	IEA				C		HPO:iea	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0008020	OMIM:304030	IEA				P		HPO:skoehler	
OMIM	304030	CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN		HP:0008275	OMIM:304030	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000175	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000204	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000252	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000324	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000463	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000518	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000541	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000568	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000588	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000639	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000648	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000826	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000892	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000902	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000921	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0000951	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001028	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001252	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001290	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001302	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001305	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001338	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0001423	OMIM:304050	IEA				I		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002036	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002126	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002187	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002188	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002190	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002282	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002308	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002389	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002414	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002650	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002884	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0002937	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0003305	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0003316	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0005338	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0005815	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0006532	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0006956	OMIM:304050	TAS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0007082	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0007858	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0008897	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0009623	OMIM:304050	IEA				P		HPO:iea	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0009792	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0010609	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0010759	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0011097	OMIM:304050	PCS				P		HPO:probinson	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0012032	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0012469	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0030731	OMIM:304050	IEA				P		HPO:skoehler	
OMIM	304050	AICARDI SYNDROME; AIC		HP:0200059	OMIM:304050	TAS				P		HPO:skoehler	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0000238	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0000252	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001249	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001250	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001257	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001321	OMIM:304100	TAS				P		HPO:probinson	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001338	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001417	OMIM:304100	IEA				I		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001419	OMIM:304100	TAS				I		HPO:skoehler	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0001999	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0002251	OMIM:304100	IEA				P		HPO:iea	
OMIM	304100	CORPUS CALLOSUM, PARTIAL AGENESIS OF, X-LINKED		HP:0007068	OMIM:304100	TAS				P		HPO:probinson	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000028	OMIM:304110	TAS				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000047	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000049	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000164	OMIM:304110	TAS				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000175	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000204	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000248	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000316	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000324	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000349	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000431	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000456	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000470	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000494	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000506	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000577	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000639	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000767	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000776	OMIM:304110	IEA				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0000912	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001060	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001156	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001252	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001263	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001274	OMIM:304110	IEA				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001290	OMIM:304110	TAS				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001388	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001423	OMIM:304110	IEA				I		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001537	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001547	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001770	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001807	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001808	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0001809	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0002007	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0002079	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0002162	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0003187	OMIM:304110	IEA				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0004209	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0004322	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0004440	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0005278	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0006585	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0010055	OMIM:304110	IEA				P		HPO:iea	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0012813	OMIM:304110	TAS				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0200021	OMIM:304110	IEA				P		HPO:skoehler	
OMIM	304110	CRANIOFRONTONASAL SYNDROME; CFNS		HP:0200053	OMIM:304110	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000028	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000047	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000126	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000160	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000175	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000238	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000260	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000272	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000283	OMIM:304120	IEA				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000316	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO	HP:0012828	HP:0000347	OMIM:304120	TAS				P		HPO:probinson	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000358	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000369	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000405	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000494	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000767	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000773	OMIM:304120	IEA				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000774	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000926	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0000946	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001162	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001249	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001374	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001423	OMIM:304120	IEA				I		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001476	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001539	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001770	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001782	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0001838	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002007	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002093	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002645	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002694	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002878	OMIM:304120	TAS				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002980	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002982	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0002986	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0003031	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0003304	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0003826	OMIM:304120	IEA				M		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0004322	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0005280	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0006160	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0006381	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0008087	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0008897	OMIM:304120	TAS				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0009467	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0009778	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010049	OMIM:304120	TAS				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010055	OMIM:304120	TAS				P		HPO:probinson	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010109	OMIM:304120	TAS				P		HPO:probinson	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010557	OMIM:304120	IEA				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010559	OMIM:304120	IEA				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010560	OMIM:304120	IEA				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0010743	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0011220	OMIM:304120	TAS				P		HPO:skoehler	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0011304	OMIM:304120	IEA				P		HPO:iea	
OMIM	304120	#304120 OTOPALATODIGITAL SYNDROME, TYPE II; OPD2;;OPD II SYNDROME;;OPD SYNDROME 2;;CRANIOORODIGITAL SYNDROME;;FACIOPALATOOSSEOUS SYNDROME; FPO		HP:0011800	OMIM:304120	TAS				P		HPO:skoehler	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000015	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000126	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000218	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000275	OMIM:304150	TAS				P		HPO:probinson	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000276	OMIM:304150	TAS				P		HPO:probinson	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000343	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000348	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000444	OMIM:304150	TAS				P		HPO:skoehler	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000472	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000767	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000768	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000774	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000885	OMIM:304150	IEA				P		HPO:skoehler	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000894	OMIM:304150	TAS				P		HPO:probinson	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000916	OMIM:304150	TAS				P		HPO:probinson	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000926	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000939	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY	HP:0012825	HP:0000974	OMIM:304150	TAS				P		HPO:probinson	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000977	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0000978	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001241	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001278	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001377	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001388	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001419	OMIM:304150	IEA				I		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001582	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0001763	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002028	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002036	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002208	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002673	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002808	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002857	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0002862	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0003066	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0003276	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0004474	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0005302	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0005792	OMIM:304150	IEA				P		HPO:iea	
OMIM	304150	#304150 OCCIPITAL HORN SYNDROME; OHS;;CUTIS LAXA, X-LINKED, FORMERLY;;EHLERS-DANLOS SYNDROME, OCCIPITAL HORN TYPE, FORMERLY;;EDS IX, FORMERLY;;EDS9, FORMERLY		HP:0006000	OMIM:304150	IEA				P		HPO:iea	
OMIM	304200	CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION		HP:0000818	OMIM:304200	IEA				P		HPO:iea	
OMIM	304200	CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION		HP:0001249	OMIM:304200	IEA				P		HPO:iea	
OMIM	304200	CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION		HP:0001417	OMIM:304200	TAS				I		HPO:skoehler	
OMIM	304200	CUTIS VERTICIS GYRATA, THYROID APLASIA, AND MENTAL RETARDATION		HP:0010541	OMIM:304200	IEA				P		HPO:skoehler	
OMIM	304300	CYANIDE, INABILITY TO SMELL		HP:0000271	OMIM:304300	IEA				P		HPO:iea	
OMIM	304300	CYANIDE, INABILITY TO SMELL		HP:0001419	OMIM:304300	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000154	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000238	OMIM:304340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	304340	PETTIGREW SYNDROME		HP:0000276	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000280	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000303	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000407	OMIM:304340	IEA				P		HPO:iea	
OMIM	304340	PETTIGREW SYNDROME		HP:0000448	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0000490	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001250	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001257	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001263	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001266	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001290	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001305	OMIM:304340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	304340	PETTIGREW SYNDROME		HP:0001347	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001371	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0001417	OMIM:304340	IEA				I		HPO:iea	
OMIM	304340	PETTIGREW SYNDROME		HP:0001419	OMIM:304340	TAS				I		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0002066	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0002134	OMIM:304340	IEA				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0002514	OMIM:304340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	304340	PETTIGREW SYNDROME		HP:0002650	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0003593	OMIM:304340	TAS				C		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0005101	OMIM:304340	IEA				P		HPO:iea	
OMIM	304340	PETTIGREW SYNDROME		HP:0010864	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0011220	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0012471	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304340	PETTIGREW SYNDROME		HP:0100716	OMIM:304340	TAS				P		HPO:skoehler	
OMIM	304400	DEAFNESS, X-LINKED 2		HP:0000381	OMIM:304400	TAS				P		HPO:probinson	
OMIM	304400	DEAFNESS, X-LINKED 2		HP:0000405	OMIM:304400	TAS				P		HPO:iea	
OMIM	304400	DEAFNESS, X-LINKED 2		HP:0000408	OMIM:304400	TAS				P		HPO:probinson	
OMIM	304400	DEAFNESS, X-LINKED 2		HP:0001419	OMIM:304400	TAS				I		HPO:probinson	
OMIM	304400	DEAFNESS, X-LINKED 2		HP:0004458	OMIM:304400	TAS				P		HPO:probinson	
OMIM	304500	DEAFNESS, X-LINKED 1		HP:0000407	PMID:20021999	PCS	HP:0003577			P		HPO:iea	
OMIM	304500	DEAFNESS, X-LINKED 1		HP:0001419	PMID:20021999	PCS				I		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0000408	OMIM:304700	PCS				P		HPO:probinson	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0000505	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0000512	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0000545	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0000613	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001133	OMIM:304700	TAS				P		HPO:skoehler	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001257	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001260	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001268	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001332	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001337	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001347	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0001419	OMIM:304700	IEA				I		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0002015	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0002533	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0002659	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0007663	OMIM:304700	TAS				P		HPO:skoehler	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0008596	OMIM:304700	IEA				P		HPO:iea	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0008596	OMIM:304700	PCS				P		HPO:probinson	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0011463	OMIM:304700	PCS				C		HPO:probinson	
OMIM	304700	#304700 MOHR-TRANEBJAERG SYNDROME; MTS;;DYSTONIA-DEAFNESS SYNDROME; DDS;;DEAFNESS-DYSTONIA-OPTIC ATROPHY SYNDROME; DDP;;DEAFNESS SYNDROME, PROGRESSIVE, WITH BLINDNESS, DYSTONIA, FRACTURES,AND MENTAL DEFICIENCY		HP:0100704	OMIM:304700	PCS				P		HPO:probinson	
OMIM	304730	DERMOIDS OF CORNEA		HP:0000478	OMIM:304730	IEA				P		HPO:iea	
OMIM	304730	DERMOIDS OF CORNEA		HP:0001417	OMIM:304730	IEA				I		HPO:iea	
OMIM	304730	DERMOIDS OF CORNEA		HP:0007957	OMIM:304730	TAS				P		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0000819	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0000821	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0000964	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0001419	OMIM:304790	IEA				I		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0001873	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0001880	OMIM:304790	TAS				P		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0001890	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0002014	OMIM:304790	IEA				P		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0002595	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0002716	OMIM:304790	IEA				P		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0002958	OMIM:304790	IEA				P		HPO:iea	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0003828	OMIM:304790	TAS				C		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0011473	OMIM:304790	TAS				P		HPO:skoehler	
OMIM	304790	IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED; IPEX		HP:0100651	OMIM:304790	TAS				P		HPO:skoehler	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0000021	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0000103	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0000737	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0000873	OMIM:304800	IEA				P		HPO:skoehler	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001249	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001250	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001419	OMIM:304800	IEA				I		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001425	OMIM:304800	TAS				I		HPO:skoehler	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001508	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001955	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001959	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0001986	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0002013	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0002019	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0003228	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0003623	OMIM:304800	IEA				C		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0004322	OMIM:304800	IEA				P		HPO:iea	
OMIM	304800	DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED		HP:0008872	OMIM:304800	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000103	OMIM:304900	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000126	OMIM:304900	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0000863	OMIM:304900	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0001417	OMIM:304900	IEA				I		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0001423	OMIM:304900	TAS				I		HPO:skoehler	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0001948	OMIM:304900	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0001959	OMIM:304900	IEA				P		HPO:iea	
OMIM	304900	DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE		HP:0002900	OMIM:304900	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000248	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000280	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000303	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000470	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000707	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000884	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0000926	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0001419	OMIM:304950	IEA				I		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0001498	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0001552	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0001822	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002650	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002651	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002684	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002812	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002857	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002938	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0002942	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0003175	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0003521	OMIM:304950	IEA				P		HPO:skoehler	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0003796	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0004590	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0005033	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0005743	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0008839	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0010049	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0010230	OMIM:304950	IEA				P		HPO:iea	
OMIM	304950	304950 DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED		HP:0100864	OMIM:304950	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000028	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000047	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000085	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000252	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000486	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000498	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000509	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000518	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000648	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000653	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000670	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000939	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000953	OMIM:305000	IEA				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0000975	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001059	OMIM:305000	IEA				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001249	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001251	OMIM:305000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001263	OMIM:305000	TAS		HP:0040284		P		HPO:skoehler	25%
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001321	OMIM:305000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001394	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001419	OMIM:305000	IEA				I		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001511	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001596	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001741	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001807	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001809	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001873	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001876	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001882	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0001903	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002043	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002091	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002165	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002206	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002216	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002721	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002745	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002860	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0002863	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0004322	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0004334	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0004808	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0005212	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0005528	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0006480	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0007427	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0008404	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0008661	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0008734	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0009926	OMIM:305000	IEA				P		HPO:iea	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0012189	OMIM:305000	TAS				P		HPO:skoehler	
OMIM	305000	DYSKERATOSIS CONGENITA, X-LINKED; DKCX		HP:0030731	OMIM:305000	IEA				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000232	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000327	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000331	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000336	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000430	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000535	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000561	OMIM:305100	IEA				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000607	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000653	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000668	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000679	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000691	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000698	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000958	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000963	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000964	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000966	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000970	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0000977	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001006	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001106	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001419	OMIM:305100	IEA				I		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001425	OMIM:305100	TAS				I		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001598	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001609	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001618	OMIM:305100	TAS				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0001945	OMIM:305100	TAS				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002007	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002046	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002098	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002223	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002299	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002557	OMIM:305100	TAS				P		HPO:probinson	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0002561	OMIM:305100	TAS				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0003196	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0005280	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0007411	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0007592	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0007607	OMIM:305100	IEA				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0010803	OMIM:305100	IEA				P		HPO:iea	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0011830	OMIM:305100	TAS				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0012384	OMIM:305100	IEA				P		HPO:skoehler	
OMIM	305100	ECTODERMAL DYSPLASIA 1, HYPOHIDROTIC, X-LINKED; XHED		HP:0012471	OMIM:305100	TAS				P		HPO:skoehler	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0000974	OMIM:305200	IEA				P		HPO:iea	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0000977	OMIM:305200	IEA				P		HPO:iea	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0000993	OMIM:305200	IEA				P		HPO:iea	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0001388	OMIM:305200	IEA				P		HPO:skoehler	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0001419	OMIM:305200	IEA				I		HPO:iea	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0002297	OMIM:305200	IEA				P		HPO:iea	
OMIM	305200	EHLERS-DANLOS SYNDROME, TYPE V		HP:0012233	OMIM:305200	TAS				P		HPO:probinson	
OMIM	305350	305350 EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED; EDVX; EDV2		HP:0001417	OMIM:305350	TAS				I		HPO:skoehler	
OMIM	305350	305350 EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED; EDVX; EDV2		HP:0006739	OMIM:305350	IEA				P		HPO:iea	
OMIM	305350	305350 EPIDERMODYSPLASIA VERRUCIFORMIS, X-LINKED; EDVX; EDV2		HP:0200043	OMIM:305350	IEA				P		HPO:skoehler	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0000490	OMIM:305390	TAS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0000541	PMID:8457509	PCS				P		HPO:skoehler	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0000568	OMIM:305390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0000639	OMIM:305390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0001419	PMID:20159112	PCS				I		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0001493	PMID:20159112	PCS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0007663	OMIM:305390	TAS				P		HPO:skoehler	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0007710	PMID:1642288	PCS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0007989	OMIM:305390	PCS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0011530	OMIM:305390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0011532	PMID:8457509	PCS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0012841	OMIM:305390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0030490	OMIM:305390	TAS				P		HPO:probinson	
OMIM	305390	#305390 EXUDATIVE VITREORETINOPATHY 2, X-LINKED; EVR2;;EXUDATIVE VITREORETINOPATHY, FAMILIAL, 2;;EVRX;;FEVR, X-LINKED; FEVRX		HP:0030666	OMIM:305390	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	305400	Aarskog-Scott syndrome		HP:0000023	OMIM:305400	IEA		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000028	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000049	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	10/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000175	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000204	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000289	OMIM:305400	IEA		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000311	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000316	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	10/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000327	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000349	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000431	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000463	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000470	OMIM:305400	TAS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:probinson	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0000486	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000494	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000508	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000540	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000668	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000767	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000823	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0000954	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001156	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001159	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001169	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:probinson	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0001187	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001256	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HP:probinson	HP:0040284
OMIM	305400	Aarskog-Scott syndrome		HP:0001263	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HP:probinson	5/11
OMIM	305400	Aarskog-Scott syndrome		HP:0001419	OMIM:305400	IEA				I	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001508	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0001544	PMID:8076412	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	2/5
OMIM	305400	Aarskog-Scott syndrome		HP:0001769	OMIM:305400	TAS				P	AARSKOG-SCOTT SYNDROME	HPO:probinson	
OMIM	305400	Aarskog-Scott syndrome		HP:0001773	OMIM:305400	TAS				P	AARSKOG-SCOTT SYNDROME	HPO:probinson	
OMIM	305400	Aarskog-Scott syndrome		HP:0002055	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0002650	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0003196	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:iea	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0003311	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0003318	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0003502	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0004279	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HPO:probinson	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0004322	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HP:probinson	11/11
OMIM	305400	Aarskog-Scott syndrome		HP:0007018	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0009237	PMID:20082460	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HP:probinson	8/11
OMIM	305400	Aarskog-Scott syndrome		HP:0009466	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0009748	OMIM:305400	IEA				P	AARSKOG-SCOTT SYNDROME	HPO:iea	
OMIM	305400	Aarskog-Scott syndrome		HP:0012774	OMIM:305400	TAS				P	AARSKOG-SCOTT SYNDROME	HPO:skoehler	
OMIM	305400	Aarskog-Scott syndrome		HP:0030084	OMIM:305400	TAS				P	AARSKOG-SCOTT SYNDROME	HPO:skoehler	
OMIM	305400	Aarskog-Scott syndrome		HP:0032277	PMID:8076412	PCS		HP:0040284		P	AARSKOG-SCOTT SYNDROME	HP:probinson	3/5
OMIM	305435	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3		HP:0001417	OMIM:305435	IEA				I		HPO:iea	
OMIM	305435	FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 3		HP:0001871	OMIM:305435	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000023	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000028	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000047	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000154	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000175	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000179	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000189	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000204	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000238	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000260	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000286	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000316	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000343	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000347	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000407	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000448	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000453	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000470	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000486	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000494	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000678	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000766	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000954	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0000960	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001159	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001171	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001212	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001249	OMIM:305450	IEA				P		HPO:skoehler	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001250	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001263	OMIM:305450	TAS				P		HPO:skoehler	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001270	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001319	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001338	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001357	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001419	OMIM:305450	IEA				I		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001476	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001537	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001545	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001620	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001627	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0001739	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002007	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002019	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002021	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002023	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002025	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002213	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002236	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002282	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002566	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002828	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0002938	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0004322	OMIM:305450	IEA	HP:0003593			P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0005490	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0007018	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0008070	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0009466	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0009473	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0009762	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0010055	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0010609	OMIM:305450	IEA				P		HPO:skoehler	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0011220	OMIM:305450	TAS				P		HPO:skoehler	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0011266	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0011304	OMIM:305450	IEA				P		HPO:iea	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0012385	OMIM:305450	TAS				P		HPO:skoehler	
OMIM	305450	#305450 OPITZ-KAVEGGIA SYNDROME; OKS;;FG SYNDROME 1; FGS1;;FG SYNDROME; FGS;;MENTAL RETARDATION, LARGE HEAD, IMPERFORATE ANUS, CONGENITAL HYPOTONIA,AND PARTIAL AGENESIS OF CORPUS CALLOSUM;;KELLER SYNDROME		HP:0030084	OMIM:305450	TAS				P		HPO:skoehler	
OMIM	305550	FINGERPRINT BODY MYOPATHY		HP:0001417	OMIM:305550	IEA				I		HPO:iea	
OMIM	305550	FINGERPRINT BODY MYOPATHY		HP:0001939	OMIM:305550	IEA				P		HPO:iea	
OMIM	305550	FINGERPRINT BODY MYOPATHY		HP:0003198	OMIM:305550	IEA				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000023	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000028	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000060	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000066	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000085	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000126	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000175	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000204	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000238	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000252	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000307	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000324	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000369	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000377	OMIM:305600	IEA				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000402	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000410	OMIM:305600	TAS				P		HPO:probinson	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000446	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000455	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000486	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000526	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000528	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000567	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000568	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000612	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000639	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000648	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000668	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000677	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000684	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000689	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000773	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0000776	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001009	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001083	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001156	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001162	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001171	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001180	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001249	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001274	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001374	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001388	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001423	OMIM:305600	IEA				I		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001537	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001539	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001540	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001545	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001600	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001770	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001802	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001817	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001829	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001839	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0001849	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002036	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002164	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002232	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002299	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002308	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002475	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002557	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002558	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002566	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0002650	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0003191	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0003298	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0004322	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0004334	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0006297	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0006608	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0006638	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0007546	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0007588	OMIM:305600	TAS				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0007663	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0008070	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0008404	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0009381	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0009803	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0010049	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0010719	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0010740	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0010743	OMIM:305600	IEA				P		HPO:iea	
OMIM	305600	FOCAL DERMAL HYPOPLASIA; FDH		HP:0030037	OMIM:305600	TAS				P		HPO:skoehler	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000072	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000126	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000218	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000280	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000307	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000316	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000331	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000336	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000407	OMIM:305620	IEA				P		HPO:skoehler	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000431	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000494	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000684	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0000689	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001007	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001166	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001239	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001249	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001419	OMIM:305620	IEA				I		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001592	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001634	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001648	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0001833	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002650	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002673	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002700	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002857	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002949	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0002987	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0003202	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0003691	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0003779	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0004608	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006155	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006207	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006335	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006380	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006440	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006466	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0006665	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0008097	OMIM:305620	IEA				P		HPO:iea	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0009768	OMIM:305620	TAS				P		HPO:probinson	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0010307	OMIM:305620	IEA				P		HPO:skoehler	
OMIM	305620	FRONTOMETAPHYSEAL DYSPLASIA		HP:0100490	OMIM:305620	IEA				P		HPO:iea	
OMIM	305690	GENITOURINARY TRACT ANOMALIES		HP:0000119	OMIM:305690	IEA				P		HPO:iea	
OMIM	305690	GENITOURINARY TRACT ANOMALIES		HP:0001417	OMIM:305690	IEA				I		HPO:iea	
OMIM	305690	GENITOURINARY TRACT ANOMALIES		HP:0003811	OMIM:305690	IEA				M		HPO:iea	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0000765	OMIM:305700	IEA				P		HPO:iea	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0000771	OMIM:305700	IEA				P		HPO:skoehler	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0001417	OMIM:305700	TAS				I		HPO:nvasilevsky	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0001475	OMIM:305700	TAS				I		HPO:nvasilevsky	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0001513	OMIM:305700	IEA				P		HPO:iea	
OMIM	305700	SERTOLI CELL-ONLY SYNDROME		HP:0001939	OMIM:305700	IEA				P		HPO:iea	
OMIM	305800	MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED		HP:0000793	OMIM:305800	IEA				P		HPO:iea	
OMIM	305800	MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED		HP:0001693	OMIM:305800	IEA				P		HPO:skoehler	
OMIM	305800	MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED		HP:0001939	OMIM:305800	IEA				P		HPO:iea	
OMIM	305800	MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS, X-LINKED		HP:0009125	OMIM:305800	IEA				P		HPO:skoehler	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0001270	OMIM:306000	IEA				P		HPO:iea	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0001419	OMIM:306000	IEA				I		HPO:iea	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0001510	OMIM:306000	IEA				P		HPO:iea	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0001943	OMIM:306000	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0001946	OMIM:306000	IEA				P		HPO:skoehler	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA	HP:0012825	HP:0002155	OMIM:306000	TAS				P		HPO:probinson	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA		HP:0002240	OMIM:306000	IEA				P		HPO:iea	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA	HP:0012825	HP:0002910	OMIM:306000	TAS				P		HPO:probinson	
OMIM	306000	GLYCOGEN STORAGE DISEASE IXA	HP:0012825	HP:0003124	OMIM:306000	TAS				P		HPO:probinson	
OMIM	306300	GRANULOMAS, CONGENITAL CEREBRAL		HP:0000707	OMIM:306300	IEA				P		HPO:iea	
OMIM	306300	GRANULOMAS, CONGENITAL CEREBRAL		HP:0001939	OMIM:306300	IEA				P		HPO:iea	
OMIM	306300	GRANULOMAS, CONGENITAL CEREBRAL		HP:0003811	OMIM:306300	IEA				M		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0000976	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0001419	OMIM:306400	IEA				I		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0001744	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002240	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002716	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002721	OMIM:306400	IEA				P		HPO:skoehler	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002723	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002724	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002726	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002740	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002741	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002742	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002754	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002840	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002842	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0002955	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0003203	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0003206	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0003514	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0003621	OMIM:306400	IEA				C		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0005224	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0005224	OMIM:306400	TAS				P		HPO:skoehler	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0005406	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0006532	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0007417	OMIM:306400	IEA				P		HPO:iea	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0100523	OMIM:306400	TAS				P		HPO:probinson	
OMIM	306400	GRANULOMATOUS DISEASE, CHRONIC, X-LINKED; CDGX		HP:0100658	OMIM:306400	TAS				P		HPO:probinson	
OMIM	306700	HEMOPHILIA A		HP:0000978	OMIM:306700	TAS				P		HPO:probinson	
OMIM	306700	HEMOPHILIA A		HP:0001419	OMIM:306700	IEA				I		HPO:iea	
OMIM	306700	HEMOPHILIA A		HP:0001934	OMIM:306700	IEA				P		HPO:iea	
OMIM	306700	HEMOPHILIA A		HP:0002758	OMIM:306700	IEA				P		HPO:iea	
OMIM	306700	HEMOPHILIA A		HP:0003125	OMIM:306700	IEA				P		HPO:iea	
OMIM	306700	HEMOPHILIA A		HP:0003645	OMIM:306700	TAS				P		HPO:probinson	
OMIM	306700	HEMOPHILIA A		HP:0005261	OMIM:306700	IEA				P		HPO:iea	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0000978	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0001417	OMIM:306800	TAS				I		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0001934	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0002239	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0002758	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0003125	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0005261	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0005542	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306800	HEMOPHILIA A WITH VASCULAR ABNORMALITY		HP:0025017	OMIM:306800	TAS				P		HPO:skoehler	
OMIM	306900	HEMOPHILIA B		HP:0001419	OMIM:306900	TAS				I		HPO:probinson	
OMIM	306900	HEMOPHILIA B		HP:0001892	OMIM:306900	TAS				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0001934	OMIM:306900	IEA				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0002239	OMIM:306900	IEA				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0002758	OMIM:306900	IEA				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0003645	OMIM:306900	TAS				P		HPO:probinson	
OMIM	306900	HEMOPHILIA B		HP:0005261	OMIM:306900	IEA				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0005542	OMIM:306900	IEA				P		HPO:iea	
OMIM	306900	HEMOPHILIA B		HP:0011858	OMIM:306900	TAS				P		HPO:probinson	
OMIM	306930	HEMOPOIETIC PROLIFERATION		HP:0001417	OMIM:306930	IEA				I		HPO:iea	
OMIM	306930	HEMOPOIETIC PROLIFERATION		HP:0001871	OMIM:306930	IEA				P		HPO:iea	
OMIM	306950	HERNIA, ANTERIOR DIAPHRAGMATIC		HP:0000776	OMIM:306950	TAS				P		HPO:skoehler	
OMIM	306950	HERNIA, ANTERIOR DIAPHRAGMATIC		HP:0003811	OMIM:306950	TAS				M		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0000085	PMID:14681828	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0000104	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0000316	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0000369	PMID:14681828	PCS		HP:0040284		P		HP:probinson	2/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001419	PMID:14681828	PCS				I		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001508	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001539	PMID:14681828	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001629	PMID:14681828	PCS				P		HPO:iea	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001631	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001640	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001642	OMIM:306955	IEA				P		HPO:iea	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001643	PMID:14681828	PCS	HP:0003577	HP:0040284		P		HPO:iea	1/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001651	OMIM:306955	IEA				P		HPO:iea	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001669	PMID:14681828	PCS		HP:0040284		P		HPO:skoehler	5/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001719	PMID:14681828	PCS	HP:0003577	HP:0040284		P		HP:probinson	4/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001746	PMID:14681828	PCS		HP:0040284		P		HPO:skoehler	4/5
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001748	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0001750	PMID:14681828	PCS		HP:0040284		P		HPO:skoehler	1/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0002023	PMID:14681828	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/9
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0003363	PMID:14681828	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0003812	OMIM:306955	IEA				C		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0011560	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0011565	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306955	HETEROTAXY, VISCERAL, 1, X-LINKED; HTX1		HP:0012890	OMIM:306955	TAS				P		HPO:skoehler	
OMIM	306960	HHHH SYNDROME		HP:0000924	OMIM:306960	IEA				P		HPO:iea	
OMIM	306960	HHHH SYNDROME		HP:0001250	OMIM:306960	IEA				P		HPO:iea	
OMIM	306960	HHHH SYNDROME		HP:0001269	OMIM:306960	IEA				P		HPO:iea	
OMIM	306960	HHHH SYNDROME		HP:0001419	OMIM:306960	TAS				I		HPO:skoehler	
OMIM	306960	HHHH SYNDROME		HP:0100556	OMIM:306960	TAS				P		HPO:skoehler	
OMIM	306980	HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY		HP:0002251	OMIM:306980	IEA				P		HPO:iea	
OMIM	306980	HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY		HP:0005627	OMIM:306980	IEA				P		HPO:iea	
OMIM	306980	HIRSCHSPRUNG DISEASE WITH TYPE D BRACHYDACTYLY		HP:0009778	OMIM:306980	TAS				P		HPO:skoehler	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0000252	OMIM:306990	IEA				P		HPO:iea	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0001360	OMIM:306990	IEA				P		HPO:iea	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0001417	OMIM:306990	IEA				I		HPO:iea	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0001511	OMIM:306990	IEA				P		HPO:iea	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0001558	OMIM:306990	IEA				P		HPO:iea	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0001989	OMIM:306990	TAS				P		HPO:probinson	
OMIM	306990	HOLOPROSENCEPHALY WITH FETAL AKINESIA/HYPOKINESIA SEQUENCE		HP:0002828	OMIM:306990	IEA				P		HPO:skoehler	
OMIM	306995	HOMOSEXUALITY 1		HP:0001417	OMIM:306995	TAS				I		HPO:skoehler	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0000238	OMIM:307000	IEA				P		HPO:iea	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0000256	OMIM:307000	IEA				P		HPO:iea	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001181	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001249	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001257	PMID:7645588	PCS				P		HPO:skoehler	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001258	PMID:7645588	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001274	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001331	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0001419	OMIM:307000	IEA				I		HPO:iea	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0002410	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0007016	OMIM:307000	IEA				P		HPO:iea	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0009600	OMIM:307000	TAS				P		HPO:probinson	
OMIM	307000	HYDROCEPHALUS DUE TO CONGENITAL STENOSIS OF AQUEDUCT OF SYLVIUS		HP:0009600	OMIM:307000	IEA				P		HPO:iea	
OMIM	307010	307010 HYDROCEPHALUS WITH CEREBELLAR AGENESIS		HP:0000238	OMIM:307010	IEA				P		HPO:iea	
OMIM	307010	307010 HYDROCEPHALUS WITH CEREBELLAR AGENESIS		HP:0001417	OMIM:307010	IEA				I		HPO:iea	
OMIM	307010	307010 HYDROCEPHALUS WITH CEREBELLAR AGENESIS		HP:0012642	OMIM:307010	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000028	OMIM:307030	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000316	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000369	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000486	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000846	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000846	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0000939	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001249	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001250	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001254	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001259	OMIM:307030	IEA				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001263	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001417	OMIM:307030	IEA				I		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001419	OMIM:307030	TAS				I		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001423	OMIM:307030	TAS				I		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001510	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001518	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001942	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001943	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001993	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0001999	OMIM:307030	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0002007	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0002155	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0002572	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0002714	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0002756	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0003198	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0003560	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0004322	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0007185	OMIM:307030	IEA				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0008182	OMIM:307030	IEA				P		HPO:iea	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0025356	OMIM:307030	IEA				P		HPO:skoehler	
OMIM	307030	GLYCEROL KINASE DEFICIENCY; GKD		HP:0040301	OMIM:307030	TAS				P		HPO:skoehler	
OMIM	307150	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG		HP:0001007	OMIM:307150	IEA				P	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME XQ27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG	HPO:skoehler	
OMIM	307150	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG		HP:0001417	OMIM:307150	IEA				I	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME XQ27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG	HPO:iea	
OMIM	307150	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG		HP:0001423	OMIM:307150	TAS				I	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME XQ27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG	HPO:skoehler	
OMIM	307150	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG		HP:0002650	OMIM:307150	TAS		HP:0040283		P	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME XQ27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG	HPO:skoehler	HP:0040283
OMIM	307150	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME Xq27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG		HP:0004540	OMIM:307150	IEA				P	#307150 HYPERTRICHOSIS, CONGENITAL GENERALIZED; HTC2;;CHROMOSOME XQ27.1 INTERCHROMOSOMAL INSERTION SYNDROME;;CGH;;HCG	HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000010	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000024	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000031	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000246	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000365	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000389	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000509	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000824	OMIM:307200	TAS				P		HPO:skoehler	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0000999	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0001287	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0001412	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0001419	OMIM:307200	IEA				I		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002014	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002090	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002383	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002718	OMIM:307200	TAS				P		HPO:probinson	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002743	OMIM:307200	TAS				P		HPO:probinson	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0002750	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0003095	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0003139	OMIM:307200	TAS				P		HPO:probinson	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0003729	OMIM:307200	IEA				P		HPO:iea	
OMIM	307200	#307200 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE III; IGHD3;;IGHD III;;GROWTH HORMONE DEFICIENCY WITH HYPOGAMMAGLOBULINEMIA;;HYPOGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;AGAMMAGLOBULINEMIA AND ISOLATED GROWTH HORMONE DEFICIENCY, X-LINKED;;FLEISHER SYNDROME		HP:0004322	OMIM:307200	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0000026	OMIM:307500	TAS				P		HPO:skoehler	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0000815	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0001249	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0001417	OMIM:307500	IEA				I		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0001952	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0002652	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0003074	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0003319	OMIM:307500	IEA				P		HPO:iea	
OMIM	307500	HYPOGONADISM, MALE, WITH MENTAL RETARDATION AND SKELETAL ANOMALIES		HP:0005820	OMIM:307500	IEA				P		HPO:iea	
OMIM	307700	HYPOPARATHYROIDISM, X-LINKED		HP:0000464	OMIM:307700	IEA				P		HPO:iea	
OMIM	307700	HYPOPARATHYROIDISM, X-LINKED		HP:0001250	OMIM:307700	IEA				P		HPO:iea	
OMIM	307700	HYPOPARATHYROIDISM, X-LINKED		HP:0001281	OMIM:307700	IEA				P		HPO:iea	
OMIM	307700	HYPOPARATHYROIDISM, X-LINKED		HP:0001417	OMIM:307700	IEA				I		HPO:iea	
OMIM	307700	HYPOPARATHYROIDISM, X-LINKED		HP:0008198	OMIM:307700	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0000117	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0000124	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0001423	OMIM:307800	IEA				I		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002007	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002148	OMIM:307800	IEA				P		HPO:skoehler	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002176	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002644	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002653	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002749	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002758	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002829	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002979	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002980	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0002982	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0003025	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0003155	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0003165	OMIM:307800	IEA				P		HPO:skoehler	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0003416	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0004322	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0004912	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0006285	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0006432	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0008117	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0008144	OMIM:307800	IEA				P		HPO:iea	
OMIM	307800	#307800 HYPOPHOSPHATEMIC RICKETS, X-LINKED DOMINANT; XLHR;;HYPOPHOSPHATEMIA, X-LINKED; XLH;;HYP;;VITAMIN D-RESISTANT RICKETS, X-LINKED;;HYPOPHOSPHATEMIC VITAMIN D-RESISTANT RICKETS; HPDR		HP:0010502	OMIM:307800	TAS				P		HPO:probinson	
OMIM	307830	HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION		HP:0001419	OMIM:307830	TAS				I		HPO:probinson	
OMIM	307830	HYPOURICEMIA, FAMILIAL RENAL, DUE TO TUBULAR HYPERSECRETION		HP:0003537	OMIM:307830	TAS				P		HPO:probinson	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0000104	OMIM:308050	IEA				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0000126	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0000204	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000347	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000365	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000773	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000835	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000882	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000894	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0000962	PMID:10710233	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0001036	PMID:10710233	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001256	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0001371	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0001374	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001423	OMIM:308050	PCS				I		HPO:iea	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001425	OMIM:308050	TAS				I		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001537	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0001596	PMID:12668600	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0001597	PMID:12668600	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001671	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0001750	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0002089	PMID:12668600	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0002650	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0002977	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0003462	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0003465	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0003826	PMID:12668600;OMIM:308050	PCS		HP:0040284		M		HPO:iea	99%
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0004322	PMID:12668600	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0005990	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0007431	PMID:12668600	PCS		HP:0040280		P		HPO:iea	HP:0040280
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0008417	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0008678	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0008839	OMIM:308050	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0008839	OMIM:308050	TAS				P		HPO:probinson	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0008883	OMIM:308050	TAS				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0009815	PMID:12668600	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0010655	PMID:12668600	PCS	HP:0003593	HP:0040281		P		HPO:iea	HP:0040281
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS		HP:0010783	OMIM:308050	IEA				P		HPO:skoehler	
OMIM	308050	CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS	HP:0012833	HP:0030680	PMID:10710233	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0000028	OMIM:308100	IEA				P		HPO:iea	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0001419	OMIM:308100	IEA				I		HPO:iea	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0001939	OMIM:308100	IEA				P		HPO:iea	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0002664	OMIM:308100	IEA				P		HPO:skoehler	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0007431	OMIM:308100	TAS				P		HPO:probinson	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0007759	OMIM:308100	IEA				P		HPO:iea	
OMIM	308100	ICHTHYOSIS, X-LINKED		HP:0008064	OMIM:308100	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0000026	OMIM:308200	IEA				P		HPO:skoehler	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0000044	OMIM:308200	TAS				P		HPO:probinson	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0000458	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0000510	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0001249	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0001250	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0001417	OMIM:308200	IEA				I		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0001939	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0004857	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0007431	OMIM:308200	IEA				P		HPO:iea	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0008213	OMIM:308200	TAS				P		HPO:probinson	
OMIM	308200	ICHTHYOSIS AND MALE HYPOGONADISM		HP:0031003	OMIM:308200	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000003	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000023	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000028	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000110	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000122	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000175	OMIM:308205	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000252	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000365	OMIM:308205	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000491	OMIM:308205	IEA				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000495	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000561	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000613	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000772	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000958	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000966	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0000968	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001019	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001162	OMIM:308205	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001249	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001250	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001263	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001419	OMIM:308205	TAS				I		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001537	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001562	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0001596	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002079	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002119	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002164	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002223	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002251	OMIM:308205	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002542	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002650	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0002827	OMIM:308205	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0003468	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0003577	OMIM:308205	TAS				C		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0003828	OMIM:308205	TAS				C		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0004322	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0005254	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0007502	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0007759	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0008404	OMIM:308205	TAS				P		HPO:probinson	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0012444	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308205	IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME		HP:0040189	OMIM:308205	TAS				P		HPO:skoehler	
OMIM	308220	IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN		HP:0001417	PMID:6499285	PCS				I		HPO:skoehler	
OMIM	308220	IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN		HP:0002718	PMID:6499285	PCS				P		HPO:probinson	
OMIM	308220	IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN		HP:0004429	PMID:6499285	PCS				P		HPO:probinson	
OMIM	308220	IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN		HP:0005386	PMID:6499285	PCS				P		HPO:probinson	
OMIM	308220	IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN		HP:0011840	PMID:6499285	PCS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0000230	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0001419	OMIM:308230	IEA				I		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0001744	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0001873	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0001875	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0001878	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002014	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002240	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002718	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1	HP:0012828	HP:0002720	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002721	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002847	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002849	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002959	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0002961	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0003496	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1	HP:0012828	HP:0004315	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0005419	OMIM:308230	IEA				P		HPO:iea	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1	HP:0012828	HP:0005479	OMIM:308230	TAS				P		HPO:probinson	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0010280	OMIM:308230	IEA				P		HPO:skoehler	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0030812	OMIM:308230	TAS				P		HPO:skoehler	
OMIM	308230	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 1		HP:0200123	OMIM:308230	TAS				P		HPO:skoehler	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001287	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001419	OMIM:308240	IEA				I		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001744	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001873	OMIM:308240	TAS				P		HPO:skoehler	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001876	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0001903	OMIM:308240	TAS				P		HPO:skoehler	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002240	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002383	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002480	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002665	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002716	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0002721	OMIM:308240	IEA				P		HPO:skoehler	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0003496	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0004315	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0004787	OMIM:308240	IEA				P		HPO:iea	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0012178	OMIM:308240	TAS				P		HPO:probinson	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0100776	OMIM:308240	TAS				P		HPO:probinson	
OMIM	308240	LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1; XLP1		HP:0100827	OMIM:308240	IEA				P		HPO:skoehler	
OMIM	308250	IMMUNOGLOBULIN M, LEVEL OF		HP:0001287	OMIM:308250	IEA				P		HPO:skoehler	
OMIM	308250	IMMUNOGLOBULIN M, LEVEL OF		HP:0001417	OMIM:308250	IEA				I		HPO:iea	
OMIM	308250	IMMUNOGLOBULIN M, LEVEL OF		HP:0002850	OMIM:308250	IEA				P		HPO:skoehler	
OMIM	308280	IMPACTED TEETH, MULTIPLE		HP:0001417	OMIM:308280	IEA				I		HPO:iea	
OMIM	308280	IMPACTED TEETH, MULTIPLE		HP:0001571	OMIM:308280	IEA				P		HPO:iea	
OMIM	308280	IMPACTED TEETH, MULTIPLE		HP:0011069	OMIM:308280	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000252	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000486	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000491	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000518	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000541	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000554	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000568	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000573	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000648	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000668	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000684	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000962	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0000980	OMIM:308300	IEA				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001000	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001249	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001250	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001257	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001423	OMIM:308300	IEA				I		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001803	OMIM:308300	PCS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001805	OMIM:308300	PCS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001807	OMIM:308300	PCS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0001880	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002164	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002208	OMIM:308300	TAS	HP:0011463			P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002213	OMIM:308300	PCS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002557	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002558	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002751	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0002937	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0003187	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0004322	OMIM:308300	PCS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0004529	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0005815	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0007750	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0007850	OMIM:308300	IEA				P		HPO:iea	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0008070	OMIM:308300	PCS	HP:0003581			P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0008404	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0010783	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0100699	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308300	INCONTINENTIA PIGMENTI; IP		HP:0100783	OMIM:308300	TAS				P		HPO:skoehler	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0000252	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001249	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001257	OMIM:308350	TAS				P		HPO:skoehler	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001266	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001276	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001332	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001347	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0001419	OMIM:308350	IEA				I		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0002015	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0002094	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0002119	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0002123	OMIM:308350	IEA				P		HPO:skoehler	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0002521	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0008936	OMIM:308350	IEA				P		HPO:iea	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0100660	OMIM:308350	IEA				P		HPO:skoehler	
OMIM	308350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1; EIEE1		HP:0200134	OMIM:308350	IEA				P		HPO:skoehler	
OMIM	308500	IRIS HYPOPLASIA WITH GLAUCOMA; IHG		HP:0000501	OMIM:308500	IEA				P		HPO:skoehler	
OMIM	308500	IRIS HYPOPLASIA WITH GLAUCOMA; IHG		HP:0001089	OMIM:308500	IEA				P		HPO:skoehler	
OMIM	308500	IRIS HYPOPLASIA WITH GLAUCOMA; IHG		HP:0001417	OMIM:308500	TAS				I		HPO:skoehler	
OMIM	308500	IRIS HYPOPLASIA WITH GLAUCOMA; IHG		HP:0007676	OMIM:308500	TAS				P		HPO:skoehler	
OMIM	308600	JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY		HP:0000952	OMIM:308600	TAS				P		HPO:skoehler	
OMIM	308600	JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY		HP:0001419	OMIM:308600	TAS				I		HPO:skoehler	
OMIM	308600	JAUNDICE, FAMILIAL OBSTRUCTIVE, OF INFANCY		HP:0003265	OMIM:308600	TAS				P		HPO:skoehler	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000027	OMIM:308700	TAS				P		HPO:skoehler	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000028	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000029	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000044	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000054	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000122	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000218	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000324	OMIM:308700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000458	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0000771	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001251	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001335	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001341	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001417	OMIM:308700	IEA				I		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001419	OMIM:308700	TAS				I		HPO:skoehler	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0001761	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0002225	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0002929	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0003164	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0003782	OMIM:308700	IEA				P		HPO:iea	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0008734	OMIM:308700	TAS				P		HPO:skoehler	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0030341	PMID:18160472	PCS				P		HPO:probinson	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0030341	OMIM:308700	TAS				P		HPO:probinson	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0030344	PMID:18160472	PCS				P		HPO:probinson	
OMIM	308700	HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA; HH1		HP:0030344	OMIM:308700	TAS				P		HPO:probinson	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000028	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000029	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000044	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000054	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000122	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000218	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000458	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0000771	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001251	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001258	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001335	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001341	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001417	OMIM:308750	IEA				I		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0001761	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0002225	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0002929	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0003164	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0003782	OMIM:308750	IEA				P		HPO:iea	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0030341	PMID:6604133	PCS				P		HPO:probinson	
OMIM	308750	KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA		HP:0030344	PMID:6604133	PCS				P		HPO:probinson	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000491	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000498	OMIM:308800	IEA				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000509	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000535	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000613	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000653	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000656	OMIM:308800	PCS				P		HPO:probinson	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000958	OMIM:308800	IEA				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0000982	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001041	OMIM:308800	TAS				P		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001131	OMIM:308800	IEA				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001417	OMIM:308800	IEA				I		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001419	OMIM:308800	TAS				I		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001425	OMIM:308800	TAS				I		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0001597	OMIM:308800	IEA				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0002164	OMIM:308800	TAS				P		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0004552	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0007502	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0008391	OMIM:308800	PCS				P		HPO:iea	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0025084	OMIM:308800	TAS				P		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0030054	OMIM:308800	TAS				P		HPO:skoehler	
OMIM	308800	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX		HP:0032152	OMIM:308800	IEA				P		HPO:skoehler	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0000252	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0000561	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0001417	OMIM:308830	PCS				I		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0002059	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0002223	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0003510	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0003819	OMIM:308830	PCS				M		HPO:probinson	
OMIM	308830	KERATOSIS FOLLICULARIS, DWARFISM, AND CEREBRAL ATROPHY		HP:0007439	OMIM:308830	PCS				P		HPO:probinson	
OMIM	308850	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001249	OMIM:308850	IEA				P		HPO:iea	
OMIM	308850	LARYNGEAL ABDUCTOR PARALYSIS		HP:0001419	OMIM:308850	IEA				I		HPO:iea	
OMIM	308850	LARYNGEAL ABDUCTOR PARALYSIS		HP:0003470	OMIM:308850	IEA				P		HPO:skoehler	
OMIM	308850	LARYNGEAL ABDUCTOR PARALYSIS		HP:0004886	OMIM:308850	IEA				P		HPO:iea	
OMIM	308905	LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO		HP:0000648	OMIM:308905	IEA				P		HPO:skoehler	
OMIM	308905	LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO		HP:0001112	OMIM:308905	IEA				P		HPO:skoehler	
OMIM	308905	LEBER OPTIC ATROPHY, SUSCEPTIBILITY TO		HP:0001417	OMIM:308905	IEA				I		HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0000093	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0000112	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0000518	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0000790	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0001142	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0001417	OMIM:308940	TAS				I	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0001508	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0001757	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0002013	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0002015	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0002019	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0002094	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0003774	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0004722	OMIM:308940	TAS	HP:0003584			P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0006524	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0006756	OMIM:308940	IEA				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:iea	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0011501	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308940	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME		HP:0030034	OMIM:308940	TAS				P	#308940 LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS;;LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY;;ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL;;CHROMOSOME XQ22.3 CENTROMERIC DELETION SYNDROME	HPO:skoehler	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0000742	OMIM:308950	IEA				P		HPO:iea	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0001249	OMIM:308950	IEA				P		HPO:iea	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0001257	OMIM:308950	IEA				P		HPO:iea	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0001266	OMIM:308950	IEA				P		HPO:iea	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0001417	OMIM:308950	IEA				I		HPO:iea	
OMIM	308950	LESCH-NYHAN PHENOTYPE WITH NORMAL HGPRT		HP:0002149	OMIM:308950	IEA				P		HPO:iea	
OMIM	308960	LEUKEMIA, ACUTE, ?X-LINKED		HP:0001417	OMIM:308960	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	308960	LEUKEMIA, ACUTE, ?X-LINKED		HP:0002488	OMIM:308960	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0000083	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0000092	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0000097	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0000114	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0000121	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0001419	OMIM:308990	IEA				I		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0002148	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0002150	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0002907	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0003076	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0003126	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0003355	OMIM:308990	IEA				P		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0003677	OMIM:308990	IEA				C		HPO:iea	
OMIM	308990	PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS		HP:0004322	OMIM:308990	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000028	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000083	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000093	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000501	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000505	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000519	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000568	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000718	OMIM:309000	IEA				P		HPO:skoehler	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000733	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0000926	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001225	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001249	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001250	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001284	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001319	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001382	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001419	OMIM:309000	IEA				I		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001482	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001508	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0001994	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002019	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002049	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002119	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002650	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002748	OMIM:309000	IEA				P		HPO:skoehler	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002749	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002756	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002808	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002827	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0002857	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0003109	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0003124	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0003148	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0003355	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0003646	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0004322	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0004639	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0005984	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0006297	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0007109	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0007663	OMIM:309000	TAS				P		HPO:skoehler	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0007948	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0009473	OMIM:309000	IEA				P		HPO:iea	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0025131	OMIM:309000	TAS				P		HPO:skoehler	
OMIM	309000	LOWE OCULOCEREBRORENAL SYNDROME		HP:0100490	OMIM:309000	TAS				P		HPO:probinson	
OMIM	309050	LUTHERAN SUPPRESSOR, X-LINKED		HP:0001419	OMIM:309050	IEA				I		HPO:iea	
OMIM	309050	LUTHERAN SUPPRESSOR, X-LINKED		HP:0001939	OMIM:309050	IEA				P		HPO:iea	
OMIM	309100	MACULAR DYSTROPHY, X-LINKED		HP:0001417	OMIM:309100	IEA				I		HPO:iea	
OMIM	309100	MACULAR DYSTROPHY, X-LINKED		HP:0007754	OMIM:309100	IEA				P		HPO:iea	
OMIM	309120	SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2		HP:0000027	OMIM:309120	TAS				P		HPO:skoehler	
OMIM	309120	SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2		HP:0000029	OMIM:309120	IEA				P		HPO:skoehler	
OMIM	309120	SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2		HP:0001419	OMIM:309120	TAS				I		HPO:skoehler	
OMIM	309120	SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2		HP:0001939	OMIM:309120	IEA				P		HPO:iea	
OMIM	309120	SPERMATOGENIC FAILURE, X-LINKED, 2; SPGFX2		HP:0003251	OMIM:309120	IEA				P		HPO:iea	
OMIM	309200	MAJOR AFFECTIVE DISORDER 2		HP:0001423	OMIM:309200	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	309200	MAJOR AFFECTIVE DISORDER 2		HP:0003593	OMIM:309200	IEA				C		HPO:iea	
OMIM	309200	MAJOR AFFECTIVE DISORDER 2		HP:0007302	OMIM:309200	IEA				P		HPO:iea	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000483	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000485	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000501	OMIM:309300	IEA				P		HPO:skoehler	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000518	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000541	OMIM:309300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309300	MEGALOCORNEA; MGC1		HP:0000616	OMIM:309300	IEA				P		HPO:skoehler	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0001084	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0001132	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0001419	OMIM:309300	TAS				I		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0007836	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0011487	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309300	MEGALOCORNEA; MGC1		HP:0100693	OMIM:309300	TAS				P		HPO:probinson	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000071	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000126	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000175	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000270	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000274	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000316	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000336	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000347	OMIM:309350	TAS				P		HPO:probinson	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000400	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000403	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000472	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000486	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000520	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000684	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000692	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000767	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000774	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000882	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0000894	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001270	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001288	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001377	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001423	OMIM:309350	IEA				I		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001508	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001539	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001609	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001634	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001704	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001762	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0001763	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002092	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002205	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002208	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002673	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002751	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002827	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002857	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0002982	OMIM:309350	TAS				P		HPO:probinson	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0003015	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0003826	OMIM:309350	TAS				M		HPO:probinson	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0004611	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0005446	OMIM:309350	TAS				P		HPO:probinson	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0005792	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0009771	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0009882	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0010230	OMIM:309350	IEA				P		HPO:iea	
OMIM	309350	MELNICK-NEEDLES SYNDROME		HP:0011335	OMIM:309350	TAS				P		HPO:probinson	
OMIM	309400	MENKES DISEASE		HP:0000248	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0000252	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0000271	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0000939	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0000973	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001010	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001249	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001250	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001276	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001388	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001419	OMIM:309400	IEA				I		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0001511	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0002045	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0002170	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0002645	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0003016	OMIM:309400	TAS				P		HPO:probinson	
OMIM	309400	MENKES DISEASE		HP:0003819	OMIM:309400	IEA				M		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0004322	OMIM:309400	IEA				P		HPO:iea	
OMIM	309400	MENKES DISEASE		HP:0005054	OMIM:309400	TAS				P		HPO:probinson	
OMIM	309400	MENKES DISEASE		HP:0008070	OMIM:309400	IEA				P		HPO:skoehler	
OMIM	309480	MENTAL RETARDATION ASSOCIATED WITH PSORIASIS		HP:0001249	OMIM:309480	IEA				P		HPO:iea	
OMIM	309480	MENTAL RETARDATION ASSOCIATED WITH PSORIASIS		HP:0001250	OMIM:309480	IEA				P		HPO:iea	
OMIM	309480	MENTAL RETARDATION ASSOCIATED WITH PSORIASIS		HP:0001417	OMIM:309480	IEA				I		HPO:iea	
OMIM	309480	MENTAL RETARDATION ASSOCIATED WITH PSORIASIS		HP:0003765	OMIM:309480	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000047	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000089	OMIM:309500	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000160	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000175	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000218	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000219	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000248	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000252	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000272	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000275	OMIM:309500	TAS				P		HPO:probinson	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000276	OMIM:309500	TAS				P		HPO:probinson	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000286	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000303	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000322	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000325	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000347	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000365	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000378	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000400	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000411	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000414	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000431	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000486	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000518	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000540	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000568	OMIM:309500	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000582	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000589	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000618	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000739	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0000767	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001249	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001250	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001257	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001347	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001419	OMIM:309500	IEA				I		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001547	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001595	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001611	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001629	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001631	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001636	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001696	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001741	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001761	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0001786	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0002023	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0002033	OMIM:309500	TAS	HP:0003593			P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0002059	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0002650	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0004209	OMIM:309500	TAS				P		HPO:probinson	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0004322	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0005338	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0008070	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0008734	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0009473	OMIM:309500	IEA				P		HPO:iea	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0012385	OMIM:309500	TAS				P		HPO:skoehler	
OMIM	309500	RENPENNING SYNDROME 1; RENS1		HP:0031013	OMIM:309500	IEA				P		HPO:skoehler	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0000325	OMIM:309510	IEA				P		HPO:skoehler	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0000750	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0001249	OMIM:309510	TAS				P		HPO:skoehler	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0001250	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0001260	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0001371	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0001419	OMIM:309510	IEA				I		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0002061	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0002353	OMIM:309510	IEA				P		HPO:iea	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0002451	OMIM:309510	IEA				P		HPO:skoehler	
OMIM	309510	#309510 PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS;;PARTINGTON SYNDROME;;MENTAL RETARDATION, X-LINKED, SYNDROMIC 1; MRXS1;;MENTAL RETARDATION, X-LINKED, WITH DYSTONIC MOVEMENTS, ATAXIA, ANDSEIZURES;;MENTAL RETARDATION, X-LINKED 36; MRX36		HP:0004373	OMIM:309510	TAS				P		HPO:probinson	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000119	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000194	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000218	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000219	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000219	OMIM:309520	TAS				P		HPO:skoehler	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000256	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000275	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000276	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000322	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000327	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000347	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000369	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000426	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000446	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000678	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000709	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000712	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000717	OMIM:309520	TAS				P		HPO:skoehler	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000718	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000722	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000735	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000744	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000752	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0000767	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001166	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001249	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001250	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001274	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001290	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001371	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001388	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001419	OMIM:309520	IEA				I		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001519	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001547	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001611	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001629	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0001631	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0002002	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0002007	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0003189	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0004970	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0008544	OMIM:309520	IEA				P		HPO:iea	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0011220	OMIM:309520	TAS				P		HPO:skoehler	
OMIM	309520	#309520 LUJAN-FRYNS SYNDROME;;MENTAL RETARDATION, X-LINKED, WITH MARFANOID HABITUS		HP:0011304	OMIM:309520	IEA				P		HPO:iea	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0000248	OMIM:309530	TAS				P		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0000486	OMIM:309530	TAS				P		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0000540	OMIM:309530	TAS				P		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0001249	OMIM:309530	IEA				P		HPO:iea	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0001250	OMIM:309530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0001290	OMIM:309530	TAS				P		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0001419	OMIM:309530	IEA				I		HPO:iea	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0001423	OMIM:309530	TAS				I		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0002465	OMIM:309530	TAS				P		HPO:skoehler	
OMIM	309530	MENTAL RETARDATION, X-LINKED 1		HP:0005484	OMIM:309530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0000248	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0000252	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0001249	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:probinson	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0001250	OMIM:309541	IEA				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0001290	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0001419	OMIM:309541	TAS				I	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0001508	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0002072	OMIM:309541	TAS		HP:0040283		P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	HP:0040283
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0002156	OMIM:309541	TAS		HP:0040283		P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	HP:0040283
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0002305	OMIM:309541	TAS		HP:0040283		P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	HP:0040283
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0002521	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0002912	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0003593	OMIM:309541	TAS				C	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0004322	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309541	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, cblX TYPE		HP:0012120	OMIM:309541	TAS				P	METHYLMALONIC ACIDEMIA AND HOMOCYSTEINEMIA, CBLX TYPE	HPO:skoehler	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000154	OMIM:309545	PCS				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000179	OMIM:309545	PCS				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000215	OMIM:309545	PCS				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000248	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000303	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000321	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0000750	OMIM:309545	PCS				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0001249	OMIM:309545	TAS				P		HPO:skoehler	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0001250	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0001417	OMIM:309545	IEA				I		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0002381	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0002719	OMIM:309545	IEA				P		HPO:iea	
OMIM	309545	%309545 MENTAL RETARDATION, X-LINKED, SYNDROMIC 12; MRXS12		HP:0008897	OMIM:309545	PCS				P		HPO:iea	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000426	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000713	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000718	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000722	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000750	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0000752	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:309548	IEA				P		HPO:iea	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0001417	OMIM:309548	IEA				I		HPO:iea	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0001419	OMIM:309548	TAS				I		HPO:skoehler	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0001939	OMIM:309548	IEA				P		HPO:iea	
OMIM	309548	#309548 MENTAL RETARDATION, X-LINKED, ASSOCIATED WITH FRAGILE SITE FRAXE;;FRAXE MENTAL RETARDATION SYNDROME		HP:0100710	OMIM:309548	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000179	OMIM:309549	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000400	OMIM:309549	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000629	OMIM:309549	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000637	OMIM:309549	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000717	OMIM:309549	IEA	HP:0003593	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0000750	OMIM:309549	IEA				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0001250	OMIM:309549	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0001256	OMIM:309549	IEA				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0001263	OMIM:309549	TAS				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0001417	OMIM:309549	IEA				I		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0001419	OMIM:309549	TAS				I		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0002194	OMIM:309549	IEA				P		HPO:skoehler	
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0005280	OMIM:309549	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309549	MENTAL RETARDATION, X-LINKED 9		HP:0009832	OMIM:309549	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0000252	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0000365	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES	HP:0012828	HP:0000365	OMIM:309555	TAS				P		HPO:probinson	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0000618	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0000648	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0001141	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0001249	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0001250	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0001257	OMIM:309555	IEA				P		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0001417	OMIM:309555	IEA				I		HPO:iea	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0003819	OMIM:309555	TAS				M		HPO:probinson	
OMIM	309555	MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES		HP:0005193	OMIM:309555	IEA				P		HPO:iea	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0000218	OMIM:309560	TAS				P		HPO:skoehler	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0000972	OMIM:309560	IEA				P		HPO:iea	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001249	OMIM:309560	IEA				P		HPO:iea	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001256	OMIM:309560	TAS				P		HPO:skoehler	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001258	OMIM:309560	IEA				P		HPO:iea	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001337	OMIM:309560	TAS				P		HPO:skoehler	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001348	OMIM:309560	TAS				P		HPO:skoehler	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001417	OMIM:309560	IEA				I		HPO:iea	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001419	OMIM:309560	TAS				I		HPO:skoehler	
OMIM	309560	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA AND PALMOPLANTAR HYPERKERATOSIS		HP:0001761	OMIM:309560	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000028	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000046	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000047	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000054	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000076	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000089	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000135	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000154	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000158	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000179	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000188	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000194	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000218	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000219	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000252	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000268	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000272	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000280	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000286	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000316	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000341	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000347	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000358	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000369	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000407	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000431	OMIM:309580	TAS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000451	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000463	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000470	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000508	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000577	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000582	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000648	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000749	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0000752	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001156	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001182	OMIM:309580	TAS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001238	OMIM:309580	TAS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001250	OMIM:309580	TAS		HP:0040284		P		HPO:probinson	35%
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001347	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001419	OMIM:309580	IEA				I		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001513	OMIM:309580	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001566	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001762	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001763	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001871	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0001884	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002013	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002019	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002020	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002307	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002750	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002751	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0002857	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0004322	OMIM:309580	TAS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0005280	OMIM:309580	TAS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0005326	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0006887	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0006895	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0008551	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0008734	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0008947	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0009466	OMIM:309580	IEA				P		HPO:iea	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0010804	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0010806	OMIM:309580	PCS				P		HPO:probinson	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0010808	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1	HP:0012829	HP:0010864	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0011800	OMIM:309580	TAS				P		HPO:skoehler	
OMIM	309580	MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1		HP:0030084	OMIM:309580	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000028	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000098	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000175	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000179	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000193	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000303	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000316	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000322	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000324	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000377	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000465	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000678	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000767	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000768	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0000939	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001187	OMIM:309583	TAS				P		HPO:probinson	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001249	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001250	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001252	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001260	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001290	OMIM:309583	TAS				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001419	OMIM:309583	IEA				I		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001611	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001762	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0001847	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0002136	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0002705	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0002751	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0002757	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0003199	OMIM:309583	IEA				P		HPO:iea	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0004283	OMIM:309583	TAS				P		HPO:probinson	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0004322	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0006610	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0011003	OMIM:309583	IEA				P		HPO:skoehler	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0011302	OMIM:309583	TAS				P		HPO:probinson	
OMIM	309583	MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE		HP:0100807	OMIM:309583	TAS				P		HPO:probinson	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000028	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000054	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000135	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000248	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000252	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000278	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000336	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000455	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000490	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000574	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000692	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000712	OMIM:309585	IEA				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000771	OMIM:309585	IEA				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0000823	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001182	OMIM:309585	IEA				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001249	OMIM:309585	PCS				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001250	OMIM:309585	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001252	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001263	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001344	OMIM:309585	IEA				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001419	OMIM:309585	IEA				I		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001423	OMIM:309585	TAS				I		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001513	OMIM:309585	IEA				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001761	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001763	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001773	OMIM:309585	IEA				P		HPO:iea	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0001956	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0002808	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0003199	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0004322	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0008734	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0200055	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309585	WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME; WTS		HP:0400005	OMIM:309585	TAS				P		HPO:skoehler	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000023	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000028	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000164	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000278	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000286	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000348	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000369	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000448	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000486	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000508	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000639	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000878	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000939	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0000951	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0001252	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0001290	OMIM:309610	TAS				P		HPO:skoehler	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0001419	OMIM:309610	IEA				I		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0001762	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0002059	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0002673	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0002999	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0009466	OMIM:309610	IEA				P		HPO:iea	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0010499	OMIM:309610	IEA				P		HPO:skoehler	
OMIM	309610	PRIETO X-LINKED MENTAL RETARDATION SYNDROME		HP:0030084	OMIM:309610	TAS				P		HPO:skoehler	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0000431	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0001249	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0001417	OMIM:309620	IEA				I		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0001952	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0002023	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0002650	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0002652	OMIM:309620	IEA				P		HPO:skoehler	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0002949	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0004322	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0005487	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0005819	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0006897	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0008467	OMIM:309620	IEA				P		HPO:iea	
OMIM	309620	%309620 MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD;;CHRISTIAN SYNDROME; CHRS		HP:0011349	OMIM:309620	TAS				P		HPO:skoehler	
OMIM	309630	#309630 METACARPAL 4-5 FUSION; MF4		HP:0001419	OMIM:309630	TAS				I		HPO:skoehler	
OMIM	309630	#309630 METACARPAL 4-5 FUSION; MF4		HP:0005867	OMIM:309630	IEA				P		HPO:iea	
OMIM	309640	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA		HP:0001249	OMIM:309640	TAS				P		HPO:probinson	
OMIM	309640	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA		HP:0001258	OMIM:309640	IEA				P		HPO:skoehler	
OMIM	309640	MENTAL RETARDATION WITH SPASTIC PARAPLEGIA		HP:0006983	OMIM:309640	TAS				P		HPO:probinson	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000028	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000047	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000072	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000089	OMIM:309800	TAS				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000202	OMIM:309800	IEA				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000204	OMIM:309800	TAS				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000252	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000365	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000369	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000396	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000403	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000465	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000482	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000508	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000528	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000567	OMIM:309800	TAS				P		HPO:probinson	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000568	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000588	OMIM:309800	TAS				P		HPO:probinson	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000612	OMIM:309800	TAS				P		HPO:probinson	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000612	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000618	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000678	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000690	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000692	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000718	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000729	OMIM:309800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000742	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000767	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000774	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0000894	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001018	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001159	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001249	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001250	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001264	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001270	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001290	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001417	OMIM:309800	IEA				I		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001510	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0001647	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002021	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002023	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002035	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002089	OMIM:309800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002251	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002705	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002751	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0002938	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0008678	OMIM:309800	IEA				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0009466	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0009473	OMIM:309800	IEA				P		HPO:iea	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0012385	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0020006	OMIM:309800	TAS				P		HPO:probinson	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0030084	OMIM:309800	TAS				P		HPO:skoehler	
OMIM	309800	MICROPHTHALMIA, SYNDROMIC 1		HP:0200021	OMIM:309800	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000013	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000041	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000047	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000054	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000238	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000252	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000365	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000518	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000568	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000580	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000612	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000647	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0000776	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001250	OMIM:309801	IEA				P		HPO:skoehler	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001274	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001331	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001423	OMIM:309801	IEA				I		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001545	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001629	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001631	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0001939	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0002023	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0002623	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0004322	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0005152	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0006887	OMIM:309801	IEA		HP:0040284		P		HPO:skoehler	24%
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0007398	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0008665	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0011675	OMIM:309801	IEA				P		HPO:iea	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0012861	OMIM:309801	TAS				P		HPO:skoehler	
OMIM	309801	#309801 MICROPHTHALMIA, SYNDROMIC 7; MCOPS7;;MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS;;MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA;;MIDAS SYNDROME		HP:0030048	OMIM:309801	TAS				P		HPO:skoehler	
OMIM	309840	MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS		HP:0000707	OMIM:309840	IEA				P		HPO:iea	
OMIM	309840	MODIFIER, X-LINKED, FOR NEUROFUNCTIONAL DEFECTS		HP:0001417	OMIM:309840	IEA				I		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000023	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000158	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000179	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000238	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000256	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000268	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000280	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000365	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000403	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000470	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000508	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000684	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000687	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000943	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0000998	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001085	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001171	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001250	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001371	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001419	OMIM:309900	IEA				I		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001537	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001609	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001635	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001654	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001744	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0001761	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002014	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002099	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002159	OMIM:309900	TAS				P		HPO:skoehler	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002180	OMIM:309900	TAS				P		HPO:probinson	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002187	OMIM:309900	TAS				P		HPO:skoehler	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002240	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002341	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002786	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002808	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0002870	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0003502	OMIM:309900	TAS				P		HPO:skoehler	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II	HP:0012825	HP:0003510	OMIM:309900	TAS				P		HPO:skoehler	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0003541	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0004389	OMIM:309900	IEA				P		HPO:iea	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0007703	OMIM:309900	TAS				P		HPO:probinson	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0008301	OMIM:309900	TAS				P		HPO:probinson	
OMIM	309900	MUCOPOLYSACCHARIDOSIS, TYPE II		HP:0030799	OMIM:309900	TAS				P		HPO:skoehler	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0001417	OMIM:309930	IEA				I		HPO:iea	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0001638	OMIM:309930	IEA				P		HPO:iea	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0003115	OMIM:309930	TAS				P		HPO:skoehler	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0003167	OMIM:309930	TAS				P		HPO:probinson	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0003236	OMIM:309930	IEA				P		HPO:iea	
OMIM	309930	MUSCULAR DYSTROPHY, CARDIAC TYPE		HP:0003560	OMIM:309930	TAS				P		HPO:skoehler	
OMIM	309950	MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE		HP:0000006	OMIM:309950	TAS				I		HPO:nvasilevsky	
OMIM	309950	MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE		HP:0001423	OMIM:309950	TAS				I		HPO:nvasilevsky	
OMIM	309950	MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE		HP:0006785	OMIM:309950	TAS				P		HPO:probinson	
OMIM	310000	MUSCULAR DYSTROPHY, MABRY TYPE		HP:0001417	OMIM:310000	IEA				I		HPO:iea	
OMIM	310000	MUSCULAR DYSTROPHY, MABRY TYPE		HP:0007081	OMIM:310000	IEA				P		HPO:iea	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0001417	OMIM:310095	IEA				I		HPO:iea	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0003236	OMIM:310095	IEA				P		HPO:iea	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0003547	OMIM:310095	IEA				P		HPO:iea	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0003560	OMIM:310095	TAS				P		HPO:skoehler	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0003691	OMIM:310095	IEA				P		HPO:iea	
OMIM	310095	MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL		HP:0011675	OMIM:310095	IEA				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001252	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001256	OMIM:310200	TAS				P		HPO:probinson	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001265	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001290	OMIM:310200	TAS				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001371	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001419	OMIM:310200	IEA				I		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001635	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001638	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0001644	OMIM:310200	TAS				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0002093	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0002515	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0002650	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0002791	OMIM:310200	IEA				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0002878	OMIM:310200	TAS				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003115	OMIM:310200	IEA				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003236	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003307	OMIM:310200	IEA				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003391	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003560	OMIM:310200	TAS				P		HPO:skoehler	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0003707	OMIM:310200	IEA				P		HPO:iea	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0011463	OMIM:310200	TAS				C		HPO:probinson	
OMIM	310200	MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD		HP:0011675	OMIM:310200	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0000464	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1	HP:0012825	HP:0000767	OMIM:310300	TAS				P		HPO:probinson	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0001419	OMIM:310300	IEA				I		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0001645	OMIM:310300	TAS				P		HPO:probinson	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0001678	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0001692	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0001771	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0002515	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0002987	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0003198	OMIM:310300	IEA				P		HPO:skoehler	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0003236	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0003621	OMIM:310300	IEA				C		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0003677	OMIM:310300	TAS				C		HPO:probinson	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0004631	OMIM:310300	IEA				P		HPO:iea	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0011463	OMIM:310300	TAS				C		HPO:probinson	
OMIM	310300	EMERY-DREIFUSS MUSCULAR DYSTROPHY 1, X-LINKED; EDMD1		HP:0011807	OMIM:310300	TAS				P		HPO:probinson	
OMIM	310350	MYELOLYMPHATIC INSUFFICIENCY		HP:0001419	OMIM:310350	TAS				I		HPO:probinson	
OMIM	310350	MYELOLYMPHATIC INSUFFICIENCY		HP:0001882	OMIM:310350	TAS				P		HPO:probinson	
OMIM	310350	MYELOLYMPHATIC INSUFFICIENCY		HP:0002718	OMIM:310350	TAS				P		HPO:probinson	
OMIM	310350	MYELOLYMPHATIC INSUFFICIENCY		HP:0004429	OMIM:310350	TAS				P		HPO:probinson	
OMIM	310350	MYELOLYMPHATIC INSUFFICIENCY		HP:0011447	OMIM:310350	TAS				P		HPO:probinson	
OMIM	310370	310370 MYOCLONIC EPILEPSY, PROGRESSIVE		HP:0001417	OMIM:310370	TAS				I		HPO:skoehler	
OMIM	310370	310370 MYOCLONIC EPILEPSY, PROGRESSIVE		HP:0002123	OMIM:310370	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000028	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000218	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000238	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000256	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000275	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000276	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000467	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0000544	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001166	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001284	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001371	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001410	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001419	OMIM:310400	IEA				I		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001558	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0001561	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0002021	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0002375	OMIM:310400	TAS				P		HPO:skoehler	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0002643	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0002878	OMIM:310400	IEA				P		HPO:skoehler	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0003324	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0003517	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0004887	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0006829	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0009110	OMIM:310400	IEA				P		HPO:iea	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0010628	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310400	MYOPATHY, CENTRONUCLEAR, X-LINKED; CNMX		HP:0011308	OMIM:310400	TAS				P		HPO:probinson	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0001270	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0001319	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0001371	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0001419	OMIM:310440	IEA				I		HPO:iea	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0002093	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0002486	OMIM:310440	IEA				P		HPO:skoehler	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0002650	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003198	OMIM:310440	TAS				P		HPO:probinson	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003202	OMIM:310440	TAS				P		HPO:skoehler	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003236	OMIM:310440	IEA				P		HPO:iea	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003391	OMIM:310440	TAS				P		HPO:skoehler	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003551	OMIM:310440	IEA				P		HPO:iea	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003677	OMIM:310440	IEA				C		HPO:iea	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0003829	OMIM:310440	TAS				C		HPO:skoehler	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0007941	OMIM:310440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0008994	OMIM:310440	IEA				P		HPO:iea	
OMIM	310440	#310440 MYOPATHY, X-LINKED, WITH EXCESSIVE AUTOPHAGY; MEAX;;XMEA		HP:0009046	OMIM:310440	TAS				P		HPO:skoehler	
OMIM	310460	%310460 MYOPIA 1, X-LINKED; MYP1		HP:0000545	OMIM:310460	IEA				P		HPO:iea	
OMIM	310460	%310460 MYOPIA 1, X-LINKED; MYP1		HP:0001417	OMIM:310460	IEA				I		HPO:iea	
OMIM	310460	%310460 MYOPIA 1, X-LINKED; MYP1		HP:0001419	OMIM:310460	TAS				I		HPO:skoehler	
OMIM	310465	N SYNDROME		HP:0000028	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0000047	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0000365	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0000505	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0001249	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0001257	OMIM:310465	IEA				P		HPO:iea	
OMIM	310465	N SYNDROME		HP:0001417	OMIM:310465	IEA				I		HPO:iea	
OMIM	310465	N SYNDROME		HP:0001909	OMIM:310465	TAS				P		HPO:skoehler	
OMIM	310465	N SYNDROME		HP:0002664	OMIM:310465	IEA				P		HPO:skoehler	
OMIM	310465	N SYNDROME		HP:0003220	OMIM:310465	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0000092	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0000096	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0000114	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0000121	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0000787	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0001419	OMIM:310468	IEA				I		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0002150	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0002907	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0003126	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0005576	OMIM:310468	IEA				P		HPO:iea	
OMIM	310468	NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE		HP:0012622	OMIM:310468	TAS				P		HPO:probinson	
OMIM	310470	NEUROPATHY, HEREDITARY SENSORY, X-LINKED		HP:0000763	OMIM:310470	TAS				P		HPO:probinson	
OMIM	310470	NEUROPATHY, HEREDITARY SENSORY, X-LINKED		HP:0001417	OMIM:310470	TAS				I		HPO:probinson	
OMIM	310470	NEUROPATHY, HEREDITARY SENSORY, X-LINKED		HP:0003380	OMIM:310470	TAS				P		HPO:probinson	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0000365	OMIM:310490	IEA				P		HPO:iea	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0000407	OMIM:310490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0000763	OMIM:310490	IEA				P		HPO:iea	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0001249	OMIM:310490	IEA				P		HPO:iea	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0001324	OMIM:310490	TAS				P		HPO:probinson	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0001419	OMIM:310490	TAS				I		HPO:probinson	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0002936	OMIM:310490	TAS				P		HPO:skoehler	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0003236	OMIM:310490	TAS				P		HPO:skoehler	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0003390	OMIM:310490	TAS				P		HPO:skoehler	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0007002	OMIM:310490	IEA				P		HPO:iea	
OMIM	310490	COWCHOCK SYNDROME; COWCK		HP:0100543	OMIM:310490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0000545	OMIM:310500	IEA				P		HPO:iea	
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0001417	OMIM:310500	IEA				I		HPO:iea	
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0001419	OMIM:310500	TAS				I		HPO:skoehler	
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0007642	OMIM:310500	IEA				P		HPO:iea	
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0011003	OMIM:310500	TAS				P		HPO:skoehler	
OMIM	310500	#310500 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A;;CSNB, COMPLETE, X-LINKED;;NIGHT BLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA;;HEMERALOPIA-MYOPIA;;MYOPIA-NIGHT BLINDNESS; NBM1NYCTALOPIA, INCLUDED		HP:0012047	OMIM:310500	TAS				P		HPO:skoehler	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000407	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000518	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000541	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000568	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000594	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000618	OMIM:310600	TAS	HP:0003593			P		HPO:probinson	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000648	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000709	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000718	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000726	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0000738	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0001250	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0001419	OMIM:310600	IEA				I		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0006887	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0007676	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0007759	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0007973	OMIM:310600	IEA				P		HPO:iea	
OMIM	310600	#310600 NORRIE DISEASE; ND;;ATROPHIA BULBORUM HEREDITARIA;;EPISKOPI BLINDNESS		HP:0008052	OMIM:310600	TAS				P		HPO:skoehler	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0000666	OMIM:310700	IEA				P		HPO:iea	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0001419	OMIM:310700	IEA				I		HPO:iea	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0001423	OMIM:310700	IEA				I		HPO:iea	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0001425	OMIM:310700	TAS				I		HPO:skoehler	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0003593	OMIM:310700	IEA				C		HPO:iea	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0006934	OMIM:310700	IEA				P		HPO:iea	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1	HP:0012825	HP:0007663	OMIM:310700	TAS				P		HPO:probinson	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0012043	OMIM:310700	TAS				P		HPO:probinson	
OMIM	310700	NYSTAGMUS 1, CONGENITAL, X-LINKED; NYS1		HP:0032037	OMIM:310700	IEA				P		HPO:skoehler	
OMIM	310800	NYSTAGMUS, MYOCLONIC		HP:0000639	OMIM:310800	IEA				P		HPO:iea	
OMIM	310800	NYSTAGMUS, MYOCLONIC		HP:0001336	OMIM:310800	IEA				P		HPO:iea	
OMIM	310800	NYSTAGMUS, MYOCLONIC		HP:0001423	OMIM:310800	IEA				I		HPO:iea	
OMIM	310900	OCCIPITAL HAIR, WHITE LOCK OF		HP:0001417	OMIM:310900	IEA				I		HPO:iea	
OMIM	310900	OCCIPITAL HAIR, WHITE LOCK OF		HP:0011364	OMIM:310900	IEA				P		HPO:skoehler	
OMIM	310980	OMPHALOCELE		HP:0001417	OMIM:310980	IEA				I		HPO:iea	
OMIM	310980	OMPHALOCELE		HP:0001539	OMIM:310980	IEA				P		HPO:iea	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0000508	OMIM:311000	IEA				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0000545	OMIM:311000	IEA				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0000546	OMIM:311000	TAS				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0000602	OMIM:311000	IEA				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0001417	OMIM:311000	IEA				I		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0002414	OMIM:311000	IEA				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0003438	OMIM:311000	TAS				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0006844	OMIM:311000	TAS				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0007686	OMIM:311000	TAS				P		HPO:probinson	
OMIM	311000	OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA		HP:0200065	OMIM:311000	TAS				P		HPO:probinson	
OMIM	311050	OPTIC ATROPHY 2		HP:0000648	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0001249	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0001260	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0001337	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0001417	OMIM:311050	TAS				I		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0002075	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0003438	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0003487	OMIM:311050	TAS				P		HPO:skoehler	
OMIM	311050	OPTIC ATROPHY 2		HP:0007083	OMIM:311050	TAS				P		HPO:probinson	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0000407	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0000510	OMIM:311070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0000529	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0000648	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0001270	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0001271	OMIM:311070	IEA				P		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0001288	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0001419	OMIM:311070	IEA				I		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0001761	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0002460	OMIM:311070	TAS				P		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0002522	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0002936	OMIM:311070	IEA				P		HPO:iea	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0003383	OMIM:311070	TAS				P		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0003481	OMIM:311070	IEA				P		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0003693	OMIM:311070	TAS				P		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0003828	OMIM:311070	TAS				C		HPO:skoehler	
OMIM	311070	CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5		HP:0011463	OMIM:311070	TAS				C		HPO:probinson	
OMIM	311100	OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME		HP:0000648	OMIM:311100	IEA				P		HPO:iea	
OMIM	311100	OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME		HP:0001258	OMIM:311100	IEA				P		HPO:iea	
OMIM	311100	OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME		HP:0001417	OMIM:311100	IEA				I		HPO:iea	
OMIM	311100	OPTIC ATROPHY--SPASTIC PARAPLEGIA SYNDROME		HP:0004924	OMIM:311100	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000093	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000113	OMIM:311200	IEA	HP:0003581			P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000138	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000161	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000175	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000180	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000199	OMIM:311200	TAS				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000218	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000238	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000252	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000286	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000308	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000316	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000324	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000365	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000369	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000430	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000431	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000494	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000506	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000670	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0000822	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001056	OMIM:311200	TAS	HP:0003593			P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001156	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001159	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001249	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001250	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001274	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001317	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001395	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001407	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001423	OMIM:311200	IEA				I		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001596	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001627	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001737	OMIM:311200	TAS		HP:0040284		P		HPO:skoehler	29%
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0001780	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002007	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002132	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002282	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002444	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002475	OMIM:311200	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002536	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0002617	OMIM:311200	IEA				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0003577	OMIM:311200	TAS				C		HPO:probinson	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0004322	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0006297	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0006349	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0008070	OMIM:311200	IEA				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0009085	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0009466	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0010297	OMIM:311200	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0010442	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0011069	OMIM:311200	IEA				P		HPO:iea	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0030084	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311200	OROFACIODIGITAL SYNDROME I; OFD1		HP:0100702	OMIM:311200	TAS				P		HPO:skoehler	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0000737	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001249	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001250	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001251	OMIM:311250	IEA				P		HPO:skoehler	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001254	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001259	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001263	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001297	OMIM:311250	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001419	OMIM:311250	IEA				I		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001508	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001950	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001951	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0001987	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0002013	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0002038	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0002131	OMIM:311250	TAS				P		HPO:skoehler	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0002181	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0003217	OMIM:311250	IEA				P		HPO:iea	
OMIM	311250	#311250 ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO;;ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY;;OTC DEFICIENCYVALPROATE SENSITIVITY, INCLUDED		HP:0003572	OMIM:311250	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000160	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000175	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000269	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000272	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000316	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000336	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000405	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000431	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000494	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0000767	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001241	OMIM:311300	TAS				P		HPO:skoehler	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001256	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001377	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001423	OMIM:311300	IEA				I		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001476	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001539	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001571	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001592	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001770	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001782	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0001852	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002007	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002164	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002650	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002673	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002688	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002737	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0002827	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0003083	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0003196	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0004232	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0004322	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0005048	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0005090	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0006389	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0008089	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0008127	OMIM:311300	IEA				P		HPO:iea	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0008404	OMIM:311300	TAS				P		HPO:skoehler	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0009642	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0009882	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0010041	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0010044	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0010047	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0010055	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0010109	OMIM:311300	TAS				P		HPO:probinson	
OMIM	311300	#311300 OTOPALATODIGITAL SYNDROME, TYPE I; OPD1;;OPD I SYNDROME;;OPD SYNDROME 1OTOPALATODIGITAL SPECTRUM DISORDER, INCLUDED;;FRONTOOTOPALATODIGITAL OSTEODYSPLASIA, INCLUDED		HP:0012368	OMIM:311300	TAS				P		HPO:skoehler	
OMIM	311350	OUABAIN RESISTANCE		HP:0001417	OMIM:311350	IEA				I		HPO:iea	
OMIM	311360	PREMATURE OVARIAN FAILURE 1		HP:0000837	OMIM:311360	IEA				P		HPO:iea	
OMIM	311360	PREMATURE OVARIAN FAILURE 1		HP:0000858	OMIM:311360	IEA				P		HPO:iea	
OMIM	311360	PREMATURE OVARIAN FAILURE 1		HP:0001417	OMIM:311360	IEA				I		HPO:iea	
OMIM	311360	PREMATURE OVARIAN FAILURE 1		HP:0001939	OMIM:311360	IEA				P		HPO:iea	
OMIM	311360	PREMATURE OVARIAN FAILURE 1		HP:0008209	OMIM:311360	IEA				P		HPO:iea	
OMIM	311400	PAINE SYNDROME		HP:0000252	OMIM:311400	IEA				P		HPO:iea	
OMIM	311400	PAINE SYNDROME		HP:0001264	OMIM:311400	IEA				P		HPO:iea	
OMIM	311400	PAINE SYNDROME		HP:0001417	OMIM:311400	IEA				I		HPO:iea	
OMIM	311400	PAINE SYNDROME		HP:0002123	OMIM:311400	IEA				P		HPO:iea	
OMIM	311400	PAINE SYNDROME		HP:0006955	OMIM:311400	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000176	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000316	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000431	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000455	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000494	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0000506	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001137	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001249	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001250	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001257	OMIM:311450	IEA				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001417	OMIM:311450	IEA				I		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001761	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001763	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0001840	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0002007	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0002236	OMIM:311450	IEA				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0002967	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0002986	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0003022	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0005280	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0006289	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0006293	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0009466	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0009473	OMIM:311450	IEA				P		HPO:iea	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0010809	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0012385	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311450	311450 PALLISTER W SYNDROME;;W SYNDROME		HP:0030084	OMIM:311450	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0000256	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0000726	OMIM:311510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001249	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001250	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001260	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001263	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001300	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001355	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0001419	OMIM:311510	TAS				I		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002007	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002067	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002322	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002362	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002396	OMIM:311510	TAS				P		HPO:probinson	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0002465	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0100315	OMIM:311510	IEA				P		HPO:skoehler	
OMIM	311510	WAISMAN SYNDROME; WSMN		HP:0100660	OMIM:311510	TAS				P		HPO:skoehler	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0000162	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0000175	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0000201	OMIM:311895	TAS				P		HPO:skoehler	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0000347	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0000348	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0001182	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0001417	OMIM:311895	IEA				I		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0001795	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0002007	OMIM:311895	TAS				P		HPO:skoehler	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0004209	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0005747	OMIM:311895	IEA				P		HPO:iea	
OMIM	311895	311895 PIERRE ROBIN SEQUENCE WITH FACIAL AND DIGITAL ANOMALIES		HP:0009882	OMIM:311895	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000085	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000126	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000162	OMIM:311900	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000175	OMIM:311900	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000199	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311900	TARP SYNDROME; TARPS		HP:0000218	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000239	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000316	OMIM:311900	IEA				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000347	OMIM:311900	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000358	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000369	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000395	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000431	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000463	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0000648	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311900	TARP SYNDROME; TARPS		HP:0000767	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311900	TARP SYNDROME; TARPS		HP:0000879	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311900	TARP SYNDROME; TARPS		HP:0000954	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001263	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001273	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001290	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001320	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001321	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001417	OMIM:311900	IEA				I		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001419	OMIM:311900	TAS				I		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001508	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001511	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0001636	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	311900	TARP SYNDROME; TARPS		HP:0001762	OMIM:311900	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS	HP:0012840	HP:0002984	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0006191	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0008551	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0009891	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0012725	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0012745	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0030084	OMIM:311900	TAS				P		HPO:skoehler	
OMIM	311900	TARP SYNDROME; TARPS		HP:0030680	OMIM:311900	IEA				P		HPO:iea	
OMIM	311900	TARP SYNDROME; TARPS		HP:0100259	OMIM:311900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	312000	PANHYPOPITUITARISM, X-LINKED		HP:0000839	OMIM:312000	IEA				P		HPO:iea	
OMIM	312000	PANHYPOPITUITARISM, X-LINKED		HP:0000871	OMIM:312000	IEA				P		HPO:iea	
OMIM	312000	PANHYPOPITUITARISM, X-LINKED		HP:0001417	OMIM:312000	IEA				I		HPO:iea	
OMIM	312060	PROPERDIN DEFICIENCY, X-LINKED		HP:0001419	OMIM:312060	IEA				I		HPO:iea	
OMIM	312060	PROPERDIN DEFICIENCY, X-LINKED		HP:0001939	OMIM:312060	IEA				P		HPO:iea	
OMIM	312060	PROPERDIN DEFICIENCY, X-LINKED		HP:0005423	OMIM:312060	IEA				P		HPO:iea	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0000252	OMIM:312080	TAS				P		HPO:iea	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0000365	OMIM:312080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0000639	PMID:3598129	PCS	HP:0003623	HP:0040280		P		HPO:iea	HP:0040280
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0000648	PMID:3598129	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0000750	http://www.ncbi.nlm.nih.gov/books/NBK1182/	TAS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001249	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001250	PMID:18485258	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001251	PMID:3598129	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001252	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001260	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001263	PMID:18485258	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001265	PMID:3598129	PCS		HP:0040284		P		HPO:iea	4/7
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001266	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001290	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001332	PMID:3598129	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001337	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001419	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS				I		HPO:iea	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001508	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0001583	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0002015	PMID:18485258	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0002168	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0002361	PMID:3598129	PCS	HP:0003593	HP:0040280		P		HPO:iea	HP:0040280
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0002478	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0002599	PMID:3598129	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0003269	PMID:3598129	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0003593	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS				C		HPO:iea	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0003677	PMID:3598129	PCS		HP:0040281		C		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0004322	http://www.ncbi.nlm.nih.gov/books/NBK1182/	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0004886	PMID:18485258;PMID:3598129	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0007256	PMID:3598129	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0007266	OMIM:312080	TAS				P		HPO:skoehler	
OMIM	312080	PELIZAEUS-MERZBACHER DISEASE		HP:0100709	http://www.ncbi.nlm.nih.gov/books/NBK1182/;PMID:11093273	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000175	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000204	OMIM:312150	TAS				P		HPO:probinson	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000286	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000316	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000347	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000369	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000457	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000476	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000883	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0000969	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001040	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001371	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001373	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001417	OMIM:312150	TAS				I		HPO:skoehler	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001511	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001561	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001961	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001989	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0001999	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0002047	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0002089	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0002659	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0002948	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0003634	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED		HP:0005905	OMIM:312150	IEA				P		HPO:iea	
OMIM	312150	%312150 MULTIPLE PTERYGIUM SYNDROME, X-LINKED;;PTERYGIUM SYNDROME, MULTIPLE, X-LINKED	HP:0012828	HP:0009381	OMIM:312150	TAS				P		HPO:probinson	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000252	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000343	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000431	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000454	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000463	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000496	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0000508	OMIM:312170	IEA				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001249	OMIM:312170	IEA				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001250	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001252	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001254	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001263	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001266	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001274	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001290	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001332	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001423	OMIM:312170	IEA				I		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001518	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0001999	OMIM:312170	IEA		HP:0040284		P		HPO:skoehler	35%
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002007	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002059	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002119	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002131	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002151	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002490	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002872	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0002928	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0003348	OMIM:312170	IEA				P		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0003593	OMIM:312170	IEA				C		HPO:iea	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0004900	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0004925	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0006799	OMIM:312170	TAS				P		HPO:skoehler	
OMIM	312170	PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD		HP:0025356	OMIM:312170	IEA				P		HPO:skoehler	
OMIM	312190	RADIAL APLASIA, X-LINKED		HP:0000238	OMIM:312190	IEA				P		HPO:iea	
OMIM	312190	RADIAL APLASIA, X-LINKED		HP:0001417	OMIM:312190	IEA				I		HPO:iea	
OMIM	312190	RADIAL APLASIA, X-LINKED		HP:0002023	OMIM:312190	IEA				P		HPO:iea	
OMIM	312190	RADIAL APLASIA, X-LINKED		HP:0003244	OMIM:312190	IEA				P		HPO:iea	
OMIM	312190	RADIAL APLASIA, X-LINKED		HP:0003974	OMIM:312190	IEA				P		HPO:iea	
OMIM	312200	RADIAL LOOP, PLAIN, ON RIGHT INDEX FINGER		HP:0001417	OMIM:312200	IEA				I		HPO:iea	
OMIM	312200	RADIAL LOOP, PLAIN, ON RIGHT INDEX FINGER		HP:0007566	OMIM:312200	IEA				P		HPO:iea	
OMIM	312210	RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY		HP:0001417	OMIM:312210	IEA				I		HPO:iea	
OMIM	312210	RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY		HP:0002715	OMIM:312210	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000027	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000028	PMID:1598912	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000037	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000048	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000051	PMID:1598912	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000054	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000135	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000771	PMID:1598912	PCS				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0000789	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0001419	PMID:1598912	PCS				I		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0001547	OMIM:312300	IEA				P		HPO:iea	
OMIM	312300	REIFENSTEIN SYNDROME		HP:0012873	OMIM:312300	TAS				P		HPO:skoehler	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0000952	OMIM:312500	IEA				P		HPO:iea	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0001417	OMIM:312500	IEA				I		HPO:iea	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0001433	OMIM:312500	IEA				P		HPO:iea	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0001903	OMIM:312500	IEA				P		HPO:iea	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0002716	OMIM:312500	IEA				P		HPO:iea	
OMIM	312500	RETICULOENDOTHELIOSIS, X-LINKED		HP:0003593	OMIM:312500	IEA				C		HPO:iea	
OMIM	312550	RETINAL DYSPLASIA, PRIMARY		HP:0001417	OMIM:312550	IEA				I		HPO:iea	
OMIM	312550	RETINAL DYSPLASIA, PRIMARY		HP:0001493	OMIM:312550	IEA				P		HPO:iea	
OMIM	312550	RETINAL DYSPLASIA, PRIMARY		HP:0007973	OMIM:312550	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0000510	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0000518	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0000545	OMIM:312600	IEA				P		HPO:skoehler	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0000580	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0000662	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0001133	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0001417	OMIM:312600	TAS				I		HPO:skoehler	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0200065	OMIM:312600	IEA				P		HPO:iea	
OMIM	312600	#312600 RETINITIS PIGMENTOSA 2; RP2		HP:0200065	OMIM:312600	TAS				P		HPO:skoehler	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0000007	OMIM:312612	IEA				I		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0000510	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0000580	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0000662	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0001133	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0001417	OMIM:312612	TAS				I		HPO:skoehler	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0002205	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0012263	OMIM:312612	TAS				P		HPO:skoehler	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0200065	OMIM:312612	IEA				P		HPO:iea	
OMIM	312612	RETINITIS PIGMENTOSA 6		HP:0200065	OMIM:312612	TAS				P		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0000529	PMID:15937075	PCS				P		HPO:probinson	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0000540	PMID:11384589	PCS				P		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0000541	PMID:15937075	PCS		HP:0040284		P		HPO:probinson	26/86
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0001105	OMIM:312700	TAS				P		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0001423	PMID:1867553	PCS				I		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0007401	PMID:7662639	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0007667	OMIM:312700	TAS				P		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0007722	PMID:7662639	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0007902	PMID:15937075	PCS		HP:0040284		P		HPO:probinson	26/86
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0007984	PMID:10922205	PCS				P		HPO:probinson	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0030502	PMID:1867553	PCS				P		HPO:skoehler	
OMIM	312700	RETINOSCHISIS 1, X-LINKED, JUVENILE		HP:0030824	PMID:1867553	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	312750	RETT SYNDROME; RTT		HP:0000164	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0000726	OMIM:312750	IEA				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0000729	OMIM:312750	TAS				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0001250	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0001257	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0001332	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0001423	OMIM:312750	IEA				I		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0001773	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002019	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002020	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002066	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002078	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002104	OMIM:312750	IEA				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0002120	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002187	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002333	OMIM:312750	TAS				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0002353	OMIM:312750	TAS				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0002376	OMIM:312750	IEA				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0002650	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0002808	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0003202	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0003763	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0004322	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0004326	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0004879	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0005135	OMIM:312750	TAS				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0005184	OMIM:312750	TAS				P		HPO:skoehler	
OMIM	312750	RETT SYNDROME; RTT		HP:0005484	OMIM:312750	IEA				P		HPO:iea	
OMIM	312750	RETT SYNDROME; RTT		HP:0010521	OMIM:312750	IEA				P		HPO:skoehler	
OMIM	312780	RUSSELL-SILVER SYNDROME, X-LINKED		HP:0000325	OMIM:312780	IEA				P		HPO:iea	
OMIM	312780	RUSSELL-SILVER SYNDROME, X-LINKED		HP:0000957	OMIM:312780	IEA				P		HPO:iea	
OMIM	312780	RUSSELL-SILVER SYNDROME, X-LINKED		HP:0001417	OMIM:312780	TAS				I		HPO:skoehler	
OMIM	312780	RUSSELL-SILVER SYNDROME, X-LINKED		HP:0001511	OMIM:312780	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000023	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000028	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000048	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000051	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000054	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000286	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000294	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000331	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000343	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000358	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000369	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000426	OMIM:312830	TAS				P		HPO:probinson	
OMIM	312830	SCARF SYNDROME		HP:0000431	OMIM:312830	TAS				P		HPO:probinson	
OMIM	312830	SCARF SYNDROME		HP:0000465	OMIM:312830	TAS				P		HPO:probinson	
OMIM	312830	SCARF SYNDROME		HP:0000470	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000474	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000486	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000494	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000508	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000768	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000879	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0000973	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0001249	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0001419	OMIM:312830	IEA				I		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0001537	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0001540	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0001552	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0002162	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0002557	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0003312	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0004440	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0004443	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0006297	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0006610	OMIM:312830	IEA				P		HPO:iea	
OMIM	312830	SCARF SYNDROME		HP:0008070	OMIM:312830	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0000365	OMIM:312840	IEA				P		HPO:skoehler	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0000544	OMIM:312840	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:312840	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0001257	OMIM:312840	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0001266	OMIM:312840	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0001417	OMIM:312840	IEA				I		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0001510	OMIM:312840	IEA				P		HPO:iea	
OMIM	312840	SCHIMKE X-LINKED MENTAL RETARDATION SYNDROME		HP:0005484	OMIM:312840	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0000246	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0000388	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0001419	OMIM:312863	IEA				I		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0002090	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0002837	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0004315	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0005387	OMIM:312863	TAS				P		HPO:probinson	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0005407	OMIM:312863	IEA				P		HPO:iea	
OMIM	312863	#312863 COMBINED IMMUNODEFICIENCY, X-LINKED; CIDX;;XCID;;IMMUNODEFICIENCY 6; IMD6		HP:0005415	OMIM:312863	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000023	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000023	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000028	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000028	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000047	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000047	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000105	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000105	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000107	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000107	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000154	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000154	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000158	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000158	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000175	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000175	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000216	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000216	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000238	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000238	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000256	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000256	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000280	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000280	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000286	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000286	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000316	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000316	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000365	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000365	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000384	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000384	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000431	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000463	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000463	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000494	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000494	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000689	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000689	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000767	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000767	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000776	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000776	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000891	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0000891	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001162	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001169	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001233	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001233	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001252	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001274	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001274	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001290	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001320	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001320	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001419	OMIM:312870	IEA				I		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001419	OMIM:312870	TAS				I		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001537	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001537	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001540	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001540	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001629	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001629	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001638	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001638	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001642	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001642	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001643	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001643	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001669	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001669	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001744	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001744	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001748	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001748	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001762	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001762	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001769	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001773	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001792	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0001837	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002101	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002240	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002240	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002245	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002245	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002558	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002558	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002566	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002566	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002650	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002650	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002667	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002667	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002869	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0002869	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003185	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003196	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003196	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003422	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003517	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0003517	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0004279	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0004467	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0004467	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0004510	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0004510	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0005280	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0005580	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0005580	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0005616	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0005616	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0006176	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0006176	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0008416	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0008416	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0008523	PMID:17223397	PCS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0008803	OMIM:312870	TAS				P		HPO:probinson	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0009101	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0009101	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0009882	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0009882	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0011304	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0011304	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0011675	OMIM:312870	IEA				P		HPO:iea	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0011675	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312870	SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1		HP:0100259	OMIM:312870	TAS				P		HPO:skoehler	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0000135	OMIM:312910	IEA				P		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0000365	OMIM:312910	IEA				P		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0000518	OMIM:312910	IEA				P		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0001337	OMIM:312910	IEA				P		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0001417	OMIM:312910	IEA				I		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0002313	OMIM:312910	IEA				P		HPO:iea	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0003621	OMIM:312910	TAS				C		HPO:probinson	
OMIM	312910	SPASTIC PARAPARESIS AND DEAFNESS		HP:0004322	OMIM:312910	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0000639	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0000648	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001249	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001258	OMIM:312920	TAS				P		HPO:skoehler	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001260	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001310	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001317	OMIM:312920	IEA				P		HPO:skoehler	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001347	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001371	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001419	OMIM:312920	IEA				I		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0001761	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0002061	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0002064	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0002313	OMIM:312920	TAS				P		HPO:skoehler	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0002314	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0002503	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0003202	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0003487	OMIM:312920	IEA				P		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0003621	OMIM:312920	IEA				C		HPO:iea	
OMIM	312920	SPASTIC PARAPLEGIA 2, X-LINKED; SPG2		HP:0007340	OMIM:312920	IEA				P		HPO:iea	
OMIM	313000	SPATIAL VISUALIZATION, APTITUDE FOR		HP:0000707	OMIM:313000	IEA				P		HPO:iea	
OMIM	313000	SPATIAL VISUALIZATION, APTITUDE FOR		HP:0001419	OMIM:313000	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0000029	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0000144	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0000153	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1	HP:0012825	HP:0000763	OMIM:313200	TAS				P		HPO:probinson	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0000771	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0001260	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0001265	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0001283	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0001337	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0001419	OMIM:313200	IEA				I		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0002015	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0002380	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0003236	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0003394	OMIM:313200	TAS				P		HPO:probinson	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0003581	OMIM:313200	TAS				C		HPO:probinson	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0003677	OMIM:313200	IEA				C		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0003690	OMIM:313200	TAS				P		HPO:probinson	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0008981	OMIM:313200	IEA				P		HPO:iea	
OMIM	313200	SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1		HP:0009830	OMIM:313200	IEA				P		HPO:skoehler	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0001171	OMIM:313350	IEA				P		HPO:iea	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0001417	OMIM:313350	IEA				I		HPO:iea	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0001839	OMIM:313350	IEA				P		HPO:iea	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0006101	OMIM:313350	IEA				P		HPO:iea	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0009803	OMIM:313350	IEA				P		HPO:iea	
OMIM	313350	SPLIT-HAND/FOOT MALFORMATION 2		HP:0010049	OMIM:313350	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0000470	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0000914	OMIM:313400	TAS				P		HPO:skoehler	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0000926	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0001376	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0001419	OMIM:313400	IEA				I		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0001552	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE	HP:0012825	HP:0002650	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002655	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002808	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002812	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002829	OMIM:313400	IEA				P		HPO:skoehler	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002866	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0002938	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0003090	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0003521	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0004594	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0007759	OMIM:313400	IEA				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0008843	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE	HP:0012825	HP:0010582	OMIM:313400	TAS				P		HPO:iea	
OMIM	313400	#313400 SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED; SEDT;;SED TARDA, X-LINKED;;SPONDYLOEPIPHYSEAL DYSPLASIA, LATE		HP:0100864	OMIM:313400	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000280	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000316	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000431	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000463	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000486	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000639	OMIM:313420	IEA				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000768	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0000926	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001182	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001187	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001256	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001417	OMIM:313420	IEA				I		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001423	OMIM:313420	TAS				I		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0001597	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002093	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002167	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002657	OMIM:313420	TAS				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002694	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002808	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002878	OMIM:313420	TAS				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0002944	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0003037	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0003273	OMIM:313420	TAS				P		HPO:probinson	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0003510	OMIM:313420	IEA				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0005280	OMIM:313420	IEA				P		HPO:iea	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0006380	OMIM:313420	TAS				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0009381	OMIM:313420	IEA				P		HPO:skoehler	
OMIM	313420	SPONDYLOMETAPHYSEAL DYSPLASIA, X-LINKED		HP:0011342	OMIM:313420	TAS				P		HPO:skoehler	
OMIM	313490	TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS		HP:0000679	OMIM:313490	TAS				P		HPO:skoehler	
OMIM	313490	TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS		HP:0000691	OMIM:313490	IEA				P		HPO:iea	
OMIM	313490	TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS		HP:0001419	OMIM:313490	IEA				I		HPO:iea	
OMIM	313490	TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS		HP:0003771	OMIM:313490	IEA				P		HPO:iea	
OMIM	313490	TAURODONTISM, MICRODONTIA, AND DENS INVAGINATUS		HP:0011088	OMIM:313490	TAS				P		HPO:skoehler	
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0000668	PMID:18657636	PCS		HP:0040284		P		HPO:lccarmody	5/5
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0000674	PMID:18657636	PCS				P		HPO:lccarmody	
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0000677	PMID:18657636	PCS				P		HPO:lccarmody	
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0001423	PMID:18657636	PCS				I		HPO:lccarmody	
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0010667	PMID:18657636	PCS		HP:0040284		P		HPO:lccarmody	5/5
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0011051	PMID:16583127	PCS	HP:0003621	HP:0040284		P		HPO:lccarmody	9/10
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0011054	PMID:16583127	PCS		HP:0040284		P		HPO:lccarmody	9/10
OMIM	313500	TOOTH AGENESIS, SELECTIVE, X-LINKED, 1		HP:0200153	PMID:18657636	PCS		HP:0040284		P		HPO:lccarmody	5/5
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000047	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000104	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000175	OMIM:313850	TAS				P		HPO:skoehler	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000204	OMIM:313850	TAS				P		HPO:skoehler	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000238	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000476	OMIM:313850	TAS				P		HPO:skoehler	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0000776	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0001417	OMIM:313850	IEA				I		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0001539	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0001643	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0001669	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0001683	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0002089	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0002323	OMIM:313850	IEA				P		HPO:iea	
OMIM	313850	THORACOABDOMINAL SYNDROME		HP:0002933	OMIM:313850	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0000421	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0000964	OMIM:313900	IEA				P		HPO:skoehler	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0000967	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0000978	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0001419	OMIM:313900	IEA				I		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0001905	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0003011	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0003212	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0003261	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0004854	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0005261	OMIM:313900	IEA				P		HPO:iea	
OMIM	313900	THROMBOCYTOPENIA 1		HP:0005537	OMIM:313900	IEA				P		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0000099	OMIM:314000	IEA				P		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0000790	OMIM:314000	IEA				P		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0001417	OMIM:314000	IEA				I		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0001873	OMIM:314000	IEA				P		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0001892	OMIM:314000	IEA				P		HPO:iea	
OMIM	314000	THROMBOCYTOPENIA WITH ELEVATED SERUM IGA AND RENAL DISEASE		HP:0003261	OMIM:314000	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0000421	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0000967	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0000978	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001007	OMIM:314050	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001419	OMIM:314050	IEA				I		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001744	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001873	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001878	OMIM:314050	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0001923	OMIM:314050	IEA				P		HPO:iea	
OMIM	314050	#314050 THROMBOCYTOPENIA WITH BETA-THALASSEMIA, X-LINKED; XLTT;;THROMBOCYTOPENIA, PLATELET DYSFUNCTION, HEMOLYSIS, AND IMBALANCEDGLOBIN SYNTHESIS		HP:0003010	OMIM:314050	IEA				P		HPO:iea	
OMIM	314100	THUMBS, CONGENITAL CLASPED		HP:0000707	OMIM:314100	IEA				P		HPO:iea	
OMIM	314100	THUMBS, CONGENITAL CLASPED		HP:0000924	OMIM:314100	IEA				P		HPO:iea	
OMIM	314100	THUMBS, CONGENITAL CLASPED		HP:0001419	OMIM:314100	IEA				I		HPO:iea	
OMIM	314240	TOOTH SIZE		HP:0000164	OMIM:314240	IEA				P		HPO:iea	
OMIM	314240	TOOTH SIZE		HP:0001417	OMIM:314240	IEA				I		HPO:iea	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0001304	OMIM:314250	TAS				P		HPO:probinson	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0001336	OMIM:314250	TAS				P		HPO:probinson	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0001337	OMIM:314250	TAS				P		HPO:skoehler	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0001419	OMIM:314250	TAS				I		HPO:probinson	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0002072	OMIM:314250	TAS				P		HPO:probinson	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0002548	OMIM:314250	TAS				P		HPO:probinson	
OMIM	314250	DYSTONIA 3, TORSION, X-LINKED		HP:0003581	OMIM:314250	TAS				C		HPO:probinson	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000028	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000110	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000324	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000473	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000798	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0000995	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0002619	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0008717	OMIM:314300	IEA				P		HPO:iea	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0010562	OMIM:314300	IEA				P		HPO:skoehler	
OMIM	314300	TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKCR		HP:0012330	OMIM:314300	IEA				P		HPO:skoehler	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000023	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000216	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000218	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000237	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000243	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000286	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000341	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000358	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000369	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000431	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000444	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0000601	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001249	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001250	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001419	OMIM:314320	IEA				I		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001518	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0001629	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0004209	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0004322	OMIM:314320	IEA				P		HPO:iea	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0004442	OMIM:314320	TAS				P		HPO:probinson	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0004443	OMIM:314320	TAS				P		HPO:probinson	
OMIM	314320	TRIGONOCEPHALY WITH SHORT STATURE AND DEVELOPMENTAL DELAY		HP:0005494	OMIM:314320	IEA				P		HPO:iea	
OMIM	314360	ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET		HP:0001159	OMIM:314360	IEA				P		HPO:skoehler	
OMIM	314360	ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET		HP:0001419	OMIM:314360	TAS				I		HPO:skoehler	
OMIM	314360	ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET		HP:0001839	OMIM:314360	TAS				P		HPO:skoehler	
OMIM	314360	ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET		HP:0003022	OMIM:314360	TAS				P		HPO:probinson	
OMIM	314360	ULNAR HYPOPLASIA WITH LOBSTER-CLAW DEFORMITY OF FEET		HP:0009381	OMIM:314360	TAS				P		HPO:skoehler	
OMIM	314380	UNIQUE GREEN PHENOMENON		HP:0000478	OMIM:314380	IEA				P		HPO:iea	
OMIM	314380	UNIQUE GREEN PHENOMENON		HP:0001417	OMIM:314380	IEA				I		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0000068	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0000105	OMIM:314390	TAS				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0000126	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0000238	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0000925	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0001161	OMIM:314390	IEA				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0001419	OMIM:314390	TAS				I		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0001669	OMIM:314390	TAS				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0002023	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0002575	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0003468	OMIM:314390	TAS				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0003974	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0005792	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0006695	OMIM:314390	TAS				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0009623	OMIM:314390	IEA				P		HPO:iea	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0030680	OMIM:314390	IEA				P		HPO:skoehler	
OMIM	314390	VACTERL ASSOCIATION, X-LINKED, WITH OR WITHOUT HYDROCEPHALUS; VACTERLX		HP:0031853	OMIM:314390	IEA				P		HPO:skoehler	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001419	OMIM:314400	IEA				I		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001634	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001635	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001653	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001659	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0001939	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0005180	OMIM:314400	IEA				P		HPO:iea	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0006692	OMIM:314400	PCS				P		HPO:probinson	
OMIM	314400	CARDIAC VALVULAR DYSPLASIA, X-LINKED		HP:0011580	OMIM:314400	PCS				P		HPO:probinson	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0000924	OMIM:314500	IEA				P		HPO:iea	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0000970	OMIM:314500	IEA				P		HPO:iea	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0001139	OMIM:314500	IEA				P		HPO:iea	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0001249	OMIM:314500	IEA				P		HPO:iea	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0001417	OMIM:314500	TAS				I		HPO:nvasilevsky	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0001466	OMIM:314500	TAS				I		HPO:nvasilevsky	
OMIM	314500	VAN DEN BOSCH SYNDROME		HP:0200016	OMIM:314500	IEA				P		HPO:skoehler	
OMIM	314550	VESICOURETERAL REFLUX, X-LINKED		HP:0000076	OMIM:314550	IEA				P		HPO:iea	
OMIM	314550	VESICOURETERAL REFLUX, X-LINKED		HP:0001417	OMIM:314550	IEA				I		HPO:iea	
OMIM	314560	VON WILLEBRAND DISEASE, X-LINKED FORM		HP:0001417	OMIM:314560	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	314560	VON WILLEBRAND DISEASE, X-LINKED FORM		HP:0003010	OMIM:314560	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000023	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000028	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000049	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000349	OMIM:314570	TAS				P		HPO:skoehler	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000358	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000369	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0000508	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0001155	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0001423	OMIM:314570	IEA				I		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0002808	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0002868	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0003365	OMIM:314570	TAS				P		HPO:probinson	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0003502	OMIM:314570	TAS				P		HPO:skoehler	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0004322	OMIM:314570	PCS				P		HPO:probinson	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0005001	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0005059	OMIM:314570	TAS				P		HPO:skoehler	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0008808	OMIM:314570	IEA				P		HPO:iea	
OMIM	314570	WIDOW&#39;S PEAK SYNDROME		HP:0008843	OMIM:314570	TAS				P		HPO:probinson	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000187	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000218	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000252	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000278	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000319	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000343	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000347	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000369	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000463	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000470	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000508	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000577	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000582	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000657	OMIM:314580	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000750	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0000774	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001250	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001256	OMIM:314580	IEA				P		HPO:iea	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001257	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001263	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001284	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001290	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001332	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001417	OMIM:314580	IEA				I		HPO:iea	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001419	OMIM:314580	TAS				I		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001558	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0001762	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002059	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002104	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002307	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002643	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002650	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002804	OMIM:314580	TAS	HP:0003577			P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002808	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0002827	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0003307	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0003577	OMIM:314580	TAS				C		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0003693	OMIM:314580	IEA				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0004322	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0005745	OMIM:314580	IEA				P		HPO:iea	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0009623	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0009890	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0010628	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0010765	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0010806	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0011968	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0012385	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314580	WIEACKER-WOLFF SYNDROME		HP:0012448	OMIM:314580	TAS				P		HPO:skoehler	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000324	OMIM:314600	IEA				P		HPO:iea	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000356	OMIM:314600	TAS				P		HPO:skoehler	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000365	OMIM:314600	IEA				P		HPO:iea	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000384	OMIM:314600	IEA				P		HPO:iea	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000465	OMIM:314600	IEA				P		HPO:skoehler	
OMIM	314600	WILDERVANCK SYNDROME		HP:0000538	OMIM:314600	IEA				P		HPO:iea	
OMIM	314600	WILDERVANCK SYNDROME		HP:0002949	OMIM:314600	IEA				P		HPO:skoehler	
OMIM	314600	WILDERVANCK SYNDROME		HP:0003745	OMIM:314600	TAS				I		HPO:skoehler	
OMIM	314600	WILDERVANCK SYNDROME		HP:0011349	OMIM:314600	IEA				P		HPO:skoehler	
OMIM	314900	XM SYSTEM		HP:0001417	OMIM:314900	IEA				I		HPO:iea	
OMIM	314900	XM SYSTEM		HP:0001939	OMIM:314900	IEA				P		HPO:iea	
OMIM	400003	DELETED IN AZOOSPERMIA		HP:0000027	OMIM:400003	IEA				P		HPO:iea	
OMIM	400003	DELETED IN AZOOSPERMIA		HP:0001450	OMIM:400003	IEA				I		HPO:iea	
OMIM	400003	DELETED IN AZOOSPERMIA		HP:0001939	OMIM:400003	IEA				P		HPO:iea	
OMIM	400004	RETINITIS PIGMENTOSA, Y-LINKED		HP:0000510	OMIM:400004	TAS				P		HPO:skoehler	
OMIM	400043	DEAFNESS, Y-LINKED 1		HP:0000360	OMIM:400043	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	400043	DEAFNESS, Y-LINKED 1		HP:0000407	OMIM:400043	IEA				P		HPO:skoehler	
OMIM	400043	DEAFNESS, Y-LINKED 1		HP:0001450	OMIM:400003	IEA				I		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0000037	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0000055	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0000098	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0000133	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0000786	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0008187	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400044	#400044 46,XY SEX REVERSAL 1; SRXY1;;46,XY SEX REVERSAL, SRY-RELATED;;46,XY GONADAL DYSGENESIS, COMPLETE, SRY-RELATED46,XY TRUE HERMAPHRODITISM, SRY-RELATED, INCLUDED;;TESTIS-DETERMINING FACTOR, X-CHROMOSOMAL, FORMERLY, INCLUDED; TDFX,FORMERLY, INCLUDED;;SEX-REVERSING LOCUS ON X, FORMERLY, INCLUDED; SRVX, FORMERLY, INCLUDED		HP:0012245	OMIM:400044	IEA				P		HPO:skoehler	
OMIM	400045	46,XX SEX REVERSAL 1		HP:0001450	OMIM:400045	TAS				I		HPO:probinson	
OMIM	400045	46,XX SEX REVERSAL 1		HP:0010459	OMIM:400045	TAS				P		HPO:probinson	
OMIM	400045	46,XX SEX REVERSAL 1		HP:0012245	OMIM:400045	TAS				P		HPO:probinson	
OMIM	415000	SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED		HP:0000027	OMIM:415000	IEA				P		HPO:skoehler	
OMIM	415000	SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED		HP:0001450	OMIM:415000	IEA				I		HPO:iea	
OMIM	424500	GONADOBLASTOMA		HP:0000150	OMIM:424500	IEA				P		HPO:iea	
OMIM	424500	GONADOBLASTOMA		HP:0001450	OMIM:424500	IEA				I		HPO:iea	
OMIM	424500	GONADOBLASTOMA		HP:0001939	OMIM:424500	IEA				P		HPO:iea	
OMIM	425500	HAIRY EARS, Y-LINKED		HP:0000598	OMIM:425500	IEA				P		HPO:iea	
OMIM	475000	GROWTH CONTROL, Y-CHROMOSOME INFLUENCED		HP:0001450	OMIM:475000	IEA				I		HPO:iea	
OMIM	475000	GROWTH CONTROL, Y-CHROMOSOME INFLUENCED		HP:0001507	OMIM:475000	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0000496	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0000572	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0000648	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0000726	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001112	OMIM:500001	TAS				P		HPO:probinson	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001249	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001257	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001260	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001332	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0001427	OMIM:500001	IEA				I		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002015	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002067	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002151	OMIM:500001	TAS				P		HPO:probinson	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002305	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002490	OMIM:500001	TAS				P		HPO:probinson	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0002650	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0003202	OMIM:500001	IEA				P		HPO:iea	
OMIM	500001	LEBER OPTIC ATROPHY AND DYSTONIA		HP:0009830	OMIM:500001	IEA				P		HPO:skoehler	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001251	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001252	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001260	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001265	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001270	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001290	OMIM:500002	TAS				P		HPO:skoehler	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0001427	OMIM:500002	TAS				I		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0003200	OMIM:500002	TAS				P		HPO:probinson	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0003236	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0003458	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0003701	OMIM:500002	IEA				P		HPO:skoehler	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0003737	OMIM:500002	TAS				P		HPO:skoehler	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0005978	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0007126	OMIM:500002	TAS				P		HPO:skoehler	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0008347	OMIM:500002	TAS				P		HPO:probinson	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0010628	OMIM:500002	IEA				P		HPO:iea	
OMIM	500002	MITOCHONDRIAL MYOPATHY WITH DIABETES		HP:0012507	OMIM:500002	TAS				P		HPO:probinson	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0000654	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0001252	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0001263	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0001290	OMIM:500003	TAS				P		HPO:skoehler	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0001427	OMIM:500003	IEA				I		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0002355	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0002359	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0003200	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0003487	OMIM:500003	IEA				P		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0003593	OMIM:500003	IEA				C		HPO:iea	
OMIM	500003	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL		HP:0007098	OMIM:500003	TAS				P		HPO:probinson	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0000252	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0000365	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0000486	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0000717	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0000980	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001249	OMIM:500007	TAS				P		HPO:skoehler	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001250	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001251	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001252	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001254	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001270	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001290	OMIM:500007	TAS				P		HPO:skoehler	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001324	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001426	OMIM:500007	IEA				I		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001427	OMIM:500007	IEA				I		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001510	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0001638	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002013	OMIM:500007	TAS				P		HPO:probinson	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002018	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002027	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002039	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002076	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0002579	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0003546	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0007018	OMIM:500007	IEA				P		HPO:iea	
OMIM	500007	CYCLIC VOMITING SYNDROME		HP:0100543	OMIM:500007	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0000158	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0000467	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0001265	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0001284	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0001290	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0001427	PMID:19720722	PCS				I		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0001508	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0002058	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0002151	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0002240	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0002747	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003128	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003200	PMID:19720722	PCS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003234	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003236	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003542	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003623	OMIM:500009	TAS				C		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003688	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003688	PMID:19720722	PCS				P		HPO:probinson	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0003737	OMIM:500009	IEA				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0009051	PMID:19720722	PCS		HP:0040284		P		HPO:skoehler	7/15
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0009058	PMID:19720722	PCS		HP:0040284		P		HPO:skoehler	12/16
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0010628	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0011968	PMID:19720722	PCS		HP:0040284		P		HPO:skoehler	16/17
OMIM	500009	#500009 MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT; MMIT;;MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT, DUE TO RESPIRATORY CHAINDEFICIENCY;;COX DEFICIENCY MYOPATHY, INFANTILE, TRANSIENT;;RESPIRATORY CHAIN DEFICIENCY, INFANTILE, TRANSIENT		HP:0100293	OMIM:500009	TAS				P		HPO:skoehler	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0000006	OMIM:502500	TAS				I		HPO:nvasilevsky	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0000726	OMIM:502500	IEA				P		HPO:skoehler	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0001300	OMIM:502500	IEA				P		HPO:iea	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0001427	OMIM:502500	TAS				I		HPO:nvasilevsky	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0002185	OMIM:502500	IEA				P		HPO:skoehler	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0002423	OMIM:502500	IEA				P		HPO:iea	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0002511	OMIM:502500	IEA				P		HPO:skoehler	
OMIM	502500	ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL		HP:0003584	OMIM:502500	IEA				C		HPO:iea	
OMIM	515000	CHLORAMPHENICOL TOXICITY		HP:0001915	OMIM:515000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0000407	OMIM:520000	TAS				P		HPO:probinson	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0000508	OMIM:520000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0000544	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0000546	OMIM:520000	IEA				P		HPO:skoehler	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0000580	PMID:8094200	PCS				P		HPO:probinson	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001133	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001133	OMIM:520000	TAS				P		HPO:probinson	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001250	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001260	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001427	OMIM:520000	TAS				I		HPO:skoehler	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001638	OMIM:520000	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0001751	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0002317	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0002321	OMIM:520000	TAS				P		HPO:skoehler	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0003074	OMIM:520000	IEA				P		HPO:iea	
OMIM	520000	#520000 DIABETES AND DEAFNESS, MATERNALLY INHERITED; MIDD;;DIABETES-DEAFNESS SYNDROME, MATERNALLY TRANSMITTED;;BALLINGER-WALLACE SYNDROME;;DIABETES MELLITUS, TYPE II, WITH DEAFNESS;;NONINSULIN-DEPENDENT DIABETES MELLITUS WITH DEAFNESS;;NIDDM WITH DEAFNESS		HP:0005978	OMIM:520000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000252	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000407	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000508	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000580	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000590	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000726	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000763	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000819	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0000829	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001250	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001251	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001324	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001427	OMIM:530000	IEA				I		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001638	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001709	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001924	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001947	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0001994	OMIM:530000	TAS				P		HPO:probinson	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0002135	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0002922	OMIM:530000	TAS				P		HPO:probinson	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0003128	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0003200	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0004322	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0008207	OMIM:530000	IEA				P		HPO:iea	
OMIM	530000	KEARNS-SAYRE SYNDROME; KSS		HP:0011675	OMIM:530000	IEA				P		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0000572	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0000576	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0000648	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001112	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001138	OMIM:535000	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001251	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001271	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001332	OMIM:535000	IEA				P		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001425	OMIM:535000	TAS				I		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0001427	OMIM:535000	TAS				I		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0002174	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0003198	OMIM:535000	IEA				P		HPO:iea	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0003829	OMIM:535000	TAS				C		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0007768	OMIM:535000	TAS				P		HPO:skoehler	
OMIM	535000	#535000 LEBER OPTIC ATROPHY;;LEBER HEREDITARY OPTIC NEUROPATHY; LHON		HP:0011675	OMIM:535000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000408	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000519	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000602	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000726	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000819	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0000822	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001269	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001298	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001427	OMIM:540000	IEA				I		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001507	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001635	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001712	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0001716	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0002069	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0002076	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0002401	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0002572	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0003128	OMIM:540000	TAS				P		HPO:probinson	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0003198	OMIM:540000	IEA				P		HPO:iea	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0003200	OMIM:540000	TAS				P		HPO:probinson	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0003737	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0003828	OMIM:540000	TAS				C		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0005162	OMIM:540000	IEA				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0008619	OMIM:540000	IEA				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0012377	OMIM:540000	TAS				P		HPO:skoehler	
OMIM	540000	MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS		HP:0100704	OMIM:540000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0000407	OMIM:545000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001250	OMIM:545000	IEA				P		HPO:skoehler	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001251	OMIM:545000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001257	OMIM:545000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001324	OMIM:545000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001336	OMIM:545000	IEA				P		HPO:skoehler	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0001427	OMIM:545000	IEA				I		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0002123	OMIM:545000	TAS				P		HPO:skoehler	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0002151	OMIM:545000	TAS				P		HPO:probinson	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0003198	OMIM:545000	IEA				P		HPO:iea	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0003200	OMIM:545000	TAS				P		HPO:probinson	
OMIM	545000	MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS		HP:0003542	OMIM:545000	TAS				P		HPO:probinson	
OMIM	550500	MYOGLOBINURIA, RECURRENT		HP:0001427	OMIM:550500	TAS				I		HPO:skoehler	
OMIM	550500	MYOGLOBINURIA, RECURRENT		HP:0003200	OMIM:550500	TAS				P		HPO:skoehler	
OMIM	550500	MYOGLOBINURIA, RECURRENT		HP:0003652	OMIM:550500	TAS				P		HPO:skoehler	
OMIM	550500	MYOGLOBINURIA, RECURRENT		HP:0008305	OMIM:550500	TAS				P		HPO:probinson	
OMIM	551000	MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE		HP:0001427	OMIM:551000	TAS				I		HPO:probinson	
OMIM	551000	MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE		HP:0003128	OMIM:551000	TAS				P		HPO:probinson	
OMIM	551000	MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE		HP:0003198	OMIM:551000	TAS				P		HPO:probinson	
OMIM	551000	MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE		HP:0009069	OMIM:551000	TAS				P		HPO:probinson	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000488	OMIM:551500	IEA				P		HPO:skoehler	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000510	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000618	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000639	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000726	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0000763	OMIM:551500	TAS				P		HPO:probinson	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0001250	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0001251	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0001263	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0001427	OMIM:551500	IEA				I		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0003198	OMIM:551500	IEA				P		HPO:skoehler	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0003701	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0003737	OMIM:551500	IEA				P		HPO:skoehler	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0007117	OMIM:551500	IEA				P		HPO:iea	
OMIM	551500	NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA		HP:0007814	OMIM:551500	IEA				P		HPO:iea	
OMIM	553000	ONCOCYTOMA		HP:0001427	OMIM:553000	IEA				I		HPO:iea	
OMIM	553000	ONCOCYTOMA		HP:0001939	OMIM:553000	IEA				P		HPO:iea	
OMIM	553000	ONCOCYTOMA		HP:0002664	OMIM:553000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0000819	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0001427	OMIM:557000	IEA				I		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0001508	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0001518	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0001942	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0001994	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0002024	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0003128	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0003344	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0004864	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0008336	OMIM:557000	IEA				P		HPO:iea	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0100651	OMIM:557000	TAS				P		HPO:skoehler	
OMIM	557000	#557000 PEARSON MARROW-PANCREAS SYNDROME;;SIDEROBLASTIC ANEMIA WITH MARROW CELL VACUOLIZATION AND EXOCRINE PANCREATICDYSFUNCTION		HP:0100732	OMIM:557000	TAS				P		HPO:skoehler	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000103	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000114	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000365	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000508	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000550	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000580	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000597	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000618	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000819	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0000939	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001251	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001252	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001290	OMIM:560000	TAS				P		HPO:skoehler	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001336	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001427	OMIM:560000	IEA				I		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001508	OMIM:560000	PCS				P		HPO:probinson	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0001944	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0002013	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0002014	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0002240	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0002376	OMIM:560000	PCS				P		HPO:probinson	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0002748	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0007511	OMIM:560000	IEA				P		HPO:iea	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0007610	OMIM:560000	TAS				P		HPO:skoehler	
OMIM	560000	RENAL TUBULOPATHY, DIABETES MELLITUS, AND CEREBELLAR ATAXIA		HP:0100651	OMIM:560000	TAS				P		HPO:skoehler	
OMIM	580000	DEAFNESS, AMINOGLYCOSIDE-INDUCED		HP:0001427	OMIM:580000	TAS				I		HPO:skoehler	
OMIM	580000	DEAFNESS, AMINOGLYCOSIDE-INDUCED		HP:0011975	OMIM:580000	TAS				P		HPO:probinson	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000007	OMIM:598500	TAS				I		HPO:nvasilevsky	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000072	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000126	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000407	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000618	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000639	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000648	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000819	OMIM:598500	IEA	HP:0003593			P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000873	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0000924	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001249	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001250	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001427	OMIM:598500	TAS				I		HPO:nvasilevsky	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001873	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001875	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001889	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0001924	OMIM:598500	IEA				P		HPO:iea	
OMIM	598500	WOLFRAM SYNDROME, MITOCHONDRIAL FORM		HP:0012332	OMIM:598500	IEA				P		HPO:iea	
OMIM	600000	SPONDYLOCAMPTODACTYLY		HP:0000006	OMIM:600000	TAS				I		HPO:nvasilevsky	
OMIM	600000	SPONDYLOCAMPTODACTYLY		HP:0000007	OMIM:600000	TAS				I		HPO:nvasilevsky	
OMIM	600000	SPONDYLOCAMPTODACTYLY		HP:0002650	OMIM:600000	TAS				P		HPO:skoehler	
OMIM	600000	SPONDYLOCAMPTODACTYLY		HP:0004558	OMIM:600000	TAS				P		HPO:skoehler	
OMIM	600000	SPONDYLOCAMPTODACTYLY		HP:0100490	OMIM:600000	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000006	OMIM:600001	IEA				I		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000023	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000073	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000252	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000776	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000819	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0000924	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001195	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001250	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001263	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001508	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001511	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001537	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001629	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001631	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001636	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001642	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001643	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001655	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001660	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0001669	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0002566	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0002594	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0003074	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0003076	OMIM:600001	IEA				P		HPO:iea	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0004388	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0004415	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0005912	OMIM:600001	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0011573	OMIM:600001	IEA				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0011611	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0011682	OMIM:600001	TAS				P		HPO:skoehler	
OMIM	600001	HEART DEFECTS, CONGENITAL, AND OTHER CONGENITAL ANOMALIES; HDCA		HP:0031369	OMIM:600001	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	600002	EIKEN SYNDROME		HP:0000007	OMIM:600002	TAS				I		HPO:probinson	
OMIM	600002	EIKEN SYNDROME		HP:0002652	OMIM:600002	IEA				P		HPO:probinson	
OMIM	600002	EIKEN SYNDROME		HP:0002663	OMIM:600002	TAS				P		HPO:probinson	
OMIM	600002	EIKEN SYNDROME		HP:0003038	OMIM:600002	TAS				P		HPO:skoehler	
OMIM	600002	EIKEN SYNDROME		HP:0003275	OMIM:600002	TAS				P		HPO:skoehler	
OMIM	600002	EIKEN SYNDROME		HP:0004322	OMIM:600002	TAS				P		HPO:skoehler	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000006	OMIM:600057	IEA				I		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000023	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000039	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000072	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000085	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0000122	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0001545	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0002644	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0002836	OMIM:600057	IEA				P		HPO:iea	
OMIM	600057	EXSTROPHY OF BLADDER		HP:0030911	OMIM:600057	TAS				P		HPO:skoehler	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0000006	OMIM:600059	TAS				I		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0000510	OMIM:600059	TAS				P		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0000546	OMIM:600059	TAS				P		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0000662	OMIM:600059	TAS	HP:0003621			P		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0001133	OMIM:600059	TAS				P		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0003829	OMIM:600059	TAS				C		HPO:skoehler	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0007894	OMIM:600059	TAS				P		HPO:probinson	
OMIM	600059	RETINITIS PIGMENTOSA 13; RP13		HP:0011505	OMIM:600059	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600060	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 2		HP:0000007	OMIM:600060	TAS				I		HPO:skoehler	
OMIM	600060	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 2		HP:0000407	OMIM:600060	TAS				P		HPO:skoehler	
OMIM	600060	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 2		HP:0002321	OMIM:600060	TAS				P		HPO:skoehler	
OMIM	600060	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 2		HP:0003577	OMIM:600060	TAS				C		HPO:skoehler	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0000006	OMIM:600072	IEA				I		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0000016	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0000651	OMIM:600072	TAS				P		HPO:skoehler	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0000726	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0000975	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0001251	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0001260	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0001336	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0001824	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0001945	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0002015	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0002019	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0002104	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0002529	OMIM:600072	TAS				P		HPO:skoehler	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0003581	OMIM:600072	TAS				C		HPO:skoehler	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0011463	OMIM:600072	TAS				C		HPO:probinson	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0012332	OMIM:600072	IEA				P		HPO:iea	
OMIM	600072	#600072 FATAL FAMILIAL INSOMNIA; FFI;;INSOMNIA, FATAL FAMILIAL		HP:0100785	OMIM:600072	TAS				P		HPO:skoehler	
OMIM	600080	MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC		HP:0000006	OMIM:600080	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600080	MYELOCYTIC LEUKEMIA-LIKE SYNDROME, FAMILIAL, CHRONIC		HP:0005506	OMIM:600080	TAS				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0000007	OMIM:600081	IEA				I		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0000886	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0000893	OMIM:600081	TAS				P		HPO:probinson	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0000920	OMIM:600081	TAS				P		HPO:probinson	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0001252	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0001290	OMIM:600081	TAS				P		HPO:skoehler	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0001324	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0001508	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0001510	OMIM:600081	TAS				P		HPO:skoehler	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002007	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002148	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002355	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002653	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002663	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002748	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002752	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002753	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002757	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002979	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002980	OMIM:600081	TAS				P		HPO:probinson	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0002982	OMIM:600081	TAS				P		HPO:probinson	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003013	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003020	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003025	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003029	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003155	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003593	OMIM:600081	IEA				C		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0003698	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0004492	OMIM:600081	IEA				P		HPO:iea	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0005469	OMIM:600081	IEA				P		HPO:skoehler	
OMIM	600081	VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B		HP:0010502	OMIM:600081	TAS				P		HPO:probinson	
OMIM	600082	PROSTATIC HYPERPLASIA, BENIGN		HP:0000006	OMIM:600082	IEA				I		HPO:iea	
OMIM	600082	PROSTATIC HYPERPLASIA, BENIGN		HP:0003593	OMIM:600082	IEA				C		HPO:iea	
OMIM	600082	PROSTATIC HYPERPLASIA, BENIGN		HP:0008711	OMIM:600082	IEA				P		HPO:iea	
OMIM	600084	MACROCYTOSIS, FAMILIAL		HP:0000006	OMIM:600084	IEA				I		HPO:iea	
OMIM	600084	MACROCYTOSIS, FAMILIAL		HP:0001871	OMIM:600084	IEA				P		HPO:iea	
OMIM	600084	MACROCYTOSIS, FAMILIAL		HP:0001939	OMIM:600084	IEA				P		HPO:iea	
OMIM	600089	PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS		HP:0000007	OMIM:600089	IEA				I		HPO:iea	
OMIM	600089	PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS		HP:0000857	OMIM:600089	IEA				P		HPO:iea	
OMIM	600089	PANCREATIC BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS		HP:0001438	OMIM:600089	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0000007	OMIM:600092	TAS				I		HPO:skoehler	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0000037	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0000252	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0000589	OMIM:600092	IEA				P		HPO:skoehler	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0000889	OMIM:600092	TAS				P		HPO:skoehler	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0001320	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0001591	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0002983	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0003510	OMIM:600092	IEA				P		HPO:skoehler	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0005621	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0007676	OMIM:600092	IEA				P		HPO:iea	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0009803	OMIM:600092	TAS				P		HPO:probinson	
OMIM	600092	CHONDRODYSPLASIA-PSEUDOHERMAPHRODITISM SYNDROME		HP:0010049	OMIM:600092	TAS				P		HPO:probinson	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000007	OMIM:600093	IEA				I		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000179	OMIM:600093	IEA				P		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000215	OMIM:600093	IEA				P		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000252	OMIM:600093	IEA				P		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000289	OMIM:600093	TAS				P		HPO:probinson	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000322	OMIM:600093	TAS				P		HPO:probinson	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000431	OMIM:600093	TAS				P		HPO:probinson	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0000455	OMIM:600093	TAS				P		HPO:probinson	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0001263	OMIM:600093	IEA				P		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0002655	OMIM:600093	TAS				P		HPO:iea	
OMIM	600093	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES		HP:0005715	OMIM:600093	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000007	OMIM:600096	TAS				I		HPO:skoehler	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000028	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000189	OMIM:600096	TAS				P		HPO:skoehler	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000194	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000218	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000316	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000343	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0000426	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001018	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001182	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001250	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001252	OMIM:600096	IEA				P		HPO:skoehler	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001263	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0001939	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0002019	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0002307	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0002353	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0003270	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0005832	OMIM:600096	IEA				P		HPO:iea	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0011344	OMIM:600096	TAS				P		HPO:skoehler	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0012450	OMIM:600096	TAS				P		HPO:skoehler	
OMIM	600096	PUERTO RICAN INFANT HYPOTONIA SYNDROME		HP:0025356	OMIM:600096	IEA				P		HPO:skoehler	
OMIM	600101	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2		HP:0000006	OMIM:600101	IEA				I		HPO:iea	
OMIM	600101	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2		HP:0000360	OMIM:600101	TAS				P		HPO:skoehler	
OMIM	600101	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2	HP:0012828	HP:0000365	OMIM:600101	TAS				P		HPO:probinson	
OMIM	600101	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2		HP:0003676	OMIM:600101	TAS				C		HPO:skoehler	
OMIM	600105	RETINITIS PIGMENTOSA 12; RP12		HP:0000007	OMIM:600105	IEA				I		HPO:iea	
OMIM	600105	RETINITIS PIGMENTOSA 12; RP12		HP:0000510	OMIM:600105	IEA				P		HPO:iea	
OMIM	600105	RETINITIS PIGMENTOSA 12; RP12		HP:0000639	OMIM:600105	IEA				P		HPO:skoehler	
OMIM	600105	RETINITIS PIGMENTOSA 12; RP12		HP:0000662	OMIM:600105	IEA				P		HPO:skoehler	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0000006	OMIM:600110	TAS				I		HPO:probinson	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0000007	OMIM:600110	TAS				I		HPO:probinson	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0007401	OMIM:600110	IEA				P		HPO:skoehler	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0007663	OMIM:600110	TAS				P		HPO:skoehler	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0007754	OMIM:600110	TAS				P		HPO:probinson	
OMIM	600110	STARGARDT DISEASE 3; STGD3		HP:0011507	OMIM:600110	TAS				P		HPO:probinson	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0000007	OMIM:600116	IEA				I		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0001288	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0001300	OMIM:600116	TAS				P		HPO:skoehler	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0001332	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0001337	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0001347	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0002063	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0002067	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0002172	OMIM:600116	IEA				P		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0003581	OMIM:600116	IEA				C		HPO:iea	
OMIM	600116	#600116 PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE; PARK2;;PARKINSON DISEASE, JUVENILE, AUTOSOMAL RECESSIVE; PDJ;;PARKINSONISM, EARLY-ONSET, WITH DIURNAL FLUCTUATION; EPDF		HP:0011960	OMIM:600116	TAS				P		HPO:skoehler	
OMIM	600117	DYSPHASIA, FAMILIAL DEVELOPMENTAL		HP:0000006	OMIM:600117	IEA				I		HPO:iea	
OMIM	600117	DYSPHASIA, FAMILIAL DEVELOPMENTAL		HP:0002357	OMIM:600117	TAS				P		HPO:probinson	
OMIM	600117	DYSPHASIA, FAMILIAL DEVELOPMENTAL		HP:0002474	OMIM:600117	TAS				P		HPO:probinson	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000007	OMIM:600118	IEA				I		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000028	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000252	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000347	OMIM:600118	TAS				P		HPO:skoehler	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000400	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000482	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000490	OMIM:600118	TAS				P		HPO:skoehler	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000508	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000519	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000568	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000648	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0000939	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001249	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001252	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001264	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001274	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001290	OMIM:600118	TAS				P		HPO:skoehler	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001321	OMIM:600118	TAS				P		HPO:skoehler	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001347	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001382	OMIM:600118	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001508	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0001845	OMIM:600118	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0002059	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0002079	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0002219	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0002751	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0003241	OMIM:600118	IEA				P		HPO:iea	
OMIM	600118	WARBURG MICRO SYNDROME 1		HP:0004322	OMIM:600118	IEA				P		HPO:iea	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3		HP:0000007	OMIM:600121	TAS				I		HPO:probinson	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3		HP:0001508	OMIM:600121	TAS				P		HPO:probinson	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3	HP:0012828	HP:0003097	OMIM:600121	TAS				P		HPO:probinson	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3	HP:0012828	HP:0005792	OMIM:600121	TAS				P		HPO:probinson	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3		HP:0008905	OMIM:600121	TAS				P		HPO:probinson	
OMIM	600121	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 3		HP:0010655	OMIM:600121	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000007	OMIM:600122	TAS				I		HPO:skoehler	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000037	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000280	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000470	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000490	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0000567	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0001249	OMIM:600122	TAS				P		HPO:skoehler	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0001344	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0001513	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0002162	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0005857	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0007633	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0008625	OMIM:600122	TAS				P		HPO:probinson	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0008897	OMIM:600122	TAS				P		HPO:skoehler	
OMIM	600122	MALE PSEUDOHERMAPHRODITISM/MENTAL RETARDATION SYNDROME, VERLOES TYPE		HP:0045025	OMIM:600122	TAS				P		HPO:skoehler	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000007	OMIM:600123	IEA				I		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000076	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000347	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000378	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000431	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000486	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000568	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000581	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0000582	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001263	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001511	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001545	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001629	OMIM:600123	TAS				P		HPO:skoehler	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001631	OMIM:600123	TAS				P		HPO:skoehler	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0001636	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0002020	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0002023	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0003022	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0003974	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0004209	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0006695	OMIM:600123	IEA				P		HPO:skoehler	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0010035	OMIM:600123	IEA				P		HPO:iea	
OMIM	600123	600123 ATRIOVENTRICULAR SEPTAL DEFECT WITH BLEPHAROPHIMOSIS AND ANAL ANDRADIAL DEFECTS		HP:0011266	OMIM:600123	IEA				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0000006	OMIM:600131	TAS				I		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0001425	OMIM:600131	TAS				I		HPO:skoehler	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0002069	OMIM:600131	TAS				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0002121	OMIM:600131	TAS				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0002373	OMIM:600131	TAS				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0002392	OMIM:600131	TAS				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0010849	OMIM:600131	TAS				P		HPO:iea	
OMIM	600131	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 1; ECA1		HP:0011463	OMIM:600131	TAS				C		HPO:iea	
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000007	PMID:17620573	PCS				I		HPO:iea	
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000510	PMID:17620573	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000543	PMID:17620573	PCS				P		HP:probinson	
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000550	PMID:17620573	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000639	PMID:17620573	PCS	HP:0003593	HP:0040284		P		HP:probinson	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0000662	PMID:17620573	PCS	HP:0003593	HP:0040284		P		HP:probinson	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0001133	PMID:17620573	PCS				P		HP:probinson	
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0007663	PMID:17620573	PCS	HP:0003593	HP:0040284		P		HP:probinson	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0007737	PMID:17620573	IEA				P		HP:probinson	
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0007787	PMID:17620573	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	600132	RETINITIS PIGMENTOSA 14		HP:0008043	PMID:17620573	TAS				P		HP:probinson	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0000006	PMID:17325180	PCS				I		HPO:iea	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0000510	PMID:20939871	PCS				P		HPO:iea	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0000543	PMID:20939871	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0000618	OMIM:600138	TAS				P		HPO:skoehler	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0000662	PMID:20939871	PCS		HP:0040284		P		HPO:skoehler	5/6
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0001133	PMID:20939871	PCS				P		HP:probinson	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0003829	PMID:23041261	PCS				C		HPO:skoehler	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0007401	OMIM:600138	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0007663	PMID:20939871	PCS				P		HP:probinson	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0007737	PMID:17325180	PCS				P		HP:probinson	
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0030629	PMID:20939871	PCS		HP:0040284		P		HP:probinson	4/6
OMIM	600138	RETINITIS PIGMENTOSA 11		HP:0040049	PMID:17325180	PCS		HP:0040284		P		HPO:skoehler	4/6
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0000007	OMIM:600142	IEA				I		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0000020	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0000639	OMIM:600142	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0000726	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001251	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001257	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001260	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001288	OMIM:600142	TAS				P		HPO:skoehler	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001297	OMIM:600142	IEA				P		HPO:skoehler	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001347	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0001596	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0002063	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0002071	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0002200	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0002352	OMIM:600142	IEA				P		HPO:skoehler	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0002448	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0003419	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0003487	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0004931	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0007162	OMIM:600142	IEA				P		HPO:iea	
OMIM	600142	CEREBRAL ARTERIOPATHY, AUTOSOMAL RECESSIVE, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY; CARASIL		HP:0007204	OMIM:600142	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0000007	OMIM:600143	IEA				I		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0000529	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0000750	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0001250	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0001251	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0001272	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0001336	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0002059	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0002074	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0002353	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0002376	OMIM:600143	IEA				P		HPO:iea	
OMIM	600143	CEROID LIPOFUSCINOSIS, NEURONAL, 8		HP:0003205	OMIM:600143	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0000006	OMIM:600145	TAS				I		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0000011	OMIM:600145	TAS				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0000016	OMIM:600145	IEA				P		HPO:skoehler	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0001287	OMIM:600145	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0002019	OMIM:600145	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0002315	OMIM:600145	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0002435	OMIM:600145	IEA				P		HPO:skoehler	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0003418	OMIM:600145	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0005224	OMIM:600145	IEA				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0007293	OMIM:600145	TAS				P		HPO:iea	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0009790	OMIM:600145	TAS				P		HPO:skoehler	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0010305	OMIM:600145	IEA				P		HPO:skoehler	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0012033	OMIM:600145	TAS				P		HPO:probinson	
OMIM	600145	SACRAL DEFECT WITH ANTERIOR MENINGOCELE		HP:0025247	OMIM:600145	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0000007	OMIM:600151	TAS				I		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0000089	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0000510	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0001156	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0001249	OMIM:600151	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0001263	OMIM:600151	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0001513	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0003241	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0003828	OMIM:600151	TAS				C		HPO:skoehler	
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0005180	OMIM:600151	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600151	BARDET-BIEDL SYNDROME 3; BBS3		HP:0010442	OMIM:600151	TAS				P		HPO:skoehler	
OMIM	600155	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2; HSCR2		HP:0000007	OMIM:600155	TAS				I		HPO:skoehler	
OMIM	600155	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 2; HSCR2		HP:0002251	OMIM:600155	IEA				P		HPO:iea	
OMIM	600156	%600156 HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 5; HSCR5		HP:0000006	OMIM:600156	TAS				I		HPO:skoehler	
OMIM	600156	%600156 HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 5; HSCR5		HP:0002251	OMIM:600156	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000248	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000316	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000358	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000369	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000411	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000465	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000508	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000537	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0000582	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0001249	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0001252	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0001290	OMIM:600159	TAS				P		HPO:skoehler	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0007514	OMIM:600159	TAS				P		HPO:probinson	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0009623	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0009836	OMIM:600159	IEA				P		HPO:iea	
OMIM	600159	PTERYGIUM COLLI AND MENTAL RETARDATION WITH FACIAL AND DIGITAL ANOMALIES		HP:0012098	OMIM:600159	TAS				P		HPO:probinson	
OMIM	600165	NANOPHTHALMOS 1		HP:0000006	OMIM:600165	IEA				I		HPO:iea	
OMIM	600165	NANOPHTHALMOS 1		HP:0007633	OMIM:600165	IEA				P		HPO:iea	
OMIM	600166	HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA		HP:0000006	OMIM:600166	IEA				I		HPO:iea	
OMIM	600166	HYPERPARATHYROIDISM, PRIMARY, CAUSED BY WATER CLEAR CELL HYPERPLASIA		HP:0008200	OMIM:600166	IEA				P		HPO:iea	
OMIM	600171	GONADAL AGENESIS		HP:0000007	OMIM:600171	IEA				I		HPO:iea	
OMIM	600171	GONADAL AGENESIS		HP:0008633	OMIM:600171	IEA				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0000006	OMIM:600175	IEA				I		HPO:iea	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0001265	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0001284	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0001558	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0001762	OMIM:600175	IEA				P		HPO:iea	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0001763	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0002460	OMIM:600175	TAS				P		HPO:probinson	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0002650	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0002804	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0002808	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0002987	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES	HP:0012825	HP:0003236	OMIM:600175	TAS				P		HPO:probinson	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003273	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003307	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003680	OMIM:600175	TAS				C		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003693	OMIM:600175	TAS				P		HPO:probinson	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003828	OMIM:600175	TAS				C		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0003829	OMIM:600175	TAS				C		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0006380	OMIM:600175	TAS				P		HPO:probinson	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0007269	OMIM:600175	TAS				P		HPO:probinson	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0008956	OMIM:600175	TAS				P		HPO:skoehler	
OMIM	600175	#600175 SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE;;SPINAL MUSCULAR ATROPHY, CONGENITAL BENIGN, WITH CONTRACTURES		HP:0008964	OMIM:600175	IEA				P		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0000007	OMIM:600176	IEA				I		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0000924	OMIM:600176	IEA				P		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0001249	OMIM:600176	IEA				P		HPO:skoehler	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0001263	OMIM:600176	TAS				P		HPO:skoehler	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0001302	OMIM:600176	TAS				P		HPO:skoehler	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0002069	OMIM:600176	IEA				P		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0007069	OMIM:600176	IEA				P		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0007270	OMIM:600176	IEA				P		HPO:iea	
OMIM	600176	%600176 PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS;;PACHYGYRIA WITH MENTAL RETARDATION AND SEIZURES		HP:0100702	OMIM:600176	TAS				P		HPO:skoehler	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0000006	OMIM:600193	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0000271	OMIM:600193	IEA				P		HPO:iea	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0000407	OMIM:600193	IEA				P		HPO:iea	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0001100	OMIM:600193	IEA				P		HPO:iea	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0002211	OMIM:600193	IEA				P		HPO:iea	
OMIM	600193	WAARDENBURG SYNDROME, TYPE IIB		HP:0002216	OMIM:600193	IEA				P		HPO:iea	
OMIM	600195	VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL		HP:0000006	OMIM:600195	IEA				I		HPO:iea	
OMIM	600195	VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL		HP:0000153	OMIM:600195	IEA				P		HPO:iea	
OMIM	600195	VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL		HP:0002584	OMIM:600195	IEA				P		HPO:skoehler	
OMIM	600195	VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL		HP:0012721	OMIM:600195	IEA				P		HPO:skoehler	
OMIM	600202	DYSLEXIA, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:600202	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600202	DYSLEXIA, SUSCEPTIBILITY TO, 2		HP:0010522	OMIM:600202	IEA				P		HPO:iea	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0000006	OMIM:600204	TAS				I		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0001425	OMIM:600204	TAS				I		HPO:skoehler	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0002515	OMIM:600204	TAS				P		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0002656	OMIM:600204	TAS				P		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0002970	OMIM:600204	TAS				P		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0003071	OMIM:600204	TAS				P		HPO:skoehler	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0003502	OMIM:600204	TAS				P		HPO:iea	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2	HP:0012825	HP:0004279	OMIM:600204	TAS				P		HPO:skoehler	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0005086	OMIM:600204	TAS				P		HPO:iea	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0010582	OMIM:600204	TAS				P		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0010585	OMIM:600204	TAS				P		HPO:probinson	
OMIM	600204	EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2		HP:0011463	OMIM:600204	TAS				C		HPO:probinson	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0000006	OMIM:600208	IEA				I		HPO:iea	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0000079	OMIM:600208	IEA				P		HPO:iea	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0000408	OMIM:600208	IEA				P		HPO:iea	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0000478	OMIM:600208	IEA				P		HPO:iea	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0000978	OMIM:600208	TAS				P		HPO:skoehler	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0001902	OMIM:600208	IEA				P		HPO:iea	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0003010	OMIM:600208	IEA				P		HPO:skoehler	
OMIM	600208	#600208 MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS		HP:0040185	OMIM:600208	IEA				P		HPO:skoehler	
OMIM	600209	EXOSTOSES, MULTIPLE, TYPE III		HP:0000006	OMIM:600209	IEA				I		HPO:iea	
OMIM	600209	EXOSTOSES, MULTIPLE, TYPE III		HP:0002762	OMIM:600209	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0000006	OMIM:600223	IEA				I		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0000763	OMIM:600223	TAS				P		HPO:skoehler	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0001260	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0001265	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0001272	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0001284	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0002073	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0002406	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0002936	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0003487	OMIM:600223	IEA				P		HPO:iea	
OMIM	600223	%600223 SPINOCEREBELLAR ATAXIA 4; SCA4;;SPINOCEREBELLAR ATAXIA, AUTOSOMAL DOMINANT, WITH SENSORY AXONAL NEUROPATHY		HP:0007772	OMIM:600223	IEA				P		HPO:skoehler	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0000006	OMIM:600224	IEA				I		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0000317	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0000640	OMIM:600224	TAS				P		HPO:probinson	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001260	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001263	OMIM:600224	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001272	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001290	OMIM:600224	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001310	OMIM:600224	TAS				P		HPO:skoehler	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0001347	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002066	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002070	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002075	OMIM:600224	TAS				P		HPO:skoehler	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002080	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002311	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002493	OMIM:600224	IEA				P		HPO:skoehler	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0002495	OMIM:600224	IEA				P		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0003593	OMIM:600224	TAS		HP:0040283		C		HPO:skoehler	HP:0040283
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0003674	OMIM:600224	IEA				C		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0003677	OMIM:600224	IEA				C		HPO:iea	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0007772	OMIM:600224	IEA				P		HPO:skoehler	
OMIM	600224	SPINOCEREBELLAR ATAXIA 5; SCA5		HP:0100543	OMIM:600224	TAS				P		HPO:skoehler	
OMIM	600231	PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE		HP:0000006	OMIM:600231	IEA				I		HPO:iea	
OMIM	600231	PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE		HP:0007435	OMIM:600231	IEA				P		HPO:iea	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0000007	OMIM:600251	IEA				I		HPO:iea	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0000175	OMIM:600251	TAS				P		HPO:skoehler	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0000204	OMIM:600251	TAS				P		HPO:skoehler	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0000589	OMIM:600251	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0000924	OMIM:600251	IEA				P		HPO:iea	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0002006	OMIM:600251	IEA				P		HPO:skoehler	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0003745	OMIM:600251	TAS				I		HPO:skoehler	
OMIM	600251	FACIAL CLEFTING, OBLIQUE, 1; OBLFC1		HP:0006191	OMIM:600251	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000006	OMIM:600252	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000175	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000252	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000444	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000501	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0000684	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0001249	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0001263	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0001363	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0001511	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0001627	OMIM:600252	TAS				P		HPO:lccarmody	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0004467	OMIM:600252	IEA				P		HPO:iea	
OMIM	600252	LOWRY-MACLEAN SYNDROME		HP:0009110	OMIM:600252	TAS				P		HPO:probinson	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0000238	OMIM:600257	IEA				P		HPO:iea	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0000478	OMIM:600257	IEA				P		HPO:iea	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0000598	OMIM:600257	IEA				P		HPO:iea	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0001452	OMIM:600257	IEA				I		HPO:iea	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0001939	OMIM:600257	IEA				P		HPO:iea	
OMIM	600257	BOR-DUANE HYDROCEPHALUS CONTIGUOUS GENE SYNDROME		HP:0003011	OMIM:600257	IEA				P		HPO:iea	
OMIM	600263	HELICOBACTER PYLORI INFECTION, SUSCEPTIBILITY TO		HP:0005202	OMIM:600263	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000006	OMIM:600268	IEA				I		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000242	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000256	OMIM:600268	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000286	OMIM:600268	IEA				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000431	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000483	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000486	OMIM:600268	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000520	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000625	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS	HP:0012825	HP:0000752	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0000953	OMIM:600268	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001004	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001057	OMIM:600268	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001140	OMIM:600268	IEA				P		HPO:iea	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001250	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001263	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001510	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0001680	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0002326	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0002836	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0005280	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0007759	OMIM:600268	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0010816	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0012803	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0100559	OMIM:600268	TAS				P		HPO:skoehler	
OMIM	600268	%600268 OCULOECTODERMAL SYNDROME; OES;;APLASIA CUTIS CONGENITA WITH EPIBULBAR DERMOIDS		HP:0100702	OMIM:600268	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600269	SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES		HP:0000006	OMIM:600269	IEA				I		HPO:iea	
OMIM	600269	SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES		HP:0007646	OMIM:600269	IEA				P		HPO:iea	
OMIM	600269	SHORT TARSUS WITH ABSENCE OF LOWER EYELASHES		HP:0007697	OMIM:600269	IEA				P		HPO:iea	
OMIM	600273	POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS		HP:0000006	OMIM:600273	TAS				I		HPO:iea	
OMIM	600273	POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS		HP:0000113	OMIM:600273	TAS	HP:0003593			P		HPO:probinson	
OMIM	600273	POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS		HP:0006772	OMIM:600273	TAS				P		HPO:probinson	
OMIM	600273	POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS		HP:0009717	OMIM:600273	TAS				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000006	OMIM:600274	IEA				I		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000710	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000727	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000734	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000737	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000741	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000748	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0000751	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0001300	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0001425	OMIM:600274	TAS				I		HPO:skoehler	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0002145	OMIM:600274	TAS				P		HPO:probinson	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0002463	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0002476	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0002529	OMIM:600274	TAS				P		HPO:probinson	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0002591	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0007354	OMIM:600274	IEA				P		HPO:iea	
OMIM	600274	FRONTOTEMPORAL DEMENTIA; FTD		HP:0008768	OMIM:600274	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000007	OMIM:600302	IEA				I		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000154	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000188	OMIM:600302	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000219	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000219	OMIM:600302	TAS				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000232	OMIM:600302	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000322	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000337	OMIM:600302	TAS				P		HPO:probinson	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000470	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000478	OMIM:600302	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0000675	OMIM:600302	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0001250	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0001256	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0001258	OMIM:600302	IEA				P		HPO:iea	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0001956	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0002059	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0005490	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0006380	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600302	600302 FRYNS MACROCEPHALY;;MACROCEPHALY WITH SPASTIC PARAPLEGIA AND DISTINCTIVE CRANIOFACIALAPPEARANCE		HP:0006610	OMIM:600302	IEA				P		HPO:skoehler	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0000006	OMIM:600309	PCS				I		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0000822	OMIM:600309	IEA				P		HPO:skoehler	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0000961	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0001635	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0002092	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0010445	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0011622	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0011705	OMIM:600309	PCS				P		HPO:probinson	
OMIM	600309	ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3		HP:0031665	OMIM:600309	IEA				P		HPO:skoehler	
OMIM	600316	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 3		HP:0000007	OMIM:600316	TAS				I		HPO:probinson	
OMIM	600316	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 3		HP:0011476	OMIM:600316	TAS	HP:0003577			P		HPO:probinson	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000007	OMIM:600325	IEA				I		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000023	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000028	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000175	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000218	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000248	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000252	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000256	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000316	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000341	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000347	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000358	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000369	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0000677	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001156	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001159	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001166	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001252	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001263	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001355	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001511	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001537	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0001999	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0002007	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0002236	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0002553	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0002943	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0004322	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0004325	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0005676	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0009473	OMIM:600325	IEA				P		HPO:iea	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0009778	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0009891	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0030084	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600325	%600325 AMINOPTERIN SYNDROME SINE AMINOPTERIN; ASSA;;PSEUDOAMINOPTERIN SYNDROME		HP:0045025	OMIM:600325	TAS				P		HPO:skoehler	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0000007	OMIM:600329	TAS				I		HPO:nvasilevsky	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0000924	OMIM:600329	IEA				P		HPO:iea	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0001274	OMIM:600329	IEA				P		HPO:iea	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0001466	OMIM:600329	TAS				I		HPO:nvasilevsky	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0001522	OMIM:600329	IEA				M		HPO:iea	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0001939	OMIM:600329	IEA				P		HPO:iea	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0002059	OMIM:600329	IEA				P		HPO:iea	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0011002	OMIM:600329	TAS	HP:0003593			P		HPO:skoehler	
OMIM	600329	OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY		HP:0025517	OMIM:600329	TAS				P		HPO:nvasilevsky	
OMIM	600331	PARC SYNDROME		HP:0000006	OMIM:600331	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600331	PARC SYNDROME		HP:0000175	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600331	PARC SYNDROME		HP:0000308	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600331	PARC SYNDROME		HP:0000561	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600331	PARC SYNDROME		HP:0001029	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600331	PARC SYNDROME		HP:0001596	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600331	PARC SYNDROME		HP:0002223	OMIM:600331	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0000006	OMIM:600332	IEA				I		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0001425	OMIM:600332	TAS				I		HPO:skoehler	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003457	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003559	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003710	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003712	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003719	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003738	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0003760	OMIM:600332	IEA				P		HPO:iea	
OMIM	600332	RIPPLING MUSCLE DISEASE 1; RMD1		HP:0008967	OMIM:600332	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0000007	OMIM:600333	IEA				I		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0000602	OMIM:600333	IEA				P		HPO:skoehler	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0000726	OMIM:600333	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0001939	OMIM:600333	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002059	OMIM:600333	IEA				P		HPO:skoehler	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002093	OMIM:600333	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002398	OMIM:600333	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002446	OMIM:600333	TAS				P		HPO:skoehler	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002483	OMIM:600333	IEA				P		HPO:iea	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0002878	OMIM:600333	TAS				P		HPO:skoehler	
OMIM	600333	600333 MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA		HP:0008361	OMIM:600333	IEA				P		HPO:iea	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0000006	OMIM:600334	IEA				I		HPO:iea	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003376	OMIM:600334	IEA				P		HPO:iea	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003458	OMIM:600334	IEA				P		HPO:iea	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003560	OMIM:600334	TAS				P		HPO:skoehler	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003581	OMIM:600334	IEA				C		HPO:iea	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003677	OMIM:600334	TAS				C		HPO:skoehler	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003805	OMIM:600334	TAS				P		HPO:skoehler	
OMIM	600334	TIBIAL MUSCULAR DYSTROPHY, TARDIVE		HP:0003829	OMIM:600334	IEA				C		HPO:iea	
OMIM	600335	SUCCINIC ACIDEMIA		HP:0000007	OMIM:600335	IEA				I		HPO:iea	
OMIM	600335	SUCCINIC ACIDEMIA		HP:0002098	OMIM:600335	IEA				P		HPO:iea	
OMIM	600335	SUCCINIC ACIDEMIA		HP:0003128	OMIM:600335	IEA				P		HPO:iea	
OMIM	600343	%600343 PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF; PDDP		HP:0000006	OMIM:600343	TAS				I		HPO:skoehler	
OMIM	600343	%600343 PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF; PDDP		HP:0000153	OMIM:600343	IEA				P		HPO:iea	
OMIM	600343	%600343 PAROTID SALIVARY GLANDS, POLYCYSTIC DYSGENETIC DISEASE OF; PDDP		HP:0000924	OMIM:600343	IEA				P		HPO:iea	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0000007	OMIM:600348	TAS				I		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0000238	OMIM:600348	IEA	HP:0003577			P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0000256	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0000924	OMIM:600348	IEA				P		HPO:iea	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0001250	OMIM:600348	IEA				P		HPO:iea	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0001257	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0001263	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0001274	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0002119	OMIM:600348	IEA				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0002126	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0002282	OMIM:600348	TAS				P		HPO:iea	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0002360	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600348	BAND HETEROTOPIA; BH		HP:0010864	OMIM:600348	TAS				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0000006	OMIM:600351	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0000969	OMIM:600351	TAS				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0001875	OMIM:600351	IEA				P		HPO:iea	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0002013	OMIM:600351	IEA				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0002039	OMIM:600351	TAS				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0002242	OMIM:600351	TAS				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0003073	OMIM:600351	IEA				P		HPO:iea	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0003075	OMIM:600351	IEA				P		HPO:iea	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0004315	OMIM:600351	IEA				P		HPO:iea	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0005208	OMIM:600351	IEA				P		HPO:skoehler	
OMIM	600351	ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY		HP:0031273	OMIM:600351	IEA				P		HPO:skoehler	
OMIM	600356	PACHYDERMODACTYLY, FAMILIAL		HP:0000006	OMIM:600356	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600356	PACHYDERMODACTYLY, FAMILIAL		HP:0000924	OMIM:600356	IEA				P		HPO:iea	
OMIM	600360	APLASIA CUTIS CONGENITA OF LIMBS, RECESSIVE		HP:0000007	OMIM:600360	IEA				I		HPO:iea	
OMIM	600360	APLASIA CUTIS CONGENITA OF LIMBS, RECESSIVE		HP:0001057	OMIM:600360	TAS				P		HPO:probinson	
OMIM	600360	APLASIA CUTIS CONGENITA OF LIMBS, RECESSIVE		HP:0007506	OMIM:600360	TAS				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0000006	OMIM:600361	IEA				I		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0000763	OMIM:600361	TAS				P		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001257	OMIM:600361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001276	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001425	OMIM:600361	TAS				I		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001618	OMIM:600361	TAS				P		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001761	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0001765	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0002355	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0002359	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0002460	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0002460	OMIM:600361	TAS				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0002936	OMIM:600361	TAS				P		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V	HP:0012825	HP:0003431	OMIM:600361	PCS				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003477	OMIM:600361	TAS				P		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003487	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003581	OMIM:600361	TAS				C		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003677	OMIM:600361	IEA				C		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003690	OMIM:600361	TAS				P		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0003693	OMIM:600361	TAS				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0009027	OMIM:600361	IEA				P		HPO:probinson	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0011463	OMIM:600361	TAS				C		HPO:skoehler	
OMIM	600361	HEREDITARY MOTOR AND SENSORY NEUROPATHY V		HP:0012514	OMIM:600361	IEA				P		HPO:skoehler	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0000006	OMIM:600363	IEA				I		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0000012	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0000020	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0001250	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0001258	OMIM:600363	TAS				P		HPO:skoehler	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0001337	OMIM:600363	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0001761	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002061	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002064	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002166	OMIM:600363	TAS				P		HPO:probinson	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002169	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002314	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0002839	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0003487	OMIM:600363	IEA				P		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0003587	OMIM:600363	IEA				C		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0003676	OMIM:600363	IEA				C		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0003828	OMIM:600363	IEA				C		HPO:iea	
OMIM	600363	SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT		HP:0007340	OMIM:600363	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0000007	PMID:25574826	PCS				I		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0000028	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	1/2
OMIM	600373	CODAS SYNDROME		HP:0000143	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	1/2
OMIM	600373	CODAS SYNDROME		HP:0000405	PMID:25574826	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	600373	CODAS SYNDROME		HP:0000407	PMID:25574826	PCS		HP:0040284		P		HPO:iea	2/4
OMIM	600373	CODAS SYNDROME		HP:0000463	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	600373	CODAS SYNDROME		HP:0000508	PMID:25574826	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	600373	CODAS SYNDROME		HP:0000518	PMID:25574826	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	600373	CODAS SYNDROME		HP:0000519	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0000684	PMID:25574826	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	600373	CODAS SYNDROME		HP:0001216	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0001249	PMID:25574826	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	600373	CODAS SYNDROME		HP:0001250	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	1/4
OMIM	600373	CODAS SYNDROME		HP:0001252	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0001263	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0001270	PMID:25574826	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	600373	CODAS SYNDROME		HP:0001290	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	600373	CODAS SYNDROME		HP:0001374	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0001539	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	1/4
OMIM	600373	CODAS SYNDROME		HP:0001561	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0001604	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	3/4
OMIM	600373	CODAS SYNDROME		HP:0001629	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0001631	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	2/4
OMIM	600373	CODAS SYNDROME		HP:0002020	PMID:25574826	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	600373	CODAS SYNDROME		HP:0002023	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	2/4
OMIM	600373	CODAS SYNDROME		HP:0002079	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0002119	OMIM:600373	IEA				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0002650	PMID:25574826	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	600373	CODAS SYNDROME		HP:0002682	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0002750	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0002761	OMIM:600373	IEA				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0002857	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	600373	CODAS SYNDROME		HP:0003177	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0003311	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	600373	CODAS SYNDROME		HP:0003417	PMID:25574826	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	600373	CODAS SYNDROME		HP:0004322	PMID:25574826	PCS		HP:0040284		P		HPO:iea	4/4
OMIM	600373	CODAS SYNDROME		HP:0004626	OMIM:600373	IEA				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0005280	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0005792	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0006297	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0006297	PMID:25574826	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	600373	CODAS SYNDROME		HP:0006695	OMIM:600373	TAS				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0008081	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	600373	CODAS SYNDROME		HP:0009623	OMIM:600373	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600373	CODAS SYNDROME		HP:0009803	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0009901	PMID:25574826	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	600373	CODAS SYNDROME		HP:0010049	OMIM:600373	IEA				P		HPO:iea	
OMIM	600373	CODAS SYNDROME		HP:0010577	OMIM:600373	IEA				P		HPO:skoehler	
OMIM	600373	CODAS SYNDROME		HP:0100255	PMID:25574826	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000006	OMIM:600376	IEA				I		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000214	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000227	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000434	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000471	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000524	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000822	OMIM:600376	IEA				P		HPO:skoehler	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0000961	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001217	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001232	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001250	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001342	OMIM:600376	TAS				P		HPO:skoehler	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001394	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001425	OMIM:600376	TAS				I		HPO:skoehler	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001694	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001901	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0001903	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002076	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002092	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002094	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002138	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002140	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002248	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002249	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002326	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002390	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002408	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002573	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002604	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002629	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0002707	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0004406	OMIM:600376	TAS	HP:0011463			P		HPO:skoehler	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0006107	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0006548	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0006574	OMIM:600376	IEA				P		HPO:iea	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0030049	OMIM:600376	TAS				P		HPO:skoehler	
OMIM	600376	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2; HHT2		HP:0030491	OMIM:600376	TAS				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000006	OMIM:600383	IEA				I		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000126	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000308	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000316	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000444	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000494	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0000508	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0001196	OMIM:600383	TAS		HP:0040284		P		HPO:probinson	3/5
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0001438	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0001611	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0001773	OMIM:600383	TAS				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0002983	OMIM:600383	TAS				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0003027	OMIM:600383	IEA				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0003468	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0005694	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0005891	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0008845	OMIM:600383	IEA				P		HPO:iea	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0009487	OMIM:600383	TAS				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0009701	OMIM:600383	TAS				P		HPO:skoehler	
OMIM	600383	MESOMELIA-SYNOSTOSES SYNDROME		HP:0010292	OMIM:600383	TAS				P		HPO:skoehler	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0000006	OMIM:600384	IEA				I		HPO:iea	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0000252	OMIM:600384	IEA				P		HPO:iea	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0001159	OMIM:600384	IEA				P		HPO:iea	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0001249	OMIM:600384	PCS				P		HPO:probinson	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0001449	OMIM:600384	PCS				P		HPO:probinson	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0001991	OMIM:600384	TAS				P		HPO:skoehler	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0002751	OMIM:600384	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0004322	OMIM:600384	PCS				P		HPO:probinson	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0010554	OMIM:600384	TAS				P		HPO:skoehler	
OMIM	600384	%600384 APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSALIV		HP:0100543	OMIM:600384	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0000006	OMIM:600399	IEA				I		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0000256	OMIM:600399	IEA				P		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0000272	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0000336	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0000767	OMIM:600399	IEA				P		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0001263	OMIM:600399	IEA				P		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0001290	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0002164	OMIM:600399	IEA				P		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0004322	OMIM:600399	IEA				P		HPO:iea	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0004482	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0005280	OMIM:600399	TAS	HP:0003593			P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0011220	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600399	PECTUS EXCAVATUM, MACROCEPHALY, SHORT STATURE, AND DYSPLASTIC NAILS		HP:0011800	OMIM:600399	TAS				P		HPO:skoehler	
OMIM	600416	600416 MUSCULAR DYSTROPHY, SCAPULOHUMERAL		HP:0000006	OMIM:600416	IEA				I		HPO:iea	
OMIM	600416	600416 MUSCULAR DYSTROPHY, SCAPULOHUMERAL		HP:0000707	OMIM:600416	IEA				P		HPO:iea	
OMIM	600416	600416 MUSCULAR DYSTROPHY, SCAPULOHUMERAL		HP:0001324	OMIM:600416	TAS				P		HPO:skoehler	
OMIM	600416	600416 MUSCULAR DYSTROPHY, SCAPULOHUMERAL		HP:0001939	OMIM:600416	IEA				P		HPO:iea	
OMIM	600416	600416 MUSCULAR DYSTROPHY, SCAPULOHUMERAL		HP:0008970	OMIM:600416	IEA				P		HPO:iea	
OMIM	600419	ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS		HP:0000006	OMIM:600419	IEA				I		HPO:iea	
OMIM	600419	ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS		HP:0000975	OMIM:600419	TAS				P		HPO:probinson	
OMIM	600419	ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS		HP:0001071	OMIM:600419	IEA				P		HPO:iea	
OMIM	600419	ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS		HP:0001528	OMIM:600419	TAS				P		HPO:probinson	
OMIM	600419	ANGIOKERATOMA CORPORIS DIFFUSUM WITH ARTERIOVENOUS FISTULAS		HP:0004947	OMIM:600419	TAS				P		HPO:probinson	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000006	OMIM:600430	TAS				I	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000248	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000272	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000280	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000283	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000311	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000407	OMIM:600430	TAS		HP:0040283		P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000445	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000455	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000490	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000581	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000718	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000752	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0000964	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001249	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001250	OMIM:600430	TAS		HP:0040283		P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001263	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001265	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001428	OMIM:600430	IEA				I	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001513	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001682	OMIM:600430	TAS		HP:0040283		P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0001831	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0002553	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0003577	OMIM:600430	IEA				C	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0004322	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0005280	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0007021	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0009803	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0010049	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0010743	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:iea	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0011675	OMIM:600430	TAS		HP:0040283		P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0011800	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0045025	OMIM:600430	IEA				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600430	CHROMOSOME 2q37 DELETION SYNDROME		HP:0100716	OMIM:600430	TAS				P	CHROMOSOME 2Q37 DELETION SYNDROME	HPO:skoehler	
OMIM	600457	HYPERTRICHOSIS, ANTERIOR CERVICAL		HP:0004535	OMIM:600457	IEA				P		HPO:iea	
OMIM	600458	ADENOMYOSIS		HP:0000006	OMIM:600458	TAS				I		HPO:nvasilevsky	
OMIM	600458	ADENOMYOSIS		HP:0000119	OMIM:600458	IEA				P		HPO:iea	
OMIM	600458	ADENOMYOSIS		HP:0001423	OMIM:600458	TAS				I		HPO:nvasilevsky	
OMIM	600458	ADENOMYOSIS		HP:0001892	OMIM:600458	IEA				P		HPO:skoehler	
OMIM	600458	ADENOMYOSIS		HP:0100607	OMIM:600458	TAS				P		HPO:skoehler	
OMIM	600459	600459 ARTERIAL DISSECTION WITH LENTIGINOSIS		HP:0000007	OMIM:600459	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600459	600459 ARTERIAL DISSECTION WITH LENTIGINOSIS		HP:0001003	OMIM:600459	IEA				P		HPO:iea	
OMIM	600459	600459 ARTERIAL DISSECTION WITH LENTIGINOSIS		HP:0001939	OMIM:600459	IEA				P		HPO:iea	
OMIM	600459	600459 ARTERIAL DISSECTION WITH LENTIGINOSIS		HP:0005294	OMIM:600459	IEA				P		HPO:iea	
OMIM	600459	600459 ARTERIAL DISSECTION WITH LENTIGINOSIS		HP:0012180	OMIM:600459	TAS				P		HPO:skoehler	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000007	OMIM:600460	TAS				I		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000028	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000047	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000049	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000054	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000175	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000204	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000316	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000369	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0000400	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001171	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001217	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001249	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001263	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001510	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001629	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001636	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001643	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0001680	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0003819	OMIM:600460	TAS				M		HPO:skoehler	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0004960	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600460	600460 CLEFT PALATE, CARDIAC DEFECT, GENITAL ANOMALIES, AND ECTRODACTYLY;;CCGE;;ACROCARDIOFACIAL SYNDROME; ACFS		HP:0008589	OMIM:600460	TAS				P		HPO:probinson	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0000047	OMIM:600461	IEA				P		HPO:skoehler	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0000054	OMIM:600461	IEA				P		HPO:skoehler	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0000363	OMIM:600461	TAS				P		HPO:probinson	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0001433	OMIM:600461	IEA				P		HPO:iea	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0001541	OMIM:600461	IEA				P		HPO:skoehler	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0001852	OMIM:600461	IEA				P		HPO:iea	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0001869	OMIM:600461	IEA				P		HPO:iea	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0001878	OMIM:600461	TAS				P		HPO:probinson	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0003577	OMIM:600461	IEA				C		HPO:skoehler	
OMIM	600461	HEMOLYTIC ANEMIA, LETHAL CONGENITAL NONSPHEROCYTIC, WITH GENITAL AND OTHER ABNORMALITIES		HP:0005469	OMIM:600461	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000007	OMIM:600462	IEA				I		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000218	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000252	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000347	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000823	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0000980	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0001249	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0001508	OMIM:600462	TAS				P		HPO:skoehler	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0001924	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0001931	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0001935	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0002151	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0003128	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0003281	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0003323	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0003546	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0003688	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0009055	OMIM:600462	IEA				P		HPO:iea	
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0009743	OMIM:600462	TAS		HP:0040284		P		HPO:iea	HP:0040284
OMIM	600462	MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1		HP:0012132	OMIM:600462	TAS				P		HPO:skoehler	
OMIM	600467	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4		HP:0000006	OMIM:600467	IEA				I		HPO:iea	
OMIM	600467	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4		HP:0001941	OMIM:600467	IEA				P		HPO:iea	
OMIM	600467	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4		HP:0002047	OMIM:600467	IEA				P		HPO:iea	
OMIM	600467	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 4		HP:0003201	OMIM:600467	IEA				P		HPO:iea	
OMIM	600496	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III		HP:0000006	OMIM:600496	IEA				I		HPO:iea	
OMIM	600496	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III		HP:0003074	OMIM:600496	IEA				P		HPO:iea	
OMIM	600496	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III		HP:0003593	OMIM:600496	IEA				C		HPO:iea	
OMIM	600496	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III		HP:0004904	OMIM:600496	IEA				P		HPO:iea	
OMIM	600496	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III		HP:0005978	OMIM:600496	IEA				P		HPO:iea	
OMIM	600501	ABCD SYNDROME		HP:0000007	OMIM:600501	TAS				I		HPO:probinson	
OMIM	600501	ABCD SYNDROME		HP:0000365	OMIM:600501	TAS				P		HPO:skoehler	
OMIM	600501	ABCD SYNDROME		HP:0001022	OMIM:600501	TAS				P		HPO:probinson	
OMIM	600501	ABCD SYNDROME		HP:0001520	OMIM:600501	TAS				P		HPO:skoehler	
OMIM	600501	ABCD SYNDROME		HP:0002251	OMIM:600501	TAS				P		HPO:skoehler	
OMIM	600501	ABCD SYNDROME		HP:0006958	OMIM:600501	TAS				P		HPO:probinson	
OMIM	600501	ABCD SYNDROME		HP:0007894	OMIM:600501	TAS				P		HPO:probinson	
OMIM	600510	GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1		HP:0000006	OMIM:600510	TAS				I		HPO:skoehler	
OMIM	600510	GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1		HP:0000545	OMIM:600510	TAS				P		HPO:skoehler	
OMIM	600510	GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1		HP:0000648	OMIM:600510	TAS				P		HPO:skoehler	
OMIM	600510	GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1		HP:0011462	OMIM:600510	TAS				C		HPO:probinson	
OMIM	600510	GLAUCOMA-RELATED PIGMENT DISPERSION SYNDROME; GPDS1		HP:0012108	OMIM:600510	TAS				P		HPO:probinson	
OMIM	600511	%600511 SCHIZOPHRENIA 3; SCZD3;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 6-RELATED		HP:0000006	OMIM:600511	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600511	%600511 SCHIZOPHRENIA 3; SCZD3;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 6-RELATED		HP:0000707	OMIM:600511	IEA				P		HPO:iea	
OMIM	600511	%600511 SCHIZOPHRENIA 3; SCZD3;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 6-RELATED		HP:0100753	OMIM:600511	TAS				P		HPO:skoehler	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:600512	TAS				I		HPO:probinson	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0002349	OMIM:600512	TAS				P		HPO:probinson	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0002384	OMIM:600512	TAS				P		HPO:probinson	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0003829	OMIM:600512	TAS				C		HPO:probinson	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0007334	OMIM:600512	TAS				P		HPO:probinson	
OMIM	600512	EPILEPSY, LATERAL TEMPORAL LOBE, AUTOSOMAL DOMINANT		HP:0011158	OMIM:600512	TAS				P		HPO:probinson	
OMIM	600513	EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1		HP:0000006	PMID:7895015	PCS				I		HPO:iea	
OMIM	600513	EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1		HP:0001249	PMID:14623738	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600513	EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1		HP:0003829	OMIM:600513	TAS				C		HPO:skoehler	
OMIM	600513	EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1		HP:0007359	PMID:7895015	PCS				P		HPO:probinson	
OMIM	600513	EPILEPSY, NOCTURNAL FRONTAL LOBE, TYPE 1		HP:0011463	PMID:7895015	PCS				C		HPO:probinson	
OMIM	600522	PHOSPHOLIPASE A2, GROUP IVA; PLA2G4A		HP:0000007	PMID:18451993	PCS		HP:0040284		I		HPO:probinson	1/1
OMIM	600522	PHOSPHOLIPASE A2, GROUP IVA; PLA2G4A		HP:0001891	PMID:18451993	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600522	PHOSPHOLIPASE A2, GROUP IVA; PLA2G4A		HP:0002584	PMID:18451993	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600522	PHOSPHOLIPASE A2, GROUP IVA; PLA2G4A		HP:0005229	PMID:18451993	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0000007	OMIM:600546	IEA				I		HPO:iea	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0000252	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0001263	OMIM:600546	IEA				P		HPO:iea	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0001511	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0001876	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0001999	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0003220	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600546	INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY		HP:0008897	OMIM:600546	PCS				P		HPO:probinson	
OMIM	600559	HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS		HP:0000519	OMIM:600559	IEA				P		HPO:iea	
OMIM	600559	HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS		HP:0001334	OMIM:600559	IEA				P		HPO:iea	
OMIM	600559	HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS		HP:0001522	OMIM:600559	IEA				M		HPO:iea	
OMIM	600559	HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS		HP:0001561	OMIM:600559	IEA				P		HPO:iea	
OMIM	600559	HYDROCEPHALUS, ENDOCARDIAL FIBROELASTOSIS, AND CATARACTS		HP:0001706	OMIM:600559	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0000006	OMIM:600561	IEA				I		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0001269	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0001283	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0001308	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0001348	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0001388	OMIM:600561	IEA				P		HPO:skoehler	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0002273	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0002655	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0002750	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0002878	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0002938	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0003090	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0003304	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0003414	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0003467	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0003690	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0004322	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0005667	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0008489	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0009130	OMIM:600561	IEA				P		HPO:iea	
OMIM	600561	SPONDYLOEPIPHYSEAL DYSPLASIA WITH ATLANTOAXIAL INSTABILITY		HP:0011448	OMIM:600561	TAS				P		HPO:probinson	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0000006	OMIM:600593	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0001363	OMIM:600593	IEA				P		HPO:iea	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0001822	OMIM:600593	IEA				P		HPO:iea	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0005776	OMIM:600593	TAS				P		HPO:probinson	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0006110	OMIM:600593	TAS				P		HPO:probinson	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0006118	OMIM:600593	IEA				P		HPO:iea	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0010164	OMIM:600593	TAS				P		HPO:probinson	
OMIM	600593	CRANIOSYNOSTOSIS, ADELAIDE TYPE		HP:0010230	OMIM:600593	TAS				P		HPO:probinson	
OMIM	600598	SETTING-SUN PHENOMENON, FAMILIAL BENIGN		HP:0000006	OMIM:600598	TAS				I		HPO:nvasilevsky	
OMIM	600598	SETTING-SUN PHENOMENON, FAMILIAL BENIGN		HP:0000478	OMIM:600598	IEA				P		HPO:iea	
OMIM	600598	SETTING-SUN PHENOMENON, FAMILIAL BENIGN		HP:0001426	OMIM:600598	TAS				I		HPO:nvasilevsky	
OMIM	600598	SETTING-SUN PHENOMENON, FAMILIAL BENIGN		HP:0500044	OMIM:600598	IEA				P		HPO:skoehler	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0000006	OMIM:600624	IEA				I		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0000135	OMIM:600624	IEA				P		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0000365	OMIM:600624	IEA				P		HPO:skoehler	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0000548	OMIM:600624	IEA				P		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0001249	OMIM:600624	IEA				P		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0001939	OMIM:600624	IEA				P		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0003621	OMIM:600624	IEA				C		HPO:iea	
OMIM	600624	CONE-ROD DYSTROPHY 1; CORD1		HP:0011463	OMIM:600624	TAS				C		HPO:skoehler	
OMIM	600625	OROFACIAL CLEFT 11; OFC11		HP:0000202	PMID:19249007	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	600625	OROFACIAL CLEFT 11; OFC11		HP:0010982	PMID:19249007	PCS				I		HP:probinson	
OMIM	600625	OROFACIAL CLEFT 11; OFC11		HP:0410030	OMIM:600625	IEA				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000007	OMIM:600627	TAS				I		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000316	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000407	OMIM:600627	TAS				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000486	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000505	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000545	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000712	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000716	OMIM:600627	TAS				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0000718	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0001181	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0001263	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0001377	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0001763	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0002342	OMIM:600627	TAS				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0002761	OMIM:600627	IEA				P		HPO:iea	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0003361	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0025268	OMIM:600627	TAS				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0030214	OMIM:600627	TAS				P		HPO:skoehler	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0100490	OMIM:600627	TAS				P		HPO:probinson	
OMIM	600627	HYPERTRYPTOPHANEMIA; HYPTRP		HP:0500134	OMIM:600627	IEA				P		HPO:skoehler	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0000006	OMIM:600628	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0002286	OMIM:600628	TAS				P		HPO:iea	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0003621	OMIM:600628	IEA				C		HPO:iea	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0008070	OMIM:600628	TAS				P		HPO:iea	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0011463	OMIM:600628	TAS				C		HPO:skoehler	
OMIM	600628	600628 LOOSE ANAGEN HAIR SYNDROME		HP:0040169	OMIM:600628	IEA				P		HPO:skoehler	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0000007	OMIM:600630	TAS				I		HPO:skoehler	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0000958	OMIM:600630	IEA				P		HPO:iea	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0000992	OMIM:600630	TAS				P		HPO:skoehler	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0001009	OMIM:600630	IEA				P		HPO:iea	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0001425	OMIM:600630	IEA				I		HPO:iea	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0001480	OMIM:600630	IEA				P		HPO:iea	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0002664	OMIM:600630	IEA				P		HPO:iea	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0003224	OMIM:600630	TAS				P		HPO:skoehler	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0003593	OMIM:600630	TAS				C		HPO:skoehler	
OMIM	600630	#600630 UV-SENSITIVE SYNDROME 1; UVSS1		HP:0007623	OMIM:600630	IEA				P		HPO:iea	
OMIM	600631	%600631 ENURESIS, NOCTURNAL, 1; ENUR1;;BEDWETTING		HP:0000006	OMIM:600631	TAS				I		HPO:skoehler	
OMIM	600631	%600631 ENURESIS, NOCTURNAL, 1; ENUR1;;BEDWETTING		HP:0010677	OMIM:600631	TAS				P		HPO:skoehler	
OMIM	600634	PITUITARY ADENOMA, PROLACTIN-SECRETING		HP:0006767	OMIM:600634	IEA				P		HPO:iea	
OMIM	600634	PITUITARY ADENOMA, PROLACTIN-SECRETING		HP:0040278	OMIM:600634	TAS				P		HPO:skoehler	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0000006	OMIM:600638	IEA				I		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0000508	OMIM:600638	TAS				P		HPO:skoehler	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0000577	OMIM:600638	IEA				P		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0000646	OMIM:600638	IEA				P		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001239	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001263	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001274	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001328	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001477	OMIM:600638	IEA				P		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0001491	OMIM:600638	IEA				P		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0003477	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0007831	OMIM:600638	IEA				P		HPO:iea	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0009473	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0010628	OMIM:600638	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0012241	OMIM:600638	TAS				P		HPO:skoehler	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0012242	OMIM:600638	TAS				P		HPO:skoehler	
OMIM	600638	#600638 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT; CFEOM3A;;FEOM3 LOCUS		HP:0100490	OMIM:600638	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0000006	OMIM:600643	IEA				I		HPO:iea	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0001409	OMIM:600643	IEA				P		HPO:iea	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0001954	OMIM:600643	IEA				P		HPO:skoehler	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0002013	OMIM:600643	IEA				P		HPO:iea	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0002040	OMIM:600643	IEA				P		HPO:skoehler	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0002240	OMIM:600643	IEA				P		HPO:iea	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0002617	OMIM:600643	IEA				P		HPO:skoehler	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0030151	OMIM:600643	TAS				P		HPO:skoehler	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0100523	OMIM:600643	TAS				P		HPO:skoehler	
OMIM	600643	CAROLI DISEASE, ISOLATED		HP:0410019	OMIM:600643	TAS				P		HPO:skoehler	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0000007	OMIM:600649	IEA				I		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001250	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001254	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001403	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001640	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001644	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001985	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0001987	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0002013	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0002240	OMIM:600649	IEA				P		HPO:iea	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0002910	PMID:1999498	PCS				P		HPO:probinson	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0003236	OMIM:600649	PCS				P		HPO:probinson	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0003593	OMIM:600649	PCS				C		HPO:probinson	
OMIM	600649	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE		HP:0005943	OMIM:600649	IEA				P		HPO:iea	
OMIM	600652	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4		HP:0000006	OMIM:600652	IEA				I		HPO:iea	
OMIM	600652	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 4		HP:0000408	OMIM:600652	IEA				P		HPO:iea	
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0000006	OMIM:600666	TAS				I		HPO:skoehler	
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0000113	OMIM:600666	IEA				P		HPO:iea	
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0000822	OMIM:600666	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0001407	OMIM:600666	TAS				P		HPO:skoehler	
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0001410	OMIM:600666	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0003828	OMIM:600666	TAS				C		HPO:skoehler	
OMIM	600666	POLYCYSTIC KIDNEY DISEASE 3		HP:0004944	OMIM:600666	TAS				P		HPO:skoehler	
OMIM	600668	CHONDROCALCINOSIS 1		HP:0000006	OMIM:600668	IEA				I		HPO:iea	
OMIM	600668	CHONDROCALCINOSIS 1		HP:0000934	OMIM:600668	IEA				P		HPO:iea	
OMIM	600668	CHONDROCALCINOSIS 1		HP:0002758	OMIM:600668	IEA				P		HPO:skoehler	
OMIM	600669	EPILEPSY, IDIOPATHIC GENERALIZED		HP:0000006	OMIM:600669	TAS				I		HPO:probinson	
OMIM	600669	EPILEPSY, IDIOPATHIC GENERALIZED		HP:0002069	OMIM:600669	TAS				P		HPO:skoehler	
OMIM	600669	EPILEPSY, IDIOPATHIC GENERALIZED		HP:0002121	OMIM:600669	TAS				P		HPO:probinson	
OMIM	600669	EPILEPSY, IDIOPATHIC GENERALIZED		HP:0002123	OMIM:600669	TAS				P		HPO:probinson	
OMIM	600669	EPILEPSY, IDIOPATHIC GENERALIZED		HP:0010849	OMIM:600669	TAS				P		HPO:probinson	
OMIM	600670	VARICELLA, SEVERE RECURRENT		HP:0000007	OMIM:600670	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600670	VARICELLA, SEVERE RECURRENT		HP:0005428	OMIM:600670	IEA				P		HPO:iea	
OMIM	600674	MICROTIA-ANOTIA		HP:0000006	OMIM:600674	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600674	MICROTIA-ANOTIA		HP:0001360	OMIM:600674	IEA				P		HPO:skoehler	
OMIM	600674	MICROTIA-ANOTIA		HP:0008551	OMIM:600674	IEA				P		HPO:skoehler	
OMIM	600674	MICROTIA-ANOTIA		HP:0009892	OMIM:600674	IEA				P		HPO:skoehler	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000006	OMIM:600679	IEA				I		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000316	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000431	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000458	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000738	OMIM:600679	TAS				P		HPO:skoehler	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000751	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0000951	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0001085	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0001742	OMIM:600679	TAS				P		HPO:skoehler	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0002015	OMIM:600679	IEA				P		HPO:skoehler	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0002357	OMIM:600679	IEA				P		HPO:skoehler	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0004411	OMIM:600679	IEA				P		HPO:iea	
OMIM	600679	DERMOID CYSTS, FAMILIAL FRONTONASAL		HP:0031951	OMIM:600679	IEA				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0000013	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0000141	OMIM:600705	IEA				P		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0001156	OMIM:600705	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600705	SATOYOSHI SYNDROME		HP:0001596	OMIM:600705	IEA				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0001763	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0002014	OMIM:600705	IEA				P		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0002024	OMIM:600705	IEA				P		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0002289	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0002857	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0003394	OMIM:600705	IEA				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0003712	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0003745	OMIM:600705	IEA				I		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0004322	OMIM:600705	IEA				P		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0008180	OMIM:600705	TAS				P		HPO:skoehler	
OMIM	600705	SATOYOSHI SYNDROME		HP:0009771	OMIM:600705	IEA				P		HPO:iea	
OMIM	600705	SATOYOSHI SYNDROME		HP:0010049	OMIM:600705	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600705	SATOYOSHI SYNDROME		HP:0010743	OMIM:600705	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600705	SATOYOSHI SYNDROME		HP:0012378	OMIM:600705	IEA				P		HPO:skoehler	
OMIM	600706	PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA		HP:0000006	OMIM:600706	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600706	PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA		HP:0003236	OMIM:600706	TAS				P		HPO:probinson	
OMIM	600706	PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA	HP:0012825	HP:0003701	OMIM:600706	TAS				P		HPO:probinson	
OMIM	600706	PROXIMAL MYOPATHY WITH FOCAL DEPLETION OF MITOCHONDRIA	HP:0012828	HP:0003738	OMIM:600706	TAS				P		HPO:probinson	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0000007	OMIM:600721	IEA				I		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0000256	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0000347	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001249	OMIM:600721	IEA				P		HPO:skoehler	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001250	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001252	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001263	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001290	OMIM:600721	TAS				P		HPO:skoehler	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001324	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001638	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0001659	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0002007	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0002104	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0002188	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0002416	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0002572	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0003150	OMIM:600721	IEA				P		HPO:skoehler	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0005348	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0006956	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0007052	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0007105	OMIM:600721	IEA				P		HPO:iea	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0011220	OMIM:600721	TAS				P		HPO:skoehler	
OMIM	600721	D-2-HYDROXYGLUTARIC ACIDURIA 1		HP:0012321	OMIM:600721	TAS				P		HPO:skoehler	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000006	OMIM:600736	IEA				I		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000286	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000316	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000358	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000426	OMIM:600736	TAS				P		HPO:probinson	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0000431	OMIM:600736	TAS				P		HPO:probinson	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0001169	OMIM:600736	TAS				P		HPO:probinson	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0001212	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0001611	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0001773	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0002705	OMIM:600736	TAS				P		HPO:skoehler	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0002750	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0004279	OMIM:600736	TAS				P		HPO:probinson	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0004322	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0005639	OMIM:600736	IEA				P		HPO:iea	
OMIM	600736	600736 VELOFACIOSKELETAL SYNDROME		HP:0009778	OMIM:600736	TAS				P		HPO:probinson	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0000006	OMIM:600740	TAS				I		HPO:skoehler	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0000083	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0000716	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0000787	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0000934	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0001012	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0001324	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0001733	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0002148	OMIM:600740	TAS				P		HPO:skoehler	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0002315	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0002653	OMIM:600740	TAS				P		HPO:skoehler	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0002749	OMIM:600740	TAS				P		HPO:skoehler	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0002918	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0003072	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0003127	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0003529	OMIM:600740	IEA				P		HPO:iea	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0004398	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0008200	OMIM:600740	IEA				P		HPO:skoehler	
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0008659	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600740	HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III		HP:0012378	OMIM:600740	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600757	OROFACIAL CLEFT 3		HP:0000006	OMIM:600757	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600757	OROFACIAL CLEFT 3		HP:0000271	OMIM:600757	IEA				P		HPO:iea	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0000007	OMIM:600771	TAS				I		HPO:nvasilevsky	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0000369	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0000400	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS	HP:0012825	HP:0000520	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0001419	OMIM:600771	TAS				I		HPO:nvasilevsky	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0002209	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0002213	OMIM:600771	TAS				P		HPO:nvasilevsky	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0003510	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0003683	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0004779	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600771	DWARFISM, FAMILIAL, WITH MUSCLE SPASMS		HP:0011964	OMIM:600771	TAS				P		HPO:probinson	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000006	OMIM:600775	TAS				I		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000256	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000272	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000278	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000316	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0000609	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0002007	OMIM:600775	IEA				P		HPO:iea	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0003196	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0004443	OMIM:600775	IEA				P		HPO:iea	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0005469	OMIM:600775	IEA				P		HPO:iea	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011220	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011325	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011326	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011327	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011755	OMIM:600775	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0011800	OMIM:600775	TAS				P		HPO:skoehler	
OMIM	600775	CRANIOSYNOSTOSIS 4; CRS4		HP:0031987	OMIM:600775	IEA				P		HPO:skoehler	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000007	OMIM:600776	IEA				I		HPO:iea	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000119	OMIM:600776	IEA				P		HPO:iea	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000400	OMIM:600776	TAS				P		HPO:skoehler	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000528	OMIM:600776	IEA				P		HPO:skoehler	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000568	OMIM:600776	IEA				P		HPO:skoehler	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000598	OMIM:600776	IEA				P		HPO:iea	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0000925	OMIM:600776	IEA				P		HPO:iea	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0002006	OMIM:600776	IEA				P		HPO:skoehler	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0002744	OMIM:600776	IEA				P		HPO:iea	
OMIM	600776	FRYNS MICROPHTHALMIA SYNDROME		HP:0045005	OMIM:600776	IEA				P		HPO:skoehler	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0001596	OMIM:600785	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002663	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002748	OMIM:600785	TAS				P		HPO:probinson	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002752	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002753	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002857	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002970	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002980	OMIM:600785	TAS				P		HPO:probinson	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0002982	OMIM:600785	TAS				P		HPO:probinson	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003013	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003025	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003152	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003155	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003165	OMIM:600785	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003593	OMIM:600785	TAS				C		HPO:probinson	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0003745	OMIM:600785	IEA				I		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0006462	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0006463	OMIM:600785	IEA				P		HPO:iea	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0010502	OMIM:600785	TAS				P		HPO:probinson	
OMIM	600785	VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR		HP:0030839	OMIM:600785	TAS				P		HPO:skoehler	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000006	OMIM:600790	TAS				I		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000505	OMIM:600790	TAS				P		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000533	OMIM:600790	TAS				P		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000541	OMIM:600790	TAS				P		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000545	OMIM:600790	TAS				P		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0000639	OMIM:600790	TAS				P		HPO:iea	
OMIM	600790	CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL		HP:0001135	OMIM:600790	TAS				P		HPO:iea	
OMIM	600791	ENLARGED VESTIBULAR AQUEDUCT		HP:0000007	OMIM:600791	TAS				I		HPO:probinson	
OMIM	600791	ENLARGED VESTIBULAR AQUEDUCT		HP:0000376	OMIM:600791	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600791	ENLARGED VESTIBULAR AQUEDUCT		HP:0000407	OMIM:600791	TAS				P		HPO:probinson	
OMIM	600791	ENLARGED VESTIBULAR AQUEDUCT		HP:0011387	OMIM:600791	TAS				P		HPO:skoehler	
OMIM	600792	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 5		HP:0000007	OMIM:600792	TAS				I		HPO:skoehler	
OMIM	600792	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 5		HP:0000407	OMIM:600792	TAS				P		HPO:skoehler	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0000006	OMIM:600794	IEA				I		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0001347	OMIM:600794	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0001761	OMIM:600794	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0001763	OMIM:600794	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0001765	OMIM:600794	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0002460	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003392	OMIM:600794	TAS				P		HPO:skoehler	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003393	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003426	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003427	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003435	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003484	OMIM:600794	IEA				P		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003674	OMIM:600794	IEA				C		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003677	OMIM:600794	IEA				C		HPO:iea	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0003693	OMIM:600794	TAS				P		HPO:probinson	
OMIM	600794	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA; HMN5A		HP:0009830	OMIM:600794	IEA				P		HPO:skoehler	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000006	OMIM:600795	IEA				I		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000020	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000710	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000711	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000718	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000719	OMIM:600795	IEA				P		HPO:skoehler	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000733	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000734	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000741	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000743	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000751	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0000757	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0001288	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0001332	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0001336	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0001347	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002063	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002120	OMIM:600795	TAS				P		HPO:probinson	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002145	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002300	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002310	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002354	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002371	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002442	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002446	OMIM:600795	IEA				P		HPO:iea	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0002529	OMIM:600795	IEA				P		HPO:skoehler	
OMIM	600795	FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3		HP:0003487	OMIM:600795	IEA				P		HPO:iea	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0000007	OMIM:600802	TAS				I		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0001287	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0001508	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0002014	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0002090	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0002733	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0002788	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0002965	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0003139	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0004430	OMIM:600802	IEA				P		HPO:skoehler	
OMIM	600802	#600802 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-NEGATIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-NEGATIVE		HP:0005214	OMIM:600802	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0000006	OMIM:600803	TAS				I		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0000007	OMIM:600803	TAS				I		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0000952	OMIM:600803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0001081	OMIM:600803	IEA				P		HPO:iea	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0001082	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0001395	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0001733	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0002910	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0003155	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0011980	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600803	#600803 GALLBLADDER DISEASE 1; GBD1;;CHOLELITHIASIS, LOW PHOSPHOLIPID-ASSOCIATED; LPAC		HP:0030151	OMIM:600803	TAS				P		HPO:skoehler	
OMIM	600807	ASTHMA, SUSCEPTIBILITY TO		HP:0000006	OMIM:600807	TAS				I		HPO:nvasilevsky	
OMIM	600807	ASTHMA, SUSCEPTIBILITY TO		HP:0001426	OMIM:600807	TAS				I		HPO:nvasilevsky	
OMIM	600807	ASTHMA, SUSCEPTIBILITY TO		HP:0002099	OMIM:600807	IEA				P		HPO:iea	
OMIM	600808	%600808 ENURESIS, NOCTURNAL, 2; ENUR2		HP:0000006	OMIM:600808	IEA				I		HPO:iea	
OMIM	600808	%600808 ENURESIS, NOCTURNAL, 2; ENUR2		HP:0001425	OMIM:600808	TAS				I		HPO:skoehler	
OMIM	600808	%600808 ENURESIS, NOCTURNAL, 2; ENUR2		HP:0010677	OMIM:600808	TAS				P		HPO:skoehler	
OMIM	600850	SCHIZOPHRENIA 4		HP:0000006	OMIM:600850	IEA				I		HPO:iea	
OMIM	600850	SCHIZOPHRENIA 4		HP:0001939	OMIM:600850	IEA				P		HPO:iea	
OMIM	600850	SCHIZOPHRENIA 4		HP:0100753	OMIM:600850	IEA				P		HPO:skoehler	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0000006	OMIM:600852	IEA				I		HPO:iea	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0000510	OMIM:600852	IEA				P		HPO:iea	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0000551	PMID:15563508	PCS				P		HPO:lccarmody	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0000613	PMID:15563508	PCS				P		HPO:lccarmody	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0000662	PMID:15563508	PCS	HP:0011462			P		HPO:lccarmody	
OMIM	600852	RETINITIS PIGMENTOSA 17		HP:0007737	PMID:15563508	PCS				P		HPO:lccarmody	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0000006	OMIM:600858	IEA				I		HPO:iea	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001425	OMIM:600858	TAS				I		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001639	OMIM:600858	IEA				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001670	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001678	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001688	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0001716	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0004309	OMIM:600858	IEA				P		HPO:iea	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0005110	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0011713	OMIM:600858	TAS				P		HPO:skoehler	
OMIM	600858	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6; CMH6		HP:0031318	OMIM:600858	IEA				P		HPO:skoehler	
OMIM	600880	BUDD-CHIARI SYNDROMEMEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA, INCLUDED		HP:0000007	OMIM:600880	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600880	BUDD-CHIARI SYNDROMEMEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA, INCLUDED		HP:0001394	OMIM:600880	IEA				P		HPO:iea	
OMIM	600880	BUDD-CHIARI SYNDROMEMEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA, INCLUDED		HP:0001402	OMIM:600880	IEA				P		HPO:iea	
OMIM	600880	BUDD-CHIARI SYNDROMEMEMBRANOUS OBSTRUCTION OF INFERIOR VENA CAVA, INCLUDED		HP:0002639	OMIM:600880	IEA				P		HPO:iea	
OMIM	600881	#600881 CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS		HP:0000006	OMIM:600881	TAS				I		HPO:skoehler	
OMIM	600881	#600881 CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS		HP:0000519	OMIM:600881	TAS				P		HPO:skoehler	
OMIM	600881	#600881 CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS		HP:0008031	OMIM:600881	TAS				P		HPO:skoehler	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0000006	OMIM:600882	IEA				I		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0000763	OMIM:600882	IEA				P		HPO:skoehler	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001265	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001284	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001761	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001763	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001765	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001810	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001868	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0001886	OMIM:600882	TAS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0002460	OMIM:600882	TAS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B	HP:0012825	HP:0002460	OMIM:600882	PCS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0003376	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0003378	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B	HP:0012825	HP:0003380	OMIM:600882	PCS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0003384	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B	HP:0012825	HP:0003431	OMIM:600882	PCS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0003474	OMIM:600882	IEA				P		HPO:skoehler	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0003693	OMIM:600882	TAS				P		HPO:probinson	
OMIM	600882	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B; CMT2B		HP:0009027	OMIM:600882	IEA				P		HPO:probinson	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0000006	OMIM:600884	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0001635	OMIM:600884	IEA				P		HPO:skoehler	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0001644	OMIM:600884	IEA				P		HPO:iea	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0002617	OMIM:600884	IEA				P		HPO:skoehler	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0004308	OMIM:600884	IEA				P		HPO:iea	
OMIM	600884	CARDIOMYOPATHY, DILATED, 1B; CMD1B		HP:0006670	OMIM:600884	IEA				P		HPO:iea	
OMIM	600886	#600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT;;HYPERFERRITINEMIA-CATARACT SYNDROME;;HYPERFERRITINEMIA, HEREDITARY, WITH CONGENITAL CATARACTS; HHCS		HP:0000006	PMID:15280904	PCS				I		HPO:iea	
OMIM	600886	#600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT;;HYPERFERRITINEMIA-CATARACT SYNDROME;;HYPERFERRITINEMIA, HEREDITARY, WITH CONGENITAL CATARACTS; HHCS		HP:0003281	PMID:15280904	PCS		HP:0040284		P		HPO:iea	7/7
OMIM	600886	#600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT;;HYPERFERRITINEMIA-CATARACT SYNDROME;;HYPERFERRITINEMIA, HEREDITARY, WITH CONGENITAL CATARACTS; HHCS		HP:0010693	OMIM:600886	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600886	#600886 HYPERFERRITINEMIA WITH OR WITHOUT CATARACT;;HYPERFERRITINEMIA-CATARACT SYNDROME;;HYPERFERRITINEMIA, HEREDITARY, WITH CONGENITAL CATARACTS; HHCS		HP:0100018	OMIM:600886	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000007	OMIM:600901	TAS				I		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000028	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000081	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000085	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000086	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000104	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000252	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000365	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000486	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000568	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000815	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000957	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0000978	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001000	OMIM:600901	TAS				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001017	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001249	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001263	OMIM:600901	TAS				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001518	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001627	OMIM:600901	TAS				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001873	OMIM:600901	TAS				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001875	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001876	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001896	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001903	OMIM:600901	TAS				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0001909	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0003213	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0003214	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0003221	OMIM:600901	IEA				P		HPO:skoehler	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0003974	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0004322	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0009777	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0009778	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0009943	OMIM:600901	IEA				P		HPO:iea	
OMIM	600901	FANCONI ANEMIA, COMPLEMENTATION GROUP E		HP:0030680	OMIM:600901	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000006	OMIM:600903	IEA				I		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000007	OMIM:600903	IEA				I		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000112	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000225	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000246	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000388	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000421	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0000964	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001287	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001873	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001878	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001888	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001891	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0001983	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002014	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002037	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002090	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002783	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002788	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002848	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002850	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002963	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0002971	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0003010	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0003212	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0003261	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0003565	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0005310	OMIM:600903	TAS				P		HPO:probinson	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0005537	OMIM:600903	IEA				P		HPO:iea	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0011944	OMIM:600903	TAS				P		HPO:probinson	
OMIM	600903	600903 WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM		HP:0040184	OMIM:600903	TAS				P		HPO:skoehler	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000007	OMIM:600906	IEA				I		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000194	OMIM:600906	IEA				P		HPO:skoehler	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000431	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000523	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000535	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000598	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000637	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000678	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000958	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY	HP:0012825	HP:0000966	OMIM:600906	TAS				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0000968	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0001249	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0001999	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0002119	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0002315	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0002410	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0003745	OMIM:600906	IEA				I		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0004691	OMIM:600906	TAS				P		HPO:skoehler	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0006097	OMIM:600906	TAS				P		HPO:skoehler	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0006358	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0007385	OMIM:600906	IEA				P		HPO:iea	
OMIM	600906	ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY		HP:0008401	OMIM:600906	IEA				P		HPO:iea	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0000523	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0000678	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0002119	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0002315	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0002410	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0003745	OMIM:600907	IEA				I		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0006297	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0006358	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600907	ENAMEL HYPOPLASIA, CATARACTS, AND AQUEDUCTAL STENOSIS		HP:0011094	OMIM:600907	IEA				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000007	OMIM:600908	IEA				I		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000013	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000104	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000218	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000377	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000444	OMIM:600908	IEA				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000470	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000490	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000527	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000601	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0000668	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001249	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001367	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001539	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001770	OMIM:600908	TAS				P		HPO:probinson	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001863	OMIM:600908	TAS				P		HPO:probinson	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0001999	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0002944	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0003186	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0003799	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0004322	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0004785	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0008633	OMIM:600908	IEA				P		HPO:iea	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0008807	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600908	KENNERKNECHT SYNDROME		HP:0012743	OMIM:600908	TAS				P		HPO:skoehler	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0000006	OMIM:600919	PCS				I		HPO:probinson	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0001279	OMIM:600919	PCS				P		HPO:probinson	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0001425	OMIM:600919	TAS				I		HPO:skoehler	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0001645	OMIM:600919	PCS				P		HPO:probinson	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0001657	OMIM:600919	PCS				P		HPO:probinson	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0001688	OMIM:600919	PCS				P		HPO:probinson	
OMIM	600919	CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED		HP:0005110	OMIM:600919	PCS				P		HPO:probinson	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000007	OMIM:600920	IEA				I		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000175	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000218	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000232	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000272	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000327	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000411	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000430	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000452	OMIM:600920	IEA				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000460	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000534	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000581	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000647	OMIM:600920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000678	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000767	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000883	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0000895	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001166	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001195	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001363	OMIM:600920	TAS				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001601	OMIM:600920	IEA				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001762	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001786	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001822	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001836	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0001847	OMIM:600920	TAS				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0002705	OMIM:600920	TAS				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0002980	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0002987	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0003031	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0003083	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0003100	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0005033	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0005280	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0006236	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0006380	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0006633	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0009473	OMIM:600920	IEA				P		HPO:iea	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0010307	OMIM:600920	IEA				P		HPO:skoehler	
OMIM	600920	VAN DEN ENDE-GUPTA SYNDROME; VDEGS		HP:0010493	OMIM:600920	TAS				P		HPO:probinson	
OMIM	600952	TRANSSEXUALITY		HP:0000707	OMIM:600952	IEA				P		HPO:iea	
OMIM	600952	TRANSSEXUALITY		HP:0030797	PMID:7477289	PCS				P		HPO:probinson	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0000044	OMIM:600955	IEA				P		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0000786	OMIM:600955	IEA				P		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0001513	OMIM:600955	TAS				P		HPO:probinson	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0002014	OMIM:600955	IEA				P		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0002024	OMIM:600955	IEA				P		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0003745	OMIM:600955	IEA				I		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0008163	OMIM:600955	IEA				P		HPO:iea	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0011473	OMIM:600955	TAS				P		HPO:skoehler	
OMIM	600955	#600955 PROPROTEIN CONVERTASE 1/3 DEFICIENCY;;OBESITY AND ENDOCRINOPATHY DUE TO IMPAIRED PROCESSING OF PROHORMONES		HP:0012051	OMIM:600955	TAS				P		HPO:probinson	
OMIM	600962	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC		HP:0000006	OMIM:600962	IEA				I		HPO:iea	
OMIM	600962	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC		HP:0007404	OMIM:600962	IEA				P		HPO:iea	
OMIM	600965	DEAFNESS, AUTOSOMAL DOMINANT 6		HP:0000006	OMIM:600965	IEA				I		HPO:iea	
OMIM	600965	DEAFNESS, AUTOSOMAL DOMINANT 6		HP:0000408	OMIM:600965	PCS				P		HPO:probinson	
OMIM	600965	DEAFNESS, AUTOSOMAL DOMINANT 6		HP:0008573	OMIM:600965	PCS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0000006	OMIM:600969	TAS				I		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0001384	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0001425	OMIM:600969	TAS				I		HPO:skoehler	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0002656	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0002663	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0002758	OMIM:600969	TAS				P		HPO:skoehler	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0003502	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0003701	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0008180	OMIM:600969	TAS				P		HPO:skoehler	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0010049	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0010582	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600969	EPIPHYSEAL DYSPLASIA, MULTIPLE, 3; EDM3		HP:0010585	OMIM:600969	TAS				P		HPO:probinson	
OMIM	600971	#600971 DEAFNESS, AUTOSOMAL RECESSIVE 6; DFNB6;;NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 6; NSRD6		HP:0000007	OMIM:600971	IEA				I		HPO:skoehler	
OMIM	600971	#600971 DEAFNESS, AUTOSOMAL RECESSIVE 6; DFNB6;;NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 6; NSRD6		HP:0000365	OMIM:600971	IEA	HP:0003577	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000007	OMIM:600972	IEA				I		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000023	OMIM:600972	TAS				P		HPO:skoehler	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000272	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000773	OMIM:600972	IEA				P		HPO:skoehler	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000774	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000946	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0000969	OMIM:600972	IEA				P		HPO:skoehler	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0001537	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0001561	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0001623	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0001789	OMIM:600972	TAS				P		HPO:skoehler	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0002093	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0002983	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0003270	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0003826	OMIM:600972	IEA				M		HPO:skoehler	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0004599	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0008921	OMIM:600972	IEA				P		HPO:iea	
OMIM	600972	#600972 ACHONDROGENESIS, TYPE IB; ACG1B;;ACHONDROGENESIS, FRACCARO TYPE		HP:0012368	OMIM:600972	TAS				P		HPO:skoehler	
OMIM	600974	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 7		HP:0000007	OMIM:600974	IEA				I		HPO:iea	
OMIM	600974	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 7		HP:0000407	OMIM:600974	TAS				P		HPO:probinson	
OMIM	600975	GLAUCOMA 3, PRIMARY INFANTILE, B		HP:0000007	OMIM:600975	IEA				I		HPO:iea	
OMIM	600975	GLAUCOMA 3, PRIMARY INFANTILE, B		HP:0008007	OMIM:600975	IEA				P		HPO:iea	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0000006	OMIM:600977	TAS				I		HPO:probinson	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0000548	OMIM:600977	IEA				P		HPO:skoehler	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0000551	OMIM:600977	TAS				P		HPO:probinson	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0000608	PMID:17377520	TAS				P		HPO:probinson	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0000613	OMIM:600977	TAS				P		HPO:probinson	
OMIM	600977	CONE-ROD DYSTROPHY 5		HP:0007663	OMIM:600977	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000006	OMIM:600987	IEA				I		HPO:iea	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000175	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000204	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000252	OMIM:600987	IEA				P		HPO:iea	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000341	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000490	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000582	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0000729	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001249	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001263	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001629	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001631	OMIM:600987	IEA				P		HPO:iea	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001680	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0001852	OMIM:600987	IEA				P		HPO:iea	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0002003	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0002020	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0002553	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0004322	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0004691	OMIM:600987	IEA				P		HPO:iea	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0009237	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0009536	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0009890	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0010055	OMIM:600987	TAS				P		HPO:probinson	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0010804	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0011230	OMIM:600987	IEA				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0011304	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0012725	OMIM:600987	IEA				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0025356	OMIM:600987	IEA				P		HPO:skoehler	
OMIM	600987	CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR		HP:0045075	OMIM:600987	TAS				P		HPO:skoehler	
OMIM	600989	INFUNDIBULOPELVIC DYSGENESIS		HP:0000003	OMIM:600989	IEA				P		HPO:iea	
OMIM	600989	INFUNDIBULOPELVIC DYSGENESIS		HP:0000006	OMIM:600989	IEA				I		HPO:iea	
OMIM	600989	INFUNDIBULOPELVIC DYSGENESIS		HP:0002027	OMIM:600989	IEA				P		HPO:iea	
OMIM	600989	INFUNDIBULOPELVIC DYSGENESIS		HP:0002907	OMIM:600989	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000006	OMIM:600991	TAS				I		HPO:nvasilevsky	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000218	OMIM:600991	TAS				P		HPO:skoehler	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000238	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000272	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000286	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000303	OMIM:600991	TAS				P		HPO:skoehler	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000316	OMIM:600991	TAS				P		HPO:skoehler	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000348	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000369	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000414	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000431	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000463	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000709	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0000912	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0001156	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0001249	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0001263	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0001423	OMIM:600991	TAS				I		HPO:nvasilevsky	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0001852	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0002194	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0002500	OMIM:600991	IEA				P		HPO:iea	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0002751	OMIM:600991	TAS				P		HPO:skoehler	
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0005280	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0006297	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600991	HYDROCEPHALUS, SKELETAL ANOMALIES, AND MENTAL DISTURBANCE		HP:0100702	OMIM:600991	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	600994	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 5		HP:0000006	OMIM:600994	TAS				I		HPO:skoehler	
OMIM	600994	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 5		HP:0000408	OMIM:600994	TAS				P		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0000007	OMIM:600995	TAS				I		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0000093	OMIM:600995	TAS				P		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0000097	OMIM:600995	TAS				P		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0000100	OMIM:600995	IEA				P		HPO:iea	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0000969	OMIM:600995	IEA				P		HPO:iea	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003073	OMIM:600995	IEA				P		HPO:iea	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003077	OMIM:600995	IEA				P		HPO:iea	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003621	OMIM:600995	IEA				C		HPO:iea	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003678	OMIM:600995	TAS				C		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003774	OMIM:600995	TAS				P		HPO:skoehler	
OMIM	600995	#600995 NEPHROTIC SYNDROME, TYPE 2; NPHS2;;NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE; SRN1		HP:0003828	OMIM:600995	TAS				C		HPO:skoehler	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0000006	OMIM:600996	TAS				I		HPO:skoehler	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0001699	OMIM:600996	TAS				M		HPO:skoehler	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0004308	OMIM:600996	TAS				P		HPO:skoehler	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0004758	OMIM:600996	IEA				P		HPO:iea	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0006698	OMIM:600996	IEA				P		HPO:iea	
OMIM	600996	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2		HP:0011663	PMID:8589694	PCS				P		HPO:probinson	
OMIM	601001	#601001 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:601001	IEA				I		HPO:skoehler	
OMIM	601001	#601001 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE		HP:0001805	OMIM:601001	IEA				P		HPO:skoehler	
OMIM	601001	#601001 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE		HP:0001807	OMIM:601001	TAS				P		HPO:skoehler	
OMIM	601001	#601001 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:601001	IEA				C		HPO:skoehler	
OMIM	601001	#601001 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE		HP:0003828	OMIM:601001	IEA				C		HPO:skoehler	
OMIM	601003	BRODY MYOPATHY		HP:0000007	OMIM:601003	TAS				I		HPO:probinson	
OMIM	601003	BRODY MYOPATHY		HP:0003394	OMIM:601003	TAS				P		HPO:probinson	
OMIM	601004	PORTAL VEIN, CAVERNOUS TRANSFORMATION OF		HP:0000006	OMIM:601004	TAS				I		HPO:probinson	
OMIM	601004	PORTAL VEIN, CAVERNOUS TRANSFORMATION OF		HP:0004941	OMIM:601004	TAS				P		HPO:probinson	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000006	OMIM:601005	TAS				I		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000219	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000311	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000691	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000717	OMIM:601005	IEA				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0000821	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001159	OMIM:601005	IEA				P		HPO:iea	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001249	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001250	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001263	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001290	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001629	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001636	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001640	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001643	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001655	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001657	OMIM:601005	IEA				P		HPO:iea	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001662	OMIM:601005	IEA				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001699	OMIM:601005	IEA				M		HPO:iea	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0001943	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0002090	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0002719	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0002901	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0005280	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0012387	OMIM:601005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601005	TIMOTHY SYNDROME; TS		HP:0012725	OMIM:601005	TAS				P		HPO:skoehler	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000007	OMIM:601016	IEA				I		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000062	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000175	OMIM:601016	TAS				P		HPO:probinson	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000204	OMIM:601016	TAS				P		HPO:probinson	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000457	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000601	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0000830	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0002983	OMIM:601016	TAS				P		HPO:skoehler	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0006989	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0009473	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0009826	OMIM:601016	IEA				P		HPO:iea	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0010557	OMIM:601016	IEA				P		HPO:skoehler	
OMIM	601016	601016 MIDLINE MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM;;DINCSOY SYNDROME		HP:0012385	OMIM:601016	TAS				P		HPO:skoehler	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0000007	OMIM:601027	IEA				I		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0000204	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0000765	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0001762	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0001830	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0001830	OMIM:601027	TAS				P		HPO:probinson	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0001841	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0001841	OMIM:601027	TAS				P		HPO:probinson	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0002190	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0002986	OMIM:601027	TAS				P		HPO:skoehler	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0005772	OMIM:601027	TAS				P		HPO:skoehler	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0007291	OMIM:601027	IEA				P		HPO:iea	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0008986	OMIM:601027	TAS				P		HPO:skoehler	
OMIM	601027	TIBIA, ABSENCE OR HYPOPLASIA OF, WITH POLYDACTYLY, RETROCEREBELLAR ARACHNOID CYST, AND OTHER ANOMALIES		HP:0100702	OMIM:601027	TAS				P		HPO:skoehler	
OMIM	601039	ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN		HP:0000007	OMIM:601039	IEA				I		HPO:iea	
OMIM	601039	ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN		HP:0001249	OMIM:601039	IEA				P		HPO:iea	
OMIM	601039	ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN		HP:0007503	OMIM:601039	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0000006	OMIM:601042	IEA				I		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0000651	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0001258	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0001260	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0001266	OMIM:601042	TAS				P		HPO:skoehler	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0001332	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0001347	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0002062	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0002076	OMIM:601042	TAS				P		HPO:skoehler	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0002131	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0002315	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0003401	OMIM:601042	IEA				P		HPO:iea	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0007256	OMIM:601042	TAS				P		HPO:skoehler	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0100543	OMIM:601042	TAS				P		HPO:skoehler	
OMIM	601042	#601042 DYSTONIA 9; DYT9;;CHOREOATHETOSIS/SPASTICITY, EPISODIC;;CSE CHOREOATHETOSIS, PAROXYSMAL, WITH EPISODIC ATAXIA;;CHOREOATHETOSIS, KINESIGENIC, WITH EPISODIC ATAXIA AND SPASTICITY		HP:0100660	OMIM:601042	TAS				P		HPO:skoehler	
OMIM	601067	USHER SYNDROME, TYPE ID		HP:0000007	OMIM:601067	TAS				I		HPO:probinson	
OMIM	601067	USHER SYNDROME, TYPE ID	HP:0012829	HP:0000365	OMIM:601067	TAS	HP:0003577			P		HPO:probinson	
OMIM	601067	USHER SYNDROME, TYPE ID		HP:0000510	OMIM:601067	TAS				P		HPO:probinson	
OMIM	601067	USHER SYNDROME, TYPE ID		HP:0001751	OMIM:601067	TAS				P		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0000006	OMIM:601068	TAS				I		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001249	OMIM:601068	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001312	OMIM:601068	TAS				P		HPO:iea	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001326	OMIM:601068	TAS				P		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001337	OMIM:601068	TAS				P		HPO:iea	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001340	OMIM:601068	TAS				P		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001351	OMIM:601068	IEA				P		HPO:iea	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0001425	OMIM:601068	TAS				I		HPO:skoehler	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0002069	OMIM:601068	TAS				P		HPO:iea	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0002123	OMIM:601068	TAS				P		HPO:iea	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0003581	OMIM:601068	TAS				C		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0003680	OMIM:601068	TAS				C		HPO:probinson	
OMIM	601068	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 1; FAME1		HP:0010852	OMIM:601068	TAS				P		HPO:probinson	
OMIM	601071	DEAFNESS, AUTOSOMAL RECESSIVE 9		HP:0000007	OMIM:601071	TAS				I		HPO:skoehler	
OMIM	601071	DEAFNESS, AUTOSOMAL RECESSIVE 9		HP:0000407	OMIM:601071	TAS				P		HPO:skoehler	
OMIM	601071	DEAFNESS, AUTOSOMAL RECESSIVE 9		HP:0004463	OMIM:601071	TAS				P		HPO:skoehler	
OMIM	601071	DEAFNESS, AUTOSOMAL RECESSIVE 9		HP:0008529	OMIM:601071	TAS				P		HPO:skoehler	
OMIM	601072	DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8		HP:0000007	OMIM:601072	TAS				I		HPO:probinson	
OMIM	601072	DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8		HP:0000407	OMIM:601072	TAS				P		HPO:skoehler	
OMIM	601072	DEAFNESS, CHILDHOOD-ONSET NEUROSENSORY, AUTOSOMAL RECESSIVE 8		HP:0011463	OMIM:601072	TAS				C		HPO:probinson	
OMIM	601075	APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION		HP:0000007	OMIM:601075	IEA				I		HPO:iea	
OMIM	601075	APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION		HP:0006934	OMIM:601075	IEA				P		HPO:iea	
OMIM	601075	APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION		HP:0007536	OMIM:601075	IEA				P		HPO:iea	
OMIM	601075	APLASIA CUTIS CONGENITA, HIGH MYOPIA, AND CONE-ROD DYSFUNCTION		HP:0011003	OMIM:601075	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000013	OMIM:601076	IEA				P		HPO:skoehler	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000027	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000086	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000122	OMIM:601076	IEA				P		HPO:skoehler	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000175	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000204	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000324	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000347	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000405	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000772	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000813	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000912	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0000925	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0002350	OMIM:601076	IEA				P		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0003745	OMIM:601076	IEA				I		HPO:iea	
OMIM	601076	MULLERIAN DUCT APLASIA, UNILATERAL RENAL AGENESIS, AND CERVICOTHORACICSOMITE ANOMALIES		HP:0004322	OMIM:601076	IEA				P		HPO:iea	
OMIM	601086	LATERALITY DEFECTS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:601086	IEA				I		HPO:iea	
OMIM	601086	LATERALITY DEFECTS, AUTOSOMAL DOMINANT		HP:0001507	OMIM:601086	IEA				P		HPO:iea	
OMIM	601086	LATERALITY DEFECTS, AUTOSOMAL DOMINANT		HP:0001696	OMIM:601086	IEA				P		HPO:iea	
OMIM	601086	LATERALITY DEFECTS, AUTOSOMAL DOMINANT		HP:0001746	OMIM:601086	IEA				P		HPO:iea	
OMIM	601086	LATERALITY DEFECTS, AUTOSOMAL DOMINANT		HP:0030853	OMIM:601086	TAS				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000006	PMID:30160832	PCS				I		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000160	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	10/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000164	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	6/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000219	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	10/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000248	OMIM:601088	IEA				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000270	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000272	OMIM:601088	IEA				P		HPO:iea	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000289	OMIM:601088	TAS				P		HPO:probinson	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000303	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000316	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	9/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000319	OMIM:601088	TAS				P		HPO:probinson	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000343	PMID:30160832	PCS		HP:0040284		P		HPO:probinson	11/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000348	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	11/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000358	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000365	PMID:30160832	PCS		HP:0040284		P		HP:probinson	15/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000369	OMIM:601088	TAS				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000407	OMIM:601088	IEA				P		HPO:iea	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000431	OMIM:601088	TAS				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000494	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000508	OMIM:601088	TAS				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000519	PMID:30160832	PCS		HP:0040284		P		HPO:iea	14/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000582	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0000767	PMID:30160832	PCS		HP:0040284		P		HP:probinson	3/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0001156	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	12/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0001182	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0001249	PMID:30160832	PCS		HP:0040284		P		HPO:iea	15/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0001250	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	8/10
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0001701	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	6/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0002059	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0002209	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0002974	OMIM:601088	IEA				P		HPO:iea	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0003196	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	13/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0004322	OMIM:601088	IEA	HP:0003593			P		HPO:iea	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0004484	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0005280	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	11/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0007099	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0008404	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0008551	OMIM:601088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0011229	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	8/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0011800	PMID:30160832	PCS		HP:0040284		P		HPO:skoehler	15/15
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0012368	OMIM:601088	TAS				P		HPO:skoehler	
OMIM	601088	AYME-GRIPP SYNDROME; AYGRP		HP:0012385	PMID:30160832	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601095	601095 HARROD SYNDROME		HP:0000007	OMIM:601095	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601095	601095 HARROD SYNDROME		HP:0000028	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000047	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000160	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000218	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000307	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000400	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000601	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0000689	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0001166	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0001249	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0001508	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0001999	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0002021	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0002251	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0002619	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0002705	OMIM:601095	TAS				P		HPO:skoehler	
OMIM	601095	601095 HARROD SYNDROME		HP:0003189	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0003241	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0004734	OMIM:601095	IEA				P		HPO:iea	
OMIM	601095	601095 HARROD SYNDROME		HP:0004794	OMIM:601095	TAS				P		HPO:skoehler	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0000470	OMIM:601096	IEA				P		HPO:iea	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0000774	OMIM:601096	TAS				P		HPO:skoehler	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0001156	OMIM:601096	IEA				P		HPO:iea	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0001249	OMIM:601096	IEA				P		HPO:iea	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0002651	OMIM:601096	TAS				P		HPO:skoehler	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0003422	OMIM:601096	IEA				P		HPO:iea	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0008873	OMIM:601096	IEA				P		HPO:iea	
OMIM	601096	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MICROMELIC		HP:0100255	OMIM:601096	IEA				P		HPO:iea	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0000006	OMIM:601098	TAS				I		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0001265	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0001425	OMIM:601098	TAS				I		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0001761	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0002460	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0002936	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003382	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003383	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003431	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003481	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003621	OMIM:601098	TAS				C		HPO:skoehler	
OMIM	601098	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1C; CMT1C		HP:0003693	OMIM:601098	TAS				P		HPO:skoehler	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000006	OMIM:601104	IEA				I		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000605	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000613	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000622	OMIM:601104	TAS				P		HPO:skoehler	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000651	OMIM:601104	PCS				P		HPO:probinson	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000658	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000737	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000741	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0000743	OMIM:601104	PCS		HP:0040284		P		HPO:probinson	45%
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0001260	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0001300	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0001337	OMIM:601104	PCS		HP:0040284		P		HPO:probinson	30%
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0001425	OMIM:601104	TAS				I		HPO:skoehler	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002015	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002063	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002067	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002141	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002171	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002185	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002300	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002304	OMIM:601104	PCS				P		HPO:probinson	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002354	OMIM:601104	PCS				P		HPO:probinson	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002439	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002451	OMIM:601104	PCS		HP:0040284		P		HPO:probinson	18%
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002527	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002528	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002529	OMIM:601104	PCS				P		HPO:probinson	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002530	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0002544	OMIM:601104	IEA				P		HPO:iea	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0003581	OMIM:601104	PCS				C		HPO:probinson	
OMIM	601104	SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1		HP:0200147	OMIM:601104	IEA				P		HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000007	OMIM:601110	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000193	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000218	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000252	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000286	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000400	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000414	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000431	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:probinson	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000486	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000612	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000648	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0000654	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001141	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001181	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001250	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001263	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001272	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001276	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001347	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001508	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001762	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001792	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:probinson	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0001864	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002013	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002014	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002059	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002164	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:probinson	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002521	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0002804	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0003642	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0005280	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:probinson	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0008936	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0009473	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:iea	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0011473	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0012537	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0025356	OMIM:601110	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0030084	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:skoehler	
OMIM	601110	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id; CDG1D		HP:0100807	OMIM:601110	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE ID; CDG1D	HPO:probinson	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0000007	OMIM:601127	IEA				I		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0000271	OMIM:601127	IEA				P		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001249	OMIM:601127	IEA				P		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001508	OMIM:601127	IEA				P		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001629	OMIM:601127	IEA				P		HPO:skoehler	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001636	OMIM:601127	IEA				P		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001642	OMIM:601127	IEA				P		HPO:iea	
OMIM	601127	FALLOT COMPLEX WITH SEVERE MENTAL AND GROWTH RETARDATION		HP:0001719	OMIM:601127	IEA				P		HPO:iea	
OMIM	601144	BRUGADA SYNDROME 1; BRGDA1		HP:0000006	OMIM:601144	IEA				I		HPO:iea	
OMIM	601144	BRUGADA SYNDROME 1; BRGDA1		HP:0001663	OMIM:601144	IEA				P		HPO:iea	
OMIM	601144	BRUGADA SYNDROME 1; BRGDA1		HP:0001695	OMIM:601144	IEA				P		HPO:iea	
OMIM	601144	BRUGADA SYNDROME 1; BRGDA1		HP:0001699	OMIM:601144	IEA				M		HPO:iea	
OMIM	601144	BRUGADA SYNDROME 1; BRGDA1		HP:0011712	OMIM:601144	IEA				P		HPO:skoehler	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000006	OMIM:601152	IEA				I		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000007	OMIM:601152	TAS				I		HPO:skoehler	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000360	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000458	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000543	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000551	OMIM:601152	TAS				P		HPO:skoehler	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000603	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000641	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000648	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0000649	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0001265	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0001284	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0001604	OMIM:601152	IEA				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0001761	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0002403	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0002460	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0002650	OMIM:601152	TAS				P		HPO:skoehler	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0002936	OMIM:601152	TAS				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0002938	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003376	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003378	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003378	OMIM:601152	TAS				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003409	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6	HP:0012825	HP:0003431	OMIM:601152	IEA				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003593	OMIM:601152	TAS				C		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003690	OMIM:601152	TAS				P		HPO:skoehler	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003693	OMIM:601152	IEA				P		HPO:iea	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003693	OMIM:601152	TAS				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0003701	OMIM:601152	IEA				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0007924	OMIM:601152	IEA				P		HPO:probinson	
OMIM	601152	#601152 HEREDITARY MOTOR AND SENSORY NEUROPATHY VI;;HMSN6;;HMSN VI;;PERIPHERAL NEUROPATHY AND OPTIC ATROPHY;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6		HP:0008587	OMIM:601152	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0000006	OMIM:601154	IEA				I		HPO:iea	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0001279	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0001297	OMIM:601154	IEA				P		HPO:iea	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0001644	OMIM:601154	IEA				P		HPO:iea	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0001678	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0001962	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0004749	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0004755	OMIM:601154	IEA				P		HPO:iea	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0005110	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0006673	OMIM:601154	IEA				P		HPO:iea	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0006682	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0006699	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0011712	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0011713	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601154	CARDIOMYOPATHY, DILATED, 1E		HP:0025478	OMIM:601154	TAS				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0000007	OMIM:601160	IEA				I		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0001274	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0001561	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0001939	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0001989	OMIM:601160	TAS				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002089	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002089	OMIM:601160	TAS				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002304	OMIM:601160	IEA				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002335	OMIM:601160	TAS				P		HPO:probinson	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002365	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002529	OMIM:601160	IEA				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002804	OMIM:601160	IEA				P		HPO:iea	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0002804	OMIM:601160	TAS				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0007009	OMIM:601160	IEA				P		HPO:skoehler	
OMIM	601160	LISSENCEPHALY TYPE III AND BONE DYSPLASIA		HP:0045028	OMIM:601160	IEA				P		HPO:skoehler	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000007	OMIM:601161	IEA				I		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000347	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000369	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000377	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000384	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000431	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000506	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0000581	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0001939	OMIM:601161	IEA				P		HPO:iea	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0030680	OMIM:601161	IEA				P		HPO:skoehler	
OMIM	601161	TRISOMY 18-LIKE SYNDROME		HP:0045025	OMIM:601161	IEA				P		HPO:skoehler	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0000006	OMIM:601162	IEA				I		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0000012	OMIM:601162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0000020	OMIM:601162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0000518	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0000639	OMIM:601162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001258	OMIM:601162	TAS				P		HPO:probinson	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001260	OMIM:601162	TAS				P		HPO:skoehler	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001288	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001317	OMIM:601162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001328	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001347	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001498	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0001761	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002013	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002020	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002036	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002061	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002127	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002495	OMIM:601162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002644	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0002750	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0003487	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0003677	OMIM:601162	TAS				C		HPO:skoehler	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0003700	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0003743	OMIM:601162	IEA				I		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0004322	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0007178	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0007299	OMIM:601162	IEA				P		HPO:iea	
OMIM	601162	SPASTIC PARAPLEGIA 9A, AUTOSOMAL DOMINANT; SPG9A		HP:0007340	OMIM:601162	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000007	OMIM:601163	TAS				I		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000029	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL	HP:0012825	HP:0000316	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000369	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000463	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000775	OMIM:601163	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0000776	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0001159	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0001539	OMIM:601163	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0001770	OMIM:601163	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0002089	OMIM:601163	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0002566	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0004209	OMIM:601163	TAS				P		HPO:skoehler	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0004331	OMIM:601163	IEA				P		HPO:iea	
OMIM	601163	DIAPHRAGMATIC DEFECTS, LIMB DEFICIENCIES, AND OSSIFICATION DEFECTS OF SKULL		HP:0009827	OMIM:601163	IEA				P		HPO:skoehler	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0000007	OMIM:601165	IEA				I		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0000157	OMIM:601165	TAS				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0000204	OMIM:601165	TAS				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0000272	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0000316	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0001169	OMIM:601165	TAS				P		HPO:probinson	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0001520	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0002566	OMIM:601165	TAS				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0002744	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0003271	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0004279	OMIM:601165	TAS				P		HPO:probinson	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0004510	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0005469	OMIM:601165	IEA				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0005922	OMIM:601165	TAS				P		HPO:probinson	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0009944	OMIM:601165	TAS				P		HPO:iea	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0012368	OMIM:601165	TAS				P		HPO:skoehler	
OMIM	601165	601165 CLEFT LIP/PALATE WITH CHARACTERISTIC FACIES, INTESTINAL MALROTATION,AND LETHAL CONGENITAL HEART DISEASE		HP:0030680	OMIM:601165	IEA				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0000007	OMIM:601170	PCS				I		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0001272	OMIM:601170	TAS				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0002059	OMIM:601170	TAS				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0002119	OMIM:601170	PCS				P		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003324	OMIM:601170	IEA				P		HPO:iea	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003327	OMIM:601170	TAS				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003429	OMIM:601170	TAS				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003431	OMIM:601170	IEA				P		HPO:iea	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003458	OMIM:601170	PCS				P		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003593	OMIM:601170	PCS				C		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003690	OMIM:601170	TAS				P		HPO:skoehler	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0003741	OMIM:601170	IEA				P		HPO:iea	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0006808	OMIM:601170	PCS				P		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0010628	OMIM:601170	IEA				P		HPO:iea	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0011344	OMIM:601170	PCS				P		HPO:probinson	
OMIM	601170	MUSCULAR DYSTROPHY, CONGENITAL, WITH SEVERE CENTRAL NERVOUS SYSTEM ATROPHY AND ABSENCE OF LARGE MYELINATED FIBERS		HP:0025356	OMIM:601170	IEA				P		HPO:skoehler	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000007	OMIM:601186	TAS				I		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000013	OMIM:601186	TAS				P		HPO:probinson	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000023	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000028	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000085	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000089	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000125	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000126	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000347	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000369	OMIM:601186	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000431	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000528	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000581	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000776	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0000813	OMIM:601186	TAS				P		HPO:probinson	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001252	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001290	OMIM:601186	TAS				P		HPO:skoehler	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001511	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001629	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001631	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001636	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001642	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001643	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001660	OMIM:601186	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001680	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0001750	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0002089	OMIM:601186	TAS				P		HPO:probinson	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0002093	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0002187	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0002627	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0004322	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0004712	OMIM:601186	TAS				P		HPO:probinson	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0004935	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0005156	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0005311	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0005944	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0006270	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0007633	OMIM:601186	IEA				P		HPO:iea	
OMIM	601186	MICROPHTHALMIA, SYNDROMIC 9		HP:0009110	OMIM:601186	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0000007	OMIM:601187	IEA				I		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0001249	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0001250	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0002652	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0002750	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0002866	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0003274	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0004322	OMIM:601187	IEA				P		HPO:iea	
OMIM	601187	GURRIERI SYNDROME		HP:0005638	OMIM:601187	IEA				P		HPO:iea	
OMIM	601195	601195 IRON OVERLOAD IN AFRICA;;AFRICAN IRON OVERLOAD;;BANTU SIDEROSIS		HP:0000006	OMIM:601195	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601195	601195 IRON OVERLOAD IN AFRICA;;AFRICAN IRON OVERLOAD;;BANTU SIDEROSIS		HP:0001939	OMIM:601195	IEA				P		HPO:iea	
OMIM	601195	601195 IRON OVERLOAD IN AFRICA;;AFRICAN IRON OVERLOAD;;BANTU SIDEROSIS		HP:0012463	OMIM:601195	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0000006	OMIM:601198	TAS				I		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0000121	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0000787	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0000848	OMIM:601198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0001250	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0001281	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0002135	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0002150	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0002900	OMIM:601198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0002901	OMIM:601198	IEA				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0002917	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0003394	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0003401	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0004322	OMIM:601198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0012211	OMIM:601198	TAS				P		HPO:skoehler	
OMIM	601198	HYPOCALCEMIA, AUTOSOMAL DOMINANT 1		HP:0025425	OMIM:601198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601200	PLEUROPULMONARY BLASTOMA		HP:0000006	PMID:19556464,OMIM:601200	TAS				I		HPO:skoehler	
OMIM	601200	PLEUROPULMONARY BLASTOMA		HP:0002859	PMID:19556464	PCS				P		HPO:skoehler	
OMIM	601200	PLEUROPULMONARY BLASTOMA		HP:0002885	PMID:21266384	TAS		HP:0040284		P		HPO:skoehler	1/86
OMIM	601200	PLEUROPULMONARY BLASTOMA		HP:0100528	PMID:21266384	PCS	HP:0011463	HP:0040284		P		HPO:skoehler	11/14
OMIM	601202	CATARACT, ANTERIOR POLAR, 2		HP:0000006	PMID:8852669	PCS				I		HPO:lccarmody	
OMIM	601202	CATARACT, ANTERIOR POLAR, 2		HP:0000646	PMID:8852669	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	16/17
OMIM	601202	CATARACT, ANTERIOR POLAR, 2		HP:0001134	PMID:8852669	PCS	HP:0003593	HP:0040284		P		HPO:lccarmody	17/17
OMIM	601214	NAXOS DISEASE		HP:0000007	OMIM:601214	IEA				I		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0000535	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601214	NAXOS DISEASE		HP:0000982	OMIM:601214	IEA				P		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0000982	PMID:11691526	PCS	HP:0003577	HP:0040284		P		HPO:probinson	28/28
OMIM	601214	NAXOS DISEASE		HP:0001030	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601214	NAXOS DISEASE		HP:0001279	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	15/26
OMIM	601214	NAXOS DISEASE		HP:0001635	PMID:11691526	PCS				P		HPO:probinson	
OMIM	601214	NAXOS DISEASE		HP:0001640	OMIM:601214	IEA				P		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0001644	OMIM:601214	IEA				P		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0001645	PMID:11691526	PCS				P		HPO:probinson	
OMIM	601214	NAXOS DISEASE		HP:0001699	OMIM:601214	IEA				M		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0001806	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601214	NAXOS DISEASE		HP:0001962	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	2/26
OMIM	601214	NAXOS DISEASE		HP:0002212	OMIM:601214	IEA				P		HPO:iea	
OMIM	601214	NAXOS DISEASE		HP:0002224	PMID:11691526	PCS	HP:0003577	HP:0040284		P		HPO:probinson	28/28
OMIM	601214	NAXOS DISEASE		HP:0004751	PMID:11691526	PCS				P		HPO:probinson	
OMIM	601214	NAXOS DISEASE		HP:0006677	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	19/26
OMIM	601214	NAXOS DISEASE		HP:0006682	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	24/26
OMIM	601214	NAXOS DISEASE		HP:0008404	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601214	NAXOS DISEASE		HP:0010872	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	20/26
OMIM	601214	NAXOS DISEASE		HP:0011663	PMID:11691526	PCS				P		HPO:probinson	
OMIM	601214	NAXOS DISEASE		HP:0011712	PMID:11691526	PCS				P		HPO:probinson	
OMIM	601214	NAXOS DISEASE		HP:0025092	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601214	NAXOS DISEASE		HP:0031193	PMID:11691526	PCS		HP:0040284		P		HPO:probinson	23/26
OMIM	601214	NAXOS DISEASE		HP:0100792	OMIM:601214	TAS				P		HPO:skoehler	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000007	OMIM:601216	IEA				I		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000303	OMIM:601216	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000327	OMIM:601216	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000677	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000687	OMIM:601216	TAS				P		HPO:skoehler	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000691	OMIM:601216	TAS				P		HPO:skoehler	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000705	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000926	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0000998	OMIM:601216	TAS				P		HPO:skoehler	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0001634	OMIM:601216	TAS				P		HPO:skoehler	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0002750	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0002945	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0004322	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0008441	OMIM:601216	IEA				P		HPO:iea	
OMIM	601216	DENTAL ANOMALIES AND SHORT STATURE; DASS		HP:0008450	OMIM:601216	IEA				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0000007	OMIM:601217	TAS				I		HPO:nvasilevsky	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0000054	OMIM:601217	TAS				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0000815	OMIM:601217	IEA				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0001256	OMIM:601217	IEA				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0001419	OMIM:601217	TAS				I		HPO:nvasilevsky	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0001596	OMIM:601217	IEA				P		HPO:skoehler	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0001939	OMIM:601217	IEA				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0002069	OMIM:601217	TAS				P		HPO:skoehler	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0002224	OMIM:601217	TAS	HP:0003621			P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0008734	OMIM:601217	TAS				P		HPO:iea	
OMIM	601217	ALOPECIA-MENTAL RETARDATION SYNDROME WITH CONVULSIONS AND HYPERGONADOTROPICHYPOGONADISM		HP:0040149	OMIM:601217	IEA				P		HPO:skoehler	
OMIM	601220	601220 OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH		HP:0000007	OMIM:601220	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601220	601220 OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH		HP:0000939	OMIM:601220	IEA				P		HPO:probinson	
OMIM	601220	601220 OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH		HP:0001010	OMIM:601220	TAS				P		HPO:probinson	
OMIM	601220	601220 OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH		HP:0001107	OMIM:601220	TAS				P		HPO:probinson	
OMIM	601220	601220 OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH		HP:0040160	OMIM:601220	TAS				P		HPO:skoehler	
OMIM	601223	NEURONAL INTESTINAL DYSPLASIA, TYPE B		HP:0000006	OMIM:601223	IEA				I		HPO:iea	
OMIM	601223	NEURONAL INTESTINAL DYSPLASIA, TYPE B		HP:0001939	OMIM:601223	IEA				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000054	PMID:8644736	PCS		HP:0040284		P		HPO:iea	5/6
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000248	PMID:8644736	PCS		HP:0040284		P		HPO:iea	6/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000262	OMIM:601224	TAS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000286	PMID:8644736	PCS		HP:0040284		P		HPO:iea	4/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000322	PMID:15852040	PCS		HP:0040284		P		HPO:iea	6/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000337	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000348	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000430	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000431	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000494	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000506	PMID:8644736	PCS		HP:0040284		P		HPO:iea	4/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0000954	PMID:8644736	PCS		HP:0040284		P		HPO:iea	5/6
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0001156	PMID:15852040	PCS		HP:0040284		P		HPO:iea	5/8
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0001249	PMID:8644736	PCS		HP:0040284		P		HPO:iea	7/10
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0001250	PMID:8644736	PCS		HP:0040284		P		HPO:iea	2/11
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0001252	PMID:8644736	PCS		HP:0040284		P		HPO:iea	5/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0001466	OMIM:601224	TAS				I		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0002645	PMID:8644736	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0002697	PMID:8644736	PCS		HP:0040284		P		HPO:iea	9/11
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0002714	PMID:15852040	PCS		HP:0040284		P		HPO:iea	8/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0002762	PMID:8644736	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0003196	PMID:8644736	PCS				P		HPO:iea	
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0004439	PMID:8644736	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0005338	PMID:15852040	PCS		HP:0040284		P		HPO:iea	6/9
OMIM	601224	POTOCKI-SHAFFER SYNDROME		HP:0005650	OMIM:601224	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	601228	POLYPOSIS SYNDROME, HEREDITARY MIXED, 1		HP:0000006	OMIM:601228	IEA				I		HPO:iea	
OMIM	601228	POLYPOSIS SYNDROME, HEREDITARY MIXED, 1		HP:0001438	OMIM:601228	IEA				P		HPO:iea	
OMIM	601230	DERMATITIS HERPETIFORMIS, FAMILIAL		HP:0000006	OMIM:601230	TAS				I		HPO:iea	
OMIM	601230	DERMATITIS HERPETIFORMIS, FAMILIAL		HP:0000989	PMID:24068131	PCS				P		HPO:skoehler	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0000007	OMIM:601238	IEA				I		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0000639	OMIM:601238	IEA				P		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0001252	OMIM:601238	IEA				P		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0001260	OMIM:601238	IEA				P		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0001263	OMIM:601238	IEA				P		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0001290	OMIM:601238	TAS				P		HPO:skoehler	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0002066	OMIM:601238	IEA				P		HPO:skoehler	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0002080	OMIM:601238	IEA				P		HPO:iea	
OMIM	601238	CEREBELLAR ATAXIA, CAYMAN TYPE		HP:0002136	OMIM:601238	TAS				P		HPO:probinson	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0000007	OMIM:601277	IEA				I		HPO:iea	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0000656	OMIM:601277	TAS				P		HPO:skoehler	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0000707	OMIM:601277	IEA				P		HPO:iea	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0000982	OMIM:601277	TAS				P		HPO:skoehler	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0001217	OMIM:601277	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0001438	OMIM:601277	IEA				P		HPO:iea	
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0001820	OMIM:601277	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601277	#601277 ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A; ARCI4A;;ICHTHYOSIS CONGENITA IIB; ICR2B;;ICHTHYOSIS, LAMELLAR, 2, FORMERLY; LI2, FORMERLY		HP:0007431	OMIM:601277	TAS				P		HPO:skoehler	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0000007	OMIM:601287	TAS				I		HPO:probinson	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0001714	OMIM:601287	TAS				P		HPO:skoehler	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0002355	OMIM:601287	TAS				P		HPO:probinson	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0003236	OMIM:601287	TAS				P		HPO:skoehler	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0003391	OMIM:601287	TAS				P		HPO:skoehler	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0003560	OMIM:601287	TAS				P		HPO:skoehler	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0003691	OMIM:601287	TAS				P		HPO:probinson	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0007126	OMIM:601287	TAS				P		HPO:probinson	
OMIM	601287	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F		HP:0008981	OMIM:601287	TAS				P		HPO:skoehler	
OMIM	601316	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 10		HP:0000006	OMIM:601316	TAS				I		HPO:probinson	
OMIM	601316	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 10		HP:0000407	OMIM:601316	TAS				P		HPO:probinson	
OMIM	601317	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 11		HP:0000006	OMIM:601317	TAS				I		HPO:probinson	
OMIM	601317	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 11		HP:0002321	OMIM:601317	TAS				P		HPO:skoehler	
OMIM	601317	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 11		HP:0008619	OMIM:601317	TAS				P		HPO:probinson	
OMIM	601319	ODONTOMICRONYCHIAL DYSPLASIA		HP:0000007	OMIM:601319	IEA				I		HPO:iea	
OMIM	601319	ODONTOMICRONYCHIAL DYSPLASIA		HP:0001799	OMIM:601319	PCS				P		HPO:probinson	
OMIM	601319	ODONTOMICRONYCHIAL DYSPLASIA		HP:0001816	OMIM:601319	PCS				P		HPO:probinson	
OMIM	601319	ODONTOMICRONYCHIAL DYSPLASIA		HP:0006337	OMIM:601319	IEA				P		HPO:iea	
OMIM	601319	ODONTOMICRONYCHIAL DYSPLASIA		HP:0008383	OMIM:601319	PCS				P		HPO:probinson	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000006	PMID:16380919	PCS				I		HPO:iea	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000028	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	1/12
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000256	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	14/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000272	PMID:16380919	PCS		HP:0040284		P		HPO:iea	5/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000286	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	12/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000316	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	20/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000358	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	22/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000369	PMID:16380919	PCS		HP:0040284		P		HPO:iea	22/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000465	PMID:16380919	PCS		HP:0040284		P		HPO:iea	14/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000470	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000494	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	18/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000508	PMID:16380919	PCS		HP:0040284		P		HPO:iea	15/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000750	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000767	PMID:16542390	PCS		HP:0040284		P		HP:probinson	4/8
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000915	OMIM:601321	IEA				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000917	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0000997	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	16/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001249	PMID:16380919	PCS		HP:0040284		P		HP:probinson	4/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS	HP:0012825	HP:0001263	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001324	OMIM:601321	IEA				P		HPO:iea	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001328	OMIM:601321	IEA				P		HPO:iea	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001328	PMID:16380919	PCS		HP:0040284		P		HP:probinson	11/20
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001642	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	4/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0001684	OMIM:601321	IEA				P		HPO:iea	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0002162	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	17/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0002650	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	9/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0002967	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	7/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0003006	PMID:16380919	PCS		HP:0040284		P		HP:probinson	1/21
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0004322	OMIM:601321	IEA		HP:0040284		P		HPO:iea	10/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0005272	OMIM:601321	IEA				P		HPO:iea	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0005280	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0007565	PMID:16380919	PCS		HP:0040284		P		HP:probinson	22/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0009732	PMID:16380919	PCS		HP:0040284		P		HP:probinson	1/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0009734	PMID:16380919	PCS		HP:0040284		P		HPO:skoehler	4/14
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0009737	PMID:16380919	PCS		HP:0040284		P		HPO:iea	12/20
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0011800	OMIM:601321	TAS				P		HPO:skoehler	
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0012471	PMID:16380919	PCS		HP:0040284		P		HP:probinson	9/22
OMIM	601321	NEUROFIBROMATOSIS-NOONAN SYNDROME; NFNS		HP:0030052	PMID:16380919	PCS				P		HPO:skoehler	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0000007	OMIM:601322	IEA				I		HPO:iea	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0001321	OMIM:601322	IEA				P		HPO:iea	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0001631	OMIM:601322	IEA				P		HPO:iea	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0001636	OMIM:601322	IEA				P		HPO:iea	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0001696	OMIM:601322	IEA				P		HPO:iea	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0002132	OMIM:601322	TAS				P		HPO:probinson	
OMIM	601322	PORENCEPHALY, CEREBELLAR HYPOPLASIA, AND INTERNAL MALFORMATIONS		HP:0002335	OMIM:601322	TAS				P		HPO:probinson	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000006	OMIM:601331	TAS				I		HPO:skoehler	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000007	OMIM:601331	IEA				I		HPO:iea	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000076	OMIM:601331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000083	OMIM:601331	TAS				P		HPO:probinson	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000110	OMIM:601331	TAS				P		HPO:probinson	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0000800	OMIM:601331	TAS				P		HPO:probinson	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0002089	OMIM:601331	IEA				P		HPO:iea	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0003577	OMIM:601331	TAS				C		HPO:skoehler	
OMIM	601331	RENAL DYSPLASIA, DIFFUSE CYSTIC		HP:0004719	OMIM:601331	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000006	OMIM:601338	TAS				I		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000407	OMIM:601338	IEA				P		HPO:iea	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000408	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000529	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000618	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000639	OMIM:601338	IEA				P		HPO:iea	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0000648	OMIM:601338	IEA				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001260	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001269	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001284	OMIM:601338	IEA				P		HPO:iea	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001310	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS	HP:0025303	HP:0001324	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001332	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0001761	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0002066	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0002078	OMIM:601338	TAS				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0002131	OMIM:601338	IEA				P		HPO:iea	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0002131	OMIM:601338	TAS				P		HPO:iea	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0002311	OMIM:601338	IEA				P		HPO:skoehler	
OMIM	601338	CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING LOSS; CAPOS		HP:0006852	OMIM:601338	IEA				P		HPO:iea	
OMIM	601341	ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL		HP:0000007	OMIM:601341	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601341	ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL		HP:0000951	OMIM:601341	IEA				P		HPO:iea	
OMIM	601341	ATROPHIA MACULOSA VARIOLIFORMIS CUTIS, FAMILIAL		HP:0007401	OMIM:601341	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0000006	OMIM:601344	IEA				I		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0002812	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0002944	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0004268	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0004322	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0008423	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0008464	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0008467	OMIM:601344	IEA				P		HPO:iea	
OMIM	601344	SPINAL DYSPLASIA, ANHALT TYPE		HP:0008473	OMIM:601344	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000006	OMIM:601345	IEA				I		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000535	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000653	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000668	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000677	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000695	OMIM:601345	TAS				P		HPO:skoehler	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000956	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0000968	OMIM:601345	TAS				P		HPO:skoehler	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0001597	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0002209	OMIM:601345	TAS				P		HPO:skoehler	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE	HP:0012825	HP:0004322	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0004437	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0004482	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0007387	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0007515	OMIM:601345	IEA				P		HPO:iea	
OMIM	601345	ECTODERMAL DYSPLASIA WITH NATAL TEETH, TURNPENNY TYPE		HP:0100038	OMIM:601345	TAS				P		HPO:skoehler	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0000007	OMIM:601346	IEA				I		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0000047	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0001511	OMIM:601346	TAS				P		HPO:probinson	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0001734	OMIM:601346	IEA				P		HPO:skoehler	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0002247	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0002566	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0002575	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0002594	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0005233	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0005235	OMIM:601346	IEA				P		HPO:skoehler	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0005242	OMIM:601346	IEA				P		HPO:iea	
OMIM	601346	MARTINEZ-FRIAS SYNDROME		HP:0005245	OMIM:601346	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000007	OMIM:601347	IEA				I		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000076	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000160	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000179	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000272	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000322	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000369	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000545	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0000963	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0001263	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0001631	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0001659	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0001875	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,	HP:0012825	HP:0001903	OMIM:601347	TAS				P		HPO:probinson	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0001999	OMIM:601347	IEA				P		HPO:skoehler	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002007	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002110	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002570	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002719	OMIM:601347	TAS				P		HPO:probinson	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002721	OMIM:601347	IEA				P		HPO:skoehler	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0002863	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0004322	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0004325	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0004808	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0005180	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0005280	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0007522	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0008734	OMIM:601347	IEA				P		HPO:iea	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0011220	OMIM:601347	TAS				P		HPO:skoehler	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0011800	OMIM:601347	TAS				P		HPO:skoehler	
OMIM	601347	MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,		HP:0030037	OMIM:601347	TAS				P		HPO:skoehler	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0000006	OMIM:601348	TAS				I		HPO:nvasilevsky	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0000007	OMIM:601348	TAS				I		HPO:nvasilevsky	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0000347	OMIM:601348	IEA				P		HPO:iea	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0000581	OMIM:601348	IEA				P		HPO:iea	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0001629	OMIM:601348	IEA				P		HPO:iea	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0001636	OMIM:601348	IEA				P		HPO:iea	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0001839	OMIM:601348	TAS				P		HPO:skoehler	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0010954	OMIM:601348	TAS				P		HPO:skoehler	
OMIM	601348	ECTRODACTYLY OF LOWER LIMBS, CONGENITAL HEART DEFECT, AND MICROGNATHIA		HP:0012745	OMIM:601348	TAS				P		HPO:skoehler	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000006	OMIM:601349	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000028	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000175	OMIM:601349	TAS				P		HPO:probinson	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000202	OMIM:601349	IEA				P		HPO:skoehler	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000204	OMIM:601349	TAS				P		HPO:probinson	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000252	OMIM:601349	IEA				P		HPO:skoehler	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000303	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000482	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000568	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0000581	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0001249	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0001566	OMIM:601349	IEA				P		HPO:iea	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0001839	OMIM:601349	TAS				P		HPO:probinson	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0012745	OMIM:601349	TAS				P		HPO:skoehler	
OMIM	601349	MICROPHTHALMIA, SYNDROMIC 8; MCOPS8		HP:0100678	OMIM:601349	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0000007	OMIM:601350	TAS				I		HPO:skoehler	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0000085	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0000308	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0000325	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0000774	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0001939	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0002663	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0004322	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0004482	OMIM:601350	IEA				P		HPO:iea	
OMIM	601350	SHORT STATURE SYNDROME, BRUSSELS TYPE		HP:0025369	OMIM:601350	IEA				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0000007	OMIM:601351	IEA				I		HPO:iea	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0000023	OMIM:601351	IEA				P		HPO:iea	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0000307	OMIM:601351	TAS				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0000325	OMIM:601351	TAS				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0000407	OMIM:601351	IEA				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0001510	OMIM:601351	IEA				P		HPO:iea	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0001537	OMIM:601351	IEA				P		HPO:iea	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0002342	OMIM:601351	IEA				P		HPO:iea	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0002656	OMIM:601351	IEA				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0004322	OMIM:601351	TAS				P		HPO:skoehler	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0006499	OMIM:601351	TAS				P		HPO:probinson	
OMIM	601351	GROWTH RETARDATION, DEAFNESS, FEMORAL EPIPHYSEAL DYSPLASIA, AND LACRIMAL DUCT OBSTRUCTION		HP:0007678	OMIM:601351	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0000007	OMIM:601352	IEA				I		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0000252	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0000280	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0001007	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0001249	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0001250	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0002650	OMIM:601352	IEA				P		HPO:iea	
OMIM	601352	MENTAL RETARDATION, MICROCEPHALY, EPILEPSY, AND COARSE FACE		HP:0002750	OMIM:601352	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000007	OMIM:601353	TAS				I		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000028	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000046	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000049	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000160	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000175	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000219	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000248	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000272	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000316	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000343	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000358	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000365	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000369	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000485	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000494	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000518	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000527	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000586	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000915	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0000917	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001156	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001182	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001249	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001250	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001263	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001290	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001510	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0001838	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0002059	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0002079	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0002221	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0002650	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0003187	OMIM:601353	IEA				P		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0003196	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0003745	OMIM:601353	IEA				I		HPO:iea	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0005280	OMIM:601353	IEA				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0008551	OMIM:601353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0012368	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0012385	OMIM:601353	TAS				P		HPO:skoehler	
OMIM	601353	BRACHYCEPHALY, DEAFNESS, CATARACT, MICROSTOMIA, AND MENTAL RETARDATION		HP:0040019	OMIM:601353	IEA				P		HPO:skoehler	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000007	OMIM:601355	IEA				I		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000122	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000175	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000252	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000430	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0000465	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0001629	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0001660	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0002086	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0002324	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0004467	OMIM:601355	IEA				P		HPO:iea	
OMIM	601355	MICROCEPHALY, CONGENITAL HEART DISEASE, UNILATERAL RENAL AGENESIS,AND HYPOSEGMENTED LUNGS		HP:0009882	OMIM:601355	TAS				P		HPO:skoehler	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0000007	OMIM:601356	IEA				I		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0000256	OMIM:601356	TAS				P		HPO:skoehler	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0000260	OMIM:601356	IEA				P		HPO:skoehler	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0000413	OMIM:601356	IEA				P		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0000926	OMIM:601356	IEA				P		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0001776	OMIM:601356	IEA				P		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0002645	OMIM:601356	IEA				P		HPO:skoehler	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0003027	OMIM:601356	IEA				P		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0005716	OMIM:601356	TAS				P		HPO:probinson	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0005720	OMIM:601356	TAS				P		HPO:probinson	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0007759	OMIM:601356	IEA				P		HPO:iea	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE	HP:0012828	HP:0009826	OMIM:601356	TAS				P		HPO:probinson	
OMIM	601356	%601356 LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE		HP:0011910	OMIM:601356	TAS				P		HPO:probinson	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0000369	OMIM:601357	TAS				P		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0000589	OMIM:601357	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0001331	OMIM:601357	TAS				P		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0001360	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0001539	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0001629	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0001849	OMIM:601357	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0002006	OMIM:601357	IEA				P		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0002650	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0002744	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0003097	OMIM:601357	IEA				P		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0003577	OMIM:601357	TAS				C		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0003745	OMIM:601357	TAS				I		HPO:skoehler	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0007035	OMIM:601357	IEA				P		HPO:iea	
OMIM	601357	BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY; ACLH		HP:0009827	OMIM:601357	IEA				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000006	OMIM:601358	TAS				I		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000028	OMIM:601358	IEA				P		HPO:iea	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000154	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000179	OMIM:601358	IEA				P		HPO:iea	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000232	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000252	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000289	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000294	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000325	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000343	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000446	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	12/22
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000463	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000494	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	6/22
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000687	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	11/21
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000718	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0000964	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	8/23
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001156	OMIM:601358	IEA				P		HPO:iea	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001249	OMIM:601358	IEA				P		HPO:iea	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001250	OMIM:601358	TAS	HP:0011463			P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001344	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001508	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001511	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0001852	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0002209	OMIM:601358	IEA				P		HPO:iea	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0002223	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0002465	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0002650	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	9/22
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0004322	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	13/23
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0006237	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0007946	OMIM:601358	TAS		HP:0040284		P		HPO:skoehler	9/22
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0009803	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0010049	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0010743	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0010864	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0012810	OMIM:601358	TAS				P		HPO:skoehler	
OMIM	601358	NICOLAIDES-BARAITSER SYNDROME; NCBRS		HP:0045025	OMIM:601358	IEA				P		HPO:skoehler	
OMIM	601360	AMELIA, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:601360	IEA				I		HPO:iea	
OMIM	601360	AMELIA, AUTOSOMAL RECESSIVE		HP:0009827	OMIM:601360	IEA				P		HPO:skoehler	
OMIM	601363	WILMS TUMOR 4		HP:0000006	OMIM:601363	IEA				I		HPO:iea	
OMIM	601363	WILMS TUMOR 4		HP:0002667	OMIM:601363	IEA				P		HPO:iea	
OMIM	601367	STROKE, ISCHEMIC		HP:0001297	OMIM:601367	IEA				P		HPO:iea	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0000006	OMIM:601369	TAS				I		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0000360	OMIM:601369	TAS				P		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0002321	OMIM:601369	TAS				P		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0003676	OMIM:601369	TAS				C		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0005102	OMIM:601369	TAS				P		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0008596	OMIM:601369	TAS				P		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0009591	OMIM:601369	TAS				P		HPO:skoehler	
OMIM	601369	#601369 DEAFNESS, AUTOSOMAL DOMINANT 9; DFNA9		HP:0011462	OMIM:601369	TAS				C		HPO:skoehler	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0000007	OMIM:601370	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0002507	OMIM:601370	IEA				P		HPO:iea	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0002673	OMIM:601370	IEA				P		HPO:iea	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0004440	OMIM:601370	IEA				P		HPO:iea	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0004443	OMIM:601370	IEA				P		HPO:iea	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0008479	OMIM:601370	IEA				P		HPO:iea	
OMIM	601370	HOLOPROSENCEPHALY, SEMILOBAR, WITH CRANIOSYNOSTOSIS		HP:0009882	OMIM:601370	PCS				P		HPO:iea	
OMIM	601371	CATARACT, AGE-RELATED NUCLEAR		HP:0000007	OMIM:601371	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601371	CATARACT, AGE-RELATED NUCLEAR		HP:0100018	OMIM:601371	TAS				P		HPO:probinson	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT		HP:0000007	OMIM:601372	TAS				I		HPO:nvasilevsky	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT		HP:0000518	OMIM:601372	TAS				P		HPO:skoehler	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT		HP:0001419	OMIM:601372	TAS				I		HPO:nvasilevsky	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT		HP:0001428	OMIM:601372	TAS				I		HPO:nvasilevsky	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT	HP:0012825	HP:0002072	OMIM:601372	TAS				P		HPO:skoehler	
OMIM	601372	CHOREA, REMITTING, WITH NYSTAGMUS AND CATARACT		HP:0007747	OMIM:601372	TAS				P		HPO:skoehler	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0000007	OMIM:601374	IEA				I		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0000193	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0001762	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0006893	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0007027	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0007265	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0007268	OMIM:601374	IEA				P		HPO:iea	
OMIM	601374	APROSENCEPHALY AND CEREBELLAR DYSGENESIS		HP:0007973	OMIM:601374	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0000006	OMIM:601375	IEA				I		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0000653	OMIM:601375	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0000653	OMIM:601375	PCS				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0001662	OMIM:601375	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0001805	OMIM:601375	TAS				P		HPO:skoehler	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0002209	OMIM:601375	PCS				P		HPO:probinson	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0002215	OMIM:601375	PCS				P		HPO:probinson	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0002223	OMIM:601375	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0002225	OMIM:601375	PCS				P		HPO:probinson	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0002286	OMIM:601375	PCS				P		HPO:probinson	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0004763	OMIM:601375	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0007529	OMIM:601375	IEA				P		HPO:skoehler	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0008404	OMIM:601375	IEA				P		HPO:iea	
OMIM	601375	601375 ECTODERMAL DYSPLASIA, HIDROTIC, CHRISTIANSON-FOURIE TYPE		HP:0010764	OMIM:601375	PCS				P		HPO:probinson	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0000007	OMIM:601376	TAS				I		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0001474	OMIM:601376	TAS				P		HPO:skoehler	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0002984	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0003022	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0003038	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0003097	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0003811	OMIM:601376	TAS				M		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0003930	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0005623	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0005736	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0005787	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0005825	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0005885	OMIM:601376	TAS				P		HPO:iea	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0008873	OMIM:601376	TAS				P		HPO:skoehler	
OMIM	601376	CHONDRODYSPLASIA, LETHAL, WITH LONG BONE ANGULATION AND MIXED BONE DENSITY		HP:0012792	OMIM:601376	TAS				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0000006	OMIM:601379	IEA				I		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0000160	OMIM:601379	PCS				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0001249	OMIM:601379	IEA				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0001363	OMIM:601379	IEA				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0002714	OMIM:601379	PCS				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0004322	OMIM:601379	IEA				P		HPO:iea	
OMIM	601379	HUNTER-MCALPINE CRANIOSYNOSTOSIS SYNDROME		HP:0007874	OMIM:601379	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0000007	OMIM:601382	IEA				I		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0001270	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0001425	OMIM:601382	TAS				I		HPO:skoehler	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0001762	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0002460	OMIM:601382	TAS				P		HPO:skoehler	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0002650	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0002936	OMIM:601382	TAS				P		HPO:skoehler	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0003431	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0003693	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0003693	OMIM:601382	TAS				P		HPO:skoehler	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0003701	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0006958	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0007208	OMIM:601382	IEA				P		HPO:iea	
OMIM	601382	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B1; CMT4B1		HP:0010628	OMIM:601382	IEA				P		HPO:iea	
OMIM	601386	#601386 DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12		HP:0000007	OMIM:601386	IEA				I		HPO:iea	
OMIM	601386	#601386 DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12		HP:0000399	OMIM:601386	IEA				P		HPO:iea	
OMIM	601386	#601386 DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12		HP:0000478	OMIM:601386	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000007	OMIM:601389	IEA				I		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000089	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000110	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000796	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000891	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0000912	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0001177	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0001539	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0001762	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0001973	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0002023	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0002944	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0004392	OMIM:601389	IEA				P		HPO:iea	
OMIM	601389	CERVICAL RIBS, SPRENGEL ANOMALY, ANAL ATRESIA, AND URETHRAL OBSTRUCTION		HP:0008635	OMIM:601389	IEA				P		HPO:iea	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000007	OMIM:601390	TAS				I		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000047	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000089	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000218	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000260	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000272	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000286	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000316	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000327	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000341	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000347	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000405	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000407	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000413	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000431	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000508	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000581	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000689	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000774	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000894	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000938	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0000960	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001249	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001290	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001302	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001388	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001510	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001545	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0001762	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002023	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002079	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002282	OMIM:601390	IEA				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002650	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002652	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002714	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0002779	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0003577	OMIM:601390	TAS				C		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0004689	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0008551	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0009879	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0010044	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0010537	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0010554	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0010804	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0011800	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0011968	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0012745	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0030084	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601390	VAN MALDERGEM SYNDROME 1; VMLDS1		HP:0040079	OMIM:601390	TAS				P		HPO:skoehler	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0000006	PMID:11830488	PCS				I		HPO:iea	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0000421	OMIM:601399	TAS				P		HPO:probinson	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0000978	OMIM:601399	IEA				P		HPO:iea	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0001873	OMIM:601399	TAS				P		HPO:probinson	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0002665	OMIM:601399	IEA				P		HPO:skoehler	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0002863	OMIM:601399	IEA				P		HPO:iea	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0003006	OMIM:601399	IEA				P		HPO:iea	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0003010	PMID:11830488	PCS		HP:0040284		P		HPO:iea	14/14
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0003540	PMID:11830488	PCS		HP:0040284		P		HPO:iea	14/14
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0004808	PMID:11830488	PCS		HP:0040284		P		HPO:iea	3/14
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0004845	OMIM:601399	IEA				P		HPO:iea	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0012527	PMID:11830488	PCS				P		HP:probinson	
OMIM	601399	PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY		HP:0012529	PMID:11830488	PCS		HP:0040284		P		HP:probinson	14/14
OMIM	601410	DIABETES MELLITUS, TRANSIENT NEONATAL, 1		HP:0001511	OMIM:601410	IEA				P		HPO:iea	
OMIM	601410	DIABETES MELLITUS, TRANSIENT NEONATAL, 1		HP:0001525	OMIM:601410	IEA				P		HPO:iea	
OMIM	601410	DIABETES MELLITUS, TRANSIENT NEONATAL, 1		HP:0001944	OMIM:601410	IEA				P		HPO:iea	
OMIM	601410	DIABETES MELLITUS, TRANSIENT NEONATAL, 1		HP:0003074	OMIM:601410	IEA				P		HPO:iea	
OMIM	601410	DIABETES MELLITUS, TRANSIENT NEONATAL, 1		HP:0008255	OMIM:601410	IEA				P		HPO:iea	
OMIM	601412	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 7		HP:0000006	OMIM:601412	TAS				I		HPO:probinson	
OMIM	601412	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 7		HP:0005101	OMIM:601412	TAS				P		HPO:probinson	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0000006	OMIM:601414	IEA				I		HPO:iea	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0000510	OMIM:601414	TAS				P		HPO:skoehler	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0000575	OMIM:601414	IEA				P		HPO:skoehler	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0000662	OMIM:601414	IEA				P		HPO:iea	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0007987	OMIM:601414	IEA				P		HPO:iea	
OMIM	601414	RETINITIS PIGMENTOSA 18		HP:0008043	OMIM:601414	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0000006	PMID:17221859	PCS				I		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0000007	PMID:9697706	PCS				I		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0000467	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001283	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001639	PMID:17221859	PCS		HP:0040284		P		HPO:iea	2/7
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001644	PMID:17221859	PCS		HP:0040284		P		HPO:skoehler	1/7
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001662	PMID:17221859	PCS		HP:0040284		P		HP:probinson	1/7
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001709	PMID:17221859	PCS		HP:0040284		P		HP:probinson	2/7
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0001723	PMID:17221859	PCS		HP:0040284		P		HP:probinson	1/7
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0002014	OMIM:601419	TAS				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0002019	OMIM:601419	TAS				P		HPO:skoehler	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0002460	OMIM:601419	TAS				P		HPO:skoehler	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0002600	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0002747	OMIM:601419	TAS				P		HPO:skoehler	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0003458	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0003694	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0003812	OMIM:601419	IEA				C		HPO:skoehler	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0010628	OMIM:601419	IEA				P		HPO:iea	
OMIM	601419	MYOPATHY, MYOFIBRILLAR, 1; MFM1		HP:0011663	PMID:10970245	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0000007	OMIM:601420	IEA				I		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0000175	OMIM:601420	TAS				P		HPO:skoehler	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0000204	OMIM:601420	TAS				P		HPO:probinson	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0000252	OMIM:601420	IEA				P		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0000520	OMIM:601420	IEA				P		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0001177	OMIM:601420	IEA				P		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0001250	OMIM:601420	IEA				P		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0001263	OMIM:601420	IEA				P		HPO:iea	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0002079	OMIM:601420	IEA				P		HPO:skoehler	
OMIM	601420	MICROCEPHALY, CORPUS CALLOSUM DYSGENESIS, AND CLEFT LIP/PALATE		HP:0025356	OMIM:601420	IEA				P		HPO:skoehler	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000007	OMIM:601427	TAS				I		HPO:skoehler	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000164	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000402	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000470	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000612	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000765	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000824	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0000851	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001305	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001321	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001385	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001510	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001595	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0001773	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0002777	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0007700	OMIM:601427	IEA				P		HPO:iea	
OMIM	601427	ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM, AND TRACHEAL STENOSIS		HP:0008736	OMIM:601427	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0000007	OMIM:601438	TAS				I		HPO:skoehler	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0000926	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0001156	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0002812	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0005687	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0005792	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0008905	OMIM:601438	IEA				P		HPO:iea	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0010049	OMIM:601438	IEA				P		HPO:skoehler	
OMIM	601438	RHIZOMELIC DYSPLASIA, PATTERSON-LOWRY TYPE		HP:0010743	OMIM:601438	TAS				P		HPO:skoehler	
OMIM	601449	DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION		HP:0000007	OMIM:601449	TAS				I		HPO:probinson	
OMIM	601449	DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION		HP:0000381	OMIM:601449	TAS				P		HPO:probinson	
OMIM	601449	DEAFNESS, PROGRESSIVE, WITH STAPES FIXATION		HP:0008513	OMIM:601449	TAS				P		HPO:probinson	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000006	OMIM:601450	IEA				I		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000023	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000076	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000272	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000286	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000316	OMIM:601450	PCS				P		HPO:probinson	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0000431	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0001374	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0001382	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM	HP:0012825	HP:0001388	OMIM:601450	PCS				P		HPO:probinson	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0001643	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0001655	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0003502	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0003502	OMIM:601450	PCS				P		HPO:probinson	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0005191	OMIM:601450	IEA				P		HPO:iea	
OMIM	601450	601450 DISLOCATION OF HIP, CONGENITAL, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM;;HIP, CONGENITAL DISLOCATION OF, WITH HYPEREXTENSIBILITY OF FINGERSAND FACIAL DYSMORPHISM		HP:0012368	OMIM:601450	TAS				P		HPO:skoehler	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0000006	OMIM:601453	IEA				I		HPO:iea	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA	HP:0012827	HP:0000252	OMIM:601453	TAS				P		HPO:probinson	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0000668	OMIM:601453	IEA				P		HPO:iea	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0000694	OMIM:601453	IEA				P		HPO:iea	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0000698	OMIM:601453	TAS				P		HPO:probinson	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0002213	OMIM:601453	TAS				P		HPO:skoehler	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0002217	OMIM:601453	IEA				P		HPO:iea	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0002299	OMIM:601453	TAS				P		HPO:skoehler	
OMIM	601453	601453 TRICHODENTAL DYSPLASIA		HP:0008070	OMIM:601453	IEA				P		HPO:iea	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0000007	OMIM:601455	IEA				I		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0000365	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0000649	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0000762	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0001155	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0001265	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0001284	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0001288	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0002460	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0002936	OMIM:601455	TAS				P		HPO:skoehler	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0003383	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0003447	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0003481	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0003621	OMIM:601455	IEA				C		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0003693	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0004696	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0006916	OMIM:601455	IEA				P		HPO:probinson	
OMIM	601455	#601455 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D; CMT4D;;NEUROPATHY, HEREDITARY MOTOR AND SENSORY, LOM TYPE; HMSNL;;CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, AUTOSOMAL RECESSIVE, TYPE4D;;CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4D;;HMSN4D		HP:0006958	OMIM:601455	TAS				P		HPO:probinson	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0000007	OMIM:601457	IEA				I		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0000265	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0000388	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0000509	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0001287	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0001369	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0001508	OMIM:601457	TAS				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0002014	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0002090	OMIM:601457	IEA				P		HPO:skoehler	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0003139	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0004430	OMIM:601457	TAS				P		HPO:probinson	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0005390	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE	HP:0012828	HP:0005403	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE		HP:0008866	OMIM:601457	IEA				P		HPO:iea	
OMIM	601457	SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-NEGATIVE, NK CELL-POSITIVE	HP:0012828	HP:0010976	OMIM:601457	TAS				P		HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000006	OMIM:601462	IEA				I	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000007	OMIM:601462	IEA				I	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000218	OMIM:601462	TAS		HP:0040283		P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:skoehler	HP:0040283
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000508	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000597	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0000602	OMIM:601462	TAS				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:skoehler	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0001260	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0002015	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003324	OMIM:601462	TAS				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003436	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003443	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003473	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003554	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0003674	OMIM:601462	IEA				C	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0004889	OMIM:601462	IEA				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:iea	
OMIM	601462	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa; CMS2A;;CMS IIa		HP:0011968	OMIM:601462	TAS				P	#601462 MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL; SCCMS;;MYASTHENIC SYNDROME, CONGENITAL, POSTSYNAPTIC SLOW-CHANNEL;;MYASTHENIC SYNDROME, CONGENITAL, TYPE IIA; CMS2A;;CMS IIA	HPO:skoehler	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0000007	OMIM:601466	TAS				I		HPO:nvasilevsky	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0001397	OMIM:601466	TAS				P		HPO:skoehler	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0001410	OMIM:601466	TAS				P		HPO:skoehler	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0001419	OMIM:601466	TAS				I		HPO:nvasilevsky	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0001987	OMIM:601466	TAS				P		HPO:skoehler	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0002480	OMIM:601466	TAS				P		HPO:skoehler	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0012021	OMIM:601466	TAS				P		HPO:probinson	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0012022	OMIM:601466	TAS				P		HPO:probinson	
OMIM	601466	PATENT DUCTUS VENOSUS		HP:0012024	OMIM:601466	TAS				P		HPO:skoehler	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0000006	OMIM:601471	IEA				I		HPO:iea	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0001425	OMIM:601471	IEA				I		HPO:skoehler	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0003680	OMIM:601471	IEA				C		HPO:iea	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0008000	PMID:8872479	PCS				P		HPO:lccarmody	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0010628	PMID:8872479	PCS				P		HPO:lccarmody	
OMIM	601471	FACIAL PARESIS, HEREDITARY CONGENITAL, 1; HCFP1		HP:0012507	OMIM:601471	TAS				P		HPO:lccarmody	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0000006	OMIM:601472	IEA				I		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0001265	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0001761	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0001765	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0002172	OMIM:601472	IEA				P		HPO:skoehler	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0002650	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0002936	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003392	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003393	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003426	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003427	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003435	OMIM:601472	IEA				P		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003484	OMIM:601472	TAS				P		HPO:probinson	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003674	OMIM:601472	IEA				C		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003677	OMIM:601472	IEA				C		HPO:iea	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0003693	OMIM:601472	TAS				P		HPO:probinson	
OMIM	601472	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2D; CMT2D		HP:0009129	OMIM:601472	TAS				P		HPO:probinson	
OMIM	601477	RIBBING DISEASE		HP:0000007	OMIM:601477	IEA				I		HPO:iea	
OMIM	601477	RIBBING DISEASE		HP:0003034	OMIM:601477	TAS				P		HPO:skoehler	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0000007	OMIM:601492	IEA				I		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0000176	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0000193	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0000403	OMIM:601492	TAS				P		HPO:skoehler	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0000951	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0002159	OMIM:601492	TAS				P		HPO:probinson	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0003170	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0004322	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0005280	OMIM:601492	IEA				P		HPO:iea	
OMIM	601492	MUCOPOLYSACCHARIDOSIS TYPE IX		HP:0012069	OMIM:601492	TAS				P		HPO:probinson	
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0000006	OMIM:601493	IEA				I		HPO:skoehler	
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0001635	OMIM:601493	IEA				P		HPO:skoehler	
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0001644	OMIM:601493	IEA				P		HPO:skoehler	
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0001645	OMIM:601493	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0001712	OMIM:601493	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0004308	OMIM:601493	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0006685	OMIM:601493	IEA				P		HPO:skoehler	
OMIM	601493	CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C		HP:0030682	OMIM:601493	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0000006	OMIM:601494	IEA				I		HPO:iea	
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0001635	OMIM:601494	TAS				P		HPO:skoehler	
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0001644	OMIM:601494	IEA				P		HPO:iea	
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0001699	OMIM:601494	TAS				M		HPO:skoehler	
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0001712	OMIM:601494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0005110	OMIM:601494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601494	#601494 CARDIOMYOPATHY, DILATED, 1D; CMD1D;;LEFT VENTRICULAR NONCOMPACTION 6, INCLUDED; LVNC6, INCLUDED		HP:0030682	OMIM:601494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0000007	OMIM:601495	TAS				I		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0000403	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0000509	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0001508	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0001875	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0002014	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0002110	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0002718	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0002743	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0003593	OMIM:601495	TAS				C		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0004432	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0006532	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0010976	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0011108	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601495	#601495 AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE; AGM1;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGHM DEFECT		HP:0100280	OMIM:601495	TAS				P		HPO:skoehler	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000006	OMIM:601499	IEA				I		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000023	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000028	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000047	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000232	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000238	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000303	OMIM:601499	IEA				P		HPO:skoehler	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000316	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000322	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000327	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000365	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000431	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000482	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000501	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000506	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000618	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000668	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0000691	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0001537	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0001627	OMIM:601499	TAS				P		HPO:skoehler	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0002025	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0007759	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0007833	OMIM:601499	IEA				P		HPO:iea	
OMIM	601499	%601499 AXENFELD-RIEGER SYNDROME, TYPE 2; RIEG2;;RIEGER SYNDROME, TYPE 2		HP:0030680	OMIM:601499	IEA				P		HPO:iea	
OMIM	601518	#601518 PROSTATE CANCER, HEREDITARY, 1; HPC1;;PRCA1		HP:0000006	OMIM:601518	TAS				I		HPO:skoehler	
OMIM	601518	#601518 PROSTATE CANCER, HEREDITARY, 1; HPC1;;PRCA1		HP:0002664	OMIM:601518	IEA				P		HPO:iea	
OMIM	601518	#601518 PROSTATE CANCER, HEREDITARY, 1; HPC1;;PRCA1		HP:0012125	OMIM:601518	TAS				P		HPO:skoehler	
OMIM	601536	#601536 ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME; ABDS;;NAVAJO BRAINSTEM SYNDROMEBOSLEY-SALIH-ALORAINY SYNDROME, INCLUDED; BSAS, INCLUDED		HP:0000407	OMIM:601536	IEA				P		HPO:skoehler	
OMIM	601536	#601536 ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME; ABDS;;NAVAJO BRAINSTEM SYNDROMEBOSLEY-SALIH-ALORAINY SYNDROME, INCLUDED; BSAS, INCLUDED		HP:0000496	OMIM:601536	IEA		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	601536	#601536 ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME; ABDS;;NAVAJO BRAINSTEM SYNDROMEBOSLEY-SALIH-ALORAINY SYNDROME, INCLUDED; BSAS, INCLUDED		HP:0002194	OMIM:601536	IEA				P		HPO:skoehler	
OMIM	601536	#601536 ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME; ABDS;;NAVAJO BRAINSTEM SYNDROMEBOSLEY-SALIH-ALORAINY SYNDROME, INCLUDED; BSAS, INCLUDED		HP:0002363	OMIM:601536	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	601536	#601536 ATHABASKAN BRAINSTEM DYSGENESIS SYNDROME; ABDS;;NAVAJO BRAINSTEM SYNDROMEBOSLEY-SALIH-ALORAINY SYNDROME, INCLUDED; BSAS, INCLUDED		HP:0009145	OMIM:601536	IEA				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000007	OMIM:601539	TAS				I		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000107	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000286	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000407	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000431	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000444	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000510	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000648	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0000750	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001250	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001263	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001290	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001319	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001394	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0001395	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0002240	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0002415	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0003159	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0010655	OMIM:601539	TAS				P		HPO:probinson	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0011800	OMIM:601539	TAS				P		HPO:skoehler	
OMIM	601539	PEROXISOME BIOGENESIS DISORDER 1B; PBD1B		HP:0025356	OMIM:601539	IEA				P		HPO:skoehler	
OMIM	601543	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 12		HP:0000006	OMIM:601543	IEA				I		HPO:iea	
OMIM	601543	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 12		HP:0000407	OMIM:601543	TAS				P		HPO:skoehler	
OMIM	601544	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 3		HP:0000006	OMIM:601544	TAS				I		HPO:skoehler	
OMIM	601544	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 3		HP:0000407	OMIM:601544	TAS				P		HPO:skoehler	
OMIM	601547	CATARACT 3, MULTIPLE TYPES; CTRCT3		HP:0000006	PMID:11424921	PCS				I		HPO:skoehler	
OMIM	601547	CATARACT 3, MULTIPLE TYPES; CTRCT3		HP:0000519	OMIM:601547	IEA				P		HPO:skoehler	
OMIM	601547	CATARACT 3, MULTIPLE TYPES; CTRCT3		HP:0007976	OMIM:601547	TAS	HP:0003577	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	601547	CATARACT 3, MULTIPLE TYPES; CTRCT3		HP:0010695	PMID:11424921	PCS				P		HPO:skoehler	
OMIM	601547	CATARACT 3, MULTIPLE TYPES; CTRCT3		HP:0010698	OMIM:601547	IEA				P		HPO:skoehler	
OMIM	601549	ALACRIMA		HP:0000007	OMIM:601549	IEA				I		HPO:iea	
OMIM	601549	ALACRIMA		HP:0000522	OMIM:601549	IEA				P		HPO:iea	
OMIM	601549	ALACRIMA		HP:0000584	OMIM:601549	IEA				P		HPO:iea	
OMIM	601549	ALACRIMA		HP:0000613	OMIM:601549	IEA				P		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000007	OMIM:601552	IEA				I		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000278	OMIM:601552	TAS				P		HPO:skoehler	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000444	OMIM:601552	TAS				P		HPO:skoehler	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000445	OMIM:601552	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000448	OMIM:601552	TAS				P		HPO:skoehler	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000494	OMIM:601552	IEA				P		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000568	OMIM:601552	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0000689	OMIM:601552	IEA				P		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0001083	OMIM:601552	IEA				P		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0001089	OMIM:601552	IEA				P		HPO:skoehler	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0001999	OMIM:601552	IEA				P		HPO:iea	
OMIM	601552	FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS		HP:0003683	OMIM:601552	IEA				P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0000007	OMIM:601553	IEA				I		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0000164	OMIM:601553	IEA				P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0000618	PMID:12445216	PCS	HP:0003581			P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0001006	PMID:11544476	PCS	HP:0003593			P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0001597	OMIM:601553	IEA				P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0003777	PMID:11544476	PCS				P		HPO:iea	
OMIM	601553	#601553 HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD;;HYPOTRICHOSIS WITH CONE-ROD DYSTROPHY		HP:0007754	PMID:11544476	PCS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000007	OMIM:601559	TAS				I		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000205	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000272	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000321	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000347	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000369	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000470	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000682	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000883	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000935	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000939	OMIM:601559	TAS				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000954	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0000963	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001181	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001252	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001290	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001609	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001611	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001883	OMIM:601559	IEA				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0001954	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002007	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002015	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002089	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002092	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002093	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002104	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002486	OMIM:601559	IEA				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002650	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002756	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002980	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002982	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0002987	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0003015	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0003037	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0003196	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0004322	OMIM:601559	TAS	HP:0003593			P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0004684	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0004964	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0004980	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0005089	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0005736	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0005830	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0006380	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0006844	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0007328	OMIM:601559	IEA				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0007610	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0007759	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0008824	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0009185	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0009465	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0009803	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0010298	OMIM:601559	IEA				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0011800	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0011968	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0012332	OMIM:601559	IEA				P		HPO:iea	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0012745	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0012810	OMIM:601559	TAS				P		HPO:skoehler	
OMIM	601559	STUVE-WIEDEMANN SYNDROME		HP:0100865	OMIM:601559	TAS				P		HPO:probinson	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000175	OMIM:601560	TAS				P		HPO:skoehler	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000316	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000347	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000358	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000369	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000455	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000582	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0000767	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0001156	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0001371	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0001511	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0001762	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0001840	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0002650	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0002654	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE	HP:0012825	HP:0002812	OMIM:601560	TAS				P		HPO:skoehler	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0002857	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003038	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003083	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003090	OMIM:601560	TAS				P		HPO:probinson	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003097	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003370	OMIM:601560	TAS				P		HPO:probinson	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0003745	OMIM:601560	IEA				I		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0005792	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0006167	OMIM:601560	TAS				P		HPO:probinson	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0008905	OMIM:601560	IEA				P		HPO:iea	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0010049	OMIM:601560	IEA				P		HPO:skoehler	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0010582	OMIM:601560	TAS				P		HPO:probinson	
OMIM	601560	MULTIPLE EPIPHYSEAL DYSPLASIA WITH ROBIN PHENOTYPE		HP:0100864	OMIM:601560	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000007	OMIM:601561	TAS				I		HPO:skoehler	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000175	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000260	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000268	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000272	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA	HP:0012828	HP:0000501	OMIM:601561	TAS				P		HPO:probinson	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000520	OMIM:601561	TAS				P		HPO:probinson	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0000926	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0002663	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0002983	OMIM:601561	IEA				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0002987	OMIM:601561	TAS				P		HPO:probinson	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0003015	OMIM:601561	TAS				P		HPO:skoehler	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0003026	OMIM:601561	TAS				P		HPO:iea	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0003273	OMIM:601561	TAS				P		HPO:probinson	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0004322	OMIM:601561	TAS				P		HPO:skoehler	
OMIM	601561	DYSSEGMENTAL DYSPLASIA WITH GLAUCOMA		HP:0005622	OMIM:601561	TAS				P		HPO:probinson	
OMIM	601583	WILMS TUMOR 5		HP:0000006	OMIM:601583	IEA				I		HPO:iea	
OMIM	601583	WILMS TUMOR 5		HP:0001428	OMIM:601583	IEA				I		HPO:iea	
OMIM	601583	WILMS TUMOR 5		HP:0002667	OMIM:601583	IEA				P		HPO:iea	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0000007	OMIM:601596	IEA				I		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0000365	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0000639	OMIM:601596	TAS				P		HPO:skoehler	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0000764	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0001270	OMIM:601596	IEA				P		HPO:iea	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0001291	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0001308	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0001425	OMIM:601596	TAS				I		HPO:skoehler	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0001761	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0002355	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0002460	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C	HP:0012828	HP:0002650	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0002936	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0003387	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0003400	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0003431	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0003484	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0003693	OMIM:601596	TAS				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0004466	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0007107	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0007695	OMIM:601596	IEA				P		HPO:probinson	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0010628	OMIM:601596	TAS				P		HPO:skoehler	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0012473	OMIM:601596	TAS				P		HPO:skoehler	
OMIM	601596	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C; CMT4C		HP:0040078	OMIM:601596	IEA				P		HPO:skoehler	
OMIM	601606	TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1		HP:0000006	OMIM:601606	IEA				I		HPO:iea	
OMIM	601606	TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1		HP:0002671	OMIM:601606	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601606	TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1		HP:0003581	OMIM:601606	IEA				C		HPO:iea	
OMIM	601608	SPASTIC PARAPLEGIA AND EVANS SYNDROME		HP:0000007	OMIM:601608	IEA				I		HPO:iea	
OMIM	601608	SPASTIC PARAPLEGIA AND EVANS SYNDROME		HP:0001258	OMIM:601608	IEA				P		HPO:iea	
OMIM	601608	SPASTIC PARAPLEGIA AND EVANS SYNDROME		HP:0001973	OMIM:601608	IEA				P		HPO:iea	
OMIM	601608	SPASTIC PARAPLEGIA AND EVANS SYNDROME		HP:0004844	OMIM:601608	IEA				P		HPO:iea	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0000007	OMIM:601612	IEA				I		HPO:iea	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0001643	OMIM:601612	TAS				P		HPO:skoehler	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0001671	OMIM:601612	TAS				P		HPO:skoehler	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0001680	OMIM:601612	TAS				P		HPO:skoehler	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0002093	OMIM:601612	TAS				P		HPO:skoehler	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0003577	OMIM:601612	TAS				C		HPO:skoehler	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0003811	OMIM:601612	IEA				M		HPO:iea	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0005944	OMIM:601612	IEA				P		HPO:iea	
OMIM	601612	%601612 LUNG AGENESIS, CONGENITAL HEART DEFECTS, AND THUMB ANOMALIES SYNDROME;LACHT;;MARDINI-NYHAN ASSOCIATION		HP:0100682	OMIM:601612	TAS				P		HPO:skoehler	
OMIM	601616	IRIS PIGMENT EPITHELIUM ANOMALIES		HP:0000006	PMID:8874445	PCS				I		HPO:iea	
OMIM	601616	IRIS PIGMENT EPITHELIUM ANOMALIES		HP:0011523	PMID:8874445	PCS				P		HPO:probinson	
OMIM	601626	LEUKEMIA, ACUTE MYELOID; AML		HP:0000006	OMIM:601626	TAS				I		HPO:skoehler	
OMIM	601626	LEUKEMIA, ACUTE MYELOID; AML		HP:0001428	OMIM:601626	IEA				I		HPO:skoehler	
OMIM	601626	LEUKEMIA, ACUTE MYELOID; AML		HP:0004808	OMIM:601626	TAS				P		HPO:skoehler	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0000006	OMIM:601631	TAS				I		HPO:probinson	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0000501	OMIM:601631	TAS	HP:0003621			P		HPO:probinson	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0000558	OMIM:601631	TAS				P		HPO:skoehler	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0000627	OMIM:601631	TAS				P		HPO:skoehler	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0000659	OMIM:601631	TAS				P		HPO:skoehler	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0001320	OMIM:601631	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0001492	OMIM:601631	TAS				P		HPO:skoehler	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0002280	OMIM:601631	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0007905	OMIM:601631	TAS	HP:0003621			P		HPO:probinson	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0007990	OMIM:601631	TAS				P		HPO:probinson	
OMIM	601631	ANTERIOR SEGMENT DYSGENESIS 3		HP:0009918	OMIM:601631	TAS				P		HPO:skoehler	
OMIM	601634	NEURAL TUBE DEFECTS, FOLATE-SENSITIVE		HP:0000007	OMIM:601634	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601634	NEURAL TUBE DEFECTS, FOLATE-SENSITIVE		HP:0001939	OMIM:601634	IEA				P		HPO:iea	
OMIM	601634	NEURAL TUBE DEFECTS, FOLATE-SENSITIVE		HP:0010301	OMIM:601634	TAS				P		HPO:skoehler	
OMIM	601650	PARAGANGLIOMAS 2		HP:0000006	OMIM:601650	TAS				I		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0001605	OMIM:601650	TAS				P		HPO:probinson	
OMIM	601650	PARAGANGLIOMAS 2		HP:0001609	OMIM:601650	TAS				P		HPO:probinson	
OMIM	601650	PARAGANGLIOMAS 2		HP:0001686	OMIM:601650	TAS				P		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0002886	OMIM:601650	TAS				P		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0003001	OMIM:601650	TAS				P		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0003581	OMIM:601650	TAS				C		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0006715	OMIM:601650	TAS				P		HPO:iea	
OMIM	601650	PARAGANGLIOMAS 2		HP:0006824	OMIM:601650	TAS				P		HPO:probinson	
OMIM	601650	PARAGANGLIOMAS 2		HP:0008629	OMIM:601650	TAS				P		HPO:probinson	
OMIM	601650	PARAGANGLIOMAS 2		HP:0030074	OMIM:601650	TAS				P		HPO:skoehler	
OMIM	601665	OBESITY		HP:0000006	OMIM:601665	TAS				I		HPO:skoehler	
OMIM	601665	OBESITY		HP:0000007	OMIM:601665	TAS				I		HPO:skoehler	
OMIM	601665	OBESITY		HP:0001513	OMIM:601665	TAS				P		HPO:iea	
OMIM	601665	OBESITY		HP:0010982	OMIM:601665	TAS				I		HPO:iea	
OMIM	601665	OBESITY		HP:0012340	OMIM:601665	TAS				P		HPO:iea	
OMIM	601665	OBESITY		HP:0031819	PMID:12872269	PCS				P		HPO:lccarmody	
OMIM	601666	%601666 DIABETES MELLITUS, INSULIN-DEPENDENT, 15; IDDM15;;INSULIN-DEPENDENT DIABETES MELLITUS 15		HP:0000819	OMIM:601666	IEA				P		HPO:iea	
OMIM	601666	%601666 DIABETES MELLITUS, INSULIN-DEPENDENT, 15; IDDM15;;INSULIN-DEPENDENT DIABETES MELLITUS 15		HP:0100651	OMIM:601666	TAS				P		HPO:skoehler	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000007	OMIM:601668	IEA				I		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000592	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000677	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000707	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000926	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0000951	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0001182	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0001238	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0002651	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0002857	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0002868	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD	HP:0012825	HP:0003015	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0003025	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0003071	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0003301	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0003508	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0006290	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0006304	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0006339	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0006429	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0009183	OMIM:601668	IEA				P		HPO:iea	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0010584	OMIM:601668	IEA				P		HPO:skoehler	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0010585	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601668	601668 SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH ABNORMAL DENTITION; SEMDAD		HP:0100864	OMIM:601668	TAS				P		HPO:probinson	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000007	OMIM:601675	IEA				I		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000135	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000252	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000271	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000278	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000411	OMIM:601675	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000482	OMIM:601675	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000486	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000518	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000568	OMIM:601675	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000613	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000639	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000750	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000765	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000958	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000962	OMIM:601675	IEA				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0000992	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001009	OMIM:601675	IEA				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001019	OMIM:601675	TAS				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001019	OMIM:601675	IEA				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001097	OMIM:601675	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001249	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001371	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001480	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001518	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001792	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0001808	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002024	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002028	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002099	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002213	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002299	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002671	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002719	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0002860	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0004315	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0004322	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0005214	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0007479	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0007519	OMIM:601675	IEA				P		HPO:iea	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0008070	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0008404	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0009886	OMIM:601675	TAS				P		HPO:skoehler	
OMIM	601675	TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE; TTD1		HP:0010719	OMIM:601675	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000007	OMIM:601678	IEA				I		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000103	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000111	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000121	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000127	OMIM:601678	TAS				P		HPO:skoehler	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000128	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000841	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000843	OMIM:601678	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000848	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000859	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000934	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0000938	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001249	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001250	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001263	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001281	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001425	OMIM:601678	TAS				I		HPO:skoehler	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001508	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001518	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001561	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001563	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001622	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001944	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001945	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0001960	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002013	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002014	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002019	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002150	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002632	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002900	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002914	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0002917	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003072	OMIM:601678	TAS				P		HPO:skoehler	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003081	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003113	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003158	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003324	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003394	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003401	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003527	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0003566	OMIM:601678	IEA				P		HPO:iea	
OMIM	601678	BARTTER SYNDROME, TYPE 1, ANTENATAL		HP:0004322	OMIM:601678	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000006	OMIM:601680	IEA				I		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000160	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000218	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000303	OMIM:601680	IEA				P		HPO:skoehler	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000325	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000343	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000347	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000431	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000465	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000494	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0000598	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0001193	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0001762	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0001838	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0001840	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0001848	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0002650	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0002804	OMIM:601680	IEA				P		HPO:skoehler	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0003049	OMIM:601680	TAS				P		HPO:probinson	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0004322	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0005272	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0005684	OMIM:601680	TAS				P		HPO:probinson	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0006109	OMIM:601680	IEA				P		HPO:iea	
OMIM	601680	ARTHROGRYPOSIS, DISTAL, TYPE 2B		HP:0100490	OMIM:601680	IEA				P		HPO:iea	
OMIM	601682	GLAUCOMA 1, OPEN ANGLE, C		HP:0000006	OMIM:601682	IEA				I		HPO:iea	
OMIM	601682	GLAUCOMA 1, OPEN ANGLE, C		HP:0007906	OMIM:601682	IEA				P		HPO:iea	
OMIM	601696	NOVELTY SEEKING PERSONALITY TRAIT		HP:0000006	OMIM:601696	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601696	NOVELTY SEEKING PERSONALITY TRAIT		HP:0000707	OMIM:601696	IEA				P		HPO:iea	
OMIM	601696	NOVELTY SEEKING PERSONALITY TRAIT		HP:0100710	OMIM:601696	TAS				P		HPO:skoehler	
OMIM	601700	SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE		HP:0000006	OMIM:601700	IEA				I		HPO:iea	
OMIM	601700	SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE		HP:0000951	OMIM:601700	IEA				P		HPO:iea	
OMIM	601700	SEBACEOUS GLAND HYPERPLASIA, FAMILIAL PRESENILE		HP:0003674	OMIM:601700	IEA				C		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000007	OMIM:601701	IEA				I		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000175	OMIM:601701	TAS				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000202	OMIM:601701	IEA				P		HPO:skoehler	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000204	OMIM:601701	TAS				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000248	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000252	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000581	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000621	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000677	OMIM:601701	TAS				P		HPO:skoehler	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000682	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000819	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000958	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000962	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000966	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000968	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0000987	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0001128	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA	HP:0012825	HP:0001999	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0002164	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0002223	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0002552	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0002751	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0002804	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0003202	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0004322	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0007477	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0007477	OMIM:601701	TAS				P		HPO:probinson	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0009473	OMIM:601701	IEA				P		HPO:iea	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0012385	OMIM:601701	TAS				P		HPO:skoehler	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0045025	OMIM:601701	IEA				P		HPO:skoehler	
OMIM	601701	ARTHROGRYPOSIS AND ECTODERMAL DYSPLASIA		HP:0100018	OMIM:601701	IEA				P		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0000007	OMIM:601705	TAS				I		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001596	OMIM:601705	TAS	HP:0003577			P		HPO:skoehler	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001803	OMIM:601705	TAS				P		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0001807	OMIM:601705	TAS				P		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0005352	OMIM:601705	TAS				P		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0008165	OMIM:601705	TAS				P		HPO:iea	
OMIM	601705	T-CELL IMMUNODEFICIENCY, CONGENITAL ALOPECIA, AND NAIL DYSTROPHY		HP:0008404	OMIM:601705	IEA				P		HPO:skoehler	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0000007	OMIM:601706	TAS				I		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0000482	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0000567	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0000612	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0000639	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0002211	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0007509	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0007587	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601706	YEMENITE DEAF-BLIND HYPOPIGMENTATION SYNDROME		HP:0008625	OMIM:601706	TAS				P		HPO:probinson	
OMIM	601707	CURRY-JONES SYNDROME		HP:0000324	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0000568	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0000581	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0000589	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0000951	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001007	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0001159	OMIM:601707	IEA				P		HPO:skoehler	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001177	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001263	OMIM:601707	TAS				P		HPO:skoehler	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001274	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001363	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0001442	OMIM:601707	TAS				I		HPO:skoehler	
OMIM	601707	CURRY-JONES SYNDROME		HP:0002025	OMIM:601707	IEA				P		HPO:iea	
OMIM	601707	CURRY-JONES SYNDROME		HP:0002119	OMIM:601707	TAS				P		HPO:skoehler	
OMIM	601707	CURRY-JONES SYNDROME		HP:0002126	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0002566	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0007099	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0007206	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0009942	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0010554	OMIM:601707	TAS				P		HPO:skoehler	
OMIM	601707	CURRY-JONES SYNDROME		HP:0010621	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0011304	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601707	CURRY-JONES SYNDROME		HP:0012450	OMIM:601707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601708	SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL		HP:0000006	OMIM:601708	TAS				I		HPO:skoehler	
OMIM	601708	SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL		HP:0011989	OMIM:601708	TAS				P		HPO:probinson	
OMIM	601708	SUPERIOR TRANSVERSE SCAPULAR LIGAMENT, CALCIFICATION OF, FAMILIAL		HP:0012216	OMIM:601708	TAS				P		HPO:probinson	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0000006	OMIM:601709	IEA				I		HPO:iea	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0000132	OMIM:601709	TAS				P		HPO:probinson	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0000421	OMIM:601709	TAS				P		HPO:probinson	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0000978	OMIM:601709	IEA				P		HPO:skoehler	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0001873	OMIM:601709	IEA				P		HPO:skoehler	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0005261	OMIM:601709	TAS				P		HPO:probinson	
OMIM	601709	#601709 QUEBEC PLATELET DISORDER; QPD;;BLEEDING DISORDER, PLATELET-TYPE, 5; BDPLT5;;FACTOR V QUEBEC		HP:0008148	OMIM:601709	IEA				P		HPO:iea	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0000007	PMID:9425888	PCS				I		HPO:probinson	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0000510	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0000512	PMID:9070931	PCS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0000543	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0000662	PMID:9070931	PCS	HP:0003621			P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0001133	PMID:9070931	PCS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0007663	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0007722	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0007737	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601718	RETINITIS PIGMENTOSA 19		HP:0007843	OMIM:601718	TAS				P		HPO:skoehler	
OMIM	601759	PREAXIAL HALLUCAL POLYDACTYLY		HP:0000819	OMIM:601759	IEA				P		HPO:skoehler	
OMIM	601759	PREAXIAL HALLUCAL POLYDACTYLY		HP:0001177	OMIM:601759	IEA				P		HPO:iea	
OMIM	601759	PREAXIAL HALLUCAL POLYDACTYLY		HP:0001841	OMIM:601759	IEA				P		HPO:iea	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0000006	OMIM:601764	TAS				I		HPO:probinson	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0000961	OMIM:601764	IEA				P		HPO:iea	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0001425	OMIM:601764	TAS				I		HPO:skoehler	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0002104	OMIM:601764	IEA				P		HPO:skoehler	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0002372	OMIM:601764	TAS				P		HPO:probinson	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0002384	OMIM:601764	IEA				P		HPO:iea	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0007334	OMIM:601764	IEA				P		HPO:iea	
OMIM	601764	SEIZURES, BENIGN FAMILIAL INFANTILE, 1; BFIS1		HP:0040168	OMIM:601764	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000007	OMIM:601776	IEA				I		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000028	OMIM:601776	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000100	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1	HP:0012832	HP:0000126	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000153	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000160	OMIM:601776	TAS	HP:0003593			P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000175	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000218	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000219	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000239	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000248	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000270	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000308	OMIM:601776	TAS	HP:0003593			P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000316	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000324	OMIM:601776	TAS	HP:0003581			P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000337	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000343	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000358	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000365	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000411	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000482	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000486	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000494	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000501	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000506	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000541	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000545	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000592	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000593	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000767	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000974	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0000978	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001030	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001166	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1	HP:0012828	HP:0001181	OMIM:601776	TAS				P		HPO:probinson	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001249	OMIM:601776	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001263	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001270	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001290	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001373	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001388	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001537	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001540	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001581	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001631	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001762	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0001999	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002019	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002036	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002107	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002119	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002246	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002566	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002650	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0002761	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1	HP:0012839	HP:0002804	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0004425	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0005684	OMIM:601776	IEA				P		HPO:iea	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0005684	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0031005	OMIM:601776	IEA				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0031364	OMIM:601776	IEA				P		HPO:skoehler	
OMIM	601776	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 1; EDSMC1		HP:0100699	OMIM:601776	TAS				P		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0000006	OMIM:601777	TAS				I		HPO:iea	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0000007	OMIM:601777	IEA				I		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0000548	OMIM:601777	TAS				P		HPO:iea	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0000613	OMIM:601777	IEA				P		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0000639	OMIM:601777	IEA				P		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0003831	OMIM:601777	IEA				C		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0007401	OMIM:601777	IEA				P		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0007663	OMIM:601777	TAS				P		HPO:iea	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0007675	OMIM:601777	IEA				P		HPO:skoehler	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0007994	OMIM:601777	TAS				P		HPO:probinson	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0011463	OMIM:601777	TAS				C		HPO:probinson	
OMIM	601777	CONE-ROD DYSTROPHY 6; CORD6		HP:0012047	OMIM:601777	IEA				P		HPO:skoehler	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0000007	OMIM:601780	IEA				I		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0000529	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0000546	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0001250	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0001311	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0002074	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0002333	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0003205	OMIM:601780	IEA				P		HPO:iea	
OMIM	601780	CEROID LIPOFUSCINOSIS, NEURONAL, 6		HP:0003208	OMIM:601780	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000006	OMIM:601794	TAS				I		HPO:skoehler	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000028	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000135	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000238	OMIM:601794	IEA				P		HPO:skoehler	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000480	OMIM:601794	TAS				P		HPO:skoehler	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000510	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000518	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000568	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0000771	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0001513	OMIM:601794	IEA				P		HPO:iea	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0006889	OMIM:601794	TAS				P		HPO:skoehler	
OMIM	601794	COLOBOMA-OBESITY-HYPOGENITALISM-MENTAL RETARDATION SYNDROME		HP:0100702	OMIM:601794	IEA				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000023	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000028	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000047	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000059	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000107	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000110	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000151	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000158	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000175	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000193	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000219	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000219	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000232	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000256	OMIM:601803	IEA				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000280	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000286	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000293	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000316	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000343	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000347	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000365	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000400	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000402	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000431	OMIM:601803	TAS				P		HPO:probinson	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000463	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000465	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000470	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000486	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000508	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000518	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000520	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000535	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000545	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000582	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000653	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000684	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000776	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000954	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000966	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0000970	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001162	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001169	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001250	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001252	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001276	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001290	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001371	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001374	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001442	OMIM:601803	IEA				I		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001513	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001537	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001539	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001545	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001629	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001631	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001639	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001643	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001650	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001680	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001769	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001830	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0001831	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002007	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002023	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002025	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002089	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002187	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002558	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002566	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002751	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0002883	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0003027	OMIM:601803	TAS				P		HPO:probinson	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0003196	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0003826	OMIM:601803	IEA				M		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0004209	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0004768	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0005026	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0005280	OMIM:601803	TAS				P		HPO:probinson	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0005484	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0007535	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0007572	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0009803	OMIM:601803	IEA				P		HPO:iea	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0011220	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0011968	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0012673	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601803	PALLISTER-KILLIAN SYNDROME		HP:0030276	OMIM:601803	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000006	OMIM:601808	IEA				I		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000023	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000028	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000047	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000054	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000175	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000193	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000204	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000219	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000219	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000252	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000272	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000286	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000294	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000303	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000316	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000322	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000400	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000402	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000405	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000407	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000413	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000448	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000452	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000470	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000486	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000494	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000510	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000581	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000639	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000648	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0000824	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001047	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001249	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001250	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001252	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001270	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001290	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001321	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001337	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001388	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001531	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001537	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001629	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001631	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001635	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001643	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001650	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001761	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001762	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001763	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001770	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001838	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0001845	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002072	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002099	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002119	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002136	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002188	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002205	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002370	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002500	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002650	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0002714	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0003745	OMIM:601808	IEA				I		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0004322	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0004433	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0004970	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0005134	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0005164	OMIM:601808	TAS				P		HPO:probinson	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0005176	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0005280	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0009623	OMIM:601808	IEA				P		HPO:iea	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0010806	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0011800	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601808	CHROMOSOME 18Q DELETION SYNDROME		HP:0012745	OMIM:601808	TAS				P		HPO:skoehler	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0000007	OMIM:601809	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0000327	OMIM:601809	IEA				P		HPO:iea	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0000347	OMIM:601809	IEA				P		HPO:iea	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0001040	OMIM:601809	IEA				P		HPO:iea	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0002089	OMIM:601809	IEA				P		HPO:iea	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0002804	OMIM:601809	IEA				P		HPO:iea	
OMIM	601809	SPONDYLOSPINAL THORACIC DYSOSTOSIS		HP:0010306	OMIM:601809	IEA				P		HPO:skoehler	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000007	OMIM:601811	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000252	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000311	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000369	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000377	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000518	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000819	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0000939	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0001507	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0001595	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0001871	OMIM:601811	IEA				P		HPO:iea	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0002664	OMIM:601811	IEA				P		HPO:skoehler	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0002669	OMIM:601811	TAS				P		HPO:skoehler	
OMIM	601811	PREMATURE AGING SYNDROME, OKAMOTO TYPE		HP:0005280	OMIM:601811	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000006	OMIM:601812	TAS				I		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000233	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000270	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000327	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000347	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000407	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000426	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000460	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000520	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000540	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000684	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000938	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000951	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0000962	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0001156	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0001507	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0002645	OMIM:601812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0002650	OMIM:601812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0002750	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0002925	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0003100	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0008070	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0009771	OMIM:601812	IEA				P		HPO:iea	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0010539	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0011800	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601812	PREMATURE AGING SYNDROME, PENTTINEN TYPE		HP:0100578	OMIM:601812	TAS				P		HPO:skoehler	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0000006	OMIM:601813	IEA				I		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0000007	OMIM:601813	IEA				I		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0000523	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0000618	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0000938	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0001147	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0001489	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0001493	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0003593	OMIM:601813	IEA				C		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0007663	OMIM:601813	TAS				P		HPO:skoehler	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0007685	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0007811	OMIM:601813	TAS				P		HPO:probinson	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0007902	OMIM:601813	TAS				P		HPO:probinson	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0007917	OMIM:601813	IEA				P		HPO:iea	
OMIM	601813	EXUDATIVE VITREORETINOPATHY 4		HP:0030490	OMIM:601813	TAS				P		HPO:skoehler	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:601815	IEA				I		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0000519	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0000639	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001181	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001249	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001250	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001510	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001873	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0001889	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0002510	OMIM:601815	IEA				P		HPO:iea	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0002521	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0007266	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0008734	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601815	PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY		HP:0011451	OMIM:601815	PCS				P		HPO:probinson	
OMIM	601816	BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1; BILIQTL1		HP:0002904	OMIM:601816	TAS				P		HPO:probinson	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0000007	OMIM:601820	IEA				I		HPO:iea	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0000825	OMIM:601820	IEA				P		HPO:iea	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0001425	OMIM:601820	TAS				I		HPO:skoehler	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0001520	OMIM:601820	IEA				P		HPO:iea	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0001943	OMIM:601820	IEA				P		HPO:iea	
OMIM	601820	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 2; HHF2		HP:0004510	OMIM:601820	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0000006	OMIM:601829	TAS				I		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0000204	OMIM:601829	IEA				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0000272	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0000677	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0001057	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0002650	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0003311	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0003468	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0003777	OMIM:601829	IEA				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0004322	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0004614	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0010044	OMIM:601829	IEA				P		HPO:iea	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0010554	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0011220	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0045075	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601829	ACROFACIAL DYSOSTOSIS, PALAGONIA TYPE		HP:0100333	OMIM:601829	TAS				P		HPO:skoehler	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0000006	OMIM:601846	IEA				I		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0001618	OMIM:601846	TAS				P		HPO:probinson	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0001761	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0002015	OMIM:601846	TAS				P		HPO:probinson	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0002460	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003236	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003547	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003555	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003560	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003581	OMIM:601846	IEA				C		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003687	OMIM:601846	TAS				P		HPO:skoehler	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003691	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003722	OMIM:601846	IEA				P		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003805	OMIM:601846	TAS				P		HPO:probinson	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0003828	OMIM:601846	IEA				C		HPO:iea	
OMIM	601846	%601846 VACUOLAR NEUROMYOPATHY;;MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV		HP:0009027	OMIM:601846	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0000007	OMIM:601847	IEA				I		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0000989	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001046	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001394	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001402	OMIM:601847	IEA				P		HPO:skoehler	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001406	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001508	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0001744	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0002014	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0002240	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0002630	OMIM:601847	TAS				P		HPO:probinson	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0002908	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0003155	OMIM:601847	IEA				P		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0003593	OMIM:601847	IEA				C		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0003819	OMIM:601847	IEA				M		HPO:iea	
OMIM	601847	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2		HP:0004322	OMIM:601847	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000218	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000233	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000248	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000260	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000262	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000272	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000316	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000319	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000358	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000369	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000463	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000486	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000716	OMIM:601853	IEA				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000752	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0000824	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001250	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001251	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001276	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001290	OMIM:601853	TAS				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001320	OMIM:601853	TAS				P		HPO:probinson	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001347	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001363	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0001596	OMIM:601853	IEA				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0002335	OMIM:601853	TAS				P		HPO:probinson	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0002645	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0002678	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0003196	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0003745	OMIM:601853	IEA				I		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0004322	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0006899	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0007302	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0007759	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0011800	OMIM:601853	TAS				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0031912	OMIM:601853	IEA				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0031913	OMIM:601853	IEA				P		HPO:skoehler	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0100543	OMIM:601853	IEA				P		HPO:iea	
OMIM	601853	GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS		HP:0100716	OMIM:601853	TAS				P		HPO:skoehler	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0000006	OMIM:601859	IEA				I		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001025	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001744	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001880	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001890	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001891	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001904	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0001973	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002240	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002633	OMIM:601859	IEA				P		HPO:skoehler	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002729	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002730	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002731	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002851	OMIM:601859	TAS				P		HPO:probinson	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002853	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002923	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0002972	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003237	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003261	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003262	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003453	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003454	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003493	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003496	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0003613	OMIM:601859	IEA				P		HPO:iea	
OMIM	601859	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME		HP:0004844	OMIM:601859	IEA				P		HPO:iea	
OMIM	601868	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 13		HP:0000006	OMIM:601868	IEA				I		HPO:iea	
OMIM	601868	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 13		HP:0000407	OMIM:601868	TAS	HP:0003577			P		HPO:probinson	
OMIM	601869	#601869 DEAFNESS, AUTOSOMAL RECESSIVE 15; DFNB15;;DEAFNESS, AUTOSOMAL RECESSIVE 72; DFNB72;;DEAFNESS, AUTOSOMAL RECESSIVE 95; DFNB95		HP:0000007	PMID:21326233	PCS				I		HPO:skoehler	
OMIM	601869	#601869 DEAFNESS, AUTOSOMAL RECESSIVE 15; DFNB15;;DEAFNESS, AUTOSOMAL RECESSIVE 72; DFNB72;;DEAFNESS, AUTOSOMAL RECESSIVE 95; DFNB95		HP:0000399	PMID:21326233	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	601884	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1		HP:0000006	OMIM:601884	IEA				I		HPO:iea	
OMIM	601884	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1		HP:0000925	OMIM:601884	IEA				P		HPO:iea	
OMIM	601884	BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1		HP:0004563	OMIM:601884	IEA				P		HPO:iea	
OMIM	601885	#601885 CATARACT, ZONULAR PULVERULENT 3; CZP3;;CAE3		HP:0000006	OMIM:601885	IEA				I		HPO:skoehler	
OMIM	601885	#601885 CATARACT, ZONULAR PULVERULENT 3; CZP3;;CAE3		HP:0010920	OMIM:601885	IEA				P		HPO:skoehler	
OMIM	601887	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5		HP:0000006	OMIM:601887	TAS				I		HPO:skoehler	
OMIM	601887	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5		HP:0001649	OMIM:601887	IEA				P		HPO:skoehler	
OMIM	601887	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5		HP:0001945	OMIM:601887	TAS				P		HPO:skoehler	
OMIM	601887	MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5		HP:0012416	OMIM:601887	IEA				P		HPO:skoehler	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0000006	OMIM:601894	TAS				I		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0000093	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0000100	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0000822	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0002907	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0003677	OMIM:601894	TAS				C		HPO:skoehler	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0003774	OMIM:601894	TAS				P		HPO:skoehler	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0004916	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0005584	OMIM:601894	TAS				P		HPO:probinson	
OMIM	601894	#601894 GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2; GFND2;;GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS;;FIBRONECTIN GLOMERULOPATHY		HP:0100820	OMIM:601894	IEA				P		HPO:skoehler	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000007	OMIM:601927	IEA				I		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000034	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000219	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000219	OMIM:601927	TAS				P		HPO:skoehler	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000286	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000311	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000348	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000455	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000506	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000582	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0000750	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001004	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001539	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001562	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001597	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001629	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001631	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0001643	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0002623	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0004749	OMIM:601927	TAS				P		HPO:skoehler	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0005099	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0005280	OMIM:601927	IEA				P		HPO:iea	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0010775	OMIM:601927	IEA				P		HPO:skoehler	
OMIM	601927	%601927 LYMPHEDEMA, CARDIAC SEPTAL DEFECTS, AND CHARACTERISTIC FACIES;;IRONS-BIANCHI SYNDROME;;LYMPHEDEMA, ATRIAL SEPTAL DEFECT, AND CHARACTERISTIC FACIES		HP:0011220	OMIM:601927	TAS				P		HPO:skoehler	
OMIM	601941	DIABETES MELLITUS, INSULIN-DEPENDENT, 6		HP:0000819	OMIM:601941	IEA				P		HPO:iea	
OMIM	601942	DIABETES MELLITUS, INSULIN-DEPENDENT, 10		HP:0000819	OMIM:601942	IEA				P		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0000007	OMIM:601952	IEA				I		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0001036	OMIM:601952	IEA				P		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0001795	OMIM:601952	IEA				P		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0001795	OMIM:601952	PCS				P		HPO:probinson	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0007465	OMIM:601952	IEA				P		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0007479	OMIM:601952	TAS				P		HPO:skoehler	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0007490	OMIM:601952	IEA				P		HPO:iea	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0008064	OMIM:601952	PCS				P		HPO:probinson	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0008404	OMIM:601952	PCS				P		HPO:probinson	
OMIM	601952	#601952 KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA;;KLICK SYNDROME		HP:0009775	OMIM:601952	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0000007	OMIM:601954	IEA				I		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0002355	OMIM:601954	TAS				P		HPO:probinson	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0002522	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0003236	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0003551	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0003557	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0003560	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0003805	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0008944	OMIM:601954	TAS				P		HPO:probinson	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0008948	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0008981	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0008994	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0008997	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0009025	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0009027	OMIM:601954	IEA				P		HPO:iea	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0009046	OMIM:601954	TAS				P		HPO:probinson	
OMIM	601954	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2G		HP:0009053	OMIM:601954	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0000006	OMIM:601957	IEA				I		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0000303	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0000689	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0000695	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0000954	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0001010	OMIM:601957	IEA				P		HPO:skoehler	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0001156	OMIM:601957	TAS				P		HPO:skoehler	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0001857	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0002164	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0006189	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0008404	OMIM:601957	TAS				P		HPO:skoehler	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0009882	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0010034	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0010105	OMIM:601957	IEA				P		HPO:iea	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0010719	OMIM:601957	TAS				P		HPO:skoehler	
OMIM	601957	601957 ODONTOTRICHOUNGUAL-DIGITAL-PALMAR SYNDROME;;OTUDP SYNDROME		HP:0012471	OMIM:601957	TAS				P		HPO:skoehler	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000007	OMIM:601976	IEA				I		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000023	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000028	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000248	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000272	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000286	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000358	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000369	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000407	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000411	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000430	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000494	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000767	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0000774	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0001762	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0002007	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0002645	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0002750	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0002857	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0004322	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0005280	OMIM:601976	TAS				P		HPO:skoehler	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0009702	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0010109	OMIM:601976	IEA				P		HPO:iea	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0011220	OMIM:601976	TAS				P		HPO:skoehler	
OMIM	601976	601976 OTOFACIOOSSEOUS-GONADAL SYNDROME		HP:0012368	OMIM:601976	TAS				P		HPO:skoehler	
OMIM	601977	#601977 THROMBOCYTHEMIA 2; THCYT2		HP:0000006	OMIM:601977	IEA				I		HPO:iea	
OMIM	601977	#601977 THROMBOCYTHEMIA 2; THCYT2		HP:0001428	OMIM:601977	TAS				I		HPO:skoehler	
OMIM	601977	#601977 THROMBOCYTHEMIA 2; THCYT2		HP:0001894	OMIM:601977	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0000006	OMIM:601979	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0000939	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0000988	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0002014	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0002240	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0002633	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0002721	OMIM:601979	IEA				P		HPO:iea	
OMIM	601979	HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION		HP:0011424	OMIM:601979	IEA				P		HPO:iea	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0000007	OMIM:601992	TAS				I		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0000639	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001251	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001260	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001315	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001635	OMIM:601992	TAS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001691	OMIM:601992	TAS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001761	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001765	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0001953	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0002062	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0002311	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0002495	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0002650	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003115	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003116	OMIM:601992	TAS				P		HPO:skoehler	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003133	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003134	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003209	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003232	OMIM:601992	IEA				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003487	OMIM:601992	TAS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0003621	OMIM:601992	PCS				C		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0005157	OMIM:601992	TAS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0011397	OMIM:601992	PCS				P		HPO:probinson	
OMIM	601992	%601992 FRIEDREICH ATAXIA 2; FRDA2		HP:0011441	OMIM:601992	PCS				P		HPO:probinson	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0000007	OMIM:602014	IEA				I		HPO:iea	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0001250	OMIM:602014	IEA				P		HPO:iea	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0001281	OMIM:602014	IEA				P		HPO:iea	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0002901	OMIM:602014	IEA				P		HPO:iea	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0002917	OMIM:602014	IEA				P		HPO:iea	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0003394	OMIM:602014	IEA				P		HPO:skoehler	
OMIM	602014	HYPOMAGNESEMIA 1, INTESTINAL; HOMG1		HP:0003593	OMIM:602014	IEA				C		HPO:iea	
OMIM	602025	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9; BMIQ9		HP:0001513	OMIM:602025	TAS				P		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0000006	OMIM:602032	IEA				I		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0000007	OMIM:602032	TAS				I		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0000561	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0001596	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0001806	OMIM:602032	IEA				P		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0002223	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0002231	OMIM:602032	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0002299	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0003777	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0004524	OMIM:602032	IEA				P		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0007436	OMIM:602032	IEA				P		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0008394	OMIM:602032	IEA				P		HPO:iea	
OMIM	602032	#602032 ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE; ECTD4;;ECTODERMAL DYSPLASIA, 'PURE' HAIR/NAIL TYPE		HP:0008404	OMIM:602032	TAS				P		HPO:skoehler	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0000006	OMIM:602066	IEA				I		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0000739	OMIM:602066	IEA				P		HPO:skoehler	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0002197	OMIM:602066	IEA				P		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0002268	OMIM:602066	IEA				P		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0002372	OMIM:602066	IEA				P		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0007098	OMIM:602066	IEA				P		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0007359	OMIM:602066	IEA				P		HPO:iea	
OMIM	602066	#602066 CONVULSIONS, FAMILIAL INFANTILE, WITH PAROXYSMAL CHOREOATHETOSIS;ICCA;;INFANTILE CONVULSIONS AND PAROXYSMAL CHOREOATHETOSIS, FAMILIAL;;ICCA SYNDROME;;PAROXYSMAL KINESIGENIC DYSKINESIA WITH INFANTILE CONVULSIONS; PKD/IC		HP:0040168	OMIM:602066	TAS				P		HPO:skoehler	
OMIM	602068	LEISHMANIASIS, TEGUMENTARY		HP:0000007	OMIM:602068	IEA				I		HPO:iea	
OMIM	602068	LEISHMANIASIS, TEGUMENTARY		HP:0001425	OMIM:602068	IEA				I		HPO:iea	
OMIM	602068	LEISHMANIASIS, TEGUMENTARY		HP:0003831	OMIM:602068	IEA				C		HPO:iea	
OMIM	602068	LEISHMANIASIS, TEGUMENTARY		HP:0007408	OMIM:602068	IEA				P		HPO:iea	
OMIM	602071	BROAD TERMINAL PHALANGES, FAMILIAL		HP:0000006	OMIM:602071	TAS				I		HPO:probinson	
OMIM	602071	BROAD TERMINAL PHALANGES, FAMILIAL		HP:0009836	OMIM:602071	TAS				P		HPO:probinson	
OMIM	602071	BROAD TERMINAL PHALANGES, FAMILIAL		HP:0010186	OMIM:602071	TAS				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0000007	OMIM:602078	IEA				I		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0000505	OMIM:602078	PCS				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0000577	OMIM:602078	TAS				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0000646	OMIM:602078	IEA				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0001488	OMIM:602078	IEA				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0001491	OMIM:602078	IEA				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0007936	OMIM:602078	IEA				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2	HP:0012828	HP:0007936	OMIM:602078	PCS				P		HPO:probinson	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0025584	OMIM:602078	IEA				P		HPO:skoehler	
OMIM	602078	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2; CFEOM2		HP:0025586	OMIM:602078	IEA				P		HPO:skoehler	
OMIM	602079	TRIMETHYLAMINURIA		HP:0000007	OMIM:602079	IEA				I		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0000716	OMIM:602079	IEA				P		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0000822	OMIM:602079	TAS				P		HPO:probinson	
OMIM	602079	TRIMETHYLAMINURIA		HP:0001649	OMIM:602079	TAS				P		HPO:probinson	
OMIM	602079	TRIMETHYLAMINURIA		HP:0001744	OMIM:602079	IEA				P		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0001875	OMIM:602079	IEA				P		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0001903	OMIM:602079	IEA				P		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0003614	OMIM:602079	IEA				P		HPO:iea	
OMIM	602079	TRIMETHYLAMINURIA		HP:0006532	OMIM:602079	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0000006	OMIM:602080	IEA				I		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0001425	OMIM:602080	TAS				I		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002273	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002385	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002423	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002512	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002644	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002653	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002659	OMIM:602080	TAS				P		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002797	OMIM:602080	IEA				P		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0002953	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0003080	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0003084	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0003155	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0003676	OMIM:602080	TAS				C		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0003828	OMIM:602080	TAS				C		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0006480	OMIM:602080	TAS				P		HPO:skoehler	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0006824	OMIM:602080	IEA				P		HPO:iea	
OMIM	602080	PAGET DISEASE OF BONE 2, EARLY-ONSET		HP:0008513	OMIM:602080	TAS		HP:0040284		P		HPO:probinson	40%
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0000006	OMIM:602081	IEA				I		HPO:iea	
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0000271	OMIM:602081	IEA				P		HPO:iea	
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0000750	OMIM:602081	IEA				P		HPO:iea	
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0002134	OMIM:602081	IEA				P		HPO:iea	
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0002546	OMIM:602081	IEA				P		HPO:iea	
OMIM	602081	SPEECH-LANGUAGE DISORDER 1		HP:0007301	OMIM:602081	TAS				P		HPO:probinson	
OMIM	602082	CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II		HP:0000006	OMIM:602082	IEA				I		HPO:iea	
OMIM	602082	CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II		HP:0000559	OMIM:602082	IEA				P		HPO:iea	
OMIM	602082	CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II		HP:0000613	OMIM:602082	IEA				P		HPO:iea	
OMIM	602082	CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II		HP:0001131	OMIM:602082	IEA				P		HPO:skoehler	
OMIM	602082	CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE II		HP:0007755	OMIM:602082	IEA				P		HPO:iea	
OMIM	602083	USHER SYNDROME, TYPE IF		HP:0000007	OMIM:602083	TAS				I		HPO:probinson	
OMIM	602083	USHER SYNDROME, TYPE IF		HP:0000510	OMIM:602083	TAS				P		HPO:probinson	
OMIM	602083	USHER SYNDROME, TYPE IF		HP:0001270	OMIM:602083	TAS				P		HPO:probinson	
OMIM	602083	USHER SYNDROME, TYPE IF		HP:0008527	OMIM:602083	TAS				P		HPO:probinson	
OMIM	602085	POLYDACTYLY, POSTAXIAL, TYPE A2		HP:0000006	OMIM:602085	IEA				I		HPO:iea	
OMIM	602085	POLYDACTYLY, POSTAXIAL, TYPE A2		HP:0001162	OMIM:602085	IEA				P		HPO:iea	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0000006	OMIM:602086	TAS				I		HPO:skoehler	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0001425	OMIM:602086	TAS				I		HPO:skoehler	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0003140	OMIM:602086	TAS				P		HPO:skoehler	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0003338	OMIM:602086	TAS				P		HPO:skoehler	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0004308	OMIM:602086	TAS				P		HPO:skoehler	
OMIM	602086	%602086 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 3; ARVC3		HP:0011663	OMIM:602086	TAS				P		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0000006	OMIM:602087	TAS				I		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0001425	OMIM:602087	TAS				I		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0001699	OMIM:602087	TAS				M		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0003140	OMIM:602087	TAS				P		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0003338	OMIM:602087	TAS				P		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0004308	OMIM:602087	TAS				P		HPO:skoehler	
OMIM	602087	%602087 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 4; ARVC4		HP:0011663	OMIM:602087	TAS				P		HPO:skoehler	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0000007	OMIM:602088	IEA				I		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0000090	OMIM:602088	IEA				P		HPO:skoehler	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0000105	OMIM:602088	TAS				P		HPO:probinson	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0000822	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0001562	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0001696	OMIM:602088	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0002089	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0002093	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0002153	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0002878	OMIM:602088	TAS				P		HPO:skoehler	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0003259	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0003774	OMIM:602088	TAS	HP:0011463			P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0004719	OMIM:602088	TAS				P		HPO:probinson	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0004734	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0004743	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0005564	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0005976	OMIM:602088	IEA				P		HPO:iea	
OMIM	602088	#602088 NEPHRONOPHTHISIS 2; NPHP2;;NPH2		HP:0010444	OMIM:602088	TAS				P		HPO:skoehler	
OMIM	602089	#602089 HEMANGIOMA, CAPILLARY INFANTILE;;HCI;;HEMANGIOMA, HEREDITARY CAPILLARY		HP:0000006	OMIM:602089	TAS				I		HPO:skoehler	
OMIM	602089	#602089 HEMANGIOMA, CAPILLARY INFANTILE;;HCI;;HEMANGIOMA, HEREDITARY CAPILLARY		HP:0005306	OMIM:602089	TAS				P		HPO:probinson	
OMIM	602092	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 18		HP:0000007	PMID:12107438	PCS				I		HPO:lccarmody	
OMIM	602092	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 18		HP:0000407	PMID:12107438	PCS				P		HPO:skoehler	
OMIM	602093	CONE DYSTROPHY 3		HP:0000006	OMIM:602093	IEA				I		HPO:iea	
OMIM	602093	CONE DYSTROPHY 3		HP:0000529	OMIM:602093	TAS				P		HPO:skoehler	
OMIM	602093	CONE DYSTROPHY 3		HP:0000548	OMIM:602093	TAS				P		HPO:skoehler	
OMIM	602093	CONE DYSTROPHY 3		HP:0000613	OMIM:602093	IEA				P		HPO:iea	
OMIM	602093	CONE DYSTROPHY 3		HP:0007401	OMIM:602093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602093	CONE DYSTROPHY 3		HP:0007663	OMIM:602093	TAS				P		HPO:skoehler	
OMIM	602096	ALZHEIMER DISEASE 5		HP:0000006	OMIM:602096	IEA				I		HPO:iea	
OMIM	602096	ALZHEIMER DISEASE 5		HP:0002511	OMIM:602096	TAS	HP:0003584			P		HPO:probinson	
OMIM	602096	ALZHEIMER DISEASE 5		HP:0003584	OMIM:602096	TAS				C		HPO:skoehler	
OMIM	602097	USHER SYNDROME, TYPE IE; USH1E		HP:0000007	OMIM:602097	IEA				I		HPO:iea	
OMIM	602097	USHER SYNDROME, TYPE IE; USH1E		HP:0000510	OMIM:602097	IEA				P		HPO:iea	
OMIM	602097	USHER SYNDROME, TYPE IE; USH1E		HP:0001284	OMIM:602097	IEA				P		HPO:skoehler	
OMIM	602097	USHER SYNDROME, TYPE IE; USH1E		HP:0008527	OMIM:602097	IEA				P		HPO:iea	
OMIM	602097	USHER SYNDROME, TYPE IE; USH1E		HP:0008568	OMIM:602097	IEA				P		HPO:iea	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0000007	OMIM:602099	IEA				I		HPO:iea	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0001257	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0001260	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0001347	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0002366	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0002380	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0002460	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0002483	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0002747	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0003487	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0003621	OMIM:602099	IEA				C		HPO:iea	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0003677	OMIM:602099	IEA				C		HPO:iea	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0003693	OMIM:602099	TAS				P		HPO:skoehler	
OMIM	602099	#602099 AMYOTROPHIC LATERAL SCLEROSIS 5, JUVENILE; ALS5		HP:0007354	OMIM:602099	IEA				P		HPO:iea	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0000006	OMIM:602107	TAS				I		HPO:skoehler	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0001284	OMIM:602107	TAS				P		HPO:skoehler	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0001324	OMIM:602107	TAS				P		HPO:skoehler	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0001945	OMIM:602107	IEA				P		HPO:skoehler	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0003401	OMIM:602107	TAS				P		HPO:skoehler	
OMIM	602107	NEUROPATHY, HEREDITARY THERMOSENSITIVE		HP:0003828	OMIM:602107	TAS				C		HPO:skoehler	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0000006	OMIM:602111	TAS				I		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED	HP:0012825	HP:0000926	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0001377	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002515	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002651	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002750	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002758	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002812	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002869	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002970	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002980	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002982	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0002986	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0003015	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0003021	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0003031	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0003071	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0004566	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0006603	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0008476	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0008905	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602111	#602111 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MISSOURI TYPE;;SEMD, MISSOURI TYPEMETAPHYSEAL ANADYSPLASIA 1, INCLUDED; MANDP1, INCLUDED		HP:0010585	OMIM:602111	TAS				P		HPO:probinson	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0000007	OMIM:602114	IEA				I		HPO:iea	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0000112	OMIM:602114	IEA				P		HPO:skoehler	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0001969	OMIM:602114	IEA				P		HPO:iea	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0002611	OMIM:602114	IEA				P		HPO:iea	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0002910	OMIM:602114	IEA				P		HPO:iea	
OMIM	602114	NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE		HP:0012622	OMIM:602114	TAS				P		HPO:probinson	
OMIM	602124	DYSTONIA 7, TORSION		HP:0000006	OMIM:602124	IEA				I		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0000473	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0000643	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0001304	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0001618	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0002312	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0002356	OMIM:602124	IEA				P		HPO:skoehler	
OMIM	602124	DYSTONIA 7, TORSION		HP:0002378	OMIM:602124	IEA				P		HPO:skoehler	
OMIM	602124	DYSTONIA 7, TORSION		HP:0003712	OMIM:602124	IEA				P		HPO:iea	
OMIM	602124	DYSTONIA 7, TORSION		HP:0012048	OMIM:602124	IEA				P		HPO:iea	
OMIM	602134	TREMOR, HEREDITARY ESSENTIAL, 2; ETM2		HP:0000006	OMIM:602134	IEA				I		HPO:iea	
OMIM	602134	TREMOR, HEREDITARY ESSENTIAL, 2; ETM2		HP:0007351	OMIM:602134	IEA				P		HPO:iea	
OMIM	602134	TREMOR, HEREDITARY ESSENTIAL, 2; ETM2		HP:0012378	OMIM:602134	IEA				P		HPO:skoehler	
OMIM	602134	TREMOR, HEREDITARY ESSENTIAL, 2; ETM2		HP:0030186	OMIM:602134	TAS				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000090	OMIM:602152	TAS				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000405	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000490	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000508	OMIM:602152	TAS				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000510	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000577	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000824	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0000938	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0001156	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0002652	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0002750	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0002986	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0008245	OMIM:602152	IEA				P		HPO:iea	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0012622	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602152	RHYNS SYNDROME; RHYNS		HP:0100864	OMIM:602152	IEA				P		HPO:skoehler	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000006	OMIM:602196	IEA				I		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000175	OMIM:602196	IEA				P		HPO:skoehler	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000201	OMIM:602196	TAS				P		HPO:probinson	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000347	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000465	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000767	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0000772	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0001252	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0001290	OMIM:602196	TAS				P		HPO:skoehler	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0001382	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0001965	OMIM:602196	IEA				P		HPO:iea	
OMIM	602196	PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES		HP:0006631	OMIM:602196	IEA				P		HPO:iea	
OMIM	602197	602197 CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3;;CDR3		HP:0001317	OMIM:602197	IEA				P		HPO:skoehler	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0000007	OMIM:602199	IEA				I		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0001410	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0001942	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0001944	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0002013	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0002913	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0003201	OMIM:602199	IEA				P		HPO:iea	
OMIM	602199	MEDIUM CHAIN 3-KETOACYL-COA THIOLASE DEFICIENCY		HP:0003811	OMIM:602199	IEA				M		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000007	OMIM:602200	IEA				I		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000073	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000085	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000086	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000104	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0000238	OMIM:602200	TAS				P		HPO:probinson	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0002119	OMIM:602200	TAS				P		HPO:probinson	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0002617	OMIM:602200	IEA				P		HPO:skoehler	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0003956	OMIM:602200	TAS				P		HPO:probinson	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0003974	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0006956	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0009777	OMIM:602200	IEA				P		HPO:iea	
OMIM	602200	VENTRICULOMEGALY WITH DEFECTS OF THE RADIUS AND KIDNEY		HP:0009821	OMIM:602200	TAS				P		HPO:probinson	
OMIM	602247	XANTHOMATOSIS, SUSCEPTIBILITY TO		HP:0000006	OMIM:602247	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	602247	XANTHOMATOSIS, SUSCEPTIBILITY TO		HP:0000991	OMIM:602247	IEA				P		HPO:skoehler	
OMIM	602247	XANTHOMATOSIS, SUSCEPTIBILITY TO		HP:0003124	OMIM:602247	IEA				P		HPO:skoehler	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0000006	OMIM:602248	TAS				I		HPO:skoehler	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0000502	OMIM:602248	IEA				P		HPO:iea	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0001297	PMID:19249895	PCS				P		HPO:probinson	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0002202	OMIM:602248	IEA				P		HPO:iea	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0002239	OMIM:602248	IEA				P		HPO:iea	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0002563	OMIM:602248	IEA				P		HPO:iea	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0005244	OMIM:602248	IEA				P		HPO:iea	
OMIM	602248	%602248 MALIGNANT ATROPHIC PAPULOSIS;;DEGOS DISEASE;;PAPULOSIS, MALIGNANT ATROPHIC		HP:0200034	PMID:19249895	PCS				P		HPO:probinson	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000006	OMIM:602249	IEA				I		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000160	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000233	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000252	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000322	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000405	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000411	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000448	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000581	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0000582	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0001015	OMIM:602249	TAS				P		HPO:skoehler	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0001166	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0001256	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0001562	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0001636	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0002007	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0003758	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0004209	OMIM:602249	TAS				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0005328	OMIM:602249	PCS				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0008070	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0009183	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0010554	OMIM:602249	IEA				P		HPO:iea	
OMIM	602249	PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES		HP:0100807	OMIM:602249	PCS				P		HPO:iea	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000007	OMIM:602271	TAS				I		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000510	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000546	OMIM:602271	IEA				P		HPO:skoehler	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000639	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000648	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0000907	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX	HP:0012825	HP:0000926	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0002657	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0002812	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0003375	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0003411	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0004322	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0005257	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0006532	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0008905	OMIM:602271	IEA				P		HPO:skoehler	
OMIM	602271	SPONDYLOMETAPHYSEAL DYSPLASIA, AXIAL; SMDAX		HP:0100864	OMIM:602271	TAS				P		HPO:probinson	
OMIM	602342	Pierpont syndrome		HP:0000006	PMID:26769062	PCS				I	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000028	PMID:28562391	PCS	HP:0003577	HP:0040284		P	PIERPONT SYNDROME	HP:probinson	1/1
OMIM	602342	Pierpont syndrome		HP:0000054	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0000232	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000233	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0000248	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000252	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000272	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0000283	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000289	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000293	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000316	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000319	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0000348	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000358	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000365	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	5/5
OMIM	602342	Pierpont syndrome		HP:0000445	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000455	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0000470	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000482	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	3/6
OMIM	602342	Pierpont syndrome		HP:0000486	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0000490	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000506	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000568	OMIM:602342	IEA				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0000687	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0000750	PMID:21834056	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	9/9
OMIM	602342	Pierpont syndrome		HP:0000759	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0001169	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:probinson	
OMIM	602342	Pierpont syndrome		HP:0001212	PMID:26769062	IEA		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0001249	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0001250	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0001252	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0001263	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0001276	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0001508	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0001769	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0001773	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0001831	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0001869	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0002265	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0002308	PMID:30365874	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	1/2
OMIM	602342	Pierpont syndrome		HP:0002650	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	5/6
OMIM	602342	Pierpont syndrome		HP:0002708	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0003196	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0004279	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:probinson	
OMIM	602342	Pierpont syndrome		HP:0004322	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0004325	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	3/6
OMIM	602342	Pierpont syndrome		HP:0006191	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0006610	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0006610	PMID:21834056	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	4/5
OMIM	602342	Pierpont syndrome		HP:0007946	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0009381	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	6/6
OMIM	602342	Pierpont syndrome		HP:0009890	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HPO:skoehler	6/6
OMIM	602342	Pierpont syndrome		HP:0011341	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0011800	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0011968	OMIM:602342	TAS		HP:0040283		P	PIERPONT SYNDROME	HPO:skoehler	HP:0040283
OMIM	602342	Pierpont syndrome		HP:0012043	OMIM:602342	IEA				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602342	Pierpont syndrome		HP:0032276	PMID:26769062	PCS				P	PIERPONT SYNDROME	HP:probinson	
OMIM	602342	Pierpont syndrome		HP:0045025	PMID:26769062	PCS		HP:0040284		P	PIERPONT SYNDROME	HP:probinson	5/6
OMIM	602342	Pierpont syndrome		HP:0100853	OMIM:602342	TAS				P	PIERPONT SYNDROME	HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0000007	OMIM:602347	IEA				I		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0000952	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0000989	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0001394	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0001406	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0001408	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0001425	OMIM:602347	TAS				I		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0001744	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0002014	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0002024	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0002240	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0002910	OMIM:602347	IEA				P		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0003593	OMIM:602347	IEA				C		HPO:skoehler	
OMIM	602347	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 3; PFIC3		HP:0006580	OMIM:602347	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0000006	OMIM:602361	TAS				I		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0000054	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0000238	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0000526	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0000568	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0001156	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0001250	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0001263	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA	HP:0012828	HP:0001508	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0001541	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0001746	OMIM:602361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0002901	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0003015	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0003100	PMID:23684011	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0004322	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0004331	OMIM:602361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0006270	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0010296	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602361	GRACILE BONE DYSPLASIA		HP:0011220	OMIM:602361	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000007	PMID:14982867	PCS				I		HPO:probinson	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000027	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000044	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000141	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000789	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0000953	PMID:14982867	PCS				P		HPO:probinson	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001254	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001369	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001394	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001635	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001638	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001644	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0001744	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0002240	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0003281	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0003452	PMID:14982867	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0011462	PMID:14982867	PCS				C		HPO:probinson	
OMIM	602390	HEMOCHROMATOSIS, TYPE 2A		HP:0011675	OMIM:602390	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000007	PMID:11519011	PCS				I		HPO:iea	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000033	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000061	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000169	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000175	PMID:12457401;PMID:9450875	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000238	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000252	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000256	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000286	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000347	PMID:12457401;PMID:9450875	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000358	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000369	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000378	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000463	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000486	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000494	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0000639	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001250	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001257	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001263	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001338	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001508	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001643	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0001776	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0002007	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0002119	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0002804	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0003107	PMID:11519011	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0003196	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0004482	OMIM:602398	TAS				P		HPO:skoehler	
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0005160	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0005281	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0005789	PMID:9450875	PCS	HP:0003577	HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0007370	PMID:12457401;PMID:9450875	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0008905	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0009085	PMID:9450875	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602398	#602398 DESMOSTEROLOSIS		HP:0009473	PMID:12457401	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000007	PMID:18445049	PCS				I		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000498	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000535	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000613	PMID:17273967	TAS		HP:0040284		P		HPO:skoehler	3/3
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000613	PMID:17273967	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000962	OMIM:602400	IEA				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0000966	OMIM:602400	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0001006	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0002212	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0002299	PMID:17273967	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0003777	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0007431	OMIM:602400	TAS				P		HPO:skoehler	
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0007957	PMID:17273967	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	602400	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11; ARCI11		HP:0008070	PMID:17273967	TAS		HP:0040284		P		HPO:skoehler	3/3
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0000007	OMIM:602401	TAS				I		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0001572	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0001810	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0002209	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0006349	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0007436	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0008391	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0040079	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0100840	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602401	ECTODERMAL DYSPLASIA 8, HAIR/TOOTH/NAIL TYPE		HP:0200102	OMIM:602401	TAS				P		HPO:skoehler	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000006	OMIM:602418	IEA				I		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000126	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000175	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000204	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000218	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000275	OMIM:602418	TAS				P		HPO:probinson	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000276	OMIM:602418	TAS				P		HPO:probinson	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000347	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0000601	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0001180	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0002984	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0003027	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0005070	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0006315	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0006495	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0009623	OMIM:602418	IEA				P		HPO:iea	
OMIM	602418	WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME		HP:0009777	OMIM:602418	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0000006	OMIM:602433	IEA				I		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0000764	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0001347	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0001761	OMIM:602433	TAS				P		HPO:probinson	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002127	OMIM:602433	TAS				P		HPO:skoehler	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002169	OMIM:602433	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002355	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002366	OMIM:602433	TAS				P		HPO:skoehler	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002398	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0002460	OMIM:602433	TAS				P		HPO:probinson	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0003405	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0003487	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0003677	OMIM:602433	IEA				C		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0006825	OMIM:602433	IEA				P		HPO:iea	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0007354	OMIM:602433	TAS				P		HPO:probinson	
OMIM	602433	#602433 AMYOTROPHIC LATERAL SCLEROSIS 4, JUVENILE; ALS4;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, WITH PYRAMIDAL FEATURES		HP:0040078	OMIM:602433	TAS				P		HPO:skoehler	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0002380	OMIM:602440	IEA				P		HPO:iea	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0003445	OMIM:602440	IEA				P		HPO:skoehler	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0003484	OMIM:602440	TAS				P		HPO:probinson	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0003587	OMIM:602440	IEA				C		HPO:iea	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0003745	OMIM:602440	IEA				I		HPO:iea	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0007181	OMIM:602440	TAS				P		HPO:probinson	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0010873	OMIM:602440	IEA				P		HPO:skoehler	
OMIM	602440	AMYOTROPHY, MONOMELIC		HP:0031372	OMIM:602440	IEA				P		HPO:skoehler	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0000007	OMIM:602450	IEA				I		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0000155	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0000388	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0001508	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0002014	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0002090	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0002732	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0002788	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0003139	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0003249	OMIM:602450	IEA				P		HPO:iea	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0004430	OMIM:602450	TAS				P		HPO:probinson	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0005359	OMIM:602450	TAS				P		HPO:probinson	
OMIM	602450	SEVERE COMBINED IMMUNODEFICIENCY WITH SENSITIVITY TO IONIZING RADIATION		HP:0030813	OMIM:602450	TAS				P		HPO:skoehler	
OMIM	602459	#602459 DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15		HP:0000006	OMIM:602459	IEA				I		HPO:skoehler	
OMIM	602459	#602459 DEAFNESS, AUTOSOMAL DOMINANT 15; DFNA15		HP:0000365	OMIM:602459	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000007	OMIM:602471	IEA				I		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000028	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000160	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000218	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000272	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000347	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000405	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000413	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000490	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000494	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000601	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0000882	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0001371	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0001762	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0002827	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0003083	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0003577	OMIM:602471	TAS				C		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0004322	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0004467	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0005792	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0006595	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0008785	OMIM:602471	IEA				P		HPO:iea	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0008905	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602471	#602471 SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, ANDSKELETAL ABNORMALITIES; SAMS		HP:0011968	OMIM:602471	TAS				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0000007	OMIM:602473	IEA				I		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0000967	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001063	OMIM:602473	IEA				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001249	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001250	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001251	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001252	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001263	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001290	OMIM:602473	TAS				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001298	OMIM:602473	IEA				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0001508	OMIM:602473	TAS				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0002028	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0002071	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0002376	OMIM:602473	TAS				P		HPO:skoehler	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0003128	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0003219	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0003688	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0007183	OMIM:602473	IEA				P		HPO:iea	
OMIM	602473	ENCEPHALOPATHY, ETHYLMALONIC; EE		HP:0008046	OMIM:602473	PCS				P		HPO:probinson	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0000007	OMIM:602475	IEA				I		HPO:iea	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0000819	OMIM:602475	IEA				P		HPO:skoehler	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0000925	OMIM:602475	IEA				P		HPO:iea	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0001347	OMIM:602475	IEA				P		HPO:iea	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0002176	OMIM:602475	IEA				P		HPO:iea	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0002196	OMIM:602475	IEA				P		HPO:iea	
OMIM	602475	OSSIFICATION OF THE POSTERIOR LONGITUDINAL LIGAMENT OF SPINE		HP:0011001	OMIM:602475	IEA				P		HPO:iea	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0000006	OMIM:602477	IEA				I		HPO:iea	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0001425	OMIM:602477	TAS				I		HPO:skoehler	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0002069	OMIM:602477	IEA				P		HPO:iea	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0002373	OMIM:602477	TAS				P		HPO:skoehler	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0003593	OMIM:602477	TAS				C		HPO:probinson	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0010818	OMIM:602477	IEA				P		HPO:iea	
OMIM	602477	FEBRILE SEIZURES, FAMILIAL, 2; FEB2		HP:0010819	OMIM:602477	TAS				P		HPO:skoehler	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0000006	OMIM:602481	IEA				I		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0000622	OMIM:602481	TAS				P		HPO:probinson	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0000651	OMIM:602481	TAS				P		HPO:probinson	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001125	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001249	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001250	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001259	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001260	OMIM:602481	TAS				P		HPO:probinson	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001269	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001289	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001425	OMIM:602481	TAS				I		HPO:skoehler	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0001945	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002077	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002131	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002186	OMIM:602481	TAS				P		HPO:probinson	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002301	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002321	OMIM:602481	IEA				P		HPO:skoehler	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002329	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002357	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0002381	OMIM:602481	IEA				P		HPO:iea	
OMIM	602481	MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2		HP:0003829	OMIM:602481	IEA				C		HPO:iea	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000006	OMIM:602482	IEA				I		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000272	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000316	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000407	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000501	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000520	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000627	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000668	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0000691	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0001320	OMIM:602482	TAS				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0001425	OMIM:602482	IEA				I		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0001631	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0001643	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0007676	OMIM:602482	IEA				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0009918	OMIM:602482	TAS				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0011120	OMIM:602482	TAS				P		HPO:skoehler	
OMIM	602482	#602482 AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3;;AXENFELD-RIEGER ANOMALY WITH OR WITHOUT CARDIAC DEFECTS AND/OR SENSORINEURALHEARING LOSS;;ANTERIOR SEGMENT MESENCHYMAL DYSGENESIS;;ANTERIOR CHAMBER CLEAVAGE SYNDROME;;RIEGER SYNDROME, TYPE 3AXENFELD ANOMALY, INCLUDED;;RIEGER ANOMALY, INCLUDED;;AXENFELD-RIEGER ANOMALY, INCLUDED		HP:0011800	OMIM:602482	TAS				P		HPO:skoehler	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000006	OMIM:602483	IEA				I		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000160	PMID:16114046	PCS		HP:0040284		P		HPO:probinson	52%
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000162	PMID:16114046	PCS		HP:0040284		P		HPO:probinson	46%
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000175	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000256	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000311	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000347	PMID:16114046	PCS		HP:0040284		P		HPO:probinson	71%
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000358	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000369	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000378	OMIM:602483	PCS				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000384	OMIM:602483	PCS				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000402	PMID:16114046	PCS		HP:0040284		P		HPO:probinson	30%
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000678	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0000689	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0002104	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0004451	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0004453	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0005216	OMIM:602483	PCS				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0007627	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0007628	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0008537	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0008559	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0009088	OMIM:602483	IEA				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0009102	OMIM:602483	PCS				P		HPO:probinson	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0025267	OMIM:602483	TAS				P		HPO:skoehler	
OMIM	602483	AURICULOCONDYLAR SYNDROME 1; ARCND1		HP:0031013	OMIM:602483	IEA				P		HPO:skoehler	
OMIM	602484	PELVIC DYSPLASIA - ARTHROGRYPOSIS OF LOWER LIMBS		HP:0002804	OMIM:602484	IEA				P		HPO:skoehler	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0000006	OMIM:602485	IEA				I		HPO:iea	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0000819	OMIM:602485	IEA	HP:0003584			P		HPO:iea	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0000825	OMIM:602485	IEA				P		HPO:iea	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0001249	OMIM:602485	IEA				P		HPO:iea	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0001325	OMIM:602485	IEA				P		HPO:iea	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0001425	OMIM:602485	TAS				I		HPO:skoehler	
OMIM	602485	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3		HP:0002173	OMIM:602485	IEA				P		HPO:iea	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000006	OMIM:602499	TAS				I		HPO:nvasilevsky	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000482	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000486	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000545	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000589	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0000639	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0007401	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0007663	OMIM:602499	IEA				P		HPO:skoehler	
OMIM	602499	MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA; MACOM		HP:0007906	OMIM:602499	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000238	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000286	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000316	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000319	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000337	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000494	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000568	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0000965	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001159	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001249	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001250	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001252	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001263	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001290	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001355	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001388	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001428	OMIM:602501	TAS				I		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001548	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001629	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0001909	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0002119	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0002126	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0002389	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0002667	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0002858	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0003745	OMIM:602501	IEA				I		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0004481	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0005280	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0009748	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0010442	OMIM:602501	IEA				P		HPO:skoehler	
OMIM	602501	MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME		HP:0100790	OMIM:602501	TAS				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000007	OMIM:602522	IEA				I		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000083	OMIM:602522	TAS				P		HPO:probinson	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000103	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000127	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000407	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000859	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000969	OMIM:602522	IEA				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001249	OMIM:602522	IEA				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001252	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001265	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001270	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001290	OMIM:602522	TAS				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001425	OMIM:602522	IEA				I		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001508	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001561	OMIM:602522	TAS				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001563	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001622	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001789	OMIM:602522	TAS				P		HPO:probinson	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002900	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002902	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002914	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003081	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003113	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003577	OMIM:602522	IEA				C		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0004737	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0004909	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0005565	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0005576	OMIM:602522	IEA				P		HPO:iea	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0012213	OMIM:602522	TAS				P		HPO:skoehler	
OMIM	602522	BARTTER SYNDROME, TYPE 4A, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0012605	OMIM:602522	IEA				P		HPO:iea	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0000007	OMIM:602531	TAS				I		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0001156	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0001159	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0001249	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0001647	OMIM:602531	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0001920	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0002757	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0004325	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0005145	OMIM:602531	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0040019	OMIM:602531	IEA				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0100546	OMIM:602531	IEA				P		HPO:skoehler	
OMIM	602531	GRANGE SYNDROME; GRNG		HP:0100817	OMIM:602531	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000006	OMIM:602535	TAS				I		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000098	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000162	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000212	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000272	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000278	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000322	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000365	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000369	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000396	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000452	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000453	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000463	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000574	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000586	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000592	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000664	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000767	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000822	OMIM:602535	IEA				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0000879	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001249	OMIM:602535	IEA				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001252	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001270	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001274	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001290	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001508	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001537	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001539	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001601	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001631	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0001643	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002007	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002059	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002092	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002100	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002104	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002650	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0002870	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003100	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003196	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003311	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003414	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003745	OMIM:602535	IEA				I		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003778	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0003819	OMIM:602535	IEA				M		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0004325	OMIM:602535	TAS				P		HPO:probinson	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0005280	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0005616	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0006048	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0006642	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0007227	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0009845	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0009882	OMIM:602535	IEA				P		HPO:iea	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0010759	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0011220	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0011800	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0012472	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602535	MARSHALL-SMITH SYNDROME; MRSHSS		HP:0040079	OMIM:602535	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000006	OMIM:602540	TAS				I		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000407	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000535	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000561	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000653	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0000982	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0001019	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0001761	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0002860	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0003593	OMIM:602540	TAS				C		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0004552	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0008064	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602540	#602540 ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS;;HID SYNDROME		HP:0011859	OMIM:602540	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0000007	OMIM:602541	TAS				I		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0000252	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0000750	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001249	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001250	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001270	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001319	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001427	OMIM:602541	TAS				I		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0001644	OMIM:602541	TAS		HP:0040284		P		HPO:skoehler	50%
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0002465	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0002515	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003198	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003236	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003391	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003560	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003577	OMIM:602541	TAS				C		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003677	OMIM:602541	TAS				C		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0003741	OMIM:602541	IEA				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0008064	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602541	#602541 MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC;;MUSCULAR DYSTROPHY, CONGENITAL, WITH MITOCHONDRIAL STRUCTURAL ABNORMALITIES		HP:0010628	OMIM:602541	TAS				P		HPO:skoehler	
OMIM	602554	TORSION DYSTONIA WITH ONSET IN INFANCY		HP:0000006	OMIM:602554	IEA				I		HPO:iea	
OMIM	602554	TORSION DYSTONIA WITH ONSET IN INFANCY		HP:0001304	OMIM:602554	IEA				P		HPO:iea	
OMIM	602554	TORSION DYSTONIA WITH ONSET IN INFANCY		HP:0003593	OMIM:602554	IEA				C		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0000007	OMIM:602557	IEA				I		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0000233	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0000470	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0000773	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0000926	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0001388	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0001591	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0001744	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002240	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002651	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002663	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002812	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002938	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002970	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0002983	OMIM:602557	TAS				P		HPO:skoehler	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0003015	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0003025	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0003099	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0003270	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0003375	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE	HP:0012828	HP:0003498	OMIM:602557	TAS				P		HPO:probinson	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0004298	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0008417	OMIM:602557	TAS	HP:0003593			P		HPO:skoehler	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE	HP:0012825	HP:0008450	OMIM:602557	TAS				P		HPO:probinson	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0008463	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0009826	OMIM:602557	IEA				P		HPO:iea	
OMIM	602557	602557 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SHOHAT TYPE;;SEMD, SHOHAT TYPE		HP:0100864	OMIM:602557	IEA				P		HPO:iea	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000154	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000239	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000311	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000316	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000319	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000343	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000347	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000358	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000403	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000431	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000463	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000491	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000494	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000509	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000574	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000637	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000656	OMIM:602562	IEA				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA	HP:0012825	HP:0000664	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0000677	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0003745	OMIM:602562	TAS				I		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0005321	OMIM:602562	IEA				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0007957	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0008551	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602562	MANDIBULOFACIAL DYSOSTOSIS WITH MACROBLEPHARON AND MACROSTOMIA		HP:0012368	OMIM:602562	TAS				P		HPO:skoehler	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0000007	OMIM:602579	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0000825	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001252	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001290	OMIM:602579	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:skoehler	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001394	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001395	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001399	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001508	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001892	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:skoehler	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001929	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001976	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0001977	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0002013	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0002014	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0002240	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0002243	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0003073	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0003642	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:iea	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0011473	OMIM:602579	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:skoehler	
OMIM	602579	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib; CDG1B		HP:0031842	OMIM:602579	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IB; CDG1B	HPO:skoehler	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000006	OMIM:602588	IEA				I		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000278	OMIM:602588	TAS				P		HPO:probinson	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000369	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000378	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000407	OMIM:602588	TAS				P		HPO:skoehler	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0000410	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0003828	OMIM:602588	IEA				C		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0003829	OMIM:602588	IEA				C		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0004458	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0004467	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0008551	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0008554	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0008586	OMIM:602588	IEA				P		HPO:iea	
OMIM	602588	#602588 BRANCHIOOTIC SYNDROME 1; BOS1;;BO SYNDROME 1;;BRANCHIOOTIC DYSPLASIAANTERIOR SEGMENT ANOMALIES WITH OR WITHOUT CATARACT, INCLUDED		HP:0009795	OMIM:602588	TAS				P		HPO:probinson	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000007	OMIM:602613	IEA				I		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000023	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000028	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000272	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000343	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000347	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000402	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000463	OMIM:602613	TAS				P		HPO:probinson	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000470	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000520	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000890	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000954	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0000965	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001156	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001193	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001250	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001321	OMIM:602613	TAS				P		HPO:skoehler	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001508	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001522	OMIM:602613	IEA				M		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001561	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001655	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0001714	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002059	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002079	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002104	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002171	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002245	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002529	OMIM:602613	IEA				P		HPO:skoehler	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0002984	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0003022	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0003100	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0003196	OMIM:602613	TAS				P		HPO:probinson	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0005043	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0005257	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0005280	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0005716	OMIM:602613	TAS				P		HPO:probinson	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0006157	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0007009	OMIM:602613	IEA				P		HPO:skoehler	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0007100	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0008070	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0008452	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0008839	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0008905	OMIM:602613	IEA				P		HPO:iea	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0009487	OMIM:602613	TAS				P		HPO:skoehler	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0012368	OMIM:602613	TAS				P		HPO:skoehler	
OMIM	602613	SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION, LETHAL		HP:0020034	OMIM:602613	TAS				C		HPO:skoehler	
OMIM	602629	DYSTONIA 6, TORSION		HP:0000006	OMIM:602629	IEA				I		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0000234	OMIM:602629	IEA				P		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0000473	OMIM:602629	IEA				P		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0001260	OMIM:602629	IEA				P		HPO:skoehler	
OMIM	602629	DYSTONIA 6, TORSION		HP:0001304	OMIM:602629	IEA				P		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0001336	OMIM:602629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602629	DYSTONIA 6, TORSION		HP:0001618	OMIM:602629	IEA				P		HPO:skoehler	
OMIM	602629	DYSTONIA 6, TORSION		HP:0002356	OMIM:602629	IEA				P		HPO:skoehler	
OMIM	602629	DYSTONIA 6, TORSION		HP:0002451	OMIM:602629	IEA				P		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0003829	OMIM:602629	TAS		HP:0040284		C		HPO:skoehler	60%
OMIM	602629	DYSTONIA 6, TORSION		HP:0012048	OMIM:602629	IEA				P		HPO:iea	
OMIM	602629	DYSTONIA 6, TORSION		HP:0012049	OMIM:602629	TAS				P		HPO:skoehler	
OMIM	602629	DYSTONIA 6, TORSION		HP:0031008	OMIM:602629	TAS				P		HPO:skoehler	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0000006	OMIM:602668	IEA				I		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0000135	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0000798	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0000819	OMIM:602668	TAS				P		HPO:skoehler	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0001649	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0001962	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0002292	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0002486	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0002850	OMIM:602668	TAS				P		HPO:skoehler	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0003236	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0003326	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0003554	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0003701	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0003722	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0004315	OMIM:602668	TAS				P		HPO:skoehler	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0007889	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0008189	OMIM:602668	IEA				P		HPO:iea	
OMIM	602668	DYSTROPHIA MYOTONICA 2		HP:0008232	OMIM:602668	IEA				P		HPO:iea	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0000007	OMIM:602722	IEA				I		HPO:skoehler	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0000121	OMIM:602722	IEA		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0001508	OMIM:602722	IEA				P		HPO:skoehler	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0001510	OMIM:602722	IEA				P		HPO:skoehler	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0001944	OMIM:602722	IEA				P		HPO:skoehler	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0002013	OMIM:602722	IEA				P		HPO:skoehler	
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0008341	OMIM:602722	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	602722	#602722 RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE; RTADR;;RTA, DISTAL, AUTOSOMAL RECESSIVE;;RENAL TUBULAR ACIDOSIS, AUTOSOMAL RECESSIVE, WITH PRESERVED HEARINGRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSETSENSORINEURAL HEARING LOSS, INCLUDED		HP:0008619	OMIM:602722	IEA				P		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0000006	OMIM:602723	TAS				I		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0000962	OMIM:602723	TAS				P		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0001036	OMIM:602723	TAS				P		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0003765	OMIM:602723	IEA				P		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0025092	OMIM:602723	TAS				P		HPO:skoehler	
OMIM	602723	PSORIASIS 2; PSORS2		HP:0040189	OMIM:602723	IEA				P		HPO:skoehler	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0000007	OMIM:602771	IEA				I		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0000218	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001252	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001270	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001290	OMIM:602771	TAS				P		HPO:skoehler	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001371	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001508	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001547	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001611	OMIM:602771	TAS				P		HPO:probinson	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0001620	OMIM:602771	TAS				P		HPO:probinson	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0002111	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0002421	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0002650	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0002792	OMIM:602771	TAS				P		HPO:probinson	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0002877	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003306	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003324	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003327	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003557	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003560	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003593	OMIM:602771	IEA				C		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003680	OMIM:602771	IEA				C		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003700	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0003787	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0004322	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0005991	OMIM:602771	IEA				P		HPO:iea	
OMIM	602771	RIGID SPINE MUSCULAR DYSTROPHY 1		HP:0010628	OMIM:602771	IEA				P		HPO:iea	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000007	PMID:18976725	PCS				I		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000510	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000533	OMIM:602772	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000543	OMIM:602772	IEA				P		HPO:skoehler	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000550	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000613	OMIM:602772	IEA				P		HPO:skoehler	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0000662	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0001133	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0007737	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0007787	OMIM:602772	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	602772	RETINITIS PIGMENTOSA 25; RP25		HP:0007843	PMID:18976725	PCS				P		HPO:probinson	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000007	OMIM:602782	TAS				I		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000407	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000520	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000815	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000819	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0000824	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001629	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001631	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001634	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001640	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001744	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001822	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0001945	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0002240	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0002594	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0002987	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0004322	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0005200	OMIM:602782	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0012385	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0025289	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0030084	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0100534	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602782	HISTIOCYTOSIS-LYMPHADENOPATHY PLUS SYNDROME		HP:0100727	OMIM:602782	TAS				P		HPO:skoehler	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000006	OMIM:602849	IEA				I		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000218	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000248	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000256	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000272	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000294	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000316	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000407	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000486	OMIM:602849	IEA				P		HPO:skoehler	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000494	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000508	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0000689	OMIM:602849	IEA				P		HPO:skoehler	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0001156	OMIM:602849	TAS				P		HPO:skoehler	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0001241	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0001249	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0001263	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0001357	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0003795	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0004440	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0005819	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0006193	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0009466	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0010055	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0010230	OMIM:602849	IEA				P		HPO:iea	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0011800	OMIM:602849	TAS				P		HPO:skoehler	
OMIM	602849	MUENKE SYNDROME; MNKES		HP:0030084	OMIM:602849	TAS				P		HPO:skoehler	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0000007	OMIM:602875	IEA				I		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001230	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001377	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001388	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001500	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001783	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001799	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001831	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001831	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0001847	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0002007	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0002938	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0002984	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0002986	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0003015	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0003086	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0003196	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0003300	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0003498	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0004568	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0004633	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0005619	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0006009	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0007516	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0008484	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0009803	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0009803	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0010049	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0010230	OMIM:602875	IEA				P		HPO:iea	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0010743	OMIM:602875	TAS				P		HPO:probinson	
OMIM	602875	#602875 ACROMESOMELIC DYSPLASIA, MAROTEAUX TYPE; AMDMST. HELENA DYSPLASIA, INCLUDED		HP:0011220	OMIM:602875	TAS				P		HPO:skoehler	
OMIM	603010	DEAFNESS, AUTOSOMAL RECESSIVE 17; DFNB17		HP:0000007	OMIM:603010	TAS				I		HPO:skoehler	
OMIM	603010	DEAFNESS, AUTOSOMAL RECESSIVE 17; DFNB17		HP:0000407	OMIM:603010	TAS				P		HPO:skoehler	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0000007	OMIM:603034	IEA				I		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0000508	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0000597	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0001252	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0001260	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0001290	OMIM:603034	TAS				P		HPO:skoehler	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0001612	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0002015	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0002093	OMIM:603034	TAS				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0002650	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0002715	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0002747	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003198	OMIM:603034	IEA				P		HPO:skoehler	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003199	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003307	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003324	OMIM:603034	TAS				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003388	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003403	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003436	OMIM:603034	TAS				P		HPO:skoehler	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003443	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003473	OMIM:603034	TAS				P		HPO:probinson	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003554	OMIM:603034	TAS				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003593	OMIM:603034	TAS				C		HPO:probinson	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0003690	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0008872	OMIM:603034	IEA				P		HPO:iea	
OMIM	603034	MYASTHENIC SYNDROME, CONGENITAL, 5; CMS5		HP:0008872	OMIM:603034	TAS				P		HPO:probinson	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0000007	OMIM:603041	IEA				I		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0000407	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0000508	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0000590	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0001284	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0001533	OMIM:603041	IEA				P		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002013	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002019	OMIM:603041	TAS				P		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002024	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002027	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002254	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002352	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002460	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002578	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002579	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0002936	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003128	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003200	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003548	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003676	OMIM:603041	TAS				C		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003688	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003689	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003693	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0003737	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0004326	OMIM:603041	TAS				P		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0004395	OMIM:603041	IEA				P		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0007103	OMIM:603041	IEA				P		HPO:iea	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0031368	OMIM:603041	IEA				P		HPO:skoehler	
OMIM	603041	MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); MTDPS1		HP:0100613	OMIM:603041	TAS				M		HPO:skoehler	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0000006	OMIM:603075	TAS				I		HPO:skoehler	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0000529	PMID:15013873	PCS	HP:0003584			P		HPO:skoehler	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0000608	PMID:15013873	PCS				P		HP:probinson	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0011506	OMIM:603075	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0012643	OMIM:603075	TAS				P		HPO:skoehler	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0025574	OMIM:603075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0030499	PMID:15013873	PCS	HP:0003584			P		HP:probinson	
OMIM	603075	MACULAR DEGENERATION, AGE-RELATED, 1; ARMD1		HP:0031609	PMID:15013873	PCS	HP:0003584			P		HP:probinson	
OMIM	603098	DEAFNESS, AUTOSOMAL RECESSIVE 13		HP:0000007	OMIM:603098	TAS				I		HPO:skoehler	
OMIM	603098	DEAFNESS, AUTOSOMAL RECESSIVE 13		HP:0000407	PMID:9781028	TAS				P		HPO:lccarmody	
OMIM	603116	CDAGS SYNDROME		HP:0000007	OMIM:603116	IEA				I		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000047	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000143	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000175	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000248	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000270	OMIM:603116	TAS				P		HPO:probinson	
OMIM	603116	CDAGS SYNDROME		HP:0000272	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000407	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000508	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000535	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000653	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000656	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000773	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0000894	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0001263	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0002007	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0002023	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0002209	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0002697	OMIM:603116	IEA				P		HPO:skoehler	
OMIM	603116	CDAGS SYNDROME		HP:0002808	OMIM:603116	IEA				P		HPO:iea	
OMIM	603116	CDAGS SYNDROME		HP:0004440	OMIM:603116	TAS				P		HPO:probinson	
OMIM	603116	CDAGS SYNDROME		HP:0004442	OMIM:603116	TAS				P		HPO:probinson	
OMIM	603116	CDAGS SYNDROME		HP:0004443	OMIM:603116	TAS				P		HPO:probinson	
OMIM	603116	CDAGS SYNDROME		HP:0011800	OMIM:603116	TAS				P		HPO:skoehler	
OMIM	603116	CDAGS SYNDROME		HP:0025407	OMIM:603116	TAS				P		HPO:skoehler	
OMIM	603116	CDAGS SYNDROME		HP:0200044	OMIM:603116	IEA				P		HPO:skoehler	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0000007	OMIM:603147	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0000486	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001250	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001251	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001263	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001284	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001929	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0001976	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0003642	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0008150	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0008936	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:iea	
OMIM	603147	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C		HP:0025356	OMIM:603147	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IC; CDG1C	HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000006	OMIM:603165	IEA				I		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000509	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000518	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000563	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000958	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000964	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000980	OMIM:603165	IEA				P		HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0000989	OMIM:603165	TAS				P		HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0001041	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0001047	OMIM:603165	TAS				P		HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0001581	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0001939	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0002099	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0003193	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0007453	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0008064	OMIM:603165	IEA				P		HPO:iea	
OMIM	603165	DERMATITIS, ATOPIC		HP:0011232	OMIM:603165	TAS				P		HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0012537	OMIM:603165	TAS				P		HPO:skoehler	
OMIM	603165	DERMATITIS, ATOPIC		HP:0032152	OMIM:603165	IEA				P		HPO:skoehler	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0000007	PMID:20512146	PCS				I		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0000107	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0000175	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0000568	OMIM:603194	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0001162	OMIM:603194	TAS				P		HPO:skoehler	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0001305	OMIM:603194	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0001408	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0001511	OMIM:603194	TAS				P		HPO:skoehler	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0002084	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0002323	OMIM:603194	TAS				P		HPO:skoehler	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0002435	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0006487	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603194	#603194 MECKEL SYNDROME, TYPE 2; MKS2;;MECKEL-GRUBER SYNDROME, TYPE 2		HP:0010442	PMID:20512146	PCS				P		HPO:probinson	
OMIM	603204	EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2		HP:0000006	OMIM:603204	TAS				I		HPO:skoehler	
OMIM	603204	EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2		HP:0000716	OMIM:603204	TAS				P		HPO:skoehler	
OMIM	603204	EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2		HP:0000718	OMIM:603204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603204	EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2		HP:0002069	OMIM:603204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603204	EPILEPSY, NOCTURNAL FRONTAL LOBE, 2; ENFL2		HP:0002133	OMIM:603204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000006	OMIM:603218	IEA				I		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000711	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000716	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000718	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000726	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000739	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000746	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0000751	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0001260	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0001310	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0002063	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0002072	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0002283	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0002311	OMIM:603218	TAS				P		HPO:skoehler	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0002317	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0006999	OMIM:603218	IEA				P		HPO:iea	
OMIM	603218	HUNTINGTON DISEASE-LIKE 1		HP:0006999	OMIM:603218	TAS				P		HPO:probinson	
OMIM	603221	MYOPIA 3		HP:0000006	OMIM:603221	IEA				I		HPO:iea	
OMIM	603221	MYOPIA 3		HP:0000541	OMIM:603221	IEA				P		HPO:iea	
OMIM	603221	MYOPIA 3		HP:0001425	OMIM:603221	IEA				I		HPO:skoehler	
OMIM	603221	MYOPIA 3		HP:0011003	OMIM:603221	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0000006	OMIM:603233	IEA				I		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0000852	OMIM:603233	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0001156	OMIM:603233	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0001513	OMIM:603233	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0002901	OMIM:603233	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0002905	OMIM:603233	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0003165	OMIM:603233	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0003456	OMIM:603233	IEA				P		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0003745	OMIM:603233	IEA				I		HPO:iea	
OMIM	603233	PSEUDOHYPOPARATHYROIDISM, TYPE IB		HP:0010049	OMIM:603233	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0000006	OMIM:603278	TAS				I		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0000093	OMIM:603278	IEA				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0000097	OMIM:603278	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0000822	OMIM:603278	TAS				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0000969	OMIM:603278	IEA				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0001903	OMIM:603278	TAS				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003073	OMIM:603278	IEA				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003077	OMIM:603278	IEA				P		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003677	OMIM:603278	TAS				C		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003774	OMIM:603278	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003828	OMIM:603278	TAS				C		HPO:skoehler	
OMIM	603278	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1		HP:0003829	OMIM:603278	TAS				C		HPO:skoehler	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0000006	OMIM:603284	IEA				I		HPO:iea	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0001009	OMIM:603284	IEA				P		HPO:skoehler	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0001250	OMIM:603284	IEA				P		HPO:iea	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0001297	OMIM:603284	IEA				P		HPO:skoehler	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0001342	OMIM:603284	TAS				P		HPO:skoehler	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0001425	OMIM:603284	TAS				I		HPO:skoehler	
OMIM	603284	CEREBRAL CAVERNOUS MALFORMATIONS 2		HP:0002315	OMIM:603284	IEA				P		HPO:skoehler	
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0001250	OMIM:603285	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0001342	OMIM:603285	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0001428	OMIM:603285	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0002060	OMIM:603285	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0002315	OMIM:603285	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	603285	#603285 CEREBRAL CAVERNOUS MALFORMATIONS 3; CCM3		HP:0003470	OMIM:603285	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0001319	PMID:12215968	PCS	HP:0003623	HP:0040284		P		HPO:probinson	3/20
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0001396	PMID:12215968	PCS	HP:0003623	HP:0040284		P		HPO:probinson	19/20
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0001511	PMID:12215968	PCS				P		HPO:probinson	
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0003281	PMID:12215968	PCS	HP:0003623			P		HPO:probinson	
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0003355	PMID:12215968	PCS	HP:0003623	HP:0040284		P		HPO:probinson	20/20
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0003452	PMID:12215968	PCS	HP:0003623			P		HPO:probinson	
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0003542	PMID:12215968	PCS	HP:0003623			P		HPO:probinson	
OMIM	603358	#603358 GRACILE SYNDROME;;GROWTH RETARDATION, AMINO ACIDURIA, CHOLESTASIS, IRON OVERLOAD, LACTICACIDOSIS, AND EARLY DEATH;;FINNISH LETHAL NEONATAL METABOLIC SYNDROME; FLNMS;;LACTIC ACIDOSIS, FINNISH, WITH HEPATIC HEMOSIDEROSIS;;FELLMAN SYNDROME		HP:0004925	PMID:12215968	PCS	HP:0003623			P		HPO:probinson	
OMIM	603373	#603373 HYPERTHYROIDISM, FAMILIAL GESTATIONAL		HP:0000006	PMID:9854118	TAS				I		HPO:probinson	
OMIM	603373	#603373 HYPERTHYROIDISM, FAMILIAL GESTATIONAL		HP:0000836	PMID:9854118	TAS				P		HPO:probinson	
OMIM	603373	#603373 HYPERTHYROIDISM, FAMILIAL GESTATIONAL		HP:0012188	PMID:9854118	TAS				P		HPO:probinson	
OMIM	603383	GLAUCOMA 1, OPEN ANGLE, F; GLC1F		HP:0000006	OMIM:603383	TAS				I		HPO:probinson	
OMIM	603383	GLAUCOMA 1, OPEN ANGLE, F; GLC1F		HP:0007854	OMIM:603383	TAS				P		HPO:probinson	
OMIM	603383	GLAUCOMA 1, OPEN ANGLE, F; GLC1F		HP:0007906	OMIM:603383	TAS				P		HPO:probinson	
OMIM	603383	GLAUCOMA 1, OPEN ANGLE, F; GLC1F		HP:0012108	OMIM:603383	TAS				P		HPO:probinson	
OMIM	603383	GLAUCOMA 1, OPEN ANGLE, F; GLC1F		HP:0012796	OMIM:603383	TAS				P		HPO:probinson	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000006	OMIM:603387	TAS				I		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000238	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000256	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000508	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000618	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0000637	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001090	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001250	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001263	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001302	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001355	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001629	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001631	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0001653	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002007	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002079	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002126	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002187	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002808	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0002943	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0003202	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0006380	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0007074	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0008936	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0010775	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603387	#603387 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME;MPPH;;MEGALENCEPHALY, POLYMICROGYRIA, MEGA CORPUS CALLOSUM SYNDROME;;MEG-PMG-MEGACC SYNDROME;;MEGALENCEPHALY, MEGA CORPUS CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT		HP:0100259	OMIM:603387	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000006	OMIM:603457	TAS				I		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000023	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000028	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000047	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000054	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000059	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000135	OMIM:603457	IEA				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000175	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000218	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000316	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000365	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000453	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000458	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000518	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000568	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000589	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000664	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000685	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000689	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0000786	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0004409	OMIM:603457	IEA				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0006349	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0007957	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0009927	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0011800	OMIM:603457	TAS				P		HPO:skoehler	
OMIM	603457	BOSMA ARHINIA MICROPHTHALMIA SYNDROME		HP:0410030	OMIM:603457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000007	OMIM:603463	IEA				I		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000047	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000232	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000272	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000303	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000316	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000410	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000636	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000689	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0000768	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0002690	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0004322	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0004492	OMIM:603463	IEA				P		HPO:iea	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0011120	OMIM:603463	TAS				P		HPO:skoehler	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0011800	OMIM:603463	TAS				P		HPO:skoehler	
OMIM	603463	603463 HYPOSPADIAS, HYPERTELORISM, UPPER LID COLOBOMA, AND MIXED-TYPE HEARINGLOSS		HP:0012471	OMIM:603463	TAS				P		HPO:skoehler	
OMIM	603467	#603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF		HP:0000007	OMIM:603467	TAS				I		HPO:probinson	
OMIM	603467	#603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF		HP:0003220	OMIM:603467	TAS				P		HPO:probinson	
OMIM	603467	#603467 FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF		HP:0005528	OMIM:603467	TAS				P		HPO:probinson	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0000007	OMIM:603471	TAS				I		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001259	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001289	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001397	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001402	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001733	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0001987	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0002155	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0002181	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603471	#603471 CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2;;CITRIN DEFICIENCY		HP:0002910	OMIM:603471	TAS				P		HPO:skoehler	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0000006	OMIM:603511	IEA				I		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0001283	OMIM:603511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0001371	OMIM:603511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0002015	OMIM:603511	IEA				P		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0002094	OMIM:603511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0002515	OMIM:603511	TAS				P		HPO:skoehler	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003236	OMIM:603511	IEA				P		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003391	OMIM:603511	TAS				P		HPO:skoehler	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003547	OMIM:603511	IEA				P		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003551	OMIM:603511	TAS				P		HPO:skoehler	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003555	OMIM:603511	TAS				P		HPO:probinson	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003560	OMIM:603511	TAS				P		HPO:probinson	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003581	OMIM:603511	IEA				C		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003677	OMIM:603511	IEA				C		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003749	OMIM:603511	IEA				P		HPO:iea	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0003805	OMIM:603511	TAS				P		HPO:skoehler	
OMIM	603511	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1E		HP:0010628	OMIM:603511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:603513	IEA				I		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001264	OMIM:603513	TAS				P		HPO:skoehler	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001371	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0001425	OMIM:603513	IEA				I		HPO:skoehler	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0002510	OMIM:603513	IEA				P		HPO:skoehler	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0002650	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:603513	IEA				P		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:603513	IEA				C		HPO:iea	
OMIM	603513	CEREBRAL PALSY, SPASTIC, SYMMETRIC, AUTOSOMAL RECESSIVE		HP:0100021	OMIM:603513	TAS				P		HPO:skoehler	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000006	OMIM:603516	IEA				I		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000012	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000020	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000639	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000716	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000726	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0000762	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0001250	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0001260	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0001272	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0001310	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0001347	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002015	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002062	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002066	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002070	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002071	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002073	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002075	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002168	OMIM:603516	IEA				P		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0002311	OMIM:603516	TAS				P		HPO:skoehler	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0003743	OMIM:603516	IEA				I		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0003829	OMIM:603516	IEA				C		HPO:iea	
OMIM	603516	#603516 SPINOCEREBELLAR ATAXIA 10; SCA10		HP:0007256	OMIM:603516	TAS				P		HPO:skoehler	
OMIM	603529	603529 DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLASTHETEROCHROMATIN		HP:0000006	OMIM:603529	TAS				I		HPO:skoehler	
OMIM	603529	603529 DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLASTHETEROCHROMATIN		HP:0004447	OMIM:603529	TAS				P		HPO:skoehler	
OMIM	603529	603529 DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLASTHETEROCHROMATIN		HP:0010972	OMIM:603529	TAS				P		HPO:skoehler	
OMIM	603529	603529 DYSERYTHROPOIESIS, CONGENITAL, WITH ULTRASTRUCTURALLY NORMAL ERYTHROBLASTHETEROCHROMATIN		HP:0011273	OMIM:603529	TAS				P		HPO:skoehler	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000006	OMIM:603543	IEA				I		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000175	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000193	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000564	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000668	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0000966	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0001159	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0001171	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0001822	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0001839	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0002164	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0002557	OMIM:603543	IEA				P		HPO:skoehler	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0009473	OMIM:603543	IEA				P		HPO:iea	
OMIM	603543	#603543 LIMB-MAMMARY SYNDROME; LMS		HP:0012385	OMIM:603543	TAS				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0000006	OMIM:603546	IEA				I		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0000272	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0000977	OMIM:603546	TAS				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0001252	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0001290	OMIM:603546	TAS				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0001374	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0001388	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0001498	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0002650	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0002651	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0002857	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003015	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003025	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003083	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003090	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003301	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0003370	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0004322	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0005008	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0005092	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0005121	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2	HP:0012828	HP:0006016	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0006127	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2	HP:0012828	HP:0006454	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0008457	OMIM:603546	IEA				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0008819	OMIM:603546	TAS				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0009836	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0010301	OMIM:603546	IEA				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0010582	PMID:12966527	PCS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0010585	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0011800	OMIM:603546	TAS				P		HPO:skoehler	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0012296	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0012297	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603546	SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 2		HP:0012299	OMIM:603546	TAS				P		HPO:probinson	
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0000007	PMID:16582076	PCS				I		HPO:probinson	
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001250	OMIM:603552	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001263	OMIM:603552	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001290	OMIM:603552	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001744	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001873	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001875	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001903	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0001945	PMID:16582076	PCS				P		HPO:probinson	
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0002155	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0002240	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0003281	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0011900	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	603552	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4		HP:0012156	PMID:16582076	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0000007	OMIM:603553	TAS				I		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0000737	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0000952	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001250	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001251	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001259	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001263	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001276	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001287	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001290	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001508	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001744	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001873	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001882	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0001903	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002155	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002240	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002301	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002383	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002445	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002516	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002716	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002902	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0002922	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0003073	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0003075	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0003281	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0003573	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0007430	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0008151	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0011900	OMIM:603553	TAS				P		HPO:skoehler	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0012156	OMIM:603553	TAS				P		HPO:probinson	
OMIM	603553	HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2		HP:0012229	OMIM:603553	TAS				P		HPO:probinson	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0000007	OMIM:603554	IEA				I		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0000778	OMIM:603554	TAS				P		HPO:probinson	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001019	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001072	OMIM:603554	TAS				P		HPO:skoehler	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001508	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001596	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001744	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001873	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001880	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0001903	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002014	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002090	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002240	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002716	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002718	OMIM:603554	TAS				P		HPO:probinson	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0002841	OMIM:603554	TAS				P		HPO:probinson	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0003075	OMIM:603554	IEA				P		HPO:iea	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0004429	OMIM:603554	TAS				P		HPO:probinson	
OMIM	603554	#603554 OMENN SYNDROME;;RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA;;SEVERE COMBINED IMMUNODEFICIENCY WITH HYPEREOSINOPHILIA		HP:0005365	OMIM:603554	TAS				P		HPO:skoehler	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0000006	OMIM:603563	IEA				I		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0000012	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0000020	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0001258	OMIM:603563	TAS				P		HPO:probinson	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0001347	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0001761	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0002061	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0002064	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0002166	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0002314	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0002839	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0003487	OMIM:603563	IEA				P		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0003581	OMIM:603563	IEA				C		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0003587	OMIM:603563	IEA				C		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0003676	OMIM:603563	IEA				C		HPO:iea	
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0006986	OMIM:603563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603563	#603563 SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT; SPG8		HP:0007340	OMIM:603563	IEA				P		HPO:iea	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000007	PMID:11157507	PCS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:iea	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000093	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000252	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000490	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000601	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0000639	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001249	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001250	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001251	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001260	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001263	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001298	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001873	PMID:11157507	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:probinson	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001875	PMID:11157507	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:probinson	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0001933	PMID:11157507	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:probinson	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0002310	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0002465	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0002718	PMID:11157507	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:iea	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0003355	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0003593	PMID:11157507	PCS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:iea	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0005469	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0031156	OMIM:603585	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:probinson	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0040185	OMIM:603585	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:skoehler	
OMIM	603585	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIf; CDG2F		HP:0040223	PMID:11157507	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIF; CDG2F	HPO:probinson	
OMIM	603592	XANTHINURIA, TYPE II		HP:0000007	OMIM:603592	TAS				I		HPO:skoehler	
OMIM	603592	XANTHINURIA, TYPE II		HP:0000083	OMIM:603592	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603592	XANTHINURIA, TYPE II		HP:0000787	OMIM:603592	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603592	XANTHINURIA, TYPE II		HP:0003537	OMIM:603592	TAS				P		HPO:skoehler	
OMIM	603622	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 17		HP:0000006	OMIM:603622	TAS				I		HPO:skoehler	
OMIM	603622	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 17		HP:0003621	OMIM:603622	TAS				C		HPO:skoehler	
OMIM	603622	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 17		HP:0005101	OMIM:603622	TAS				P		HPO:skoehler	
OMIM	603629	#603629 DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21		HP:0000007	PMID:9949200	PCS				I		HPO:probinson	
OMIM	603629	#603629 DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21		HP:0000407	PMID:9949200	PCS	HP:0003593			P		HPO:probinson	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0000006	OMIM:603641	IEA				I		HPO:iea	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0000407	OMIM:603641	IEA				P		HPO:iea	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0000705	OMIM:603641	IEA				P		HPO:skoehler	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0006297	OMIM:603641	IEA				P		HPO:iea	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0009590	OMIM:603641	IEA				P		HPO:iea	
OMIM	603641	NEUROENDOCRINE CARCINOMA OF SALIVARY GLANDS, SENSORINEURAL HEARING LOSS, AND ENAMEL HYPOPLASIA		HP:0030731	OMIM:603641	IEA				P		HPO:skoehler	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0000006	OMIM:603649	IEA				I		HPO:probinson	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0000505	OMIM:603649	IEA	HP:0003581			P		HPO:probinson	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0000548	OMIM:603649	IEA				P		HPO:skoehler	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0000551	OMIM:603649	IEA				P		HPO:probinson	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0011504	OMIM:603649	IEA				P		HPO:probinson	
OMIM	603649	#603649 CONE-ROD DYSTROPHY 7; CORD7		HP:0012045	OMIM:603649	IEA				P		HPO:probinson	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000006	OMIM:603671	IEA				I		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000028	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000175	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000204	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000248	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000316	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000431	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000455	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000456	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000494	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000501	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000506	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000508	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0000545	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001159	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001249	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001250	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001274	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001762	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0001805	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002079	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002084	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002119	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002190	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002282	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002690	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0002781	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0004122	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0006951	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0010442	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0010559	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0010806	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0011803	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0012032	OMIM:603671	IEA				P		HPO:skoehler	
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0040075	OMIM:603671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603671	ACROMELIC FRONTONASAL DYSOSTOSIS; AFND		HP:0100258	OMIM:603671	TAS				P		HPO:skoehler	
OMIM	603678	DEAFNESS, AUTOSOMAL RECESSIVE 14		HP:0000007	OMIM:603678	TAS				I		HPO:skoehler	
OMIM	603678	DEAFNESS, AUTOSOMAL RECESSIVE 14		HP:0000407	PMID:9887371	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	603688	#603688 PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY;;PCBC;;CAPB		HP:0012125	OMIM:603688	IEA				P		HPO:skoehler	
OMIM	603688	#603688 PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY;;PCBC;;CAPB		HP:0100006	OMIM:603688	IEA				P		HPO:skoehler	
OMIM	603689	#603689 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE; HMERF;;MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM;;EDSTROM MYOPATHY		HP:0000006	OMIM:603689	TAS				I		HPO:probinson	
OMIM	603689	#603689 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE; HMERF;;MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM;;EDSTROM MYOPATHY		HP:0003701	OMIM:603689	TAS	HP:0003581			P		HPO:probinson	
OMIM	603689	#603689 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE; HMERF;;MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM;;EDSTROM MYOPATHY		HP:0003722	OMIM:603689	TAS	HP:0003581			P		HPO:probinson	
OMIM	603689	#603689 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE; HMERF;;MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM;;EDSTROM MYOPATHY		HP:0009027	OMIM:603689	TAS	HP:0003581			P		HPO:probinson	
OMIM	603689	#603689 HEREDITARY MYOPATHY WITH EARLY RESPIRATORY FAILURE; HMERF;;MYOPATHY, PROXIMAL, WITH EARLY RESPIRATORY MUSCLE INVOLVEMENT; MPRM;;EDSTROM MYOPATHY		HP:0009113	OMIM:603689	TAS	HP:0003581			P		HPO:probinson	
OMIM	603720	DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16		HP:0000006	OMIM:603720	IEA		HP:0040280		I		HPO:skoehler	HP:0040280
OMIM	603720	DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16		HP:0000007	OMIM:603720	TAS				I		HPO:skoehler	
OMIM	603720	DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16		HP:0000407	OMIM:603720	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000252	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000269	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000347	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000358	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000369	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000414	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000537	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000581	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0000691	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0001270	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0001290	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0001644	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0005280	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603736	OHDO SYNDROME, SBBYS VARIANT; SBBYSS		HP:0010864	OMIM:603736	IEA				P		HPO:skoehler	
OMIM	603776	#603776 HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3; HCHOLA3;;FH3LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS1, INCLUDED; LDLCQ1, INCLUDED		HP:0000006	OMIM:603776	IEA		HP:0040280		I		HPO:skoehler	HP:0040280
OMIM	603776	#603776 HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, 3; HCHOLA3;;FH3LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS1, INCLUDED; LDLCQ1, INCLUDED		HP:0003124	OMIM:603776	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	603786	#603786 STARGARDT DISEASE 4; STGD4		HP:0000006	OMIM:603786	TAS				I		HPO:skoehler	
OMIM	603786	#603786 STARGARDT DISEASE 4; STGD4		HP:0000608	OMIM:603786	TAS				P		HPO:skoehler	
OMIM	603786	#603786 STARGARDT DISEASE 4; STGD4		HP:0007663	OMIM:603786	TAS				P		HPO:skoehler	
OMIM	603786	#603786 STARGARDT DISEASE 4; STGD4		HP:0012045	OMIM:603786	TAS				P		HPO:skoehler	
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0000007	OMIM:603813	IEA		HP:0040280		I		HPO:skoehler	HP:0040280
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0002155	OMIM:603813	IEA				P		HPO:skoehler	
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0002621	OMIM:603813	IEA				P		HPO:skoehler	
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0003124	OMIM:603813	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0003362	OMIM:603813	IEA				P		HPO:skoehler	
OMIM	603813	HYPERCHOLESTEROLEMIA, AUTOSOMAL RECESSIVE; ARH		HP:0010874	OMIM:603813	IEA				P		HPO:skoehler	
OMIM	603829	#603829 VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITYTO;;VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1		HP:0001279	PMID:4834245	PCS				P		HPO:lccarmody	
OMIM	603829	#603829 VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITYTO;;VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1		HP:0001649	PMID:4834245	PCS				P		HPO:lccarmody	
OMIM	603829	#603829 VENTRICULAR FIBRILLATION DURING MYOCARDIAL INFARCTION, SUSCEPTIBILITYTO;;VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 1; VF1		HP:0001663	OMIM:603829	TAS				P		HPO:skoehler	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0000006	OMIM:603830	IEA				I		HPO:iea	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001279	OMIM:603830	IEA				P		HPO:iea	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001425	OMIM:603830	TAS				I		HPO:skoehler	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001645	OMIM:603830	IEA				P		HPO:iea	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001657	OMIM:603830	IEA				P		HPO:iea	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001663	OMIM:603830	TAS				P		HPO:skoehler	
OMIM	603830	LONG QT SYNDROME 3; LQT3		HP:0001664	OMIM:603830	IEA				P		HPO:iea	
OMIM	603855	%603855 CYSTIC FIBROSIS, MODIFIER OF, 1; CFM1MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO, INCLUDED		HP:0004401	OMIM:603855	IEA				P		HPO:skoehler	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0000006	PMID:12471200	PCS				I		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0000006	OMIM:603860	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0000092	PMID:14569098	IEA				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0000108	PMID:12471200	PCS				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0000805	PMID:12471200	PCS				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0001970	PMID:14569098	IEA		HP:0040284		P		HP:probinson	6/9
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0001997	PMID:12471200	PCS				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0001997	PMID:14569098	PCS		HP:0040284		P		HP:probinson	18/39
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0002149	PMID:12471200	PCS				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0003774	PMID:12471200	PCS				P		HP:probinson	
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0003774	PMID:14569098	PCS		HP:0040284		P		HP:probinson	17/39
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0005562	PMID:14569098	PCS		HP:0040284		P		HP:probinson	9/12
OMIM	603860	#603860 MEDULLARY CYSTIC KIDNEY DISEASE 2; MCKD2;;MEDULLARY CYSTIC KIDNEY DISEASE 2, AUTOSOMAL DOMINANT; ADMCKD2		HP:0008659	PMID:12471200	PCS				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000007	OMIM:603896	IEA				I		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000256	OMIM:603896	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000618	OMIM:603896	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000648	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000712	OMIM:603896	PCS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000746	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000751	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000786	OMIM:603896	IEA				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0000869	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001250	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001252	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001254	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001257	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001260	OMIM:603896	TAS				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001288	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001290	OMIM:603896	TAS				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0001945	OMIM:603896	IEA				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0002171	OMIM:603896	IEA				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0002317	OMIM:603896	TAS				P		HPO:skoehler	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM	HP:0012828	HP:0002352	OMIM:603896	TAS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0002354	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0002376	OMIM:603896	PCS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0003621	OMIM:603896	PCS		HP:0040282		C		HPO:probinson	HP:0040282
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0004485	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0006808	OMIM:603896	PCS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0007305	OMIM:603896	PCS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0008193	OMIM:603896	IEA				P		HPO:iea	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0008209	OMIM:603896	PCS				P		HPO:probinson	
OMIM	603896	LEUKOENCEPHALOPATHY WITH VANISHING WHITE MATTER; VWM		HP:0008233	OMIM:603896	IEA				P		HPO:iea	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000007	OMIM:603903	TAS				I		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000083	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000488	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000790	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000822	OMIM:603903	IEA				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0000952	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001081	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001297	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001640	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001744	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001878	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0001974	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0002027	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0002240	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0002718	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0008346	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0012418	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603903	SICKLE CELL ANEMIA		HP:0200023	OMIM:603903	TAS				P		HPO:skoehler	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0000006	OMIM:603909	IEA				I		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0000100	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0000123	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001025	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001744	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001880	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001890	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001891	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001904	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0001973	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002240	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002633	OMIM:603909	IEA				P		HPO:skoehler	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002729	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002730	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002731	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002851	OMIM:603909	TAS				P		HPO:probinson	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002853	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002923	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0002972	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003237	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003261	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003262	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003453	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003454	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003493	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003496	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003613	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0003621	OMIM:603909	IEA				C		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0004844	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0005404	OMIM:603909	IEA				P		HPO:iea	
OMIM	603909	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA		HP:0025300	OMIM:603909	TAS				P		HPO:skoehler	
OMIM	603956	#603956 CERVICAL CANCER		HP:0001428	OMIM:603956	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	603956	#603956 CERVICAL CANCER		HP:0002664	OMIM:603956	IEA				P		HPO:skoehler	
OMIM	603956	#603956 CERVICAL CANCER		HP:0003319	OMIM:603956	IEA				P		HPO:skoehler	
OMIM	603964	%603964 DEAFNESS, AUTOSOMAL DOMINANT 16; DFNA16		HP:0000006	OMIM:603964	IEA				I		HPO:skoehler	
OMIM	603964	%603964 DEAFNESS, AUTOSOMAL DOMINANT 16; DFNA16		HP:0000360	OMIM:603964	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	603964	%603964 DEAFNESS, AUTOSOMAL DOMINANT 16; DFNA16		HP:0008615	OMIM:603964	IEA				P		HPO:skoehler	
OMIM	603965	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2		HP:0000093	OMIM:603965	TAS				P		HPO:skoehler	
OMIM	603965	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2		HP:0000097	OMIM:603965	TAS				P		HPO:skoehler	
OMIM	603965	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2		HP:0000100	OMIM:603965	TAS				P		HPO:skoehler	
OMIM	603965	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2		HP:0003774	OMIM:603965	IEA				P		HPO:skoehler	
OMIM	603965	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2		HP:0012622	OMIM:603965	TAS				P		HPO:probinson	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0000007	OMIM:604004	IEA				I		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0000256	OMIM:604004	TAS				P		HPO:skoehler	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001250	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001251	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001256	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001257	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001270	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0001355	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0003593	OMIM:604004	IEA				C		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0006943	OMIM:604004	IEA				P		HPO:iea	
OMIM	604004	#604004 MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 1; MLC1;;VACUOLATING MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS;;LVM;;VL;;LEUKOENCEPHALOPATHY WITH SWELLING AND CYSTS;;VAN DER KNAAP DISEASE		HP:0007341	OMIM:604004	IEA				P		HPO:iea	
OMIM	604060	DEAFNESS, AUTOSOMAL RECESSIVE 20; DFNB20		HP:0000007	OMIM:604060	TAS				I		HPO:skoehler	
OMIM	604060	DEAFNESS, AUTOSOMAL RECESSIVE 20; DFNB20		HP:0000365	OMIM:604060	IEA	HP:0003593			P		HPO:skoehler	
OMIM	604060	DEAFNESS, AUTOSOMAL RECESSIVE 20; DFNB20		HP:0000407	OMIM:604060	TAS				P		HPO:skoehler	
OMIM	604091	HYPOALPHALIPOPROTEINEMIA, PRIMARY		HP:0000006	PMID:9888879	PCS				I		HPO:probinson	
OMIM	604091	HYPOALPHALIPOPROTEINEMIA, PRIMARY		HP:0001658	PMID:10431236	PCS				P		HPO:lccarmody	
OMIM	604091	HYPOALPHALIPOPROTEINEMIA, PRIMARY		HP:0003233	PMID:9888879	PCS				P		HPO:probinson	
OMIM	604091	HYPOALPHALIPOPROTEINEMIA, PRIMARY		HP:0005181	PMID:7627690	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0000007	OMIM:604093	TAS				I		HPO:skoehler	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0000561	PMID:26142438	PCS	HP:0011463			P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0009926	PMID:26142438	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0009938	PMID:26142438	PCS				P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0010783	PMID:26142438	PCS				P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0010783	OMIM:604093	IEA				P		HPO:skoehler	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0025249	OMIM:604093	IEA				P		HPO:skoehler	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0031285	PMID:26142438	PCS				P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0045075	PMID:26142438	PCS	HP:0011463			P		HPO:lccarmody	
OMIM	604093	KERATOSIS PILARIS ATROPHICANS; KPA		HP:0200034	PMID:26142438	PCS				P		HPO:lccarmody	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000006	OMIM:604116	TAS				I		HPO:nvasilevsky	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000007	OMIM:604116	TAS				I		HPO:nvasilevsky	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000548	OMIM:604116	IEA				P		HPO:skoehler	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000551	OMIM:604116	IEA	HP:0003593			P		HPO:skoehler	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000572	OMIM:604116	IEA	HP:0003593			P		HPO:skoehler	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0000603	OMIM:604116	IEA	HP:0003593			P		HPO:skoehler	
OMIM	604116	#604116 CONE-ROD DYSTROPHY 3; CORD3		HP:0001419	OMIM:604116	TAS				I		HPO:nvasilevsky	
OMIM	604117	VOHWINKEL SYNDROME, VARIANT FORM		HP:0000006	OMIM:604117	TAS				I		HPO:skoehler	
OMIM	604117	VOHWINKEL SYNDROME, VARIANT FORM		HP:0000962	OMIM:604117	TAS				P		HPO:skoehler	
OMIM	604117	VOHWINKEL SYNDROME, VARIANT FORM		HP:0001036	OMIM:604117	TAS				P		HPO:skoehler	
OMIM	604117	VOHWINKEL SYNDROME, VARIANT FORM		HP:0025114	OMIM:604117	TAS				P		HPO:skoehler	
OMIM	604117	VOHWINKEL SYNDROME, VARIANT FORM		HP:0040162	OMIM:604117	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000006	OMIM:604121	TAS				I		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000407	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000648	OMIM:604121	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000709	OMIM:604121	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000716	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0000726	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0001251	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0001257	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0001272	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0001347	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0002189	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0002354	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0002476	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0002524	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0003581	OMIM:604121	TAS				C		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0003676	OMIM:604121	TAS				C		HPO:skoehler	
OMIM	604121	CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN		HP:0030050	OMIM:604121	TAS				P		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0000006	OMIM:604129	IEA				I		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0000007	OMIM:604129	IEA				I		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0001030	OMIM:604129	IEA				P		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0001056	OMIM:604129	IEA				P		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0002164	OMIM:604129	IEA				P		HPO:skoehler	
OMIM	604129	#604129 EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DYSTROPHIC EPIDERMOLYSIS BULLOSA PRURIGINOSA;;DEB, PRURIGINOSA		HP:0008404	OMIM:604129	TAS				P		HPO:skoehler	
OMIM	604131	#604131 ALPHA-THALASSEMIA		HP:0004840	OMIM:604131	TAS				P		HPO:probinson	
OMIM	604131	#604131 ALPHA-THALASSEMIA		HP:0011907	OMIM:604131	TAS				P		HPO:probinson	
OMIM	604145	#604145 CARDIOMYOPATHY, DILATED, 1G; CMD1G		HP:0000006	OMIM:604145	IEA				I		HPO:skoehler	
OMIM	604145	#604145 CARDIOMYOPATHY, DILATED, 1G; CMD1G		HP:0001644	OMIM:604145	IEA				P		HPO:skoehler	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000007	OMIM:604168	IEA				I		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000044	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000164	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000482	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000519	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000639	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000786	OMIM:604168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0000815	OMIM:604168	TAS				P		HPO:skoehler	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001171	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001249	OMIM:604168	TAS				P		HPO:skoehler	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001251	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001263	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001263	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001270	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001761	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001762	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0001999	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0002059	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0002072	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0002751	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0002816	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0003431	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0003487	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0003593	OMIM:604168	TAS				C		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0004322	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0007178	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0007182	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0008214	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0008734	OMIM:604168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0008942	OMIM:604168	IEA				P		HPO:iea	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0010620	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0011096	OMIM:604168	TAS				P		HPO:probinson	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0040078	OMIM:604168	IEA				P		HPO:skoehler	
OMIM	604168	CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN		HP:0100543	OMIM:604168	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0000006	PMID:11238270	TAS				I		HPO:probinson	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001629	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001635	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001643	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001645	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001653	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0001712	PMID:11238270	TAS				P		HPO:probinson	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0004308	PMID:11238270	TAS				P		HPO:probinson	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0004383	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0005110	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0011664	OMIM:604169	TAS				P		HPO:probinson	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0030682	OMIM:604169	TAS				P		HPO:skoehler	
OMIM	604169	LEFT VENTRICULAR NONCOMPACTION 1; LVNC1		HP:0030682	OMIM:604169	IEA				P		HPO:skoehler	
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000007	PMID:20004881	PCS				I		HPO:skoehler	
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000272	OMIM:604173	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000316	OMIM:604173	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000403	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000498	OMIM:604173	TAS				P		HPO:skoehler	
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0000509	OMIM:604173	TAS				P		HPO:skoehler	
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0001029	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0001744	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0001875	PMID:20004881	PCS				P		HPO:skoehler	
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0001875	PMID:20503306	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0003236	PMID:20004881	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0004322	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0006532	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0007556	PMID:20004881	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0011108	PMID:20004881	PCS		HP:0040284		P		HP:probinson	2/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0011800	PMID:20004881	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	604173	#604173 POIKILODERMA WITH NEUTROPENIA; PN;;POIKILODERMA WITH NEUTROPENIA, CLERICUZIO-TYPE		HP:0025435	PMID:20004881	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	604185	FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2		HP:0000006	OMIM:604185	IEA				I		HPO:iea	
OMIM	604185	FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2		HP:0000365	OMIM:604185	IEA				P		HPO:skoehler	
OMIM	604185	FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2		HP:0001425	OMIM:604185	TAS				I		HPO:skoehler	
OMIM	604185	FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2		HP:0003680	OMIM:604185	IEA				C		HPO:iea	
OMIM	604185	FACIAL PARESIS, HEREDITARY CONGENITAL, 2; HCFP2		HP:0010628	OMIM:604185	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0000006	OMIM:604187	IEA				I		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0000012	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0000020	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0001251	OMIM:604187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0001258	OMIM:604187	IEA				P		HPO:skoehler	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0001300	OMIM:604187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0001347	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0001761	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0002064	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0002166	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0002650	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0002839	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0002936	OMIM:604187	TAS				P		HPO:skoehler	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0003487	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0003676	OMIM:604187	IEA				C		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0007340	OMIM:604187	IEA				P		HPO:iea	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0011448	OMIM:604187	TAS				P		HPO:probinson	
OMIM	604187	#604187 SPASTIC PARAPLEGIA 10, AUTOSOMAL DOMINANT; SPG10;;SPASTIC PARAPLEGIA 10 WITH OR WITHOUT PERIPHERAL NEUROPATHY		HP:0011449	OMIM:604187	TAS				P		HPO:probinson	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0000007	OMIM:604213	TAS				I		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0000238	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0001250	OMIM:604213	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0001256	OMIM:604213	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0001321	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0001338	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0002079	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0002119	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0002126	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0002282	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0002700	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0006989	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0007033	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0008625	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604213	#604213 CHUDLEY-MCCULLOUGH SYNDROME; CMCS;;DEAFNESS, SENSORINEURAL, WITH PARTIAL AGENESIS OF THE CORPUS CALLOSUMAND ARACHNOID CYSTS;;DEAFNESS, AUTOSOMAL RECESSIVE 82; DFNB82		HP:0100702	OMIM:604213	TAS				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0000006	OMIM:604218	IEA				I		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0000639	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0000651	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0000726	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0001250	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0001260	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0001298	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0001336	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0002059	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0002071	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0002171	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0002529	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604218	ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB		HP:0002936	OMIM:604218	IEA				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000006	OMIM:604219	TAS				I		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000007	OMIM:604219	IEA				I		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000482	OMIM:604219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000486	OMIM:604219	TAS				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000501	OMIM:604219	TAS				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000519	OMIM:604219	TAS				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000568	OMIM:604219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000612	OMIM:604219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000639	OMIM:604219	TAS				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0000646	OMIM:604219	TAS				P		HPO:skoehler	
OMIM	604219	CATARACT 9, MULTIPLE TYPES; CTRCT9		HP:0007834	OMIM:604219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604229	PETERS ANOMALY		HP:0000007	PMID:10051017	PCS				I		HPO:curators	
OMIM	604229	PETERS ANOMALY		HP:0000486	PMID:14711722	PCS		HP:0040284		P		HPO:curators	16%
OMIM	604229	PETERS ANOMALY		HP:0000639	PMID:14711722	PCS		HP:0040284		P		HPO:curators	32%
OMIM	604229	PETERS ANOMALY		HP:0000659	OMIM:604229	IEA				P		HPO:skoehler	
OMIM	604229	PETERS ANOMALY		HP:0001087	PMID:11403040;PMID:14711722	PCS		HP:0040282		P		HPO:curators	HP:0040282
OMIM	604229	PETERS ANOMALY		HP:0007957	PMID:10051017;PMID:8162071	PCS		HP:0040281		P		HPO:curators	HP:0040281
OMIM	604232	#604232 LEBER CONGENITAL AMAUROSIS 3; LCA3RETINITIS PIGMENTOSA, JUVENILE, SPATA7-RELATED, INCLUDED		HP:0000007	PMID:21310915	PCS				I		HPO:probinson	
OMIM	604232	#604232 LEBER CONGENITAL AMAUROSIS 3; LCA3RETINITIS PIGMENTOSA, JUVENILE, SPATA7-RELATED, INCLUDED		HP:0000572	PMID:21310915	PCS		HP:0040284		P		HPO:probinson	10/10
OMIM	604232	#604232 LEBER CONGENITAL AMAUROSIS 3; LCA3RETINITIS PIGMENTOSA, JUVENILE, SPATA7-RELATED, INCLUDED		HP:0000639	PMID:21310915	PCS		HP:0040284		P		HPO:probinson	10/10
OMIM	604232	#604232 LEBER CONGENITAL AMAUROSIS 3; LCA3RETINITIS PIGMENTOSA, JUVENILE, SPATA7-RELATED, INCLUDED		HP:0000662	PMID:21310915	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	604232	#604232 LEBER CONGENITAL AMAUROSIS 3; LCA3RETINITIS PIGMENTOSA, JUVENILE, SPATA7-RELATED, INCLUDED		HP:0001133	PMID:21310915	PCS				P		HPO:probinson	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0000006	OMIM:604233	TAS				I		HPO:skoehler	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0002069	OMIM:604233	TAS				P		HPO:skoehler	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0002121	OMIM:604233	TAS				P		HPO:skoehler	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0002373	OMIM:604233	TAS				P		HPO:skoehler	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0003829	OMIM:604233	TAS				C		HPO:skoehler	
OMIM	604233	#604233 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 1; GEFSP1;;GEFS+, TYPE 1; GEFS+1		HP:0010819	OMIM:604233	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000007	PMID:11313241	PCS				I		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000044	PMID:12130528	PCS				P		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000141	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000802	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000953	PMID:12130528	PCS				P		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0000979	OMIM:604250	IEA				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001369	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001394	PMID:11313241	PCS				P		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001638	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001875	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001888	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0001903	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0002910	PMID:11313241	PCS				P		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0003281	PMID:11313241	PCS				P		HPO:probinson	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0003452	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604250	HEMOCHROMATOSIS, TYPE 3; HFE3		HP:0012378	OMIM:604250	TAS				P		HPO:skoehler	
OMIM	604271	SHORT STATURE, IDIOPATHIC, AUTOSOMAL		HP:0004322	OMIM:604271	IEA				P		HPO:iea	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000007	OMIM:604273	IEA				I		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000028	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000047	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000252	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000278	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000369	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0000426	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001251	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001252	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001263	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001290	OMIM:604273	TAS				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001508	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001639	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0001987	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0002151	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0002240	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0003128	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0003535	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0003593	OMIM:604273	IEA				C		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0004322	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604273	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1		HP:0025356	OMIM:604273	IEA				P		HPO:skoehler	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0000007	OMIM:604278	IEA				I		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0000501	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0000518	OMIM:604278	IEA				P		HPO:skoehler	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0000585	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0001249	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0001510	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0001995	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0002049	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0004910	OMIM:604278	IEA				P		HPO:iea	
OMIM	604278	RENAL TUBULAR ACIDOSIS, PROXIMAL, WITH OCULAR ABNORMALITIES AND MENTALRETARDATION		HP:0005546	OMIM:604278	IEA				P		HPO:iea	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0000007	OMIM:604286	TAS				I		HPO:probinson	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0001644	OMIM:604286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003236	OMIM:604286	TAS				P		HPO:skoehler	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003325	OMIM:604286	TAS				P		HPO:probinson	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003560	OMIM:604286	TAS				P		HPO:skoehler	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003621	OMIM:604286	TAS				C		HPO:probinson	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003691	OMIM:604286	TAS				P		HPO:skoehler	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003707	OMIM:604286	TAS				P		HPO:skoehler	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0003724	OMIM:604286	TAS				P		HPO:probinson	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0007126	OMIM:604286	TAS				P		HPO:skoehler	
OMIM	604286	#604286 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E		HP:0008988	OMIM:604286	TAS				P		HPO:probinson	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000007	OMIM:604290	IEA				I		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000473	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000546	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000643	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000726	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0000819	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0001251	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0001260	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0001903	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0002071	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0002072	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0002168	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0002396	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0003281	OMIM:604290	IEA				P		HPO:iea	
OMIM	604290	ACERULOPLASMINEMIA		HP:0003581	OMIM:604290	TAS				C		HPO:probinson	
OMIM	604290	ACERULOPLASMINEMIA		HP:0025498	OMIM:604290	TAS				P		HPO:skoehler	
OMIM	604290	ACERULOPLASMINEMIA		HP:0040303	OMIM:604290	TAS				P		HPO:skoehler	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000006	OMIM:604292	IEA				I		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000015	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000021	OMIM:604292	IEA				P		HPO:skoehler	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000028	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000044	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000054	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000070	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000072	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000076	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000081	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000104	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000110	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000126	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000145	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000175	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000198	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000204	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000217	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000272	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000327	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000365	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000437	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000453	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000498	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000535	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000581	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000613	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000620	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000635	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000653	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000670	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000691	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000824	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000863	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000962	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0000968	OMIM:604292	TAS				P		HPO:probinson	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001171	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001249	OMIM:604292	TAS		HP:0040284		P		HPO:probinson	7%
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001592	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001739	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001770	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001803	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0001839	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0002209	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0002215	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0002225	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0002286	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0002557	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0007513	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0008404	OMIM:604292	TAS				P		HPO:skoehler	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0008551	OMIM:604292	IEA				P		HPO:iea	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0008661	OMIM:604292	IEA				P		HPO:skoehler	
OMIM	604292	ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 3; EEC3		HP:0100257	OMIM:604292	TAS				P		HPO:iea	
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000006	OMIM:604307	TAS				I		HPO:probinson	
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000482	OMIM:604307	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000519	OMIM:604307	IEA				P		HPO:skoehler	
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000613	OMIM:604307	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000639	OMIM:604307	TAS				P		HPO:skoehler	
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0000646	OMIM:604307	TAS				P		HPO:skoehler	
OMIM	604307	CATARACT 2, MULTIPLE TYPES; CTRCT2		HP:0100018	OMIM:604307	TAS				P		HPO:probinson	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD		HP:0000006	OMIM:604308	TAS				I		HPO:skoehler	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD		HP:0000766	OMIM:604308	TAS				P		HPO:skoehler	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD		HP:0001065	OMIM:604308	TAS				P		HPO:skoehler	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD		HP:0001519	OMIM:604308	TAS				P		HPO:skoehler	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD		HP:0001634	OMIM:604308	TAS				P		HPO:skoehler	
OMIM	604308	#604308 MASS SYNDROME;;MASS PHENOTYPE;;OVERLAP CONNECTIVE TISSUE DISEASE; OCTD	HP:0012825	HP:0004942	OMIM:604308	TAS				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000007	OMIM:604314	IEA				I		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000049	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000059	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000160	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000189	OMIM:604314	TAS				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000218	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000243	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000252	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000269	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000272	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000278	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000294	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000311	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000319	OMIM:604314	TAS				P		HPO:probinson	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000343	OMIM:604314	TAS				P		HPO:probinson	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000358	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000369	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000391	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000395	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000403	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000407	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000414	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000437	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000474	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000506	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000508	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000527	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000581	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000807	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0000996	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001181	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001249	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001250	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001252	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001290	OMIM:604314	TAS				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001601	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001762	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0001810	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0002162	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0002558	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0004209	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0005989	OMIM:604314	TAS				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0006191	OMIM:604314	IEA				P		HPO:skoehler	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0008872	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0009623	OMIM:604314	IEA				P		HPO:iea	
OMIM	604314	BLEPHAROPHIMOSIS WITH FACIAL AND GENITAL ANOMALIES AND MENTAL RETARDATION		HP:0011800	OMIM:604314	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000007	OMIM:604317	TAS				I		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000252	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000340	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000718	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000750	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0000752	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001249	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001250	OMIM:604317	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001263	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001269	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001285	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001302	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001347	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0001558	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0002079	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0002126	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0002282	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0003577	OMIM:604317	TAS				C		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0009879	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0010636	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604317	#604317 MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS; MCPH2		HP:0100710	OMIM:604317	TAS				P		HPO:skoehler	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0000007	OMIM:604320	IEA				I		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0000020	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0000762	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0000764	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0000975	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001265	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001508	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001511	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001518	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001558	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001612	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001622	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0001762	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0002019	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0002398	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0002460	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0002789	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0002878	OMIM:604320	TAS				P		HPO:skoehler	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0003445	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0003690	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0003693	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0005348	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0005946	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0006597	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0007269	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0009109	OMIM:604320	IEA				P		HPO:iea	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0009110	OMIM:604320	TAS				P		HPO:probinson	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0040078	OMIM:604320	IEA				P		HPO:skoehler	
OMIM	604320	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1; DSMA1		HP:0100490	OMIM:604320	IEA				P		HPO:iea	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000007	OMIM:604321	TAS				I		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000252	OMIM:604321	TAS				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000316	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000340	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000347	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000574	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000664	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000718	OMIM:604321	TAS				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0000750	OMIM:604321	IEA				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0001249	OMIM:604321	TAS				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0001335	OMIM:604321	TAS				P		HPO:skoehler	
OMIM	604321	MICROCEPHALY 4, PRIMARY, AUTOSOMAL RECESSIVE; MCPH4		HP:0100710	OMIM:604321	TAS				P		HPO:skoehler	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000006	OMIM:604326	IEA				I		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000317	OMIM:604326	IEA				P		HPO:skoehler	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000496	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000716	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000726	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000739	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0000746	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0001260	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0001272	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0001300	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0001310	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0001347	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002073	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002075	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002120	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002345	OMIM:604326	IEA				P		HPO:skoehler	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002346	OMIM:604326	IEA				P		HPO:iea	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0002530	OMIM:604326	IEA				P		HPO:skoehler	
OMIM	604326	SPINOCEREBELLAR ATAXIA 12		HP:0007141	OMIM:604326	IEA				P		HPO:skoehler	
OMIM	604348	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1; FASPS1		HP:0000006	OMIM:604348	PCS				I		HPO:iea	
OMIM	604348	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1; FASPS1		HP:0000716	OMIM:604348	TAS				P		HPO:skoehler	
OMIM	604348	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1; FASPS1		HP:0006979	PMID:10470086	PCS	HP:0003621	HP:0040281		P		HPO:iea	HP:0040281
OMIM	604348	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1; FASPS1		HP:0031873	OMIM:604348	IEA				P		HPO:skoehler	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0000006	OMIM:604352	IEA				I		HPO:iea	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0001425	OMIM:604352	TAS				I		HPO:skoehler	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0002069	OMIM:604352	IEA				P		HPO:iea	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0002373	OMIM:604352	TAS				P		HPO:probinson	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0003593	OMIM:604352	TAS				C		HPO:probinson	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0010818	OMIM:604352	IEA				P		HPO:iea	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0010819	OMIM:604352	IEA				P		HPO:iea	
OMIM	604352	FEBRILE SEIZURES, FAMILIAL, 4; FEB4		HP:0011463	OMIM:604352	TAS				C		HPO:probinson	
OMIM	604356	#604356 DUANE RETRACTION SYNDROME 2; DURS2		HP:0000006	OMIM:604356	TAS				I		HPO:probinson	
OMIM	604356	#604356 DUANE RETRACTION SYNDROME 2; DURS2		HP:0000646	OMIM:604356	TAS		HP:0040284		P		HPO:probinson	48%
OMIM	604356	#604356 DUANE RETRACTION SYNDROME 2; DURS2		HP:0009921	OMIM:604356	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000007	OMIM:604360	IEA				I		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000012	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000020	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000505	OMIM:604360	TAS	HP:0003581			P		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000608	OMIM:604360	TAS	HP:0003581			P		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000640	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0000763	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001249	OMIM:604360	TAS	HP:0003584			P		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001251	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001258	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001260	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001268	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001274	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001328	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001347	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001513	OMIM:604360	TAS				P		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0001761	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002015	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002061	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002064	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002079	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002120	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002166	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002314	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002518	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0002839	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0003380	OMIM:604360	TAS				P		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0003393	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0003487	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0003581	OMIM:604360	TAS				C		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0003676	OMIM:604360	IEA				C		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0007067	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0007178	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0007340	OMIM:604360	IEA				P		HPO:iea	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0011448	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0011449	OMIM:604360	TAS				P		HPO:probinson	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0011463	OMIM:604360	TAS				C		HPO:skoehler	
OMIM	604360	#604360 SPASTIC PARAPLEGIA 11, AUTOSOMAL RECESSIVE; SPG11;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, WITH MENTAL IMPAIRMENT ANDTHIN CORPUS CALLOSUM;;SPASTIC PARAPLEGIA, AUTOSOMAL RECESSIVE, COMPLICATED, WITH THIN CORPUSCALLOSUM;;HSP-TCC		HP:0030051	OMIM:604360	IEA				P		HPO:iea	
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0000006	OMIM:604364	TAS				I		HPO:skoehler	
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0000729	OMIM:604364	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0001249	OMIM:604364	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0003829	OMIM:604364	TAS				C		HPO:skoehler	
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0031951	OMIM:604364	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0032047	PMID:25623524	PCS		HP:0040284		P		HPO:nvasilevsky	2/7
OMIM	604364	#604364 EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI; FFEVF;;EPILEPSY, PARTIAL, WITH VARIABLE FOCI; FPEVF		HP:0032052	PMID:25623524	PCS		HP:0040284		P		HPO:nvasilevsky	2/7
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000006	OMIM:604367	IEA				I		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000147	OMIM:604367	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000271	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000464	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000786	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000822	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000831	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000842	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000876	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0000956	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0001007	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0001015	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0001394	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0001397	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0002149	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0002155	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0003011	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0003074	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0003233	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0003635	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0003758	OMIM:604367	TAS				P		HPO:skoehler	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0009017	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0009125	OMIM:604367	TAS				P		HPO:skoehler	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0009800	OMIM:604367	IEA				P		HPO:iea	
OMIM	604367	#604367 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS		HP:0100602	OMIM:604367	TAS				P		HPO:skoehler	
OMIM	604369	SALLA DISEASE		HP:0000007	OMIM:604369	IEA				I		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0000577	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0000639	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0000750	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001249	OMIM:604369	TAS				P		HPO:skoehler	
OMIM	604369	SALLA DISEASE		HP:0001250	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001251	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001252	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001257	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001260	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001263	OMIM:604369	TAS				P		HPO:skoehler	
OMIM	604369	SALLA DISEASE		HP:0001290	OMIM:604369	TAS				P		HPO:skoehler	
OMIM	604369	SALLA DISEASE		HP:0001510	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0001922	OMIM:604369	TAS				P		HPO:skoehler	
OMIM	604369	SALLA DISEASE		HP:0001939	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0002305	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0002540	OMIM:604369	IEA				P		HPO:iea	
OMIM	604369	SALLA DISEASE		HP:0002684	OMIM:604369	IEA				P		HPO:iea	
OMIM	604370	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1		HP:0000006	OMIM:604370	IEA				I		HPO:skoehler	
OMIM	604370	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1		HP:0001426	OMIM:604370	IEA				I		HPO:skoehler	
OMIM	604370	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1		HP:0003002	OMIM:604370	IEA				P		HPO:skoehler	
OMIM	604370	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1		HP:0100615	OMIM:604370	IEA				P		HPO:skoehler	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0000007	OMIM:604377	IEA				I	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0001252	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0001263	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0001290	OMIM:604377	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:skoehler	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0001522	OMIM:604377	IEA				M	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0001639	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0002098	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0002151	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0002490	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0002529	OMIM:604377	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:probinson	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0003128	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0003577	OMIM:604377	IEA				C	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0006999	OMIM:604377	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:probinson	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0007941	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0008872	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:iea	
OMIM	604377	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 1; CEMCOX1		HP:0200147	OMIM:604377	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 1; CEMCOX1	HPO:skoehler	
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0000007	OMIM:604379	TAS				I		HPO:skoehler	
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0000535	OMIM:604379	TAS				P		HPO:skoehler	
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0000653	OMIM:604379	TAS				P		HPO:skoehler	
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0001006	OMIM:604379	IEA				P		HPO:skoehler	
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0002224	OMIM:604379	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604379	HYPOTRICHOSIS 7; HYPT7		HP:0025249	OMIM:604379	IEA				P		HPO:skoehler	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0000006	OMIM:604381	TAS				I		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0001156	OMIM:604381	TAS				P		HPO:skoehler	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0001643	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0001647	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0001831	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0004209	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0005295	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0009381	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604381	604381 PATENT DUCTUS ARTERIOSUS AND BICUSPID AORTIC VALVE WITH HAND ANOMALIES		HP:0010047	OMIM:604381	TAS				P		HPO:probinson	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000007	OMIM:604387	IEA				I		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000083	OMIM:604387	TAS	HP:0011462			P		HPO:probinson	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000090	OMIM:604387	IEA				P		HPO:skoehler	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000092	OMIM:604387	IEA				P		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000103	OMIM:604387	IEA				P		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000108	OMIM:604387	IEA				P		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0000805	OMIM:604387	IEA				P		HPO:skoehler	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0001395	OMIM:604387	IEA				P		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0001959	OMIM:604387	IEA				P		HPO:iea	
OMIM	604387	#604387 NEPHRONOPHTHISIS 3; NPHP3;;NPH3		HP:0005576	OMIM:604387	IEA				P		HPO:iea	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0000007	OMIM:604391	TAS				I		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0000571	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0000640	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0000657	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0001009	OMIM:604391	IEA				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0001260	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0001265	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0001272	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0001332	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1	HP:0012825	HP:0002061	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0002066	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0002072	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0002075	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0002359	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0003676	OMIM:604391	TAS				C		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1	HP:0012825	HP:0003693	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0003828	OMIM:604391	TAS				C		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0007772	OMIM:604391	TAS				P		HPO:skoehler	
OMIM	604391	ATAXIA-TELANGIECTASIA-LIKE DISORDER 1; ATLD1		HP:0011133	OMIM:604391	IEA				P		HPO:skoehler	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0000007	OMIM:604393	TAS				I		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0000543	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0000548	OMIM:604393	IEA				P		HPO:skoehler	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0000563	OMIM:604393	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0000618	OMIM:604393	IEA				P		HPO:skoehler	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4	HP:0012828	HP:0000662	OMIM:604393	TAS				P		HPO:skoehler	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0007401	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0007663	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0007688	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4	HP:0012828	HP:0007843	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604393	LEBER CONGENITAL AMAUROSIS 4; LCA4		HP:0012043	OMIM:604393	TAS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0000006	PMID:18313022	PCS				I		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0001635	OMIM:604400	TAS				P		HPO:skoehler	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0001645	PMID:18313022	PCS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0001962	OMIM:604400	TAS				P		HPO:skoehler	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0004756	PMID:18313022	PCS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0006677	PMID:18313022	PCS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0006682	PMID:18313022	PCS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0011663	PMID:18313022	PCS				P		HPO:probinson	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0031972	OMIM:604400	IEA				P		HPO:skoehler	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0100660	OMIM:604400	IEA				P		HPO:skoehler	
OMIM	604400	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5; ARVD5		HP:0100749	OMIM:604400	TAS				P		HPO:skoehler	
OMIM	604401	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6		HP:0000006	PMID:10631146	IEA				I		HPO:probinson	
OMIM	604401	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6		HP:0001645	PMID:10631146	IEA		HP:0040284		P		HPO:probinson	2/12
OMIM	604401	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6		HP:0006682	PMID:10631146	IEA		HP:0040284		P		HPO:probinson	5/12
OMIM	604401	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 6		HP:0011663	PMID:10631146	IEA				P		HPO:probinson	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0000006	OMIM:604403	IEA				I		HPO:iea	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0002069	OMIM:604403	IEA				P		HPO:iea	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0002121	OMIM:604403	TAS				P		HPO:skoehler	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0002123	OMIM:604403	TAS				P		HPO:skoehler	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0002373	OMIM:604403	IEA				P		HPO:iea	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0003828	OMIM:604403	TAS				C		HPO:skoehler	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0006813	OMIM:604403	TAS				P		HPO:skoehler	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0010818	OMIM:604403	IEA				P		HPO:iea	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0010819	OMIM:604403	IEA				P		HPO:iea	
OMIM	604403	#604403 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 2; GEFSP2;;GEFS+, TYPE 2; GEFS+2FEBRILE SEIZURES, FAMILIAL, 3A, INCLUDED; FEB3A, INCLUDED		HP:0011463	OMIM:604403	IEA				C		HPO:iea	
OMIM	604416	PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE		HP:0000006	OMIM:604416	IEA				I		HPO:iea	
OMIM	604416	PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE		HP:0000999	OMIM:604416	IEA				P		HPO:skoehler	
OMIM	604416	PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE		HP:0001061	OMIM:604416	TAS				P		HPO:skoehler	
OMIM	604416	PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE		HP:0001369	OMIM:604416	TAS				P		HPO:probinson	
OMIM	604416	PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE		HP:0025452	OMIM:604416	TAS				P		HPO:skoehler	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0000006	OMIM:604432	IEA				I		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0000639	OMIM:604432	IEA				P		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0001260	OMIM:604432	IEA				P		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0001272	OMIM:604432	IEA				P		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0001347	OMIM:604432	IEA				P		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0002073	OMIM:604432	IEA				P		HPO:iea	
OMIM	604432	#604432 SPINOCEREBELLAR ATAXIA 11; SCA11		HP:0003581	OMIM:604432	TAS				C		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0000006	OMIM:604454	TAS				I		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0000007	OMIM:604454	TAS				I		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0002460	OMIM:604454	TAS				P		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0003376	OMIM:604454	TAS				P		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0003581	OMIM:604454	TAS				C		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0003677	OMIM:604454	TAS				C		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0003693	OMIM:604454	TAS				P		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0003805	OMIM:604454	TAS				P		HPO:skoehler	
OMIM	604454	WELANDER DISTAL MYOPATHY; WDM		HP:0008180	OMIM:604454	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0000006	OMIM:604484	IEA				I		HPO:iea	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0000763	OMIM:604484	IEA				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0001284	OMIM:604484	IEA				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0001288	OMIM:604484	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002171	OMIM:604484	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002378	OMIM:604484	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002380	OMIM:604484	IEA				P		HPO:iea	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002398	OMIM:604484	TAS				P		HPO:probinson	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002445	OMIM:604484	TAS				P		HPO:probinson	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0002936	OMIM:604484	IEA				P		HPO:iea	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003077	OMIM:604484	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003380	OMIM:604484	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003394	OMIM:604484	IEA				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003581	OMIM:604484	IEA				C		HPO:iea	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003677	OMIM:604484	IEA				C		HPO:iea	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0003701	OMIM:604484	TAS				P		HPO:probinson	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0007126	OMIM:604484	TAS				P		HPO:probinson	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0008180	OMIM:604484	TAS				P		HPO:skoehler	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0009830	OMIM:604484	TAS				P		HPO:probinson	
OMIM	604484	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, OKINAWA TYPE; HMSNO		HP:0040078	OMIM:604484	IEA				P		HPO:skoehler	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0000007	OMIM:604498	TAS				I		HPO:probinson	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0001320	OMIM:604498	TAS				P		HPO:probinson	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0001873	OMIM:604498	IEA				P		HPO:probinson	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0001876	OMIM:604498	TAS				P		HPO:probinson	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0004859	OMIM:604498	TAS				P		HPO:probinson	
OMIM	604498	AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL		HP:0005548	OMIM:604498	TAS				P		HPO:probinson	
OMIM	604519	INFLAMMATORY BOWEL DISEASE 3		HP:0000006	OMIM:604519	TAS				I		HPO:skoehler	
OMIM	604519	INFLAMMATORY BOWEL DISEASE 3		HP:0100279	OMIM:604519	TAS				P		HPO:skoehler	
OMIM	604536	ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME		HP:0000968	OMIM:604536	IEA				P		HPO:skoehler	
OMIM	604536	ECTODERMAL DYSPLASIA/SKIN FRAGILITY SYNDROME		HP:0001030	OMIM:604536	IEA				P		HPO:skoehler	
OMIM	604537	#604537 LEBER CONGENITAL AMAUROSIS 5; LCA5		HP:0000007	PMID:17546029	PCS				I		HPO:skoehler	
OMIM	604537	#604537 LEBER CONGENITAL AMAUROSIS 5; LCA5		HP:0000505	PMID:17546029	PCS	HP:0003577			P		HPO:skoehler	
OMIM	604537	#604537 LEBER CONGENITAL AMAUROSIS 5; LCA5		HP:0000540	PMID:17546029	PCS				P		HPO:skoehler	
OMIM	604537	#604537 LEBER CONGENITAL AMAUROSIS 5; LCA5		HP:0000550	PMID:17546029	PCS				P		HPO:skoehler	
OMIM	604537	#604537 LEBER CONGENITAL AMAUROSIS 5; LCA5		HP:0000639	PMID:17546029	PCS				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0000006	OMIM:604559	TAS				I		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0001279	OMIM:604559	TAS				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0001657	OMIM:604559	TAS				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0001662	OMIM:604559	TAS				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0001678	OMIM:604559	IEA				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0005165	OMIM:604559	TAS				P		HPO:probinson	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0011711	OMIM:604559	TAS				P		HPO:skoehler	
OMIM	604559	PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IB; PFHB1B		HP:0011712	OMIM:604559	IEA				P		HPO:skoehler	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0000007	OMIM:604563	IEA				I		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0000407	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0000501	OMIM:604563	TAS				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001171	OMIM:604563	TAS				P		HPO:skoehler	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001178	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001265	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001284	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001425	OMIM:604563	TAS				I		HPO:skoehler	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001761	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001762	OMIM:604563	IEA				P		HPO:skoehler	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0001765	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0002355	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0002460	OMIM:604563	TAS				P		HPO:probinson	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0002751	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0002936	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003376	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003380	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003383	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003431	OMIM:604563	IEA				P		HPO:skoehler	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003481	OMIM:604563	IEA				P		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003621	OMIM:604563	IEA				C		HPO:iea	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0003693	OMIM:604563	TAS				P		HPO:probinson	
OMIM	604563	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2		HP:0009027	OMIM:604563	IEA				P		HPO:iea	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0000007	OMIM:604571	TAS				I		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0000389	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0001083	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0002097	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0002110	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0002837	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0011109	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0011950	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0100582	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604571	#604571 BARE LYMPHOCYTE SYNDROME, TYPE I;;BLS, TYPE I;;HLA CLASS I DEFICIENCY		HP:0200042	OMIM:604571	TAS				P		HPO:skoehler	
OMIM	604625	#604625 TOOTH AGENESIS, SELECTIVE, 3; STHAG3;;HYPODONTIA/OLIGODONTIA 3		HP:0000006	OMIM:604625	TAS				I		HPO:probinson	
OMIM	604625	#604625 TOOTH AGENESIS, SELECTIVE, 3; STHAG3;;HYPODONTIA/OLIGODONTIA 3		HP:0000677	OMIM:604625	TAS				P		HPO:probinson	
OMIM	604625	#604625 TOOTH AGENESIS, SELECTIVE, 3; STHAG3;;HYPODONTIA/OLIGODONTIA 3		HP:0000691	OMIM:604625	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604715	#604715 ORTHOSTATIC INTOLERANCE;;NEUROCIRCULATORY ASTHENIA;;MITRAL VALVE PROLAPSE SYNDROME;;IRRITABLE HEART;;SOLDIERS HEART		HP:0000006	OMIM:604715	TAS				I		HPO:probinson	
OMIM	604715	#604715 ORTHOSTATIC INTOLERANCE;;NEUROCIRCULATORY ASTHENIA;;MITRAL VALVE PROLAPSE SYNDROME;;IRRITABLE HEART;;SOLDIERS HEART		HP:0012173	OMIM:604715	TAS				P		HPO:probinson	
OMIM	604717	DEAFNESS, AUTOSOMAL DOMINANT 20		HP:0000006	OMIM:604717	TAS				I		HPO:probinson	
OMIM	604717	DEAFNESS, AUTOSOMAL DOMINANT 20		HP:0000408	OMIM:604717	TAS				P		HPO:probinson	
OMIM	604717	DEAFNESS, AUTOSOMAL DOMINANT 20		HP:0008619	OMIM:604717	TAS				P		HPO:probinson	
OMIM	604717	DEAFNESS, AUTOSOMAL DOMINANT 20		HP:0011462	OMIM:604717	TAS				C		HPO:probinson	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000006	OMIM:604757	TAS				I		HPO:skoehler	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000185	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000243	OMIM:604757	TAS				P		HPO:skoehler	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000244	OMIM:604757	TAS				P		HPO:skoehler	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000540	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000545	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0000601	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0001123	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0001156	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0001199	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0001250	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0002007	OMIM:604757	TAS				P		HPO:skoehler	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0002315	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0011069	OMIM:604757	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0011315	OMIM:604757	TAS				P		HPO:skoehler	
OMIM	604757	CRANIOSYNOSTOSIS 2		HP:0011318	OMIM:604757	TAS				P		HPO:skoehler	
OMIM	604765	#604765 CARDIOMYOPATHY, DILATED, 1I; CMD1I		HP:0000006	PMID:10430757	PCS				I		HPO:probinson	
OMIM	604765	#604765 CARDIOMYOPATHY, DILATED, 1I; CMD1I		HP:0001635	PMID:10430757	PCS				P		HPO:probinson	
OMIM	604765	#604765 CARDIOMYOPATHY, DILATED, 1I; CMD1I		HP:0001644	PMID:10430757	PCS				P		HPO:probinson	
OMIM	604765	#604765 CARDIOMYOPATHY, DILATED, 1I; CMD1I		HP:0006673	PMID:10430757	PCS				P		HPO:probinson	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0000006	OMIM:604772	TAS				I		HPO:skoehler	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0001250	OMIM:604772	TAS				P		HPO:skoehler	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0001279	OMIM:604772	TAS				P		HPO:skoehler	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0001699	OMIM:604772	TAS				M		HPO:skoehler	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0004756	OMIM:604772	IEA				P		HPO:skoehler	
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0005110	OMIM:604772	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0005162	OMIM:604772	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	604772	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1		HP:0025478	OMIM:604772	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0000007	OMIM:604777	TAS				I		HPO:skoehler	
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0000982	OMIM:604777	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0001019	OMIM:604777	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5	HP:0012826	HP:0001036	OMIM:604777	TAS				P		HPO:skoehler	
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0001927	OMIM:604777	TAS				P		HPO:probinson	
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0007479	OMIM:604777	TAS				P		HPO:probinson	
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5	HP:0012826	HP:0025092	OMIM:604777	TAS				P		HPO:skoehler	
OMIM	604777	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5		HP:0040162	OMIM:604777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0000007	OMIM:604801	IEA				I		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0001270	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0001290	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0001771	OMIM:604801	TAS				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0002878	PMID:10677302	PCS	HP:0011463			P		HPO:probinson	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003236	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003306	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003391	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003547	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003720	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0003741	OMIM:604801	TAS				P		HPO:probinson	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0009113	PMID:10677302	PCS	HP:0011463			P		HPO:probinson	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0010628	OMIM:604801	IEA				P		HPO:iea	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0012036	OMIM:604801	TAS				P		HPO:probinson	
OMIM	604801	MUSCULAR DYSTROPHY, CONGENITAL, 1B		HP:0012037	OMIM:604801	TAS				P		HPO:probinson	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:604802	IEA				I		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0000020	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001251	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001257	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001268	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001332	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0001371	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002062	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002071	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002072	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002167	OMIM:604802	TAS				P		HPO:skoehler	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002300	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002317	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002340	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0002607	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0006913	OMIM:604802	IEA				P		HPO:iea	
OMIM	604802	%604802 HUNTINGTON DISEASE-LIKE 3; HDL3;;HUNTINGTON DISEASE-LIKE NEURODEGENERATIVE DISORDER, AUTOSOMAL RECESSIVE		HP:0007256	OMIM:604802	TAS				P		HPO:skoehler	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0000007	OMIM:604804	IEA				I		HPO:iea	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0000252	OMIM:604804	TAS				P		HPO:skoehler	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0000340	OMIM:604804	TAS				P		HPO:skoehler	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0000407	OMIM:604804	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0000520	OMIM:604804	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0001263	OMIM:604804	TAS				P		HPO:skoehler	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0002342	OMIM:604804	IEA				P		HPO:skoehler	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0002472	OMIM:604804	IEA				P		HPO:iea	
OMIM	604804	#604804 MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE; MCPH3		HP:0009879	OMIM:604804	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0000006	OMIM:604805	IEA				I		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0000012	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0000020	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0001258	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0001347	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0001761	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0002064	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0002166	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0002839	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0003487	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0003676	OMIM:604805	IEA				C		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0007340	OMIM:604805	IEA				P		HPO:iea	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0011448	OMIM:604805	TAS				P		HPO:probinson	
OMIM	604805	SPASTIC PARAPLEGIA 12, AUTOSOMAL DOMINANT		HP:0011449	OMIM:604805	TAS				P		HPO:probinson	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0002110	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0003651	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0003676	OMIM:604809	TAS				C		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0012418	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0012735	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0030828	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0030830	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604809	PANBRONCHIOLITIS, DIFFUSE		HP:0030831	OMIM:604809	TAS				P		HPO:skoehler	
OMIM	604827	MYOCLONIC EPILEPSY, JUVENILE, 2		HP:0000007	OMIM:604827	IEA				I		HPO:iea	
OMIM	604827	MYOCLONIC EPILEPSY, JUVENILE, 2		HP:0001336	OMIM:604827	TAS				P		HPO:probinson	
OMIM	604827	MYOCLONIC EPILEPSY, JUVENILE, 2		HP:0002069	OMIM:604827	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000006	OMIM:604841	TAS				I		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000175	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000193	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000201	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000272	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000347	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000407	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000463	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000501	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000518	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000541	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0000545	OMIM:604841	TAS	HP:0011463			P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0001166	OMIM:604841	IEA				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0001382	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE	HP:0012825	HP:0002655	OMIM:604841	TAS				P		HPO:iea	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0003040	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0004327	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0005280	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0011800	OMIM:604841	TAS				P		HPO:skoehler	
OMIM	604841	#604841 STICKLER SYNDROME, TYPE II; STL2;;STICKLER SYNDROME, VITREOUS TYPE 2;;STICKLER SYNDROME, BEADED VITREOUS TYPE		HP:0100807	OMIM:604841	TAS				P		HPO:probinson	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0000006	OMIM:604864	IEA				I		HPO:iea	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0000926	OMIM:604864	IEA				P		HPO:iea	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0001387	OMIM:604864	IEA				P		HPO:iea	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0003301	OMIM:604864	IEA				P		HPO:iea	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0004322	OMIM:604864	TAS				P		HPO:skoehler	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0004568	OMIM:604864	IEA				P		HPO:iea	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0005086	OMIM:604864	TAS				P		HPO:skoehler	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0008843	OMIM:604864	TAS				P		HPO:skoehler	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0012313	OMIM:604864	TAS				P		HPO:probinson	
OMIM	604864	#604864 OSTEOARTHRITIS WITH MILD CHONDRODYSPLASIA		HP:0030041	OMIM:604864	TAS				P		HPO:skoehler	
OMIM	604901	#604901 NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS; NAIC		HP:0000007	PMID:12417987	IEA				I		HPO:probinson	
OMIM	604901	#604901 NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS; NAIC		HP:0001409	PMID:12417987	IEA				P		HPO:probinson	
OMIM	604901	#604901 NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS; NAIC		HP:0002613	PMID:12417987	IEA				P		HPO:probinson	
OMIM	604901	#604901 NORTH AMERICAN INDIAN CHILDHOOD CIRRHOSIS; NAIC		HP:0006579	PMID:12417987	IEA				P		HPO:probinson	
OMIM	604919	BECKER NEVUS SYNDROME		HP:0003764	OMIM:604919	IEA				P		HPO:skoehler	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000006	OMIM:604922	IEA				I		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000268	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000316	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000629	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000670	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000703	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0000883	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0001377	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0001476	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0001555	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0002645	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0002659	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0004322	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0004990	OMIM:604922	IEA				P		HPO:iea	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0008115	OMIM:604922	TAS				P		HPO:probinson	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0011918	OMIM:604922	TAS				P		HPO:probinson	
OMIM	604922	CORTICAL DEFECTS, WORMIAN BONES, AND DENTINOGENESIS IMPERFECTA		HP:0100774	OMIM:604922	IEA				P		HPO:skoehler	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0000007	PMID:10739754	PCS				I		HPO:probinson	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0000407	PMID:10739754	PCS				P		HPO:probinson	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0000648	PMID:10739754	PCS				P		HPO:probinson	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0000716	OMIM:604928	TAS				P		HPO:skoehler	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0000819	PMID:10739754	PCS				P		HPO:probinson	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0001138	OMIM:604928	TAS				P		HPO:skoehler	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0001892	PMID:11317648	PCS				P		HPO:probinson	
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0002592	PMID:10739754	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	604928	WOLFRAM SYNDROME 2; WFS2		HP:0008320	PMID:11317648	PCS				P		HPO:probinson	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0000007	OMIM:604931	TAS				I		HPO:skoehler	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0000789	OMIM:604931	TAS				P		HPO:skoehler	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0000876	OMIM:604931	TAS				P		HPO:skoehler	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0001007	OMIM:604931	TAS				P		HPO:skoehler	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0001061	OMIM:604931	TAS				P		HPO:skoehler	
OMIM	604931	#604931 CORTISONE REDUCTASE DEFICIENCY 1; CORTRD1		HP:0001513	OMIM:604931	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000007	OMIM:605013	IEA				I		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000252	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000340	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000400	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000426	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000520	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0000742	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0001274	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0001302	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0001321	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0001347	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0001762	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002119	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002123	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002305	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002324	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002365	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002510	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0002828	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0003202	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0004322	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0006887	OMIM:605013	IEA				P		HPO:iea	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0010864	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605013	MICROHYDRANENCEPHALY; MHAC		HP:0012736	OMIM:605013	TAS				P		HPO:skoehler	
OMIM	605019	#605019 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2;;HYPOLIPIDEMIA, FAMILIAL, COMBINED		HP:0000006	PMID:20942659	IEA				I		HPO:probinson	
OMIM	605019	#605019 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2;;HYPOLIPIDEMIA, FAMILIAL, COMBINED		HP:0000007	OMIM:605019	TAS				I		HPO:skoehler	
OMIM	605019	#605019 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2;;HYPOLIPIDEMIA, FAMILIAL, COMBINED		HP:0003563	PMID:20942659	IEA				P		HPO:probinson	
OMIM	605019	#605019 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 2; FHBL2;;HYPOLIPIDEMIA, FAMILIAL, COMBINED		HP:0012153	PMID:20942659	IEA				P		HPO:probinson	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0000007	OMIM:605021	IEA				I		HPO:iea	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0001260	OMIM:605021	TAS				P		HPO:skoehler	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0002069	OMIM:605021	TAS				P		HPO:probinson	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0002123	OMIM:605021	TAS				P		HPO:probinson	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0002373	OMIM:605021	IEA				P		HPO:iea	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0002373	OMIM:605021	TAS				P		HPO:probinson	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0003593	OMIM:605021	TAS				C		HPO:probinson	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0003828	OMIM:605021	TAS				C		HPO:skoehler	
OMIM	605021	MYOCLONIC EPILEPSY, FAMILIAL INFANTILE		HP:0007359	OMIM:605021	TAS				P		HPO:skoehler	
OMIM	605027	LYMPHOMA, NON-HODGKIN, FAMILIAL		HP:0002665	OMIM:605027	IEA				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000006	OMIM:605039	TAS				I		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000007	OMIM:605039	IEA				I		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000076	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000175	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000187	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000189	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000204	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000243	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000252	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000276	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000278	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000294	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000316	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000329	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000341	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000347	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000358	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000369	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000431	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000486	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000520	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000545	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000582	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000587	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0000960	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001007	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001052	OMIM:605039	TAS				P		HPO:probinson	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001159	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001169	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001182	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001250	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001252	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001263	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001274	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001290	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001305	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001373	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001508	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001511	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001561	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001629	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001631	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001831	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001845	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0001869	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002020	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002079	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002187	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002282	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002365	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002558	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0002566	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0003049	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0003083	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0004322	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0005026	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0005487	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0006191	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0006276	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0006610	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0011220	OMIM:605039	IEA				P		HPO:iea	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0011401	OMIM:605039	PCS				P		HPO:probinson	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0011968	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0012385	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605039	BOHRING-OPITZ SYNDROME		HP:0100874	OMIM:605039	TAS				P		HPO:skoehler	
OMIM	605041	BROOKE-SPIEGLER SYNDROME; BSS		HP:0000006	OMIM:605041	IEA				I		HPO:skoehler	
OMIM	605041	BROOKE-SPIEGLER SYNDROME; BSS		HP:0001056	OMIM:605041	IEA				P		HPO:skoehler	
OMIM	605041	BROOKE-SPIEGLER SYNDROME; BSS		HP:0002664	OMIM:605041	IEA				P		HPO:skoehler	
OMIM	605041	BROOKE-SPIEGLER SYNDROME; BSS		HP:0003581	OMIM:605041	IEA				C		HPO:skoehler	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0000006	OMIM:605055	IEA				I		HPO:iea	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0001250	OMIM:605055	IEA				P		HPO:iea	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0002185	OMIM:605055	IEA				P		HPO:iea	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0002511	OMIM:605055	IEA				P		HPO:iea	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0006790	OMIM:605055	IEA				P		HPO:iea	
OMIM	605055	ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID AND PRION PATHOLOGY		HP:0100256	OMIM:605055	IEA				P		HPO:skoehler	
OMIM	605074	#605074 RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1		HP:0000006	OMIM:605074	TAS				I		HPO:skoehler	
OMIM	605074	#605074 RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1		HP:0003829	OMIM:605074	TAS				C		HPO:skoehler	
OMIM	605074	#605074 RENAL CELL CARCINOMA, PAPILLARY, 1; RCCP1		HP:0006766	OMIM:605074	TAS				P		HPO:skoehler	
OMIM	605115	#605115 HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATIONIN PREGNANCY		HP:0000006	OMIM:605115	TAS				I		HPO:probinson	
OMIM	605115	#605115 HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATIONIN PREGNANCY		HP:0000822	OMIM:605115	TAS				P		HPO:probinson	
OMIM	605115	#605115 HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATIONIN PREGNANCY		HP:0003351	OMIM:605115	TAS				P		HPO:probinson	
OMIM	605115	#605115 HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATIONIN PREGNANCY		HP:0004319	OMIM:605115	TAS				P		HPO:probinson	
OMIM	605115	#605115 HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH SEVERE EXACERBATIONIN PREGNANCY		HP:0008071	PMID:10884226	PCS				P		HPO:probinson	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000006	OMIM:605130	TAS				I		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000218	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000219	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000286	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000316	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000343	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000369	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000431	OMIM:605130	IEA				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000437	OMIM:605130	IEA				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000445	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000486	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000494	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000527	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000574	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000581	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000664	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000718	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000750	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0000960	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001182	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001249	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001250	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001252	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001252	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001263	OMIM:605130	IEA				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001290	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001290	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001508	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0001831	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0002019	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0002136	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0002750	OMIM:605130	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0004209	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0004322	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0005819	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0012368	OMIM:605130	TAS				P		HPO:skoehler	
OMIM	605130	WIEDEMANN-STEINER SYNDROME; WDSTS		HP:0045025	OMIM:605130	IEA				P		HPO:skoehler	
OMIM	605192	DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23		HP:0000006	PMID:10777717	PCS				I		HPO:probinson	
OMIM	605192	DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23		HP:0000076	OMIM:605192	TAS				P		HPO:skoehler	
OMIM	605192	DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23		HP:0000405	PMID:10777717	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	605192	DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23		HP:0000407	PMID:10777717	PCS				P		HPO:probinson	
OMIM	605192	DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23		HP:0004467	OMIM:605192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:605229	IEA				I		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0001256	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:605229	TAS				P		HPO:probinson	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0001761	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0002061	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0002064	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0003581	OMIM:605229	TAS				C		HPO:probinson	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:605229	IEA				C		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0007002	OMIM:605229	IEA				P		HPO:iea	
OMIM	605229	SPASTIC PARAPLEGIA 14, AUTOSOMAL RECESSIVE		HP:0007340	OMIM:605229	IEA				P		HPO:iea	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0000007	OMIM:605231	TAS				I		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0000047	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0000107	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0000510	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0000819	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0001159	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0001249	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0001513	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0003241	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605231	BARDET-BIEDL SYNDROME 6; BBS6		HP:0010442	OMIM:605231	TAS				P		HPO:skoehler	
OMIM	605249	SEBASTIAN SYNDROME		HP:0000006	OMIM:605249	IEA				I		HPO:iea	
OMIM	605249	SEBASTIAN SYNDROME		HP:0000421	OMIM:605249	PCS				P		HPO:probinson	
OMIM	605249	SEBASTIAN SYNDROME		HP:0001873	OMIM:605249	PCS				P		HPO:probinson	
OMIM	605249	SEBASTIAN SYNDROME		HP:0001902	OMIM:605249	IEA				P		HPO:iea	
OMIM	605249	SEBASTIAN SYNDROME	HP:0012825	HP:0003010	OMIM:605249	PCS				P		HPO:probinson	
OMIM	605249	SEBASTIAN SYNDROME		HP:0008264	OMIM:605249	IEA				P		HPO:iea	
OMIM	605249	SEBASTIAN SYNDROME		HP:0040235	OMIM:605249	TAS				P		HPO:skoehler	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0000006	OMIM:605253	TAS				I		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0000007	OMIM:605253	TAS				I		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0001270	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0001284	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0001291	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0001319	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0002460	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0003383	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING	HP:0012828	HP:0003431	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0003484	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0003577	OMIM:605253	TAS				C		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0003693	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING	HP:0012828	HP:0007182	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605253	NEUROPATHY, CONGENITAL HYPOMYELINATING		HP:0009830	OMIM:605253	TAS				P		HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0000007	OMIM:605258	TAS				I	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0002716	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0002718	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0002720	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0002721	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0002959	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0004315	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0004798	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:probinson	
OMIM	605258	#605258 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 2; HIGM2;;HYPER-IgM SYNDROME 2		HP:0200117	OMIM:605258	TAS				P	#605258 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 2; HIGM2;;HYPER-IGM SYNDROME 2	HPO:skoehler	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0000006	OMIM:605259	IEA				I		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0000365	OMIM:605259	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0000639	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0000648	OMIM:605259	TAS				P		HPO:skoehler	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001249	OMIM:605259	IEA				P		HPO:skoehler	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001252	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001260	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001270	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001272	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001290	OMIM:605259	TAS				P		HPO:skoehler	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0001347	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0002062	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0002066	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0002070	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0002073	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0002406	OMIM:605259	IEA				P		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0003677	OMIM:605259	IEA				C		HPO:iea	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0007256	OMIM:605259	TAS				P		HPO:skoehler	
OMIM	605259	SPINOCEREBELLAR ATAXIA 13		HP:0008003	OMIM:605259	TAS				P		HPO:skoehler	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0000006	OMIM:605274	IEA				I		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0000765	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0001263	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0001476	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0001760	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0001772	OMIM:605274	TAS				P		HPO:probinson	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0002827	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0002990	OMIM:605274	TAS				P		HPO:probinson	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0003027	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0003083	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0004322	OMIM:605274	IEA				P		HPO:iea	
OMIM	605274	MESOMELIC DYSPLASIA, SAVARIRAYAN TYPE		HP:0005736	OMIM:605274	IEA				P		HPO:iea	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0000316	OMIM:605275	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0000494	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0000508	OMIM:605275	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001263	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001638	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001642	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001671	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001680	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0001718	OMIM:605275	IEA				P		HPO:skoehler	
OMIM	605275	NOONAN SYNDROME 2; NS2		HP:0004322	OMIM:605275	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0000006	OMIM:605280	IEA				I		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0000012	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0000020	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0001258	OMIM:605280	TAS				P		HPO:skoehler	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0001347	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0002061	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0002064	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0002166	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0002839	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0003487	OMIM:605280	IEA				P		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0003676	OMIM:605280	IEA				C		HPO:iea	
OMIM	605280	SPASTIC PARAPLEGIA 13, AUTOSOMAL DOMINANT		HP:0007340	OMIM:605280	IEA				P		HPO:iea	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000007	OMIM:605282	TAS				I		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000175	OMIM:605282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000592	OMIM:605282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000648	OMIM:605282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000664	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000691	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0000699	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0001156	OMIM:605282	IEA				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0001159	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0001234	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0002002	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0002553	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0002974	OMIM:605282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0008368	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0008619	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0009702	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0010049	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0010743	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0011087	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605282	TEMTAMY PREAXIAL BRACHYDACTYLY SYNDROME; TPBS		HP:0030084	OMIM:605282	TAS				P		HPO:skoehler	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0000007	OMIM:605285	IEA				I		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0001155	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0001265	OMIM:605285	TAS				P		HPO:skoehler	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0001760	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0002355	OMIM:605285	TAS				P		HPO:skoehler	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0002460	OMIM:605285	TAS				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0002650	OMIM:605285	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0003387	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0003431	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0003450	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0003470	OMIM:605285	IEA				P		HPO:skoehler	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0003676	OMIM:605285	IEA				C		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0007182	OMIM:605285	IEA				P		HPO:iea	
OMIM	605285	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR		HP:0009830	OMIM:605285	TAS				P		HPO:skoehler	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0000006	PMID:10839977	PCS				I		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0001159	OMIM:605289	TAS				P		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0001171	OMIM:605289	IEA				P		HPO:skoehler	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0001199	OMIM:605289	TAS				P		HPO:skoehler	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0001839	OMIM:605289	IEA				P		HPO:skoehler	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0001964	PMID:10839977	PCS				P		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0005914	PMID:10839977	PCS				P		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0009767	PMID:10839977	PCS				P		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0010173	PMID:10839977	PCS				P		HPO:probinson	
OMIM	605289	SPLIT-HAND/FOOT MALFORMATION 4; SHFM4		HP:0100257	OMIM:605289	TAS				P		HPO:probinson	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0000006	OMIM:605309	IEA				I		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0000337	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0000343	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0000717	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0001249	OMIM:605309	IEA				P		HPO:skoehler	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0001263	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0001513	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0001888	OMIM:605309	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0002007	OMIM:605309	TAS				P		HPO:skoehler	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0002719	OMIM:605309	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0003196	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0004313	OMIM:605309	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0004422	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0005280	OMIM:605309	IEA				P		HPO:iea	
OMIM	605309	MACROCEPHALY/AUTISM SYNDROME		HP:0005490	OMIM:605309	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000006	OMIM:605321	IEA				I		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000160	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000218	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000243	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000286	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000347	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000358	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000369	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000426	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000486	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000508	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000520	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000545	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000581	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000582	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000601	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0000767	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001052	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001076	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001256	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001263	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001631	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0001642	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0003186	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0004440	OMIM:605321	TAS				P		HPO:skoehler	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0005306	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0009891	OMIM:605321	IEA				P		HPO:iea	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0011829	OMIM:605321	TAS				P		HPO:skoehler	
OMIM	605321	FRONTOOCULAR SYNDROME		HP:0012745	OMIM:605321	TAS				P		HPO:skoehler	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0000007	OMIM:605355	IEA				I		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY	HP:0012828	HP:0000768	OMIM:605355	IEA				P		HPO:probinson	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0001337	OMIM:605355	TAS				P		HPO:probinson	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0001547	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0002063	OMIM:605355	IEA				P		HPO:skoehler	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0002093	OMIM:605355	IEA				P		HPO:skoehler	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0002194	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003044	OMIM:605355	TAS				P		HPO:probinson	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003184	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003198	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003273	OMIM:605355	TAS				P		HPO:probinson	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003323	OMIM:605355	IEA				P		HPO:probinson	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003593	OMIM:605355	IEA				C		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003798	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0003803	OMIM:605355	IEA				P		HPO:iea	
OMIM	605355	#605355 NEMALINE MYOPATHY 5; NEM5;;NEMALINE MYOPATHY, AMISH TYPE; ANM;;AMISH NEMALINE MYOPATHY		HP:0007126	OMIM:605355	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0000006	OMIM:605361	IEA				I		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0000317	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0000639	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0000716	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0001260	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0001268	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0001272	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0001310	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0001347	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0002015	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0002066	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0002073	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0002354	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0003677	OMIM:605361	IEA				C		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0003829	OMIM:605361	IEA				C		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0004373	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0006938	OMIM:605361	IEA				P		HPO:iea	
OMIM	605361	SPINOCEREBELLAR ATAXIA 14		HP:0007018	OMIM:605361	IEA				P		HPO:iea	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0000006	PMID:10769282	IEA				I		HPO:probinson	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0000407	PMID:10769282	IEA	HP:0003621			P		HPO:probinson	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0001635	PMID:10769282	IEA				P		HPO:probinson	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0001644	PMID:10769282	IEA	HP:0003581			P		HPO:probinson	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0001645	PMID:10769282	IEA				P		HPO:probinson	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0001699	OMIM:605362	IEA				M		HPO:skoehler	
OMIM	605362	CARDIOMYOPATHY, DILATED, 1J; CMD1J		HP:0005162	OMIM:605362	IEA				P		HPO:skoehler	
OMIM	605373	PARAGANGLIOMAS 3		HP:0000006	OMIM:605373	IEA				I		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0000740	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0000975	OMIM:605373	TAS				P		HPO:probinson	
OMIM	605373	PARAGANGLIOMAS 3		HP:0001605	OMIM:605373	TAS				P		HPO:probinson	
OMIM	605373	PARAGANGLIOMAS 3		HP:0001609	OMIM:605373	TAS				P		HPO:probinson	
OMIM	605373	PARAGANGLIOMAS 3		HP:0001649	OMIM:605373	TAS				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0001686	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0001962	OMIM:605373	TAS				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0002331	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0002640	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0003001	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0003334	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0003581	OMIM:605373	TAS				C		HPO:skoehler	
OMIM	605373	PARAGANGLIOMAS 3		HP:0006737	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0006748	OMIM:605373	IEA				P		HPO:iea	
OMIM	605373	PARAGANGLIOMAS 3		HP:0006824	OMIM:605373	TAS				P		HPO:probinson	
OMIM	605373	PARAGANGLIOMAS 3		HP:0008629	OMIM:605373	TAS				P		HPO:probinson	
OMIM	605373	PARAGANGLIOMAS 3		HP:0030074	OMIM:605373	TAS				P		HPO:skoehler	
OMIM	605375	#605375 EPILEPSY, NOCTURNAL FRONTAL LOBE, 3; ENFL3		HP:0000006	OMIM:605375	IEA				I		HPO:skoehler	
OMIM	605375	#605375 EPILEPSY, NOCTURNAL FRONTAL LOBE, 3; ENFL3		HP:0001250	OMIM:605375	IEA				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0000006	OMIM:605376	TAS				I		HPO:probinson	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0001669	OMIM:605376	TAS				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0001696	OMIM:605376	TAS				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0001719	OMIM:605376	TAS				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0001748	OMIM:605376	TAS				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0002566	OMIM:605376	TAS				P		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0003363	OMIM:605376	TAS				P		HPO:probinson	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0003829	OMIM:605376	TAS				C		HPO:skoehler	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0006695	OMIM:605376	TAS				P		HPO:probinson	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0011537	OMIM:605376	TAS				P		HPO:probinson	
OMIM	605376	HETEROTAXY, VISCERAL, 2, AUTOSOMAL		HP:0011599	OMIM:605376	TAS				P		HPO:probinson	
OMIM	605387	CATARACT 31, MULTIPLE TYPES		HP:0000006	PMID:17701905	PCS				I		HPO:probinson	
OMIM	605387	CATARACT 31, MULTIPLE TYPES		HP:0007787	PMID:17701905	PCS				P		HPO:probinson	
OMIM	605387	CATARACT 31, MULTIPLE TYPES		HP:0010923	OMIM:605387	TAS				P		HPO:skoehler	
OMIM	605387	CATARACT 31, MULTIPLE TYPES		HP:0100018	OMIM:605387	TAS				P		HPO:skoehler	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:605388	IEA				I		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0000666	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0001270	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0001272	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0002075	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0002136	OMIM:605388	IEA				P		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:605388	IEA				C		HPO:iea	
OMIM	605388	CEREBRAL PALSY, ATAXIC, AUTOSOMAL RECESSIVE		HP:0100021	OMIM:605388	IEA				P		HPO:skoehler	
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0000006	OMIM:605389	IEA				I		HPO:skoehler	
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0000007	OMIM:605389	IEA				I		HPO:skoehler	
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0000653	OMIM:605389	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0001006	OMIM:605389	IEA	HP:0011463	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0002215	OMIM:605389	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0002225	OMIM:605389	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0002231	OMIM:605389	IEA				P		HPO:skoehler	
OMIM	605389	HYPOTRICHOSIS 1; HYPT1		HP:0045075	OMIM:605389	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0000007	OMIM:605407	IEA				I		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0000298	OMIM:605407	TAS				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0000508	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0000750	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0001270	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0001300	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0001336	PMID:8817341	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0001337	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0002063	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0002066	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0002375	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0002451	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0002548	OMIM:605407	TAS				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0003593	OMIM:605407	IEA				C		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0003785	OMIM:605407	IEA				P		HPO:iea	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0003828	OMIM:605407	TAS				C		HPO:skoehler	
OMIM	605407	#605407 SEGAWA SYNDROME, AUTOSOMAL RECESSIVE;;PARKINSONISM, INFANTILE, AUTOSOMAL RECESSIVE;;DYSTONIA, DOPA-RESPONSIVE, AUTOSOMAL RECESSIVE;;DOPA-RESPONSIVE DYSTONIA, AUTOSOMAL RECESSIVE;;TYROSINE HYDROXYLASE DEFICIENCY		HP:0008936	OMIM:605407	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0000006	OMIM:605419	IEA				I		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0000298	OMIM:605419	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0000725	OMIM:605419	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0000738	OMIM:605419	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0000746	OMIM:605419	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0005324	OMIM:605419	IEA				P		HPO:iea	
OMIM	605419	SCHIZOPHRENIA 10		HP:0100753	OMIM:605419	IEA				P		HPO:skoehler	
OMIM	605428	DEAFNESS, AUTOSOMAL RECESSIVE 26		HP:0000007	OMIM:605428	TAS				I		HPO:skoehler	
OMIM	605428	DEAFNESS, AUTOSOMAL RECESSIVE 26		HP:0000407	OMIM:605428	TAS				P		HPO:skoehler	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0000006	OMIM:605432	IEA				I		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0000407	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0000967	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0001159	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0001905	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0001915	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0002827	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0002986	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0003031	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0003182	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0004209	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0004859	OMIM:605432	IEA				P		HPO:skoehler	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0005037	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0005548	OMIM:605432	IEA				P		HPO:iea	
OMIM	605432	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA		HP:0006394	OMIM:605432	IEA				P		HPO:iea	
OMIM	605462	BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 1; BCC1		HP:0002671	OMIM:605462	IEA				P		HPO:skoehler	
OMIM	605472	USHER SYNDROME, TYPE IIC		HP:0000007	OMIM:605472	IEA				I		HPO:iea	
OMIM	605472	USHER SYNDROME, TYPE IIC		HP:0000510	OMIM:605472	IEA				P		HPO:iea	
OMIM	605472	USHER SYNDROME, TYPE IIC		HP:0008527	OMIM:605472	IEA				P		HPO:iea	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0000007	OMIM:605479	IEA				I		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0000952	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0000989	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0001081	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0001406	OMIM:605479	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0002240	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0002908	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605479	CHOLESTASIS, BENIGN RECURRENT INTRAHEPATIC, 2; BRIC2		HP:0003155	OMIM:605479	IEA				P		HPO:skoehler	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0000006	OMIM:605543	TAS				I		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0000726	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0000738	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0001278	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0001300	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0001824	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0003596	OMIM:605543	IEA				C		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0003678	OMIM:605543	IEA				C		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0011999	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605543	PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY		HP:0100315	OMIM:605543	TAS				P		HPO:probinson	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000007	OMIM:605549	TAS				I		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000548	OMIM:605549	IEA				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000587	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000608	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000613	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000618	OMIM:605549	IEA				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000662	OMIM:605549	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0000980	OMIM:605549	IEA				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0007703	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0007994	OMIM:605549	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0008043	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605549	CONE-ROD DYSTROPHY 8; CORD8		HP:0009926	OMIM:605549	TAS				P		HPO:skoehler	
OMIM	605552	ABDOMINAL OBESITY-METABOLIC SYNDROME 1		HP:0000006	OMIM:605552	TAS				I		HPO:skoehler	
OMIM	605552	ABDOMINAL OBESITY-METABOLIC SYNDROME 1		HP:0000822	OMIM:605552	TAS				P		HPO:skoehler	
OMIM	605552	ABDOMINAL OBESITY-METABOLIC SYNDROME 1		HP:0012743	OMIM:605552	TAS				P		HPO:skoehler	
OMIM	605572	ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2		HP:0000006	OMIM:605572	TAS				I		HPO:skoehler	
OMIM	605572	ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2		HP:0000822	OMIM:605572	TAS				P		HPO:skoehler	
OMIM	605572	ABDOMINAL OBESITY-METABOLIC SYNDROME QUANTITATIVE TRAIT LOCUS 2		HP:0012743	OMIM:605572	TAS				P		HPO:skoehler	
OMIM	605583	DEAFNESS, AUTOSOMAL DOMINANT 25		HP:0000006	OMIM:605583	IEA				I		HPO:skoehler	
OMIM	605583	DEAFNESS, AUTOSOMAL DOMINANT 25		HP:0000407	OMIM:605583	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	605583	DEAFNESS, AUTOSOMAL DOMINANT 25		HP:0003828	OMIM:605583	TAS				C		HPO:skoehler	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0000007	OMIM:605588	IEA				I		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0001265	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0001284	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0001425	OMIM:605588	TAS				I		HPO:skoehler	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0001761	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0002460	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0002751	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0002936	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003376	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003378	OMIM:605588	TAS				P		HPO:probinson	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003380	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003383	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003384	OMIM:605588	TAS				P		HPO:probinson	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1	HP:0012825	HP:0003431	OMIM:605588	PCS				P		HPO:probinson	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003484	OMIM:605588	IEA				P		HPO:probinson	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003674	OMIM:605588	IEA				C		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003693	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0003701	OMIM:605588	IEA				P		HPO:iea	
OMIM	605588	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B1; CMT2B1		HP:0009027	OMIM:605588	IEA				P		HPO:iea	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0000007	OMIM:605589	IEA				I		HPO:iea	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0001265	OMIM:605589	IEA				P		HPO:iea	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0001284	OMIM:605589	IEA				P		HPO:iea	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0002460	OMIM:605589	TAS				P		HPO:probinson	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0002936	OMIM:605589	IEA				P		HPO:iea	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2	HP:0012825	HP:0003431	OMIM:605589	IEA				P		HPO:probinson	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0003581	OMIM:605589	TAS				C		HPO:probinson	
OMIM	605589	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B2		HP:0003693	OMIM:605589	TAS				P		HPO:probinson	
OMIM	605594	DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1		HP:0000006	OMIM:605594	TAS				I		HPO:skoehler	
OMIM	605594	DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1		HP:0000360	OMIM:605594	TAS				P		HPO:skoehler	
OMIM	605594	DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1		HP:0000703	OMIM:605594	TAS				P		HPO:skoehler	
OMIM	605594	DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1		HP:0005101	OMIM:605594	TAS				P		HPO:skoehler	
OMIM	605594	DEAFNESS, AUTOSOMAL DOMINANT 39, WITH DENTINOGENESIS IMPERFECTA 1		HP:0008619	OMIM:605594	TAS				P		HPO:skoehler	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000006	OMIM:605627	IEA				I		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000050	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000175	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000189	OMIM:605627	TAS				P		HPO:skoehler	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000218	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000238	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000248	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000256	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000272	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000286	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000289	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000316	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000358	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000369	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000426	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000463	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000528	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000535	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0000653	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0001162	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0001249	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0001320	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0001363	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0002007	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0002079	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0002084	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0002714	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0003196	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0006315	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0009891	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0010806	OMIM:605627	IEA				P		HPO:iea	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0011220	OMIM:605627	TAS				P		HPO:skoehler	
OMIM	605627	CEREBROOCULONASAL SYNDROME		HP:0012806	OMIM:605627	IEA				P		HPO:skoehler	
OMIM	605635	HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2		HP:0002900	OMIM:605635	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	605635	HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2		HP:0003828	OMIM:605635	IEA				C		HPO:skoehler	
OMIM	605635	HYPERALDOSTERONISM, FAMILIAL, TYPE II; HALD2		HP:0003829	OMIM:605635	IEA				C		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000006	OMIM:605637	TAS				I		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000007	OMIM:605637	IEA				I		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000218	OMIM:605637	TAS				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000467	OMIM:605637	TAS				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000508	OMIM:605637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0000602	OMIM:605637	IEA				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0002058	OMIM:605637	TAS				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0002460	OMIM:605637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0002515	OMIM:605637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0002650	OMIM:605637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0002803	OMIM:605637	IEA				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0003198	OMIM:605637	IEA				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0003324	OMIM:605637	TAS				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0003691	OMIM:605637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0003701	OMIM:605637	TAS				P		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0003828	OMIM:605637	TAS				C		HPO:skoehler	
OMIM	605637	MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA		HP:0100299	OMIM:605637	IEA				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000006	OMIM:605670	TAS				I		HPO:iea	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000488	OMIM:605670	IEA				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000510	OMIM:605670	TAS				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000546	OMIM:605670	IEA				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000572	OMIM:605670	TAS				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000575	OMIM:605670	TAS				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0000618	OMIM:605670	IEA				P		HPO:skoehler	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0007830	OMIM:605670	TAS				P		HPO:iea	
OMIM	605670	LATE-ONSET RETINAL DEGENERATION; LORD		HP:0031531	OMIM:605670	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0000006	OMIM:605676	IEA				I		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0000007	OMIM:605676	TAS				I		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0000969	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0000982	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0001635	OMIM:605676	TAS				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0001644	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0002224	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0004756	OMIM:605676	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0007475	OMIM:605676	TAS				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0009804	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605676	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK		HP:0031319	OMIM:605676	IEA				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0000007	OMIM:605711	TAS				I		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0000822	OMIM:605711	IEA				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0001254	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0001263	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0001324	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0001508	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0002092	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0002878	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0003128	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0008972	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0011968	OMIM:605711	TAS				P		HPO:skoehler	
OMIM	605711	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1; MMDS1		HP:0025356	OMIM:605711	IEA				P		HPO:skoehler	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0000006	OMIM:605714	PCS				I		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0000726	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0001297	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0002637	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0004938	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0004968	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0011695	OMIM:605714	PCS				P		HPO:probinson	
OMIM	605714	#605714 CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED;;AMYLOIDOSIS, CEREBROARTERIAL, APP-RELATED;;AMYLOIDOSIS, HEREDITARY, WITH CEREBRAL HEMORRHAGE, DUTCH VARIANT;HCHWAD;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, DUTCH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT;;CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT		HP:0011970	OMIM:605714	TAS				P		HPO:skoehler	
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0000007	PMID:15070707	PCS				I		HPO:probinson	
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0000252	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	3/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0000957	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0001508	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0001511	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0002023	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0003221	PMID:15070707	PCS				P		HPO:probinson	
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0004322	OMIM:605724	TAS				P		HPO:skoehler	
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0004808	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0005528	OMIM:605724	TAS				P		HPO:skoehler	
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0006727	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	605724	FANCONI ANEMIA, COMPLEMENTATION GROUP D1		HP:0009778	PMID:15070707	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0000007	OMIM:605726	IEA				I		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0001171	OMIM:605726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0001265	OMIM:605726	IEA				P		HPO:skoehler	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0001761	OMIM:605726	IEA				P		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0001765	OMIM:605726	TAS				P		HPO:skoehler	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0002460	OMIM:605726	IEA				P		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0003431	OMIM:605726	IEA				P		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0003487	OMIM:605726	IEA				P		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0003676	OMIM:605726	IEA				C		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0003693	OMIM:605726	TAS				P		HPO:skoehler	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0007269	OMIM:605726	TAS				P		HPO:iea	
OMIM	605726	#605726 SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 2; DSMA2;;NEURONOPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE;;NEUROPATHY, DISTAL HEREDITARY MOTOR, JERASH TYPE; HMNJ;;SPINAL MUSCULAR ATROPHY, JERASH TYPE		HP:0009027	OMIM:605726	TAS				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0000006	OMIM:605735	IEA				I		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0000132	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0000421	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0000978	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0002584	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0003540	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0003577	OMIM:605735	TAS				C		HPO:skoehler	
OMIM	605735	%605735 BLEEDING DISORDER, PLATELET-TYPE, 12; BDPLT12;;PROSTAGLANDIN-ENDOPEROXIDE SYNTHASE 1 DEFICIENCY, PLATELET;;PGHS1 DEFICIENCY;;PLATELET CYCLOOXYGENASE 1 DEFICIENCY;;PLATELET COX1 DEFICIENCY		HP:0005261	OMIM:605735	IEA				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0000006	OMIM:605750	TAS				I		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0000541	OMIM:605750	TAS				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0001147	OMIM:605750	TAS				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0007663	OMIM:605750	TAS				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0008052	OMIM:605750	TAS				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0011530	OMIM:605750	TAS				P		HPO:skoehler	
OMIM	605750	EXUDATIVE VITREORETINOPATHY 3; EVR3		HP:0030490	OMIM:605750	IEA				P		HPO:skoehler	
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0000006	OMIM:605751	IEA				I		HPO:iea	
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0002076	OMIM:605751	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0002197	OMIM:605751	IEA				P		HPO:iea	
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0003829	OMIM:605751	TAS				C		HPO:skoehler	
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0007359	OMIM:605751	IEA				P		HPO:iea	
OMIM	605751	#605751 SEIZURES, BENIGN FAMILIAL INFANTILE, 2; BFIS2;;CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; BFIC2		HP:0040168	OMIM:605751	TAS				P		HPO:skoehler	
OMIM	605779	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7		HP:0000006	OMIM:605779	IEA				I		HPO:iea	
OMIM	605779	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7		HP:0001598	OMIM:605779	TAS				P		HPO:probinson	
OMIM	605779	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 7		HP:0030803	OMIM:605779	TAS				P		HPO:skoehler	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0000006	OMIM:605808	TAS				I		HPO:probinson	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0000505	PMID:10896989	PCS				P		HPO:probinson	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0000532	OMIM:605808	TAS				P		HPO:probinson	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0007722	PMID:18378316	PCS				P		HPO:probinson	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0011531	PMID:10896989	PCS				P		HPO:probinson	
OMIM	605808	BIRDSHOT CHORIORETINOPATHY		HP:0012123	PMID:10896989	PCS				P		HPO:probinson	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0000006	OMIM:605809	TAS				I		HPO:skoehler	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0000007	OMIM:605809	IEA				I		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0000486	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0000508	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0000597	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0001283	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0001290	OMIM:605809	TAS				P		HPO:probinson	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0001612	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002015	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002033	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002098	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002747	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002872	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0002882	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003198	OMIM:605809	IEA				P		HPO:skoehler	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003388	OMIM:605809	TAS				P		HPO:skoehler	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003397	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003402	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003403	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003473	OMIM:605809	TAS				P		HPO:probinson	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003554	OMIM:605809	IEA				P		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003577	OMIM:605809	IEA				C		HPO:iea	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0003690	OMIM:605809	TAS				P		HPO:skoehler	
OMIM	605809	MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL; CMS4A		HP:0008872	OMIM:605809	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0000007	OMIM:605814	TAS				I		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0001394	OMIM:605814	TAS				P		HPO:skoehler	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0001406	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0001508	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0001510	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0002155	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0002904	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0003124	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0003233	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0003235	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605814	#605814 CITRULLINEMIA, TYPE II, NEONATAL-ONSET;;CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY; NICCD		HP:0011966	OMIM:605814	TAS				P		HPO:probinson	
OMIM	605818	%605818 DEAFNESS, AUTOSOMAL RECESSIVE 27; DFNB27		HP:0000007	OMIM:605818	TAS				I		HPO:skoehler	
OMIM	605818	%605818 DEAFNESS, AUTOSOMAL RECESSIVE 27; DFNB27		HP:0000407	OMIM:605818	TAS				P		HPO:skoehler	
OMIM	605820	NONAKA MYOPATHY		HP:0000007	OMIM:605820	IEA				I		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0001288	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0002460	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003236	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003458	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003581	OMIM:605820	IEA				C		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003693	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003791	OMIM:605820	IEA				P		HPO:iea	
OMIM	605820	NONAKA MYOPATHY		HP:0003805	OMIM:605820	IEA				P		HPO:iea	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000007	OMIM:605822	TAS				I		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000358	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000369	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000407	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000465	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000518	OMIM:605822	IEA				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000541	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000639	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000646	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000914	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0000938	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0001324	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0001631	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0001634	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0001763	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0002162	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0002953	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0004322	OMIM:605822	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0004325	OMIM:605822	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0010511	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0012741	OMIM:605822	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605822	SPONDYLOOCULAR SYNDROME; SOS		HP:0100807	OMIM:605822	TAS				P		HPO:skoehler	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0000006	OMIM:605827	IEA				I		HPO:iea	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0000966	OMIM:605827	IEA				P		HPO:iea	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0004782	OMIM:605827	IEA				P		HPO:iea	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0010566	OMIM:605827	IEA				P		HPO:skoehler	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0010610	OMIM:605827	IEA				P		HPO:skoehler	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0025249	OMIM:605827	IEA				P		HPO:skoehler	
OMIM	605827	BASALOID FOLLICULAR HAMARTOMA SYNDROME, GENERALIZED, AUTOSOMAL DOMINANT; GBFHS		HP:0200034	OMIM:605827	IEA				P		HPO:skoehler	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0000007	PMID:10102904	PCS				I		HPO:iea	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0003236	PMID:10102904	PCS				P		HPO:iea	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0003750	PMID:10102904	PCS				P		HPO:iea	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0031945	PMID:10102904	PCS				P		HP:probinson	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0031946	PMID:10102904	PCS				P		HP:probinson	
OMIM	605850	DIMETHYLGLYCINE DEHYDROGENASE DEFICIENCY		HP:0410020	PMID:10102904	PCS				P		HP:probinson	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0000007	OMIM:605899	IEA				I		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0000711	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0000718	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0000737	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0000752	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001249	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001250	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001252	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001254	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001265	OMIM:605899	IEA				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001274	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001290	OMIM:605899	TAS				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001298	OMIM:605899	IEA				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001336	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001347	OMIM:605899	IEA				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0001522	OMIM:605899	TAS				M		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0002154	OMIM:605899	TAS				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0003108	OMIM:605899	IEA				P		HPO:iea	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0100247	OMIM:605899	TAS				P		HPO:skoehler	
OMIM	605899	GLYCINE ENCEPHALOPATHY; GCE		HP:0100710	OMIM:605899	TAS				P		HPO:skoehler	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000007	OMIM:605909	IEA				I		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000012	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000716	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000726	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000739	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001300	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001332	OMIM:605909	TAS				P		HPO:probinson	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001347	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002063	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002067	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002172	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002322	OMIM:605909	IEA				P		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003593	OMIM:605909	IEA				C		HPO:iea	
OMIM	605909	PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003677	OMIM:605909	IEA				C		HPO:iea	
OMIM	605911	3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE-2 DEFICIENCY		HP:0000007	OMIM:605911	TAS				I		HPO:skoehler	
OMIM	605911	3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE-2 DEFICIENCY		HP:0002013	OMIM:605911	TAS				P		HPO:skoehler	
OMIM	605911	3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE-2 DEFICIENCY		HP:0002014	OMIM:605911	TAS				P		HPO:skoehler	
OMIM	605911	3-HYDROXY-3-METHYLGLUTARYL-COA SYNTHASE-2 DEFICIENCY		HP:0002240	OMIM:605911	TAS				P		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0000006	OMIM:605967	TAS				I		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0000767	OMIM:605967	TAS				P		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0000768	OMIM:605967	TAS				P		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0001199	OMIM:605967	TAS				P		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0002342	OMIM:605967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0009944	OMIM:605967	TAS				P		HPO:skoehler	
OMIM	605967	%605967 ACROPECTORAL SYNDROME; ACRPS;;ACRP SYNDROME;;SYNDACTYLY, PREAXIAL POLYDACTYLY, AND STERNAL DEFORMITY		HP:0100258	OMIM:605967	TAS				P		HPO:skoehler	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000007	OMIM:606002	TAS				I		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000486	OMIM:606002	TAS		HP:0040284		P		HPO:iea	30%
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000524	OMIM:606002	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000639	PMID:16636238,PMID:19141356	PCS		HP:0040284		P		HPO:iea	8/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000640	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0000657	PMID:16636238,PMID:14736755,PMID:19141356	PCS		HP:0040284		P		HPO:iea	2/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001152	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001260	PMID:16636238	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001265	PMID:14736755	PCS		HP:0040284		P		HPO:iea	4/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001271	OMIM:606002	TAS				P		HPO:skoehler	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001272	PMID:16636238,PMID:14736755,PMID:19141356	PCS		HP:0040284		P		HPO:iea	8/8
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001284	PMID:16636238,PMID:19141356,PMID:14736755	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001332	PMID:14736755	PCS		HP:0040284		P		HPO:iea	5/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001337	OMIM:606002	TAS		HP:0040284		P		HPO:iea	57%
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0001761	PMID:14736755	PCS		HP:0040284		P		HPO:iea	12/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002015	PMID:16636238	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002066	PMID:16636238,PMID:14736755	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002070	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002072	OMIM:606002	TAS		HP:0040284		P		HPO:iea	4/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002346	PMID:14736755,PMID:19141356	PCS		HP:0040284		P		HPO:iea	2/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002460	PMID:16636238	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0002650	PMID:14736755	PCS		HP:0040284		P		HPO:iea	7/18
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003236	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003431	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003477	PMID:16636238	PCS		HP:0040284		P		HPO:iea	8/8
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003676	OMIM:606002	TAS				C		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003693	PMID:16636238	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0003828	OMIM:606002	TAS				C		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0006254	PMID:16636238,PMID:14736755,PMID:19141356	PCS		HP:0040284		P		HPO:iea	6/6
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0006879	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0006886	PMID:16636238	PCS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0006937	OMIM:606002	TAS		HP:0040284		P		HPO:iea	57%
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0007240	OMIM:606002	TAS				P		HPO:skoehler	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0007256	OMIM:606002	TAS				P		HPO:skoehler	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0007267	OMIM:606002	IEA				P		HPO:skoehler	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0010702	OMIM:606002	TAS				P		HPO:iea	
OMIM	606002	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1; SCAR1		HP:0010831	PMID:16636238	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000007	PMID:11283793	PCS				I		HPO:probinson	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000154	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000233	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000260	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000322	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000325	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000369	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0000664	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001009	PMID:11283793	PCS				P		HPO:probinson	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001394	PMID:11283793	PCS				P		HPO:probinson	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001395	OMIM:606003	TAS	HP:0003577			P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001410	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001413	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001433	PMID:11283793	PCS				P		HPO:probinson	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001508	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001511	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001518	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001562	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001629	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001643	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001655	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001680	PMID:11283793	PCS				P		HPO:probinson	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001744	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001873	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001876	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0001903	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0002002	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0002033	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0002099	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0002240	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0005280	OMIM:606003	TAS				P		HPO:skoehler	
OMIM	606003	TRANSALDOLASE DEFICIENCY		HP:0008665	PMID:11283793	PCS				P		HPO:probinson	
OMIM	606012	%606012 DEAFNESS, AUTOSOMAL DOMINANT 18; DFNA18		HP:0000006	OMIM:606012	IEA				I		HPO:skoehler	
OMIM	606012	%606012 DEAFNESS, AUTOSOMAL DOMINANT 18; DFNA18		HP:0001730	OMIM:606012	TAS				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000006	OMIM:606053	IEA				I		HPO:iea	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000007	OMIM:606053	IEA				I		HPO:iea	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000717	OMIM:606053	IEA				P		HPO:iea	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000733	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000735	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0000750	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0001263	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0001302	OMIM:606053	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0002540	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0003593	OMIM:606053	IEA				C		HPO:skoehler	
OMIM	606053	INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISM AND SPEECH DELAY; IDDAS		HP:0031936	OMIM:606053	IEA				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0000007	OMIM:606054	IEA				I		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0000939	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0000964	OMIM:606054	IEA				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001250	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001254	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001259	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001263	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001332	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001508	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001638	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001733	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001873	OMIM:606054	TAS				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001875	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001876	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001903	OMIM:606054	TAS				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001942	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001943	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001944	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0001987	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002013	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002019	OMIM:606054	IEA				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002059	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002104	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002154	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002240	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002509	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0002789	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0003108	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0003128	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0003353	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0004322	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0004396	OMIM:606054	TAS				P		HPO:probinson	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0006846	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0008872	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0008936	OMIM:606054	IEA				P		HPO:iea	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0011695	OMIM:606054	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606054	PROPIONIC ACIDEMIA		HP:0025356	OMIM:606054	IEA				P		HPO:skoehler	
OMIM	606054	PROPIONIC ACIDEMIA		HP:0410066	PMID:22626821,PMID:19551947	PCS				P		HPO:NicoleVasilevsky	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000007	OMIM:606056	IEA				I		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000218	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000269	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000278	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000407	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000445	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000527	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000581	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0000648	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001188	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001250	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001252	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001263	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001290	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0001939	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002059	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002079	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002240	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002757	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002791	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0002943	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0003577	OMIM:606056	TAS				C		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0004313	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0008872	OMIM:606056	IEA				P		HPO:iea	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0010557	OMIM:606056	IEA				P		HPO:skoehler	
OMIM	606056	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIB		HP:0012745	OMIM:606056	TAS				P		HPO:skoehler	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0000007	PMID:20705278	IEA				I		HPO:probinson	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0000510	PMID:20705278	IEA				P		HPO:probinson	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0000543	PMID:20705278	IEA				P		HPO:probinson	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0000662	PMID:20705278	IEA				P		HPO:probinson	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0001133	PMID:20705278	IEA				P		HPO:probinson	
OMIM	606068	#606068 RETINITIS PIGMENTOSA 28; RP28		HP:0007737	PMID:20705278	IEA				P		HPO:probinson	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0000006	OMIM:606069	TAS				I		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0000518	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0000802	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0001638	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0001952	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0002758	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0002829	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0003281	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0011675	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606069	HEMOCHROMATOSIS, TYPE 4		HP:0012378	OMIM:606069	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0000006	OMIM:606070	IEA				I		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0000726	OMIM:606070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0000762	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0001260	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0001283	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0001347	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0001609	OMIM:606070	IEA				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0001739	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002015	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002127	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002366	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002460	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002483	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002747	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002835	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0002936	OMIM:606070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0003236	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0003547	OMIM:606070	IEA				P		HPO:iea	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0003581	OMIM:606070	TAS				C		HPO:probinson	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0003805	OMIM:606070	TAS				P		HPO:probinson	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0003828	OMIM:606070	TAS				C		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0007354	OMIM:606070	TAS				P		HPO:skoehler	
OMIM	606070	#606070 AMYOTROPHIC LATERAL SCLEROSIS 21; ALS21;;MYOPATHY, DISTAL, 2, FORMERLY; MPD2, FORMERLY;;VOCAL CORD AND PHARYNGEAL DYSFUNCTION WITH DISTAL MYOPATHY, FORMERLY;VCPDM, FORMERLY		HP:0008756	OMIM:606070	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0000006	OMIM:606071	IEA				I		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0000012	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0000020	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0000407	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0000763	OMIM:606071	IEA				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0001265	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0001284	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0001604	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0001761	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0001765	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0002460	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0002650	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0002870	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0002878	OMIM:606071	TAS				P		HPO:probinson	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0002936	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0003674	OMIM:606071	IEA				C		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0003724	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0003829	OMIM:606071	TAS				C		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0004322	OMIM:606071	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0004878	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0006897	OMIM:606071	IEA				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0007230	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0009027	OMIM:606071	IEA				P		HPO:iea	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0009113	OMIM:606071	TAS				P		HPO:probinson	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0009130	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0010307	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0011349	OMIM:606071	TAS				P		HPO:probinson	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0012246	OMIM:606071	TAS				P		HPO:probinson	
OMIM	606071	HEREDITARY MOTOR AND SENSORY NEUROPATHY, TYPE IIC; HMSN2C		HP:0200021	OMIM:606071	TAS				P		HPO:skoehler	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0000006	PMID:11431690	PCS				I		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0001425	OMIM:606072	TAS				I		HPO:skoehler	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003236	PMID:11431690	PCS				P		HPO:skoehler	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003457	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003559	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003581	OMIM:606072	IEA		HP:0040282		C		HPO:iea	HP:0040282
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003710	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003712	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003719	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003738	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0003760	OMIM:606072	IEA				P		HPO:iea	
OMIM	606072	RIPPLING MUSCLE DISEASE; RMD		HP:0008967	OMIM:606072	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000023	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000054	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000154	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000218	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000260	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000316	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000319	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000358	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000484	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000621	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000668	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000695	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000696	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0000964	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0001263	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0001537	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0001545	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0001561	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0001643	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0002028	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0002079	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0002208	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0003745	OMIM:606156	IEA				I		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0008551	OMIM:606156	IEA				P		HPO:iea	
OMIM	606156	606156 SENER SYNDROME;;FRONTONASAL DYSPLASIA AND DILATED VIRCHOW-ROBIN SPACES		HP:0012520	OMIM:606156	TAS				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0000006	OMIM:606159	IEA				I		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0000338	OMIM:606159	TAS				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0000643	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0000712	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0000734	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001251	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001257	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001260	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001266	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001300	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001317	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001337	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001347	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001618	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0001939	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002015	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002063	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002067	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002180	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002300	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002356	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0002425	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0003487	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0003676	OMIM:606159	IEA				C		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0007007	OMIM:606159	IEA				P		HPO:iea	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0007123	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0012049	OMIM:606159	TAS				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0012343	OMIM:606159	TAS				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0031908	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606159	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3		HP:0100660	OMIM:606159	IEA				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000006	OMIM:606164	TAS				I		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000286	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000347	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000358	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000410	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000475	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000494	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000535	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0000776	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0001263	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0001913	OMIM:606164	IEA				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0001972	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0002098	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0003593	OMIM:606164	TAS				C		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0004322	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0008551	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0011800	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606164	DIAMOND-BLACKFAN ANEMIA 15 WITH MANDIBULOFACIAL DYSOSTOSIS; DBA15		HP:0011968	OMIM:606164	TAS				P		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000003	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000006	OMIM:606170	TAS				I		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000007	OMIM:606170	IEA				I		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000028	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000046	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000054	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000126	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000252	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000280	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000347	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000365	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000426	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000445	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000448	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000494	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0000684	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001156	OMIM:606170	TAS				P		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001252	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001263	OMIM:606170	TAS				P		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001274	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001290	OMIM:606170	TAS				P		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001374	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001561	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001601	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001629	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001631	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0001762	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0002015	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0002089	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0002209	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0002974	OMIM:606170	TAS		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0002999	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0003175	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0003273	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0006380	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0006443	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0006887	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0007165	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0008665	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0008683	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0008823	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0009803	OMIM:606170	IEA				P		HPO:iea	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0025356	OMIM:606170	IEA				P		HPO:skoehler	
OMIM	606170	GENITOPATELLAR SYNDROME; GTPTS		HP:0030048	OMIM:606170	TAS				P		HPO:skoehler	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000006	OMIM:606176	IEA				I		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000007	OMIM:606176	IEA				I		HPO:skoehler	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000343	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000463	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000508	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000598	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0000819	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001250	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001263	OMIM:606176	TAS				P		HPO:skoehler	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001270	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001324	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001511	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001518	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0001993	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0002521	OMIM:606176	IEA				P		HPO:skoehler	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0002714	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0002715	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0003074	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0003121	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0003196	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0003196	OMIM:606176	TAS				P		HPO:probinson	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0005487	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0006279	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0008936	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0009466	OMIM:606176	IEA				P		HPO:iea	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0009830	OMIM:606176	IEA				P		HPO:skoehler	
OMIM	606176	DIABETES MELLITUS, PERMANENT NEONATAL; PNDM		HP:0030084	OMIM:606176	TAS				P		HPO:skoehler	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0000007	OMIM:606183	IEA				I		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0000639	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0001272	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0001310	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0001609	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0001618	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0002066	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0002073	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0002094	OMIM:606183	IEA				P		HPO:skoehler	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0003445	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0003470	OMIM:606183	IEA				P		HPO:skoehler	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0003581	OMIM:606183	IEA				C		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY	HP:0012825	HP:0003693	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0006511	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0007289	OMIM:606183	IEA				P		HPO:iea	
OMIM	606183	LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY		HP:0008003	OMIM:606183	IEA				P		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:606217	IEA				I		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0001425	OMIM:606217	TAS				I		HPO:skoehler	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0001651	OMIM:606217	TAS				P		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0002627	OMIM:606217	IEA				P		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0003829	OMIM:606217	IEA				C		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0004935	OMIM:606217	IEA				P		HPO:iea	
OMIM	606217	ATRIOVENTRICULAR SEPTAL DEFECT, SUSCEPTIBILITY TO, 2		HP:0006695	OMIM:606217	TAS				P		HPO:probinson	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000076	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000098	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040281		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040281
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000113	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000164	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000218	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000252	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040284
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000256	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000268	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000272	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000286	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000293	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000307	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000331	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000336	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000343	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000365	PMID:18505557	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	20%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000400	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000411	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000414	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000431	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000486	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000490	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000508	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000527	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000574	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000689	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000710	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000717	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000718	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	25%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000750	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040281		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040281
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000817	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000960	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0000966	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001004	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001176	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001250	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001263	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	100%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001265	OMIM:606232	TAS	HP:0003623			P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001270	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001290	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001319	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040281		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040281
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001629	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001643	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0001800	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002020	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002046	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002119	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002136	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002188	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002317	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002342	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002518	ISBN-13:978-0721606156	PCS		HP:0040283		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040283
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0002572	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0003745	http://www.ncbi.nlm.nih.gov/books/NBK1198/#gr_22q13_3.Genetic_Counseling	PCS				I	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0003763	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0004209	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0004691	PMID:18505557	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0007328	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0011120	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0011968	OMIM:606232	TAS	HP:0003623			P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100540	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040282		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	HP:0040282
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100658	PMID:18505557	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	10%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100702	PMID:18505557	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	15%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100703	PMID:18505557	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	15%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100704	http://www.ncbi.nlm.nih.gov/books/NBK1198/	PCS		HP:0040284		P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:iea	6%
OMIM	606232	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22q13.3 DELETION SYNDROME;;TELOMERIC 22q13 MONOSOMY SYNDROME		HP:0100797	OMIM:606232	TAS				P	#606232 PHELAN-MCDERMID SYNDROME; PHMDS;;CHROMOSOME 22Q13.3 DELETION SYNDROME;;TELOMERIC 22Q13 MONOSOMY SYNDROME	HPO:skoehler	
OMIM	606240	THYROID CANCER, NONMEDULLARY, 3; NMTC3		HP:0000006	OMIM:606240	TAS				I		HPO:skoehler	
OMIM	606240	THYROID CANCER, NONMEDULLARY, 3; NMTC3		HP:0040198	OMIM:606240	TAS				P		HPO:skoehler	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000007	OMIM:606242	IEA				I		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000219	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000219	OMIM:606242	TAS				P		HPO:skoehler	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000252	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000343	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000349	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000447	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000508	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0000574	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001047	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001177	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001220	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001249	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001511	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0001999	OMIM:606242	IEA				P		HPO:skoehler	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0004322	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0006380	OMIM:606242	IEA				P		HPO:iea	
OMIM	606242	%606242 MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM;;KONDOH SYNDROME		HP:0008070	OMIM:606242	IEA				P		HPO:iea	
OMIM	606243	#606243 ALVEOLAR SOFT PART SARCOMA; ASPS		HP:0001428	OMIM:606243	TAS				I		HPO:probinson	
OMIM	606243	#606243 ALVEOLAR SOFT PART SARCOMA; ASPS		HP:0012218	OMIM:606243	TAS				P		HPO:probinson	
OMIM	606263	PAGET DISEASE OF BONE 4; PDB4		HP:0000006	OMIM:606263	TAS				I		HPO:skoehler	
OMIM	606263	PAGET DISEASE OF BONE 4; PDB4		HP:0000365	OMIM:606263	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606263	PAGET DISEASE OF BONE 4; PDB4		HP:0002653	OMIM:606263	TAS				P		HPO:skoehler	
OMIM	606263	PAGET DISEASE OF BONE 4; PDB4		HP:0002797	OMIM:606263	IEA				P		HPO:skoehler	
OMIM	606263	PAGET DISEASE OF BONE 4; PDB4		HP:0003155	OMIM:606263	TAS				P		HPO:skoehler	
OMIM	606282	DEAFNESS, AUTOSOMAL DOMINANT 24		HP:0000006	OMIM:606282	TAS				I		HPO:skoehler	
OMIM	606282	DEAFNESS, AUTOSOMAL DOMINANT 24		HP:0000365	OMIM:606282	TAS				P		HPO:skoehler	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000007	OMIM:606324	IEA				I		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000643	OMIM:606324	IEA				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000725	OMIM:606324	IEA				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000739	OMIM:606324	IEA				P		HPO:skoehler	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002063	OMIM:606324	TAS				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002067	OMIM:606324	IEA				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002174	OMIM:606324	IEA				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002322	OMIM:606324	IEA				P		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003581	OMIM:606324	IEA				C		HPO:iea	
OMIM	606324	PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003677	OMIM:606324	IEA				C		HPO:iea	
OMIM	606346	DEAFNESS, AUTOSOMAL DOMINANT 22; DFNA22		HP:0000006	OMIM:606346	TAS				I		HPO:probinson	
OMIM	606346	DEAFNESS, AUTOSOMAL DOMINANT 22; DFNA22		HP:0000408	OMIM:606346	TAS				P		HPO:skoehler	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0000007	OMIM:606353	IEA				I		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0000183	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0000980	OMIM:606353	IEA				P		HPO:skoehler	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0001152	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0001285	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0001347	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002015	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002064	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002120	OMIM:606353	TAS				P		HPO:skoehler	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002127	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002193	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002464	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002491	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0002501	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0003487	OMIM:606353	IEA				P		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0003621	OMIM:606353	IEA				C		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0003677	OMIM:606353	IEA				C		HPO:iea	
OMIM	606353	PRIMARY LATERAL SCLEROSIS, JUVENILE; PLSJ		HP:0011463	OMIM:606353	TAS				C		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0000007	PMID:9096364	PCS				I		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0000819	OMIM:606367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0000821	OMIM:606367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0000964	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0001433	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0001596	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0001744	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0001890	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002028	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002205	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002240	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002716	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002718	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002720	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002721	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0002841	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0004429	PMID:9096364	PCS				P		HPO:probinson	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0005403	PMID:9096364	PCS				P		HPO:skoehler	
OMIM	606367	#606367 IMMUNODEFICIENCY 41 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY; IMD41;;INTERLEUKIN 2 RECEPTOR, ALPHA, DEFICIENCY OF;;IL2RA DEFICIENCY;;CD25 DEFICIENCY		HP:0011473	OMIM:606367	TAS				P		HPO:skoehler	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000007	OMIM:606369	IEA				I		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000164	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000212	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000256	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000348	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000358	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000369	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000494	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0000508	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0001263	OMIM:606369	TAS				P		HPO:skoehler	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002015	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002020	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002079	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002123	OMIM:606369	TAS				P		HPO:probinson	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002205	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002280	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0002518	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0003676	OMIM:606369	IEA				C		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0005280	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0006887	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0006892	OMIM:606369	IEA				P		HPO:iea	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0010804	OMIM:606369	TAS				P		HPO:skoehler	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0010864	OMIM:606369	TAS				P		HPO:skoehler	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0025356	OMIM:606369	IEA				P		HPO:skoehler	
OMIM	606369	MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY		HP:0200134	OMIM:606369	IEA				P		HPO:skoehler	
OMIM	606392	#606392 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4; MODY4;;MODY, TYPE 4		HP:0000006	OMIM:606392	TAS				I		HPO:skoehler	
OMIM	606392	#606392 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4; MODY4;;MODY, TYPE 4		HP:0004904	OMIM:606392	IEA				P		HPO:skoehler	
OMIM	606392	#606392 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 4; MODY4;;MODY, TYPE 4		HP:0005978	OMIM:606392	TAS	HP:0011462			P		HPO:skoehler	
OMIM	606394	#606394 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6; MODY6;;MODY, TYPE 6		HP:0000006	OMIM:606394	TAS				I		HPO:probinson	
OMIM	606394	#606394 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6; MODY6;;MODY, TYPE 6		HP:0004904	OMIM:606394	TAS	HP:0011462			P		HPO:probinson	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000007	OMIM:606407	IEA				I		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000268	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000358	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000400	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000508	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000527	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000787	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000815	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0000824	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001252	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001263	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001290	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001319	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001466	OMIM:606407	IEA				I		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001508	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001558	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001611	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0001998	OMIM:606407	IEA				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0002007	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0002591	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0002901	OMIM:606407	IEA				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0003128	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0003131	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0005280	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0008872	OMIM:606407	IEA				P		HPO:iea	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0010628	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0010804	OMIM:606407	TAS				P		HPO:probinson	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0010864	OMIM:606407	IEA				P		HPO:skoehler	
OMIM	606407	HYPOTONIA-CYSTINURIA SYNDROME		HP:0011398	OMIM:606407	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000007	OMIM:606408	IEA				I		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000061	OMIM:606408	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000076	OMIM:606408	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000813	OMIM:606408	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000974	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000977	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0000978	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0001382	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0001634	OMIM:606408	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0002036	OMIM:606408	TAS				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0002829	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0003555	OMIM:606408	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0003701	OMIM:606408	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0007126	OMIM:606408	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0009025	OMIM:606408	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0031655	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606408	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE; EDSCLL		HP:0032153	OMIM:606408	IEA				P		HPO:skoehler	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000006	OMIM:606438	IEA				I		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000716	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000726	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000737	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000738	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000739	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000741	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0000746	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0001260	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0001332	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0001347	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0001824	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0002063	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0002067	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0002072	OMIM:606438	IEA				P		HPO:iea	
OMIM	606438	HUNTINGTON DISEASE-LIKE 2		HP:0002345	OMIM:606438	IEA				P		HPO:iea	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0000006	OMIM:606445	TAS				I		HPO:skoehler	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0001744	OMIM:606445	TAS				P		HPO:skoehler	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0002240	OMIM:606445	TAS				P		HPO:skoehler	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0002719	OMIM:606445	TAS				P		HPO:skoehler	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0002850	OMIM:606445	TAS				P		HPO:skoehler	
OMIM	606445	PERSISTENT POLYCLONAL B-CELL LYMPHOCYTOSIS; PPBL		HP:0100827	OMIM:606445	IEA				P		HPO:skoehler	
OMIM	606451	DEAFNESS, AUTOSOMAL DOMINANT 30		HP:0000006	OMIM:606451	TAS				I		HPO:skoehler	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0000006	OMIM:606482	IEA				I		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0000764	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0001265	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0001284	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0001425	OMIM:606482	TAS				I		HPO:skoehler	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0001761	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0002460	OMIM:606482	TAS				P		HPO:skoehler	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0002460	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0002936	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003380	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003383	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003481	OMIM:606482	IEA				P		HPO:skoehler	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003621	OMIM:606482	IEA				C		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003693	OMIM:606482	IEA				P		HPO:iea	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0003693	OMIM:606482	TAS				P		HPO:skoehler	
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0007107	OMIM:606482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606482	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE B; CMTDIB		HP:0040078	OMIM:606482	TAS				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0000006	OMIM:606483	IEA				I		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0001265	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0001284	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0001425	OMIM:606483	TAS				I		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0001761	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0002460	OMIM:606483	TAS				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0002460	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0002936	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003376	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003378	OMIM:606483	TAS				P		HPO:probinson	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003383	OMIM:606483	IEA				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003394	OMIM:606483	TAS				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003481	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003674	OMIM:606483	IEA				C		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003693	OMIM:606483	IEA				P		HPO:iea	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0003693	OMIM:606483	TAS				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0007107	OMIM:606483	TAS				P		HPO:skoehler	
OMIM	606483	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE A; CMTDIA		HP:0009027	OMIM:606483	IEA				P		HPO:iea	
OMIM	606519	PHACE ASSOCIATION		HP:0000519	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0000568	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0000609	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0000648	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0000851	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001250	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001263	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001305	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001321	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001423	OMIM:606519	TAS				I		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001629	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001643	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0001680	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0002076	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0002277	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0003745	OMIM:606519	TAS				I		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0004942	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0005314	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0007434	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0007486	OMIM:606519	TAS				P		HPO:probinson	
OMIM	606519	PHACE ASSOCIATION		HP:0007986	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0100029	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606519	PHACE ASSOCIATION		HP:0100545	OMIM:606519	TAS				P		HPO:skoehler	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0000007	OMIM:606528	IEA				I		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0000124	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0000842	OMIM:606528	TAS				P		HPO:probinson	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0001508	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0001943	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0002013	OMIM:606528	IEA				P		HPO:skoehler	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0002014	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0002242	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0002909	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0008527	OMIM:606528	IEA				P		HPO:iea	
OMIM	606528	HOMOZYGOUS 11P15-P14 DELETION SYNDROME		HP:0008872	OMIM:606528	IEA				P		HPO:iea	
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0000007	OMIM:606545	TAS				I		HPO:probinson	
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0000656	OMIM:606545	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0000966	OMIM:606545	TAS				P		HPO:skoehler	
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0000982	OMIM:606545	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0007479	OMIM:606545	TAS				P		HPO:probinson	
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0010783	OMIM:606545	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606545	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3		HP:0012472	OMIM:606545	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0000006	OMIM:606552	IEA				I		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0000360	OMIM:606552	TAS				P		HPO:probinson	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0000617	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0000640	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0000651	OMIM:606552	TAS				P		HPO:probinson	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0001257	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0002018	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0002131	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0002321	OMIM:606552	IEA				P		HPO:iea	
OMIM	606552	EPISODIC ATAXIA, TYPE 4		HP:0025312	OMIM:606552	TAS				P		HPO:skoehler	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0000006	OMIM:606554	IEA				I		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0000360	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0000651	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0001324	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002013	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002018	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002131	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002315	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002321	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0002411	OMIM:606554	IEA				P		HPO:iea	
OMIM	606554	EPISODIC ATAXIA, TYPE 3		HP:0003674	OMIM:606554	IEA				C		HPO:iea	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0000007	PMID:11574907	PCS				I		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0000505	OMIM:606574	TAS				P		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0000635	PMID:14961451	PCS				P		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0000639	PMID:14961451	PCS				P		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0001022	OMIM:606574	IEA				P		HPO:skoehler	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0001104	OMIM:606574	TAS				P		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0005599	PMID:11574907	PCS				P		HPO:probinson	
OMIM	606574	#606574 ALBINISM, OCULOCUTANEOUS, TYPE IV; OCA4;;OCULOCUTANEOUS ALBINISM, TYPE IV		HP:0007894	PMID:11574907	PCS				P		HPO:probinson	
OMIM	606579	#606579 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1;VAMAS1;;VITILIGO; VTLG;;SYSTEMIC LUPUS ERYTHEMATOSUS, VITILIGO-RELATED; SLEV1		HP:0001045	OMIM:606579	IEA				P		HPO:probinson	
OMIM	606579	#606579 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1;VAMAS1;;VITILIGO; VTLG;;SYSTEMIC LUPUS ERYTHEMATOSUS, VITILIGO-RELATED; SLEV1		HP:0010982	OMIM:606579	IEA				I		HPO:probinson	
OMIM	606593	LIG4 SYNDROME		HP:0000750	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0000992	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0001009	OMIM:606593	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	606593	LIG4 SYNDROME		HP:0001263	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0001873	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0001876	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0002863	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606593	LIG4 SYNDROME		HP:0003765	OMIM:606593	IEA				P		HPO:skoehler	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0000006	OMIM:606595	IEA				I		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001171	OMIM:606595	TAS				P		HPO:skoehler	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001178	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001265	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001284	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001425	OMIM:606595	TAS				I		HPO:skoehler	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0001761	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0002380	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0002460	OMIM:606595	TAS				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0002936	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0003376	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0003394	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F	HP:0012825	HP:0003431	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0003693	OMIM:606595	TAS				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0007267	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606595	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F; CMT2F		HP:0009027	OMIM:606595	IEA				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0000007	OMIM:606612	IEA				I		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0000158	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0000252	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0001249	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0001272	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0001302	OMIM:606612	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0001319	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0001771	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002111	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002119	OMIM:606612	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002194	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002350	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002355	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002359	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002500	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002650	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002808	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0002948	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003236	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003307	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003324	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003326	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003394	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003458	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003547	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003551	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003577	OMIM:606612	IEA				C		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003701	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003724	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003733	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003741	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0003828	OMIM:606612	TAS				C		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0007126	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0008872	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0008981	OMIM:606612	IEA				P		HPO:iea	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0010628	OMIM:606612	PCS				P		HPO:probinson	
OMIM	606612	#606612 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5; MDDGB5;;MUSCULAR DYSTROPHY, CONGENITAL, 1C; MDC1C;;MUSCULAR DYSTROPHY, CONGENITAL, FKRP-RELATED		HP:0040083	OMIM:606612	TAS				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0000006	OMIM:606631	TAS				I		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0000135	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0000823	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0000938	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0001324	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0001634	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0001653	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0002515	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0002944	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0003155	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0003202	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0003273	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0003565	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0006380	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0012514	PMID:11807860	PCS				P		HPO:probinson	
OMIM	606631	CAMURATI-ENGELMANN DISEASE, TYPE 2		HP:0100774	OMIM:606631	IEA				P		HPO:skoehler	
OMIM	606640	AMYOTROPHIC LATERAL SCLEROSIS 3		HP:0000006	PMID:11706389	PCS				I		HPO:probinson	
OMIM	606640	AMYOTROPHIC LATERAL SCLEROSIS 3		HP:0002483	PMID:11706389	PCS				P		HPO:probinson	
OMIM	606640	AMYOTROPHIC LATERAL SCLEROSIS 3		HP:0007340	PMID:11706389	PCS				P		HPO:probinson	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0000006	OMIM:606658	IEA				I		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0000641	OMIM:606658	TAS				P		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0001260	OMIM:606658	IEA				P		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0001272	OMIM:606658	IEA				P		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0001347	OMIM:606658	IEA				P		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0002066	OMIM:606658	IEA				P		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0002070	OMIM:606658	TAS				P		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0002078	OMIM:606658	TAS				P		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0002168	OMIM:606658	TAS				P		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0002174	OMIM:606658	IEA				P		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0003581	OMIM:606658	TAS				C		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0003621	OMIM:606658	TAS				C		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0003677	OMIM:606658	IEA				C		HPO:iea	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0007772	OMIM:606658	IEA				P		HPO:skoehler	
OMIM	606658	SPINOCEREBELLAR ATAXIA 15		HP:0007979	OMIM:606658	TAS				P		HPO:skoehler	
OMIM	606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:606664	IEA				I		HPO:iea	
OMIM	606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0002240	OMIM:606664	IEA				P		HPO:iea	
OMIM	606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0002910	OMIM:606664	IEA				P		HPO:iea	
OMIM	606664	GLYCINE N-METHYLTRANSFERASE DEFICIENCY		HP:0003235	OMIM:606664	IEA				P		HPO:iea	
OMIM	606685	#606685 CARDIOMYOPATHY, DILATED, 1L; CMD1L		HP:0000006	PMID:10974018	PCS				I		HPO:probinson	
OMIM	606685	#606685 CARDIOMYOPATHY, DILATED, 1L; CMD1L		HP:0001635	PMID:10974018	PCS				P		HPO:probinson	
OMIM	606685	#606685 CARDIOMYOPATHY, DILATED, 1L; CMD1L		HP:0001644	PMID:10974018	PCS				P		HPO:probinson	
OMIM	606685	#606685 CARDIOMYOPATHY, DILATED, 1L; CMD1L		HP:0006673	PMID:10974018	PCS				P		HPO:probinson	
OMIM	606688	#606688 SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES		HP:0000006	OMIM:606688	IEA				I		HPO:iea	
OMIM	606688	#606688 SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES		HP:0000726	OMIM:606688	IEA				P		HPO:iea	
OMIM	606688	#606688 SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES		HP:0000751	OMIM:606688	IEA				P		HPO:iea	
OMIM	606688	#606688 SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES		HP:0001298	OMIM:606688	IEA				P		HPO:skoehler	
OMIM	606688	#606688 SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES		HP:0002171	OMIM:606688	IEA				P		HPO:skoehler	
OMIM	606690	LYMPHANGIOLEIOMYOMATOSIS		HP:0001428	OMIM:606690	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	606690	LYMPHANGIOLEIOMYOMATOSIS		HP:0012798	OMIM:606690	IEA				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000007	OMIM:606693	IEA				I		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000298	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000458	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000473	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000514	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000605	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000718	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000725	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000726	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0000738	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001250	OMIM:606693	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001251	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001257	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001258	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001260	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001288	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001300	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001336	OMIM:606693	IEA				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001337	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0001347	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002063	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002172	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002304	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002375	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002385	OMIM:606693	IEA				P		HPO:skoehler	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002425	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002548	OMIM:606693	TAS				P		HPO:probinson	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0002936	OMIM:606693	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0003487	OMIM:606693	IEA				P		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0003678	OMIM:606693	IEA				C		HPO:iea	
OMIM	606693	KUFOR-RAKEB SYNDROME		HP:0004409	OMIM:606693	TAS				P		HPO:skoehler	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0000006	OMIM:606703	IEA				I		HPO:iea	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0000317	OMIM:606703	TAS				P		HPO:probinson	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0000739	OMIM:606703	IEA				P		HPO:skoehler	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001260	OMIM:606703	TAS				P		HPO:skoehler	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001270	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001332	OMIM:606703	IEA				P		HPO:iea	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001347	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001635	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0001644	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0002072	OMIM:606703	IEA				P		HPO:iea	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0002322	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0002509	OMIM:606703	TAS				P		HPO:skoehler	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0003621	OMIM:606703	IEA				C		HPO:iea	
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0008936	OMIM:606703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606703	#606703 DYSKINESIA, FAMILIAL, WITH FACIAL MYOKYMIA; FDFM		HP:0100660	OMIM:606703	IEA				P		HPO:skoehler	
OMIM	606705	#606705 DEAFNESS, AUTOSOMAL DOMINANT 36; DFNA36		HP:0000006	OMIM:606705	TAS				I		HPO:probinson	
OMIM	606705	#606705 DEAFNESS, AUTOSOMAL DOMINANT 36; DFNA36		HP:0000360	OMIM:606705	TAS				P		HPO:skoehler	
OMIM	606705	#606705 DEAFNESS, AUTOSOMAL DOMINANT 36; DFNA36		HP:0000407	OMIM:606705	TAS	HP:0003621			P		HPO:probinson	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0000750	OMIM:606711	IEA				P		HPO:iea	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0001425	OMIM:606711	TAS				I		HPO:skoehler	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0001426	OMIM:606711	IEA				I		HPO:iea	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0002463	OMIM:606711	TAS				P		HPO:skoehler	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0002526	OMIM:606711	IEA				P		HPO:iea	
OMIM	606711	SPECIFIC LANGUAGE IMPAIRMENT 1; SLI1		HP:0002549	OMIM:606711	IEA				P		HPO:iea	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0001425	OMIM:606712	TAS				I		HPO:skoehler	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0001426	OMIM:606712	IEA				I		HPO:iea	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0002463	OMIM:606712	IEA				P		HPO:skoehler	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0002474	OMIM:606712	IEA				P		HPO:iea	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0002526	OMIM:606712	IEA				P		HPO:iea	
OMIM	606712	SPECIFIC LANGUAGE IMPAIRMENT 2; SLI2		HP:0002549	OMIM:606712	IEA				P		HPO:iea	
OMIM	606713	#606713 VAN DER WOUDE SYNDROME 2; VWS2		HP:0000006	OMIM:606713	TAS				I		HPO:skoehler	
OMIM	606713	#606713 VAN DER WOUDE SYNDROME 2; VWS2		HP:0000175	OMIM:606713	TAS				P		HPO:skoehler	
OMIM	606713	#606713 VAN DER WOUDE SYNDROME 2; VWS2		HP:0000204	OMIM:606713	TAS				P		HPO:skoehler	
OMIM	606713	#606713 VAN DER WOUDE SYNDROME 2; VWS2		HP:0000674	OMIM:606713	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0000006	OMIM:606719	IEA				I		HPO:skoehler	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0002860	OMIM:606719	IEA				P		HPO:skoehler	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0002861	OMIM:606719	IEA				P		HPO:skoehler	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0006725	OMIM:606719	TAS				P		HPO:skoehler	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0012142	OMIM:606719	TAS				P		HPO:probinson	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0012182	OMIM:606719	TAS				P		HPO:skoehler	
OMIM	606719	#606719 MELANOMA-PANCREATIC CANCER SYNDROME;;FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA-PANCREATIC CARCINOMA SYNDROME;FAMMMPC		HP:0100242	OMIM:606719	TAS				P		HPO:skoehler	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000006	OMIM:606721	IEA				I		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000271	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000519	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000580	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000639	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0000855	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0001278	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0001310	OMIM:606721	IEA				P		HPO:skoehler	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0001733	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0001952	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0002066	OMIM:606721	IEA				P		HPO:skoehler	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0002155	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0002169	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0002936	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0003124	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0003487	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0003635	PMID:11781404	PCS				P		HPO:probinson	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0003828	OMIM:606721	TAS				C		HPO:skoehler	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0005320	PMID:11781404	PCS				P		HPO:probinson	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0005995	PMID:11781404	PCS				P		HPO:probinson	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0007340	OMIM:606721	IEA				P		HPO:iea	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0007485	OMIM:606721	TAS				P		HPO:probinson	
OMIM	606721	LIPODYSTROPHY WITH CONGENITAL CATARACTS AND NEURODEGENERATION		HP:0009125	OMIM:606721	TAS				P		HPO:iea	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000007	PMID:21998596	PCS				I		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2	HP:0012825	HP:0000047	PMID:11781686	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000086	OMIM:606744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000171	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000252	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000341	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000347	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000448	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000568	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0000691	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0001321	PMID:11781686	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0001510	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0001518	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2	HP:0012825	HP:0001620	PMID:11781686	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0004209	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0007429	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0011342	PMID:21998596	PCS				P		HPO:probinson	
OMIM	606744	#606744 SECKEL SYNDROME 2; SCKL2;;SECKEL-TYPE DWARFISM 2;;MICROCEPHALIC PRIMORDIAL DWARFISM 2		HP:0030148	OMIM:606744	TAS				P		HPO:skoehler	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0000006	OMIM:606762	IEA				I		HPO:iea	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0000825	OMIM:606762	IEA				P		HPO:iea	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0001249	OMIM:606762	IEA				P		HPO:iea	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0001325	OMIM:606762	TAS				P		HPO:probinson	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0001425	OMIM:606762	TAS				I		HPO:skoehler	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0002173	OMIM:606762	IEA				P		HPO:iea	
OMIM	606762	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 6; HHF6		HP:0008162	OMIM:606762	IEA				P		HPO:iea	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:606763	TAS				I		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0000246	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0000365	OMIM:606763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0000388	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0000789	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0002098	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0002205	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0003577	OMIM:606763	TAS				C		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0012259	PMID:22387996	PCS				P		HPO:probinson	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0012263	OMIM:606763	TAS				P		HPO:probinson	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:606763	IEA				P		HPO:skoehler	
OMIM	606763	#606763 CILIARY DYSKINESIA, PRIMARY, 2; CILD2;;CILIARY DYSKINESIA, PRIMARY, 2, WITH OR WITHOUT SITUS INVERSUS		HP:0100582	OMIM:606763	TAS				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0000006	OMIM:606764	IEA				I		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0000953	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0001025	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0001067	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0001176	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0002015	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0002019	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0003745	OMIM:606764	IEA				I		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0005214	OMIM:606764	IEA				P		HPO:skoehler	
OMIM	606764	#606764 GASTROINTESTINAL STROMAL TUMOR; GIST		HP:0100723	OMIM:606764	TAS				P		HPO:skoehler	
OMIM	606766	SPERMATOGENIC FAILURE 3; SPGF3		HP:0000006	OMIM:606766	TAS				I		HPO:skoehler	
OMIM	606766	SPERMATOGENIC FAILURE 3; SPGF3		HP:0000789	OMIM:606766	IEA				P		HPO:skoehler	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0000007	OMIM:606768	IEA				I		HPO:iea	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0002460	OMIM:606768	TAS				P		HPO:probinson	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0003198	OMIM:606768	IEA				P		HPO:skoehler	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0003236	OMIM:606768	TAS				P		HPO:skoehler	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0003678	OMIM:606768	IEA				C		HPO:iea	
OMIM	606768	MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET; DMAT		HP:0003693	OMIM:606768	TAS				P		HPO:probinson	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000007	OMIM:606772	IEA				I		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000256	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000303	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000484	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000505	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000506	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000508	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000565	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000581	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000678	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0000750	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0001047	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0001249	OMIM:606772	TAS				P		HPO:skoehler	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0001513	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0001822	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0007663	OMIM:606772	TAS				P		HPO:skoehler	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0010579	OMIM:606772	IEA				P		HPO:iea	
OMIM	606772	%606772 MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES;;MOMES SYNDROME		HP:0011349	OMIM:606772	TAS				P		HPO:skoehler	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000006	OMIM:606777	IEA				I		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000007	OMIM:606777	TAS		HP:0040283		I		HPO:skoehler	HP:0040283
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000750	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001249	OMIM:606777	TAS				P		HPO:skoehler	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001250	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001250	OMIM:606777	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001251	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001257	OMIM:606777	IEA				P		HPO:skoehler	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001260	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001263	OMIM:606777	TAS				P		HPO:skoehler	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001266	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001269	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001289	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001328	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001336	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001347	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001939	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002268	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002353	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002360	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0003470	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0003487	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0003593	OMIM:606777	IEA				C		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0005484	OMIM:606777	TAS				P		HPO:probinson	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0007704	OMIM:606777	IEA				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0011972	OMIM:606777	TAS				P		HPO:iea	
OMIM	606777	#606777 GLUT1 DEFICIENCY SYNDROME 1; GLUT1DS1;;GLUCOSE TRANSPORT DEFECT, BLOOD-BRAIN BARRIERGLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE, INCLUDED		HP:0011973	OMIM:606777	TAS				P		HPO:iea	
OMIM	606785	CRIGLER-NAJJAR SYNDROME, TYPE II		HP:0000007	OMIM:606785	IEA				I		HPO:iea	
OMIM	606785	CRIGLER-NAJJAR SYNDROME, TYPE II		HP:0000952	OMIM:606785	IEA				P		HPO:iea	
OMIM	606785	CRIGLER-NAJJAR SYNDROME, TYPE II		HP:0008282	OMIM:606785	TAS				P		HPO:probinson	
OMIM	606798	BLEPHAROSPASM, BENIGN ESSENTIAL		HP:0000643	OMIM:606798	TAS				P		HPO:probinson	
OMIM	606798	BLEPHAROSPASM, BENIGN ESSENTIAL		HP:0003596	OMIM:606798	TAS				C		HPO:probinson	
OMIM	606798	BLEPHAROSPASM, BENIGN ESSENTIAL		HP:0003745	OMIM:606798	TAS				I		HPO:probinson	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000007	OMIM:606812	IEA				I		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000218	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000252	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000316	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000463	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000505	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000648	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0000980	OMIM:606812	IEA				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001252	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001263	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001274	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001290	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001396	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001399	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001508	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001901	OMIM:606812	TAS				P		HPO:probinson	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0001942	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002007	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002059	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002126	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002133	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002167	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002187	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002190	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002365	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0002904	OMIM:606812	IEA				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0003128	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0003355	OMIM:606812	IEA				P		HPO:skoehler	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0003758	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0004482	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0005280	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0007620	OMIM:606812	IEA				P		HPO:iea	
OMIM	606812	FUMARASE DEFICIENCY; FMRD		HP:0100954	OMIM:606812	TAS				P		HPO:skoehler	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0000007	OMIM:606824	TAS				I		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0001508	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0001942	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0001986	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0002024	OMIM:606824	IEA				P		HPO:skoehler	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0002028	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0003076	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0003270	OMIM:606824	TAS				P		HPO:skoehler	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0004924	OMIM:606824	TAS				P		HPO:probinson	
OMIM	606824	GLUCOSE/GALACTOSE MALABSORPTION; GGM		HP:0030143	OMIM:606824	TAS				P		HPO:skoehler	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0000006	OMIM:606835	TAS				I		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0001857	OMIM:606835	TAS				P		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0003040	OMIM:606835	IEA				P		HPO:skoehler	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0003621	OMIM:606835	TAS				C		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0003795	OMIM:606835	TAS				P		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0005819	OMIM:606835	TAS				P		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0005872	OMIM:606835	TAS				P		HPO:skoehler	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0009466	OMIM:606835	TAS				P		HPO:probinson	
OMIM	606835	#606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL; FDAB		HP:0009882	OMIM:606835	TAS				P		HPO:probinson	
OMIM	606840	FACIOMANDIBULAR MYOCLONUS, NOCTURNAL		HP:0001336	OMIM:606840	TAS				P		HPO:skoehler	
OMIM	606840	FACIOMANDIBULAR MYOCLONUS, NOCTURNAL		HP:0003763	OMIM:606840	TAS				P		HPO:probinson	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0001265	OMIM:606842	TAS				P		HPO:probinson	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0001284	OMIM:606842	IEA				P		HPO:skoehler	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0001638	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0002093	OMIM:606842	IEA				P		HPO:skoehler	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0002093	OMIM:606842	TAS				P		HPO:probinson	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0002094	OMIM:606842	TAS				P		HPO:probinson	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0002936	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0003690	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0003745	OMIM:606842	IEA				I		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0003798	OMIM:606842	IEA				P		HPO:skoehler	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0004571	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0004575	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0005185	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0005986	OMIM:606842	IEA				P		HPO:iea	
OMIM	606842	CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS		HP:0008483	OMIM:606842	IEA				P		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0000007	OMIM:606843	IEA				I		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0001875	OMIM:606843	IEA				P		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0002718	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3	HP:0012828	HP:0002720	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0002721	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0002847	OMIM:606843	IEA				P		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0002849	OMIM:606843	IEA				P		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0002959	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3		HP:0003496	OMIM:606843	IEA				P		HPO:iea	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3	HP:0012828	HP:0004315	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606843	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 3	HP:0012828	HP:0005479	OMIM:606843	TAS				P		HPO:probinson	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:606851	IEA				I		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000028	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000047	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000048	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000185	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000239	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000248	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000316	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000325	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000347	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000358	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000369	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000465	OMIM:606851	IEA				P		HPO:skoehler	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000494	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000508	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000589	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0000767	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:606851	TAS				P		HPO:skoehler	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0001263	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0001838	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0006712	OMIM:606851	IEA				P		HPO:iea	
OMIM	606851	CREE MENTAL RETARDATION SYNDROME		HP:0010554	OMIM:606851	TAS				P		HPO:probinson	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0000007	PMID:11845408	PCS				I		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0000565	PMID:11845408	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0000577	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0000639	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001249	PMID:11845408	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001250	PMID:11845408	PCS		HP:0040284		P		HPO:iea	4/5
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001263	PMID:11845408	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001276	PMID:11845408	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001310	PMID:11845408	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001321	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0001347	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0002078	PMID:11845408	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0002119	PMID:11845408	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0002136	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0002365	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0003487	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0006821	PMID:11845408	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0007095	OMIM:606854	IEA				P		HPO:iea	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0007266	OMIM:606854	TAS				P		HPO:probinson	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL		HP:0011448	OMIM:606854	TAS				P		HPO:probinson	
OMIM	606854	POLYMICROGYRIA, BILATERAL FRONTOPARIETAL	HP:0012825	HP:0012110	PMID:11845408	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	606864	CARNEY-STRATAKIS SYNDROME		HP:0002668	OMIM:606864	TAS				P		HPO:skoehler	
OMIM	606864	CARNEY-STRATAKIS SYNDROME		HP:0007378	OMIM:606864	TAS				P		HPO:skoehler	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0000006	OMIM:606889	TAS				I		HPO:probinson	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0000726	OMIM:606889	TAS				P		HPO:probinson	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0002511	OMIM:606889	IEA				P		HPO:skoehler	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0003596	OMIM:606889	TAS				C		HPO:probinson	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0006979	OMIM:606889	TAS				P		HPO:probinson	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0011970	OMIM:606889	TAS				P		HPO:probinson	
OMIM	606889	ALZHEIMER DISEASE 4		HP:0100256	OMIM:606889	IEA				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0000007	OMIM:606893	TAS				I		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0000225	OMIM:606893	TAS				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0000324	OMIM:606893	IEA				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0000520	OMIM:606893	TAS				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0000572	OMIM:606893	TAS				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0001537	OMIM:606893	TAS				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0001540	OMIM:606893	IEA				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0002516	OMIM:606893	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0003155	OMIM:606893	TAS				P		HPO:skoehler	
OMIM	606893	VASCULAR MALFORMATION, PRIMARY INTRAOSSEOUS		HP:0410276	OMIM:606893	IEA				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0000006	OMIM:606895	IEA				I		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0000691	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0001204	OMIM:606895	IEA				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0001792	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0001798	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0001859	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0003771	OMIM:606895	TAS				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0004253	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0005819	OMIM:606895	TAS				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0006106	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0009803	OMIM:606895	IEA				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0009843	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0009882	OMIM:606895	TAS				P		HPO:skoehler	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0010259	OMIM:606895	IEA				P		HPO:iea	
OMIM	606895	606895 SYMPHALANGISM, DISTAL, WITH MICRODONTIA, DENTAL PULP STONES, AND NARROWEDZYGOMATIC ARCH		HP:0011835	OMIM:606895	TAS				P		HPO:skoehler	
OMIM	606943	USHER SYNDROME, TYPE IG		HP:0000007	OMIM:606943	IEA				I		HPO:iea	
OMIM	606943	USHER SYNDROME, TYPE IG		HP:0000407	OMIM:606943	TAS				P		HPO:skoehler	
OMIM	606943	USHER SYNDROME, TYPE IG		HP:0000510	OMIM:606943	IEA				P		HPO:iea	
OMIM	606943	USHER SYNDROME, TYPE IG		HP:0001751	OMIM:606943	IEA				P		HPO:iea	
OMIM	606943	USHER SYNDROME, TYPE IG		HP:0004646	OMIM:606943	IEA				P		HPO:iea	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0000007	OMIM:606952	TAS				I		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0000505	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0000613	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0000639	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0001010	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0001022	OMIM:606952	IEA				P		HPO:skoehler	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0005599	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606952	#606952 ALBINISM, OCULOCUTANEOUS, TYPE IB; OCA1B;;OCULOCUTANEOUS ALBINISM, TYPE IB;;ALBINISM, YELLOW MUTANT TYPE;;YELLOW ALBINISMALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE, INCLUDED;;OCA1-TS, INCLUDED		HP:0007894	OMIM:606952	TAS				P		HPO:probinson	
OMIM	606960	%606960 INSULINOMA TUMOR SUPPRESSOR GENE LOCUS		HP:0001428	OMIM:606960	TAS				I		HPO:probinson	
OMIM	606960	%606960 INSULINOMA TUMOR SUPPRESSOR GENE LOCUS		HP:0012197	OMIM:606960	TAS				P		HPO:probinson	
OMIM	606963	%606963 PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPDPULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET, INCLUDED;;COPD, SEVERE EARLY-ONSET, INCLUDED;;PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, RATE OF DECLINE OF LUNG FUNCTIONIN, INCLUDED		HP:0006510	OMIM:606963	TAS				P		HPO:skoehler	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0000007	OMIM:606966	IEA				I		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0000090	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0000092	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0000103	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0000108	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0001510	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0001903	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0001959	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0003774	OMIM:606966	IEA				P		HPO:iea	
OMIM	606966	NEPHRONOPHTHISIS 4		HP:0005576	OMIM:606966	TAS				P		HPO:probinson	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000007	OMIM:606995	IEA				I		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000090	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000103	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000108	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000550	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000572	OMIM:606995	IEA				P		HPO:skoehler	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000639	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0000805	OMIM:606995	IEA				P		HPO:skoehler	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0001959	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0003774	OMIM:606995	IEA				P		HPO:iea	
OMIM	606995	SENIOR-LOKEN SYNDROME 3		HP:0007875	OMIM:606995	IEA				P		HPO:skoehler	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0000007	OMIM:606996	IEA				I		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0000090	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0000103	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0000510	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0000646	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0001141	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0001425	OMIM:606996	TAS				I		HPO:skoehler	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0001583	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0001903	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0001959	OMIM:606996	IEA				P		HPO:iea	
OMIM	606996	SENIOR-LOKEN SYNDROME 4; SLSN4		HP:0003774	OMIM:606996	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0000006	OMIM:607004	IEA				I		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0001425	OMIM:607004	TAS				I		HPO:skoehler	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0004322	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0005819	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0008111	OMIM:607004	TAS				P		HPO:probinson	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0009370	OMIM:607004	TAS				P		HPO:probinson	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0009466	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0009882	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0010047	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0010230	OMIM:607004	IEA				P		HPO:iea	
OMIM	607004	%607004 BRACHYDACTYLY, TYPE A1, B; BDA1B		HP:0030084	OMIM:607004	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000007	OMIM:607014	TAS				I		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0000023	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000212	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000238	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000256	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000280	OMIM:607014	TAS	HP:0003593			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0000293	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000365	OMIM:607014	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607014	HURLER SYNDROME		HP:0000455	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000470	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0000501	OMIM:607014	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607014	HURLER SYNDROME		HP:0000546	OMIM:607014	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607014	HURLER SYNDROME		HP:0000691	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0000894	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0000943	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0001007	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0001249	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0001263	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0001371	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0001387	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0001433	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0001537	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0001638	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0001653	OMIM:607014	TAS		HP:0040284		P		HPO:probinson	10/12
OMIM	607014	HURLER SYNDROME		HP:0001659	OMIM:607014	TAS		HP:0040284		P		HPO:probinson	4/12
OMIM	607014	HURLER SYNDROME		HP:0001706	OMIM:607014	TAS		HP:0040284		P		HPO:probinson	11/58
OMIM	607014	HURLER SYNDROME		HP:0001744	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0002180	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0002205	OMIM:607014	TAS		HP:0040284		P		HPO:probinson	4/12
OMIM	607014	HURLER SYNDROME		HP:0002240	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0002344	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0002673	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0002680	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0002808	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0002869	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0003311	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0003320	OMIM:607014	TAS		HP:0040284		P		HPO:probinson	38%
OMIM	607014	HURLER SYNDROME		HP:0003541	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0004322	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0004490	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0004586	OMIM:607014	TAS	HP:0011463			P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0005019	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0005280	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0007759	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0008802	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0011400	OMIM:607014	TAS				P		HPO:probinson	
OMIM	607014	HURLER SYNDROME		HP:0012185	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0012471	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0030812	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607014	HURLER SYNDROME		HP:0410018	OMIM:607014	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0000007	OMIM:607015	TAS				I		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0000347	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0000943	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001007	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001387	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001537	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001653	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001659	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0001744	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS	HP:0012825	HP:0002092	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002205	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002240	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002650	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002777	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002808	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0002870	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0004322	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0005280	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0007957	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607015	#607015 HURLER-SCHEIE SYNDROME;;MUCOPOLYSACCHARIDOSIS TYPE IH/S; MPS1-HS		HP:0012471	OMIM:607015	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000007	OMIM:607016	TAS				I		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000283	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000293	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000303	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000445	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000470	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0000501	OMIM:607016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607016	SCHEIE SYNDROME		HP:0000546	OMIM:607016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607016	SCHEIE SYNDROME		HP:0000943	OMIM:607016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607016	SCHEIE SYNDROME		HP:0001650	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0001659	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0001761	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0002341	OMIM:607016	IEA				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0002857	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0002870	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0005280	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME	HP:0003676	HP:0007957	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607016	SCHEIE SYNDROME		HP:0012185	OMIM:607016	TAS				P		HPO:skoehler	
OMIM	607017	%607017 DEAFNESS, AUTOSOMAL DOMINANT 21; DFNA21		HP:0000006	OMIM:607017	TAS				I		HPO:skoehler	
OMIM	607017	%607017 DEAFNESS, AUTOSOMAL DOMINANT 21; DFNA21		HP:0000407	OMIM:607017	TAS				P		HPO:skoehler	
OMIM	607039	#607039 DEAFNESS, AUTOSOMAL RECESSIVE 22; DFNB22		HP:0000007	OMIM:607039	TAS				I		HPO:probinson	
OMIM	607039	#607039 DEAFNESS, AUTOSOMAL RECESSIVE 22; DFNB22		HP:0000407	OMIM:607039	TAS				P		HPO:probinson	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0000006	OMIM:607060	IEA				I		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0000726	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0002063	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0002067	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0002172	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0002322	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0002548	OMIM:607060	IEA				P		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0003677	OMIM:607060	IEA				C		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0003829	OMIM:607060	TAS				C		HPO:iea	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0004409	OMIM:607060	IEA				P		HPO:skoehler	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0011960	OMIM:607060	TAS				P		HPO:probinson	
OMIM	607060	PARKINSON DISEASE 8, AUTOSOMAL DOMINANT; PARK8		HP:0100315	OMIM:607060	TAS				P		HPO:skoehler	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0000006	OMIM:607078	TAS				I		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0001216	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0001425	OMIM:607078	TAS				I		HPO:skoehler	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0002654	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0002656	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0002812	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0002829	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0002857	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5	HP:0012825	HP:0003025	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0003088	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0003090	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0003365	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0006429	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0008103	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0010582	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0010585	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607078	EPIPHYSEAL DYSPLASIA, MULTIPLE, 5; EDM5		HP:0100864	OMIM:607078	TAS				P		HPO:probinson	
OMIM	607080	46,XY GONADAL DYSGENESIS, PARTIAL, WITH MINIFASCICULAR NEUROPATHY		HP:0000133	PMID:11017805	PCS				P		HPO:iea	
OMIM	607080	46,XY GONADAL DYSGENESIS, PARTIAL, WITH MINIFASCICULAR NEUROPATHY		HP:0001271	PMID:11017805	PCS				P		HPO:iea	
OMIM	607080	46,XY GONADAL DYSGENESIS, PARTIAL, WITH MINIFASCICULAR NEUROPATHY		HP:0003380	PMID:11017805	PCS				P		HPO:iea	
OMIM	607080	46,XY GONADAL DYSGENESIS, PARTIAL, WITH MINIFASCICULAR NEUROPATHY		HP:0008668	OMIM:607080	IEA				P		HPO:skoehler	
OMIM	607084	#607084 DEAFNESS, AUTOSOMAL RECESSIVE 31; DFNB31;;WHIRLER, MOUSE, HOMOLOG OF		HP:0000007	OMIM:607084	TAS				I		HPO:probinson	
OMIM	607084	#607084 DEAFNESS, AUTOSOMAL RECESSIVE 31; DFNB31;;WHIRLER, MOUSE, HOMOLOG OF		HP:0000407	OMIM:607084	TAS				P		HPO:probinson	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0000007	OMIM:607088	IEA				I		HPO:iea	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0002792	OMIM:607088	TAS				P		HPO:probinson	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0003307	OMIM:607088	IEA				P		HPO:iea	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0003445	OMIM:607088	IEA				P		HPO:iea	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0003677	OMIM:607088	IEA				C		HPO:iea	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0003693	OMIM:607088	TAS				P		HPO:probinson	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0007181	OMIM:607088	IEA				P		HPO:iea	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0007269	OMIM:607088	TAS				P		HPO:probinson	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0009053	OMIM:607088	TAS				P		HPO:probinson	
OMIM	607088	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 3		HP:0009113	OMIM:607088	TAS				P		HPO:probinson	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0000007	OMIM:607091	IEA				I		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0000256	OMIM:607091	IEA				P		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0001252	OMIM:607091	IEA				P		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0001263	OMIM:607091	IEA				P		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0001290	OMIM:607091	TAS				P		HPO:skoehler	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0001305	OMIM:607091	IEA				P		HPO:skoehler	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0001928	OMIM:607091	IEA				P		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0003198	OMIM:607091	IEA				P		HPO:iea	
OMIM	607091	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IID		HP:0003236	OMIM:607091	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000007	OMIM:607095	IEA				I		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000316	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000470	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000668	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000926	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0000946	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0001156	OMIM:607095	TAS				P		HPO:skoehler	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0001216	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0001249	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0001831	OMIM:607095	TAS				P		HPO:probinson	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0002341	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0002680	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0003015	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0003308	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0008905	OMIM:607095	IEA				P		HPO:iea	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0009381	OMIM:607095	TAS				P		HPO:probinson	
OMIM	607095	#607095 ANAUXETIC DYSPLASIA;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, ANAUXETIC TYPE;;SPONDYLOMETAEPIPHYSEAL DYSPLASIA, MENGER TYPE		HP:0010585	OMIM:607095	IEA				P		HPO:iea	
OMIM	607101	DEAFNESS, AUTOSOMAL RECESSIVE 30; DFNB30		HP:0000007	PMID:12032315	PCS				I		HPO:probinson	
OMIM	607101	DEAFNESS, AUTOSOMAL RECESSIVE 30; DFNB30		HP:0000408	OMIM:607101	TAS				P		HPO:skoehler	
OMIM	607101	DEAFNESS, AUTOSOMAL RECESSIVE 30; DFNB30		HP:0001730	PMID:12032315	PCS				P		HPO:probinson	
OMIM	607107	%607107 NASOPHARYNGEAL CARCINOMA;;NPCA;;NPC;;NASOPHARYNGEAL CANCERNASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 1, INCLUDED; NPCA1, INCLUDED		HP:0010982	OMIM:607107	TAS				I		HPO:probinson	
OMIM	607107	%607107 NASOPHARYNGEAL CARCINOMA;;NPCA;;NPC;;NASOPHARYNGEAL CANCERNASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 1, INCLUDED; NPCA1, INCLUDED		HP:0100630	OMIM:607107	TAS				P		HPO:probinson	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0000006	OMIM:607115	TAS				I		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0000408	OMIM:607115	TAS				P		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0000520	OMIM:607115	TAS				P		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0001369	OMIM:607115	IEA				P		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0001510	OMIM:607115	TAS				P		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA	HP:0031796	HP:0001945	OMIM:607115	TAS				P		HPO:skoehler	
OMIM	607115	CINCA SYNDROME; CINCA		HP:0002007	OMIM:607115	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000007	OMIM:607131	TAS				I		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000023	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000256	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000272	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000316	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000470	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000767	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0000768	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0001004	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0001270	OMIM:607131	IEA				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0001274	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0001999	OMIM:607131	IEA				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0002007	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0002419	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0002654	OMIM:607131	IEA				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0002857	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0012444	OMIM:607131	IEA				P		HPO:skoehler	
OMIM	607131	AL-GAZALI-BAKALINOVA SYNDROME; AGBK		HP:0030084	OMIM:607131	TAS				P		HPO:skoehler	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000006	OMIM:607136	IEA				I		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000020	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000640	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000716	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000718	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000727	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000738	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000743	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0000757	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001250	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001260	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001272	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001289	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001300	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001310	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001332	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0001336	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002015	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002063	OMIM:607136	IEA				P		HPO:skoehler	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002066	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002067	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002070	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002072	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002080	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002136	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002171	OMIM:607136	TAS				P		HPO:skoehler	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002186	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002300	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002403	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002506	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0002529	OMIM:607136	TAS				P		HPO:skoehler	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0003676	OMIM:607136	IEA				C		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0007668	OMIM:607136	IEA				P		HPO:iea	
OMIM	607136	#607136 SPINOCEREBELLAR ATAXIA 17; SCA17;;HUNTINGTON DISEASE-LIKE 4; HDL4		HP:0011999	OMIM:607136	TAS				P		HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000046	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000047	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000054	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000253	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000322	PMID:12093361	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000377	PMID:12093361	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0000407	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001263	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001290	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001508	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001762	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001852	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0001999	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0002205	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0002901	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0002984	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0003097	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0003316	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0003645	PMID:12093361	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0004313	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0005736	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0005792	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0008905	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0011800	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0011947	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0011968	PMID:11983712	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:probinson	
OMIM	607143	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G		HP:0025356	OMIM:607143	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IG; CDG1G	HPO:skoehler	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0000006	OMIM:607152	IEA				I		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0000012	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0000020	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0001258	OMIM:607152	TAS				P		HPO:probinson	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0001347	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0002061	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0002064	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0002166	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0002839	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0003487	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0003677	OMIM:607152	IEA				C		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0007340	OMIM:607152	IEA				P		HPO:iea	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0011448	OMIM:607152	TAS				P		HPO:probinson	
OMIM	607152	SPASTIC PARAPLEGIA 19, AUTOSOMAL DOMINANT		HP:0011449	OMIM:607152	TAS				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0000007	OMIM:607155	IEA				I		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0000158	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0001644	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0001771	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002111	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002355	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002359	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002515	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002650	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002808	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002877	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0002948	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003236	OMIM:607155	TAS				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003307	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003326	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003394	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003547	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003551	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003701	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003733	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003741	OMIM:607155	TAS				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003749	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0003828	OMIM:607155	TAS				C		HPO:skoehler	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0005162	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0008305	OMIM:607155	TAS		HP:0040284		P		HPO:probinson	25%
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0008981	OMIM:607155	IEA				P		HPO:probinson	
OMIM	607155	#607155 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 5; MDDGC5;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, FRKP-RELATED		HP:0040083	OMIM:607155	TAS				P		HPO:skoehler	
OMIM	607174	#607174 MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO		HP:0000006	OMIM:607174	TAS				I		HPO:skoehler	
OMIM	607174	#607174 MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO		HP:0002858	OMIM:607174	TAS				P		HPO:skoehler	
OMIM	607174	#607174 MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO		HP:0003581	OMIM:607174	TAS				C		HPO:skoehler	
OMIM	607174	#607174 MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO		HP:0003829	OMIM:607174	TAS				C		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0000007	OMIM:607196	TAS				I		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0000253	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0000347	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0000737	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0001321	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0001338	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0001371	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0002240	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0002509	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0003128	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0003577	OMIM:607196	TAS				C		HPO:skoehler	
OMIM	607196	#607196 MICROCEPHALY, AMISH TYPE; MCPHA;;AMISH LETHAL MICROCEPHALY;;THIAMINE METABOLISM DYSFUNCTION SYNDROME 3 (MICROCEPHALY TYPE); THMD3		HP:0008936	OMIM:607196	TAS				P		HPO:skoehler	
OMIM	607200	THYROID DYSHORMONOGENESIS 6; TDH6		HP:0000007	OMIM:607200	IEA				I		HPO:skoehler	
OMIM	607200	THYROID DYSHORMONOGENESIS 6; TDH6		HP:0000851	OMIM:607200	IEA				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0000006	OMIM:607208	IEA				I		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0001251	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0001263	OMIM:607208	TAS				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0001268	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0001270	OMIM:607208	IEA				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0002059	OMIM:607208	TAS				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0002121	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0002123	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0002133	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0002384	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0003593	OMIM:607208	IEA				C		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0005484	OMIM:607208	TAS				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0006813	OMIM:607208	IEA				P		HPO:iea	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0100704	OMIM:607208	TAS				P		HPO:skoehler	
OMIM	607208	#607208 DRAVET SYNDROME;;EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 6; EIEE6;;SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI		HP:0200134	OMIM:607208	IEA				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0000007	OMIM:607225	IEA				I		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0000020	OMIM:607225	IEA				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0000478	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0000514	OMIM:607225	TAS				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001258	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001260	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001270	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001324	OMIM:607225	TAS				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001347	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001761	OMIM:607225	TAS				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0001771	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002015	OMIM:607225	IEA				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002366	OMIM:607225	IEA				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002425	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002445	OMIM:607225	IEA				P		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002492	OMIM:607225	TAS	HP:0003593			P		HPO:probinson	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002510	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0002650	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0003487	OMIM:607225	IEA				P		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0003593	OMIM:607225	TAS				C		HPO:probinson	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0003676	OMIM:607225	TAS				C		HPO:skoehler	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0003677	OMIM:607225	IEA				C		HPO:iea	
OMIM	607225	SPASTIC PARALYSIS, INFANTILE-ONSET ASCENDING; IAHSP		HP:0005216	OMIM:607225	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0000007	OMIM:607236	IEA				I		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0000510	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0000726	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0001257	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0001260	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0001332	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0001927	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0002015	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0002310	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0002454	OMIM:607236	IEA				P		HPO:iea	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0003563	OMIM:607236	TAS				P		HPO:probinson	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0003621	OMIM:607236	IEA				C		HPO:skoehler	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0003677	OMIM:607236	IEA				C		HPO:skoehler	
OMIM	607236	HYPOPREBETALIPOPROTEINEMIA, ACANTHOCYTOSIS, RETINITIS PIGMENTOSA,AND PALLIDAL DEGENERATION		HP:0007132	OMIM:607236	IEA				P		HPO:iea	
OMIM	607239	DEAFNESS, AUTOSOMAL RECESSIVE 33		HP:0000007	OMIM:607239	TAS				I		HPO:skoehler	
OMIM	607239	DEAFNESS, AUTOSOMAL RECESSIVE 33		HP:0000365	OMIM:607239	TAS				P		HPO:skoehler	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0000007	OMIM:607250	TAS				I		HPO:probinson	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0001251	OMIM:607250	TAS				P		HPO:probinson	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0001761	OMIM:607250	TAS				P		HPO:probinson	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0003376	OMIM:607250	TAS				P		HPO:probinson	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0003477	OMIM:607250	TAS				P		HPO:probinson	
OMIM	607250	#607250 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY;SCAN1		HP:0003693	OMIM:607250	TAS				P		HPO:probinson	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000006	OMIM:607259	TAS				I		HPO:skoehler	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000007	OMIM:607259	IEA				I		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000012	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000020	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000639	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0000648	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0001258	OMIM:607259	TAS				P		HPO:probinson	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0001260	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0001272	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0001347	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0001761	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002015	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002061	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002064	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002066	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002120	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002166	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002314	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002354	OMIM:607259	TAS				P		HPO:probinson	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002650	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0002839	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0003487	OMIM:607259	IEA				P		HPO:iea	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0003581	OMIM:607259	TAS				C		HPO:probinson	
OMIM	607259	#607259 SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG7		HP:0007340	OMIM:607259	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0000007	OMIM:607271	IEA				I		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0000964	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0001508	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0001744	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0002028	OMIM:607271	TAS				P		HPO:probinson	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0002090	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0002099	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0002716	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0004322	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0005384	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0005419	OMIM:607271	IEA				P		HPO:iea	
OMIM	607271	CASPASE 8 DEFICIENCY		HP:0005425	OMIM:607271	TAS				P		HPO:probinson	
OMIM	607278	OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO; OSFD		HP:0000006	OMIM:607278	TAS				I		HPO:skoehler	
OMIM	607278	OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO; OSFD		HP:0000767	OMIM:607278	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607278	OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO; OSFD		HP:0003038	OMIM:607278	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607278	OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO; OSFD		HP:0005864	OMIM:607278	IEA				P		HPO:skoehler	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0000007	OMIM:607313	TAS				I		HPO:probinson	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0001321	OMIM:607313	IEA				P		HPO:skoehler	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0002944	OMIM:607313	TAS				P		HPO:probinson	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0003577	OMIM:607313	TAS				C		HPO:probinson	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0007650	OMIM:607313	TAS				P		HPO:probinson	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0007817	OMIM:607313	TAS				P		HPO:probinson	
OMIM	607313	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 1; HGPPS1		HP:0012110	OMIM:607313	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0000007	OMIM:607317	IEA				I		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0000639	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001251	OMIM:607317	TAS				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001256	OMIM:607317	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001257	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001260	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001270	OMIM:607317	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001332	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001336	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001337	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001347	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0001761	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0002066	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0002359	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0002380	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0002460	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0002500	OMIM:607317	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0003477	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0003487	OMIM:607317	IEA				P		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0003581	OMIM:607317	IEA				C		HPO:iea	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0003693	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0003828	OMIM:607317	IEA				C		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0007338	OMIM:607317	TAS				P		HPO:probinson	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0008936	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607317	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 4; SCAR4		HP:0032105	OMIM:607317	IEA				P		HPO:skoehler	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000006	PMID:23234485	PCS				I		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000076	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000085	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000089	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000104	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000126	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS	HP:0012825	HP:0000286	OMIM:607323	PCS				P		HPO:probinson	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS	HP:0012825	HP:0000316	OMIM:607323	PCS				P		HPO:probinson	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000324	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000407	OMIM:607323	PCS				P		HPO:probinson	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000452	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000453	PMID:23234485	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000480	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000486	OMIM:607323	TAS	HP:0003577			P		HP:probinson	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000518	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000542	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000568	OMIM:607323	IEA		HP:0040284		P		HPO:iea	95%
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000612	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000619	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000634	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0000661	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001159	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001199	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001245	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001629	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001631	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001739	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001763	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0001852	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002023	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002025	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002251	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002617	OMIM:607323	IEA				P		HPO:skoehler	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002650	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002949	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0002984	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0003022	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0003298	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0003974	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0004712	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0004736	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0005792	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0007766	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0008588	PMID:12843316	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0008998	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0009016	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0009486	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0009777	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0009778	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0009921	PMID:23234485	PCS		HP:0040284		P		HPO:iea	95%
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0010048	OMIM:607323	IEA				P		HPO:iea	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0010628	OMIM:607323	PCS				P		HPO:probinson	
OMIM	607323	DUANE-RADIAL RAY SYNDROME; DRRS		HP:0100258	OMIM:607323	TAS				P		HPO:skoehler	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000007	OMIM:607326	IEA				I		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000252	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000268	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000882	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000884	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0000926	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0001552	OMIM:607326	IEA				P		HPO:skoehler	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002515	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002650	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002681	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002692	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002808	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002857	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0002970	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0003025	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0003274	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0003311	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0003467	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0003521	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0004568	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0008829	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0008835	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0009803	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0010049	OMIM:607326	IEA				P		HPO:iea	
OMIM	607326	#607326 SMITH-MCCORT DYSPLASIA 1; SMC1;;SMC		HP:0010582	OMIM:607326	IEA				P		HPO:iea	
OMIM	607330	LATHOSTEROLOSIS		HP:0000007	PMID:12812989;PMID:17853487;PMID:12189593	PCS				I		HPO:iea	
OMIM	607330	LATHOSTEROLOSIS		HP:0000033	PMID:12812989	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000085	PMID:17853487;PMID:15580635	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000212	PMID:2309789;PMID:17853487	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000215	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000218	PMID:12812989;PMID:12189593	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000233	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000252	PMID:12812989;PMID:17853487	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000286	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000340	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000341	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000343	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000347	PMID:12812989;PMID:12189593	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000405	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	607330	LATHOSTEROLOSIS		HP:0000431	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000463	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000494	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000508	PMID:12812989;PMID:17853487	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000518	PMID:12812989;PMID:19123163	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0000939	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001162	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001249	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001250	PMID:2309789	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001252	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001290	OMIM:607330	TAS				P		HPO:skoehler	
OMIM	607330	LATHOSTEROLOSIS		HP:0001406	PMID:15580635	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001433	PMID:2309789	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001510	PMID:17853487	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	607330	LATHOSTEROLOSIS		HP:0001762	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001770	PMID:12812989;PMID:17853487;PMID:12189593	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001830	PMID:12812989;PMID:17853487;PMID:12189593	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001927	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0001981	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002059	PMID:2309789	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002308	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002475	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002756	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002904	PMID:12812989;PMID:15580635	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0002910	PMID:12189593;PMID:15580635	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0003107	PMID:12812989;PMID:12189593	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	607330	LATHOSTEROLOSIS		HP:0003155	PMID:12189593;PMID:15580635	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0003196	PMID:12812989;PMID:17853487	PCS		HP:0040284		P		HPO:iea	2/3
OMIM	607330	LATHOSTEROLOSIS		HP:0003316	PMID:17853487;PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0003609	PMID:2309789;PMID:17853487	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	607330	LATHOSTEROLOSIS		HP:0004823	PMID:17853487	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0005608	PMID:12189593	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0007759	PMID:2309789	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607330	LATHOSTEROLOSIS		HP:0011877	OMIM:607330	TAS				P		HPO:skoehler	
OMIM	607330	LATHOSTEROLOSIS		HP:0200133	OMIM:607330	TAS				P		HPO:skoehler	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0001249	OMIM:607341	TAS				P		HPO:skoehler	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0001269	OMIM:607341	IEA				P		HPO:skoehler	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0001428	OMIM:607341	TAS				I		HPO:skoehler	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0002384	OMIM:607341	TAS				P		HPO:probinson	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0002446	OMIM:607341	TAS				P		HPO:probinson	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0002539	OMIM:607341	IEA				P		HPO:skoehler	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0003581	OMIM:607341	IEA				C		HPO:iea	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0003593	OMIM:607341	IEA				C		HPO:iea	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0003745	OMIM:607341	TAS				I		HPO:iea	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0007042	OMIM:607341	IEA				P		HPO:iea	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0032051	PMID:25799227	PCS				P		HPO:nvasilevsky	
OMIM	607341	FOCAL CORTICAL DYSPLASIA OF TAYLOR		HP:0100543	OMIM:607341	TAS				P		HPO:probinson	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0000006	OMIM:607346	IEA				I		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0001260	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0001265	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0001272	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0001336	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0001347	OMIM:607346	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002015	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002066	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002070	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002073	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002078	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002174	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0002396	OMIM:607346	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0003677	OMIM:607346	TAS				C		HPO:skoehler	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0007944	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0007979	OMIM:607346	IEA				P		HPO:iea	
OMIM	607346	#607346 SPINOCEREBELLAR ATAXIA 19; SCA19;;SPINOCEREBELLAR ATAXIA 22; SCA22		HP:0100543	OMIM:607346	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0000003	OMIM:607361	TAS				P		HPO:probinson	
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0000007	OMIM:607361	TAS				I		HPO:probinson	
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0000175	OMIM:607361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0000238	OMIM:607361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0001162	OMIM:607361	TAS				P		HPO:skoehler	
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0001305	OMIM:607361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0001395	OMIM:607361	TAS				P		HPO:skoehler	
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0001408	OMIM:607361	TAS				P		HPO:skoehler	
OMIM	607361	#607361 MECKEL SYNDROME, TYPE 3; MKS3;;MECKEL-GRUBER SYNDROME, TYPE 3		HP:0002084	OMIM:607361	TAS				P		HPO:probinson	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000007	OMIM:607364	IEA				I		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000103	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000127	OMIM:607364	TAS				P		HPO:skoehler	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000128	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000591	OMIM:607364	IEA				P		HPO:skoehler	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000610	OMIM:607364	IEA				P		HPO:skoehler	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000841	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000848	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0000859	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0001944	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0001960	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0002615	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0002900	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0002914	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0003081	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0003127	OMIM:607364	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0003324	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0005579	OMIM:607364	IEA				P		HPO:iea	
OMIM	607364	#607364 BARTTER SYNDROME, TYPE 3;;BARTTER SYNDROME, CLASSICBARTTER SYNDROME, TYPE 3, WITH HYPOCALCIURIA, INCLUDED		HP:0008046	OMIM:607364	IEA				P		HPO:skoehler	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000006	OMIM:607371	IEA				I		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000175	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000204	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000348	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000407	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000518	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0000882	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0001256	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0001518	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0002571	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0002751	OMIM:607371	IEA				P		HPO:iea	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0007325	OMIM:607371	TAS				P		HPO:probinson	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0008796	OMIM:607371	TAS				P		HPO:probinson	
OMIM	607371	DYSTONIA, JUVENILE-ONSET		HP:0011342	OMIM:607371	TAS				P		HPO:probinson	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000717	OMIM:607373	TAS				P		HPO:skoehler	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000721	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000723	OMIM:607373	TAS				P		HPO:skoehler	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000728	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000732	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000733	OMIM:607373	TAS				P		HPO:skoehler	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000750	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0000758	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0001249	OMIM:607373	IEA				P		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0001250	OMIM:607373	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0001425	OMIM:607373	TAS				I		HPO:skoehler	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0001426	OMIM:607373	IEA				I		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0002353	OMIM:607373	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0003144	OMIM:607373	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0003745	OMIM:607373	IEA				I		HPO:iea	
OMIM	607373	AUTISM, SUSCEPTIBILITY TO, 8; AUTS8		HP:0011463	OMIM:607373	IEA				C		HPO:iea	
OMIM	607398	#607398 GLUCOCORTICOID DEFICIENCY 2; GCCD2;;FAMILIAL GLUCOCORTICOID DEFICIENCY 2; FGD2		HP:0000007	OMIM:607398	IEA				I		HPO:iea	
OMIM	607398	#607398 GLUCOCORTICOID DEFICIENCY 2; GCCD2;;FAMILIAL GLUCOCORTICOID DEFICIENCY 2; FGD2		HP:0000953	OMIM:607398	IEA				P		HPO:iea	
OMIM	607398	#607398 GLUCOCORTICOID DEFICIENCY 2; GCCD2;;FAMILIAL GLUCOCORTICOID DEFICIENCY 2; FGD2		HP:0001988	OMIM:607398	IEA				P		HPO:iea	
OMIM	607398	#607398 GLUCOCORTICOID DEFICIENCY 2; GCCD2;;FAMILIAL GLUCOCORTICOID DEFICIENCY 2; FGD2		HP:0003154	OMIM:607398	IEA				P		HPO:iea	
OMIM	607398	#607398 GLUCOCORTICOID DEFICIENCY 2; GCCD2;;FAMILIAL GLUCOCORTICOID DEFICIENCY 2; FGD2		HP:0008163	OMIM:607398	IEA				P		HPO:iea	
OMIM	607411	PATENT DUCTUS ARTERIOSUS 1		HP:0000007	OMIM:607411	TAS				I		HPO:skoehler	
OMIM	607411	PATENT DUCTUS ARTERIOSUS 1		HP:0001643	OMIM:607411	TAS				P		HPO:skoehler	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0000007	OMIM:607417	IEA				I		HPO:iea	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0001250	OMIM:607417	IEA				P		HPO:skoehler	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0001256	OMIM:607417	IEA				P		HPO:iea	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0001263	OMIM:607417	IEA				P		HPO:iea	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0007018	OMIM:607417	IEA				P		HPO:skoehler	
OMIM	607417	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2		HP:0010864	OMIM:607417	IEA				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000007	OMIM:607426	IEA				I		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000096	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000100	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000407	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000510	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000572	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000639	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0000815	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001249	OMIM:607426	TAS				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001250	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001251	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001260	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001270	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001272	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001298	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001328	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001399	OMIM:607426	TAS				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001639	OMIM:607426	TAS				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001876	OMIM:607426	TAS				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0001903	OMIM:607426	TAS				P		HPO:skoehler	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0002168	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0002172	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003128	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003200	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003236	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003323	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003652	OMIM:607426	IEA				P		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0003674	OMIM:607426	IEA				C		HPO:iea	
OMIM	607426	COENZYME Q10 DEFICIENCY, PRIMARY, 1; COQ10D1		HP:0012378	OMIM:607426	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001249	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001250	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001263	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001285	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001302	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0001321	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0002119	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0002282	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0002365	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0002500	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0003745	OMIM:607432	IEA				I		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0003828	OMIM:607432	IEA				C		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0005484	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0008936	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0012520	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607432	LISSENCEPHALY 1; LIS1		HP:0031882	OMIM:607432	IEA				P		HPO:skoehler	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0000006	OMIM:607450	IEA				I		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0001425	OMIM:607450	TAS				I		HPO:skoehler	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0001635	OMIM:607450	IEA				P		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0001645	OMIM:607450	IEA				P		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0001663	OMIM:607450	TAS				P		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0004756	OMIM:607450	TAS				P		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0006682	OMIM:607450	TAS				P		HPO:probinson	
OMIM	607450	#607450 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8; ARVC8		HP:0011663	OMIM:607450	TAS				P		HPO:probinson	
OMIM	607453	#607453 DEAFNESS, AUTOSOMAL DOMINANT 44; DFNA44		HP:0000006	PMID:17503326	PCS				I		HPO:probinson	
OMIM	607453	#607453 DEAFNESS, AUTOSOMAL DOMINANT 44; DFNA44		HP:0000407	PMID:17503326	PCS	HP:0003621			P		HPO:probinson	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0000006	OMIM:607454	IEA				I		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0000514	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0000639	OMIM:607454	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0000718	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0000741	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001249	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001260	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001263	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001265	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001272	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0001300	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002066	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002070	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002071	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002073	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002168	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002174	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002304	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0002396	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0003677	OMIM:607454	IEA				C		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0007792	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0010526	OMIM:607454	IEA				P		HPO:skoehler	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0100543	OMIM:607454	IEA				P		HPO:iea	
OMIM	607454	#607454 SPINOCEREBELLAR ATAXIA 21; SCA21		HP:0100710	OMIM:607454	TAS				P		HPO:skoehler	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0000006	OMIM:607458	IEA				I		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0000639	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001265	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001272	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001284	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001310	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001337	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0001761	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0002075	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0003202	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0003390	OMIM:607458	IEA				P		HPO:skoehler	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0003487	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0003674	OMIM:607458	IEA				C		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0003690	OMIM:607458	IEA				P		HPO:iea	
OMIM	607458	SPINOCEREBELLAR ATAXIA 18		HP:0007240	OMIM:607458	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000007	PMID:12565911	PCS				I		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000407	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000508	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000518	OMIM:607459	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000590	OMIM:607459	TAS				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000639	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0000716	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001250	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001260	PMID:12565911	PCS				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001265	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001284	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001336	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001644	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0001751	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0002076	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO	HP:0012825	HP:0002151	OMIM:607459	TAS				P		HPO:probinson	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0002403	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0002578	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003200	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO	HP:0012825	HP:0003236	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003390	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003434	PMID:12565911	PCS				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003548	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003557	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003581	OMIM:607459	TAS				C		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003688	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003689	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003701	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0003713	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0004389	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0006858	OMIM:607459	TAS				P		HPO:probinson	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0006886	OMIM:607459	TAS				P		HPO:probinson	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0007240	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0007344	OMIM:607459	IEA				P		HPO:iea	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0008180	OMIM:607459	TAS				P		HPO:skoehler	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0031987	OMIM:607459	IEA				P		HPO:skoehler	
OMIM	607459	SENSORY ATAXIC NEUROPATHY, DYSARTHRIA, AND OPHTHALMOPARESIS; SANDO		HP:0100543	OMIM:607459	IEA				P		HPO:iea	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0000007	PMID:11154138	PCS				I		HPO:probinson	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0001892	OMIM:607473	TAS				P		HPO:probinson	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0008169	OMIM:607473	TAS				P		HPO:probinson	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0008321	OMIM:607473	TAS				P		HPO:probinson	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0011858	OMIM:607473	TAS				P		HPO:probinson	
OMIM	607473	#607473 VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2; VKCFD2		HP:0040250	PMID:11154138	PCS				P		HPO:probinson	
OMIM	607475	BOTHNIA RETINAL DYSTROPHY		HP:0000007	OMIM:607475	IEA				I		HPO:iea	
OMIM	607475	BOTHNIA RETINAL DYSTROPHY		HP:0000512	OMIM:607475	IEA				P		HPO:iea	
OMIM	607475	BOTHNIA RETINAL DYSTROPHY		HP:0000556	OMIM:607475	TAS				P		HPO:skoehler	
OMIM	607475	BOTHNIA RETINAL DYSTROPHY		HP:0000608	OMIM:607475	IEA				P		HPO:iea	
OMIM	607475	BOTHNIA RETINAL DYSTROPHY		HP:0000662	OMIM:607475	TAS				P		HPO:skoehler	
OMIM	607476	#607476 NEWFOUNDLAND ROD-CONE DYSTROPHY; NFRCD		HP:0000007	PMID:11868161	PCS				I		HPO:probinson	
OMIM	607476	#607476 NEWFOUNDLAND ROD-CONE DYSTROPHY; NFRCD		HP:0000551	PMID:11868161	PCS				P		HPO:probinson	
OMIM	607476	#607476 NEWFOUNDLAND ROD-CONE DYSTROPHY; NFRCD		HP:0000556	PMID:11868161	PCS				P		HPO:probinson	
OMIM	607476	#607476 NEWFOUNDLAND ROD-CONE DYSTROPHY; NFRCD		HP:0000575	PMID:11868161	PCS				P		HPO:probinson	
OMIM	607476	#607476 NEWFOUNDLAND ROD-CONE DYSTROPHY; NFRCD		HP:0000662	PMID:11868161	PCS	HP:0003593			P		HPO:probinson	
OMIM	607482	#607482 CARDIOMYOPATHY, DILATED, 1M; CMD1M		HP:0000006	PMID:12507422	PCS				I		HPO:probinson	
OMIM	607482	#607482 CARDIOMYOPATHY, DILATED, 1M; CMD1M		HP:0001644	PMID:12507422	PCS				P		HPO:probinson	
OMIM	607482	#607482 CARDIOMYOPATHY, DILATED, 1M; CMD1M		HP:0001706	PMID:14567970	PCS				P		HPO:probinson	
OMIM	607482	#607482 CARDIOMYOPATHY, DILATED, 1M; CMD1M		HP:0006670	PMID:12507422	PCS				P		HPO:probinson	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0000007	OMIM:607483	IEA				I		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0000508	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0000544	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0000639	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0000737	OMIM:607483	TAS				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001250	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001259	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001260	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001263	OMIM:607483	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001276	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001289	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001298	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001332	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0001945	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002015	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002062	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002063	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002066	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002134	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002300	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002385	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0002540	OMIM:607483	IEA				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0003487	OMIM:607483	TAS				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0003621	OMIM:607483	IEA				C		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0008936	OMIM:607483	TAS				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0012179	OMIM:607483	TAS				P		HPO:skoehler	
OMIM	607483	THIAMINE METABOLISM DYSFUNCTION SYNDROME 2 (BIOTIN- OR THIAMINE-RESPONSIVE TYPE); THMD2		HP:0025356	OMIM:607483	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000006	OMIM:607485	IEA				I		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000710	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000713	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000734	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000738	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000741	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0000751	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0001300	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002120	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002145	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002171	OMIM:607485	IEA				P		HPO:skoehler	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002185	OMIM:607485	IEA				P		HPO:skoehler	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002186	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002300	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002354	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002357	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002381	OMIM:607485	TAS				P		HPO:probinson	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002529	OMIM:607485	IEA				P		HPO:skoehler	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0002591	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0006956	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0007064	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0008762	OMIM:607485	IEA				P		HPO:iea	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0030214	OMIM:607485	TAS				P		HPO:skoehler	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0030223	OMIM:607485	TAS				P		HPO:skoehler	
OMIM	607485	FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED		HP:0100315	OMIM:607485	IEA				P		HPO:skoehler	
OMIM	607487	#607487 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25		HP:0000006	OMIM:607487	TAS				I		HPO:probinson	
OMIM	607487	#607487 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25		HP:0001644	OMIM:607487	TAS				P		HPO:probinson	
OMIM	607487	#607487 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25		HP:0001712	OMIM:607487	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607487	#607487 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 25; CMH25		HP:0001716	OMIM:607487	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607488	DYSTONIA 15, MYOCLONIC; DYT15		HP:0000006	OMIM:607488	IEA				I		HPO:iea	
OMIM	607488	DYSTONIA 15, MYOCLONIC; DYT15		HP:0001332	OMIM:607488	TAS				P		HPO:probinson	
OMIM	607488	DYSTONIA 15, MYOCLONIC; DYT15		HP:0001336	OMIM:607488	IEA				P		HPO:iea	
OMIM	607488	DYSTONIA 15, MYOCLONIC; DYT15		HP:0001425	OMIM:607488	TAS				I		HPO:skoehler	
OMIM	607488	DYSTONIA 15, MYOCLONIC; DYT15		HP:0002356	OMIM:607488	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0000006	OMIM:607498	IEA				I		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0000613	OMIM:607498	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0002013	OMIM:607498	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0002018	OMIM:607498	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0002077	OMIM:607498	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0002083	OMIM:607498	IEA				P		HPO:iea	
OMIM	607498	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3		HP:0002183	OMIM:607498	IEA				P		HPO:iea	
OMIM	607499	BULIMIA NERVOSA, SUSCEPTIBILITY TO, 1		HP:0001426	OMIM:607499	IEA				I		HPO:iea	
OMIM	607499	BULIMIA NERVOSA, SUSCEPTIBILITY TO, 1		HP:0100739	OMIM:607499	TAS				P		HPO:probinson	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0000006	OMIM:607501	IEA				I		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0000613	OMIM:607501	IEA				P		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0001347	OMIM:607501	IEA				P		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0002013	OMIM:607501	IEA				P		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0002018	OMIM:607501	IEA				P		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0002083	OMIM:607501	IEA				P		HPO:iea	
OMIM	607501	MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4		HP:0002183	OMIM:607501	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0000006	OMIM:607508	IEA				I		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0000613	OMIM:607508	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0002013	OMIM:607508	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0002018	OMIM:607508	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0002077	OMIM:607508	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0002083	OMIM:607508	IEA				P		HPO:iea	
OMIM	607508	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5		HP:0002183	OMIM:607508	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0000006	OMIM:607516	IEA				I		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0000613	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0001269	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002013	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002018	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002077	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002083	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002183	OMIM:607516	IEA				P		HPO:iea	
OMIM	607516	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6		HP:0002301	OMIM:607516	IEA				P		HPO:iea	
OMIM	607523	#607523 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 8; NDNC8;;TOENAIL DYSTROPHY, ISOLATED		HP:0000006	OMIM:607523	TAS				I		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0000007	OMIM:607539	TAS				I		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0001792	OMIM:607539	TAS				P		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0010442	OMIM:607539	TAS				P		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0012385	OMIM:607539	TAS				P		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0012725	OMIM:607539	TAS				P		HPO:skoehler	
OMIM	607539	CAMPTOSYNPOLYDACTYLY, COMPLEX		HP:0100797	OMIM:607539	TAS				P		HPO:skoehler	
OMIM	607541	#607541 CORNEAL DYSTROPHY, AVELLINO TYPE; CDA;;ACD;;AVELLINO CORNEAL DYSTROPHY;;COMBINED GRANULAR-LATTICE CORNEAL DYSTROPHY;;GRANULAR CORNEAL DYSTROPHY, TYPE II; CGD2		HP:0000006	OMIM:607541	TAS				I		HPO:probinson	
OMIM	607541	#607541 CORNEAL DYSTROPHY, AVELLINO TYPE; CDA;;ACD;;AVELLINO CORNEAL DYSTROPHY;;COMBINED GRANULAR-LATTICE CORNEAL DYSTROPHY;;GRANULAR CORNEAL DYSTROPHY, TYPE II; CGD2		HP:0001149	OMIM:607541	TAS				P		HPO:probinson	
OMIM	607541	#607541 CORNEAL DYSTROPHY, AVELLINO TYPE; CDA;;ACD;;AVELLINO CORNEAL DYSTROPHY;;COMBINED GRANULAR-LATTICE CORNEAL DYSTROPHY;;GRANULAR CORNEAL DYSTROPHY, TYPE II; CGD2		HP:0007663	OMIM:607541	TAS				P		HPO:skoehler	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0000006	OMIM:607554	PCS				I		HPO:probinson	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0001297	OMIM:607554	IEA				P		HPO:skoehler	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0001425	OMIM:607554	TAS				I		HPO:skoehler	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0001649	OMIM:607554	IEA				P		HPO:iea	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0001727	OMIM:607554	IEA				P		HPO:iea	
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0001727	OMIM:607554	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	607554	ATRIAL FIBRILLATION, FAMILIAL, 3; ATFB3		HP:0005110	OMIM:607554	PCS				P		HPO:probinson	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0000006	OMIM:607565	IEA				I		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0000012	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0000020	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0000496	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001249	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001251	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001258	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001260	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001272	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001332	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0001347	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0002064	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0002166	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0002839	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0003487	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0007340	OMIM:607565	IEA				P		HPO:iea	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0011448	OMIM:607565	TAS				P		HPO:probinson	
OMIM	607565	SPASTIC PARAPLEGIA, ATAXIA, AND MENTAL RETARDATION		HP:0011449	OMIM:607565	TAS				P		HPO:probinson	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:607569	IEA				I		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0002093	OMIM:607569	TAS				P		HPO:probinson	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0002792	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0002877	OMIM:607569	TAS		HP:0040284		P		HPO:probinson	5/11
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0002878	OMIM:607569	IEA				P		HPO:skoehler	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003236	OMIM:607569	TAS				P		HPO:probinson	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003458	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003547	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003555	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003581	OMIM:607569	TAS				C		HPO:probinson	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003676	OMIM:607569	IEA				C		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003722	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003731	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003749	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003805	OMIM:607569	IEA				P		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT		HP:0003828	OMIM:607569	IEA				C		HPO:iea	
OMIM	607569	MYOPATHY, DISTAL, WITH EARLY RESPIRATORY FAILURE, AUTOSOMAL DOMINANT	HP:0012832	HP:0009027	OMIM:607569	TAS				P		HPO:probinson	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0000006	OMIM:607578	IEA				I		HPO:iea	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0000708	OMIM:607578	IEA				P		HPO:iea	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0000961	OMIM:607578	TAS				P		HPO:iea	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0000980	OMIM:607578	TAS				P		HPO:iea	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0001891	OMIM:607578	IEA				P		HPO:skoehler	
OMIM	607578	BREATH-HOLDING SPELLS		HP:0007185	OMIM:607578	IEA				P		HPO:iea	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:607584	IEA				I		HPO:iea	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0001257	OMIM:607584	IEA				P		HPO:skoehler	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:607584	TAS				P		HPO:skoehler	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0002169	OMIM:607584	IEA				P		HPO:iea	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:607584	IEA				C		HPO:iea	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0003698	OMIM:607584	IEA				P		HPO:iea	
OMIM	607584	SPASTIC PARAPLEGIA 24, AUTOSOMAL RECESSIVE		HP:0030051	OMIM:607584	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0000007	OMIM:607594	IEA				I		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0000403	OMIM:607594	TAS				P		HPO:probinson	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0000509	OMIM:607594	TAS				P		HPO:probinson	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0001744	OMIM:607594	TAS				P		HPO:skoehler	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0001904	OMIM:607594	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002014	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002090	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002110	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002240	OMIM:607594	TAS				P		HPO:skoehler	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002716	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002718	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002720	OMIM:607594	TAS				P		HPO:probinson	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002721	OMIM:607594	IEA				P		HPO:skoehler	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002837	OMIM:607594	TAS				P		HPO:skoehler	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0002850	OMIM:607594	TAS				P		HPO:probinson	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0004315	OMIM:607594	TAS				P		HPO:probinson	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0005435	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0006532	OMIM:607594	TAS				P		HPO:skoehler	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0010976	OMIM:607594	IEA				P		HPO:iea	
OMIM	607594	#607594 IMMUNODEFICIENCY, COMMON VARIABLE, 1; CVID1;;ANTIBODY DEFICIENCY DUE TO ICOS DEFECTIMMUNODEFICIENCY, COMMON VARIABLE, INCLUDED; CVID, INCLUDED		HP:0011108	OMIM:607594	IEA				P		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000006	OMIM:607595	IEA				I		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000482	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000483	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000486	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000501	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000519	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000540	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000541	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000545	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000568	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000575	OMIM:607595	TAS				P		HPO:probinson	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000622	OMIM:607595	TAS				P		HPO:skoehler	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0000646	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0001136	OMIM:607595	IEA				P		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0001250	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0001256	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0001269	OMIM:607595	IEA				P		HPO:skoehler	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0002077	OMIM:607595	IEA				P		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0002132	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0006859	OMIM:607595	IEA				P		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0007676	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0007894	OMIM:607595	IEA				P		HPO:iea	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0007957	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0009918	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0011496	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0011500	OMIM:607595	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0012520	OMIM:607595	IEA				P		HPO:skoehler	
OMIM	607595	BRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIES; BSVD		HP:0500087	OMIM:607595	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0000007	OMIM:607596	IEA				I		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001249	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001251	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001252	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001263	OMIM:607596	TAS				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001290	OMIM:607596	TAS				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001321	OMIM:607596	TAS				P		HPO:probinson	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001324	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001347	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0001760	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0002093	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0002380	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0002398	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0002803	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0003445	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0003577	OMIM:607596	TAS				C		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0003676	OMIM:607596	IEA				C		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0006850	OMIM:607596	IEA				P		HPO:iea	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0006999	OMIM:607596	TAS				P		HPO:probinson	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0007269	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0008872	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0012110	OMIM:607596	TAS				P		HPO:probinson	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0025356	OMIM:607596	IEA				P		HPO:skoehler	
OMIM	607596	PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A		HP:0200147	OMIM:607596	TAS				P		HPO:skoehler	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000175	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000204	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000244	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000358	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000369	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000453	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000457	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000506	OMIM:607597	TAS				P		HPO:probinson	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000609	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0000625	OMIM:607597	TAS				P		HPO:probinson	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0001263	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0001382	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0001595	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0001773	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0002006	OMIM:607597	TAS				P		HPO:skoehler	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0002007	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0002705	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0003745	OMIM:607597	IEA				I		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0004478	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0007481	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0007633	OMIM:607597	IEA				P		HPO:iea	
OMIM	607597	MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES		HP:0009852	OMIM:607597	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0000007	OMIM:607598	IEA				I		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0000126	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0000347	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0000969	OMIM:607598	IEA				P		HPO:skoehler	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0001558	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0001561	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0001629	OMIM:607598	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0001644	OMIM:607598	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0002304	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0002804	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0002878	OMIM:607598	TAS	HP:0003593			P		HPO:probinson	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0003202	OMIM:607598	TAS				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0007964	OMIM:607598	IEA				P		HPO:iea	
OMIM	607598	LETHAL CONGENITAL CONTRACTURE SYNDROME 2		HP:0011003	OMIM:607598	IEA				P		HPO:iea	
OMIM	607602	ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS		HP:0000006	OMIM:607602	TAS				I		HPO:probinson	
OMIM	607602	ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS		HP:0000972	OMIM:607602	TAS				P		HPO:probinson	
OMIM	607602	ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS		HP:0007475	OMIM:607602	TAS				P		HPO:skoehler	
OMIM	607602	ICHTHYOSIS, CYCLIC, WITH EPIDERMOLYTIC HYPERKERATOSIS		HP:0010783	OMIM:607602	TAS				P		HPO:skoehler	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0000007	OMIM:607616	IEA				I		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0001103	OMIM:607616	IEA				P		HPO:skoehler	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0001744	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0001982	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0002094	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0002155	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0002205	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0002207	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0002240	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0003141	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0003233	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0003609	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0003621	OMIM:607616	IEA				C		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0004322	OMIM:607616	IEA				P		HPO:iea	
OMIM	607616	NIEMANN-PICK DISEASE, TYPE B		HP:0004333	OMIM:607616	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0000007	OMIM:607624	IEA				I		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0001008	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0001010	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0001250	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0001257	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0001317	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0002218	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0002220	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0002344	OMIM:607624	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0002718	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0002972	OMIM:607624	IEA				P		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0003593	OMIM:607624	IEA				C		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0003819	OMIM:607624	IEA				M		HPO:iea	
OMIM	607624	GRISCELLI SYNDROME, TYPE 2; GS2		HP:0012156	OMIM:607624	IEA				P		HPO:skoehler	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0000007	OMIM:607625	IEA				I		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0000511	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0000709	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0000726	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0000733	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001249	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001250	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001251	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001252	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001257	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001260	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001263	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001290	OMIM:607625	TAS				P		HPO:skoehler	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001332	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001425	OMIM:607625	TAS				I		HPO:skoehler	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001744	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001791	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0001982	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002015	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002093	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002185	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002240	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002371	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002524	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0002878	OMIM:607625	TAS				P		HPO:skoehler	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0003107	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0003349	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0003640	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0003674	OMIM:607625	IEA				C		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0004333	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0006579	OMIM:607625	IEA				P		HPO:iea	
OMIM	607625	NIEMANN-PICK DISEASE, TYPE C2		HP:0030223	OMIM:607625	TAS				P		HPO:skoehler	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000007	OMIM:607626	IEA				I		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000653	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000668	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000677	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000952	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0000958	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0001006	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0001036	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0001596	OMIM:607626	TAS				P		HPO:probinson	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0001871	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0002240	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0006297	OMIM:607626	IEA				P		HPO:iea	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0008064	OMIM:607626	TAS				P		HPO:probinson	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0025092	OMIM:607626	TAS				P		HPO:skoehler	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0030151	OMIM:607626	TAS				P		HPO:skoehler	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0040162	OMIM:607626	TAS				P		HPO:skoehler	
OMIM	607626	ICHTHYOSIS, LEUKOCYTE VACUOLES, ALOPECIA, AND SCLEROSING CHOLANGITIS; ILVASC		HP:0100874	OMIM:607626	IEA				P		HPO:skoehler	
OMIM	607628	EPILEPSY WITH GRAND MAL SEIZURES ON AWAKENING		HP:0000006	OMIM:607628	TAS				I		HPO:probinson	
OMIM	607628	EPILEPSY WITH GRAND MAL SEIZURES ON AWAKENING		HP:0002121	OMIM:607628	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607628	EPILEPSY WITH GRAND MAL SEIZURES ON AWAKENING		HP:0002123	OMIM:607628	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607628	EPILEPSY WITH GRAND MAL SEIZURES ON AWAKENING		HP:0007193	OMIM:607628	TAS				P		HPO:probinson	
OMIM	607631	EPILEPSY, JUVENILE ABSENCE		HP:0000006	OMIM:607631	IEA				I		HPO:iea	
OMIM	607631	EPILEPSY, JUVENILE ABSENCE		HP:0002121	OMIM:607631	IEA				P		HPO:iea	
OMIM	607631	EPILEPSY, JUVENILE ABSENCE		HP:0002123	OMIM:607631	IEA				P		HPO:iea	
OMIM	607631	EPILEPSY, JUVENILE ABSENCE		HP:0007193	OMIM:607631	TAS				P		HPO:skoehler	
OMIM	607631	EPILEPSY, JUVENILE ABSENCE		HP:0010849	OMIM:607631	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0000006	OMIM:607634	IEA				I		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0000405	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0000925	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0001425	OMIM:607634	TAS				I		HPO:skoehler	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0002315	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0002644	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0002684	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0005789	OMIM:607634	IEA				P		HPO:iea	
OMIM	607634	OSTEOPETROSIS, AUTOSOMAL DOMINANT 1; OPTA1		HP:0011002	OMIM:607634	IEA				P		HPO:skoehler	
OMIM	607636	VAN BUCHEM DISEASE, TYPE 2		HP:0000006	OMIM:607636	TAS				I		HPO:iea	
OMIM	607636	VAN BUCHEM DISEASE, TYPE 2		HP:0000303	OMIM:607636	TAS				P		HPO:iea	
OMIM	607636	VAN BUCHEM DISEASE, TYPE 2		HP:0000935	OMIM:607636	TAS				P		HPO:probinson	
OMIM	607636	VAN BUCHEM DISEASE, TYPE 2		HP:0002684	OMIM:607636	TAS				P		HPO:skoehler	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0000006	OMIM:607641	TAS				I		HPO:probinson	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0001605	OMIM:607641	IEA				P		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0001605	OMIM:607641	TAS				P		HPO:probinson	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0002366	OMIM:607641	IEA				P		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0002460	OMIM:607641	TAS				P		HPO:probinson	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0003581	OMIM:607641	TAS				C		HPO:probinson	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0003677	OMIM:607641	IEA				C		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0003693	OMIM:607641	TAS				P		HPO:probinson	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0007340	OMIM:607641	IEA				P		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0009130	OMIM:607641	IEA				P		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0010628	OMIM:607641	IEA				P		HPO:iea	
OMIM	607641	#607641 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB; HMN7B;;HMN VIIB;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB;;DHMN7B;;NEUROPATHY, DISTAL HEREDITARY MOTOR, WITH VOCAL CORD PARALYSIS, TYPEVIIB;;LOWER MOTOR NEURON DISEASE, DYNACTIN TYPE		HP:0030237	OMIM:607641	TAS				P		HPO:skoehler	
OMIM	607644	%607644 CANDIDIASIS, FAMILIAL, 3; CANDF3;;CANDIDIASIS, FAMILIAL CHRONIC NAIL, WITH ICAM1 DEFICIENCY; CANDN1;;FCNC		HP:0000006	OMIM:607644	TAS				I		HPO:skoehler	
OMIM	607654	#607654 KERATOSIS PALMOPLANTARIS STRIATA III; PPKS3;;STRIATE PALMOPLANTAR KERATODERMA III; SPPK3;;KERATODERMA, PALMOPLANTAR, STRIATE FORM III; KPPS3		HP:0000006	OMIM:607654	TAS				I		HPO:skoehler	
OMIM	607654	#607654 KERATOSIS PALMOPLANTARIS STRIATA III; PPKS3;;STRIATE PALMOPLANTAR KERATODERMA III; SPPK3;;KERATODERMA, PALMOPLANTAR, STRIATE FORM III; KPPS3		HP:0000982	OMIM:607654	TAS				P		HPO:skoehler	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0000007	OMIM:607655	IEA				I		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0000535	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0000653	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0001030	OMIM:607655	IEA				P		HPO:skoehler	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0001508	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0001596	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0001626	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0002164	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0002224	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0007548	OMIM:607655	IEA				P		HPO:iea	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0008404	OMIM:607655	TAS				P		HPO:skoehler	
OMIM	607655	SKIN FRAGILITY-WOOLLY HAIR SYNDROME; SFWHS		HP:0100792	OMIM:607655	IEA				P		HPO:skoehler	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0000099	OMIM:607665	TAS				P		HPO:skoehler	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0000153	OMIM:607665	IEA				P		HPO:iea	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0000554	OMIM:607665	IEA				P		HPO:skoehler	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0003259	OMIM:607665	TAS				P		HPO:skoehler	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0003745	OMIM:607665	IEA				I		HPO:iea	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0004713	OMIM:607665	IEA				P		HPO:iea	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0004729	OMIM:607665	TAS				P		HPO:iea	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0012121	OMIM:607665	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0012122	OMIM:607665	TAS				P		HPO:skoehler	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0012220	OMIM:607665	TAS				P		HPO:probinson	
OMIM	607665	TUBULOINTERSTITIAL NEPHRITIS WITH UVEITIS; TINU		HP:0012224	OMIM:607665	TAS				P		HPO:probinson	
OMIM	607671	DYSTONIA 13, TORSION		HP:0000006	OMIM:607671	IEA				I		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0000473	OMIM:607671	IEA				P		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0000643	OMIM:607671	IEA				P		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0001304	OMIM:607671	IEA				P		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0001337	OMIM:607671	IEA				P		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0002356	OMIM:607671	IEA				P		HPO:iea	
OMIM	607671	DYSTONIA 13, TORSION		HP:0002451	OMIM:607671	IEA				P		HPO:skoehler	
OMIM	607671	DYSTONIA 13, TORSION		HP:0012048	OMIM:607671	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000006	OMIM:607674	IEA				I		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000519	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000618	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000639	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000709	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000712	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000726	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0000751	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0001288	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0002015	OMIM:607674	IEA				P		HPO:iea	
OMIM	607674	CATARACT, CONGENITAL, WITH MENTAL IMPAIRMENT AND DENTATE GYRUS ATROPHY		HP:0002072	OMIM:607674	IEA				P		HPO:iea	
OMIM	607676	IMMUNODEFICIENCY DUE TO INTERLEUKIN-1 RECEPTOR-ASSOCIATED KINASE-4 DEFICIENCY		HP:0002721	OMIM:607676	IEA				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0000006	OMIM:607677	TAS				I		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0001265	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0001284	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0001761	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0002460	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0002936	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0003376	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0003378	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0003380	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0003484	OMIM:607677	TAS				P		HPO:probinson	
OMIM	607677	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I		HP:0003693	OMIM:607677	TAS				P		HPO:skoehler	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0000006	OMIM:607678	IEA				I		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0001425	OMIM:607678	TAS				I		HPO:skoehler	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0002460	OMIM:607678	IEA				P		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003376	OMIM:607678	IEA				P		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003431	OMIM:607678	IEA				P		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003484	OMIM:607678	IEA				P		HPO:probinson	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003621	OMIM:607678	IEA				C		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003693	OMIM:607678	IEA				P		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0003828	OMIM:607678	TAS				C		HPO:skoehler	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0009027	OMIM:607678	IEA				P		HPO:iea	
OMIM	607678	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1D; CMT1D		HP:0009830	OMIM:607678	IEA				P		HPO:skoehler	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0000006	OMIM:607681	TAS				I		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0001425	OMIM:607681	TAS				I		HPO:skoehler	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0002069	OMIM:607681	TAS				P		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0002121	OMIM:607681	TAS				P		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0002373	OMIM:607681	TAS				P		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0002392	OMIM:607681	TAS				P		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0010849	OMIM:607681	TAS				P		HPO:probinson	
OMIM	607681	EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2; ECA2		HP:0011463	OMIM:607681	TAS				C		HPO:probinson	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0000006	OMIM:607682	TAS				I		HPO:probinson	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0001425	OMIM:607682	TAS				I		HPO:skoehler	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0002121	OMIM:607682	TAS				P		HPO:probinson	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0002392	OMIM:607682	TAS				P		HPO:probinson	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0003621	OMIM:607682	TAS				C		HPO:probinson	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0007000	OMIM:607682	TAS				P		HPO:skoehler	
OMIM	607682	#607682 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 9; EIG9EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 6, INCLUDED; EJM6,INCLUDED		HP:0007193	OMIM:607682	TAS				P		HPO:skoehler	
OMIM	607683	%607683 DEAFNESS, AUTOSOMAL DOMINANT 52; DFNA52;;DEAFNESS, AUTOSOMAL DOMINANT 42; DFNA42		HP:0000006	OMIM:607683	TAS				I		HPO:skoehler	
OMIM	607683	%607683 DEAFNESS, AUTOSOMAL DOMINANT 52; DFNA52;;DEAFNESS, AUTOSOMAL DOMINANT 42; DFNA42		HP:0000365	OMIM:607683	IEA				P		HPO:skoehler	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0000006	OMIM:607684	TAS				I		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0000218	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0000508	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001171	OMIM:607684	TAS				P		HPO:skoehler	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001178	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001265	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001270	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001284	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001371	OMIM:607684	TAS				P		HPO:skoehler	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001761	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0001765	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0002460	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0002650	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0002936	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0003376	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E	HP:0012825	HP:0003431	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0003693	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0003798	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0003828	OMIM:607684	TAS				C		HPO:skoehler	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0006006	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0009025	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0009027	OMIM:607684	TAS				P		HPO:probinson	
OMIM	607684	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E; CMT2E		HP:0010628	OMIM:607684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0000707	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0000989	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0001428	OMIM:607685	IEA				I		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0001723	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0001744	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0001880	OMIM:607685	TAS				P		HPO:skoehler	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0002113	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0002240	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0003326	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0003745	OMIM:607685	IEA				I		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0004936	OMIM:607685	IEA				P		HPO:iea	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0005547	OMIM:607685	TAS				P		HPO:skoehler	
OMIM	607685	HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC		HP:0006685	OMIM:607685	IEA				P		HPO:iea	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0000006	PMID:18358451	PCS				I		HPO:probinson	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0002063	PMID:18358451	PCS				P		HPO:probinson	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0002067	PMID:18358451	PCS				P		HPO:probinson	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0002172	PMID:18358451	PCS				P		HPO:probinson	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0002322	PMID:18358451	PCS				P		HPO:probinson	
OMIM	607688	#607688 PARKINSON DISEASE 11, AUTOSOMAL DOMINANT; PARK11		HP:0002548	PMID:18358451	PCS				P		HPO:probinson	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000007	OMIM:607694	TAS				I		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000044	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000545	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000639	OMIM:607694	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000648	OMIM:607694	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000668	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000677	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0000823	OMIM:607694	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001257	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001260	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001263	OMIM:607694	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001272	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001310	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001332	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0001347	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002015	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002079	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002120	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002127	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002174	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002307	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0002415	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0003429	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0003487	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0003676	OMIM:607694	TAS				C		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0004322	OMIM:607694	TAS				P		HPO:skoehler	
OMIM	607694	#607694 LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/ORHYPOGONADOTROPIC HYPOGONADISM; HLD7;;LEUKOENCEPHALOPATHY, HYPOMYELINATING, WITH ATAXIA AND DELAYED DENTITION;;ATAXIA, DELAYED DENTITION, AND HYPOMYELINATION; ADDH;;LEUKODYSTROPHY, HYPOMYELINATING, WITH HYPODONTIA AND HYPOGONADOTROPICHYPOGONADISM;;4H SYNDROME		HP:0009830	OMIM:607694	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0000007	OMIM:607706	IEA				I		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0001171	OMIM:607706	TAS				P		HPO:skoehler	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0001284	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0001371	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0001604	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0001761	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0002460	OMIM:607706	TAS				P		HPO:probinson	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0002936	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0003378	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0003380	OMIM:607706	IEA				P		HPO:iea	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0003383	OMIM:607706	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE	HP:0012825	HP:0003431	OMIM:607706	TAS				P		HPO:probinson	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0003623	OMIM:607706	TAS				C		HPO:probinson	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0003693	OMIM:607706	TAS				P		HPO:probinson	
OMIM	607706	#607706 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE;;CMT2 WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE;;CHARCOT-MARIE-TOOTH DISEASE, TYPE 4A, AXONAL FORM;;CHARCOT-MARIE-TOOTH NEUROPATHY, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE		HP:0008443	OMIM:607706	IEA				P		HPO:iea	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000006	OMIM:607721	TAS				I		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000256	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000316	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000358	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000369	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000465	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000470	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000486	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000527	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000752	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0000964	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001249	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001290	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001388	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001561	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001611	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001629	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001631	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001639	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0001642	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0002079	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0002209	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0004322	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0006191	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0008064	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0011220	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0011968	OMIM:607721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0032152	OMIM:607721	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	607721	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 1; NSLH1		HP:0040169	OMIM:607721	TAS				P		HPO:skoehler	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0000007	OMIM:607731	IEA				I		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0001761	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0002460	OMIM:607731	TAS				P		HPO:probinson	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0002460	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0002936	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003376	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003380	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003438	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003450	OMIM:607731	IEA				P		HPO:skoehler	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003621	OMIM:607731	IEA				C		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0003693	OMIM:607731	TAS				P		HPO:probinson	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0007083	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0007350	OMIM:607731	IEA				P		HPO:iea	
OMIM	607731	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H		HP:0009027	OMIM:607731	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0000006	OMIM:607734	IEA				I		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0000007	OMIM:607734	TAS				I		HPO:skoehler	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0001265	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0001270	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0001284	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0001425	OMIM:607734	TAS				I		HPO:skoehler	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0001761	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0002460	OMIM:607734	TAS				P		HPO:probinson	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0002936	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003380	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003383	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003431	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003481	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003621	OMIM:607734	IEA				C		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003693	OMIM:607734	TAS				P		HPO:probinson	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0003828	OMIM:607734	TAS				C		HPO:skoehler	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0004336	OMIM:607734	IEA				P		HPO:iea	
OMIM	607734	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1F; CMT1F		HP:0007233	OMIM:607734	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0000006	OMIM:607736	IEA				I		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0000407	OMIM:607736	PCS				P		HPO:probinson	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0000408	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0000478	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0001265	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0001284	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0001761	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0002015	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0002086	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0002460	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0002936	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0003376	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0003378	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0003693	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0003693	OMIM:607736	PCS				P		HPO:probinson	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0009027	OMIM:607736	IEA				P		HPO:iea	
OMIM	607736	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J		HP:0011096	OMIM:607736	PCS				P		HPO:probinson	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0000006	OMIM:607745	TAS				I		HPO:iea	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0000961	OMIM:607745	TAS				P		HPO:skoehler	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0002104	OMIM:607745	IEA				P		HPO:skoehler	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0002372	OMIM:607745	TAS				P		HPO:iea	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0002384	OMIM:607745	IEA				P		HPO:iea	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0007334	OMIM:607745	IEA				P		HPO:iea	
OMIM	607745	SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3		HP:0040168	OMIM:607745	TAS				P		HPO:skoehler	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0000007	OMIM:607748	TAS				I		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0000989	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0001508	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0002570	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0002748	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0011892	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607748	#607748 HYPERCHOLANEMIA, FAMILIAL; FHCA		HP:0012202	OMIM:607748	TAS				P		HPO:probinson	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0000007	OMIM:607765	IEA				I		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0000952	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0001394	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0001399	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0001406	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0001508	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0001744	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0002014	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0002240	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0002570	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0002904	OMIM:607765	TAS				P		HPO:probinson	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0002910	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0003146	OMIM:607765	TAS				P		HPO:probinson	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0003256	OMIM:607765	IEA				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0003623	OMIM:607765	TAS				C		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0011985	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607765	#607765 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 1; CBAS1;;3-@BETA-HYDROXY-DELTA-5-C27-STEROID OXIDOREDUCTASE DEFICIENCY		HP:0200084	OMIM:607765	TAS				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000007	OMIM:607778	TAS				I		HPO:probinson	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000767	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000768	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000773	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000774	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0000887	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0001156	OMIM:607778	TAS				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0001216	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0001821	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002650	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002812	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002866	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002869	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002938	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002970	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002983	OMIM:607778	TAS				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0002984	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0003022	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0003097	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0003099	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0003300	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0003498	PMID:12624140	PCS	HP:0011463			P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0004279	OMIM:607778	TAS				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0004482	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0005736	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0005792	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0006438	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0008789	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0008873	OMIM:607778	TAS				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0009638	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0009882	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0010017	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0010049	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0010241	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0010575	PMID:12624140	PCS				P		HPO:iea	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0030033	OMIM:607778	IEA				P		HPO:skoehler	
OMIM	607778	ACROCAPITOFEMORAL DYSPLASIA; ACFD		HP:0100864	PMID:12624140	PCS				P		HPO:iea	
OMIM	607785	JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000006	OMIM:607785	TAS				I		HPO:skoehler	
OMIM	607785	JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001428	OMIM:607785	TAS				I		HPO:probinson	
OMIM	607785	JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0012209	OMIM:607785	TAS				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0000006	OMIM:607791	IEA				I		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0001265	OMIM:607791	IEA				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0001284	OMIM:607791	IEA				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0002460	OMIM:607791	TAS				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0002936	OMIM:607791	IEA				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0003378	OMIM:607791	IEA				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0003481	OMIM:607791	TAS				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0003484	OMIM:607791	IEA				P		HPO:probinson	
OMIM	607791	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D		HP:0003693	OMIM:607791	TAS				P		HPO:probinson	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000007	OMIM:607812	IEA				I		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000028	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000154	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000175	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000193	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000219	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000219	OMIM:607812	TAS				P		HPO:skoehler	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000256	OMIM:607812	TAS				P		HPO:skoehler	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000260	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000272	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000316	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000319	OMIM:607812	TAS				P		HPO:probinson	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000336	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000343	OMIM:607812	TAS				P		HPO:probinson	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000431	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000463	OMIM:607812	TAS				P		HPO:skoehler	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000565	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000648	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000670	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000684	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000685	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0000938	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0001388	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0001476	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0001763	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002007	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002020	OMIM:607812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002208	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002299	OMIM:607812	TAS				P		HPO:skoehler	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002650	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0002868	OMIM:607812	TAS				P		HPO:probinson	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0004322	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0005306	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0005336	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0007648	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0008070	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0008444	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0008808	OMIM:607812	IEA				P		HPO:iea	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0010695	OMIM:607812	IEA				P		HPO:skoehler	
OMIM	607812	CRANIOLENTICULOSUTURAL DYSPLASIA		HP:0011800	OMIM:607812	TAS				P		HPO:skoehler	
OMIM	607821	DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37		HP:0000007	OMIM:607821	TAS				I		HPO:probinson	
OMIM	607821	DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37		HP:0000510	OMIM:607821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607821	DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37		HP:0001751	OMIM:607821	TAS		HP:0040284		P		HPO:probinson	1/6
OMIM	607821	DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37		HP:0007642	OMIM:607821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607821	DEAFNESS, AUTOSOMAL RECESSIVE 37; DFNB37		HP:0008619	OMIM:607821	TAS				P		HPO:skoehler	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0000006	OMIM:607822	IEA				I		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0000726	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0000751	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001250	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001260	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001285	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001288	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001332	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0001336	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002015	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002071	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002120	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002185	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002186	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002354	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002395	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0002511	OMIM:607822	IEA	HP:0003593			P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0003487	OMIM:607822	IEA				P		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0003581	OMIM:607822	TAS				C		HPO:probinson	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0003678	OMIM:607822	IEA				C		HPO:iea	
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0010524	OMIM:607822	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607822	ALZHEIMER DISEASE 3; AD		HP:0031868	OMIM:607822	IEA				P		HPO:skoehler	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000006	OMIM:607823	IEA				I		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000007	OMIM:607823	IEA				I		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000034	OMIM:607823	IEA				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000164	OMIM:607823	IEA				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000561	OMIM:607823	PCS				P		HPO:probinson	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0000963	OMIM:607823	TAS				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0001006	OMIM:607823	IEA				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS	HP:0003676	HP:0001596	OMIM:607823	TAS				P		HPO:skoehler	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0001597	OMIM:607823	IEA				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0001790	OMIM:607823	IEA				P		HPO:iea	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0002223	OMIM:607823	PCS				P		HPO:probinson	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0003550	OMIM:607823	TAS				P		HPO:probinson	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0100540	OMIM:607823	TAS				P		HPO:skoehler	
OMIM	607823	HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA SYNDROME; HLTS		HP:0100869	OMIM:607823	TAS				P		HPO:probinson	
OMIM	607829	MITRAL VALVE PROLAPSE, MYXOMATOUS 2		HP:0000006	OMIM:607829	IEA				I		HPO:iea	
OMIM	607829	MITRAL VALVE PROLAPSE, MYXOMATOUS 2		HP:0001634	OMIM:607829	IEA				P		HPO:iea	
OMIM	607829	MITRAL VALVE PROLAPSE, MYXOMATOUS 2		HP:0001653	OMIM:607829	IEA				P		HPO:iea	
OMIM	607829	MITRAL VALVE PROLAPSE, MYXOMATOUS 2		HP:0003831	OMIM:607829	IEA				C		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0000006	OMIM:607831	IEA				I		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0000007	OMIM:607831	IEA				I		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0001171	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0001284	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0001425	OMIM:607831	TAS				I		HPO:skoehler	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0001762	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0002460	OMIM:607831	TAS				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0002751	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0002936	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003380	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003431	OMIM:607831	TAS				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003450	OMIM:607831	IEA				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003593	OMIM:607831	TAS				C		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003693	OMIM:607831	TAS				P		HPO:iea	
OMIM	607831	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2K; CMT2K		HP:0003701	OMIM:607831	IEA				P		HPO:iea	
OMIM	607832	#607832 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO		HP:0000083	PMID:17713465	PCS				P		HPO:probinson	
OMIM	607832	#607832 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO		HP:0000093	PMID:17713465	PCS				P		HPO:probinson	
OMIM	607832	#607832 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO		HP:0000097	PMID:17713465	PCS				P		HPO:probinson	
OMIM	607832	#607832 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO		HP:0000790	PMID:17713465	PCS				P		HPO:probinson	
OMIM	607832	#607832 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 3, SUSCEPTIBILITY TO		HP:0000822	PMID:17713465	PCS				P		HPO:probinson	
OMIM	607836	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1		HP:0000006	OMIM:607836	TAS				I		HPO:skoehler	
OMIM	607836	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1		HP:0000872	OMIM:607836	TAS				P		HPO:skoehler	
OMIM	607836	AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 1	HP:0012837	HP:0001045	OMIM:607836	TAS				P		HPO:skoehler	
OMIM	607841	#607841 DEAFNESS, AUTOSOMAL DOMINANT 48; DFNA48		HP:0000006	PMID:12736868	IEA				I		HPO:probinson	
OMIM	607841	#607841 DEAFNESS, AUTOSOMAL DOMINANT 48; DFNA48		HP:0000407	PMID:12736868	IEA				P		HPO:probinson	
OMIM	607842	#607842 AURAL ATRESIA, CONGENITAL; CAA;;AURAL ATRESIA, CONGENITAL, WITH HYPOSMIA		HP:0000006	PMID:22152683	PCS				I		HPO:probinson	
OMIM	607842	#607842 AURAL ATRESIA, CONGENITAL; CAA;;AURAL ATRESIA, CONGENITAL, WITH HYPOSMIA	HP:0012832	HP:0000405	OMIM:607842	TAS				P		HPO:skoehler	
OMIM	607842	#607842 AURAL ATRESIA, CONGENITAL; CAA;;AURAL ATRESIA, CONGENITAL, WITH HYPOSMIA		HP:0000413	PMID:22152683	PCS				P		HPO:probinson	
OMIM	607842	#607842 AURAL ATRESIA, CONGENITAL; CAA;;AURAL ATRESIA, CONGENITAL, WITH HYPOSMIA		HP:0004409	OMIM:607842	TAS				P		HPO:skoehler	
OMIM	607847	#607847 NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS;;NONIMMUNE CHRONIC IDIOPATHIC NEUTROPENIA OF ADULTS;;NI-CINA		HP:0000006	OMIM:607847	TAS				I		HPO:probinson	
OMIM	607847	#607847 NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS;;NONIMMUNE CHRONIC IDIOPATHIC NEUTROPENIA OF ADULTS;;NI-CINA	HP:0012825	HP:0001875	OMIM:607847	TAS				P		HPO:probinson	
OMIM	607847	#607847 NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS;;NONIMMUNE CHRONIC IDIOPATHIC NEUTROPENIA OF ADULTS;;NI-CINA		HP:0004808	OMIM:607847	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	607850	HAND OSTEOARTHRITIS		HP:0000006	OMIM:607850	TAS				I		HPO:probinson	
OMIM	607850	HAND OSTEOARTHRITIS		HP:0001387	OMIM:607850	TAS				P		HPO:probinson	
OMIM	607850	HAND OSTEOARTHRITIS		HP:0002829	OMIM:607850	TAS				P		HPO:probinson	
OMIM	607850	HAND OSTEOARTHRITIS		HP:0006226	OMIM:607850	TAS				P		HPO:probinson	
OMIM	607850	HAND OSTEOARTHRITIS		HP:0006233	OMIM:607850	TAS				P		HPO:probinson	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0000007	OMIM:607855	IEA				I		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0000602	OMIM:607855	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001249	OMIM:607855	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001250	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001252	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001270	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001284	OMIM:607855	IEA				P		HPO:skoehler	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001290	OMIM:607855	TAS				P		HPO:skoehler	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0001371	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0002536	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0002747	OMIM:607855	IEA				P		HPO:skoehler	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0002751	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0003236	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0003560	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0003577	OMIM:607855	IEA				C		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0003741	OMIM:607855	TAS				P		HPO:skoehler	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0007103	OMIM:607855	IEA				P		HPO:iea	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0008872	OMIM:607855	IEA				P		HPO:skoehler	
OMIM	607855	MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A		HP:0100297	OMIM:607855	IEA				P		HPO:skoehler	
OMIM	607859	ANGIOMA, TUFTED		HP:0000006	OMIM:607859	TAS				I		HPO:probinson	
OMIM	607859	ANGIOMA, TUFTED		HP:0001000	OMIM:607859	IEA				P		HPO:skoehler	
OMIM	607859	ANGIOMA, TUFTED		HP:0003829	OMIM:607859	TAS				C		HPO:skoehler	
OMIM	607859	ANGIOMA, TUFTED		HP:0011276	OMIM:607859	TAS				P		HPO:skoehler	
OMIM	607859	ANGIOMA, TUFTED		HP:0012329	OMIM:607859	TAS				P		HPO:probinson	
OMIM	607864	CAUDAL DUPLICATION ANOMALY		HP:0000073	OMIM:612229	TAS				P		HPO:probinson	
OMIM	607864	CAUDAL DUPLICATION ANOMALY		HP:0003762	OMIM:612229	TAS				P		HPO:probinson	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000028	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000047	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000077	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000176	PMID:12687501	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000193	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000204	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000218	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000238	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000248	PMID:12687501	PCS		HP:0040284		P		HPO:probinson	18/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000252	PMID:12687501	PCS		HP:0040284		P		HPO:probinson	18/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000260	PMID:12687501	PCS		HP:0040284		P		HPO:probinson	22/26
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000272	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000286	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000307	PMID:12687501	PCS		HP:0040284		P		HPO:probinson	20/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000316	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000343	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000358	PMID:12687501	PCS		HP:0040284		P		HPO:iea	7/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000369	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000391	PMID:17918734	PCS		HP:0040284		P		HPO:iea	16/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000405	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000407	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000457	PMID:12687501	PCS		HP:0040284		P		HPO:iea	20/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000486	PMID:12687501	PCS		HP:0040284		P		HPO:probinson	9/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000490	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	24/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000494	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000505	PMID:18245432;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000518	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000540	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	20/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000543	PMID:10507720	PCS				P		HPO:probinson	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000545	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:probinson	5/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000581	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000582	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000588	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000639	PMID:12687501;ISBN-13:978-0721606156	PCS		HP:0040284		P		HPO:iea	4/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000648	PMID:10507720	PCS				P		HPO:probinson	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000664	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000718	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000735	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000742	http://www.ncbi.nlm.nih.gov/books/NBK1191/;ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000750	PMID:18245432;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000851	PMID:18245432;PMID:12687501	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000878	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000892	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0000902	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001156	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001249	PMID:18245432;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001250	PMID:18031548	PCS	HP:0003593	HP:0040284		P		HPO:iea	15/31
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001252	PMID:12687501	PCS	HP:0003577	HP:0040284		P		HPO:probinson	26/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001263	PMID:18245432;PMID:17918734	PCS		HP:0040284		P		HPO:iea	30/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001274	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001290	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001302	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001385	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001476	http://www.ncbi.nlm.nih.gov/books/NBK1191/	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001510	ISBN-13:978-0721606156	PCS	HP:0003593			P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001513	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001629	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:probinson	4/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001643	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:probinson	5/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001644	PMID:12687501	PCS	HP:0003593	HP:0040284		P		HPO:probinson	7/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001647	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	2/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001655	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001761	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001773	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0001840	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002007	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002015	PMID:12687501;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002019	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002020	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002079	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002101	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002120	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002126	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002188	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002352	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002521	http://www.ncbi.nlm.nih.gov/books/NBK1191/	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002591	PMID:20034100	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002616	PMID:12687501	PCS		HP:0040284		P		HPO:iea	3/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002650	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0002750	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0003745	OMIM:607872	TAS				I		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0004209	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	12/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0004378	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0005280	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	23/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0006897	ISBN-13:978-0721606156	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0006956	PMID:18245432;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0008551	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0008872	PMID:12687501;PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0009237	ISBN-13:978-0721606156	PCS		HP:0040284		P		HPO:iea	26/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0009553	PMID:17918734	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0010316	PMID:12687501;PMID:17918734	PCS		HP:0040284		P		HPO:iea	1/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0010722	PMID:17918734	PCS		HP:0040284		P		HPO:iea	16/30
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0010865	PMID:18245432	PCS				P		HPO:iea	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0011220	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0011228	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0011800	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0012469	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0012817	OMIM:607872	TAS				P		HPO:skoehler	
OMIM	607872	CHROMOSOME 1P36 DELETION SYNDROME		HP:0100490	PMID:18245432	PCS				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0000006	OMIM:607876	TAS				I		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0000643	OMIM:607876	TAS				P		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001249	OMIM:607876	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001312	OMIM:607876	IEA				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001326	OMIM:607876	IEA				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001336	OMIM:607876	TAS				P		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001337	OMIM:607876	IEA				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001337	OMIM:607876	TAS				P		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001340	OMIM:607876	IEA				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0001351	OMIM:607876	IEA				P		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0002069	OMIM:607876	TAS				P		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0003581	OMIM:607876	IEA				C		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0003680	OMIM:607876	IEA				C		HPO:iea	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0010852	OMIM:607876	TAS				P		HPO:skoehler	
OMIM	607876	#607876 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 2; FAME2;;BENIGN ADULT FAMILIAL MYOCLONIC EPILEPSY 2; BAFME2;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 2; FCMTE2;;CORTICAL MYOCLONUS AND EPILEPSY, AUTOSOMAL DOMINANT; ADCME		HP:0100543	OMIM:607876	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0000007	OMIM:607903	TAS				I		HPO:skoehler	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0000535	OMIM:607903	TAS				P		HPO:probinson	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0000653	OMIM:607903	TAS				P		HPO:probinson	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0000989	OMIM:607903	TAS				P		HPO:skoehler	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0001006	OMIM:607903	IEA				P		HPO:skoehler	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0002299	PMID:16439973	TAS				P		HPO:probinson	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0003777	OMIM:607903	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0007502	OMIM:607903	TAS				P		HPO:skoehler	
OMIM	607903	#607903 HYPOTRICHOSIS 6; HYPT6;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE 1; LAH1;;HYPOTRICHOSIS, LOCALIZED, AUTOSOMAL RECESSIVE; LAH;;HTL		HP:0010783	OMIM:607903	TAS				P		HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0000007	OMIM:607906	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0000505	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0000518	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0000589	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0000639	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0001249	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0001250	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I	HP:0012828	HP:0001263	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0001347	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0001928	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0002240	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607906	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I		HP:0002521	OMIM:607906	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE II; CDG1I	HPO:skoehler	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000006	PMID:11527955	PCS				I		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000505	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000510	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000533	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000648	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0000662	PMID:11527955	PCS	HP:0011463			P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0007737	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607921	#607921 RETINITIS PIGMENTOSA 30; RP30		HP:0007843	PMID:11527955	PCS				P		HPO:probinson	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000006	PMID:12794703;PMID:18252212	PCS				I		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000028	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000047	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000048	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000054	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000089	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000134	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/5
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000171	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000175	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000193	OMIM:607932	IEA				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000218	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000248	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000252	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000272	OMIM:607932	IEA				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000278	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000324	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/10
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000347	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000348	OMIM:607932	IEA				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000358	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000365	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000369	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000400	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000411	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000482	PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000528	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	9/10
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000545	PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/3
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000556	PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000568	PMID:12794703;PMID:18252212	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000589	PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/5
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000618	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	8/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000639	PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000647	PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/5
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000821	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000830	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000835	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0000954	OMIM:607932	IEA				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001144	PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001156	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001177	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001252	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001263	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	5/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001321	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001344	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001357	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001508	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0001770	OMIM:607932	IEA				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0002119	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0002120	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0002188	PMID:12794703;PMID:18252212	PCS				P		HPO:iea	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0003319	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/10
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0004209	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0004443	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/10
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0005819	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0006101	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0006829	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0007068	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0007370	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	3/9
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0009600	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/11
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0009909	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0010538	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	1/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0010999	PMID:12794703;PMID:18252212	PCS		HP:0040284		P		HPO:iea	2/6
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0011800	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0025356	OMIM:607932	IEA				P		HPO:skoehler	
OMIM	607932	MICROPHTHALMIA, SYNDROMIC 6; MCOPS6		HP:0030276	OMIM:607932	TAS				P		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0000007	OMIM:607936	TAS				I		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0000982	OMIM:607936	TAS				P		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0008064	OMIM:607936	IEA				P		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0008404	OMIM:607936	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0025092	OMIM:607936	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0040162	OMIM:607936	IEA				P		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0040189	OMIM:607936	IEA				P		HPO:skoehler	
OMIM	607936	PEELING SKIN SYNDROME 4; PSS4		HP:0100725	OMIM:607936	TAS				P		HPO:skoehler	
OMIM	607941	#607941 ATRIAL SEPTAL DEFECT 2; ASD2		HP:0000006	OMIM:607941	TAS				I		HPO:skoehler	
OMIM	607941	#607941 ATRIAL SEPTAL DEFECT 2; ASD2		HP:0001629	OMIM:607941	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607941	#607941 ATRIAL SEPTAL DEFECT 2; ASD2		HP:0001631	OMIM:607941	TAS				P		HPO:skoehler	
OMIM	607941	#607941 ATRIAL SEPTAL DEFECT 2; ASD2		HP:0006695	OMIM:607941	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000007	OMIM:607944	IEA				I		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000369	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000403	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000460	OMIM:607944	TAS				P		HPO:probinson	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000821	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000926	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0000979	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0001034	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0001045	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0001256	OMIM:607944	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0001264	OMIM:607944	TAS				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0001973	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002090	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002091	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002205	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002478	OMIM:607944	TAS				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002657	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002716	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002751	OMIM:607944	TAS				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002938	OMIM:607944	TAS				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0002958	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0003025	OMIM:607944	TAS				P		HPO:probinson	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0003301	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0003621	OMIM:607944	IEA				C		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0004322	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0004979	OMIM:607944	TAS				P		HPO:probinson	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0005374	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0005387	OMIM:607944	TAS				P		HPO:probinson	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0005403	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0005576	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0005681	OMIM:607944	IEA				P		HPO:skoehler	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0007526	OMIM:607944	IEA				P		HPO:iea	
OMIM	607944	SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION; SPENCDI		HP:0011108	OMIM:607944	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000007	OMIM:608013	IEA				I		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000160	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000194	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000232	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000252	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000278	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000316	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000325	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000347	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000369	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000463	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000486	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000741	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000962	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0000967	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001250	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001399	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001433	PMID:10649495	PCS				P		HP:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001511	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001541	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001558	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001561	PMID:3415310	PCS				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001622	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001640	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001744	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001790	PMID:10649495	PCS				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001873	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0001903	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002015	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002098	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002104	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002119	OMIM:608013	TAS				P		HPO:skoehler	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002179	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002240	PMID:10649495	PCS				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002304	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002344	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002375	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0002804	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0003196	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0003656	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0004325	PMID:10352942	PCS	HP:0003577			P		HP:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0005257	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0005280	OMIM:608013	IEA				P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0007479	PMID:10685993	PCS	HP:0003577	HP:0040284		P		HPO:probinson	6/6
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0007549	OMIM:608013	IEA	HP:0003577			P		HPO:iea	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0008064	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0008551	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608013	GAUCHER DISEASE, PERINATAL LETHAL		HP:0010803	OMIM:608013	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000007	OMIM:608022	TAS				I		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000023	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000105	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000175	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000239	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000286	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000316	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000347	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000369	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000457	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000465	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000470	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000800	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0000921	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001263	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001290	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001511	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001538	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001562	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001591	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001762	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001765	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0001804	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0002089	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0002093	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0002098	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0002126	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0002779	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0003196	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0003275	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0003422	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0003521	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0005257	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0005280	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0006615	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0008435	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0008643	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0010880	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0030290	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0100752	OMIM:608022	TAS				P		HPO:probinson	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0100880	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608022	DIAPHANOSPONDYLODYSOSTOSIS		HP:0200133	OMIM:608022	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000007	OMIM:608027	IEA				I		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000248	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000253	OMIM:608027	IEA				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000293	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000343	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000365	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000369	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000400	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000520	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000637	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0000648	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001250	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001257	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001263	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001272	OMIM:608027	IEA				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001319	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001321	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0001347	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002059	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002079	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002365	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002421	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002705	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0002714	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0003577	OMIM:608027	IEA				C		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0003676	OMIM:608027	IEA				C		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0004322	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0004325	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0005280	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0008936	OMIM:608027	IEA				P		HPO:iea	
OMIM	608027	#608027 PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3;;CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM;;PCH WITH OPTIC ATROPHY		HP:0012110	OMIM:608027	TAS				P		HPO:skoehler	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000218	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000268	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000289	OMIM:608028	TAS				P		HPO:skoehler	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000385	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000426	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000431	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000508	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0000668	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0001156	OMIM:608028	TAS				P		HPO:skoehler	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0001162	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0001204	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0001830	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0001831	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0003745	OMIM:608028	IEA				I		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0004322	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0006152	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0008589	OMIM:608028	IEA				P		HPO:iea	
OMIM	608028	608028 THAI SYMPHALANGISM SYNDROME		HP:0009381	OMIM:608028	TAS				P		HPO:probinson	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0000007	OMIM:608029	IEA				I		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0000750	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001251	OMIM:608029	TAS				P		HPO:skoehler	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001252	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001257	OMIM:608029	TAS				P		HPO:skoehler	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001270	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001272	OMIM:608029	TAS				P		HPO:skoehler	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001290	OMIM:608029	TAS				P		HPO:skoehler	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001310	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001347	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0001763	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0002066	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0002080	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0002312	OMIM:608029	IEA				P		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0003577	OMIM:608029	IEA				C		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0003680	OMIM:608029	IEA				C		HPO:iea	
OMIM	608029	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 6		HP:0004322	OMIM:608029	IEA				P		HPO:iea	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000006	PMID:20668259	PCS				I		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001265	OMIM:608030	TAS				P		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001288	PMID:20668259	PCS				P		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002380	OMIM:608030	TAS				P		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0002529	OMIM:608030	TAS				P		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0007126	OMIM:608030	TAS				P		HPO:probinson	
OMIM	608030	#608030 AMYOTROPHIC LATERAL SCLEROSIS 6, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS6AMYOTROPHIC LATERAL SCLEROSIS 6, AUTOSOMAL RECESSIVE, INCLUDED		HP:0007354	OMIM:608030	IEA				P		HPO:skoehler	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0000006	OMIM:608033	IEA				I		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0001250	OMIM:608033	IEA				P		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0001259	OMIM:608033	IEA				P		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0001276	OMIM:608033	IEA				P		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0001298	OMIM:608033	TAS				P		HPO:skoehler	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002090	OMIM:608033	IEA				P		HPO:skoehler	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002171	OMIM:608033	IEA				P		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002181	OMIM:608033	IEA				P		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002445	OMIM:608033	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002510	OMIM:608033	TAS				P		HPO:skoehler	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0002922	OMIM:608033	TAS				P		HPO:probinson	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0003593	OMIM:608033	IEA				C		HPO:iea	
OMIM	608033	#608033 ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3; IIAE3;;ENCEPHALOPATHY, ACUTE NECROTIZING, SUSCEPTIBILITY TO; ANE		HP:0003829	OMIM:608033	TAS				C		HPO:skoehler	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000717	OMIM:608049	TAS				P		HPO:probinson	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000721	OMIM:608049	IEA				P		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000723	OMIM:608049	TAS				P		HPO:skoehler	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000728	OMIM:608049	IEA				P		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000732	OMIM:608049	IEA				P		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000733	OMIM:608049	TAS				P		HPO:probinson	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000750	OMIM:608049	IEA				P		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0000758	OMIM:608049	TAS				P		HPO:probinson	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0001249	OMIM:608049	IEA				P		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0001250	OMIM:608049	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0001425	OMIM:608049	TAS				I		HPO:skoehler	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0001426	OMIM:608049	IEA				I		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0002353	OMIM:608049	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0002919	OMIM:608049	IEA				P		HPO:skoehler	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0003144	OMIM:608049	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0003745	OMIM:608049	IEA				I		HPO:iea	
OMIM	608049	AUTISM, SUSCEPTIBILITY TO, 3; AUTS3		HP:0011463	OMIM:608049	IEA				C		HPO:iea	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0000006	OMIM:608051	TAS				I		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0000603	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0007641	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0007663	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0007722	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0007754	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0007793	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608051	MACULAR DYSTROPHY, RETINAL, 2		HP:0030629	OMIM:608051	TAS				P		HPO:probinson	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0000006	OMIM:608088	IEA				I		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0000407	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0000522	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0000802	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0001279	OMIM:608088	IEA				P		HPO:skoehler	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0001609	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0002020	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0002936	OMIM:608088	IEA				P		HPO:iea	
OMIM	608088	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH ANDGASTROESOPHAGEAL REFLUX		HP:0003390	OMIM:608088	IEA				P		HPO:iea	
OMIM	608089	ENDOMETRIAL CANCER		HP:0001428	OMIM:608089	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	608089	ENDOMETRIAL CANCER		HP:0012114	OMIM:608089	IEA				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000007	OMIM:608091	IEA				I		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000050	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000090	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000107	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000218	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000238	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000256	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000268	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000316	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000369	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000505	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000556	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000565	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000567	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000568	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000570	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000588	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000617	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000639	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0000657	OMIM:608091	PCS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001162	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001249	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001251	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001252	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001263	OMIM:608091	PCS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001273	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001290	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001425	OMIM:608091	TAS				I		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001508	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0001760	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002007	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002084	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002195	OMIM:608091	TAS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002335	OMIM:608091	TAS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002365	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002404	OMIM:608091	TAS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002419	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002508	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002790	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002871	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0002876	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0005280	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0007772	OMIM:608091	TAS				P		HPO:skoehler	
OMIM	608091	JOUBERT SYNDROME 2		HP:0011933	OMIM:608091	TAS				P		HPO:probinson	
OMIM	608091	JOUBERT SYNDROME 2		HP:0012211	OMIM:608091	IEA				P		HPO:iea	
OMIM	608091	JOUBERT SYNDROME 2		HP:0100951	OMIM:608091	PCS				P		HPO:probinson	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000007	OMIM:608093	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000028	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000252	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000347	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000518	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000577	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000639	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000718	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000952	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0000954	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001249	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001250	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001252	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001263	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001276	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001290	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001337	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001347	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001371	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0001976	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0002093	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0002104	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0002910	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0003075	OMIM:608093	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	HP:0040283
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0003186	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0003577	OMIM:608093	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0003642	OMIM:608093	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0003828	OMIM:608093	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0004209	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:iea	
OMIM	608093	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J		HP:0010781	OMIM:608093	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IJ; CDG1J	HPO:skoehler	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0000006	OMIM:608096	IEA				I		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0002069	OMIM:608096	IEA				P		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0002133	OMIM:608096	IEA				P		HPO:skoehler	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0002349	OMIM:608096	IEA				P		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0002373	OMIM:608096	IEA				P		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0002384	OMIM:608096	IEA				P		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0003674	OMIM:608096	IEA				C		HPO:iea	
OMIM	608096	EPILEPSY, FAMILIAL TEMPORAL LOBE, 2; ETL2		HP:0003829	OMIM:608096	IEA				C		HPO:iea	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0000007	PMID:12682315	PCS				I		HPO:probinson	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0000253	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0000817	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0001250	PMID:12682315	PCS				P		HPO:probinson	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0001263	PMID:12682315	PCS				P		HPO:probinson	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0001290	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0001508	OMIM:608097	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0002079	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0002273	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0002521	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:608097	TAS				C		HPO:skoehler	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0007165	PMID:12682315	PCS				P		HPO:probinson	
OMIM	608097	PERIVENTRICULAR HETEROTOPIA WITH MICROCEPHALY, AUTOSOMAL RECESSIVE		HP:0010864	OMIM:608097	TAS				P		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0000007	OMIM:608099	IEA				I		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0001371	OMIM:608099	TAS				P		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0001638	OMIM:608099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0002317	OMIM:608099	IEA				P		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0002650	OMIM:608099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003236	OMIM:608099	IEA				P		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003325	OMIM:608099	IEA				P		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003458	OMIM:608099	IEA				P		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003621	OMIM:608099	IEA				C		HPO:iea	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003676	OMIM:608099	TAS				C		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003797	OMIM:608099	IEA				P		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0003828	OMIM:608099	TAS				C		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0006785	OMIM:608099	TAS				P		HPO:skoehler	
OMIM	608099	#608099 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D;;DUCHENNE-LIKE AUTOSOMAL RECESSIVE MUSCULAR DYSTROPHY, TYPE 2; DMDA2;;ADHALINOPATHY, PRIMARY		HP:0008981	OMIM:608099	IEA				P		HPO:iea	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0000316	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0000343	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001290	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001396	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001410	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001508	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001511	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001541	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001643	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001671	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001873	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001903	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0001999	OMIM:608104	IEA		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	HP:0040284
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0002013	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0002014	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0002240	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0002243	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0003073	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608104	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG1H		HP:0003160	OMIM:608104	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IH; CDG1H	HPO:skoehler	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0000007	OMIM:608105	TAS				I		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0000666	OMIM:608105	TAS				P		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0002268	OMIM:608105	TAS				P		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0002356	OMIM:608105	TAS				P		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0003593	OMIM:608105	TAS				C		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0007104	OMIM:608105	TAS				P		HPO:probinson	
OMIM	608105	EPILEPSY, ROLANDIC, WITH PAROXYSMAL EXERCISE-INDUCED DYSTONIA ANDWRITER'S CRAMP		HP:0007332	OMIM:608105	TAS				P		HPO:probinson	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0000007	OMIM:608106	TAS				I	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:iea	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0000031	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:skoehler	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0002716	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:iea	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0002718	OMIM:608106	IEA				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:iea	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0002720	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:probinson	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0002721	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:probinson	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0002959	OMIM:608106	IEA				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:iea	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0003496	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:probinson	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0004315	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:probinson	
OMIM	608106	#608106 IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5;;HYPER-IgM SYNDROME 5		HP:0200117	OMIM:608106	TAS				P	#608106 IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 5; HIGM5;;HYPER-IGM SYNDROME 5	HPO:skoehler	
OMIM	608115	OVARIAN HYPERSTIMULATION SYNDROME		HP:0000006	OMIM:608115	IEA				I		HPO:iea	
OMIM	608115	OVARIAN HYPERSTIMULATION SYNDROME		HP:0000119	OMIM:608115	IEA				P		HPO:iea	
OMIM	608115	OVARIAN HYPERSTIMULATION SYNDROME		HP:0001541	OMIM:608115	IEA				P		HPO:iea	
OMIM	608115	OVARIAN HYPERSTIMULATION SYNDROME		HP:0002018	OMIM:608115	IEA				P		HPO:iea	
OMIM	608115	OVARIAN HYPERSTIMULATION SYNDROME		HP:0002027	OMIM:608115	IEA				P		HPO:iea	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0000006	OMIM:608118	TAS				I		HPO:skoehler	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0000007	OMIM:608118	IEA				I		HPO:iea	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0000951	OMIM:608118	IEA				P		HPO:iea	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0000964	OMIM:608118	TAS				P		HPO:skoehler	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0002242	OMIM:608118	IEA				P		HPO:skoehler	
OMIM	608118	ZINC DEFICIENCY, TRANSIENT NEONATAL; TNZD		HP:0008277	OMIM:608118	IEA				P		HPO:skoehler	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000006	PMID:25447119	PCS				I		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000007	OMIM:608133	TAS				I		HPO:skoehler	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000510	OMIM:608133	TAS				P		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000512	OMIM:608133	TAS				P		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000533	OMIM:608133	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000580	PMID:25447119	PCS				P		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0000662	PMID:25447119	PCS	HP:0003581			P		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0001133	OMIM:608133	TAS				P		HPO:skoehler	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0007830	OMIM:608133	TAS				P		HPO:probinson	
OMIM	608133	#608133 RETINITIS PIGMENTOSA 7; RP7RETINITIS PIGMENTOSA 7, DIGENIC, INCLUDED;;RETINITIS PIGMENTOSA 7 WITH BULL'S-EYE MACULOPATHY, INCLUDED		HP:0007843	PMID:25447119	PCS				P		HPO:probinson	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000023	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000278	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000327	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000343	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000347	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000347	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000463	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000581	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000883	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0000890	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001250	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001263	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001290	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001371	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001539	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001540	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001561	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001601	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001622	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001629	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001631	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001642	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001643	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0001744	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002007	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002089	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002092	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002240	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002673	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0002751	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0003745	OMIM:608149	TAS				I		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0005280	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0008551	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0009826	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0011335	OMIM:608149	TAS				P		HPO:skoehler	
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0012745	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608149	KAGAMI-OGATA SYNDROME		HP:0100807	OMIM:608149	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0000007	OMIM:608154	IEA				I		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0000327	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0000407	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0000490	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES	HP:0003676	HP:0000938	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001249	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001250	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001508	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001511	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001518	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001533	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0001547	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0002215	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0002750	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0002857	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0002967	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0004322	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0004993	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0005328	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0006153	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0007464	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0009059	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0009064	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0031367	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0100818	OMIM:608154	TAS				P		HPO:skoehler	
OMIM	608154	LIPODYSTROPHY, GENERALIZED, WITH MENTAL RETARDATION, DEAFNESS, SHORT STATURE, AND SLENDER BONES		HP:0100864	OMIM:608154	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000006	OMIM:608156	IEA				I		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000007	OMIM:608156	IEA				I		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000028	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000054	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000066	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000160	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000164	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000218	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000219	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000219	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000278	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000294	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000298	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000316	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000319	OMIM:608156	TAS				P		HPO:probinson	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000327	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000341	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000343	OMIM:608156	TAS				P		HPO:probinson	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000358	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000369	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000431	OMIM:608156	TAS				P		HPO:probinson	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000470	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000475	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000535	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000581	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0000653	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0001182	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0001263	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0001363	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0002007	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0002057	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0002236	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0002553	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0002557	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0003196	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0003745	OMIM:608156	IEA				I		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0005280	OMIM:608156	TAS				P		HPO:probinson	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0005484	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0009473	OMIM:608156	IEA				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0012385	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0012745	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0030084	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608156	NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS		HP:0040082	OMIM:608156	TAS				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0000006	OMIM:608161	TAS				I		HPO:probinson	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0000613	OMIM:608161	TAS				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0007401	OMIM:608161	TAS				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0007663	OMIM:608161	TAS				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0007677	OMIM:608161	TAS				P		HPO:probinson	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0007754	OMIM:608161	IEA				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0011506	OMIM:608161	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0011510	OMIM:608161	IEA				P		HPO:skoehler	
OMIM	608161	MACULAR DYSTROPHY, VITELLIFORM, 3; VMD3		HP:0012508	OMIM:608161	TAS				P		HPO:skoehler	
OMIM	608175	AUTOIMMUNE THYROID DISEASE, SUSCEPTIBILITY TO, 3		HP:0100646	OMIM:608175	IEA				P		HPO:probinson	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0000006	OMIM:608180	IEA				I		HPO:iea	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0001440	OMIM:608180	IEA				P		HPO:iea	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0001770	OMIM:608180	IEA				P		HPO:iea	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0008368	OMIM:608180	IEA				P		HPO:skoehler	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0009701	OMIM:608180	IEA				P		HPO:iea	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0009702	OMIM:608180	IEA				P		HPO:skoehler	
OMIM	608180	SYNPOLYDACTYLY 2		HP:0010442	OMIM:608180	IEA				P		HPO:skoehler	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0000007	OMIM:608184	IEA				I		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0001890	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0001973	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002110	OMIM:608184	TAS				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002718	OMIM:608184	TAS				P		HPO:skoehler	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002721	OMIM:608184	TAS				P		HPO:skoehler	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002754	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002788	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002849	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002863	OMIM:608184	IEA				P		HPO:iea	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0002959	OMIM:608184	TAS				P		HPO:skoehler	
OMIM	608184	IMMUNODEFICIENCY WITH HYPER-IGM, TYPE 4		HP:0004798	OMIM:608184	TAS				P		HPO:skoehler	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0000006	OMIM:608189	IEA				I		HPO:iea	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0000007	OMIM:608189	IEA				I		HPO:iea	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0002027	OMIM:608189	TAS				P		HPO:skoehler	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0002894	OMIM:608189	IEA				P		HPO:iea	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0005213	OMIM:608189	IEA				P		HPO:iea	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0005213	OMIM:608189	TAS				P		HPO:probinson	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0006280	OMIM:608189	TAS				P		HPO:probinson	
OMIM	608189	TROPICAL CALCIFIC PANCREATITIS		HP:0008205	OMIM:608189	IEA				P		HPO:iea	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0000007	OMIM:608194	TAS				I		HPO:probinson	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0000548	OMIM:608194	IEA				P		HPO:skoehler	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0000551	OMIM:608194	TAS				P		HPO:probinson	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0000608	OMIM:608194	TAS				P		HPO:probinson	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0000613	OMIM:608194	TAS				P		HPO:probinson	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0007663	OMIM:608194	TAS				P		HPO:probinson	
OMIM	608194	#608194 CONE-ROD DYSTROPHY 13; CORD13		HP:0007688	OMIM:608194	TAS				P		HPO:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0001058	PMID:10758162	PCS				P		HP:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0003203	PMID:10758162	PCS				P		HP:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0005224	PMID:10758162	PCS				P		HP:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0005400	PMID:10758162	PCS				P		HP:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0011897	PMID:10758162	PCS				P		HP:probinson	
OMIM	608203	NEUTROPHIL IMMUNODEFICIENCY SYNDROME		HP:0012618	PMID:10758162	PCS				P		HP:probinson	
OMIM	608217	EPILEPSY, BENIGN NEONATAL, 3		HP:0000006	OMIM:608217	IEA				I		HPO:iea	
OMIM	608217	EPILEPSY, BENIGN NEONATAL, 3		HP:0002069	OMIM:608217	IEA				P		HPO:iea	
OMIM	608217	EPILEPSY, BENIGN NEONATAL, 3		HP:0003593	OMIM:608217	IEA				C		HPO:iea	
OMIM	608219	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 38		HP:0000007	OMIM:608219	TAS				I		HPO:probinson	
OMIM	608219	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 38	HP:0012828	HP:0000399	OMIM:608219	TAS				P		HPO:probinson	
OMIM	608220	SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25		HP:0000007	OMIM:608220	TAS				I		HPO:skoehler	
OMIM	608220	SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25		HP:0001258	OMIM:608220	TAS				P		HPO:skoehler	
OMIM	608220	SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25		HP:0002176	OMIM:608220	IEA				P		HPO:skoehler	
OMIM	608220	SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25		HP:0003418	OMIM:608220	TAS				P		HPO:skoehler	
OMIM	608220	SPASTIC PARAPLEGIA 25, AUTOSOMAL RECESSIVE; SPG25		HP:0030833	OMIM:608220	TAS				P		HPO:skoehler	
OMIM	608224	DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41		HP:0000006	OMIM:608224	TAS				I		HPO:skoehler	
OMIM	608224	DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41		HP:0000360	OMIM:608224	TAS				P		HPO:skoehler	
OMIM	608224	DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41		HP:0000365	OMIM:608224	IEA				P		HPO:skoehler	
OMIM	608224	DEAFNESS, AUTOSOMAL DOMINANT 41; DFNA41		HP:0000408	OMIM:608224	TAS				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000007	OMIM:608227	IEA				I		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000179	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000294	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000322	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000347	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000501	OMIM:608227	IEA				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000518	OMIM:608227	TAS				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000540	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0000960	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001252	OMIM:608227	IEA				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001263	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001276	OMIM:608227	IEA				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001566	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001629	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001631	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0001999	OMIM:608227	IEA				P		HPO:skoehler	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0002650	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0002750	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0003186	OMIM:608227	IEA				P		HPO:iea	
OMIM	608227	608227 CRANIOFACIAL ABNORMALITIES, CATARACTS, CONGENITAL HEART DISEASE, SACRALNEURAL TUBE DEFECTS, AND GROWTH AND DEVELOPMENTAL RETARDATION		HP:0011398	OMIM:608227	TAS				P		HPO:skoehler	
OMIM	608232	#608232 LEUKEMIA, CHRONIC MYELOID; CML;;LEUKEMIA, CHRONIC MYELOGENOUS		HP:0001428	OMIM:608232	TAS				I		HPO:skoehler	
OMIM	608232	#608232 LEUKEMIA, CHRONIC MYELOID; CML;;LEUKEMIA, CHRONIC MYELOGENOUS		HP:0004848	OMIM:608232	TAS				P		HPO:skoehler	
OMIM	608232	#608232 LEUKEMIA, CHRONIC MYELOID; CML;;LEUKEMIA, CHRONIC MYELOGENOUS		HP:0004852	OMIM:608232	TAS				P		HP:probinson	
OMIM	608232	#608232 LEUKEMIA, CHRONIC MYELOID; CML;;LEUKEMIA, CHRONIC MYELOGENOUS		HP:0005506	OMIM:608232	TAS				P		HPO:skoehler	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000007	OMIM:608233	IEA				I		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000219	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000219	OMIM:608233	TAS				P		HPO:skoehler	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000252	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000280	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000319	OMIM:608233	TAS				P		HPO:probinson	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000343	OMIM:608233	TAS				P		HPO:probinson	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000358	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000369	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000431	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000486	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000505	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000582	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000613	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000639	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000670	OMIM:608233	TAS				P		HPO:skoehler	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0000704	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001022	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001107	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001256	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001270	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001385	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001744	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001873	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0001875	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0002206	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0002240	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0002286	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0002718	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0003577	OMIM:608233	IEA				C		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0007384	OMIM:608233	IEA				P		HPO:iea	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0007663	OMIM:608233	TAS				P		HPO:skoehler	
OMIM	608233	#608233 HERMANSKY-PUDLAK SYNDROME 2; HPS2		HP:0008807	OMIM:608233	IEA				P		HPO:iea	
OMIM	608236	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:608236	PCS				I		HPO:probinson	
OMIM	608236	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT		HP:0000762	OMIM:608236	PCS				P		HPO:probinson	
OMIM	608236	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT		HP:0003383	OMIM:608236	PCS				P		HPO:probinson	
OMIM	608236	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT		HP:0003581	OMIM:608236	PCS				C		HPO:probinson	
OMIM	608236	SLOWED NERVE CONDUCTION VELOCITY, AUTOSOMAL DOMINANT		HP:0011096	OMIM:608236	PCS				P		HPO:probinson	
OMIM	608244	OTOSCLEROSIS 3; OTSC3		HP:0000006	OMIM:608244	IEA				I		HPO:skoehler	
OMIM	608244	OTOSCLEROSIS 3; OTSC3		HP:0000362	OMIM:608244	IEA				P		HPO:skoehler	
OMIM	608244	OTOSCLEROSIS 3; OTSC3		HP:0000365	OMIM:608244	IEA				P		HPO:skoehler	
OMIM	608244	OTOSCLEROSIS 3; OTSC3		HP:0003829	OMIM:608244	IEA				C		HPO:skoehler	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:608257	IEA				I		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000272	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000347	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000402	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000405	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000413	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000494	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0000689	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0001792	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0005321	OMIM:608257	TAS				P		HPO:probinson	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0007911	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0009473	OMIM:608257	IEA				P		HPO:iea	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0009892	OMIM:608257	IEA				P		HPO:skoehler	
OMIM	608257	MANDIBULOFACIAL DYSOSTOSIS WITH PTOSIS, AUTOSOMAL DOMINANT		HP:0012385	OMIM:608257	TAS				P		HPO:skoehler	
OMIM	608264	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 40		HP:0000007	OMIM:608264	TAS				I		HPO:probinson	
OMIM	608264	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 40	HP:0012829	HP:0000399	OMIM:608264	TAS				P		HPO:probinson	
OMIM	608265	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 39		HP:0000007	OMIM:608265	TAS				I		HPO:probinson	
OMIM	608265	DEAFNESS, CONGENITAL NEUROSENSORY, AUTOSOMAL RECESSIVE 39		HP:0000399	OMIM:608265	TAS				P		HPO:probinson	
OMIM	608266	#608266 PARATHYROID CARCINOMA;;PRTC		HP:0000006	PMID:14585940	PCS				I		HPO:probinson	
OMIM	608266	#608266 PARATHYROID CARCINOMA;;PRTC		HP:0000843	OMIM:608266	TAS				P		HPO:probinson	
OMIM	608266	#608266 PARATHYROID CARCINOMA;;PRTC		HP:0001428	PMID:14585940	PCS				I		HPO:probinson	
OMIM	608266	#608266 PARATHYROID CARCINOMA;;PRTC		HP:0003072	OMIM:608266	TAS				P		HPO:probinson	
OMIM	608266	#608266 PARATHYROID CARCINOMA;;PRTC		HP:0006780	OMIM:608266	TAS				P		HPO:probinson	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0000007	OMIM:608278	IEA				I		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0000252	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0000336	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0000519	OMIM:608278	PCS				P		HPO:probinson	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0000939	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0001270	OMIM:608278	PCS				P		HPO:probinson	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0001272	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0002069	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0002539	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0004322	OMIM:608278	PCS				P		HPO:probinson	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0005781	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0006887	OMIM:608278	IEA				P		HPO:iea	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0008897	OMIM:608278	PCS				P		HPO:probinson	
OMIM	608278	608278 GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY		HP:0010864	OMIM:608278	TAS				P		HPO:skoehler	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000006	OMIM:608279	IEA				I		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000268	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000444	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000482	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000508	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000518	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000646	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0000768	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0001263	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0001363	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0001840	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0002007	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0010760	OMIM:608279	IEA				P		HPO:iea	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0011220	OMIM:608279	TAS				P		HPO:skoehler	
OMIM	608279	608279 CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS		HP:0012386	OMIM:608279	TAS				P		HPO:skoehler	
OMIM	608320	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1		HP:0000006	OMIM:608320	IEA				I		HPO:iea	
OMIM	608320	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1		HP:0000822	OMIM:608320	IEA				P		HPO:skoehler	
OMIM	608320	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1		HP:0001658	OMIM:608320	IEA				P		HPO:iea	
OMIM	608320	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1		HP:0003124	OMIM:608320	IEA				P		HPO:skoehler	
OMIM	608320	CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1; ADCAD1		HP:0100749	OMIM:608320	IEA				P		HPO:skoehler	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0000006	OMIM:608323	IEA				I		HPO:iea	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0001425	OMIM:608323	TAS				I		HPO:skoehler	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0001760	OMIM:608323	IEA				P		HPO:iea	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0002460	OMIM:608323	IEA				P		HPO:iea	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0002936	OMIM:608323	IEA				P		HPO:iea	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0003450	OMIM:608323	IEA				P		HPO:iea	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0003484	OMIM:608323	IEA				P		HPO:probinson	
OMIM	608323	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE C; CMTDIC		HP:0003693	OMIM:608323	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000006	OMIM:608328	IEA				I		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000189	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000248	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000327	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000501	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000518	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000586	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000594	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000618	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000692	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0000885	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001083	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001156	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001169	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001230	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001256	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001387	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001629	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001642	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001643	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001650	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001653	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0001783	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0002650	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0002682	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0002753	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0002938	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0003416	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0003508	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0005280	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0006482	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0009768	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0011003	OMIM:608328	IEA				P		HPO:iea	
OMIM	608328	WEILL-MARCHESANI SYNDROME 2		HP:0030961	OMIM:608328	TAS				P		HPO:skoehler	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0000007	OMIM:608340	PCS				I		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0001178	OMIM:608340	TAS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0001265	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0001284	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0001761	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0001762	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0002650	OMIM:608340	TAS				P		HPO:skoehler	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0002936	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003376	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003383	OMIM:608340	PCS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003387	OMIM:608340	PCS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003445	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003690	OMIM:608340	TAS				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0003693	OMIM:608340	TAS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0009027	OMIM:608340	IEA				P		HPO:iea	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0009830	OMIM:608340	PCS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0011096	OMIM:608340	PCS				P		HPO:probinson	
OMIM	608340	#608340 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE A; CMTRIA;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE A;;RI-CMTA		HP:0011463	OMIM:608340	PCS				C		HPO:probinson	
OMIM	608345	NYSTAGMUS 3, CONGENITAL, AUTOSOMAL DOMINANT; NYS3		HP:0000006	OMIM:608345	TAS				I		HPO:probinson	
OMIM	608345	NYSTAGMUS 3, CONGENITAL, AUTOSOMAL DOMINANT; NYS3		HP:0001425	OMIM:608345	TAS				I		HPO:skoehler	
OMIM	608345	NYSTAGMUS 3, CONGENITAL, AUTOSOMAL DOMINANT; NYS3		HP:0007286	OMIM:608345	TAS				P		HPO:probinson	
OMIM	608354	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION; CMAVM		HP:0000006	PMID:14639529	IEA				I		HPO:probinson	
OMIM	608354	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION; CMAVM		HP:0004947	OMIM:608354	TAS				P		HPO:skoehler	
OMIM	608354	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION; CMAVM		HP:0005306	PMID:14639529	IEA				P		HPO:probinson	
OMIM	608354	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION; CMAVM		HP:0100026	OMIM:608354	IEA				P		HPO:skoehler	
OMIM	608355	PARKES WEBER SYNDROME; PKWS		HP:0004947	OMIM:608355	IEA				P		HPO:skoehler	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:608358	IEA				I		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0001626	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0002515	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0002792	OMIM:608358	TAS				P		HPO:probinson	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003236	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003324	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003458	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003674	OMIM:608358	IEA				C		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003677	OMIM:608358	IEA				C		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003687	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003691	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003697	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003704	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003707	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0003803	OMIM:608358	IEA				P		HPO:iea	
OMIM	608358	#608358 MYOPATHY, MYOSIN STORAGE;;MYOPATHY, HYALINE BODY, AUTOSOMAL DOMINANT		HP:0009055	OMIM:608358	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0000006	OMIM:608361	IEA				I		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0000926	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0002655	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0002750	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0002857	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0002970	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0003370	OMIM:608361	IEA				P		HPO:iea	
OMIM	608361	SPONDYLOEPIPHYSEAL DYSPLASIA, KIMBERLEY TYPE		HP:0003508	OMIM:608361	IEA				P		HPO:iea	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000006	OMIM:608363	IEA				I		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000218	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000220	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000252	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000286	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000316	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000347	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000369	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000377	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000457	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000494	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0000750	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001249	OMIM:608363	TAS				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001252	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001263	OMIM:608363	TAS				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001290	OMIM:608363	TAS				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001328	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001510	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0001611	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0003745	OMIM:608363	IEA				I		HPO:skoehler	
OMIM	608363	CHROMOSOME 22Q11.2 DUPLICATION SYNDROME		HP:0030680	OMIM:608363	IEA				P		HPO:skoehler	
OMIM	608367	MYOPIA 17		HP:0000006	OMIM:608367	PCS				I		HPO:probinson	
OMIM	608367	MYOPIA 17		HP:0007819	OMIM:608367	PCS				P		HPO:probinson	
OMIM	608367	MYOPIA 17		HP:0011003	OMIM:608367	PCS				P		HPO:probinson	
OMIM	608367	MYOPIA 17		HP:0011530	OMIM:608367	PCS				P		HPO:probinson	
OMIM	608372	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 49		HP:0000006	OMIM:608372	IEA				I		HPO:iea	
OMIM	608372	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 49		HP:0000407	OMIM:608372	IEA				P		HPO:skoehler	
OMIM	608372	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 49		HP:0001730	OMIM:608372	IEA				P		HPO:iea	
OMIM	608372	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 49		HP:0003621	OMIM:608372	IEA				C		HPO:iea	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0000007	PMID:14681825	PCS				I		HPO:probinson	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0000510	OMIM:608380	TAS				P		HPO:skoehler	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0000543	PMID:14681825	PCS				P		HPO:probinson	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0001133	PMID:14681825	PCS				P		HPO:probinson	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0007688	PMID:14681825	PCS				P		HPO:probinson	
OMIM	608380	#608380 RETINITIS PIGMENTOSA 26; RP26		HP:0007843	PMID:14681825	PCS				P		HPO:probinson	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0000006	PMID:10762556	PCS				I		HPO:probinson	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0000384	OMIM:608389	TAS				P		HPO:skoehler	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0000407	PMID:10762556	PCS				P		HPO:probinson	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0002710	PMID:10762556	PCS				P		HPO:probinson	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0004467	PMID:10762556	PCS				P		HPO:probinson	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0007678	OMIM:608389	TAS				P		HPO:skoehler	
OMIM	608389	#608389 BRANCHIOOTIC SYNDROME 3; BOS3;;BO SYNDROME 3		HP:0009796	OMIM:608389	TAS				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0000006	OMIM:608390	IEA				I		HPO:iea	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0002486	OMIM:608390	TAS				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0003236	OMIM:608390	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0003326	OMIM:608390	IEA				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0003552	OMIM:608390	IEA				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0003712	OMIM:608390	IEA				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0005949	OMIM:608390	TAS				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0010307	OMIM:608390	IEA				P		HPO:skoehler	
OMIM	608390	MYOTONIA, POTASSIUM-AGGRAVATED		HP:0025425	OMIM:608390	TAS	HP:0003623			P		HPO:skoehler	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0000007	OMIM:608393	IEA				I		HPO:iea	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0000252	OMIM:608393	IEA				P		HPO:iea	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0001425	OMIM:608393	IEA				I		HPO:iea	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0002342	OMIM:608393	IEA				P		HPO:iea	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0002472	OMIM:608393	IEA				P		HPO:iea	
OMIM	608393	#608393 MICROCEPHALY 6, PRIMARY, AUTOSOMAL RECESSIVE; MCPH6		HP:0003577	OMIM:608393	TAS				C		HPO:skoehler	
OMIM	608394	DEAFNESS, AUTOSOMAL DOMINANT 43		HP:0000006	OMIM:608394	TAS				I		HPO:skoehler	
OMIM	608394	DEAFNESS, AUTOSOMAL DOMINANT 43		HP:0000360	OMIM:608394	TAS				P		HPO:skoehler	
OMIM	608394	DEAFNESS, AUTOSOMAL DOMINANT 43		HP:0000407	OMIM:608394	TAS				P		HPO:skoehler	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0000006	OMIM:608404	IEA				I		HPO:iea	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0000007	OMIM:608404	TAS				I		HPO:skoehler	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0000818	OMIM:608404	IEA				P		HPO:iea	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0001873	OMIM:608404	IEA				P		HPO:iea	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0001902	OMIM:608404	IEA				P		HPO:iea	
OMIM	608404	#608404 PLATELET GLYCOPROTEIN IV DEFICIENCY;;BLEEDING DISORDER, PLATELET-TYPE, 10; BDPLT10;;CD36 DEFICIENCY		HP:0003010	OMIM:608404	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000007	OMIM:608406	IEA				I		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000122	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000286	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000316	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000358	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000592	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000767	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000822	OMIM:608406	IEA				P		HPO:skoehler	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0000913	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001177	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001511	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001595	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001600	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001629	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001631	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0001643	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0002092	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0002937	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0004322	OMIM:608406	IEA				P		HPO:iea	
OMIM	608406	VATER-LIKE DEFECTS WITH PULMONARY HYPERTENSION, LARYNGEAL WEBS, AND GROWTH DEFICIENCY		HP:0005950	OMIM:608406	TAS				P		HPO:skoehler	
OMIM	608415	BRADYOPSIA		HP:0030511	OMIM:608415	IEA				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0000006	OMIM:608423	IEA				I		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0000980	OMIM:608423	IEA				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0001371	OMIM:608423	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0001939	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0002747	OMIM:608423	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003306	OMIM:608423	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003458	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003547	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003560	OMIM:608423	TAS				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003581	OMIM:608423	TAS				C		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003621	OMIM:608423	TAS				C		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003687	OMIM:608423	TAS				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003691	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003736	OMIM:608423	TAS				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003749	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003805	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0003810	OMIM:608423	IEA				P		HPO:iea	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0009025	OMIM:608423	TAS				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0009046	OMIM:608423	IEA				P		HPO:skoehler	
OMIM	608423	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 2; LGMDD2		HP:0031936	OMIM:608423	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0000007	OMIM:608432	IEA				I		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0000252	OMIM:608432	IEA				P		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0000327	OMIM:608432	IEA				P		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0000336	OMIM:608432	IEA				P		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0000426	OMIM:608432	IEA				P		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM	HP:0012825	HP:0000520	OMIM:608432	TAS				P		HPO:probinson	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0001363	OMIM:608432	IEA				P		HPO:iea	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0001999	OMIM:608432	IEA				P		HPO:skoehler	
OMIM	608432	608432 CRANIOSYNOSTOSIS, CALCIFICATION OF BASAL GANGLIA, AND FACIAL DYSMORPHISM		HP:0002135	OMIM:608432	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0000007	OMIM:608443	IEA				I		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0000338	OMIM:608443	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0000736	OMIM:608443	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0000752	OMIM:608443	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0001263	OMIM:608443	TAS				P		HPO:skoehler	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0002546	OMIM:608443	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0003621	OMIM:608443	IEA				C		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0006887	OMIM:608443	IEA				P		HPO:iea	
OMIM	608443	#608443 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3		HP:0010864	OMIM:608443	TAS				P		HPO:skoehler	
OMIM	608456	#608456 FAMILIAL ADENOMATOUS POLYPOSIS, 2; FAP2;;COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE;;ADENOMAS, MULTIPLE COLORECTAL, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:608456	TAS				I		HPO:probinson	
OMIM	608456	#608456 FAMILIAL ADENOMATOUS POLYPOSIS, 2; FAP2;;COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE;;ADENOMAS, MULTIPLE COLORECTAL, AUTOSOMAL RECESSIVE		HP:0003003	PMID:12606733	TAS		HP:0040284		P		HPO:probinson	5/12
OMIM	608456	#608456 FAMILIAL ADENOMATOUS POLYPOSIS, 2; FAP2;;COLORECTAL ADENOMATOUS POLYPOSIS, AUTOSOMAL RECESSIVE;;ADENOMAS, MULTIPLE COLORECTAL, AUTOSOMAL RECESSIVE		HP:0005227	OMIM:608456	TAS				P		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0000006	PMID:9054935	PCS				I		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0000486	OMIM:608470	TAS				P		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0000613	PMID:16606891	PCS				P		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0001131	OMIM:608470	TAS				P		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0007759	OMIM:608470	TAS				P		HPO:probinson	
OMIM	608470	#608470 CORNEAL DYSTROPHY OF BOWMAN LAYER, TYPE I; CDB1;;CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE; CDRB;;REIS-BUCKLERS CORNEAL DYSTROPHY; RBCD;;CORNEAL DYSTROPHY, GEOGRAPHIC;;GRANULAR CORNEAL DYSTROPHY, TYPE III		HP:0200020	PMID:16606891	PCS				P		HPO:probinson	
OMIM	608471	#608471 CORNEAL DYSTROPHY, LATTICE TYPE IIIA; CDL3A;;LATTICE CORNEAL DYSTROPHY, TYPE IIIA		HP:0000006	OMIM:608471	IEA				I		HPO:iea	
OMIM	608471	#608471 CORNEAL DYSTROPHY, LATTICE TYPE IIIA; CDL3A;;LATTICE CORNEAL DYSTROPHY, TYPE IIIA		HP:0000505	OMIM:608471	IEA				P		HPO:iea	
OMIM	608471	#608471 CORNEAL DYSTROPHY, LATTICE TYPE IIIA; CDL3A;;LATTICE CORNEAL DYSTROPHY, TYPE IIIA		HP:0001149	OMIM:608471	IEA				P		HPO:iea	
OMIM	608471	#608471 CORNEAL DYSTROPHY, LATTICE TYPE IIIA; CDL3A;;LATTICE CORNEAL DYSTROPHY, TYPE IIIA		HP:0007663	OMIM:608471	TAS				P		HPO:skoehler	
OMIM	608471	#608471 CORNEAL DYSTROPHY, LATTICE TYPE IIIA; CDL3A;;LATTICE CORNEAL DYSTROPHY, TYPE IIIA		HP:0200020	OMIM:608471	TAS				P		HPO:probinson	
OMIM	608474	MYOPIA 5		HP:0000006	OMIM:608474	IEA				I		HPO:iea	
OMIM	608474	MYOPIA 5		HP:0000541	OMIM:608474	IEA				P		HPO:iea	
OMIM	608474	MYOPIA 5		HP:0001425	OMIM:608474	IEA				I		HPO:skoehler	
OMIM	608474	MYOPIA 5		HP:0011003	OMIM:608474	IEA				P		HPO:iea	
OMIM	608484	608484 CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA;;CORNEAL OPACITIES, CONGENITAL, WITH CORNEA GUTTATA AND CORECTOPIA		HP:0000006	OMIM:608484	TAS				I		HPO:skoehler	
OMIM	608484	608484 CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA;;CORNEAL OPACITIES, CONGENITAL, WITH CORNEA GUTTATA AND CORECTOPIA		HP:0007957	OMIM:608484	IEA				P		HPO:skoehler	
OMIM	608484	608484 CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA;;CORNEAL OPACITIES, CONGENITAL, WITH CORNEA GUTTATA AND CORECTOPIA		HP:0009918	OMIM:608484	TAS				P		HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000007	OMIM:608540	IEA				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000135	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000233	OMIM:608540	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000239	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000252	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000316	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0000347	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001250	OMIM:608540	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001252	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001263	OMIM:608540	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001284	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001290	OMIM:608540	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001371	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001511	OMIM:608540	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001522	OMIM:608540	IEA				M	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001560	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001638	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001744	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0001790	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0002059	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0002240	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0003642	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:iea	
OMIM	608540	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ik; CDG1K		HP:0025356	OMIM:608540	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IK; CDG1K	HPO:skoehler	
OMIM	608542	ANEURYSM, INTRACRANIAL BERRY, 2		HP:0002138	OMIM:608542	TAS				P		HPO:probinson	
OMIM	608542	ANEURYSM, INTRACRANIAL BERRY, 2		HP:0007029	OMIM:608542	TAS				P		HPO:probinson	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000175	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000248	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000256	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000260	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000272	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000316	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000369	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000403	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000405	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0000689	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001252	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001263	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001290	OMIM:608545	TAS				P		HPO:skoehler	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001373	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001388	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001762	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0001939	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0002007	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0002750	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0002751	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0003745	OMIM:608545	IEA				I		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0004209	OMIM:608545	TAS				P		HPO:probinson	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0004322	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0005285	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0008127	OMIM:608545	IEA				P		HPO:iea	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0009279	OMIM:608545	TAS				P		HPO:probinson	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0011220	OMIM:608545	TAS				P		HPO:skoehler	
OMIM	608545	LARSEN-LIKE SYNDROME		HP:0012368	OMIM:608545	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000007	OMIM:608553	TAS				I		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000540	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000543	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000613	OMIM:608553	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000639	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000648	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0000662	OMIM:608553	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0001116	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608553	#608553 LEBER CONGENITAL AMAUROSIS 9; LCA9		HP:0007843	OMIM:608553	TAS				P		HPO:skoehler	
OMIM	608565	#608565 DEAFNESS, AUTOSOMAL RECESSIVE 35; DFNB35		HP:0000007	PMID:18179891	PCS				I		HPO:probinson	
OMIM	608565	#608565 DEAFNESS, AUTOSOMAL RECESSIVE 35; DFNB35		HP:0000407	PMID:18179891	PCS				P		HPO:probinson	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0000006	OMIM:608567	TAS				I		HPO:skoehler	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0000007	OMIM:608567	PCS				I		HPO:probinson	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0001657	OMIM:608567	TAS				P		HPO:skoehler	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0001678	OMIM:608567	TAS				P		HPO:skoehler	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0001688	OMIM:608567	PCS				P		HPO:probinson	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0003577	OMIM:608567	TAS				C		HPO:skoehler	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0005155	OMIM:608567	PCS				P		HPO:probinson	
OMIM	608567	#608567 SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE; SSS1;;SINUS RHYTHM, CONGENITAL ABSENCE OF;;SINUS NODE DISEASE, FAMILIAL, AUTOSOMAL RECESSIVE;;SICK SINUS SYNDROME, CONGENITAL;;SINUS BRADYCARDIA SYNDROME, FAMILIAL		HP:0011704	OMIM:608567	PCS				P		HPO:probinson	
OMIM	608569	#608569 CARDIOMYOPATHY, DILATED, 1O; CMD1O;;CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA		HP:0000006	PMID:15034580	PCS				I		HPO:probinson	
OMIM	608569	#608569 CARDIOMYOPATHY, DILATED, 1O; CMD1O;;CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA		HP:0001644	PMID:15034580	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	608569	#608569 CARDIOMYOPATHY, DILATED, 1O; CMD1O;;CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA		HP:0004756	PMID:15034580	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	608569	#608569 CARDIOMYOPATHY, DILATED, 1O; CMD1O;;CARDIOMYOPATHY, DILATED, WITH VENTRICULAR TACHYCARDIA		HP:0006670	PMID:15034580	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0000006	OMIM:608571	IEA				I		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0000272	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0000311	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0001028	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0001156	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0001631	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0001770	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0001776	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0002007	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0003038	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0004322	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0005036	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0006210	OMIM:608571	IEA				P		HPO:iea	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0011220	OMIM:608571	TAS				P		HPO:skoehler	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0011800	OMIM:608571	TAS				P		HPO:skoehler	
OMIM	608571	ULNAR/FIBULAR RAY DEFECT AND BRACHYDACTYLY		HP:0100559	OMIM:608571	TAS				P		HPO:skoehler	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000007	OMIM:608572	IEA				I		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000089	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000160	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000175	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000193	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000204	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000233	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000303	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000316	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000322	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000338	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000347	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000384	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000405	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000411	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000426	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000430	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000581	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0000652	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0001629	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0001631	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0001939	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0004502	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0004691	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0008872	OMIM:608572	IEA				P		HPO:iea	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0012745	OMIM:608572	TAS				P		HPO:skoehler	
OMIM	608572	%608572 BURN-MCKEOWN SYNDROME		HP:0200138	OMIM:608572	TAS				P		HPO:skoehler	
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0000006	OMIM:608583	IEA				I		HPO:probinson	
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0001297	OMIM:608583	IEA				P		HPO:skoehler	
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0001425	OMIM:608583	TAS				I		HPO:skoehler	
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0001649	OMIM:608583	IEA				P		HPO:skoehler	
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0001727	OMIM:608583	IEA		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	608583	ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1		HP:0005110	OMIM:608583	IEA				P		HPO:probinson	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000007	OMIM:608594	IEA				I	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000065	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000098	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000147	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000303	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000325	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000400	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000787	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000842	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000868	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:probinson	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000868	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000877	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0000956	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001007	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001176	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001394	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001397	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001425	OMIM:608594	TAS				I	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001537	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001544	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001638	OMIM:608594	TAS		HP:0040283		P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	HP:0040283
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001735	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001744	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0001833	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0002155	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0002240	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0002591	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0002833	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0002910	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:skoehler	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0003292	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0003716	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0003758	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HP:probinson	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0003809	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0005616	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0008665	OMIM:608594	IEA				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:iea	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0009125	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HPO:probinson	
OMIM	608594	Lipodystrophy, congenital generalized, type 1		HP:0025128	OMIM:608594	TAS				P	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1	HP:probinson	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000006	OMIM:608600	IEA				I		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000287	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000468	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000822	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000831	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000956	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0000991	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0001015	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0001677	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0001735	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0002155	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0002240	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0003011	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0003074	OMIM:608600	IEA				P		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0003621	OMIM:608600	IEA				C		HPO:iea	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0003635	OMIM:608600	TAS				P		HPO:probinson	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0009003	OMIM:608600	TAS				P		HPO:probinson	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0009017	OMIM:608600	TAS				P		HPO:probinson	
OMIM	608600	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 1		HP:0009125	OMIM:608600	TAS				P		HPO:probinson	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0000007	OMIM:608611	IEA				I		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0000639	OMIM:608611	IEA				P		HPO:skoehler	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0000648	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001250	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001251	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001257	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001260	OMIM:608611	IEA				P		HPO:skoehler	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001263	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0001271	OMIM:608611	TAS				P		HPO:skoehler	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0002352	OMIM:608611	IEA				P		HPO:iea	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0007141	OMIM:608611	IEA				P		HPO:skoehler	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0025356	OMIM:608611	IEA				P		HPO:skoehler	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0025550	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410055	PMID:14988808	IEA				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410056	PMID:14988808	IEA				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410057	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410058	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410059	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410070	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410071	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410072	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410073	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410074	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608611	RIBOSE 5-PHOSPHATE ISOMERASE DEFICIENCY		HP:0410075	PMID:14988808	PCS				P		HPO:NicoleVasilevsky	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000007	OMIM:608612	IEA				I		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000160	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000218	OMIM:608612	TAS				P		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000270	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000292	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000320	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000347	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000418	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000464	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000520	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000678	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000685	OMIM:608612	TAS				P		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000831	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000842	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000894	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0000905	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0001070	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0001371	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0001425	OMIM:608612	TAS				I		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0001596	OMIM:608612	IEA				P		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0001870	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0002299	OMIM:608612	TAS				P		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0002645	OMIM:608612	TAS				P		HPO:skoehler	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0003074	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0003077	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0003635	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0004334	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0005995	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0006480	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0008070	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0009002	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0009064	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0009803	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0009839	OMIM:608612	IEA				P		HPO:iea	
OMIM	608612	MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY; MADB		HP:0010719	OMIM:608612	IEA				P		HPO:iea	
OMIM	608615	#608615 OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS;;TOOTH AGENESIS-COLORECTAL CANCER SYNDROME		HP:0000006	PMID:15042511	PCS				I		HPO:probinson	
OMIM	608615	#608615 OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS;;TOOTH AGENESIS-COLORECTAL CANCER SYNDROME		HP:0000677	PMID:15042511	PCS				P		HPO:probinson	
OMIM	608615	#608615 OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS;;TOOTH AGENESIS-COLORECTAL CANCER SYNDROME		HP:0002209	OMIM:608615	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608615	#608615 OLIGODONTIA-COLORECTAL CANCER SYNDROME; ODCRCS;;TOOTH AGENESIS-COLORECTAL CANCER SYNDROME		HP:0005227	PMID:15042511	PCS		HP:0040284		P		HPO:probinson	2/12
OMIM	608622	HYPERTENSION, DIASTOLIC, RESISTANCE TO		HP:0000006	OMIM:608622	IEA				I		HPO:iea	
OMIM	608622	HYPERTENSION, DIASTOLIC, RESISTANCE TO		HP:0005117	OMIM:608622	TAS				P		HPO:probinson	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000007	OMIM:608624	IEA				I		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000160	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000179	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000272	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000286	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000369	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000396	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000410	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000463	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0000508	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001156	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001263	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001290	OMIM:608624	TAS				P		HPO:skoehler	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001319	OMIM:608624	TAS				P		HPO:probinson	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001328	OMIM:608624	IEA				P		HPO:skoehler	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001513	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0001943	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0002007	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0002750	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0005280	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0007933	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0008551	OMIM:608624	IEA				P		HPO:iea	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0011220	OMIM:608624	TAS				P		HPO:skoehler	
OMIM	608624	MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA		HP:0011800	OMIM:608624	TAS				P		HPO:skoehler	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0000006	PMID:15372378	PCS				I		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0001260	OMIM:608627	TAS				P		HPO:skoehler	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0001284	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002015	PMID:15372378	PCS		HP:0040284		P		HPO:probinson	11/24
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002062	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002174	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002380	PMID:15372378	PCS		HP:0040284		P		HPO:probinson	23/24
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002460	PMID:15372378	PCS		HP:0040284		P		HPO:probinson	10/24
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0002529	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0003202	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0003323	PMID:15372378	PCS				P		HPO:probinson	
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0003394	PMID:15372378	PCS		HP:0040284		P		HPO:probinson	21/23
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0003701	PMID:15372378	PCS		HP:0040284		P		HPO:probinson	19/24
OMIM	608627	#608627 AMYOTROPHIC LATERAL SCLEROSIS 8; ALS8		HP:0007354	OMIM:608627	IEA				P		HPO:skoehler	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000007	OMIM:608629	IEA				I		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000090	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000194	OMIM:608629	IEA				P		HPO:skoehler	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000286	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000369	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000431	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000463	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000505	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000508	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000512	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000556	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000580	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000639	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0000657	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001249	OMIM:608629	IEA				P		HPO:skoehler	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001251	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001252	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001290	OMIM:608629	TAS				P		HPO:skoehler	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001320	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0001425	OMIM:608629	IEA				I		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0002419	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0002553	OMIM:608629	TAS				P		HPO:probinson	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0002790	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0002871	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0002876	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0003774	OMIM:608629	IEA				P		HPO:iea	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0011933	OMIM:608629	TAS				P		HPO:probinson	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0031936	OMIM:608629	IEA				P		HPO:skoehler	
OMIM	608629	JOUBERT SYNDROME 3; JBTS3		HP:0100951	OMIM:608629	IEA				P		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000717	OMIM:608631	IEA				P		HPO:skoehler	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000721	OMIM:608631	IEA				P		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000723	OMIM:608631	TAS				P		HPO:skoehler	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000728	OMIM:608631	IEA				P		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000732	OMIM:608631	IEA				P		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000733	OMIM:608631	TAS				P		HPO:skoehler	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0000758	OMIM:608631	IEA				P		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0001425	OMIM:608631	TAS				I		HPO:skoehler	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0001426	OMIM:608631	IEA				I		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0003621	OMIM:608631	IEA				C		HPO:iea	
OMIM	608631	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 2; ASPG2		HP:0003745	OMIM:608631	IEA				I		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0000006	OMIM:608634	IEA				I		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0002355	OMIM:608634	IEA				P		HPO:skoehler	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0002522	OMIM:608634	IEA				P		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0002600	OMIM:608634	IEA				P		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0002601	OMIM:608634	IEA				P		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0003445	OMIM:608634	IEA				P		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0003470	OMIM:608634	IEA				P		HPO:skoehler	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0003581	OMIM:608634	IEA				C		HPO:iea	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0003677	OMIM:608634	IEA				C		HPO:skoehler	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0009053	OMIM:608634	TAS				P		HPO:probinson	
OMIM	608634	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIB; HMN2B		HP:0009830	OMIM:608634	IEA				P		HPO:skoehler	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000006	OMIM:608636	TAS				I	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000721	OMIM:608636	IEA				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000723	OMIM:608636	TAS				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000728	OMIM:608636	IEA				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000732	OMIM:608636	IEA				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000733	OMIM:608636	TAS				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:probinson	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000750	OMIM:608636	IEA				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0000758	OMIM:608636	TAS				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:probinson	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0001249	OMIM:608636	IEA				P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0001250	OMIM:608636	IEA		HP:0040282		P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	HP:0040282
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0001425	OMIM:608636	TAS				I	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0001426	OMIM:608636	IEA				I	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0002353	OMIM:608636	IEA		HP:0040282		P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	HP:0040282
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0003144	OMIM:608636	IEA		HP:0040282		P	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	HP:0040282
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0003745	OMIM:608636	IEA				I	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0003829	OMIM:608636	TAS				C	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	608636	CHROMOSOME 15q11-q13 DUPLICATION SYNDROME		HP:0011463	OMIM:608636	IEA				C	CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME	HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000717	OMIM:608638	IEA				P		HPO:skoehler	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000721	OMIM:608638	IEA				P		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000723	OMIM:608638	TAS				P		HPO:skoehler	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000728	OMIM:608638	IEA				P		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000732	OMIM:608638	IEA				P		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000733	OMIM:608638	TAS				P		HPO:probinson	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000753	OMIM:608638	IEA				P		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0000758	OMIM:608638	TAS				P		HPO:probinson	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0001425	OMIM:608638	TAS				I		HPO:skoehler	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0001426	OMIM:608638	IEA				I		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0003621	OMIM:608638	IEA				C		HPO:iea	
OMIM	608638	ASPERGER SYNDROME, SUSCEPTIBILITY TO, 1; ASPG1		HP:0003745	OMIM:608638	IEA				I		HPO:iea	
OMIM	608641	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 28		HP:0000006	OMIM:608641	TAS				I		HPO:skoehler	
OMIM	608641	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 28		HP:0000407	OMIM:608641	TAS				P		HPO:skoehler	
OMIM	608641	DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 28		HP:0003676	OMIM:608641	TAS				C		HPO:probinson	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000007	OMIM:608643	IEA				I		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000271	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000508	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000616	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000712	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000737	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0000975	OMIM:608643	IEA				P		HPO:skoehler	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0001263	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0001266	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0001336	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0001347	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0001742	OMIM:608643	TAS				P		HPO:skoehler	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002014	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002019	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002020	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002360	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002451	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002509	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0002615	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0003487	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0003593	OMIM:608643	IEA				C		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0003785	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0005964	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0005968	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0008872	OMIM:608643	IEA				P		HPO:iea	
OMIM	608643	AROMATIC L-AMINO ACID DECARBOXYLASE DEFICIENCY		HP:0008936	OMIM:608643	IEA				P		HPO:iea	
OMIM	608644	#608644 CILIARY DYSKINESIA, PRIMARY, 3; CILD3;;CILIARY DYSKINESIA, PRIMARY, 3, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:608644	TAS				I		HPO:probinson	
OMIM	608644	#608644 CILIARY DYSKINESIA, PRIMARY, 3; CILD3;;CILIARY DYSKINESIA, PRIMARY, 3, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:608644	TAS				P		HPO:probinson	
OMIM	608644	#608644 CILIARY DYSKINESIA, PRIMARY, 3; CILD3;;CILIARY DYSKINESIA, PRIMARY, 3, WITH OR WITHOUT SITUS INVERSUS		HP:0002205	OMIM:608644	TAS				P		HPO:probinson	
OMIM	608644	#608644 CILIARY DYSKINESIA, PRIMARY, 3; CILD3;;CILIARY DYSKINESIA, PRIMARY, 3, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:608644	IEA				P		HPO:skoehler	
OMIM	608645	%608645 DEAFNESS, AUTOSOMAL DOMINANT 31; DFNA31		HP:0000006	OMIM:608645	TAS				I		HPO:skoehler	
OMIM	608645	%608645 DEAFNESS, AUTOSOMAL DOMINANT 31; DFNA31		HP:0040113	OMIM:608645	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0000007	OMIM:608647	TAS				I		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0000403	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0002110	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0002837	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0003593	OMIM:608647	TAS				C		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0011108	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0012265	OMIM:608647	TAS				P		HPO:probinson	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS	HP:0031796	HP:0012384	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0100582	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608647	#608647 CILIARY DYSKINESIA, PRIMARY, 5; CILD5;;CILIARY DYSKINESIA, PRIMARY, 5, WITHOUT SITUS INVERSUS		HP:0200073	OMIM:608647	TAS				P		HPO:skoehler	
OMIM	608652	DEAFNESS, AUTOSOMAL DOMINANT 47		HP:0000006	PMID:12634859	PCS				I		HPO:skoehler	
OMIM	608652	DEAFNESS, AUTOSOMAL DOMINANT 47		HP:0000407	PMID:12634859	PCS				P		HP:probinson	
OMIM	608653	DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM; DFNB32	HP:0012829	HP:0000007	OMIM:608653	TAS				I		HPO:skoehler	
OMIM	608653	DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM; DFNB32	HP:0012829	HP:0000365	OMIM:608653	TAS				P		HPO:skoehler	
OMIM	608653	DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM; DFNB32		HP:0000789	OMIM:608653	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	608653	DEAFNESS, AUTOSOMAL RECESSIVE 32, WITH OR WITHOUT IMMOTILE SPERM; DFNB32		HP:0012864	OMIM:608653	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0000007	PMID:14976160	PCS				I		HPO:iea	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0000970	OMIM:608654	TAS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0001256	OMIM:608654	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0001954	OMIM:608654	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0002661	OMIM:608654	TAS				P		HPO:iea	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0002754	PMID:14976160	PCS				P		HP:probinson	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0003593	OMIM:608654	IEA				C		HPO:iea	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0006121	PMID:3472625	PCS				P		HP:probinson	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V	HP:0012839	HP:0007021	PMID:14976160	PCS				P		HPO:skoehler	
OMIM	608654	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V		HP:0007328	OMIM:608654	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0000006	OMIM:608673	IEA				I		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0001265	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0001284	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0001425	OMIM:608673	TAS				I		HPO:skoehler	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0001761	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0002460	OMIM:608673	TAS				P		HPO:probinson	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0002650	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0002936	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0003387	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0003444	OMIM:608673	TAS				P		HPO:probinson	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0003477	OMIM:608673	IEA				P		HPO:iea	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0003693	OMIM:608673	TAS				P		HPO:probinson	
OMIM	608673	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2L; CMT2L		HP:0007078	OMIM:608673	IEA				P		HPO:iea	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0000007	OMIM:608681	TAS				I		HPO:probinson	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0000470	OMIM:608681	TAS				P		HPO:probinson	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0000902	PMID:15214000	PCS				P		HPO:probinson	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0002111	OMIM:608681	TAS		HP:0040284		P		HPO:probinson	44%
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0002205	OMIM:608681	TAS				P		HPO:probinson	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0003422	PMID:15214000	TAS				P		HPO:probinson	
OMIM	608681	#608681 SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE; SCDO2		HP:0003521	OMIM:608681	TAS				P		HPO:probinson	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0000006	OMIM:608687	IEA				I		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20	HP:0012825	HP:0000639	OMIM:608687	TAS				P		HPO:probinson	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0001260	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0001618	OMIM:608687	TAS				P		HPO:probinson	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0001620	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0002066	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0002070	OMIM:608687	IEA				P		HPO:skoehler	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0002174	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0003581	OMIM:608687	TAS				C		HPO:probinson	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0003677	OMIM:608687	IEA				C		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0007256	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0007338	OMIM:608687	IEA				P		HPO:iea	
OMIM	608687	SPINOCEREBELLAR ATAXIA 20		HP:0010530	OMIM:608687	IEA				P		HPO:skoehler	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000007	OMIM:608688	IEA				I		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000063	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000154	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000219	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000219	OMIM:608688	TAS				P		HPO:skoehler	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000248	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000369	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000426	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000463	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000648	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0000951	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0001250	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0001252	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0001290	OMIM:608688	TAS				P		HPO:skoehler	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0001631	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0001939	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0002007	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0002187	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0007875	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0008665	OMIM:608688	IEA				P		HPO:iea	
OMIM	608688	AICAR TRANSFORMYLASE/IMP CYCLOHYDROLASE DEFICIENCY		HP:0011220	OMIM:608688	TAS				P		HPO:skoehler	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000006	OMIM:608703	IEA				I		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000012	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000317	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000486	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000505	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000639	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0000763	OMIM:608703	TAS				P		HPO:skoehler	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0001251	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0001260	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0001272	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0001761	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0002013	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0002522	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0002650	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0003380	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0003487	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0006944	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0007328	OMIM:608703	IEA				P		HPO:iea	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0007663	OMIM:608703	TAS				P		HPO:skoehler	
OMIM	608703	%608703 SPINOCEREBELLAR ATAXIA 25; SCA25		HP:0011468	OMIM:608703	TAS				P		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000006	OMIM:608709	IEA				I		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000093	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000100	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000147	OMIM:608709	TAS				P		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000790	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000793	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0000819	OMIM:608709	TAS				P		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0001007	OMIM:608709	TAS				P		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0002719	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0003119	OMIM:608709	TAS				P		HPO:skoehler	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0003621	OMIM:608709	IEA				C		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0003745	OMIM:608709	IEA				I		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0005421	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0009002	OMIM:608709	TAS				P		HPO:probinson	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0009019	OMIM:608709	IEA				P		HPO:iea	
OMIM	608709	#608709 LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD;;APLD, SUSCEPTIBILITY TO;;BARRAQUER-SIMONS SYNDROME;;LIPODYSTROPHY, CEPHALOTHORACIC TYPE;;LIPODYSTROPHY, PARTIAL, PROGRESSIVE		HP:0009056	OMIM:608709	TAS				P		HPO:iea	
OMIM	608710	GRANULOMATOSIS WITH POLYANGIITIS		HP:0002955	OMIM:608710	IEA				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:608716	TAS				I		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000340	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000341	OMIM:608716	TAS				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000365	OMIM:608716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000520	OMIM:608716	TAS				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000750	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:608716	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001270	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001274	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001321	OMIM:608716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002079	OMIM:608716	TAS				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002119	OMIM:608716	TAS				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002472	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002539	OMIM:608716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002553	OMIM:608716	TAS				P		HPO:skoehler	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:608716	TAS				C		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0007018	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608716	MICROCEPHALY 5, PRIMARY, AUTOSOMAL RECESSIVE		HP:0009879	OMIM:608716	TAS				P		HPO:probinson	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0000007	OMIM:608720	IEA				I		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0000224	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0000458	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0000764	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0000970	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0001278	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0002936	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0003380	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0003581	OMIM:608720	IEA				C		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0004409	OMIM:608720	IEA				P		HPO:iea	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0009830	OMIM:608720	TAS				P		HPO:skoehler	
OMIM	608720	608720 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA		HP:0040078	OMIM:608720	TAS				P		HPO:skoehler	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0000007	OMIM:608728	TAS				I		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0000922	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0000926	PMID:15121775	PCS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0001377	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002515	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002651	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002868	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002938	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002979	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0002983	OMIM:608728	TAS				P		HPO:skoehler	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0003016	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0003026	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0003173	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0003180	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0003300	PMID:15121775	PCS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0005054	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0005257	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0008794	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0008873	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0010582	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608728	#608728 SPONDYLOEPIMETAPHYSEAL DYSPLASIA, MATRILIN-3 RELATED;;SEMD, MATN3-RELATED		HP:0010585	OMIM:608728	TAS				P		HPO:probinson	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000007	OMIM:608747	IEA				I		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000252	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000347	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000407	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000508	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000736	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000752	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0000938	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0001249	OMIM:608747	IEA				P		HPO:skoehler	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0001270	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0001511	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0001939	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0002750	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0003577	OMIM:608747	IEA				C		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0004322	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0004325	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0009466	OMIM:608747	IEA				P		HPO:iea	
OMIM	608747	#608747 INSULIN-LIKE GROWTH FACTOR I DEFICIENCY;;IGF1 DEFICIENCY;;GROWTH RETARDATION WITH SENSORINEURAL DEAFNESS AND MENTAL RETARDATION		HP:0030084	OMIM:608747	TAS				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0000006	OMIM:608751	TAS				I		HPO:probinson	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0000007	OMIM:608751	TAS				I		HPO:probinson	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001635	OMIM:608751	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001639	PMID:12021217	PCS				P		HPO:probinson	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001645	OMIM:608751	TAS				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001663	OMIM:608751	TAS				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001712	OMIM:608751	IEA				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001723	PMID:12021217	PCS				P		HPO:probinson	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0001962	OMIM:608751	TAS				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0002875	OMIM:608751	TAS				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0006685	PMID:12021217	PCS				P		HPO:probinson	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0010872	OMIM:608751	IEA				P		HPO:skoehler	
OMIM	608751	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8; CMH8		HP:0031295	OMIM:608751	IEA				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0000006	PMID:12404107	PCS				I		HPO:probinson	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0001645	OMIM:608758	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0001663	OMIM:608758	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0001670	OMIM:608758	TAS				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0001712	OMIM:608758	IEA				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0001962	OMIM:608758	TAS				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0002094	OMIM:608758	TAS				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0002321	OMIM:608758	TAS				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0004755	OMIM:608758	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0004756	OMIM:608758	TAS				P		HPO:probinson	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0005144	OMIM:608758	TAS				P		HPO:probinson	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0010872	OMIM:608758	IEA				P		HPO:skoehler	
OMIM	608758	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10; CMH10		HP:0100749	OMIM:608758	TAS				P		HPO:skoehler	
OMIM	608762	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3; EIG3		HP:0000007	OMIM:608762	TAS				I		HPO:skoehler	
OMIM	608762	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3; EIG3		HP:0000992	OMIM:608762	TAS				P		HPO:skoehler	
OMIM	608762	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3; EIG3		HP:0001250	OMIM:608762	IEA				P		HPO:skoehler	
OMIM	608762	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 3; EIG3		HP:0002069	OMIM:608762	TAS				P		HPO:skoehler	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000007	OMIM:608763	IEA				I		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000023	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000275	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000365	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000518	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0000974	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0001073	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0001249	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0001388	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0001763	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0002816	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0002827	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0003199	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0007407	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0007633	OMIM:608763	IEA				P		HPO:iea	
OMIM	608763	EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE		HP:0045025	OMIM:608763	TAS				P		HPO:skoehler	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0000006	OMIM:608768	IEA				I		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0000514	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0000639	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0000641	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0000763	OMIM:608768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0001257	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0001260	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0001272	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0001337	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0002015	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0002062	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0002073	OMIM:608768	IEA				P		HPO:iea	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0002311	OMIM:608768	TAS				P		HPO:skoehler	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0007256	OMIM:608768	TAS				P		HPO:skoehler	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0007772	OMIM:608768	IEA				P		HPO:skoehler	
OMIM	608768	#608768 SPINOCEREBELLAR ATAXIA 8; SCA8		HP:0009830	OMIM:608768	IEA				P		HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000007	PMID:15945070	PCS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000248	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000252	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000316	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000343	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000565	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0000969	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001249	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001250	PMID:15148656	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001263	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001272	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001290	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001347	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001433	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001508	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001541	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001671	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001698	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0001999	OMIM:608776	IEA		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	HP:0040284
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002007	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002188	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002283	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002465	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002652	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0002750	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0003186	PMID:15945070	PCS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:probinson	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0003196	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0005280	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0006610	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608776	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Il; CDG1L		HP:0200134	OMIM:608776	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL; CDG1L	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000126	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000160	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000278	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000294	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000319	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000341	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000347	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000365	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000369	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000377	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000445	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000582	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000952	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0000998	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001181	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001250	OMIM:608779	IEA		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	HP:0040284
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001272	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001290	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001410	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001508	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001511	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001627	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001635	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001943	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0001999	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0002020	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0002059	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0002079	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0002240	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0002910	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0003196	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0003202	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0003236	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0004425	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0010557	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0010808	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0011968	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0012448	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0012471	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0012736	OMIM:608779	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HP:probinson	
OMIM	608779	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E		HP:0012745	OMIM:608779	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIE; CDG2E	HPO:skoehler	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0000007	OMIM:608782	IEA				I		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0000639	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0001249	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0001250	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0001252	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0001263	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0001290	OMIM:608782	TAS				P		HPO:skoehler	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0002015	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0002066	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0002928	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0003128	OMIM:608782	IEA				P		HPO:iea	
OMIM	608782	PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY		HP:0003593	OMIM:608782	IEA				C		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000007	OMIM:608799	IEA				I		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000316	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000319	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000347	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000486	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000488	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000494	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000639	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0000648	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001009	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001028	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001103	PMID:16641202	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001250	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001251	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001252	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001290	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001337	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001508	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001643	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001744	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0001976	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002098	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002164	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002240	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002353	OMIM:608799	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002395	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002705	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002910	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0002910	PMID:10642602	PCS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003236	OMIM:608799	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003560	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003593	OMIM:608799	TAS				C		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003642	OMIM:608799	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003645	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003676	OMIM:608799	TAS				C		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0003828	OMIM:608799	TAS				C		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0004279	OMIM:608799	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0004855	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0005280	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0005469	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0005484	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0005543	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0006380	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0006466	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0006879	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0009824	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0011344	OMIM:608799	TAS				P		HPO:probinson	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0012385	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0100704	OMIM:608799	IEA				P		HPO:iea	
OMIM	608799	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IE		HP:0200055	OMIM:608799	TAS				P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0000007	OMIM:608800	IEA				I		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0000028	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0000033	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0000478	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0001308	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0001510	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0001608	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0001662	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0001939	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME	HP:0012828	HP:0002020	OMIM:608800	TAS				P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0002104	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0006543	OMIM:608800	TAS	HP:0003593			P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0008708	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0008715	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0008733	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0008872	OMIM:608800	IEA				P		HPO:iea	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0010307	OMIM:608800	TAS				P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0025425	OMIM:608800	TAS				P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0025428	OMIM:608800	TAS				P		HPO:skoehler	
OMIM	608800	SUDDEN INFANT DEATH WITH DYSGENESIS OF THE TESTES SYNDROME		HP:0025431	OMIM:608800	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0000007	OMIM:608804	IEA				I		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0000545	OMIM:608804	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0000648	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001250	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001251	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001260	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001263	OMIM:608804	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001266	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001270	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001332	OMIM:608804	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0001583	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002059	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002063	OMIM:608804	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002080	OMIM:608804	TAS				P		HPO:probinson	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002191	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002313	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002415	OMIM:608804	TAS				P		HPO:probinson	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002465	OMIM:608804	TAS				P		HPO:skoehler	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0002599	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0003390	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0003431	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0003487	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0003593	OMIM:608804	IEA				C		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0006808	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0007220	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0008936	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0010628	OMIM:608804	IEA				P		HPO:iea	
OMIM	608804	#608804 LEUKODYSTROPHY, HYPOMYELINATING, 2; HLD2;;PELIZAEUS-MERZBACHER-LIKE DISEASE, 1; PMLD1		HP:0100543	OMIM:608804	TAS				P		HPO:probinson	
OMIM	608805	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1		HP:0000006	OMIM:608805	TAS				I		HPO:skoehler	
OMIM	608805	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1		HP:0005743	OMIM:608805	TAS				P		HPO:skoehler	
OMIM	608805	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 1		HP:0040160	OMIM:608805	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0000007	OMIM:608807	IEA				I		HPO:iea	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0002460	OMIM:608807	IEA				P		HPO:iea	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J	HP:0012825	HP:0003236	OMIM:608807	TAS				P		HPO:probinson	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0003236	OMIM:608807	IEA				P		HPO:skoehler	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0003458	OMIM:608807	IEA				P		HPO:iea	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0003560	OMIM:608807	IEA				P		HPO:iea	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0003701	OMIM:608807	IEA				P		HPO:iea	
OMIM	608807	#608807 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J; LGMD2J		HP:0011463	OMIM:608807	TAS				C		HPO:probinson	
OMIM	608808	TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 1		HP:0000006	OMIM:608808	TAS				I		HPO:skoehler	
OMIM	608808	TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 1		HP:0001669	PMID:14638541	PCS				P		HPO:probinson	
OMIM	608808	TRANSPOSITION OF THE GREAT ARTERIES, DEXTRO-LOOPED 1		HP:0003829	OMIM:608808	TAS				C		HPO:skoehler	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0000007	OMIM:608809	IEA				I		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0000666	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0000964	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001252	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001285	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001290	OMIM:608809	TAS				P		HPO:skoehler	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001369	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001417	OMIM:608809	IEA				I		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001508	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0001875	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002014	OMIM:608809	PCS				P		HPO:probinson	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002015	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002069	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002104	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002119	OMIM:608809	PCS				P		HPO:probinson	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002352	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002583	OMIM:608809	IEA				P		HPO:skoehler	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0002719	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0003429	OMIM:608809	TAS				P		HPO:skoehler	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0003565	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0004315	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0005231	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0005484	OMIM:608809	IEA				P		HPO:iea	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0006808	OMIM:608809	PCS				P		HPO:probinson	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0007371	OMIM:608809	PCS				P		HPO:probinson	
OMIM	608809	LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA		HP:0011344	OMIM:608809	PCS				P		HPO:probinson	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0000006	OMIM:608810	IEA				I		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0000467	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0000518	OMIM:608810	TAS				P		HPO:probinson	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0001639	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0002460	OMIM:608810	TAS				P		HPO:probinson	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0002747	OMIM:608810	TAS				P		HPO:skoehler	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003236	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003325	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003458	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003555	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003560	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003581	OMIM:608810	IEA				C		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003677	OMIM:608810	IEA				C		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003694	OMIM:608810	TAS				P		HPO:probinson	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0003736	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0009027	OMIM:608810	IEA				P		HPO:iea	
OMIM	608810	#608810 MYOPATHY, MYOFIBRILLAR, 2, MFM2;;MYOPATHY, MYOFIBRILLAR, ALPHA-B CRYSTALLIN-RELATED;;MYOPATHY, DESMIN-RELATED, ASSOCIATED WITH MUTATION IN THE CRYAB GENE;;ALPHA-B CRYSTALLINOPATHY		HP:0009072	OMIM:608810	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000007	OMIM:608836	IEA				I		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000073	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000083	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000105	OMIM:608836	TAS	HP:0003577			P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000113	OMIM:608836	TAS	HP:0003577			P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000126	OMIM:608836	IEA				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000189	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000218	OMIM:608836	IEA				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000252	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000340	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000348	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000358	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000369	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000396	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000414	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0000518	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001182	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001250	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001254	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001274	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001319	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001403	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001562	OMIM:608836	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001640	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001644	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001760	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001800	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001958	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0001987	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002093	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002098	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002104	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002119	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002126	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002240	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002878	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002910	PMID:11389301	PCS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0002987	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0003455	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0003455	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0003573	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0006380	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0006559	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0006610	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0006799	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0007023	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0007229	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0008293	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0008315	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0008872	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0009058	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0010511	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0011220	OMIM:608836	PCS				P		HPO:probinson	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0011309	OMIM:608836	TAS				P		HPO:skoehler	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0011675	OMIM:608836	IEA				P		HPO:iea	
OMIM	608836	#608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL;;CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL;;CPT II DEFICIENCY, LETHAL NEONATAL;;CPT2 DEFICIENCY, LETHAL NEONATAL		HP:0011936	OMIM:608836	TAS				P		HPO:probinson	
OMIM	608837	#608837 CARNEY COMPLEX VARIANT		HP:0000006	PMID:15282353	PCS				I		HPO:probinson	
OMIM	608837	#608837 CARNEY COMPLEX VARIANT		HP:0000211	PMID:15282353	PCS				P		HPO:probinson	
OMIM	608837	#608837 CARNEY COMPLEX VARIANT		HP:0005684	PMID:15282353	PCS				P		HPO:probinson	
OMIM	608837	#608837 CARNEY COMPLEX VARIANT		HP:0011672	PMID:15282353	PCS				P		HPO:probinson	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0000007	OMIM:608840	IEA				I		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0000158	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0000654	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0000666	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001252	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001263	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001270	OMIM:608840	IEA				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001290	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001302	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001321	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0001771	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002187	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002269	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002365	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002395	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002518	OMIM:608840	IEA				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0002987	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003236	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003458	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003487	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003560	OMIM:608840	TAS				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003593	OMIM:608840	IEA				C		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003701	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0003741	OMIM:608840	IEA				P		HPO:skoehler	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0004322	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0009473	OMIM:608840	IEA				P		HPO:iea	
OMIM	608840	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6		HP:0010628	OMIM:608840	IEA				P		HPO:iea	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0000006	OMIM:608850	TAS				I		HPO:probinson	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0000551	OMIM:608850	TAS				P		HPO:probinson	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0000603	OMIM:608850	TAS				P		HPO:probinson	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0007663	OMIM:608850	TAS				P		HPO:probinson	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0007722	OMIM:608850	TAS				P		HPO:probinson	
OMIM	608850	MACULAR DYSTROPHY, RETINAL, 3; MCDR3		HP:0030499	OMIM:608850	TAS				P		HPO:probinson	
OMIM	608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6		HP:0000175	OMIM:608864	TAS				P		HPO:skoehler	
OMIM	608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6		HP:0000204	OMIM:608864	TAS				P		HPO:skoehler	
OMIM	608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6		HP:0001425	OMIM:608864	TAS				I		HPO:skoehler	
OMIM	608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6		HP:0003745	OMIM:608864	TAS				I		HPO:skoehler	
OMIM	608864	OROFACIAL CLEFT 6, SUSCEPTIBILITY TO; OFC6		HP:0010982	OMIM:608864	TAS				I		HPO:skoehler	
OMIM	608874	#608874 OROFACIAL CLEFT 5; OFC5;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 5		HP:0000006	PMID:10742093	TAS				I		HPO:probinson	
OMIM	608874	#608874 OROFACIAL CLEFT 5; OFC5;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 5		HP:0000175	OMIM:608874	TAS				P		HPO:probinson	
OMIM	608874	#608874 OROFACIAL CLEFT 5; OFC5;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 5		HP:0000204	OMIM:608874	TAS				P		HPO:probinson	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0000006	OMIM:608885	TAS				I		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0000252	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0000518	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0000639	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0000952	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001249	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001250	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001251	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001257	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001263	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001344	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001347	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0001744	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN	HP:0025303	HP:0001878	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0002153	OMIM:608885	IEA				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0002240	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0002540	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0003593	OMIM:608885	TAS				C		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0004322	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0011972	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608885	STOMATIN-DEFICIENT CRYOHYDROCYTOSIS WITH NEUROLOGIC DEFECTS; SDCHCN		HP:0012448	OMIM:608885	TAS				P		HPO:skoehler	
OMIM	608890	WAARDENBURG SYNDROME, TYPE 2D; WS2D		HP:0000007	OMIM:608890	IEA				I		HPO:skoehler	
OMIM	608890	WAARDENBURG SYNDROME, TYPE 2D; WS2D		HP:0000506	OMIM:608890	IEA				P		HPO:skoehler	
OMIM	608890	WAARDENBURG SYNDROME, TYPE 2D; WS2D		HP:0001100	OMIM:608890	IEA				P		HPO:skoehler	
OMIM	608890	WAARDENBURG SYNDROME, TYPE 2D; WS2D		HP:0001425	OMIM:608890	IEA				I		HPO:skoehler	
OMIM	608890	WAARDENBURG SYNDROME, TYPE 2D; WS2D		HP:0008527	OMIM:608890	IEA				P		HPO:skoehler	
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0000006	OMIM:608895	TAS				I		HPO:skoehler	
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0000608	PMID:15269314	PCS	HP:0003584	HP:0040284		P		HPO:probinson	9/19
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0000762	OMIM:608895	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0000974	PMID:21576112	PCS		HP:0040284		P		HPO:skoehler	4/18
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0001382	PMID:21576112	PCS		HP:0040284		P		HPO:skoehler	2/18
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0001761	PMID:21576112	PCS				P		HPO:probinson	
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0002460	PMID:21576112	PCS		HP:0040284		P		HPO:probinson	18/22
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0002936	PMID:21576112	PCS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0003477	PMID:21576112	PCS		HP:0040284		P		HPO:skoehler	18/18
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0003693	PMID:21576112	PCS		HP:0040284		P		HPO:probinson	18/22
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0011506	PMID:21576112	PCS				P		HPO:probinson	
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0011510	PMID:15269314	PCS				P		HPO:probinson	
OMIM	608895	#608895 MACULAR DEGENERATION, AGE-RELATED, 3; ARMD3		HP:0011808	PMID:21576112	PCS		HP:0040284		P		HPO:probinson	18/23
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0000007	PMID:16825436	PCS				I		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0001433	PMID:16825436	PCS				P		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0001903	PMID:16825436	PCS		HP:0040284		P		HPO:probinson	12/14
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0001913	PMID:16825436	PCS		HP:0040284		P		HPO:probinson	11/14
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0001945	PMID:16825436	PCS				P		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0002155	PMID:16825436	PCS				P		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0011900	PMID:16825436	PCS				P		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0012156	PMID:16825436	PCS				P		HPO:probinson	
OMIM	608898	#608898 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3; FHL3;;HPLH3;;HLH3		HP:0012178	PMID:16825436	PCS		HP:0040284		P		HPO:probinson	13/13
OMIM	608902	DRUG METABOLISM, POOR, CYP2D6-RELATEDDRUG METABOLISM, ULTRARAPID, CYP2D6-RELATED, INCLUDED		HP:0000007	OMIM:608902	TAS				I		HPO:probinson	
OMIM	608902	DRUG METABOLISM, POOR, CYP2D6-RELATEDDRUG METABOLISM, ULTRARAPID, CYP2D6-RELATED, INCLUDED		HP:0001939	OMIM:608902	IEA				P		HPO:iea	
OMIM	608902	DRUG METABOLISM, POOR, CYP2D6-RELATEDDRUG METABOLISM, ULTRARAPID, CYP2D6-RELATED, INCLUDED		HP:0002664	OMIM:608902	IEA				P		HPO:iea	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0000006	OMIM:608907	TAS				I		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0000716	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0000734	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0002071	OMIM:608907	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0002120	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0002185	OMIM:608907	IEA				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9	HP:0003676	HP:0002354	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0002511	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0100256	OMIM:608907	TAS				P		HPO:skoehler	
OMIM	608907	ALZHEIMER DISEASE 9, SUSCEPTIBILITY TO; AD9		HP:0410170	OMIM:608907	IEA				P		HPO:skoehler	
OMIM	608908	#608908 MYOPIA 6; MYP6		HP:0000006	OMIM:608908	TAS				I		HPO:skoehler	
OMIM	608908	#608908 MYOPIA 6; MYP6		HP:0000545	OMIM:608908	TAS				P		HPO:skoehler	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000006	OMIM:608930	IEA				I		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000007	OMIM:608930	IEA				I		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000218	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000347	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000400	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000467	OMIM:608930	TAS				P		HPO:skoehler	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000508	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0000597	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0001260	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0001270	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0001283	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0001319	OMIM:608930	TAS				P		HPO:skoehler	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0001612	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0002015	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0002033	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0002650	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0002747	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0002804	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003324	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003388	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003391	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003402	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003554	OMIM:608930	IEA				P		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003593	OMIM:608930	IEA				C		HPO:iea	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0003828	OMIM:608930	TAS				C		HPO:skoehler	
OMIM	608930	MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL; CMS1B		HP:0010628	OMIM:608930	TAS				P		HPO:skoehler	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000007	OMIM:608931	IEA				I		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000218	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000276	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000303	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000486	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000508	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000597	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0000689	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0001260	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0001270	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0001290	OMIM:608931	TAS				P		HPO:skoehler	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0001558	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0001612	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0002015	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0002715	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0002747	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0002804	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003199	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003202	OMIM:608931	TAS				P		HPO:skoehler	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003388	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003391	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003394	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003403	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003443	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003473	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY	HP:0012837	HP:0003473	OMIM:608931	TAS				P		HPO:probinson	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003554	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003593	OMIM:608931	IEA				C		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003680	OMIM:608931	IEA				C		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0003828	OMIM:608931	IEA				C		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0010628	OMIM:608931	IEA				P		HPO:iea	
OMIM	608931	MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY		HP:0011968	OMIM:608931	TAS				P		HPO:skoehler	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000007	OMIM:608940	TAS				I		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000403	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000529	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000548	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000639	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000689	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0000887	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0001156	OMIM:608940	TAS				P		HPO:skoehler	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0001387	PMID:24387990	PCS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0002650	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0002657	OMIM:608940	TAS				P		HPO:skoehler	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0002812	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0002980	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0002982	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0003016	PMID:24387990	PCS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0003021	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0003025	PMID:24387990	PCS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0003300	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0003375	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0004565	OMIM:608940	TAS	HP:0011463			P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0008002	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0008821	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0008897	OMIM:608940	TAS				P		HPO:skoehler	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0008905	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0009381	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608940	#608940 SPONDYLOMETAPHYSEAL DYSPLASIA WITH CONE-ROD DYSTROPHY; SMDCRD		HP:0010049	OMIM:608940	TAS				P		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0000007	OMIM:608957	TAS				I		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0002110	OMIM:608957	TAS				P		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0002205	OMIM:608957	TAS				P		HPO:skoehler	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0002718	OMIM:608957	TAS				P		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0003577	OMIM:608957	TAS				C		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0004429	OMIM:608957	TAS				P		HPO:probinson	
OMIM	608957	CD8 DEFICIENCY, FAMILIAL		HP:0005422	OMIM:608957	TAS				P		HPO:probinson	
OMIM	608970	MACULAR DYSTROPHY, PATTERNED, 2; MDPT2		HP:0000006	OMIM:608970	TAS				I		HPO:skoehler	
OMIM	608970	MACULAR DYSTROPHY, PATTERNED, 2; MDPT2		HP:0008001	OMIM:608970	IEA				P		HPO:skoehler	
OMIM	608970	MACULAR DYSTROPHY, PATTERNED, 2; MDPT2		HP:0011510	OMIM:608970	IEA				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000007	PMID:11023514	PCS				I		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000155	PMID:11023514	PCS				P		HPO:probinson	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000388	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000964	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0001744	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002014	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002240	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002716	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0004430	OMIM:608971	IEA				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0005390	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0005403	PMID:11023514	PCS				P		HPO:probinson	
OMIM	608971	#608971 SEVERE COMBINED IMMUNODEFICIENCY, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE,B CELL-POSITIVE, NK CELL-POSITIVE;;SCID, AUTOSOMAL RECESSIVE, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0008866	OMIM:608971	TAS				P		HPO:skoehler	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0000007	PMID:19732862	PCS				I		HPO:probinson	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0000077	OMIM:608980	IEA				P		HPO:skoehler	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0000143	OMIM:608980	TAS				P		HPO:probinson	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0000322	OMIM:608980	TAS				P		HPO:probinson	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0000414	OMIM:608980	TAS				P		HPO:probinson	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0001545	OMIM:608980	TAS				P		HPO:probinson	
OMIM	608980	#608980 BIFID NOSE WITH OR WITHOUT ANORECTAL AND RENAL ANOMALIES; BNAR		HP:0011803	PMID:19732862	PCS				P		HPO:probinson	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:608984	IEA				I		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0001265	OMIM:608984	IEA				P		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0001284	OMIM:608984	IEA				P		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0002403	OMIM:608984	IEA				P		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0003409	OMIM:608984	TAS				P		HPO:skoehler	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0003487	OMIM:608984	IEA				P		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0003581	OMIM:608984	IEA				C		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0006962	OMIM:608984	IEA				P		HPO:iea	
OMIM	608984	ATAXIA, SENSORY, AUTOSOMAL DOMINANT		HP:0010871	OMIM:608984	IEA				P		HPO:skoehler	
OMIM	608995	DYSLEXIA, SUSCEPTIBILITY TO, 8		HP:0000006	OMIM:608995	IEA				I		HPO:iea	
OMIM	608995	DYSLEXIA, SUSCEPTIBILITY TO, 8		HP:0001426	OMIM:608995	IEA				I		HPO:iea	
OMIM	608995	DYSLEXIA, SUSCEPTIBILITY TO, 8		HP:0010522	OMIM:608995	IEA				P		HPO:skoehler	
OMIM	608996	PREMATURE OVARIAN FAILURE 3		HP:0000006	PMID:19429596	PCS				I		HPO:probinson	
OMIM	608996	PREMATURE OVARIAN FAILURE 3		HP:0000013	OMIM:608996	TAS				P		HPO:skoehler	
OMIM	608996	PREMATURE OVARIAN FAILURE 3		HP:0000869	OMIM:608996	TAS				P		HPO:skoehler	
OMIM	608996	PREMATURE OVARIAN FAILURE 3		HP:0008209	PMID:19429596	PCS				P		HPO:probinson	
OMIM	609006	#609006 DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT;DFNB36DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT, INCLUDED		HP:0000007	OMIM:609006	TAS				I		HPO:probinson	
OMIM	609006	#609006 DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT;DFNB36DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT, INCLUDED		HP:0000407	OMIM:609006	TAS	HP:0003593			P		HPO:probinson	
OMIM	609006	#609006 DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT;DFNB36DEAFNESS, AUTOSOMAL DOMINANT, WITHOUT VESTIBULAR INVOLVEMENT, INCLUDED		HP:0008568	OMIM:609006	TAS				P		HPO:probinson	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0000276	OMIM:609008	TAS				P		HPO:probinson	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0000303	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0000545	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0000768	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001132	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001166	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001187	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001519	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001634	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001642	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001659	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0001696	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002058	OMIM:609008	TAS				P		HPO:probinson	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002616	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002650	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002808	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002816	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0002870	OMIM:609008	IEA				P		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0003745	OMIM:609008	IEA				I		HPO:iea	
OMIM	609008	MARFANOID HABITUS WITH SITUS INVERSUS		HP:0005301	OMIM:609008	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0000007	OMIM:609015	IEA				I		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0000580	PMID:12838198	PCS		HP:0040284		P		HPO:probinson	2/16
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001252	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001263	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001290	OMIM:609015	TAS				P		HPO:skoehler	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001508	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001518	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001560	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001635	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001644	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001789	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001985	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0001987	OMIM:609015	TAS				P		HPO:skoehler	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0002093	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0002686	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0002878	OMIM:609015	TAS				P		HPO:skoehler	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0002910	OMIM:609015	TAS				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0002913	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003128	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003198	OMIM:609015	IEA				P		HPO:skoehler	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003201	OMIM:609015	TAS				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003324	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003326	OMIM:609015	TAS				P		HPO:skoehler	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0003326	OMIM:609015	IEA				P		HPO:iea	
OMIM	609015	MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MTPD		HP:0009830	OMIM:609015	IEA				P		HPO:skoehler	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0000007	OMIM:609016	TAS				I	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0000580	OMIM:609016	TAS				P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0001252	OMIM:609016	TAS	HP:0003593			P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0001638	OMIM:609016	TAS	HP:0003593			P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0001699	OMIM:609016	TAS				M	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0001943	OMIM:609016	TAS	HP:0003593			P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0002240	OMIM:609016	TAS	HP:0003593			P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609016	#609016 LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY		HP:0100950	OMIM:609016	TAS				P	#609016 LONG-CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY;;LCHAD DEFICIENCY	HPO:probinson	
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0000007	OMIM:609021	TAS				I		HPO:probinson	
OMIM	609021	PERIPHERAL CONE DYSTROPHY	HP:0012825	HP:0000543	OMIM:609021	TAS				P		HPO:probinson	
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0000548	OMIM:609021	IEA				P		HPO:skoehler	
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0000648	OMIM:609021	TAS		HP:0040284		P		HPO:probinson	2/3
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0000980	OMIM:609021	IEA				P		HPO:skoehler	
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0007761	OMIM:609021	TAS		HP:0040284		P		HPO:probinson	2/3
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0007769	OMIM:609021	TAS				P		HPO:probinson	
OMIM	609021	PERIPHERAL CONE DYSTROPHY		HP:0030528	OMIM:609021	IEA				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000023	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000028	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000054	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000089	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000104	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000175	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000218	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000252	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000324	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000343	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000347	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000365	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000369	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000384	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000400	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000403	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000474	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0000486	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000490	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000545	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000582	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000678	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000680	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000750	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0000776	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001195	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001249	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001250	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0001252	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001263	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0001290	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0001374	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001511	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001629	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001631	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001642	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001643	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001650	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001660	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0001939	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0002019	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002020	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002023	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0002059	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002079	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002205	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002562	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0002650	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0002808	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0004467	OMIM:609029	IEA				P		HPO:iea	
OMIM	609029	EMANUEL SYNDROME		HP:0009765	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0011968	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609029	EMANUEL SYNDROME		HP:0012802	OMIM:609029	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000007	OMIM:609033	IEA				I		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000010	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000020	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000510	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000550	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000575	OMIM:609033	IEA				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000618	OMIM:609033	TAS	HP:0003581			P		HPO:probinson	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000648	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0000662	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0001249	OMIM:609033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0001251	OMIM:609033	IEA				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0001284	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002136	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002166	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002403	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002460	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002571	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0002650	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0003202	OMIM:609033	TAS				P		HPO:probinson	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0003448	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0003677	OMIM:609033	TAS				C		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0007737	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0009473	OMIM:609033	IEA				P		HPO:iea	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0010871	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0011463	OMIM:609033	TAS				C		HPO:probinson	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0012385	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0030529	OMIM:609033	TAS				P		HPO:skoehler	
OMIM	609033	POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA; AXPC1		HP:0031936	OMIM:609033	IEA				P		HPO:skoehler	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000219	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000219	OMIM:609037	TAS				P		HPO:skoehler	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000252	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000276	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000316	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000319	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000387	OMIM:609037	TAS				P		HPO:skoehler	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000455	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000508	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000598	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0000648	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0001250	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0001263	OMIM:609037	TAS				P		HPO:skoehler	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0002136	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0002353	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0003745	OMIM:609037	IEA				I		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0004322	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0006887	OMIM:609037	IEA				P		HPO:iea	
OMIM	609037	MENTAL RETARDATION WITH OPTIC ATROPHY, FACIAL DYSMORPHISM, MICROCEPHALY, AND SHORT STATURE		HP:0010864	OMIM:609037	TAS				P		HPO:skoehler	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0000006	OMIM:609039	IEA				I		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0001425	OMIM:609039	TAS				I		HPO:skoehler	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0002189	OMIM:609039	IEA				P		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0002330	OMIM:609039	IEA				P		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0002494	OMIM:609039	IEA				P		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0002519	OMIM:609039	IEA				P		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0002524	OMIM:609039	IEA				P		HPO:iea	
OMIM	609039	NARCOLEPSY 3; NRCLP3		HP:0030050	OMIM:609039	TAS				P		HPO:skoehler	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0000006	OMIM:609040	IEA				I		HPO:iea	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0001279	OMIM:609040	IEA				P		HPO:iea	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0001645	OMIM:609040	IEA				P		HPO:iea	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0001962	OMIM:609040	IEA				P		HPO:iea	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0002617	OMIM:609040	IEA				P		HPO:skoehler	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0004308	OMIM:609040	IEA				P		HPO:iea	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0006698	OMIM:609040	TAS				P		HPO:probinson	
OMIM	609040	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 9		HP:0011663	OMIM:609040	TAS				P		HPO:probinson	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:609041	IEA				I		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:609041	TAS				P		HPO:skoehler	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:609041	IEA				P		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0002061	OMIM:609041	IEA				P		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0002395	OMIM:609041	IEA				P		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:609041	IEA				P		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0003581	OMIM:609041	IEA				C		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0005340	OMIM:609041	IEA				P		HPO:iea	
OMIM	609041	SPASTIC PARAPLEGIA 27, AUTOSOMAL RECESSIVE		HP:0006938	OMIM:609041	IEA				P		HPO:iea	
OMIM	609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3		HP:0000006	OMIM:609048	TAS				I		HPO:probinson	
OMIM	609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3		HP:0001054	OMIM:609048	TAS				P		HPO:probinson	
OMIM	609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3		HP:0001062	OMIM:609048	TAS				P		HPO:probinson	
OMIM	609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3		HP:0001074	OMIM:609048	TAS				P		HPO:probinson	
OMIM	609048	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3		HP:0012056	OMIM:609048	TAS				P		HPO:probinson	
OMIM	609049	PIERSON SYNDROME		HP:0000007	OMIM:609049	IEA				I		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0000093	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0000100	OMIM:609049	TAS	HP:0003623			P		HPO:probinson	
OMIM	609049	PIERSON SYNDROME		HP:0000618	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0000969	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0001252	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0001284	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0001290	OMIM:609049	TAS				P		HPO:skoehler	
OMIM	609049	PIERSON SYNDROME		HP:0001967	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0003075	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0003623	OMIM:609049	TAS				C		HPO:probinson	
OMIM	609049	PIERSON SYNDROME		HP:0003774	OMIM:609049	IEA	HP:0003593			P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0007676	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0007774	OMIM:609049	IEA				P		HPO:iea	
OMIM	609049	PIERSON SYNDROME		HP:0011502	OMIM:609049	TAS				P		HPO:probinson	
OMIM	609049	PIERSON SYNDROME		HP:0025492	OMIM:609049	IEA				P		HPO:skoehler	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0000007	OMIM:609052	IEA				I		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0000268	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0000768	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0000920	OMIM:609052	TAS				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0000926	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0001156	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0002657	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0002673	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003016	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003025	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003090	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003180	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003300	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003375	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003510	OMIM:609052	IEA				P		HPO:skoehler	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0003918	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0004699	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0004979	OMIM:609052	TAS				P		HPO:probinson	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0005041	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0006369	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0006623	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0008076	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0008873	OMIM:609052	IEA				P		HPO:iea	
OMIM	609052	%609052 SPONDYLOMETAPHYSEAL DYSPLASIA, TYPE A4		HP:0100865	OMIM:609052	TAS				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000007	PMID:17452773	PCS				I		HPO:probinson	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000085	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000089	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000325	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000405	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000483	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000545	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000568	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000609	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000821	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000824	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0000980	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001263	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001274	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001331	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001511	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001629	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0001655	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0002308	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0002949	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0003221	PMID:17452773	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0004322	PMID:17452773	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0005528	PMID:17452773	PCS	HP:0011463	HP:0040284		P		HPO:probinson	7/7
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0009777	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0010034	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0012210	PMID:17452773	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0030048	OMIM:609053	IEA				P		HPO:skoehler	
OMIM	609053	FANCONI ANEMIA, COMPLEMENTATION GROUP I; FANCI		HP:0030680	PMID:17452773	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0000007	PMID:16116424	PCS				I		HPO:probinson	
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0000568	PMID:16116424	PCS		HP:0040284		P		HPO:probinson	4/11
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0001263	PMID:16116424	PCS				P		HPO:probinson	
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0001511	PMID:16116424	PCS		HP:0040284		P		HPO:probinson	3/11
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0003221	PMID:16116424	PCS				P		HPO:probinson	
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0005528	PMID:16116424	PCS				P		HPO:probinson	
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0007565	PMID:16116424	PCS		HP:0040284		P		HPO:probinson	8/11
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0008897	PMID:16116424	PCS				P		HPO:probinson	
OMIM	609054	#609054 FANCONI ANEMIA, COMPLEMENTATION GROUP J; FANCJ		HP:0009778	PMID:16116424	PCS		HP:0040284		P		HPO:probinson	3/11
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0000007	OMIM:609055	IEA				I		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0000510	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0000529	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0000648	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0000654	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0001249	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0001250	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0001251	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0001260	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0001922	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002059	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002063	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002168	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002300	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002361	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0002505	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0003205	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0003208	OMIM:609055	IEA				P		HPO:iea	
OMIM	609055	CEROID LIPOFUSCINOSIS, NEURONAL, 9		HP:0003819	OMIM:609055	IEA				M		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000007	OMIM:609056	IEA				I		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000252	OMIM:609056	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000365	OMIM:609056	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000572	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000648	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0000737	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001034	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001252	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001263	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001266	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001290	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001336	OMIM:609056	IEA				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001344	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0001508	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002013	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002069	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002133	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002283	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002376	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0002395	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0006834	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0008872	OMIM:609056	IEA				P		HPO:iea	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0010841	OMIM:609056	IEA				P		HPO:skoehler	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0012391	OMIM:609056	TAS				P		HPO:probinson	
OMIM	609056	SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS		HP:0100704	OMIM:609056	TAS				P		HPO:skoehler	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0000007	PMID:15265795	PCS				I		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0000112	OMIM:609057	IEA				P		HPO:skoehler	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0000123	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0000407	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0003774	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0007678	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0008404	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0011906	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609057	#609057 NEPHROPATHY WITH PRETIBIAL EPIDERMOLYSIS BULLOSA AND DEAFNESS		HP:0012221	PMID:15265795	PCS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0000007	OMIM:609060	IEA				I		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE	HP:0012825	HP:0000252	OMIM:609060	TAS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0000639	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0000817	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE	HP:0031375	HP:0001250	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0001257	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0001270	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0001347	OMIM:609060	TAS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0001396	OMIM:609060	TAS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0001511	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE	HP:0012828	HP:0001942	OMIM:609060	TAS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002079	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002151	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002240	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002283	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002375	OMIM:609060	TAS				P		HPO:probinson	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0002490	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0003577	OMIM:609060	IEA				C		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0004448	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0006799	OMIM:609060	IEA				P		HPO:iea	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0008936	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0011968	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609060	#609060 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 1; COXPD1;;HEPATOENCEPHALOPATHY, EARLY FATAL PROGRESSIVE		HP:0012448	OMIM:609060	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000007	OMIM:609069	TAS				I		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000252	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000325	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000331	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000369	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000377	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000444	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000609	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000768	OMIM:609069	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0000819	OMIM:609069	IEA				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001250	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001265	OMIM:609069	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001321	OMIM:609069	IEA				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001387	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001508	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001522	OMIM:609069	TAS				M		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001684	OMIM:609069	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0001943	OMIM:609069	IEA				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0002104	OMIM:609069	IEA				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0003074	OMIM:609069	IEA				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0003758	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0010557	OMIM:609069	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609069	PANCREATIC AND CEREBELLAR AGENESIS; PACA		HP:0012642	OMIM:609069	TAS				P		HPO:skoehler	
OMIM	609070	HEMOGLOBIN, HIGH OXYGEN SATURATION OF		HP:0000006	OMIM:609070	IEA				I		HPO:iea	
OMIM	609070	HEMOGLOBIN, HIGH OXYGEN SATURATION OF		HP:0001871	OMIM:609070	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0000006	OMIM:609115	TAS				I		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0000518	OMIM:609115	TAS				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0001265	OMIM:609115	IEA				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003198	OMIM:609115	TAS				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003236	OMIM:609115	TAS				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003547	OMIM:609115	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003581	OMIM:609115	IEA				C		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003677	OMIM:609115	IEA				C		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003749	OMIM:609115	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003805	OMIM:609115	TAS				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0003829	OMIM:609115	TAS				C		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0006203	OMIM:609115	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0006785	OMIM:609115	TAS				P		HPO:skoehler	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0008116	OMIM:609115	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0008948	OMIM:609115	IEA				P		HPO:iea	
OMIM	609115	LIMB-GIRDLE MUSCULAR DYSTROPHY, TYPE 1G; LGMD1G		HP:0008956	OMIM:609115	IEA				P		HPO:iea	
OMIM	609122	ANEURYSM, INTRACRANIAL BERRY, 3		HP:0000006	OMIM:609122	TAS				I		HPO:probinson	
OMIM	609122	ANEURYSM, INTRACRANIAL BERRY, 3		HP:0007029	OMIM:609122	TAS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000006	PMID:3565478	PCS				I		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000059	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000267	OMIM:609128	TAS				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000294	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000473	OMIM:609128	TAS				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000666	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000938	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0000954	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0001215	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0001762	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0002162	OMIM:609128	TAS				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0002650	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0002808	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0004626	OMIM:609128	TAS				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0005280	OMIM:609128	TAS				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0005650	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0005684	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0008110	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0008589	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0010326	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0010864	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0100499	OMIM:609128	IEA				P		HPO:skoehler	
OMIM	609128	ARTHROGRYPOSIS, DISTAL, TYPE 4; DA4		HP:0100500	PMID:3565478	PCS				P		HPO:probinson	
OMIM	609129	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1		HP:0000006	OMIM:609129	IEA				I		HPO:iea	
OMIM	609129	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1		HP:0000407	OMIM:609129	IEA				P		HPO:iea	
OMIM	609129	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1		HP:0001963	OMIM:609129	IEA				P		HPO:iea	
OMIM	609129	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1		HP:0006958	OMIM:609129	IEA				P		HPO:iea	
OMIM	609129	AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT, 1		HP:0008529	OMIM:609129	IEA				P		HPO:iea	
OMIM	609135	#609135 APLASTIC ANEMIA;;APLASTIC ANEMIA, SUSCEPTIBILITY TO, INCLUDED		HP:0001915	PMID:12090986	PCS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	609135	#609135 APLASTIC ANEMIA;;APLASTIC ANEMIA, SUSCEPTIBILITY TO, INCLUDED		HP:0005528	PMID:12090986	PCS				P		HPO:skoehler	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000006	OMIM:609136	IEA				I		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000028	OMIM:609136	TAS		HP:0040284		P		HPO:skoehler	2/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000407	OMIM:609136	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000458	OMIM:609136	TAS				P		HPO:skoehler	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000522	PMID:10762540	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000639	PMID:10762540	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000762	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0000966	PMID:10762540	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001053	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001100	PMID:10762540	PCS				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001249	OMIM:609136	TAS				P		HPO:skoehler	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001250	PMID:10762540	PCS		HP:0040284		P		HP:probinson	1/3
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001251	PMID:10762540	PCS		HP:0040284		P		HPO:iea	2/2
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001263	PMID:10762540	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001265	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001284	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001319	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0001761	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002211	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002226	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002227	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002313	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002460	PMID:10762540	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002510	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0002936	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0003693	OMIM:609136	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0004336	OMIM:609136	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0004463	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0006978	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0007108	OMIM:609136	IEA				P		HPO:iea	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0007182	OMIM:609136	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0007266	OMIM:609136	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0011096	OMIM:609136	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0011285	PMID:10762540	PCS				P		HPO:probinson	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0011382	OMIM:609136	TAS				P		HPO:skoehler	
OMIM	609136	PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH		HP:0012332	OMIM:609136	IEA				P		HPO:skoehler	
OMIM	609140	#609140 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2; PPCD2		HP:0000006	OMIM:609140	TAS				I		HPO:probinson	
OMIM	609140	#609140 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2; PPCD2		HP:0001131	OMIM:609140	TAS				P		HPO:probinson	
OMIM	609140	#609140 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2; PPCD2		HP:0007957	OMIM:609140	TAS				P		HPO:probinson	
OMIM	609141	#609141 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3		HP:0000006	OMIM:609141	TAS				I		HPO:probinson	
OMIM	609141	#609141 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3		HP:0000023	PMID:16252232	PCS		HP:0040284		P		HPO:probinson	11/14
OMIM	609141	#609141 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3		HP:0001131	OMIM:609141	TAS				P		HPO:probinson	
OMIM	609141	#609141 CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3; PPCD3		HP:0012038	OMIM:609141	TAS				P		HPO:probinson	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0000006	OMIM:609152	IEA				I		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0000750	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0000752	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0000836	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0000853	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001249	OMIM:609152	TAS				P		HPO:skoehler	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001270	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001518	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001622	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001649	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0001939	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0003745	OMIM:609152	IEA				I		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0005616	OMIM:609152	IEA				P		HPO:iea	
OMIM	609152	#609152 HYPERTHYROIDISM, NONAUTOIMMUNE;;HYPERTHYROIDISM, CONGENITAL NONAUTOIMMUNE;;HYPERTHYROIDISM, NONAUTOIMMUNE, AUTOSOMAL DOMINANT;;TOXIC THYROID HYPERPLASIA, AUTOSOMAL DOMINANT		HP:0008249	OMIM:609152	IEA				P		HPO:iea	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0000006	OMIM:609153	TAS				I		HPO:skoehler	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0002153	PMID:2766660	PCS				P		HPO:lccarmody	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0002378	PMID:2766660	PCS				P		HPO:lccarmody	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0003324	PMID:2766660	PCS				P		HPO:lccarmody	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0003394	PMID:2766660	PCS				P		HPO:lccarmody	
OMIM	609153	PSEUDOHYPERKALEMIA, FAMILIAL, 2, DUE TO RED CELL LEAK		HP:0003768	PMID:2766660	PCS				P		HPO:lccarmody	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0000006	OMIM:609161	IEA				I		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0001260	OMIM:609161	TAS				P		HPO:skoehler	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0001288	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0002063	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0002067	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0002075	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0002375	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0002395	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0003677	OMIM:609161	IEA				C		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0007039	OMIM:609161	IEA				P		HPO:iea	
OMIM	609161	#609161 STRIATAL DEGENERATION, AUTOSOMAL DOMINANT; ADSD		HP:0040140	OMIM:609161	TAS				P		HPO:skoehler	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0000006	OMIM:609162	IEA				I		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0000926	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0001371	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0001507	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0001831	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002515	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002650	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002812	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002829	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002868	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002942	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0002945	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0003301	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0003370	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0008819	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0010049	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0010743	OMIM:609162	IEA				P		HPO:iea	
OMIM	609162	CZECH DYSPLASIA, METATARSAL TYPE		HP:0100864	OMIM:609162	TAS				P		HPO:probinson	
OMIM	609165	#609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR; CRIE;;ICHTHYOSIS WITH CONFETTI; IWC;;ICHTHYOSIS VARIEGATAERYTHROKERATODERMA, RETICULAR, INCLUDED;;AARAU DISEASE, INCLUDED		HP:0000006	OMIM:609165	TAS				I		HPO:skoehler	
OMIM	609165	#609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR; CRIE;;ICHTHYOSIS WITH CONFETTI; IWC;;ICHTHYOSIS VARIEGATAERYTHROKERATODERMA, RETICULAR, INCLUDED;;AARAU DISEASE, INCLUDED		HP:0000972	OMIM:609165	TAS				P		HPO:skoehler	
OMIM	609165	#609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR; CRIE;;ICHTHYOSIS WITH CONFETTI; IWC;;ICHTHYOSIS VARIEGATAERYTHROKERATODERMA, RETICULAR, INCLUDED;;AARAU DISEASE, INCLUDED		HP:0000998	OMIM:609165	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609165	#609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR; CRIE;;ICHTHYOSIS WITH CONFETTI; IWC;;ICHTHYOSIS VARIEGATAERYTHROKERATODERMA, RETICULAR, INCLUDED;;AARAU DISEASE, INCLUDED		HP:0001019	OMIM:609165	TAS				P		HPO:skoehler	
OMIM	609165	#609165 ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR; CRIE;;ICHTHYOSIS WITH CONFETTI; IWC;;ICHTHYOSIS VARIEGATAERYTHROKERATODERMA, RETICULAR, INCLUDED;;AARAU DISEASE, INCLUDED		HP:0001217	OMIM:609165	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000006	OMIM:609166	IEA				I		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000176	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000211	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000384	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000407	OMIM:609166	TAS				P		HPO:skoehler	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000410	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000413	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0000486	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0001760	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0004322	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0004452	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0004467	OMIM:609166	IEA				P		HPO:iea	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0009795	OMIM:609166	TAS				P		HPO:skoehler	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0009796	OMIM:609166	TAS				P		HPO:skoehler	
OMIM	609166	%609166 BRANCHIOGENIC-DEAFNESS SYNDROME		HP:0009882	OMIM:609166	IEA				P		HPO:iea	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000007	OMIM:609180	TAS				I		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000252	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000486	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000639	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000648	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000958	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0000962	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001019	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001250	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001251	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF	HP:0012828	HP:0001263	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001276	OMIM:609180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001290	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001344	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001371	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0001508	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0002059	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0003256	OMIM:609180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0003577	OMIM:609180	TAS				C		HPO:skoehler	
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0011968	OMIM:609180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609180	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IF		HP:0040189	OMIM:609180	TAS				P		HPO:skoehler	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000006	PMID:16928994	PCS				I		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000175	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000193	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000238	PMID:16928994	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000272	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000278	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000316	PMID:16928994	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000347	PMID:16928994	PCS				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000520	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000577	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000592	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000766	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0000977	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001162	PMID:16928994	PCS				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001166	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001249	PMID:16928994	PCS				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001263	PMID:16928994	PCS		HP:0040284		P		HPO:iea	15%
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001363	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001388	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001425	PMID:16928994	PCS				I		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001519	PMID:16928994	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001631	PMID:16928994	PCS		HP:0040284		P		HPO:iea	22%
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001634	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001643	PMID:16928994	PCS		HP:0040284		P		HPO:iea	35%
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001647	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0001762	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0002308	PMID:16928994	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0002650	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004933	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004937	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004944	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004955	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004959	OMIM:609192	IEA				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0004970	PMID:16928994	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0005182	OMIM:609192	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0009473	PMID:16928994	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0010648	PMID:16928994	PCS				P		HPO:iea	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0012385	OMIM:609192	TAS				P		HPO:skoehler	
OMIM	609192	LOEYS-DIETZ SYNDROME, TYPE 1A LOEYS-DIETZ AORTIC ANEURYSM SYNDROME		HP:0410151	PMID:23608731	PCS				P		HPO:lccarmody	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0000007	OMIM:609195	IEA				I		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0000012	OMIM:609195	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0000518	OMIM:609195	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0000639	OMIM:609195	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0000712	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001256	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001258	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001260	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001265	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001310	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001317	OMIM:609195	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001332	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001347	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0001761	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002061	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002064	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002120	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002355	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002359	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0002650	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0003487	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0003676	OMIM:609195	IEA				C		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0003677	OMIM:609195	TAS				C		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0003693	OMIM:609195	IEA				P		HPO:iea	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0040083	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0040171	OMIM:609195	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609195	SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26		HP:0100660	OMIM:609195	TAS				P		HPO:skoehler	
OMIM	609197	%609197 GLUCOCORTICOID DEFICIENCY 3; GCCD3;;FAMILIAL GLUCOCORTICOID DEFICIENCY 3; FGD3;;GLUCOCORTICOID DEFICIENCY 2, FORMERLY; GCCD2, FORMERLY		HP:0000007	OMIM:609197	IEA				I		HPO:iea	
OMIM	609197	%609197 GLUCOCORTICOID DEFICIENCY 3; GCCD3;;FAMILIAL GLUCOCORTICOID DEFICIENCY 3; FGD3;;GLUCOCORTICOID DEFICIENCY 2, FORMERLY; GCCD2, FORMERLY		HP:0000953	OMIM:609197	IEA				P		HPO:iea	
OMIM	609197	%609197 GLUCOCORTICOID DEFICIENCY 3; GCCD3;;FAMILIAL GLUCOCORTICOID DEFICIENCY 3; FGD3;;GLUCOCORTICOID DEFICIENCY 2, FORMERLY; GCCD2, FORMERLY		HP:0001988	OMIM:609197	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0000006	OMIM:609200	IEA				I		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0001271	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0001284	OMIM:609200	TAS				P		HPO:probinson	
OMIM	609200	MYOTILINOPATHY		HP:0001638	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0001771	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0002600	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003236	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003326	OMIM:609200	TAS				P		HPO:probinson	
OMIM	609200	MYOTILINOPATHY		HP:0003552	OMIM:609200	TAS				P		HPO:probinson	
OMIM	609200	MYOTILINOPATHY		HP:0003581	OMIM:609200	IEA				C		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003677	OMIM:609200	IEA				C		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003693	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003701	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0003715	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0009063	OMIM:609200	IEA				P		HPO:iea	
OMIM	609200	MYOTILINOPATHY		HP:0100303	OMIM:609200	IEA				P		HPO:iea	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0000007	OMIM:609218	TAS				I		HPO:skoehler	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0000568	OMIM:609218	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0000627	OMIM:609218	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0000639	OMIM:609218	TAS				P		HPO:skoehler	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0001137	OMIM:609218	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0001492	OMIM:609218	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0007663	OMIM:609218	TAS				P		HPO:skoehler	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0007750	OMIM:609218	TAS				P		HPO:skoehler	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0008001	OMIM:609218	IEA				P		HPO:skoehler	
OMIM	609218	FOVEAL HYPOPLASIA 2; FVH2		HP:0025551	OMIM:609218	IEA				P		HPO:skoehler	
OMIM	609220	BRUCK SYNDROME 2		HP:0000007	OMIM:609220	IEA				I		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0000023	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0000768	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0000926	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0000938	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0001059	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0001371	OMIM:609220	IEA				P		HPO:skoehler	
OMIM	609220	BRUCK SYNDROME 2		HP:0001762	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0002645	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0002659	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0002980	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0002987	OMIM:609220	TAS	HP:0003577			P		HPO:probinson	
OMIM	609220	BRUCK SYNDROME 2		HP:0003080	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0004322	OMIM:609220	IEA				P		HPO:iea	
OMIM	609220	BRUCK SYNDROME 2		HP:0006380	OMIM:609220	TAS	HP:0003577			P		HPO:probinson	
OMIM	609222	DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:609222	TAS				I		HPO:probinson	
OMIM	609222	DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT		HP:0001305	OMIM:609222	TAS				P		HPO:probinson	
OMIM	609222	DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT		HP:0003829	OMIM:609222	TAS				C		HPO:probinson	
OMIM	609222	DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT		HP:0004470	OMIM:609222	TAS				P		HPO:probinson	
OMIM	609222	DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT		HP:0004488	OMIM:609222	TAS				P		HPO:probinson	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0000007	OMIM:609223	IEA				I		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0000768	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0000926	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002650	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002655	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002655	OMIM:609223	TAS				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002857	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002938	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002942	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002945	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0002970	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0003184	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0003301	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0003370	OMIM:609223	IEA				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0003521	OMIM:609223	TAS				P		HPO:iea	
OMIM	609223	SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, AUTOSOMAL RECESSIVE, LEROY-SPRANGERTYPE		HP:0006429	OMIM:609223	IEA				P		HPO:iea	
OMIM	609227	#609227 GRISCELLI SYNDROME, TYPE 3; GS3		HP:0000007	OMIM:609227	TAS				I		HPO:skoehler	
OMIM	609227	#609227 GRISCELLI SYNDROME, TYPE 3; GS3		HP:0001425	OMIM:609227	TAS				I		HPO:skoehler	
OMIM	609227	#609227 GRISCELLI SYNDROME, TYPE 3; GS3		HP:0002218	OMIM:609227	TAS				P		HPO:skoehler	
OMIM	609227	#609227 GRISCELLI SYNDROME, TYPE 3; GS3		HP:0002227	OMIM:609227	TAS				P		HPO:probinson	
OMIM	609227	#609227 GRISCELLI SYNDROME, TYPE 3; GS3		HP:0004527	OMIM:609227	TAS				P		HPO:skoehler	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0000007	OMIM:609241	IEA				I		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0000486	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0000639	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0000648	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0000938	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001250	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001252	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001257	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001263	OMIM:609241	TAS				P		HPO:probinson	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001290	OMIM:609241	TAS				P		HPO:skoehler	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001336	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0001347	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0002376	OMIM:609241	TAS				P		HPO:probinson	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0003461	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0003593	OMIM:609241	TAS				C		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0003700	OMIM:609241	IEA				P		HPO:iea	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0010864	OMIM:609241	TAS				P		HPO:probinson	
OMIM	609241	SCHINDLER DISEASE, TYPE I		HP:0100704	OMIM:609241	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000007	OMIM:609242	IEA				I		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000179	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000214	OMIM:609242	TAS				P		HPO:probinson	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000280	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000407	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000478	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000958	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0000962	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0001004	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0001071	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0001256	OMIM:609242	TAS				P		HPO:probinson	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0002059	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0002321	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0002460	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0002936	OMIM:609242	TAS				P		HPO:probinson	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0003355	OMIM:609242	IEA				P		HPO:skoehler	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0003409	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0003461	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0003477	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0003581	OMIM:609242	IEA				C		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0005280	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0006812	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0007428	OMIM:609242	IEA				P		HPO:iea	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II		HP:0040078	OMIM:609242	TAS				P		HPO:skoehler	
OMIM	609242	#609242 KANZAKI DISEASE;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, TYPE II;;ALPHA-N-ACETYLGALACTOSAMINIDASE DEFICIENCY, ADULT-ONSET;;NAGA DEFICIENCY, TYPE II;;SCHINDLER DISEASE, TYPE II	HP:0012825	HP:0100543	OMIM:609242	TAS				P		HPO:skoehler	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0000006	OMIM:609253	IEA				I		HPO:iea	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0001425	OMIM:609253	TAS				I		HPO:skoehler	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0002069	OMIM:609253	IEA				P		HPO:iea	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0002373	OMIM:609253	IEA				P		HPO:iea	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0002373	OMIM:609253	TAS				P		HPO:skoehler	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0010818	OMIM:609253	IEA				P		HPO:iea	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0010819	OMIM:609253	IEA				P		HPO:iea	
OMIM	609253	FEBRILE SEIZURES, FAMILIAL, 6; FEB6		HP:0011463	OMIM:609253	IEA				C		HPO:iea	
OMIM	609254	SENIOR-LOKEN SYNDROME 5; SLSN5		HP:0000007	OMIM:609254	IEA				I		HPO:iea	
OMIM	609254	SENIOR-LOKEN SYNDROME 5; SLSN5		HP:0000090	OMIM:609254	IEA				P		HPO:iea	
OMIM	609254	SENIOR-LOKEN SYNDROME 5; SLSN5		HP:0000510	OMIM:609254	IEA				P		HPO:iea	
OMIM	609254	SENIOR-LOKEN SYNDROME 5; SLSN5		HP:0001425	OMIM:609254	TAS				I		HPO:skoehler	
OMIM	609254	SENIOR-LOKEN SYNDROME 5; SLSN5		HP:0003774	OMIM:609254	IEA				P		HPO:iea	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0000006	OMIM:609255	TAS				I		HPO:skoehler	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0001425	OMIM:609255	TAS				I		HPO:skoehler	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0002069	OMIM:609255	TAS				P		HPO:skoehler	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0002373	OMIM:609255	TAS				P		HPO:skoehler	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0010818	OMIM:609255	TAS				P		HPO:probinson	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0010819	OMIM:609255	TAS				P		HPO:probinson	
OMIM	609255	FEBRILE SEIZURES, FAMILIAL, 5; FEB5		HP:0011463	OMIM:609255	TAS				C		HPO:skoehler	
OMIM	609256	%609256 MYOPIA 7; MYP7		HP:0000545	OMIM:609256	TAS				P		HPO:skoehler	
OMIM	609257	%609257 MYOPIA 8; MYP8		HP:0000545	OMIM:609257	TAS				P		HPO:skoehler	
OMIM	609258	%609258 MYOPIA 9; MYP9		HP:0000545	OMIM:609258	TAS				P		HPO:skoehler	
OMIM	609259	%609259 MYOPIA 10; MYP10		HP:0000545	OMIM:609259	TAS				P		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0000006	OMIM:609260	TAS				I		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0000007	OMIM:609260	TAS				I		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0000365	OMIM:609260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0000648	OMIM:609260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001257	OMIM:609260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001265	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001268	OMIM:609260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001276	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001284	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001337	OMIM:609260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001347	OMIM:609260	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001371	OMIM:609260	TAS				P		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001761	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0001765	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0002460	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0002650	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0002936	OMIM:609260	TAS				P		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003376	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003378	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003380	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003383	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003384	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2	HP:0012825	HP:0003431	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003487	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003677	OMIM:609260	TAS				C		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003690	OMIM:609260	TAS				P		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003693	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003693	OMIM:609260	TAS				P		HPO:probinson	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003828	OMIM:609260	TAS				C		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0003829	OMIM:609260	TAS				C		HPO:skoehler	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0009027	OMIM:609260	IEA				P		HPO:iea	
OMIM	609260	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A2; CMT2A2		HP:0012531	OMIM:609260	TAS				P		HPO:skoehler	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0000006	PMID:10617473	PCS				I		HPO:probinson	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0002858	PMID:11479205	PCS				P		HPO:probinson	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0003002	PMID:11479205	PCS				P		HPO:probinson	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0009733	PMID:10617473	PCS				P		HPO:probinson	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0012126	PMID:11479205	PCS				P		HPO:probinson	
OMIM	609265	#609265 LI-FRAUMENI SYNDROME 2; LFS2		HP:0100242	PMID:10617473	PCS				P		HPO:probinson	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0000007	OMIM:609270	IEA				I		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0000639	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0000651	OMIM:609270	TAS				P		HPO:skoehler	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0001152	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0001251	OMIM:609270	TAS				P		HPO:probinson	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0001260	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0001272	OMIM:609270	TAS				P		HPO:skoehler	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0001347	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0002066	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0002070	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0002174	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0002312	OMIM:609270	TAS				P		HPO:probinson	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0002495	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0003487	OMIM:609270	IEA				P		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0003621	OMIM:609270	IEA				C		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0003677	OMIM:609270	IEA				C		HPO:iea	
OMIM	609270	#609270 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7; SCAR7		HP:0007338	OMIM:609270	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0000006	OMIM:609273	TAS				I		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0001288	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003198	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003546	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003551	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003552	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003677	OMIM:609273	TAS				C		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003690	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003722	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0003798	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609273	NEMALINE MYOPATHY 6		HP:0009046	OMIM:609273	TAS				P		HPO:skoehler	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000006	OMIM:609283	IEA				I		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000407	OMIM:609283	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000407	OMIM:609283	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000508	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000590	OMIM:609283	TAS				P		HPO:skoehler	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0000590	OMIM:609283	IEA				P		HPO:skoehler	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0001425	OMIM:609283	TAS				I		HPO:skoehler	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003200	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003324	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003458	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003546	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003548	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003581	OMIM:609283	IEA				C		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003676	OMIM:609283	IEA				C		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003688	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0003689	OMIM:609283	IEA				P		HPO:iea	
OMIM	609283	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2		HP:0010628	OMIM:609283	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000006	OMIM:609284	IEA				I		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000007	OMIM:609284	IEA				I		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000218	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000275	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000276	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000467	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0000767	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0001270	OMIM:609284	TAS				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0001349	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0001371	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0001425	OMIM:609284	TAS				I		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0001761	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0002015	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0002093	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0002650	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003324	OMIM:609284	TAS				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003458	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003621	OMIM:609284	IEA				C		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003701	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003724	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0003798	OMIM:609284	IEA				P		HPO:skoehler	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0008944	OMIM:609284	IEA				P		HPO:iea	
OMIM	609284	NEMALINE MYOPATHY 1; NEM1		HP:0009053	OMIM:609284	IEA				P		HPO:iea	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0000006	OMIM:609285	IEA				I		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0000218	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0000467	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001252	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001265	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001270	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001290	OMIM:609285	TAS				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001349	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001371	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0001425	OMIM:609285	TAS				I		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0002058	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0002355	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0002515	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0002751	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0002792	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003202	OMIM:609285	TAS				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003391	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003690	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003691	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003798	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003803	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0003828	OMIM:609285	IEA				C		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0008872	OMIM:609285	IEA				P		HPO:skoehler	
OMIM	609285	NEMALINE MYOPATHY 4		HP:0011463	OMIM:609285	TAS				C		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000006	OMIM:609286	IEA				I		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000135	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000508	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000518	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000590	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000590	OMIM:609286	IEA				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000716	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000726	OMIM:609286	TAS	HP:0003584			P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000819	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0000820	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001250	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001260	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001263	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001265	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001284	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001288	OMIM:609286	TAS	HP:0003584			P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001300	OMIM:609286	TAS		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001618	OMIM:609286	TAS	HP:0003584			P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001638	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001662	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0001730	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0002015	OMIM:609286	TAS	HP:0003584			P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0002059	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0002151	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003200	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003323	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003326	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003390	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003458	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003546	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003548	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003581	OMIM:609286	TAS				C		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003676	OMIM:609286	IEA				C		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003688	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003689	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003690	OMIM:609286	IEA				P		HPO:iea	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0003701	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0008209	OMIM:609286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0010871	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0012378	OMIM:609286	TAS				P		HPO:skoehler	
OMIM	609286	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 3; PEOA3		HP:0025356	OMIM:609286	IEA				P		HPO:skoehler	
OMIM	609289	SYNCOPE, FAMILIAL VASOVAGAL; VVS		HP:0000006	OMIM:609289	TAS				I		HPO:skoehler	
OMIM	609289	SYNCOPE, FAMILIAL VASOVAGAL; VVS		HP:0001279	OMIM:609289	IEA				P		HPO:skoehler	
OMIM	609289	SYNCOPE, FAMILIAL VASOVAGAL; VVS		HP:0002321	OMIM:609289	TAS				P		HPO:skoehler	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0000007	OMIM:609304	IEA				I		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0000253	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0000649	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0001257	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0001319	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0002059	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0002123	OMIM:609304	IEA				P		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0003819	OMIM:609304	IEA				M		HPO:iea	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0012448	OMIM:609304	TAS				P		HPO:skoehler	
OMIM	609304	#609304 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 3; EIEE3		HP:0200134	OMIM:609304	IEA				P		HPO:skoehler	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0000006	OMIM:609306	IEA				I		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0000639	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0000641	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0001151	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0001260	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0001272	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0002066	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0002070	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0002078	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0002311	OMIM:609306	IEA				P		HPO:iea	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0003581	OMIM:609306	TAS				C		HPO:probinson	
OMIM	609306	SPINOCEREBELLAR ATAXIA 26		HP:0003677	OMIM:609306	IEA				C		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0000006	OMIM:609307	TAS				I		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0000486	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0000640	PMID:12489043	PCS		HP:0040284		P		HPO:iea	12/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0000641	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0000716	PMID:12489043	PCS		HP:0040284		P		HPO:iea	2/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0001256	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0001260	PMID:16211615	PCS		HP:0040284		P		HPO:iea	11/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0001272	PMID:16211615	PCS		HP:0040284		P		HPO:iea	2/9
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0001425	OMIM:609307	TAS				I		HPO:skoehler	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0001761	PMID:19471976	PCS		HP:0040284		P		HPO:iea	3/17
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002066	PMID:16211615	PCS		HP:0040284		P		HPO:iea	11/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002070	PMID:16211615	PCS		HP:0040284		P		HPO:iea	12/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002078	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002174	PMID:16211615	PCS		HP:0040284		P		HPO:iea	12/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002310	PMID:16211615	PCS		HP:0040284		P		HPO:iea	8/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002346	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002354	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0002495	PMID:16211615	PCS		HP:0040284		P		HPO:iea	9/14
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0003390	OMIM:609307	TAS				P		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0003677	OMIM:609307	TAS				C		HPO:iea	
OMIM	609307	SPINOCEREBELLAR ATAXIA 27; SCA27		HP:0007772	OMIM:609307	TAS				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0000007	OMIM:609308	IEA				I		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0000252	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0001249	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0001270	OMIM:609308	TAS				P		HPO:probinson	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0001371	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0001638	OMIM:609308	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0002355	OMIM:609308	TAS				P		HPO:probinson	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0002938	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003236	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003306	OMIM:609308	TAS				P		HPO:skoehler	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003325	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003388	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003551	OMIM:609308	TAS				P		HPO:probinson	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003560	OMIM:609308	IEA				P		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003593	OMIM:609308	IEA				C		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003677	OMIM:609308	IEA				C		HPO:iea	
OMIM	609308	#609308 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 1; MDDGC1;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K; LGMD2K		HP:0003828	OMIM:609308	TAS				C		HPO:skoehler	
OMIM	609310	#609310 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2;;COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 2; FCC2;;COCA2		HP:0000006	OMIM:609310	TAS				I		HPO:probinson	
OMIM	609310	#609310 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 2; HNPCC2;;COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 2; FCC2;;COCA2		HP:0003003	OMIM:609310	TAS				P		HPO:probinson	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0000007	OMIM:609311	IEA				I		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001265	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001270	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001284	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001425	OMIM:609311	TAS				I		HPO:skoehler	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001761	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0001762	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0002515	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0002650	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0002936	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0003380	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0003383	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0003431	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0003484	OMIM:609311	IEA				P		HPO:probinson	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0003593	OMIM:609311	IEA				C		HPO:probinson	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0008944	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0009053	OMIM:609311	IEA				P		HPO:iea	
OMIM	609311	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H; CMT4H		HP:0011096	OMIM:609311	PCS				P		HPO:probinson	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0000007	OMIM:609313	TAS				I		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0000348	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0000365	OMIM:609313	IEA				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0000518	OMIM:609313	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0000582	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001249	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001263	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001290	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001394	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001395	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001396	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0001510	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0002014	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0002242	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0003577	OMIM:609313	TAS				C		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0008064	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0009830	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609313	MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA		HP:0010783	OMIM:609313	TAS				P		HPO:skoehler	
OMIM	609322	#609322 RHABDOID TUMOR PREDISPOSITION SYNDROME 1; RTPS1;;BRAIN TUMOR, POSTERIOR FOSSA, OF INFANCY, FAMILIALMALIGNANT RHABDOID TUMOR, SOMATIC, INCLUDED;;RHABDOID TUMOR, INCLUDED; RDT, INCLUDED;;TERATOID TUMOR, ATYPICAL, INCLUDED;;AT/RT, INCLUDED		HP:0000006	OMIM:609322	IEA				I		HPO:skoehler	
OMIM	609322	#609322 RHABDOID TUMOR PREDISPOSITION SYNDROME 1; RTPS1;;BRAIN TUMOR, POSTERIOR FOSSA, OF INFANCY, FAMILIALMALIGNANT RHABDOID TUMOR, SOMATIC, INCLUDED;;RHABDOID TUMOR, INCLUDED; RDT, INCLUDED;;TERATOID TUMOR, ATYPICAL, INCLUDED;;AT/RT, INCLUDED		HP:0002885	OMIM:609322	IEA				P		HPO:skoehler	
OMIM	609322	#609322 RHABDOID TUMOR PREDISPOSITION SYNDROME 1; RTPS1;;BRAIN TUMOR, POSTERIOR FOSSA, OF INFANCY, FAMILIALMALIGNANT RHABDOID TUMOR, SOMATIC, INCLUDED;;RHABDOID TUMOR, INCLUDED; RDT, INCLUDED;;TERATOID TUMOR, ATYPICAL, INCLUDED;;AT/RT, INCLUDED		HP:0030392	OMIM:609322	TAS				P		HPO:skoehler	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0000006	OMIM:609324	IEA				I		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0000926	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0001155	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0002656	OMIM:609324	TAS				P		HPO:probinson	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0002812	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0002829	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0002834	OMIM:609324	TAS				P		HPO:probinson	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0002857	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0003365	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0003411	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0004322	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA	HP:0012825	HP:0004582	OMIM:609324	TAS				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0006398	OMIM:609324	IEA				P		HPO:iea	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0006429	OMIM:609324	TAS				P		HPO:probinson	
OMIM	609324	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH SEVERE PROXIMAL FEMORAL DYSPLASIA		HP:0100864	OMIM:609324	TAS				P		HPO:probinson	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0000007	OMIM:609325	IEA				I		HPO:iea	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0002656	OMIM:609325	TAS				P		HPO:skoehler	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0002761	OMIM:609325	IEA				P		HPO:iea	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0002938	OMIM:609325	IEA				P		HPO:iea	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0002970	OMIM:609325	IEA				P		HPO:iea	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0003065	OMIM:609325	TAS				P		HPO:probinson	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0004322	OMIM:609325	IEA				P		HPO:iea	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0006369	OMIM:609325	IEA				P		HPO:skoehler	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0006429	PMID:15523498	PCS				P		HPO:probinson	
OMIM	609325	EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MINIEPIPHYSES		HP:0100864	PMID:15523498	PCS				P		HPO:probinson	
OMIM	609338	#609338 CAROTID INTIMAL MEDIAL THICKNESS 1;;CIMT1;;INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY		HP:0010982	OMIM:609338	TAS				I		HPO:skoehler	
OMIM	609338	#609338 CAROTID INTIMAL MEDIAL THICKNESS 1;;CIMT1;;INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY		HP:0012273	OMIM:609338	TAS				P		HPO:skoehler	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0000007	OMIM:609340	IEA				I		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0001258	OMIM:609340	TAS				P		HPO:skoehler	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0001347	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0001761	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0002061	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0002355	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0002650	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0002936	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0003477	OMIM:609340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0003487	OMIM:609340	IEA				P		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0003621	OMIM:609340	IEA				C		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0003677	OMIM:609340	IEA				C		HPO:iea	
OMIM	609340	#609340 SPASTIC PARAPLEGIA 28, AUTOSOMAL RECESSIVE; SPG28		HP:0007340	OMIM:609340	IEA				P		HPO:iea	
OMIM	609376	%609376 CATARACT 35; CTRCT35;;CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 1; CATCN1		HP:0000007	OMIM:609376	TAS				I		HPO:skoehler	
OMIM	609376	%609376 CATARACT 35; CTRCT35;;CATARACT, CONGENITAL NUCLEAR, AUTOSOMAL RECESSIVE 1; CATCN1		HP:0000518	OMIM:609376	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0000006	OMIM:609384	IEA				I		HPO:iea	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0000219	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0000767	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0001249	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0001491	OMIM:609384	TAS				P		HPO:probinson	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0002553	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0002808	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0007867	OMIM:609384	IEA				P		HPO:iea	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0007911	OMIM:609384	IEA				P		HPO:iea	
OMIM	609384	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B		HP:0009891	OMIM:609384	IEA				P		HPO:skoehler	
OMIM	609404	#609404 PREECLAMPSIA/ECLAMPSIA 4; PEE4		HP:0010982	PMID:17290274	PCS				I		HPO:probinson	
OMIM	609404	#609404 PREECLAMPSIA/ECLAMPSIA 4; PEE4		HP:0100601	OMIM:609404	IEA				P		HPO:skoehler	
OMIM	609404	#609404 PREECLAMPSIA/ECLAMPSIA 4; PEE4		HP:0100602	PMID:17290274	PCS				P		HPO:probinson	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000006	OMIM:609425	IEA				I	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000219	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000252	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000275	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000276	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000322	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000358	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000369	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000400	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000426	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000709	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000717	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000718	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000733	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000739	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000752	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000767	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0000768	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0001182	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:probinson	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0001249	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:probinson	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0001263	PMID:15918153	PCS	HP:0003593			P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0001508	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0001518	OMIM:609425	TAS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:skoehler	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0002066	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0003745	OMIM:609425	IEA				I	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609425	#609425 CHROMOSOME 3q29 DELETION SYNDROME;;MICRODELETION 3q29 SYNDROME		HP:0004209	PMID:15918153	PCS				P	#609425 CHROMOSOME 3Q29 DELETION SYNDROME;;MICRODELETION 3Q29 SYNDROME	HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0000007	OMIM:609428	IEA				I		HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0000508	OMIM:609428	TAS				P		HPO:skoehler	
OMIM	609428	TUKEL SYNDROME		HP:0001159	OMIM:609428	IEA				P		HPO:skoehler	
OMIM	609428	TUKEL SYNDROME		HP:0001477	OMIM:609428	IEA				P		HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0001491	OMIM:609428	IEA				P		HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0004231	OMIM:609428	IEA				P		HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0006210	OMIM:609428	TAS				P		HPO:skoehler	
OMIM	609428	TUKEL SYNDROME		HP:0007831	OMIM:609428	IEA				P		HPO:iea	
OMIM	609428	TUKEL SYNDROME		HP:0007936	OMIM:609428	TAS				P		HPO:skoehler	
OMIM	609428	TUKEL SYNDROME		HP:0009702	OMIM:609428	IEA				P		HPO:iea	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0000007	OMIM:609432	IEA				I		HPO:iea	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION	HP:0012832	HP:0000954	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0004209	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0006097	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0008362	OMIM:609432	IEA				P		HPO:iea	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0009161	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0009177	OMIM:609432	IEA				P		HPO:iea	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0009568	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0009601	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609432	SYNDACTYLY, MESOAXIAL SYNOSTOTIC, WITH PHALANGEAL REDUCTION		HP:0010064	OMIM:609432	TAS				P		HPO:probinson	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0000007	OMIM:609438	IEA				I		HPO:iea	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK	HP:0012832	HP:0000563	OMIM:609438	TAS				P		HPO:skoehler	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0000572	OMIM:609438	IEA				P		HPO:iea	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0002373	OMIM:609438	IEA				P		HPO:iea	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0006887	OMIM:609438	IEA				P		HPO:iea	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0010864	OMIM:609438	TAS				P		HPO:skoehler	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0011702	OMIM:609438	IEA				P		HPO:iea	
OMIM	609438	609438 MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK		HP:0012723	OMIM:609438	TAS				P		HPO:skoehler	
OMIM	609439	DEAFNESS, AUTOSOMAL RECESSIVE 48		HP:0000007	OMIM:609439	TAS				I		HPO:probinson	
OMIM	609439	DEAFNESS, AUTOSOMAL RECESSIVE 48		HP:0001751	PMID:18505454	TAS				P		HPO:probinson	
OMIM	609439	DEAFNESS, AUTOSOMAL RECESSIVE 48	HP:0012832	HP:0011476	OMIM:609439	TAS	HP:0003577			P		HPO:probinson	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0000007	OMIM:609441	IEA				I		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0000013	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0000786	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0000815	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0001156	OMIM:609441	IEA				P		HPO:skoehler	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0001762	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0001769	OMIM:609441	IEA				P		HPO:skoehler	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0001831	OMIM:609441	TAS				P		HPO:probinson	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0002990	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0003022	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0005028	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0005914	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0008368	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0008873	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD	HP:0012828	HP:0009381	OMIM:609441	TAS				P		HPO:probinson	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0009466	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0009702	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0009803	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0010242	OMIM:609441	IEA				P		HPO:iea	
OMIM	609441	ACROMESOMELIC DYSPLASIA, DEMIRHAN TYPE; AMDD		HP:0100864	OMIM:609441	IEA				P		HPO:iea	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0000006	OMIM:609446	TAS				I		HPO:probinson	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0001263	OMIM:609446	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0002069	OMIM:609446	TAS				P		HPO:probinson	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0002121	OMIM:609446	TAS				P		HPO:probinson	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0007166	OMIM:609446	TAS				P		HPO:probinson	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0010849	OMIM:609446	TAS				P		HPO:probinson	
OMIM	609446	PAROXYSMAL NONKINESIGENIC DYSKINESIA, 3, WITH OR WITHOUT GENERALIZED EPILEPSY; PNKD3		HP:0100660	OMIM:609446	IEA				P		HPO:skoehler	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0000006	OMIM:609452	IEA				I		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0001271	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0001638	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0002600	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003236	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED	HP:0012839	HP:0003323	OMIM:609452	TAS				P		HPO:skoehler	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003445	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003458	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003555	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003584	OMIM:609452	TAS				C		HPO:skoehler	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003715	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0003736	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0009063	OMIM:609452	IEA				P		HPO:iea	
OMIM	609452	#609452 MYOPATHY, MYOFIBRILLAR, 4; MFM4;;MYOPATHY, MYOFIBRILLAR, ZASP-RELATED		HP:0009073	OMIM:609452	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000006	OMIM:609454	IEA				I		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000605	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000613	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000622	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000651	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000658	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000737	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000741	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0000743	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0001260	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0001300	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0001425	OMIM:609454	TAS				I		HPO:skoehler	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002015	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002063	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002067	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002141	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002171	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002174	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002185	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002304	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002354	OMIM:609454	PCS				P		HPO:probinson	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002439	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002527	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002528	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002529	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002529	OMIM:609454	PCS				P		HPO:probinson	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002530	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0002544	OMIM:609454	IEA				P		HPO:iea	
OMIM	609454	SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2		HP:0200147	OMIM:609454	IEA				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0000007	OMIM:609456	IEA				I		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0000467	OMIM:609456	TAS				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0001319	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0001371	OMIM:609456	TAS				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0001388	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0001558	OMIM:609456	TAS				P		HPO:probinson	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0002650	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0002747	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003198	OMIM:609456	IEA				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003547	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003557	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003577	OMIM:609456	IEA				C		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003701	OMIM:609456	TAS				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003741	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0003828	OMIM:609456	IEA				C		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0008180	OMIM:609456	TAS				P		HPO:skoehler	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0010628	OMIM:609456	IEA				P		HPO:iea	
OMIM	609456	MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE		HP:0031936	OMIM:609456	IEA				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000007	OMIM:609460	IEA				I		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000232	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000252	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000322	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000327	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000369	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000414	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000426	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000431	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000470	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000485	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000494	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000506	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000508	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000574	OMIM:609460	PCS				P		HPO:probinson	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000592	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0000664	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0001182	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0001249	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0001263	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0001290	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0001302	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0002079	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0002126	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0002251	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0002365	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0002553	OMIM:609460	PCS				P		HPO:probinson	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0003577	OMIM:609460	TAS				C		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0006610	OMIM:609460	IEA				P		HPO:iea	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0008070	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0012471	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0012804	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0030084	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0200020	OMIM:609460	TAS				P		HPO:probinson	
OMIM	609460	GOLDBERG-SHPRINTZEN SYNDROME		HP:0200055	OMIM:609460	TAS				P		HPO:skoehler	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0000007	OMIM:609500	TAS				I		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0001263	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0001319	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0001639	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0003198	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0003236	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0003736	OMIM:609500	TAS				P		HPO:iea	
OMIM	609500	MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET		HP:0003745	OMIM:609500	TAS				I		HPO:iea	
OMIM	609508	#609508 STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR;;STICKLER SYNDROME, TYPE I, PREDOMINANTLY OCULAR;;STICKLER SYNDROME, ATYPICALRHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT, INCLUDED; DRRD,INCLUDED		HP:0000006	PMID:17721977	PCS				I		HPO:probinson	
OMIM	609508	#609508 STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR;;STICKLER SYNDROME, TYPE I, PREDOMINANTLY OCULAR;;STICKLER SYNDROME, ATYPICALRHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT, INCLUDED; DRRD,INCLUDED		HP:0000545	PMID:15671297	PCS				P		HPO:probinson	
OMIM	609508	#609508 STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR;;STICKLER SYNDROME, TYPE I, PREDOMINANTLY OCULAR;;STICKLER SYNDROME, ATYPICALRHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT, INCLUDED; DRRD,INCLUDED		HP:0004327	PMID:15671297	PCS				P		HPO:probinson	
OMIM	609508	#609508 STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR;;STICKLER SYNDROME, TYPE I, PREDOMINANTLY OCULAR;;STICKLER SYNDROME, ATYPICALRHEGMATOGENOUS RETINAL DETACHMENT, AUTOSOMAL DOMINANT, INCLUDED; DRRD,INCLUDED		HP:0012230	PMID:15671297	PCS				P		HPO:probinson	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:609524	IEA				I		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0000759	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0002093	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0002515	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003236	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003551	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003555	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003581	OMIM:609524	IEA				C		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003677	OMIM:609524	IEA				C		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003701	OMIM:609524	TAS				P		HPO:skoehler	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0003715	OMIM:609524	IEA				P		HPO:iea	
OMIM	609524	FILAMINOPATHY, AUTOSOMAL DOMINANT		HP:0100303	OMIM:609524	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000007	OMIM:609528	IEA				I		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000253	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000276	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000316	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000407	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000431	OMIM:609528	TAS				P		HPO:probinson	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000494	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0000982	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001252	OMIM:609528	IEA				P		HPO:skoehler	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001263	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001271	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001273	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001284	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001302	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0001508	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0002126	OMIM:609528	TAS				P		HPO:skoehler	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0002421	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0002539	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0003593	OMIM:609528	IEA				C		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0005280	OMIM:609528	TAS				P		HPO:probinson	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0006887	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0007766	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0008064	OMIM:609528	IEA				P		HPO:iea	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0009830	OMIM:609528	TAS				P		HPO:probinson	
OMIM	609528	#609528 CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMASYNDROME;;CEDNIK SYNDROME		HP:0010864	OMIM:609528	TAS				P		HPO:skoehler	
OMIM	609529	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED		HP:0002720	OMIM:609529	IEA				P	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IGA, SELECTIVE DEFICIENCY OF, TACI-RELATED	HPO:skoehler	
OMIM	609529	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED		HP:0002960	OMIM:609529	IEA				P	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IGA, SELECTIVE DEFICIENCY OF, TACI-RELATED	HPO:skoehler	
OMIM	609529	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED		HP:0004332	OMIM:609529	IEA				P	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IGA, SELECTIVE DEFICIENCY OF, TACI-RELATED	HPO:skoehler	
OMIM	609529	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED		HP:0004798	OMIM:609529	IEA				P	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IGA, SELECTIVE DEFICIENCY OF, TACI-RELATED	HPO:skoehler	
OMIM	609529	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IgA, SELECTIVE DEFICIENCY OF, TACI-RELATED		HP:0005425	OMIM:609529	IEA				P	#609529 IMMUNOGLOBULIN A DEFICIENCY 2; IGAD2;;IMMUNOGLOBULIN A, SELECTIVE DEFICIENCY OF, TACI-RELATED;;IGA, SELECTIVE DEFICIENCY OF, TACI-RELATED	HPO:skoehler	
OMIM	609533	DEAFNESS, AUTOSOMAL RECESSIVE 23		HP:0000007	OMIM:609533	IEA				I		HPO:iea	
OMIM	609533	DEAFNESS, AUTOSOMAL RECESSIVE 23		HP:0000407	OMIM:609533	TAS				P		HPO:skoehler	
OMIM	609533	DEAFNESS, AUTOSOMAL RECESSIVE 23		HP:0003593	OMIM:609533	IEA				C		HPO:iea	
OMIM	609535	#609535 DRUG METABOLISM, POOR, CYP2C19-RELATEDMEPHENYTOIN, POOR METABOLISM OF, INCLUDED;;OMEPRAZOLE, POOR METABOLISM OF, INCLUDED;;PROGUANIL, POOR METABOLISM OF, INCLUDED;;CLOPIDOGREL, POOR METABOLISM OF, INCLUDED		HP:0000007	OMIM:609535	TAS				I		HPO:skoehler	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0000007	OMIM:609536	TAS				I		HPO:probinson	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0002041	OMIM:609536	TAS				P		HPO:probinson	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0002719	OMIM:609536	TAS				P		HPO:probinson	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0004431	OMIM:609536	TAS				P		HPO:probinson	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0006946	OMIM:609536	TAS				P		HPO:probinson	
OMIM	609536	#609536 COMPLEMENT COMPONENT 5 DEFICIENCY; C5D;;C5 DEFICIENCY		HP:0007569	OMIM:609536	TAS				P		HPO:probinson	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0000007	OMIM:609541	IEA				I		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0000543	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0000639	OMIM:609541	IEA				P		HPO:skoehler	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0000648	OMIM:609541	TAS				P		HPO:probinson	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0000975	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001258	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001260	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001265	OMIM:609541	TAS				P		HPO:probinson	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001270	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001371	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0001761	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0002267	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0002650	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0002808	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0003390	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0003676	OMIM:609541	TAS				C		HPO:skoehler	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0003693	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0007002	OMIM:609541	IEA				P		HPO:iea	
OMIM	609541	SPASTIC PARAPLEGIA, OPTIC ATROPHY, AND NEUROPATHY; SPOAN		HP:0007054	OMIM:609541	IEA				P		HPO:iea	
OMIM	609549	#609549 NANOPHTHALMOS 2; NNO2;;NANOPHTHALMIA 2;;NANOPHTHALMOS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:609549	TAS				I		HPO:probinson	
OMIM	609549	#609549 NANOPHTHALMOS 2; NNO2;;NANOPHTHALMIA 2;;NANOPHTHALMOS, AUTOSOMAL RECESSIVE		HP:0000568	OMIM:609549	TAS				P		HPO:probinson	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0000007	OMIM:609560	IEA				I		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0000365	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0000737	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0001250	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0001252	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0001290	OMIM:609560	TAS				P		HPO:skoehler	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0001349	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0002059	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0002134	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0002194	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0002747	OMIM:609560	TAS				P		HPO:skoehler	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003128	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003200	OMIM:609560	TAS				P		HPO:probinson	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003236	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003355	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003391	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003458	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003593	OMIM:609560	TAS				C		HPO:probinson	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003676	OMIM:609560	TAS				C		HPO:skoehler	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003690	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003700	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0003828	OMIM:609560	TAS				C		HPO:skoehler	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0006887	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0008945	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0008972	OMIM:609560	IEA				P		HPO:iea	
OMIM	609560	MITOCHONDRIAL DNA DEPLETION SYNDROME 2 (MYOPATHIC TYPE)		HP:0009141	OMIM:609560	IEA				P		HPO:iea	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0000006	OMIM:609566	IEA				I		HPO:iea	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0001425	OMIM:609566	TAS				I		HPO:skoehler	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0002084	OMIM:609566	IEA				P		HPO:iea	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0002695	OMIM:609566	IEA				P		HPO:iea	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0002697	OMIM:609566	TAS				P		HPO:skoehler	
OMIM	609566	PARIETAL FORAMINA 3; PFM3		HP:0007385	OMIM:609566	IEA				P		HPO:iea	
OMIM	609579	FAMILIAL SCAPHOCEPHALY SYNDROME, MCGILLIVRAY TYPE		HP:0000268	OMIM:609579	IEA				P		HPO:skoehler	
OMIM	609579	FAMILIAL SCAPHOCEPHALY SYNDROME, MCGILLIVRAY TYPE		HP:0001249	OMIM:609579	IEA				P		HPO:skoehler	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000007	OMIM:609583	IEA				I		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000083	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000090	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000571	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000639	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0000657	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0001251	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0001290	OMIM:609583	TAS				P		HPO:skoehler	
OMIM	609583	JOUBERT SYNDROME 4		HP:0001320	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0001425	OMIM:609583	TAS				I		HPO:skoehler	
OMIM	609583	JOUBERT SYNDROME 4		HP:0002194	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0002404	OMIM:609583	TAS				P		HPO:probinson	
OMIM	609583	JOUBERT SYNDROME 4		HP:0002419	OMIM:609583	IEA				P		HPO:iea	
OMIM	609583	JOUBERT SYNDROME 4		HP:0011933	OMIM:609583	TAS				P		HPO:probinson	
OMIM	609583	JOUBERT SYNDROME 4	HP:0012825	HP:0100543	OMIM:609583	TAS				P		HPO:skoehler	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0000006	OMIM:609597	IEA				I		HPO:iea	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0000316	OMIM:609597	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0002084	OMIM:609597	IEA				P		HPO:iea	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0002695	OMIM:609597	IEA				P		HPO:iea	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0002697	OMIM:609597	IEA				P		HPO:skoehler	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0005280	OMIM:609597	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0007385	OMIM:609597	IEA				P		HPO:iea	
OMIM	609597	#609597 PARIETAL FORAMINA 2; PFM2		HP:0012811	OMIM:609597	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609612	609612 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE;;CONGENITAL FIBROSIS SYNDROME WITH SYNERGISTIC DIVERGENCE;;EXTERNAL OPHTHALMOPLEGIA WITH SYNERGISTIC DIVERGENCEEXTERNAL OPHTHALMOPLEGIA, SYNERGISTIC DIVERGENCE, JAW WINKING, ANDOCULOCUTANEOUS HYPOPIGMENTATION, INCLUDED		HP:0000006	OMIM:609612	TAS				I		HPO:skoehler	
OMIM	609612	609612 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE;;CONGENITAL FIBROSIS SYNDROME WITH SYNERGISTIC DIVERGENCE;;EXTERNAL OPHTHALMOPLEGIA WITH SYNERGISTIC DIVERGENCEEXTERNAL OPHTHALMOPLEGIA, SYNERGISTIC DIVERGENCE, JAW WINKING, ANDOCULOCUTANEOUS HYPOPIGMENTATION, INCLUDED		HP:0000508	OMIM:609612	TAS				P		HPO:skoehler	
OMIM	609612	609612 FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE;;CONGENITAL FIBROSIS SYNDROME WITH SYNERGISTIC DIVERGENCE;;EXTERNAL OPHTHALMOPLEGIA WITH SYNERGISTIC DIVERGENCEEXTERNAL OPHTHALMOPLEGIA, SYNERGISTIC DIVERGENCE, JAW WINKING, ANDOCULOCUTANEOUS HYPOPIGMENTATION, INCLUDED		HP:0000577	OMIM:609612	TAS				P		HPO:skoehler	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0000407	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0000541	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0000887	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0000926	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0001156	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0001216	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0001763	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0001773	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0001837	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0002650	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0002866	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0002938	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003026	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003173	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003180	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003301	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003375	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003498	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0003745	OMIM:609616	IEA				I		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0004568	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0005011	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0006134	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0006370	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0010230	OMIM:609616	IEA				P		HPO:iea	
OMIM	609616	SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS		HP:0010231	OMIM:609616	IEA				P		HPO:iea	
OMIM	609620	#609620 SHORT QT SYNDROME 1; SQT1		HP:0000006	OMIM:609620	TAS				I		HPO:probinson	
OMIM	609620	#609620 SHORT QT SYNDROME 1; SQT1		HP:0001279	OMIM:609620	TAS				P		HPO:probinson	
OMIM	609620	#609620 SHORT QT SYNDROME 1; SQT1		HP:0001695	OMIM:609620	TAS				P		HPO:probinson	
OMIM	609620	#609620 SHORT QT SYNDROME 1; SQT1		HP:0001962	OMIM:609620	TAS				P		HPO:probinson	
OMIM	609620	#609620 SHORT QT SYNDROME 1; SQT1		HP:0012232	OMIM:609620	TAS				P		HPO:probinson	
OMIM	609621	SHORT QT SYNDROME 2		HP:0000006	PMID:15890322	PCS				I		HPO:probinson	
OMIM	609621	SHORT QT SYNDROME 2		HP:0001279	PMID:15890322	PCS				P		HPO:probinson	
OMIM	609621	SHORT QT SYNDROME 2		HP:0001645	PMID:15890322	PCS				P		HPO:probinson	
OMIM	609621	SHORT QT SYNDROME 2		HP:0001662	OMIM:609621	TAS				P		HPO:skoehler	
OMIM	609621	SHORT QT SYNDROME 2		HP:0001663	OMIM:609621	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609621	SHORT QT SYNDROME 2		HP:0005110	PMID:15890322	PCS				P		HPO:probinson	
OMIM	609621	SHORT QT SYNDROME 2		HP:0012232	PMID:15890322	PCS				P		HPO:probinson	
OMIM	609622	#609622 SHORT QT SYNDROME 3; SQT3		HP:0000006	PMID:15761194	PCS				I		HPO:probinson	
OMIM	609622	#609622 SHORT QT SYNDROME 3; SQT3		HP:0001649	PMID:15761194	PCS				P		HPO:probinson	
OMIM	609622	#609622 SHORT QT SYNDROME 3; SQT3		HP:0001962	PMID:15761194	PCS				P		HPO:probinson	
OMIM	609622	#609622 SHORT QT SYNDROME 3; SQT3		HP:0012232	PMID:15761194	PCS				P		HPO:probinson	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000006	OMIM:609625	IEA				I		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000028	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000046	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000054	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000076	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000219	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000219	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000252	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000268	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000286	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000316	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000324	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000325	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000343	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000347	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000369	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000407	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000411	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000431	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000444	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000448	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000454	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000465	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000470	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000486	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000494	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000582	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000718	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000736	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000750	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0000752	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001249	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001250	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001252	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001263	OMIM:609625	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001290	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001328	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001363	OMIM:609625	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001377	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001518	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001547	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001631	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001643	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001770	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001792	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0001939	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0002007	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0002136	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0002162	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0003745	OMIM:609625	IEA				I		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0004322	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0006610	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0008897	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0009466	OMIM:609625	IEA				P		HPO:iea	
OMIM	609625	CHROMOSOME 10Q26 DELETION SYNDROME		HP:0030084	OMIM:609625	TAS				P		HPO:skoehler	
OMIM	609628	MAJEED SYNDROME		HP:0000007	PMID:15994876	PCS				I		HPO:probinson	
OMIM	609628	MAJEED SYNDROME		HP:0001371	PMID:15994876	PCS				P		HPO:probinson	
OMIM	609628	MAJEED SYNDROME		HP:0001510	PMID:15994876	PCS				P		HPO:probinson	
OMIM	609628	MAJEED SYNDROME		HP:0001935	PMID:15994876	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	609628	MAJEED SYNDROME		HP:0001954	PMID:15994876	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	609628	MAJEED SYNDROME		HP:0002653	PMID:15994876	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	609628	MAJEED SYNDROME		HP:0002754	PMID:15994876	PCS				P		HPO:probinson	
OMIM	609628	MAJEED SYNDROME		HP:0002829	PMID:15994876	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	609628	MAJEED SYNDROME		HP:0011123	PMID:15994876	PCS				P		HPO:probinson	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0000006	OMIM:609634	IEA				I		HPO:iea	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0000613	OMIM:609634	IEA				P		HPO:iea	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0000618	OMIM:609634	IEA				P		HPO:skoehler	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0001250	OMIM:609634	IEA				P		HPO:iea	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0001269	OMIM:609634	IEA				P		HPO:iea	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0002077	OMIM:609634	IEA				P		HPO:iea	
OMIM	609634	MIGRAINE, FAMILIAL HEMIPLEGIC, 3		HP:0002301	OMIM:609634	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0000006	OMIM:609636	IEA				I		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0000726	OMIM:609636	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0000751	OMIM:609636	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0002120	OMIM:609636	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0002167	OMIM:609636	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0002354	OMIM:609636	IEA				P		HPO:iea	
OMIM	609636	ALZHEIMER DISEASE 10		HP:0002511	OMIM:609636	IEA				P		HPO:skoehler	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000006	OMIM:609637	TAS				I		HPO:skoehler	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000202	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	10%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000218	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	17%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000238	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000243	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000252	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000316	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	12%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000337	OMIM:609637	IEA				P		HPO:skoehler	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000341	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	53%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000400	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	37%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000582	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	97%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000601	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	19%
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0000664	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0001249	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0001263	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0001360	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0001999	OMIM:609637	TAS				P		PATOC:PS	
OMIM	609637	HOLOPROSENCEPHALY 5; HPE5		HP:0005280	OMIM:609637	TAS		HP:0040284		P		HPO:skoehler	33%
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0000007	OMIM:609638	IEA				I		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0000695	OMIM:609638	IEA				P		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001057	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001159	OMIM:609638	IEA				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001596	OMIM:609638	IEA				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001597	OMIM:609638	IEA				P		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001640	OMIM:609638	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001741	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001798	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0001852	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0002289	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0003811	OMIM:609638	IEA				M		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0004057	OMIM:609638	TAS				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0008094	OMIM:609638	IEA				P		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0009884	OMIM:609638	IEA				P		HPO:iea	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0040019	OMIM:609638	IEA				P		HPO:skoehler	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0100792	OMIM:609638	TAS				P		HPO:probinson	
OMIM	609638	EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA		HP:0200041	OMIM:609638	IEA				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000006	OMIM:609640	TAS				I		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000316	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000347	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000358	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000378	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0000494	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME	HP:0012832	HP:0000508	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME	HP:0012825	HP:0000520	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0001263	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609640	FRIAS SYNDROME		HP:0004322	OMIM:609640	TAS				P		HPO:skoehler	
OMIM	609646	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 42		HP:0000007	OMIM:609646	IEA				I		HPO:iea	
OMIM	609646	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 42		HP:0000407	OMIM:609646	IEA				P		HPO:skoehler	
OMIM	609646	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 42		HP:0003593	OMIM:609646	IEA				C		HPO:iea	
OMIM	609646	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 42		HP:0003680	OMIM:609646	IEA				C		HPO:iea	
OMIM	609647	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 46		HP:0000007	PMID:15637723	PCS				I		HPO:probinson	
OMIM	609647	DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE 46		HP:0011476	PMID:15637723	PCS	HP:0003593			P		HPO:skoehler	
OMIM	609649	TRICHILEMMAL CYST 1		HP:0000006	OMIM:609649	IEA				I		HPO:iea	
OMIM	609649	TRICHILEMMAL CYST 1		HP:0000951	OMIM:609649	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000007	OMIM:609654	IEA				I		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000175	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000204	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000218	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000252	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000369	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000378	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000396	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000470	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000508	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000767	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000768	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0000891	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0001629	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0003310	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0003508	OMIM:609654	IEA				P		HPO:iea	
OMIM	609654	SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS		HP:0008551	OMIM:609654	IEA				P		HPO:iea	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0000007	OMIM:609655	TAS				I		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0003621	OMIM:609655	TAS				C		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0006202	OMIM:609655	TAS				P		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0006378	OMIM:609655	TAS				P		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0008095	OMIM:609655	TAS				P		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0010044	OMIM:609655	TAS				P		HPO:probinson	
OMIM	609655	TALO-PATELLO-SCAPHOID OSTEOLYSIS, SYNOVITIS, AND SHORT FOURTH METACARPALS		HP:0100769	OMIM:609655	IEA				P		HPO:skoehler	
OMIM	609698	#609698 THYROID HORMONE METABOLISM, ABNORMAL		HP:0000007	OMIM:609698	TAS				I		HPO:probinson	
OMIM	609698	#609698 THYROID HORMONE METABOLISM, ABNORMAL		HP:0002750	OMIM:609698	TAS				P		HPO:probinson	
OMIM	609698	#609698 THYROID HORMONE METABOLISM, ABNORMAL		HP:0002925	OMIM:609698	TAS				P		HPO:probinson	
OMIM	609706	#609706 DEAFNESS, AUTOSOMAL RECESSIVE 53; DFNB53		HP:0000007	OMIM:609706	TAS				I		HPO:probinson	
OMIM	609706	#609706 DEAFNESS, AUTOSOMAL RECESSIVE 53; DFNB53		HP:0000407	OMIM:609706	TAS				P		HPO:probinson	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000006	OMIM:609727	IEA				I		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000012	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000017	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000019	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000020	OMIM:609727	IEA				P		HPO:skoehler	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000407	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0000752	OMIM:609727	IEA				P		HPO:skoehler	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0001258	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0001761	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0002013	OMIM:609727	IEA				P		HPO:skoehler	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0002036	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0002169	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0002495	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0003265	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0003487	OMIM:609727	IEA				P		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0003743	OMIM:609727	IEA				I		HPO:iea	
OMIM	609727	SPASTIC PARAPLEGIA 29, AUTOSOMAL DOMINANT		HP:0006986	OMIM:609727	IEA				P		HPO:iea	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0000007	OMIM:609734	TAS				I		HPO:probinson	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0000824	OMIM:609734	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0000835	OMIM:609734	IEA				P		HPO:skoehler	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0000846	OMIM:609734	IEA				P		HPO:skoehler	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0001396	OMIM:609734	TAS				P		HPO:probinson	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0001513	OMIM:609734	TAS				P		HPO:probinson	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0002173	OMIM:609734	TAS				P		HPO:probinson	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0002297	OMIM:609734	TAS				P		HPO:probinson	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0002904	OMIM:609734	IEA				P		HPO:skoehler	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0003593	OMIM:609734	IEA				C		HPO:skoehler	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0008213	OMIM:609734	IEA				P		HPO:skoehler	
OMIM	609734	OBESITY, EARLY-ONSET, WITH ADRENAL INSUFFICIENCY AND RED HAIR; OBAIRH		HP:0011748	OMIM:609734	TAS				P		HPO:probinson	
OMIM	609741	CATARACT 22, MULTIPLE TYPES; CTRCT22		HP:0000006	OMIM:609741	TAS				I		HPO:skoehler	
OMIM	609741	CATARACT 22, MULTIPLE TYPES; CTRCT22		HP:0000007	OMIM:609741	TAS				I		HPO:probinson	
OMIM	609741	CATARACT 22, MULTIPLE TYPES; CTRCT22		HP:0000501	OMIM:609741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609741	CATARACT 22, MULTIPLE TYPES; CTRCT22		HP:0000519	OMIM:609741	TAS				P		HPO:skoehler	
OMIM	609741	CATARACT 22, MULTIPLE TYPES; CTRCT22		HP:0100018	OMIM:609741	TAS	HP:0003577			P		HPO:probinson	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000006	OMIM:609637	TAS				I		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000028	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000122	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000126	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000218	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000238	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000248	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000256	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000322	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000324	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000337	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000347	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000348	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000389	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000396	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000455	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000490	OMIM:609757	IEA				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000527	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000699	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000729	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000739	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000824	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0000965	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001250	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001252	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001263	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001288	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001290	OMIM:609757	IEA				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001320	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0001643	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0002079	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0002119	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0004322	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0007018	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0011228	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609757	WILLIAMS-BEUREN REGION DUPLICATION SYNDROME		HP:0012450	OMIM:609637	TAS				P		HPO:skoehler	
OMIM	609796	PEELING SKIN SYNDROME, ACRAL TYPE		HP:0000007	OMIM:609796	TAS				I		HPO:skoehler	
OMIM	609796	PEELING SKIN SYNDROME, ACRAL TYPE		HP:0008066	OMIM:609796	TAS				P		HPO:probinson	
OMIM	609796	PEELING SKIN SYNDROME, ACRAL TYPE		HP:0010783	OMIM:609796	IEA				P		HPO:skoehler	
OMIM	609796	PEELING SKIN SYNDROME, ACRAL TYPE		HP:0040189	OMIM:609796	IEA				P		HPO:skoehler	
OMIM	609800	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4; GEFSP4		HP:0000006	OMIM:609800	IEA				I		HPO:iea	
OMIM	609800	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4; GEFSP4		HP:0001425	OMIM:609800	TAS				I		HPO:skoehler	
OMIM	609800	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4; GEFSP4		HP:0002069	OMIM:609800	IEA				P		HPO:iea	
OMIM	609800	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 4; GEFSP4		HP:0002373	OMIM:609800	IEA				P		HPO:iea	
OMIM	609808	HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS		HP:0000006	OMIM:609808	IEA				I		HPO:iea	
OMIM	609808	HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS		HP:0000951	OMIM:609808	IEA				P		HPO:iea	
OMIM	609808	HAMARTOMA, PRECALCANEAL CONGENITAL FIBROLIPOMATOUS		HP:0010566	OMIM:609808	IEA				P		HPO:skoehler	
OMIM	609812	#609812 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION;MODY8;;DIABETES AND PANCREATIC EXOCRINE DYSFUNCTION; DPED;;DIABETES-PANCREATIC EXOCRINE DYSFUNCTION SYNDROME		HP:0000006	OMIM:609812	TAS				I		HPO:probinson	
OMIM	609812	#609812 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION;MODY8;;DIABETES AND PANCREATIC EXOCRINE DYSFUNCTION; DPED;;DIABETES-PANCREATIC EXOCRINE DYSFUNCTION SYNDROME		HP:0002027	OMIM:609812	TAS				P		HPO:skoehler	
OMIM	609812	#609812 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION;MODY8;;DIABETES AND PANCREATIC EXOCRINE DYSFUNCTION; DPED;;DIABETES-PANCREATIC EXOCRINE DYSFUNCTION SYNDROME		HP:0004904	OMIM:609812	TAS				P		HPO:probinson	
OMIM	609812	#609812 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 8, WITH EXOCRINE DYSFUNCTION;MODY8;;DIABETES AND PANCREATIC EXOCRINE DYSFUNCTION; DPED;;DIABETES-PANCREATIC EXOCRINE DYSFUNCTION SYNDROME		HP:0012092	OMIM:609812	TAS				P		HPO:probinson	
OMIM	609813	#609813 SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE; SCDO3		HP:0000007	OMIM:609813	TAS				I		HPO:probinson	
OMIM	609813	#609813 SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE; SCDO3		HP:0001238	OMIM:609813	TAS				P		HPO:probinson	
OMIM	609813	#609813 SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE; SCDO3		HP:0002650	OMIM:609813	TAS				P		HPO:probinson	
OMIM	609813	#609813 SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE; SCDO3		HP:0003422	OMIM:609813	TAS				P		HPO:probinson	
OMIM	609813	#609813 SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE; SCDO3		HP:0004598	OMIM:609813	TAS				P		HPO:probinson	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0000006	OMIM:609814	IEA				I		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0000007	OMIM:609814	IEA				I		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0000790	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0002718	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0003621	OMIM:609814	IEA				C		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0004722	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0004746	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0005369	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0005389	OMIM:609814	IEA				P		HPO:iea	
OMIM	609814	COMPLEMENT FACTOR H DEFICIENCY		HP:0012622	OMIM:609814	TAS				P		HPO:probinson	
OMIM	609820	ERYTHROCYTOSIS, FAMILIAL, 3		HP:0000006	OMIM:609820	IEA				I		HPO:iea	
OMIM	609820	ERYTHROCYTOSIS, FAMILIAL, 3		HP:0001898	OMIM:609820	IEA				P		HPO:iea	
OMIM	609820	ERYTHROCYTOSIS, FAMILIAL, 3		HP:0001899	OMIM:609820	IEA				P		HPO:iea	
OMIM	609820	ERYTHROCYTOSIS, FAMILIAL, 3		HP:0001900	OMIM:609820	IEA				P		HPO:iea	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0000007	PMID:20966167	PCS				I		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0000421	PMID:10816552	PCS				P		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0000978	PMID:1333302	PCS				P		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0001934	PMID:20966167	PCS				P		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0004846	PMID:20966167	PCS				P		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0004866	PMID:20966167	PCS				P		HPO:probinson	
OMIM	609821	BLEEDING DISORDER, PLATELET-TYPE, 8; BDPLT8		HP:0031364	OMIM:609821	IEA				P		HPO:skoehler	
OMIM	609823	DEAFNESS, AUTOSOMAL RECESSIVE 28		HP:0000007	OMIM:609823	IEA				I		HPO:iea	
OMIM	609823	DEAFNESS, AUTOSOMAL RECESSIVE 28		HP:0003593	OMIM:609823	IEA				C		HPO:iea	
OMIM	609823	DEAFNESS, AUTOSOMAL RECESSIVE 28		HP:0008625	OMIM:609823	TAS				P		HPO:skoehler	
OMIM	609886	Glomerulocystic kidney disease with hyperuricemia and isosthenuria		HP:0000006	PMID:9013451	PCS				I	GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA	HPO:probinson	
OMIM	609886	Glomerulocystic kidney disease with hyperuricemia and isosthenuria		HP:0000083	PMID:9013451	PCS				P	GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA	HPO:probinson	
OMIM	609886	Glomerulocystic kidney disease with hyperuricemia and isosthenuria		HP:0000091	OMIM:609886	TAS				P	GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA	HPO:probinson	
OMIM	609886	Glomerulocystic kidney disease with hyperuricemia and isosthenuria		HP:0002149	OMIM:609886	PCS				P	GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA	HPO:probinson	
OMIM	609886	Glomerulocystic kidney disease with hyperuricemia and isosthenuria		HP:0100611	PMID:9013451	PCS				P	GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA	HPO:skoehler	
OMIM	609887	#609887 GLAUCOMA 1, OPEN ANGLE, G; GLC1G		HP:0012108	OMIM:609887	TAS				P		HPO:probinson	
OMIM	609909	#609909 CARDIOMYOPATHY, DILATED, 1P; CMD1P		HP:0000006	OMIM:609909	TAS				I		HPO:probinson	
OMIM	609909	#609909 CARDIOMYOPATHY, DILATED, 1P; CMD1P		HP:0001635	OMIM:609909	TAS				P		HPO:probinson	
OMIM	609909	#609909 CARDIOMYOPATHY, DILATED, 1P; CMD1P		HP:0001644	OMIM:609909	TAS				P		HPO:probinson	
OMIM	609909	#609909 CARDIOMYOPATHY, DILATED, 1P; CMD1P		HP:0004308	OMIM:609909	TAS				P		HPO:probinson	
OMIM	609909	#609909 CARDIOMYOPATHY, DILATED, 1P; CMD1P		HP:0006673	OMIM:609909	TAS				P		HPO:probinson	
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0000006	PMID:17924349	PCS				I		HPO:probinson	
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0000510	OMIM:609923	IEA				P		HPO:skoehler	
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0000512	PMID:17924349	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0001123	PMID:17924349	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0007722	PMID:17924349	PCS				P		HPO:probinson	
OMIM	609923	#609923 RETINITIS PIGMENTOSA 31; RP31		HP:0007843	PMID:17924349	PCS				P		HPO:probinson	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0000007	OMIM:609924	IEA				I		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0000316	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0000407	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0000431	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0000752	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001250	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001252	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001263	OMIM:609924	TAS				P		HPO:skoehler	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001272	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001290	OMIM:609924	TAS				P		HPO:skoehler	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0001324	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0002059	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0002188	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0006846	OMIM:609924	IEA				P		HPO:iea	
OMIM	609924	AMINOACYLASE 1 DEFICIENCY; ACY1D		HP:0025356	OMIM:609924	IEA				P		HPO:skoehler	
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0000707	PMID:16642431	PCS		HP:0040284		P		HPO:lccarmody	24.3%
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0000992	PMID:16642431	PCS		HP:0040284		P		HPO:lccarmody	76.3%
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0001369	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	85/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0001701	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	18/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0002102	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	53/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0002725	PMID:9843983	PCS		HP:0040284		P		HPO:probinson	76.3%
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0003493	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	98/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0005268	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	13/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0010982	OMIM:609939	TAS				I		HPO:probinson	
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0012211	PMID:9843983	PCS		HP:0040284		P		HPO:lccarmody	30/220
OMIM	609939	%609939 SYSTEMIC LUPUS ERYTHEMATOSUS, SUSCEPTIBILITY TO, 6; SLEB6		HP:0025300	PMID:16642431	PCS		HP:0040284		P		HPO:lccarmody	66%
OMIM	609941	DEAFNESS, AUTOSOMAL RECESSIVE 51		HP:0000007	PMID:16158433	PCS				I		HPO:probinson	
OMIM	609941	DEAFNESS, AUTOSOMAL RECESSIVE 51		HP:0000407	PMID:16158433	PCS	HP:0003593			P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000006	OMIM:609942	TAS				I		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000256	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000286	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000316	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000358	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000369	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000463	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000465	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000476	OMIM:609942	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0000494	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001263	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001629	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001631	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001634	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001639	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001642	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0001643	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0002007	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0003196	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0004322	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0004442	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0005281	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0011995	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0012209	OMIM:609942	TAS				P		HPO:probinson	
OMIM	609942	NOONAN SYNDROME 3; NS3		HP:0030799	OMIM:609942	IEA				P		HPO:skoehler	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000154	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000187	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000212	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000294	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000322	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000331	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000358	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000369	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000377	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000455	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000574	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000581	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000582	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000718	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000962	OMIM:609943	TAS				P		HPO:skoehler	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000998	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001212	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001249	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001500	OMIM:609943	IEA				P		HPO:skoehler	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001769	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002162	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002208	OMIM:609943	IEA				P		HPO:skoehler	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002553	OMIM:609943	IEA				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0003745	OMIM:609943	IEA				I		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0007074	OMIM:609943	TAS				P		HPO:probinson	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0007099	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0012745	OMIM:609943	TAS				P		HPO:skoehler	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0200012	OMIM:609943	IEA				P		HPO:iea	
OMIM	609943	HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0200012	OMIM:609943	TAS				P		HPO:skoehler	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000007	OMIM:609944	IEA				I		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000023	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000047	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000218	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000272	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000276	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000322	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000347	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000407	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000426	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000486	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000490	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000535	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000613	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000621	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000767	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0000968	OMIM:609944	TAS				P		HPO:probinson	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0001128	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0001939	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0002808	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0009466	OMIM:609944	IEA				P		HPO:iea	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0011800	OMIM:609944	TAS				P		HPO:skoehler	
OMIM	609944	ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVE FACIAL FEATURES		HP:0030084	OMIM:609944	TAS				P		HPO:skoehler	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000006	OMIM:609945	IEA				I		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000023	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000028	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000047	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000048	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000054	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000060	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000085	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000218	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000233	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000252	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000286	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000316	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000347	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000365	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000378	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000384	OMIM:609945	TAS				P		HPO:skoehler	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000396	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000431	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000470	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000473	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000508	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000568	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000581	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000767	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0000894	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001156	OMIM:609945	TAS				P		HPO:skoehler	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001162	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001171	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001263	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001363	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001631	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001762	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001770	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001831	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001839	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001840	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0001841	OMIM:609945	TAS				P		HPO:probinson	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002697	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002750	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002827	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002866	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002869	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0002984	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003022	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003038	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003065	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003083	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003175	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003182	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0003196	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0004058	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0004987	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0005160	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0005613	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0006380	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0006507	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0007385	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0008362	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0008386	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0008830	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0009556	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0009623	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0009756	OMIM:609945	TAS				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0009760	OMIM:609945	TAS				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0009803	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0010049	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0010561	OMIM:609945	IEA				P		HPO:skoehler	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0010743	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0010781	OMIM:609945	IEA				P		HPO:skoehler	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0010806	OMIM:609945	IEA				P		HPO:iea	
OMIM	609945	609945 BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA		HP:0011304	OMIM:609945	IEA				P		HPO:iea	
OMIM	609946	DEAFNESS, AUTOSOMAL RECESSIVE 47		HP:0000007	PMID:16261342	PCS				I		HPO:skoehler	
OMIM	609946	DEAFNESS, AUTOSOMAL RECESSIVE 47		HP:0000365	PMID:16261342	PCS	HP:0003593	HP:0040284		P		HP:probinson	5/5
OMIM	609952	DEAFNESS, AUTOSOMAL RECESSIVE 55		HP:0000007	PMID:16098016	PCS				I		HPO:skoehler	
OMIM	609952	DEAFNESS, AUTOSOMAL RECESSIVE 55		HP:0000365	PMID:16098016	PCS	HP:0003593			P		HP:probinson	
OMIM	609965	DEAFNESS, AUTOSOMAL DOMINANT 53		HP:0000006	PMID:15958501	PCS				I		HPO:skoehler	
OMIM	609965	DEAFNESS, AUTOSOMAL DOMINANT 53		HP:0000407	PMID:15958501	PCS	HP:0003621	HP:0040284		P		HP:probinson	16/16
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0000006	OMIM:609968	IEA				I		HPO:iea	
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0000825	OMIM:609968	IEA				P		HPO:iea	
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0001325	OMIM:609968	IEA				P		HPO:iea	
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0001425	OMIM:609968	TAS				I		HPO:skoehler	
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0002173	OMIM:609968	IEA				P		HPO:iea	
OMIM	609968	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5		HP:0008283	OMIM:609968	IEA				P		HPO:iea	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0000007	OMIM:609975	IEA				I		HPO:iea	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0000825	OMIM:609975	IEA				P		HPO:iea	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0001249	OMIM:609975	IEA				P		HPO:iea	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0001325	OMIM:609975	IEA				P		HPO:iea	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0001425	OMIM:609975	TAS				I		HPO:skoehler	
OMIM	609975	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 4; HHF4		HP:0002173	OMIM:609975	IEA				P		HPO:iea	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0000007	OMIM:609981	TAS				I		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0000252	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0000846	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0001263	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0001511	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0001744	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0002205	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0002240	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0002716	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0002878	OMIM:609981	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0004429	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0005523	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609981	NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT		HP:0008897	OMIM:609981	TAS				P		HPO:skoehler	
OMIM	609993	OSTEOSCLEROSIS - ICHTHYOSIS - PREMATURE OVARIAN FAILURE		HP:0008209	OMIM:609993	IEA				P		HPO:skoehler	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0000007	OMIM:610003	IEA				I		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0000711	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0000737	OMIM:610003	TAS				P		HPO:probinson	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0001249	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0001268	OMIM:610003	TAS				P		HPO:probinson	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0001272	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002059	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002069	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002074	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002312	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002353	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0002384	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0003205	OMIM:610003	IEA				P		HPO:iea	
OMIM	610003	CEROID LIPOFUSCINOSIS, NEURONAL, 8, NORTHERN EPILEPSY VARIANT		HP:0003677	OMIM:610003	IEA				C		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:610006	IEA				I		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0000252	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0000577	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001250	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001252	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001254	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001263	OMIM:610006	TAS				P		HPO:probinson	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001270	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:610006	TAS				P		HPO:skoehler	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0001943	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0002045	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0003593	OMIM:610006	IEA				C		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0003700	OMIM:610006	IEA				P		HPO:iea	
OMIM	610006	2-METHYLBUTYRYL-COA DEHYDROGENASE DEFICIENCY		HP:0005949	OMIM:610006	IEA				P		HPO:iea	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0000007	OMIM:610015	TAS				I		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0000369	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0000431	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0000988	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001250	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001290	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001298	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001347	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001371	OMIM:610015	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001522	OMIM:610015	TAS		HP:0040283		M		HPO:skoehler	HP:0040283
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001662	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0001987	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002079	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002093	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002104	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002119	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002416	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0002983	OMIM:610015	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0003429	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0005280	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0007109	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0011344	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610015	GLUTAMINE DEFICIENCY, CONGENITAL		HP:0012444	OMIM:610015	TAS				P		HPO:skoehler	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0000006	PMID:16532400	PCS				I		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0000445	PMID:16532400	PCS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0001156	OMIM:610017	TAS				P		HPO:skoehler	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0001762	OMIM:610017	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0002948	PMID:16532400	PCS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0003041	OMIM:610017	TAS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0008368	PMID:16532400	PCS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0009700	PMID:16532400	PCS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0009702	PMID:16532400	PCS				P		HPO:probinson	
OMIM	610017	MULTIPLE SYNOSTOSES SYNDROME 2		HP:0100264	OMIM:610017	TAS				P		HPO:skoehler	
OMIM	610019	#610019 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2; CATC2		HP:0000007	OMIM:610019	TAS				I		HPO:skoehler	
OMIM	610019	#610019 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 2; CATC2		HP:0000518	OMIM:610019	IEA				P		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0000006	OMIM:610021	TAS				I		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0000825	OMIM:610021	TAS				P		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0001325	OMIM:610021	TAS				P		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0001425	OMIM:610021	TAS				I		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0002173	OMIM:610021	TAS				P		HPO:skoehler	
OMIM	610021	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7		HP:0004510	OMIM:610021	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0000006	OMIM:610023	TAS				I		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS	HP:0012825	HP:0000365	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0000568	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0000612	OMIM:610023	IEA				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0000659	OMIM:610023	IEA				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0001156	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0001159	OMIM:610023	IEA				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS	HP:0012825	HP:0001263	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0004322	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0007906	OMIM:610023	IEA				P		HPO:skoehler	
OMIM	610023	BRACHYDACTYLY, COLOBOMA, AND ANTERIOR SEGMENT DYSGENESIS		HP:0030084	OMIM:610023	TAS				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000006	OMIM:610024	TAS				I		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000007	OMIM:610024	TAS				I		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000548	OMIM:610024	IEA				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000613	OMIM:610024	TAS				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000639	OMIM:610024	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0000662	OMIM:610024	TAS				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0007641	OMIM:610024	TAS				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0007663	OMIM:610024	TAS				P		HPO:skoehler	
OMIM	610024	#610024 RETINAL CONE DYSTROPHY 3A; RCD3A;;CONE DYSTROPHY WITH NIGHT BLINDNESS AND SUPERNORMAL ROD RESPONSES,PDE6H-RELATEDACHROMATOPSIA 6, INCLUDED; ACHM6, INCLUDED		HP:0008020	OMIM:610024	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0000006	OMIM:610031	IEA				I		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0000007	OMIM:610031	IEA				I		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0000252	OMIM:610031	IEA				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0000478	OMIM:610031	IEA				P		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001249	OMIM:610031	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001250	OMIM:610031	IEA				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001263	OMIM:610031	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001269	OMIM:610031	TAS				P		HPO:probinson	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001270	OMIM:610031	IEA				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001274	OMIM:610031	IEA				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001302	OMIM:610031	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001321	OMIM:610031	IEA				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001328	OMIM:610031	IEA				P		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0001491	OMIM:610031	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0002079	OMIM:610031	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0002307	OMIM:610031	TAS				P		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0003828	OMIM:610031	TAS				C		HPO:skoehler	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0006927	OMIM:610031	IEA				P		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0006930	OMIM:610031	IEA				P		HPO:iea	
OMIM	610031	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7		HP:0007941	OMIM:610031	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0000718	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0000733	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0000735	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0000752	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001249	OMIM:610042	TAS	HP:0011463			P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001250	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001251	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001257	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001263	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001315	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0001344	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0002194	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0002197	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0002353	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0002463	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0002465	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0007064	OMIM:610042	TAS				P		HPO:probinson	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0007359	OMIM:610042	IEA				P		HPO:skoehler	
OMIM	610042	PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1		HP:0032046	OMIM:610042	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0000006	PMID:15671264	PCS				I		HPO:probinson	
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0000486	PMID:15671264	IEA		HP:0040284		P		HPO:probinson	4/11
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0000501	PMID:15671264	IEA		HP:0040284		P		HPO:probinson	3/11
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0000529	OMIM:610048	TAS				P		HPO:skoehler	
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0008005	PMID:15671264	IEA				P		HPO:probinson	
OMIM	610048	#610048 CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD;;CONGENITAL STROMAL CORNEAL DYSTROPHY		HP:0011487	OMIM:610048	TAS				P		HPO:skoehler	
OMIM	610069	#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2		HP:0000006	PMID:16525031	PCS				I		HPO:skoehler	
OMIM	610069	#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2		HP:0003003	PMID:16525031	PCS				P		HPO:skoehler	
OMIM	610069	#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2		HP:0005227	PMID:16525031	PCS				P		HPO:skoehler	
OMIM	610069	#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2		HP:0012183	PMID:16525031	PCS				P		HPO:probinson	
OMIM	610069	#610069 POLYPOSIS SYNDROME, HEREDITARY MIXED, 2; HMPS2		HP:0012198	PMID:16525031	PCS				P		HPO:probinson	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0000007	OMIM:610090	IEA				I		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0000253	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001250	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001263	OMIM:610090	TAS				P		HPO:skoehler	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001276	OMIM:610090	TAS				P		HPO:skoehler	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001298	OMIM:610090	IEA				P		HPO:skoehler	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001336	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001508	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001583	PMID:12200739	PCS				P		HPO:lccarmody	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001622	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001903	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001942	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0001943	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0002151	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0002317	OMIM:610090	TAS				P		HPO:skoehler	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0003785	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0008872	OMIM:610090	IEA				P		HPO:iea	
OMIM	610090	PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY		HP:0008936	OMIM:610090	TAS				P		HPO:skoehler	
OMIM	610092	#610092 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3; MCOPCB3;;MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 3MICROPHTHALMIA, CATARACTS, AND IRIS ABNORMALITIES, INCLUDED		HP:0000007	OMIM:610092	TAS				I		HPO:probinson	
OMIM	610092	#610092 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3; MCOPCB3;;MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 3MICROPHTHALMIA, CATARACTS, AND IRIS ABNORMALITIES, INCLUDED		HP:0000518	OMIM:610092	TAS	HP:0003577			P		HPO:probinson	
OMIM	610092	#610092 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3; MCOPCB3;;MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 3MICROPHTHALMIA, CATARACTS, AND IRIS ABNORMALITIES, INCLUDED		HP:0000568	OMIM:610092	TAS				P		HPO:probinson	
OMIM	610092	#610092 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 3; MCOPCB3;;MICROPHTHALMIA, COLOBOMATOUS, ISOLATED 3MICROPHTHALMIA, CATARACTS, AND IRIS ABNORMALITIES, INCLUDED		HP:0000589	OMIM:610092	TAS				P		HPO:probinson	
OMIM	610093	#610093 MICROPHTHALMIA, ISOLATED 2; MCOP2;;ANOPHTHALMIA, CLINICAL, ISOLATED		HP:0000007	OMIM:610093	TAS				I		HPO:probinson	
OMIM	610093	#610093 MICROPHTHALMIA, ISOLATED 2; MCOP2;;ANOPHTHALMIA, CLINICAL, ISOLATED	HP:0012828	HP:0000568	OMIM:610093	TAS				P		HPO:probinson	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0000006	OMIM:610099	IEA				I		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0001171	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0001760	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0002312	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0002460	OMIM:610099	TAS				P		HPO:skoehler	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003376	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003458	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003560	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003677	OMIM:610099	IEA				C		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003693	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003694	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0003805	OMIM:610099	IEA				P		HPO:skoehler	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0008180	OMIM:610099	IEA				P		HPO:skoehler	
OMIM	610099	MYOPATHY, DISTAL 3		HP:0009473	OMIM:610099	IEA				P		HPO:iea	
OMIM	610099	MYOPATHY, DISTAL 3	HP:0012825	HP:0009473	OMIM:610099	TAS				P		HPO:skoehler	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:610100	IEA				I		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0001265	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0001284	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0001638	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0001761	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0001765	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0002460	OMIM:610100	TAS				P		HPO:probinson	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0003376	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0003383	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT	HP:0012825	HP:0003431	OMIM:610100	TAS				P		HPO:probinson	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0003444	OMIM:610100	IEA				P		HPO:iea	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0003477	OMIM:610100	IEA				P		HPO:skoehler	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0003693	OMIM:610100	TAS				P		HPO:probinson	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0006886	OMIM:610100	TAS				P		HPO:probinson	
OMIM	610100	GIANT AXONAL NEUROPATHY, AUTOSOMAL DOMINANT		HP:0006937	OMIM:610100	IEA				P		HPO:iea	
OMIM	610102	#610102 COMPLEMENT COMPONENT 7 DEFICIENCY; C7D;;C7 DEFICIENCY		HP:0000007	OMIM:610102	TAS				I		HPO:probinson	
OMIM	610102	#610102 COMPLEMENT COMPONENT 7 DEFICIENCY; C7D;;C7 DEFICIENCY		HP:0004431	OMIM:610102	TAS				P		HPO:probinson	
OMIM	610102	#610102 COMPLEMENT COMPONENT 7 DEFICIENCY; C7D;;C7 DEFICIENCY		HP:0005381	PMID:15831990	PCS				P		HPO:probinson	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000006	OMIM:610125	TAS				I		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000028	OMIM:610125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000054	OMIM:610125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000175	OMIM:610125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000482	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000518	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000528	OMIM:610125	IEA				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000556	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000568	OMIM:610125	IEA				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000589	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0000609	OMIM:610125	IEA				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0001250	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0001263	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0001290	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0001388	OMIM:610125	TAS				P		HPO:skoehler	
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0004322	OMIM:610125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610125	MICROPHTHALMIA, SYNDROMIC 5; MCOPS5		HP:0011755	OMIM:610125	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000007	OMIM:610127	IEA				I		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000252	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000340	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000369	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000431	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000510	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0000572	OMIM:610127	TAS				P		HPO:probinson	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001105	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001251	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001257	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001268	OMIM:610127	TAS				P		HPO:skoehler	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001272	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0001939	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002059	OMIM:610127	IEA				P		HPO:skoehler	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002063	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002074	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002093	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002104	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002133	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002529	OMIM:610127	TAS				P		HPO:probinson	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0002878	OMIM:610127	TAS				P		HPO:skoehler	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0003390	OMIM:610127	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0003577	OMIM:610127	IEA				C		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0005458	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0006887	OMIM:610127	IEA				P		HPO:iea	
OMIM	610127	#610127 CEROID LIPOFUSCINOSIS, NEURONAL, 10; CLN10;;CEROID LIPOFUSCINOSIS, NEURONAL, CATHEPSIN D-DEFICIENT;;NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCYNEURONAL CEROID LIPOFUSCINOSIS, CONGENITAL, INCLUDED		HP:0010864	OMIM:610127	TAS				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0000006	OMIM:610131	IEA				I		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0000508	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0000590	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001250	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001263	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001272	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001290	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001508	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0001952	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0002019	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0002020	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0002151	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0002578	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0002910	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003236	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003323	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003326	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003546	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003581	OMIM:610131	IEA				C		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003676	OMIM:610131	IEA				C		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003688	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003689	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003690	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0003828	OMIM:610131	TAS				C		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0010628	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0011675	OMIM:610131	IEA				P		HPO:skoehler	
OMIM	610131	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 4		HP:0100704	OMIM:610131	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0000006	OMIM:610140	IEA				I		HPO:skoehler	
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0001156	OMIM:610140	TAS				P		HPO:skoehler	
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0001159	OMIM:610140	IEA				P		HPO:skoehler	
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0001644	OMIM:610140	IEA				P		HPO:skoehler	
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0003198	OMIM:610140	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0010239	OMIM:610140	IEA				P		HPO:skoehler	
OMIM	610140	#610140 HEART-HAND SYNDROME, SLOVENIAN TYPE		HP:0030084	OMIM:610140	TAS				P		HPO:skoehler	
OMIM	610143	DEAFNESS, AUTOSOMAL RECESSIVE 62		HP:0000007	OMIM:610143	IEA				I		HPO:iea	
OMIM	610143	DEAFNESS, AUTOSOMAL RECESSIVE 62		HP:0000399	OMIM:610143	IEA				P		HPO:iea	
OMIM	610153	DEAFNESS, AUTOSOMAL RECESSIVE 49		HP:0000007	OMIM:610153	IEA				I		HPO:iea	
OMIM	610153	DEAFNESS, AUTOSOMAL RECESSIVE 49		HP:0000399	OMIM:610153	IEA				P		HPO:iea	
OMIM	610154	DEAFNESS, AUTOSOMAL RECESSIVE 44		HP:0000007	OMIM:610154	IEA				I		HPO:iea	
OMIM	610154	DEAFNESS, AUTOSOMAL RECESSIVE 44		HP:0000399	OMIM:610154	IEA				P		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0000007	PMID:16493448	PCS				I		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0000054	OMIM:610156	IEA				P		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0000518	PMID:16493448	PCS				P		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0000556	OMIM:610156	TAS	HP:0003577			P		HPO:probinson	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0000750	OMIM:610156	TAS				P		HPO:probinson	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0001956	PMID:16493448	PCS	HP:0011463			P		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0002342	OMIM:610156	IEA				P		HPO:iea	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0007663	OMIM:610156	IEA				P		HPO:skoehler	
OMIM	610156	MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME; MORMS		HP:0008915	OMIM:610156	TAS				P		HPO:skoehler	
OMIM	610158	%610158 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2;;FCD1 LOCUS;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0000006	OMIM:610158	TAS				I		HPO:skoehler	
OMIM	610158	%610158 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2;;FCD1 LOCUS;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0000969	OMIM:610158	TAS				P		HPO:skoehler	
OMIM	610158	%610158 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2;;FCD1 LOCUS;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0001131	OMIM:610158	IEA				P		HPO:skoehler	
OMIM	610158	%610158 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2;;FCD1 LOCUS;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0007705	OMIM:610158	TAS				P		HPO:skoehler	
OMIM	610158	%610158 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2; FECD2;;FCD1 LOCUS;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0012038	OMIM:610158	TAS				P		HPO:skoehler	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0000007	PMID:16672702	PCS				I		HPO:probinson	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0001880	PMID:16672702	PCS				P		HPO:probinson	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0002721	PMID:16672702	PCS				P		HPO:probinson	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0003593	OMIM:610163	TAS				C		HPO:skoehler	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0004385	PMID:16672702	PCS				P		HPO:probinson	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0005353	PMID:16672702	PCS				P		HPO:probinson	
OMIM	610163	IMMUNODEFICIENCY 25		HP:0005403	PMID:16672702	PCS				P		HPO:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000006	OMIM:610168	IEA				I		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000023	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000175	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000193	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000238	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000272	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000278	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000316	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000347	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000520	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000577	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000592	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000767	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000768	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0000939	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001065	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001156	OMIM:610168	TAS				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001159	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001166	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001249	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001263	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001363	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001388	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001425	OMIM:610168	TAS				I		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001519	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001537	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001631	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001634	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001643	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001647	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001762	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0001763	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0002108	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0002308	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0002650	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0003179	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0003302	PMID:24344637	PCS				P		HP:probinson	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004933	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004937	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004944	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004955	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004959	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0004970	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0005182	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0005807	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0009473	OMIM:610168	IEA				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0010442	OMIM:610168	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0010648	OMIM:610168	TAS				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0012385	OMIM:610168	TAS				P		HPO:skoehler	
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0100259	OMIM:610168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610168	#610168 LOEYS-DIETZ SYNDROME 2; LDS2;;AORTIC ANEURYSM, FAMILIAL THORACIC 3; AAT3;;MARFAN SYNDROME, TYPE II, FORMERLY		HP:0410151	PMID:23608731	PCS				P		HPO:lccarmody	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0000007	PMID:15908569	PCS				I		HPO:probinson	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0000252	OMIM:610181	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0001258	OMIM:610181	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0001298	PMID:15908569	PCS				P		HPO:probinson	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0001332	OMIM:610181	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0002059	PMID:15908569	PCS				P		HPO:probinson	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0002135	PMID:15908569	PCS				P		HPO:probinson	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0003828	OMIM:610181	TAS				C		HPO:skoehler	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0009704	PMID:15908569	PCS				P		HPO:probinson	
OMIM	610181	AICARDI-GOUTIERES SYNDROME 2; AGS2		HP:0100827	OMIM:610181	IEA				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0000007	OMIM:610185	IEA				I		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0000280	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0000464	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0000486	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0000750	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001007	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001260	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001263	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001265	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001272	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001310	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001321	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001337	OMIM:610185	IEA				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0001773	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002075	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002078	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002079	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002283	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002942	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0002943	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0003593	OMIM:610185	IEA				C		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0004279	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0004322	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0006887	OMIM:610185	IEA				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0007047	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0007063	OMIM:610185	IEA				P		HPO:iea	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0010864	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610185	#610185 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2; CAMRQ2;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 2		HP:0200055	OMIM:610185	TAS				P		HPO:skoehler	
OMIM	610187	#610187 DIAPHRAGMATIC HERNIA 3;;DIH3		HP:0000776	PMID:17568391	PCS				P		HPO:probinson	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000007	OMIM:610188	IEA				I		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000090	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000480	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000510	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000639	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000657	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0000803	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0001249	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0001251	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0001252	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0001290	OMIM:610188	TAS				P		HPO:skoehler	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002335	OMIM:610188	TAS				P		HPO:probinson	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002404	OMIM:610188	TAS				P		HPO:probinson	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002419	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002790	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002871	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0002876	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0003774	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0004727	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0006817	OMIM:610188	IEA				P		HPO:iea	
OMIM	610188	JOUBERT SYNDROME 5		HP:0007875	OMIM:610188	IEA				P		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0000007	OMIM:610189	IEA				I		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0000505	OMIM:610189	IEA				P		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0000510	OMIM:610189	IEA				P		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0000707	OMIM:610189	IEA				P		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0003774	OMIM:610189	IEA				P		HPO:iea	
OMIM	610189	#610189 SENIOR-LOKEN SYNDROME 6; SLSN6		HP:0007663	OMIM:610189	TAS				P		HPO:skoehler	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0000006	OMIM:610193	IEA				I		HPO:iea	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0001425	OMIM:610193	TAS				I		HPO:skoehler	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0001645	OMIM:610193	IEA				P		HPO:iea	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0001962	OMIM:610193	IEA				P		HPO:iea	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0004756	OMIM:610193	TAS				P		HPO:probinson	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0006682	OMIM:610193	TAS				P		HPO:skoehler	
OMIM	610193	#610193 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10; ARVC10		HP:0011663	OMIM:610193	TAS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0000007	OMIM:610198	IEA				I		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0000028	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0000047	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0000648	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001249	OMIM:610198	TAS				P		HPO:skoehler	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001324	OMIM:610198	TAS				P		HPO:skoehler	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001414	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001511	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001635	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001644	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001645	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0001657	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0002470	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0003150	OMIM:610198	TAS				P		HPO:skoehler	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0003344	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0004856	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0008734	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0008897	OMIM:610198	IEA				P		HPO:iea	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0008897	OMIM:610198	PCS				P		HPO:probinson	
OMIM	610198	#610198 3-@METHYLGLUTACONIC ACIDURIA, TYPE V; MGCA5;;CARDIOMYOPATHY, DILATED, WITH ATAXIA; DCMA;;MGA, TYPE V; MGA5		HP:0012817	OMIM:610198	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000007	OMIM:610199	TAS				I		HPO:probinson	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000113	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000219	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000260	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000286	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000343	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000369	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000407	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000453	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000557	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000819	OMIM:610199	TAS	HP:0003623			P		HPO:probinson	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000851	OMIM:610199	TAS	HP:0003623			P		HPO:probinson	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0000938	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001263	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001395	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001396	OMIM:610199	TAS				P		HPO:probinson	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001409	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001409	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001511	OMIM:610199	TAS				P		HPO:probinson	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001537	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001737	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0001744	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0002036	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0002240	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0002594	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0002719	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0002944	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0004442	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0005280	OMIM:610199	TAS				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0012115	OMIM:610199	IEA				P		HPO:skoehler	
OMIM	610199	DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH		HP:0030423	OMIM:610199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0000006	OMIM:610202	IEA				I		HPO:iea	
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0000482	OMIM:610202	IEA				P		HPO:iea	
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0000541	OMIM:610202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0000612	OMIM:610202	IEA				P		HPO:iea	
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0001104	OMIM:610202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0007780	OMIM:610202	IEA	HP:0003621			P		HPO:iea	
OMIM	610202	#610202 CATARACT 21, MULTIPLE TYPES; CTRCT21;;CATARACT 21, MULTIPLE TYPES, WITH OR WITHOUT MICROCORNEA;;CATARACT, CONGENITAL, CERULEAN TYPE, 4; CCA4;;CATARACT, PULVERULENT, JUVENILE-ONSET		HP:0007976	OMIM:610202	IEA				P		HPO:iea	
OMIM	610204	PONTOCEREBELLAR HYPOPLASIA, TYPE 5; PCH5		HP:0000007	OMIM:610204	TAS				I		HPO:skoehler	
OMIM	610204	PONTOCEREBELLAR HYPOPLASIA, TYPE 5; PCH5		HP:0000252	OMIM:610204	TAS				P		HPO:skoehler	
OMIM	610204	PONTOCEREBELLAR HYPOPLASIA, TYPE 5; PCH5		HP:0001250	OMIM:610204	TAS				P		HPO:skoehler	
OMIM	610204	PONTOCEREBELLAR HYPOPLASIA, TYPE 5; PCH5		HP:0003577	OMIM:610204	TAS				C		HPO:skoehler	
OMIM	610204	PONTOCEREBELLAR HYPOPLASIA, TYPE 5; PCH5	HP:0012828	HP:0006955	OMIM:610204	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000006	OMIM:610205	TAS				I		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000083	PMID:16773578	PCS				P		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000089	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000093	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000107	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000307	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000325	PMID:16773578	PCS				P		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000337	PMID:16773578	PCS				P		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000627	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000790	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0000822	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0001631	OMIM:610205	TAS				P		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0001636	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0001642	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0001947	OMIM:610205	TAS				P		HPO:probinson	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0002611	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0003189	OMIM:610205	TAS				P		HPO:skoehler	
OMIM	610205	ALAGILLE SYNDROME 2		HP:0004969	OMIM:610205	TAS				P		HPO:probinson	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0000006	OMIM:610208	IEA				I		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0000613	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0002013	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0002018	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0002077	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0002083	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610208	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10		HP:0002183	OMIM:610208	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0000006	OMIM:610209	IEA				I		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0000613	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0002013	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0002018	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0002077	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0002083	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610209	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11		HP:0002183	OMIM:610209	IEA				P		HPO:skoehler	
OMIM	610212	DEAFNESS, AUTOSOMAL RECESSIVE 66; DFNB66		HP:0000007	OMIM:610212	TAS				I		HPO:skoehler	
OMIM	610212	DEAFNESS, AUTOSOMAL RECESSIVE 66; DFNB66	HP:0012829	HP:0000407	OMIM:610212	TAS				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000007	OMIM:610217	IEA				I		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000639	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000648	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000712	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000736	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000750	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0000752	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001250	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001257	OMIM:610217	TAS				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001260	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001268	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001272	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001276	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001310	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001332	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0001884	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002015	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002059	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002066	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002067	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002072	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002075	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002080	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002180	OMIM:610217	TAS				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0002185	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0003487	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0003676	OMIM:610217	IEA				C		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0007772	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0011463	OMIM:610217	TAS				C		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0011968	OMIM:610217	TAS				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0100315	OMIM:610217	IEA				P		HPO:skoehler	
OMIM	610217	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B; NBIA2B		HP:0100710	OMIM:610217	TAS				P		HPO:skoehler	
OMIM	610220	#610220 DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59		HP:0000007	OMIM:610220	IEA				I		HPO:probinson	
OMIM	610220	#610220 DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59		HP:0000407	OMIM:610220	IEA				P		HPO:probinson	
OMIM	610227	#610227 SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS		HP:0000006	OMIM:610227	TAS				I		HPO:probinson	
OMIM	610227	#610227 SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS		HP:0000962	OMIM:610227	TAS				P		HPO:probinson	
OMIM	610227	#610227 SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS		HP:0001051	OMIM:610227	TAS				P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0000006	OMIM:610244	TAS				I		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0001258	OMIM:610244	IEA				P		HPO:skoehler	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0001762	OMIM:610244	TAS				P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0002061	OMIM:610244	TAS				P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0002064	OMIM:610244	TAS	HP:0003581			P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0003487	OMIM:610244	TAS				P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0007340	OMIM:610244	TAS				P		HPO:probinson	
OMIM	610244	SPASTIC PARAPLEGIA 33, AUTOSOMAL DOMINANT		HP:0011448	OMIM:610244	TAS				P		HPO:probinson	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0000006	OMIM:610245	TAS				I		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0000514	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001260	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001271	OMIM:610245	IEA				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001272	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001274	OMIM:610245	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001310	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001337	OMIM:610245	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0001347	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0002066	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0002070	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0002166	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0002529	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0003487	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0003677	OMIM:610245	TAS				C		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0007141	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610245	SPINOCEREBELLAR ATAXIA 23; SCA23		HP:0007305	OMIM:610245	TAS				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000006	OMIM:610246	IEA				I		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000508	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000514	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000597	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000640	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0000641	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001257	OMIM:610246	TAS				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001260	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001272	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001276	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001300	OMIM:610246	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0001332	OMIM:610246	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0002066	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0002070	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0002395	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0003487	OMIM:610246	IEA				P		HPO:skoehler	
OMIM	610246	#610246 SPINOCEREBELLAR ATAXIA 28; SCA28		HP:0003677	OMIM:610246	IEA				C		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0001508	OMIM:610247	TAS				P		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0001880	OMIM:610247	IEA				P		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0002013	OMIM:610247	TAS				P		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0002015	OMIM:610247	TAS				P		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0100633	OMIM:610247	IEA				P		HPO:skoehler	
OMIM	610247	ESOPHAGITIS, EOSINOPHILIC, 1; EOE1		HP:0410019	OMIM:610247	TAS				P		HPO:skoehler	
OMIM	610248	DEAFNESS, AUTOSOMAL RECESSIVE 65; DFNB65		HP:0000007	OMIM:610248	IEA				I		HPO:skoehler	
OMIM	610248	DEAFNESS, AUTOSOMAL RECESSIVE 65; DFNB65		HP:0000365	OMIM:610248	IEA				P		HPO:skoehler	
OMIM	610248	DEAFNESS, AUTOSOMAL RECESSIVE 65; DFNB65		HP:0003593	OMIM:610248	IEA				C		HPO:skoehler	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0000006	OMIM:610250	TAS				I		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0000012	OMIM:610250	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0001258	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0001260	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0001761	OMIM:610250	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0002015	OMIM:610250	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0002064	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0002936	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0003202	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0003487	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0003828	OMIM:610250	TAS				C		HPO:skoehler	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0007340	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610250	#610250 SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT; SPG31		HP:0011448	OMIM:610250	TAS				P		HPO:probinson	
OMIM	610251	ALCOHOL SENSITIVITY, ACUTE		HP:0000006	OMIM:610251	TAS				I		HPO:skoehler	
OMIM	610251	ALCOHOL SENSITIVITY, ACUTE		HP:0001033	OMIM:610251	TAS				P		HPO:skoehler	
OMIM	610251	ALCOHOL SENSITIVITY, ACUTE		HP:0003533	OMIM:610251	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000006	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS				I		HPO:sdoelken	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000028	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000047	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000054	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000158	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000232	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000248	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000252	PMID:19264732	PCS		HP:0040284		P		HPO:sdoelken	8/22
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000272	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000280	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0003621	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000303	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000316	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000365	PMID:19264732	PCS		HP:0040284		P		HPO:sdoelken	3/22
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000377	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000463	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000582	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000664	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000695	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0003577	HP:0040283		P		HPO:sdoelken	HP:0040283
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000717	http://www.ncbi.nlm.nih.gov/books/NBK47079/	PCS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000718	OMIM:610253	PCS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000722	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000733	http://www.ncbi.nlm.nih.gov/books/NBK47079/	PCS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000741	http://www.ncbi.nlm.nih.gov/books/NBK47079/	PCS	HP:0003621	HP:0040284		P		HPO:sdoelken	HP:0040284
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000750	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0000954	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001156	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001250	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040284		P		HPO:sdoelken	30%
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001290	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001513	PMID:19264732	PCS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001710	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040284		P		HPO:sdoelken	50%
OMIM	610253	KLEEFSTRA SYNDROME		HP:0001762	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040283		P		HPO:sdoelken	HP:0040283
OMIM	610253	KLEEFSTRA SYNDROME		HP:0002020	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040283		P		HPO:sdoelken	HP:0040283
OMIM	610253	KLEEFSTRA SYNDROME		HP:0002205	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0002360	http://www.ncbi.nlm.nih.gov/books/NBK47079/	PCS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0002786	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040284		P		HPO:sdoelken	HP:0040284
OMIM	610253	KLEEFSTRA SYNDROME		HP:0003745	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS				I		HPO:sdoelken	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0006335	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0003621	HP:0040283		P		HPO:sdoelken	HP:0040283
OMIM	610253	KLEEFSTRA SYNDROME		HP:0010806	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS	HP:0011463	HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0010808	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040282		P		HPO:sdoelken	HP:0040282
OMIM	610253	KLEEFSTRA SYNDROME		HP:0010864	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0011800	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610253	KLEEFSTRA SYNDROME		HP:0012210	http://www.ncbi.nlm.nih.gov/books/NBK47079/	TAS		HP:0040284		P		HPO:sdoelken	15%
OMIM	610253	KLEEFSTRA SYNDROME		HP:0012368	OMIM:610253	TAS				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000007	OMIM:610256	TAS				I		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000482	OMIM:610256	TAS				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000518	OMIM:610256	TAS				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000526	OMIM:610256	TAS				P		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000568	OMIM:610256	TAS				P		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000589	OMIM:610256	IEA				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000639	OMIM:610256	TAS				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000647	OMIM:610256	TAS				P		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0000659	OMIM:610256	TAS				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0007707	OMIM:610256	TAS				P		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0007779	OMIM:610256	TAS				P		HPO:probinson	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0007906	OMIM:610256	IEA				P		HPO:skoehler	
OMIM	610256	ANTERIOR SEGMENT DYSGENESIS 2; ASGD2		HP:0011484	OMIM:610256	TAS				P		HPO:skoehler	
OMIM	610265	#610265 DEAFNESS, AUTOSOMAL RECESSIVE 67; DFNB67		HP:0000007	PMID:16459341	PCS				I		HPO:probinson	
OMIM	610265	#610265 DEAFNESS, AUTOSOMAL RECESSIVE 67; DFNB67		HP:0008619	PMID:16752389	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	610271	Glycosylphosphatidylinositol biosynthesis defect 18		HP:0000007	PMID:30269814	TAS				I	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18	HP:probinson	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0000007	OMIM:610279	IEA				I		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0000316	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0000506	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0000565	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0001250	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0001302	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610279	PACHYGYRIA, FRONTOTEMPORAL		HP:0002342	OMIM:610279	IEA				P		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000006	OMIM:610282	IEA				I		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000007	OMIM:610282	IEA				I		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000510	OMIM:610282	IEA				P		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000548	OMIM:610282	IEA				P		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000618	OMIM:610282	IEA				P		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0000662	OMIM:610282	IEA				P		HPO:skoehler	
OMIM	610282	RETINITIS PIGMENTOSA 35; RP35		HP:0001000	OMIM:610282	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000007	OMIM:610283	IEA				I		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000510	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10	HP:0003676	HP:0000529	OMIM:610283	TAS				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000548	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000608	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000613	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0000662	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0001000	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0007994	OMIM:610283	TAS				P		HPO:skoehler	
OMIM	610283	CONE-ROD DYSTROPHY 10		HP:0009926	OMIM:610283	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0000007	OMIM:610293	IEA				I		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0001250	OMIM:610293	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0001409	OMIM:610293	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0001744	OMIM:610293	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0002121	PMID:26996948	TAS				P		HPO:nvasilevsky	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0002240	OMIM:610293	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0004936	OMIM:610293	IEA				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0010819	PMID:26996948	TAS				P		HPO:nvasilevsky	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0030242	OMIM:610293	TAS				P		HPO:skoehler	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0030243	OMIM:610293	TAS				P		HPO:nvasilevsky	
OMIM	610293	GLYCOSYLPHOSPHATIDYLINOSITOL DEFICIENCY		HP:0031555	PMID:17442906	TAS				P		HPO:nvasilevsky	
OMIM	610297	#610297 PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13		HP:0000006	OMIM:610297	TAS				I		HPO:probinson	
OMIM	610297	#610297 PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13		HP:0001337	OMIM:610297	TAS				P		HPO:probinson	
OMIM	610297	#610297 PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13		HP:0002063	OMIM:610297	TAS				P		HPO:probinson	
OMIM	610297	#610297 PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13		HP:0002067	OMIM:610297	TAS				P		HPO:probinson	
OMIM	610297	#610297 PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO; PARK13		HP:0002548	OMIM:610297	TAS				P		HPO:probinson	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0000007	OMIM:610313	IEA				I		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0000218	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0000411	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0000975	OMIM:610313	TAS				P		HPO:skoehler	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0001377	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0001760	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0002938	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0002944	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0002967	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0004691	OMIM:610313	TAS				P		HPO:probinson	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0007141	OMIM:610313	TAS				P		HPO:skoehler	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0008872	OMIM:610313	TAS				P		HPO:skoehler	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0009466	OMIM:610313	IEA				P		HPO:iea	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0010628	OMIM:610313	TAS				P		HPO:skoehler	
OMIM	610313	#610313 COLD-INDUCED SWEATING SYNDROME 2; CISS2		HP:0030084	OMIM:610313	TAS				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000007	OMIM:610319	IEA				I		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000470	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000486	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000505	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000510	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000613	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000705	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000773	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000885	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0000894	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0002650	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0003890	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0004586	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0005792	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0007663	OMIM:610319	TAS				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0008905	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610319	610319 RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA		HP:0100864	OMIM:610319	IEA				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0000007	PMID:16845400	PCS				I		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0000253	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0000639	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001257	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001290	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001298	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001332	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001347	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001433	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0001873	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0002079	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0002514	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0002910	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0003676	OMIM:610329	TAS				C		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0003819	PMID:16845400	PCS				M		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0011344	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0012448	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610329	AICARDI-GOUTIERES SYNDROME 3		HP:0200149	OMIM:610329	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0000007	PMID:16845400	PCS				I		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0000238	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0000253	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0000369	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0000444	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001250	OMIM:610333	IEA				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001257	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001272	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001332	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001433	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001511	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001744	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001873	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0001876	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002059	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002119	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002240	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002415	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002514	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0002910	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0003593	OMIM:610333	TAS				C		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0003819	PMID:16845400	PCS				M		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0011344	PMID:16845400	PCS				P		HPO:probinson	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0011968	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610333	AICARDI-GOUTIERES SYNDROME 4; AGS4		HP:0200149	OMIM:610333	TAS				P		HPO:skoehler	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0000006	OMIM:610338	IEA				I		HPO:iea	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0001629	OMIM:610338	IEA				P		HPO:iea	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0001643	OMIM:610338	IEA				P		HPO:iea	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0001655	OMIM:610338	IEA				P		HPO:iea	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0001680	OMIM:610338	IEA				P		HPO:iea	
OMIM	610338	RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL		HP:0005143	OMIM:610338	IEA				P		HPO:iea	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0000006	OMIM:610353	IEA				I		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0000708	OMIM:610353	IEA				P		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0001250	OMIM:610353	IEA				P		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0001289	OMIM:610353	IEA				P		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0001332	OMIM:610353	IEA				P		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0001425	OMIM:610353	TAS				I		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0003829	OMIM:610353	IEA				C		HPO:skoehler	
OMIM	610353	EPILEPSY, NOCTURNAL FRONTAL LOBE, 4; ENFL4		HP:0025144	OMIM:610353	IEA				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000007	OMIM:610356	TAS				I		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000483	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000486	OMIM:610356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000545	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000548	OMIM:610356	IEA				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000575	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000613	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000662	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0000666	OMIM:610356	TAS				P		HPO:skoehler	
OMIM	610356	RETINAL CONE DYSTROPHY 3B		HP:0007401	OMIM:610356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0000007	OMIM:610357	IEA				I		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0001258	OMIM:610357	TAS				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0001272	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0001310	OMIM:610357	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0001347	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0002061	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0002064	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0002839	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0003477	OMIM:610357	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0003487	OMIM:610357	IEA				P		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0003677	OMIM:610357	IEA				C		HPO:skoehler	
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0007210	OMIM:610357	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0007340	OMIM:610357	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	610357	#610357 SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE; SPG30		HP:0011448	OMIM:610357	TAS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0000006	PMID:19878916	PCS				I		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0000505	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0000510	OMIM:610359	IEA				P		HPO:skoehler	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0000543	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0000662	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0007722	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0007737	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610359	#610359 RETINITIS PIGMENTOSA 33; RP33		HP:0007843	PMID:19878916	PCS				P		HPO:probinson	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0000007	OMIM:610370	IEA				I		HPO:iea	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0001508	OMIM:610370	IEA				P		HPO:iea	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0001944	OMIM:610370	IEA				P		HPO:iea	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0002013	OMIM:610370	IEA				P		HPO:iea	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0002014	OMIM:610370	TAS				P		HPO:skoehler	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0003623	OMIM:610370	IEA				C		HPO:iea	
OMIM	610370	DIARRHEA 4, MALABSORPTIVE, CONGENITAL		HP:0004918	OMIM:610370	IEA				P		HPO:iea	
OMIM	610374	#610374 DIABETES MELLITUS, TRANSIENT NEONATAL, 2;;TNDM2		HP:0000006	PMID:16885549	PCS				I		HPO:probinson	
OMIM	610374	#610374 DIABETES MELLITUS, TRANSIENT NEONATAL, 2;;TNDM2		HP:0005978	PMID:16885549	PCS	HP:0003581	HP:0040284		P		HPO:probinson	2/7
OMIM	610374	#610374 DIABETES MELLITUS, TRANSIENT NEONATAL, 2;;TNDM2		HP:0008255	PMID:16885549	PCS	HP:0003623			P		HPO:probinson	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000007	OMIM:610377	IEA				I		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000239	OMIM:610377	TAS				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000252	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000268	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000325	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000358	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000369	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000494	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000518	OMIM:610377	IEA				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000592	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000639	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0000969	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001252	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001263	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001272	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001290	OMIM:610377	TAS				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001508	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001873	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0001974	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002013	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002014	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002059	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002073	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002335	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002716	OMIM:610377	TAS				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002751	OMIM:610377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002829	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0002910	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0003236	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0004322	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0004819	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0006268	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0006564	OMIM:610377	IEA				P		HPO:iea	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0012072	OMIM:610377	IEA				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0012282	OMIM:610377	TAS				P		HPO:skoehler	
OMIM	610377	MEVALONIC ACIDURIA; MEVA		HP:0025356	OMIM:610377	IEA				P		HPO:skoehler	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0000006	PMID:15028672	PCS				I		HPO:probinson	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0000548	PMID:15028672	PCS				P		HPO:probinson	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0000608	PMID:15028672	PCS				P		HPO:probinson	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0000613	OMIM:610381	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0000980	OMIM:610381	IEA				P		HPO:skoehler	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11	HP:0003676	HP:0007401	OMIM:610381	TAS				P		HPO:skoehler	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0007924	OMIM:610381	TAS				P		HPO:skoehler	
OMIM	610381	CONE-ROD DYSTROPHY 11; CORD11		HP:0011504	OMIM:610381	TAS				P		HPO:skoehler	
OMIM	610382	%610382 PROSOPAGNOSIA, HEREDITARY;;FACE BLINDNESS;;PROSOPAGNOSIA, DEVELOPMENTAL;;PROSOPAGNOSIA, CONGENITAL		HP:0000006	OMIM:610382	TAS				I		HPO:skoehler	
OMIM	610382	%610382 PROSOPAGNOSIA, HEREDITARY;;FACE BLINDNESS;;PROSOPAGNOSIA, DEVELOPMENTAL;;PROSOPAGNOSIA, CONGENITAL		HP:0010528	OMIM:610382	IEA				P		HPO:skoehler	
OMIM	610419	DEAFNESS, AUTOSOMAL RECESSIVE 68		HP:0000007	OMIM:610419	TAS				I		HPO:iea	
OMIM	610419	DEAFNESS, AUTOSOMAL RECESSIVE 68		HP:0000407	OMIM:610419	TAS				P		HPO:iea	
OMIM	610419	DEAFNESS, AUTOSOMAL RECESSIVE 68		HP:0003593	OMIM:610419	TAS				C		HPO:iea	
OMIM	610420	PREAURICULAR TAG, ISOLATED, AUTOSOMAL DOMINANT, 1		HP:0000006	OMIM:610420	IEA				I		HPO:iea	
OMIM	610420	PREAURICULAR TAG, ISOLATED, AUTOSOMAL DOMINANT, 1		HP:0000384	OMIM:610420	IEA				P		HPO:iea	
OMIM	610422	ALOPECIA-MENTAL RETARDATION SYNDROME 2		HP:0000007	OMIM:610422	IEA				I		HPO:iea	
OMIM	610422	ALOPECIA-MENTAL RETARDATION SYNDROME 2		HP:0001249	OMIM:610422	IEA				P		HPO:iea	
OMIM	610422	ALOPECIA-MENTAL RETARDATION SYNDROME 2		HP:0002289	OMIM:610422	IEA				P		HPO:iea	
OMIM	610425	#610425 CATARACT, LAMELLAR 2		HP:0000006	PMID:16960806	PCS				I		HPO:probinson	
OMIM	610425	#610425 CATARACT, LAMELLAR 2		HP:0007971	PMID:16960806	PCS	HP:0003577			P		HPO:probinson	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000007	PMID:16960802	PCS				I		HPO:probinson	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000486	OMIM:610427	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000505	PMID:16960802	PCS				P		HPO:probinson	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000551	OMIM:610427	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000613	OMIM:610427	TAS				P		HPO:skoehler	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0000639	PMID:16960802	PCS				P		HPO:probinson	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0007642	PMID:16960802	PCS				P		HPO:probinson	
OMIM	610427	#610427 CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD;;NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B, FORMERLY; CSNB2B,FORMERLY;;NIGHT BLINDNESS, CONGENITAL STATIONARY, INCOMPLETE, AUTOSOMAL RECESSIVE,FORMERLY		HP:0007984	PMID:16960802	PCS				P		HPO:probinson	
OMIM	610441	%610441 TESTICULAR MICROLITHIASIS		HP:0012215	PMID:16960801	TAS				P		HPO:probinson	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000007	OMIM:610442	IEA				I		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000179	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000248	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000252	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000280	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000286	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000294	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000377	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000445	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000470	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000486	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000639	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000664	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000926	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0000951	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001007	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001249	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001250	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001251	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001252	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001290	OMIM:610442	TAS				P		HPO:skoehler	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001388	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0001498	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002059	OMIM:610442	IEA				P		HPO:skoehler	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002079	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002119	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002162	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002651	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0002868	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0003015	OMIM:610442	TAS				P		HPO:probinson	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0003025	OMIM:610442	TAS				P		HPO:probinson	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0003085	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0003180	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0003301	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0005121	OMIM:610442	IEA				P		HPO:iea	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0010582	OMIM:610442	TAS				P		HPO:probinson	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0010585	OMIM:610442	TAS				P		HPO:probinson	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0010864	OMIM:610442	TAS				P		HPO:skoehler	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0011220	OMIM:610442	TAS				P		HPO:skoehler	
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0012697	OMIM:610442	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610442	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, GENEVIEVE TYPE; SEMDG		HP:0100864	OMIM:610442	IEA				P		HPO:iea	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000006	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA				I		HPO:iea	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000028	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040284		P		HPO:iea	71%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000076	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000079	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040284		P		HPO:iea	37%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000126	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000164	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000175	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000189	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000194	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000204	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000218	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000232	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000252	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000276	OMIM:610443	TAS		HP:0040284		P		HPO:skoehler	74%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000286	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000337	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000348	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000396	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000400	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000414	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000426	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000447	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000486	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000508	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000540	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000581	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000582	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000601	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000687	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000739	OMIM:610443	IEA				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000750	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000752	OMIM:610443	IEA				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000767	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000958	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000960	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0000964	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001166	OMIM:610443	TAS		HP:0040284		P		HPO:skoehler	61%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001212	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001238	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001249	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001250	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040284		P		HPO:iea	55%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001263	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001290	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040281		P		HPO:iea	HP:0040281
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001382	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001385	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001466	OMIM:610443	TAS				I		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001508	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001511	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001518	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001611	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001629	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001631	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001642	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0001647	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002021	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002079	OMIM:610443	IEA				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002119	OMIM:610443	TAS		HP:0040284		P		HPO:skoehler	38%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002282	OMIM:610443	IEA				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002465	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002650	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002705	OMIM:610443	TAS		HP:0040284		P		HPO:skoehler	50%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002808	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002827	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0002948	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0003302	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0003745	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA				I		HPO:iea	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0003828	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA				C		HPO:iea	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0004283	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0004322	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0004942	OMIM:610443	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0005487	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0005656	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0006006	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0006610	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0008872	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0009887	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0010719	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0011822	OMIM:610443	TAS		HP:0040284		P		HPO:skoehler	42%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0030680	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040284		P		HPO:iea	39%
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0040080	OMIM:610443	TAS				P		HPO:skoehler	
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0100024	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=mdel17q21_31	IEA		HP:0040282		P		HPO:iea	HP:0040282
OMIM	610443	KOOLEN-DE VRIES SYNDROME; KDVS		HP:0100710	OMIM:610443	IEA				P		HPO:skoehler	
OMIM	610444	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3		HP:0000006	OMIM:610444	TAS				I		HPO:probinson	
OMIM	610444	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3		HP:0000618	OMIM:610444	IEA				P		HPO:skoehler	
OMIM	610444	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3		HP:0007642	OMIM:610444	TAS				P		HPO:probinson	
OMIM	610445	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1		HP:0000006	OMIM:610445	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	610445	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1		HP:0000654	OMIM:610445	IEA				P		HPO:probinson	
OMIM	610445	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1		HP:0001123	OMIM:610445	IEA				P		HPO:probinson	
OMIM	610445	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1		HP:0007642	OMIM:610445	IEA				P		HPO:probinson	
OMIM	610445	NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1		HP:0007737	OMIM:610445	IEA				P		HPO:probinson	
OMIM	610448	CHILBLAIN LUPUS 1		HP:0000006	OMIM:610448	TAS				I		HPO:iea	
OMIM	610448	CHILBLAIN LUPUS 1		HP:0001597	OMIM:610448	IEA		HP:0040283		P		HPO:iea	HP:0040283
OMIM	610448	CHILBLAIN LUPUS 1		HP:0002829	OMIM:610448	TAS				P		HPO:iea	
OMIM	610448	CHILBLAIN LUPUS 1		HP:0003493	OMIM:610448	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610448	CHILBLAIN LUPUS 1		HP:0003621	OMIM:610448	IEA				C		HPO:iea	
OMIM	610448	CHILBLAIN LUPUS 1		HP:0200042	OMIM:610448	TAS				P		HPO:iea	
OMIM	610455	TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL		HP:0000007	OMIM:610455	IEA				I		HPO:iea	
OMIM	610455	TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL		HP:0000230	OMIM:610455	IEA				P		HPO:iea	
OMIM	610455	TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL		HP:0000509	OMIM:610455	IEA				P		HPO:iea	
OMIM	610455	TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL		HP:0000951	OMIM:610455	IEA				P		HPO:iea	
OMIM	610455	TUMORAL CALCINOSIS, NORMOPHOSPHATEMIC, FAMILIAL		HP:0003761	OMIM:610455	IEA				P		HPO:skoehler	
OMIM	610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0000007	OMIM:610460	TAS				I		HPO:iea	
OMIM	610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0001871	OMIM:610460	IEA				P		HPO:iea	
OMIM	610460	THIOPURINE S-METHYLTRANSFERASE DEFICIENCY		HP:0001939	OMIM:610460	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000006	OMIM:610474	IEA				I		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000007	OMIM:610474	TAS				I		HPO:skoehler	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000098	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000218	OMIM:610474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000252	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000407	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0000767	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0001166	OMIM:610474	TAS				P		HPO:skoehler	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0001249	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0001263	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0001836	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0002650	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0004570	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0006417	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0009473	OMIM:610474	IEA				P		HPO:iea	
OMIM	610474	CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME		HP:0030431	OMIM:610474	TAS				P		HPO:skoehler	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000006	OMIM:610475	IEA				I		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000311	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000709	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000713	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000716	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000739	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000822	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000938	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000939	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000963	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0000978	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001065	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001268	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001575	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001579	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001580	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0001956	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0002808	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0002920	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0003466	OMIM:610475	IEA				P		HPO:iea	
OMIM	610475	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2		HP:0003674	OMIM:610475	IEA				C		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0000006	OMIM:610476	IEA				I		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0000007	OMIM:610476	TAS				I		HPO:skoehler	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0000982	OMIM:610476	TAS				P		HPO:skoehler	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0001279	OMIM:610476	IEA				P		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0001645	OMIM:610476	IEA				P		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0001962	OMIM:610476	IEA				P		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0002094	OMIM:610476	IEA				P		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0002224	OMIM:610476	TAS				P		HPO:skoehler	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0004308	OMIM:610476	IEA				P		HPO:iea	
OMIM	610476	#610476 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11; ARVC11ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, WITH MILDPALMOPLANTAR KERATODERMA AND WOOLLY HAIR, INCLUDED		HP:0011663	OMIM:610476	TAS				P		HPO:probinson	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0000007	PMID:17033974	PCS				I		HPO:probinson	
OMIM	610478	RETINAL CONE DYSTROPHY 4	HP:0012825	HP:0000505	PMID:17033974	PCS				P		HPO:probinson	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0000548	PMID:17033974	PCS				P		HPO:skoehler	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0000613	OMIM:610478	TAS				P		HPO:skoehler	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0001133	OMIM:610478	TAS				P		HPO:skoehler	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0007663	OMIM:610478	TAS				P		HPO:skoehler	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0007814	PMID:17033974	PCS				P		HPO:probinson	
OMIM	610478	RETINAL CONE DYSTROPHY 4		HP:0007984	PMID:17033974	PCS				P		HPO:probinson	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000006	OMIM:610489	IEA				I		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000311	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000709	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000713	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000716	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000739	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000822	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000938	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000939	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000963	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0000978	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001065	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001268	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001575	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001579	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001580	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0001956	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0002808	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0002920	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0003466	OMIM:610489	IEA				P		HPO:iea	
OMIM	610489	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1		HP:0003674	OMIM:610489	IEA				C		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0000007	OMIM:610498	IEA				I		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0000369	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0000969	OMIM:610498	TAS				P		HPO:probinson	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001156	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001254	OMIM:610498	TAS				P		HPO:probinson	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001274	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001319	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001425	OMIM:610498	TAS				I		HPO:skoehler	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001518	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001643	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0001999	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0002119	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0002151	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0002375	OMIM:610498	TAS				P		HPO:skoehler	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0002910	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0003128	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0003577	OMIM:610498	IEA				C		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0005989	OMIM:610498	IEA				P		HPO:iea	
OMIM	610498	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 2; COXPD2		HP:0008872	OMIM:610498	IEA				P		HPO:iea	
OMIM	610504	#610504 PRETERM PREMATURE RUPTURE OF THE MEMBRANES; PPROM		HP:0001788	OMIM:610504	TAS				P		HPO:skoehler	
OMIM	610504	#610504 PRETERM PREMATURE RUPTURE OF THE MEMBRANES; PPROM		HP:0010982	OMIM:610504	TAS				I		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0000007	OMIM:610505	IEA				I		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0000505	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0000648	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001138	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001250	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001251	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001263	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001290	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001298	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001319	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001324	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001332	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001337	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001511	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001558	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001643	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001644	OMIM:610505	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0001655	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0002093	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0002119	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0002151	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0002240	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0002878	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0003128	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0003201	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0003236	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0003819	OMIM:610505	IEA				M		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0005157	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0008347	OMIM:610505	TAS				P		HPO:probinson	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0008872	OMIM:610505	IEA				P		HPO:iea	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0011923	OMIM:610505	TAS				P		HPO:probinson	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0011924	OMIM:610505	TAS				P		HPO:probinson	
OMIM	610505	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 3		HP:0100543	OMIM:610505	TAS				P		HPO:skoehler	
OMIM	610508	#610508 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7; MODY7		HP:0000006	PMID:15774581	PCS				I		HPO:probinson	
OMIM	610508	#610508 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7; MODY7		HP:0004904	OMIM:610508	IEA				P		HPO:skoehler	
OMIM	610508	#610508 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 7; MODY7		HP:0005978	PMID:15774581	PCS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0000007	OMIM:610532	IEA				I		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0000519	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001249	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001250	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001260	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001263	OMIM:610532	TAS				P		HPO:skoehler	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001270	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001271	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001317	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0001347	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0002080	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0002415	OMIM:610532	TAS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0002650	OMIM:610532	TAS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0003383	OMIM:610532	IEA				P		HPO:skoehler	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0003431	OMIM:610532	TAS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0003487	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0003593	OMIM:610532	IEA				C		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0003828	OMIM:610532	TAS				C		HPO:skoehler	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0006957	OMIM:610532	IEA				P		HPO:skoehler	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0007210	OMIM:610532	TAS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0007340	OMIM:610532	TAS				P		HPO:probinson	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0008936	OMIM:610532	IEA				P		HPO:iea	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5	HP:0003676	HP:0012762	OMIM:610532	TAS				P		HPO:skoehler	
OMIM	610532	LEUKODYSTROPHY, HYPOMYELINATING, 5; HLD5		HP:0030147	OMIM:610532	TAS				P		HPO:skoehler	
OMIM	610535	GLAUCOMA 1, OPEN ANGLE, M		HP:0000006	OMIM:610535	TAS				I		HPO:skoehler	
OMIM	610535	GLAUCOMA 1, OPEN ANGLE, M		HP:0001133	OMIM:610535	TAS				P		HPO:probinson	
OMIM	610535	GLAUCOMA 1, OPEN ANGLE, M		HP:0012108	OMIM:610535	TAS				P		HPO:probinson	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000006	OMIM:610536	TAS				I		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000007	OMIM:610536	IEA				I		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000175	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000243	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000252	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000253	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000272	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000286	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000347	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000369	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000384	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000396	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000405	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000413	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000453	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000463	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000494	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000506	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000582	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0000750	OMIM:610536	IEA				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001177	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001238	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001250	OMIM:610536	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001263	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001629	OMIM:610536	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0001631	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0002002	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0002032	OMIM:610536	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0002098	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0003196	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0004322	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0005321	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0008551	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0008872	OMIM:610536	IEA				P		HPO:iea	
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0009623	OMIM:610536	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610536	MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA		HP:0011800	OMIM:610536	TAS				P		HPO:skoehler	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0000007	OMIM:610539	TAS				I		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0000938	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0001250	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0001336	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0001433	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0001873	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0001903	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0004975	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610539	#610539 GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY		HP:0011813	OMIM:610539	TAS				P		HPO:probinson	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0000007	OMIM:610542	IEA				I		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0000467	OMIM:610542	TAS				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0000508	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0000597	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0001270	OMIM:610542	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0002515	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003388	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003391	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003394	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003403	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003473	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0003621	OMIM:610542	IEA				C		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0007126	OMIM:610542	TAS				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0008180	OMIM:610542	IEA				P		HPO:skoehler	
OMIM	610542	#610542 MYASTHENIC SYNDROME, CONGENITAL, WITH TUBULAR AGGREGATES 1; CMSTA1		HP:0010628	OMIM:610542	TAS				P		HPO:skoehler	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000077	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000218	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000252	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000329	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000347	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000444	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000448	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000486	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000494	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0000545	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001249	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001250	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001252	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001263	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001442	PMID:16783566;PMID:17855048	PCS				I	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001452	PMID:16783566	PCS				I	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001508	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001513	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001522	PMID:16783566;PMID:17855048	PCS				M	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001748	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0001999	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0002219	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0002360	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0002650	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0002719	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0004209	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0004383	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0008872	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0009553	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0009765	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0010055	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0010815	PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610543	CHROMOSOME 16p13.3 DELETION SYNDROME		HP:0011304	PMID:16783566;PMID:17855048	PCS				P	CHROMOSOME 16P13.3 DELETION SYNDROME	HPO:iea	
OMIM	610551	#610551 HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1;;ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 1; IIAE1		HP:0000007	PMID:16973841	PCS				I		HPO:probinson	
OMIM	610551	#610551 HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1;;ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 1; IIAE1		HP:0005353	PMID:16973841	PCS				P		HPO:probinson	
OMIM	610551	#610551 HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 1;;ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 1; IIAE1		HP:0012302	OMIM:610551	IEA				P		HPO:skoehler	
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0000006	OMIM:610582	TAS				I		HPO:probinson	
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0003074	OMIM:610582	TAS				P		HPO:skoehler	
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0003623	OMIM:610582	TAS		HP:0040283		C		HPO:skoehler	HP:0040283
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0008255	OMIM:610582	TAS				P		HPO:probinson	
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0009800	OMIM:610582	TAS				P		HPO:skoehler	
OMIM	610582	DIABETES MELLITUS, TRANSIENT NEONATAL, 3		HP:0040217	OMIM:610582	TAS				P		HPO:skoehler	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0000007	OMIM:610599	TAS				I		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0000510	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0000543	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0000550	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0000608	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0007737	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610599	#610599 RETINITIS PIGMENTOSA 36; RP36		HP:0007843	OMIM:610599	TAS				P		HPO:probinson	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0000007	OMIM:610600	IEA				I		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0000127	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0000848	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0001278	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0001508	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0001510	OMIM:610600	TAS				P		HPO:skoehler	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0001944	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0002153	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0002902	OMIM:610600	IEA				P		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0003623	OMIM:610600	IEA				C		HPO:iea	
OMIM	610600	#610600 CORTICOSTERONE METHYLOXIDASE TYPE II DEFICIENCY;;CMO II DEFICIENCY;;ALDOSTERONE DEFICIENCY II;;HYPERRENINEMIC HYPOALDOSTERONISM, FAMILIAL, 1; FHHA1B;;ALDOSTERONE DEFICIENCY DUE TO DEFICIENCY OF STEROID 18-OXIDASE;;STEROID 18-OXIDASE DEFICIENCY;;18-@OXIDASE DEFICIENCY		HP:0004319	OMIM:610600	IEA				P		HPO:iea	
OMIM	610612	LEBER CONGENITAL AMAUROSIS 12; LCA12		HP:0000007	OMIM:610612	TAS				I		HPO:skoehler	
OMIM	610612	LEBER CONGENITAL AMAUROSIS 12; LCA12		HP:0000639	OMIM:610612	IEA				P		HPO:skoehler	
OMIM	610612	LEBER CONGENITAL AMAUROSIS 12; LCA12		HP:0007875	OMIM:610612	IEA	HP:0003577			P		HPO:skoehler	
OMIM	610612	LEBER CONGENITAL AMAUROSIS 12; LCA12		HP:0008002	OMIM:610612	IEA				P		HPO:skoehler	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0000006	OMIM:610618	TAS				I		HPO:probinson	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0000282	OMIM:610618	TAS				P		HPO:skoehler	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III	HP:0025303	HP:0002013	OMIM:610618	TAS				P		HPO:skoehler	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0002574	OMIM:610618	TAS				P		HPO:probinson	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III	HP:0025303	HP:0005225	OMIM:610618	TAS				P		HPO:skoehler	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0011855	OMIM:610618	TAS				P		HPO:skoehler	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0012271	OMIM:610618	TAS				P		HPO:probinson	
OMIM	610618	ANGIOEDEMA, HEREDITARY, TYPE III		HP:0100665	OMIM:610618	TAS				P		HPO:probinson	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0000006	OMIM:610623	TAS				I		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0000007	OMIM:610623	IEA				I		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0000518	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0000568	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0000618	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0001249	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0001276	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0001315	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610623	CATARACT 11, MULTIPLE TYPES; CTRCT11		HP:0002072	OMIM:610623	IEA				P		HPO:skoehler	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000006	OMIM:610628	TAS				I		HPO:probinson	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000028	OMIM:610628	TAS				P		HPO:skoehler	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000044	OMIM:610628	TAS				P		HPO:probinson	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000054	OMIM:610628	TAS				P		HPO:skoehler	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000458	OMIM:610628	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000786	OMIM:610628	TAS				P		HPO:skoehler	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000819	OMIM:610628	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0000939	OMIM:610628	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0001250	OMIM:610628	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0001513	OMIM:610628	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0003829	OMIM:610628	TAS				C		HPO:skoehler	
OMIM	610628	HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4		HP:0008734	OMIM:610628	TAS				P		HPO:skoehler	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0000006	PMID:17186470	TAS				I		HPO:probinson	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0000465	OMIM:610629	TAS				P		HPO:skoehler	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0001896	PMID:17186470	TAS				P		HPO:probinson	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0001972	PMID:17186470	TAS				P		HPO:probinson	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0005518	PMID:17186470	TAS				P		HPO:probinson	
OMIM	610629	DIAMOND-BLACKFAN ANEMIA 3		HP:0011904	PMID:17186470	TAS				P		HPO:probinson	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0000007	OMIM:610644	TAS				I		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0000047	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0000771	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0000982	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0001792	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0002155	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0003124	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0006357	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0007410	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0008404	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0008665	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0008734	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0011838	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0012118	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0012861	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0025080	OMIM:610644	TAS				P		HPO:skoehler	
OMIM	610644	PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL		HP:0030731	OMIM:610644	IEA				P		HPO:skoehler	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000007	OMIM:610651	IEA				I		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000135	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000252	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000407	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000518	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000568	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000580	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000648	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000762	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0000992	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0001249	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0001251	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0001272	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0001347	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0001480	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0002119	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0002135	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0002671	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0003224	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0004322	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0004334	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0005328	OMIM:610651	IEA				P		HPO:iea	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0006739	OMIM:610651	TAS				P		HPO:probinson	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0011400	OMIM:610651	TAS				P		HPO:probinson	
OMIM	610651	XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B		HP:0012056	OMIM:610651	TAS				P		HPO:probinson	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000006	OMIM:610655	IEA				I		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000214	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000227	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000434	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000524	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0000961	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0001342	OMIM:610655	TAS				P		HPO:skoehler	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0001425	OMIM:610655	TAS				I		HPO:skoehler	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0001694	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0001722	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002076	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002094	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002138	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002140	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002326	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002390	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002408	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002626	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002642	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0002707	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0004406	OMIM:610655	IEA	HP:0003621			P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0006548	OMIM:610655	IEA				P		HPO:iea	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0011934	OMIM:610655	TAS				P		HPO:probinson	
OMIM	610655	TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4; HHT4		HP:0100858	OMIM:610655	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0000007	PMID:17160893	TAS				I		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0000252	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0000639	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001298	OMIM:610678	TAS				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001319	OMIM:610678	TAS				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001511	OMIM:610678	TAS				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001522	PMID:17160893	TAS				M		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001942	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0001987	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002126	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002151	OMIM:610678	TAS				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002179	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002240	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002376	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002415	OMIM:610678	IEA				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0002878	OMIM:610678	TAS				P		HPO:skoehler	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0003128	PMID:17160893	TAS				P		HPO:probinson	
OMIM	610678	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4		HP:0003593	OMIM:610678	TAS				C		HPO:skoehler	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000006	OMIM:610680	IEA				I		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000028	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000054	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000248	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000252	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000286	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000340	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0000377	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001156	OMIM:610680	TAS				P		HPO:skoehler	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001182	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001274	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001360	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001508	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001581	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001831	OMIM:610680	TAS				P		HPO:probinson	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0001999	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0002719	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0003186	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0006887	OMIM:610680	IEA				P		HPO:iea	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0009381	OMIM:610680	TAS				P		HPO:probinson	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0010864	OMIM:610680	TAS				P		HPO:skoehler	
OMIM	610680	610680 HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS		HP:0012311	OMIM:610680	TAS				P		HPO:skoehler	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000007	OMIM:610682	TAS				I		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000126	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000260	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000270	OMIM:610682	TAS				P		HPO:skoehler	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000311	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000343	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000520	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000592	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000767	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000774	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0000938	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0001522	OMIM:610682	TAS				M		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0001623	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002645	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002650	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002757	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002812	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002953	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002979	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0002983	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0003179	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0003783	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0004960	OMIM:610682	TAS				P		HPO:skoehler	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0005304	OMIM:610682	TAS				P		HPO:skoehler	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0005474	OMIM:610682	TAS				P		HPO:skoehler	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0005855	OMIM:610682	IEA				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0006367	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0006640	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0008905	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610682	#610682 OSTEOGENESIS IMPERFECTA, TYPE VII; OI7;;OI, TYPE VII;;OSTEOGENESIS IMPERFECTA, TYPE IIB, FORMERLY; OI2B, FORMERLY		HP:0010537	OMIM:610682	TAS				P		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0000007	PMID:17160903	PCS				I		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0000218	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0000467	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001252	PMID:17160903	PCS				P		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001284	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001288	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001290	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001324	PMID:17160903	PCS				P		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0001382	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0002194	PMID:17160903	PCS				P		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0002747	OMIM:610687	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0003391	OMIM:610687	TAS				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0003677	OMIM:610687	TAS				C		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0003715	OMIM:610687	IEA				P		HPO:skoehler	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0003789	PMID:17160903	PCS				P		HPO:probinson	
OMIM	610687	NEMALINE MYOPATHY 7; NEM7		HP:0003798	PMID:17160903	PCS				P		HPO:probinson	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000007	OMIM:610688	IEA				I		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000090	OMIM:610688	TAS				P		HPO:probinson	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000546	OMIM:610688	TAS				P		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000567	OMIM:610688	TAS				P		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000618	OMIM:610688	TAS				P		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0000657	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001249	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001251	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001252	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001263	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001290	OMIM:610688	TAS				P		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001320	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001395	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001408	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0001425	OMIM:610688	TAS				I		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0002404	OMIM:610688	TAS				P		HPO:probinson	
OMIM	610688	JOUBERT SYNDROME 6		HP:0002419	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0003774	OMIM:610688	TAS				P		HPO:skoehler	
OMIM	610688	JOUBERT SYNDROME 6		HP:0005957	OMIM:610688	IEA				P		HPO:iea	
OMIM	610688	JOUBERT SYNDROME 6		HP:0011933	OMIM:610688	TAS				P		HPO:probinson	
OMIM	610688	JOUBERT SYNDROME 6		HP:0100951	OMIM:610688	IEA				P		HPO:iea	
OMIM	610698	MACULAR DEGENERATION, AGE-RELATED, 4		HP:0000608	OMIM:610698	TAS	HP:0003584			P		HP:probinson	
OMIM	610698	MACULAR DEGENERATION, AGE-RELATED, 4		HP:0010982	OMIM:610698	IEA				I		HPO:probinson	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000007	OMIM:610706	IEA				I		HPO:iea	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000276	OMIM:610706	IEA				P		HPO:iea	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000347	OMIM:610706	IEA				P		HPO:iea	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000687	OMIM:610706	IEA				P		HPO:iea	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000691	OMIM:610706	IEA				P		HPO:iea	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0000698	OMIM:610706	IEA				P		HPO:skoehler	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0002194	OMIM:610706	TAS				P		HPO:probinson	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0010609	OMIM:610706	IEA				P		HPO:skoehler	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0011266	OMIM:610706	TAS				P		HPO:probinson	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0011372	OMIM:610706	TAS				P		HPO:skoehler	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0011476	OMIM:610706	TAS	HP:0003577			P		HPO:probinson	
OMIM	610706	#610706 DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA;;DEAFNESS, CONGENITAL, WITH LABYRINTHINE APLASIA, MICROTIA, AND MICRODONTIA;;DEAFNESS WITH LAMM		HP:0040080	OMIM:610706	TAS				P		HPO:skoehler	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0000006	OMIM:610708	IEA				I		HPO:iea	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0000552	OMIM:610708	IEA				P		HPO:iea	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0000603	OMIM:610708	IEA				P		HPO:iea	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0000648	OMIM:610708	IEA				P		HPO:iea	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0003677	OMIM:610708	IEA				C		HPO:skoehler	
OMIM	610708	OPTIC ATROPHY 5; OPA5		HP:0007924	OMIM:610708	IEA				P		HPO:iea	
OMIM	610713	BRACHYDACTYLY-SYNDACTYLY SYNDROME		HP:0001156	PMID:23995701	PCS				P		HPO:probinson	
OMIM	610713	BRACHYDACTYLY-SYNDACTYLY SYNDROME		HP:0006101	PMID:23995701	PCS				P		HPO:probinson	
OMIM	610713	BRACHYDACTYLY-SYNDACTYLY SYNDROME		HP:0009803	PMID:23995701	PCS				P		HPO:probinson	
OMIM	610713	BRACHYDACTYLY-SYNDACTYLY SYNDROME		HP:0012165	PMID:23995701	PCS				P		HPO:probinson	
OMIM	610713	BRACHYDACTYLY-SYNDACTYLY SYNDROME		HP:0012385	PMID:23995701	PCS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0000007	OMIM:610717	TAS				I		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0000407	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0000467	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0000819	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0001284	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0001290	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0001397	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0001638	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0002155	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0002240	OMIM:610717	TAS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0002355	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0002380	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0002910	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003198	OMIM:610717	TAS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003236	OMIM:610717	TAS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003326	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003388	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003391	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003546	PMID:18952067	PCS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003581	OMIM:610717	TAS				C		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003677	OMIM:610717	TAS				C		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003701	PMID:18952067	PCS				P		HPO:probinson	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0003828	OMIM:610717	TAS				C		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0004322	OMIM:610717	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0009046	OMIM:610717	TAS				P		HPO:skoehler	
OMIM	610717	NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY		HP:0009058	PMID:18952067	PCS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0000007	OMIM:610725	TAS				I		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0000093	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0000097	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0000100	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0000969	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0001967	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0003073	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0003676	OMIM:610725	TAS				C		HPO:skoehler	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0003774	OMIM:610725	TAS				P		HPO:probinson	
OMIM	610725	#610725 NEPHROTIC SYNDROME, TYPE 3; NPHS3;;NEPHROTIC SYNDROME, EARLY-ONSET, TYPE 3		HP:0011463	OMIM:610725	TAS				C		HPO:probinson	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000006	OMIM:610733	TAS				I		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000028	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000179	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000256	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000286	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000316	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000368	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000465	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000470	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000494	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000508	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000535	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000635	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000689	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0000915	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0001629	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0001639	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0001642	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0002212	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0002650	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0002967	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0003010	OMIM:610733	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0004322	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0005280	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0006610	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0009890	OMIM:610733	TAS				P		HPO:skoehler	
OMIM	610733	NOONAN SYNDROME 4; NS4		HP:0032152	OMIM:610733	IEA				P		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0000007	OMIM:610738	IEA				I		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0001250	OMIM:610738	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0001263	OMIM:610738	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0001875	OMIM:610738	IEA				P		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0001909	OMIM:610738	IEA				P		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0002718	OMIM:610738	IEA				P		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0002863	OMIM:610738	IEA				P		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0003593	OMIM:610738	IEA				C		HPO:skoehler	
OMIM	610738	NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3		HP:0025356	OMIM:610738	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0000007	OMIM:610743	TAS				I		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0000639	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0001260	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0001272	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0001310	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0002066	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0002070	OMIM:610743	TAS				P		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0003581	OMIM:610743	TAS				C		HPO:skoehler	
OMIM	610743	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 8; SCAR8		HP:0003677	OMIM:610743	TAS				C		HPO:skoehler	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0000006	OMIM:610753	IEA				I		HPO:skoehler	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0000007	OMIM:610753	IEA				I		HPO:skoehler	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0001426	PMID:17236136	PCS				I		HPO:lccarmody	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0002232	PMID:17236136	PCS				P		HPO:lccarmody	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0002289	PMID:17236136	PCS				P		HPO:skoehler	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0002293	PMID:17236136	PCS				P		HPO:lccarmody	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0003829	PMID:17236136	PCS				C		HPO:skoehler	
OMIM	610753	ALOPECIA AREATA 2; AA2		HP:0007418	PMID:17236136	PCS				P		HPO:lccarmody	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0000006	OMIM:610755	IEA				I		HPO:iea	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0000079	OMIM:610755	IEA				P		HPO:iea	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0000845	OMIM:610755	IEA				P		HPO:iea	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0002893	OMIM:610755	IEA				P		HPO:iea	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0002897	OMIM:610755	TAS				P		HPO:skoehler	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0006772	OMIM:610755	TAS				P		HPO:skoehler	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0030731	OMIM:610755	IEA				P		HPO:skoehler	
OMIM	610755	MULTIPLE ENDOCRINE NEOPLASIA, TYPE IV; MEN4		HP:0100570	OMIM:610755	TAS				P		HPO:skoehler	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000007	PMID:11443545	PCS				I		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000046	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000054	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000252	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000347	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000365	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000490	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000518	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000519	OMIM:610756	IEA				P		HPO:skoehler	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000568	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0000992	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0001263	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0001511	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0001522	OMIM:610756	IEA				M		HPO:skoehler	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0001838	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0002751	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0003683	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0003819	PMID:11443545	PCS				M		HPO:probinson	
OMIM	610756	CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2		HP:0100490	PMID:11443545	PCS				P		HPO:probinson	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000007	OMIM:610758	TAS				I		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000252	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000322	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000347	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000368	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000426	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000490	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000581	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0000639	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001181	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001263	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001276	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001321	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001347	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001511	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001531	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0001838	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0002126	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0002353	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0002751	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0002804	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0002827	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0003015	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0003083	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0003100	OMIM:610758	TAS				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0003577	OMIM:610758	TAS				C		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0003828	OMIM:610758	TAS				C		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0004322	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0005458	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0005830	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0007633	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0009879	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610758	#610758 CEREBROOCULOFACIOSKELETAL SYNDROME 4; COFS4		HP:0100490	OMIM:610758	IEA				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000006	PMID:25655089	PCS				I		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000028	PMID:25655089	PCS		HP:0040284		P		HP:probinson	2/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000072	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000175	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000218	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	5/11
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000219	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	13/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000248	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	11/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000294	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	7/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000319	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	10/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000324	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000343	PMID:25655089	PCS		HP:0040284		P		HP:probinson	10/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000347	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	6/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000358	PMID:25655089	PCS		HP:0040284		P		HP:probinson	3/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000365	PMID:25655089	PCS		HP:0040284		P		HP:probinson	7/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000414	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	12/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000426	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000463	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	8/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000470	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	6/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000508	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	4/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000527	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	15/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000545	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	5/11
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000574	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	9/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000579	PMID:25655089	PCS		HP:0040284		P		HP:probinson	4/12
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000664	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	11/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000691	PMID:25655089	PCS		HP:0040284		P		HP:probinson	2/9
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000954	PMID:25655089	PCS		HP:0040284		P		HP:probinson	5/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0000965	PMID:25655089	TAS		HP:0040284		P		HPO:skoehler	4/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001007	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001007	PMID:25655089	PCS		HP:0040284		P		HP:probinson	14/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001052	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/12
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001156	OMIM:610759	TAS				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001249	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001249	PMID:25655089	PCS		HP:0040284		P		HP:probinson	13/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001250	PMID:25655089	PCS		HP:0040284		P		HP:probinson	3/12
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001263	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001357	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001476	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001629	PMID:25655089	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001631	PMID:25655089	PCS	HP:0003577	HP:0040284		P		HP:probinson	4/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001642	OMIM:610759	TAS				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001643	PMID:25655089	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001647	PMID:25655089	PCS		HP:0040284		P		HP:probinson	2/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001770	PMID:25655089	PCS		HP:0040284		P		HP:probinson	4/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001773	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0001773	PMID:25655089	PCS		HP:0040284		P		HP:probinson	11/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002007	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002020	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002020	PMID:25655089	PCS		HP:0040284		P		HP:probinson	10/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002465	OMIM:610759	TAS				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002553	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002553	PMID:25655089	PCS		HP:0040284		P		HP:probinson	14/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002714	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	9/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002996	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0002996	PMID:25655089	PCS		HP:0040284		P		HP:probinson	5/11
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0004209	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	9/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0004322	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0005280	PMID:25655089	PCS		HP:0040284		P		HPO:skoehler	7/15
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0005484	PMID:25655089	PCS		HP:0040284		P		HP:probinson	12/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0008872	PMID:17273969	PCS				P		HPO:probinson	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0008872	PMID:25655089	PCS		HP:0040284		P		HP:probinson	11/14
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0009237	PMID:25655089	PCS		HP:0040284		P		HP:probinson	9/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0009623	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	12/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0011230	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0011451	PMID:25655089	PCS	HP:0003577	HP:0040284		P		HP:probinson	5/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0012368	PMID:25655089	PCS		HP:0040284		P		HP:probinson	1/16
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0030820	PMID:25655089	PCS		HP:0040284		P		HP:probinson	2/13
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0100543	OMIM:610759	TAS				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0100874	OMIM:610759	TAS				P		HPO:skoehler	
OMIM	610759	CORNELIA DE LANGE SYNDROME 3		HP:0200055	PMID:25655089	PCS		HP:0040284		P		HPO:probinson	11/14
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0000007	OMIM:610768	IEA				I	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0000535	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0000653	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001250	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001252	OMIM:610768	TAS		HP:0040283		P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:probinson	HP:0040283
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001508	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001522	OMIM:610768	IEA				M	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001644	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0001985	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0002521	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0003160	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0005484	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610768	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Im; CDG1M;;CDG Im; CDGIm;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY		HP:0008064	OMIM:610768	IEA				P	#610768 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IM; CDG1M;;CDG IM; CDGIM;;DOLICHOL KINASE DEFICIENCY;;DK1 DEFICIENCY	HPO:iea	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0000007	PMID:17273968	PCS				I		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0000961	PMID:17273968	PCS	HP:0003623			P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0001252	PMID:17273968	PCS				P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0001639	PMID:17273968	PCS				P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0001942	PMID:17273968	PCS	HP:0003623			P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0002093	PMID:17273968	PCS				P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0003128	PMID:17273968	PCS	HP:0003623			P		HPO:probinson	
OMIM	610773	#610773 MITOCHONDRIAL PHOSPHATE CARRIER DEFICIENCY;;MPCD		HP:0012087	PMID:17273968	PCS				P		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0000007	OMIM:610797	TAS				I		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0001388	OMIM:610797	TAS				P		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0001507	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0001763	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0002656	OMIM:610797	TAS				P		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0002857	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE	HP:0012825	HP:0003025	OMIM:610797	TAS				P		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0003275	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0003799	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0004209	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0004231	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0008802	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0009196	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0009465	OMIM:610797	IEA				P		HPO:iea	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0010048	OMIM:610797	TAS				P		HPO:probinson	
OMIM	610797	EPIPHYSEAL DYSPLASIA, BAUMANN TYPE		HP:0100807	OMIM:610797	TAS				P		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0000007	OMIM:610798	TAS				I		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0000280	OMIM:610798	TAS				P		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0001010	OMIM:610798	TAS				P		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0001875	OMIM:610798	TAS				P		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0002721	OMIM:610798	TAS				P		HPO:skoehler	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0002850	OMIM:610798	TAS				P		HPO:skoehler	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0004322	OMIM:610798	TAS				P		HPO:probinson	
OMIM	610798	IMMUNODEFICIENCY DUE TO DEFECT IN MAPBP-INTERACTING PROTEIN		HP:0006538	OMIM:610798	IEA				P		HPO:skoehler	
OMIM	610799	#610799 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 1; IPD1INVASIVE PNEUMOCOCCAL DISEASE, PROTECTION AGAINST, INCLUDED		HP:0000007	PMID:16950813	PCS				I		HPO:probinson	
OMIM	610799	#610799 INVASIVE PNEUMOCOCCAL DISEASE, RECURRENT ISOLATED, 1; IPD1INVASIVE PNEUMOCOCCAL DISEASE, PROTECTION AGAINST, INCLUDED		HP:0005366	PMID:16950813	PCS				P		HPO:probinson	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0000006	OMIM:610805	TAS				I		HPO:skoehler	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0000074	OMIM:610805	TAS				P		HPO:skoehler	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0000076	OMIM:610805	TAS				P		HPO:skoehler	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0003577	OMIM:610805	TAS				C		HPO:skoehler	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0003774	OMIM:610805	TAS				P		HPO:skoehler	
OMIM	610805	%610805 CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO;CAKUT;;RENAL HYPODYSPLASIA, NONSYNDROMIC, 1; RHDNS1		HP:0003829	OMIM:610805	TAS				C		HPO:skoehler	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000006	PMID:11941477	PCS				I		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000238	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000242	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000256	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000283	PMID:18830227	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000400	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000437	PMID:17001668	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000582	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000601	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000612	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0000871	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0001250	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0001263	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0001274	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0001539	PMID:11941477	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0002007	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0002507	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0002744	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0003196	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0003829	OMIM:610828	TAS				C		HPO:skoehler	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0004122	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0005273	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0005469	PMID:18830227	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0006315	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0006988	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0007633	PMID:17001668	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0008501	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0010649	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0010650	OMIM:610828	TAS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0010664	PMID:11941477	PCS				P		HPO:probinson	
OMIM	610828	HOLOPROSENCEPHALY 7		HP:0011800	OMIM:610828	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000006	PMID:17096318	PCS				I		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000028	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000054	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000238	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000252	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000272	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000322	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000327	PMID:14581620,PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000395	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000400	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000528	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000568	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000601	PMID:14581620,PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000609	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000689	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000824	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0000871	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0001162	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0001250	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0001263	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0001338	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0001360	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0002536	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0002744	PMID:14581620,PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0003745	PMID:17096318	PCS				I		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0003828	PMID:17096318	PCS				C		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0003829	PMID:17096318	PCS				C		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0004322	OMIM:610829	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0005280	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0006315	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0006485	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0009932	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0010290	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0010626	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0010627	PMID:14581620	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0010650	PMID:17096318	PCS				P		HPO:iea	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0011272	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610829	#610829 HOLOPROSENCEPHALY 9; HPE9;;PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES;;HOLOPROSENCEPHALY WITH MICROPHTHALMIA AND FIRST BRANCHIAL ARCH ANOMALIES		HP:0011800	OMIM:610829	TAS				P		HPO:skoehler	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000007	OMIM:610832	TAS				I		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000252	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000286	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000316	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000470	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0000957	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0001629	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0001915	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0002667	OMIM:610832	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0002885	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0003006	OMIM:610832	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0003221	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0008897	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610832	#610832 FANCONI ANEMIA, COMPLEMENTATION GROUP N; FANCN		HP:0009778	OMIM:610832	TAS				P		HPO:probinson	
OMIM	610840	MITRAL VALVE PROLAPSE, MYXOMATOUS 3		HP:0000006	OMIM:610840	IEA				I		HPO:iea	
OMIM	610840	MITRAL VALVE PROLAPSE, MYXOMATOUS 3		HP:0001634	OMIM:610840	IEA				P		HPO:iea	
OMIM	610840	MITRAL VALVE PROLAPSE, MYXOMATOUS 3		HP:0001653	OMIM:610840	IEA				P		HPO:iea	
OMIM	610840	MITRAL VALVE PROLAPSE, MYXOMATOUS 3		HP:0003831	OMIM:610840	IEA				C		HPO:iea	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000007	OMIM:610842	TAS				I	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000421	OMIM:610842	TAS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0000973	OMIM:610842	TAS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0001102	OMIM:610842	TAS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0001102	PMID:17110937	PCS		HP:0040284		P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	4/10
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0001892	PMID:17110937	PCS		HP:0040284		P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	5/10
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0002621	OMIM:610842	TAS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008151	PMID:18800149	PCS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008169	PMID:17110937	PCS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0008321	PMID:17110937	PCS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610842	Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency		HP:0011858	PMID:17110937	PCS				P	PSEUDOXANTHOMA ELASTICUM-LIKE DISORDER WITH MULTIPLE COAGULATION FACTOR DEFICIENCY	HPO:probinson	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0000007	OMIM:610852	IEA				I		HPO:skoehler	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0000246	OMIM:610852	IEA				P		HPO:skoehler	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0002205	OMIM:610852	IEA				P		HPO:skoehler	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0011108	OMIM:610852	TAS				P		HPO:skoehler	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0012262	OMIM:610852	TAS				P		HPO:probinson	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0012265	OMIM:610852	IEA				P		HPO:skoehler	
OMIM	610852	#610852 CILIARY DYSKINESIA, PRIMARY, 6; CILD6		HP:0200109	OMIM:610852	TAS				P		HPO:skoehler	
OMIM	610878	#610878 VESICOURETERAL REFLUX 2; VUR2		HP:0000006	PMID:17357069	PCS				I		HPO:probinson	
OMIM	610878	#610878 VESICOURETERAL REFLUX 2; VUR2		HP:0000076	PMID:17357069	PCS				P		HPO:probinson	
OMIM	610878	#610878 VESICOURETERAL REFLUX 2; VUR2		HP:0000089	PMID:17357069	PCS				P		HPO:probinson	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000154	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000218	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000243	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000252	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000303	PMID:17357070	PCS	HP:0003593			P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000316	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000319	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000325	PMID:17357070	PCS	HP:0003593			P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000337	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000347	PMID:17357070	PCS	HP:0003593			P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000365	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000494	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000540	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000678	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000689	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000717	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000733	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000752	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000817	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0000821	OMIM:610883	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001250	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001256	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001263	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001290	PMID:17357070	PCS	HP:0003593			P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001508	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001518	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001626	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0001655	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002020	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002079	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002353	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002357	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002463	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002474	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0002650	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0003146	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0003745	OMIM:610883	TAS				I		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0004322	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0005274	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0008872	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0010529	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0010535	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0010863	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0012210	PMID:17357070	PCS				P		HPO:iea	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0012448	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610883	POTOCKI-LUPSKI SYNDROME		HP:0200136	OMIM:610883	TAS				P		HPO:skoehler	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0000006	OMIM:610896	TAS				I		HPO:probinson	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0000083	OMIM:610896	TAS				P		HPO:probinson	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0000110	OMIM:610896	TAS				P		HPO:probinson	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0000365	OMIM:610896	TAS				P		HPO:probinson	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0000384	OMIM:610896	TAS				P		HPO:probinson	
OMIM	610896	#610896 BRANCHIOOTORENAL SYNDROME 2; BOR2		HP:0011332	OMIM:610896	TAS				P		HPO:probinson	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0000961	OMIM:610910	IEA		HP:0040284		P		HPO:skoehler	25%
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0001217	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0001901	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0002090	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0002091	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0002094	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0002105	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0002205	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0003587	OMIM:610910	IEA				C		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0003745	OMIM:610910	IEA				I		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0006517	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0012418	OMIM:610910	TAS				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0012735	OMIM:610910	TAS				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0031996	OMIM:610910	IEA				P		HPO:skoehler	
OMIM	610910	PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED		HP:0100749	OMIM:610910	TAS				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0000006	OMIM:610913	IEA				I		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0000961	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0001217	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0001425	OMIM:610913	IEA				I		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0001508	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0002098	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0002205	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0002789	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0003829	OMIM:610913	IEA				C		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0005576	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0006515	OMIM:610913	IEA				P		HPO:skoehler	
OMIM	610913	#610913 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 2; SMDP2;;INTERSTITIAL LUNG DISEASE DUE TO SURFACTANT PROTEIN C DEFICIENCY;;DESQUAMATIVE INTERSTITIAL PNEUMONITIS DUE TO SURFACTANT PROTEIN CDEFICIENCY;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 2		HP:0006517	OMIM:610913	TAS				P		HPO:skoehler	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000007	OMIM:610915	IEA				I		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000023	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000260	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000270	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000311	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000520	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000883	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000926	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0000938	OMIM:610915	IEA				P		HPO:skoehler	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0001263	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0001388	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0001552	OMIM:610915	IEA				P		HPO:skoehler	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002645	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002650	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002757	OMIM:610915	TAS				P		HPO:probinson	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002808	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002953	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002980	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002982	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0002986	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0003100	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0003783	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0003784	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0004331	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0005855	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0008873	OMIM:610915	IEA				P		HPO:iea	
OMIM	610915	#610915 OSTEOGENESIS IMPERFECTA, TYPE VIII; OI8;;OI, TYPE VIII		HP:0010049	OMIM:610915	IEA				P		HPO:iea	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0000007	OMIM:610921	IEA				I		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0001425	OMIM:610921	IEA				I		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0001508	OMIM:610921	IEA				P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0002098	OMIM:610921	IEA				P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0002104	OMIM:610921	IEA				P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0002789	OMIM:610921	IEA				P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0002878	OMIM:610921	TAS	HP:0003623			P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0003577	OMIM:610921	IEA				C		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0005942	OMIM:610921	IEA				P		HPO:skoehler	
OMIM	610921	#610921 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 3; SMDP3;;PULMONARY ALVEOLAR PROTEINOSIS, CONGENITAL, 3;;INTERSTITIAL LUNG DISEASE DUE TO ABCA3 DEFICIENCY		HP:0006517	OMIM:610921	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0000006	OMIM:610947	TAS				I		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0000819	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0000822	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0000939	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0001645	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0001658	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0001997	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0002155	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610947	#610947 CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2		HP:0003124	OMIM:610947	TAS				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000007	OMIM:610951	IEA				I		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000488	OMIM:610951	TAS				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000572	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000580	PMID:19277732	PCS				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000618	OMIM:610951	IEA				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000648	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0000750	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0001251	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0001263	OMIM:610951	TAS				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0001268	OMIM:610951	IEA				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0001272	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0002059	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0002123	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0002180	OMIM:610951	IEA				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0002353	OMIM:610951	IEA				P		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0002360	OMIM:610951	TAS				P		HPO:skoehler	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0003621	OMIM:610951	IEA				C		HPO:iea	
OMIM	610951	#610951 CEROID LIPOFUSCINOSIS, NEURONAL, 7; CLN7		HP:0003678	OMIM:610951	TAS				C		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000006	OMIM:610954	IEA				I		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000028	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000054	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000194	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000252	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000280	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000293	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000322	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000341	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000378	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000431	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000470	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000483	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000486	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000490	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000545	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000582	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000687	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000718	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0000954	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001182	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001217	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001250	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001252	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001270	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001290	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001298	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001344	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001763	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0001786	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0002019	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0002020	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0002066	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0002079	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0002311	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0004879	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0006887	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0008081	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0010864	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0012332	OMIM:610954	IEA				P		HPO:skoehler	
OMIM	610954	PITT-HOPKINS SYNDROME		HP:0030084	OMIM:610954	TAS				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000083	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000093	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000252	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000275	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000336	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000365	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000490	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000505	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000648	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000822	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0000958	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0001256	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0001541	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0001620	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0002119	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0002370	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS	HP:0012825	HP:0002910	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0003510	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0004326	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0004334	OMIM:610965	IEA				P		HPO:skoehler	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0006297	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0007495	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610965	XFE PROGEROID SYNDROME; XFEPS		HP:0007519	OMIM:610965	TAS				P		HPO:probinson	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000006	OMIM:610967	IEA				I		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000164	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000325	OMIM:610967	TAS				P		HPO:skoehler	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000478	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000592	OMIM:610967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000703	OMIM:610967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000926	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0000938	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0001382	OMIM:610967	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0001939	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0002644	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0002645	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0002757	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0004322	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0004586	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0005084	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0006394	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0008422	OMIM:610967	IEA				P		HPO:iea	
OMIM	610967	#610967 OSTEOGENESIS IMPERFECTA, TYPE V; OI5;;OI, TYPE V		HP:0030268	OMIM:610967	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000006	OMIM:610968	TAS				I		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000007	OMIM:610968	IEA				I		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000164	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000248	OMIM:610968	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000325	OMIM:610968	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000592	OMIM:610968	IEA				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000703	OMIM:610968	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000938	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0000951	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0001388	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002645	OMIM:610968	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002650	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002659	OMIM:610968	TAS				P		HPO:probinson	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002751	OMIM:610968	TAS				P		HPO:skoehler	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002812	OMIM:610968	TAS		HP:0040284		P		HPO:probinson	5/8
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0002953	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0003155	OMIM:610968	TAS				P		HPO:probinson	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0003179	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0004322	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0004586	OMIM:610968	IEA				P		HPO:iea	
OMIM	610968	OSTEOGENESIS IMPERFECTA, TYPE XI; OI11		HP:0008422	OMIM:610968	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0000006	OMIM:610978	IEA				I		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0000851	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001251	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001252	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001260	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001263	OMIM:610978	TAS				P		HPO:skoehler	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001266	PMID:24714694	PCS				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001270	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001290	OMIM:610978	TAS				P		HPO:skoehler	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001332	OMIM:610978	TAS				P		HPO:skoehler	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001629	PMID:24714694	PCS				P		HPO:probinson	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001631	PMID:24714694	PCS				P		HPO:probinson	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0001671	OMIM:610978	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002098	OMIM:610978	TAS	HP:0003623			P		HPO:skoehler	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002099	OMIM:610978	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002205	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002355	OMIM:610978	TAS				P		HPO:probinson	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002360	OMIM:610978	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002643	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0002925	OMIM:610978	IEA				P		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0003577	OMIM:610978	IEA				C		HPO:iea	
OMIM	610978	CHOREOATHETOSIS, HYPOTHYROIDISM, AND NEONATAL RESPIRATORY DISTRESSCHOREOATHETOSIS AND CONGENITAL HYPOTHYROIDISM, INCLUDED		HP:0008223	OMIM:610978	TAS				P		HPO:skoehler	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000007	OMIM:610984	IEA				I		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000010	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000083	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000099	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000246	OMIM:610984	IEA				P		HPO:skoehler	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0000403	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0001369	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0001581	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0002633	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0003621	OMIM:610984	IEA				C		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005356	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005366	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005369	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005376	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005381	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005416	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0005421	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0006946	OMIM:610984	IEA				P		HPO:iea	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0011108	OMIM:610984	TAS				P		HPO:skoehler	
OMIM	610984	#610984 COMPLEMENT FACTOR I DEFICIENCY; CFID;;COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY;;C3 INACTIVATOR DEFICIENCY		HP:0012330	OMIM:610984	TAS				P		HPO:skoehler	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0000007	OMIM:610992	IEA				I		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0001250	OMIM:610992	TAS				P		HPO:probinson	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0001263	OMIM:610992	IEA				P		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0001276	OMIM:610992	IEA				P		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0001320	OMIM:610992	IEA				P		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0003593	OMIM:610992	IEA				C		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0005484	OMIM:610992	IEA				P		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0008872	OMIM:610992	IEA				P		HPO:iea	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0012277	OMIM:610992	TAS				P		HPO:probinson	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0012279	OMIM:610992	TAS				P		HPO:probinson	
OMIM	610992	PHOSPHOSERINE AMINOTRANSFERASE DEFICIENCY; PSATD		HP:0025356	OMIM:610992	IEA				P		HPO:skoehler	
OMIM	611022	DEAFNESS, AUTOSOMAL RECESSIVE, 24		HP:0000007	OMIM:611022	TAS				I		HPO:probinson	
OMIM	611022	DEAFNESS, AUTOSOMAL RECESSIVE, 24		HP:0003593	OMIM:611022	TAS				C		HPO:probinson	
OMIM	611022	DEAFNESS, AUTOSOMAL RECESSIVE, 24		HP:0011476	OMIM:611022	TAS				P		HPO:probinson	
OMIM	611031	%611031 EPISODIC KINESIGENIC DYSKINESIA 2; EKD2;;DYSTONIA 19; DYT19		HP:0000006	OMIM:611031	IEA				I		HPO:iea	
OMIM	611031	%611031 EPISODIC KINESIGENIC DYSKINESIA 2; EKD2;;DYSTONIA 19; DYT19		HP:0001332	OMIM:611031	TAS				P		HPO:probinson	
OMIM	611031	%611031 EPISODIC KINESIGENIC DYSKINESIA 2; EKD2;;DYSTONIA 19; DYT19		HP:0002072	OMIM:611031	IEA				P		HPO:iea	
OMIM	611031	%611031 EPISODIC KINESIGENIC DYSKINESIA 2; EKD2;;DYSTONIA 19; DYT19		HP:0007166	OMIM:611031	TAS				P		HPO:probinson	
OMIM	611031	%611031 EPISODIC KINESIGENIC DYSKINESIA 2; EKD2;;DYSTONIA 19; DYT19	HP:0025303	HP:0100660	OMIM:611031	TAS				P		HPO:skoehler	
OMIM	611038	MICROPHTHALMIA, ISOLATED 3		HP:0000007	OMIM:611038	IEA				I		HPO:iea	
OMIM	611038	MICROPHTHALMIA, ISOLATED 3		HP:0000528	OMIM:611038	IEA				P		HPO:iea	
OMIM	611038	MICROPHTHALMIA, ISOLATED 3		HP:0000568	OMIM:611038	IEA				P		HPO:iea	
OMIM	611038	MICROPHTHALMIA, ISOLATED 3		HP:0000647	OMIM:611038	IEA				P		HPO:iea	
OMIM	611038	MICROPHTHALMIA, ISOLATED 3		HP:0009755	OMIM:611038	IEA				P		HPO:iea	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000007	OMIM:611040	TAS				I		HPO:probinson	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000510	OMIM:611040	IEA				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000518	OMIM:611040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000540	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000568	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000613	OMIM:611040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0000662	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0001000	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0007663	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0007722	OMIM:611040	TAS				P		HPO:probinson	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0007737	OMIM:611040	TAS				P		HPO:probinson	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0008323	OMIM:611040	TAS				P		HPO:probinson	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0011505	OMIM:611040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0012152	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0012426	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611040	MICROPHTHALMIA, ISOLATED 5		HP:0030823	OMIM:611040	TAS				P		HPO:skoehler	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0000007	OMIM:611067	IEA				I		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0001284	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0001762	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002355	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002366	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002460	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002515	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002650	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0002747	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003307	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003445	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003551	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003678	OMIM:611067	IEA				C		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003693	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003697	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0003701	OMIM:611067	IEA				P		HPO:iea	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0007269	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0009473	OMIM:611067	TAS				P		HPO:probinson	
OMIM	611067	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 4		HP:0011463	OMIM:611067	TAS				C		HPO:probinson	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000007	PMID:17522105	IEA				I		HPO:probinson	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000121	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	2/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000154	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000179	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000194	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000215	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000256	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	15/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000276	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000297	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000316	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000431	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000486	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0000873	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	2/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001249	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE	HP:0031375	HP:0001250	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001252	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001263	PMID:17522105	IEA				P		HPO:probinson	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001290	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001344	OMIM:611087	IEA				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001355	OMIM:611087	IEA				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001388	OMIM:611087	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001561	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001622	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	15/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0001631	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	4/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0002003	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0002119	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0002355	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0002446	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0002540	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0011968	OMIM:611087	TAS				P		HPO:skoehler	
OMIM	611087	POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY; PMSE		HP:0012371	PMID:17522105	IEA		HP:0040284		P		HPO:probinson	16/16
OMIM	611090	#611090 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12; MRT12		HP:0000007	OMIM:611090	TAS				I		HPO:probinson	
OMIM	611090	#611090 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12; MRT12		HP:0001249	OMIM:611090	TAS				P		HPO:probinson	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000007	OMIM:611091	TAS				I		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000215	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000252	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000275	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000276	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000316	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000319	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000322	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000331	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000426	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000430	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000431	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000448	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000486	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000506	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000574	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000581	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000601	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000664	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000750	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0000964	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001249	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001250	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001257	OMIM:611091	TAS	HP:0003584			P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001260	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001263	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001347	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001518	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001761	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0001771	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0003236	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0004322	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0008070	OMIM:611091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0008897	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611091	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5		HP:0008936	OMIM:611091	TAS				P		HPO:skoehler	
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0000007	OMIM:611092	TAS				I		HPO:probinson	
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001249	OMIM:611092	TAS				P		HPO:probinson	
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001250	OMIM:611092	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001263	OMIM:611092	TAS				P		HPO:skoehler	
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001332	OMIM:611092	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001336	OMIM:611092	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0001337	OMIM:611092	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611092	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6		HP:0003593	OMIM:611092	TAS				C		HPO:skoehler	
OMIM	611093	#611093 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7; MRT7;;MENTAL RETARDATION, AUTOSOMAL RECESSIVE 22; MRT22		HP:0000007	OMIM:611093	TAS				I		HPO:probinson	
OMIM	611093	#611093 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7; MRT7;;MENTAL RETARDATION, AUTOSOMAL RECESSIVE 22; MRT22		HP:0001249	OMIM:611093	TAS				P		HPO:probinson	
OMIM	611095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9		HP:0000007	OMIM:611095	TAS				I		HPO:probinson	
OMIM	611095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9		HP:0001257	OMIM:611095	IEA				P		HPO:skoehler	
OMIM	611095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9		HP:0001270	OMIM:611095	TAS				P		HPO:skoehler	
OMIM	611095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9		HP:0001510	OMIM:611095	TAS				P		HPO:skoehler	
OMIM	611095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 9; MRT9		HP:0010864	OMIM:611095	TAS				P		HPO:skoehler	
OMIM	611096	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10		HP:0000007	OMIM:611096	TAS				I		HPO:skoehler	
OMIM	611096	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10		HP:0001250	OMIM:611096	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611096	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10		HP:0001270	OMIM:611096	TAS				P		HPO:skoehler	
OMIM	611096	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 10		HP:0002342	OMIM:611096	TAS				P		HPO:skoehler	
OMIM	611097	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 11		HP:0000007	OMIM:611097	TAS				I		HPO:skoehler	
OMIM	611097	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 11		HP:0002342	OMIM:611097	TAS				P		HPO:skoehler	
OMIM	611102	DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY		HP:0000007	OMIM:611102	TAS				I		HPO:probinson	
OMIM	611102	DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY		HP:0003251	OMIM:611102	IEA				P		HPO:skoehler	
OMIM	611102	DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY		HP:0008619	OMIM:611102	TAS				P		HPO:probinson	
OMIM	611102	DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY		HP:0008669	OMIM:611102	TAS				P		HPO:probinson	
OMIM	611102	DEAFNESS, SENSORINEURAL, AND MALE INFERTILITY		HP:0012207	OMIM:611102	TAS				P		HPO:probinson	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0000007	OMIM:611105	TAS				I		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0000639	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001251	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001257	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001260	OMIM:611105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001265	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001270	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001324	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001337	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001347	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0001371	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0002352	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0003202	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0003477	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0003487	OMIM:611105	TAS				P		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0003677	OMIM:611105	TAS				C		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0003828	OMIM:611105	TAS				C		HPO:skoehler	
OMIM	611105	LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION; LBSL		HP:0100543	OMIM:611105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0000007	OMIM:611107	TAS				I		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0000252	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0000272	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0000582	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0001249	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0001263	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611107	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 4		HP:0012448	OMIM:611107	TAS				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0000007	OMIM:611126	IEA				I		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001290	OMIM:611126	TAS				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001297	OMIM:611126	IEA				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001298	OMIM:611126	TAS				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001324	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001399	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001414	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001635	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001639	OMIM:611126	TAS				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001644	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001873	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0001943	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0002181	OMIM:611126	IEA				P		HPO:iea	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0002910	OMIM:611126	TAS				P		HPO:probinson	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0003128	OMIM:611126	TAS				P		HPO:skoehler	
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0003215	OMIM:611126	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611126	MITOCHONDRIAL COMPLEX I DEFICIENCY DUE TO ACAD9 DEFICIENCY		HP:0003546	OMIM:611126	TAS				P		HPO:skoehler	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000006	OMIM:611131	IEA				I		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000007	OMIM:611131	IEA				I		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000510	OMIM:611131	IEA				P		HPO:skoehler	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000518	OMIM:611131	IEA				P		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000552	OMIM:611131	TAS				P		HPO:skoehler	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000580	OMIM:611131	IEA				P		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000613	OMIM:611131	IEA				P		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000642	OMIM:611131	TAS				P		HPO:skoehler	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0000662	OMIM:611131	IEA				P		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0007688	OMIM:611131	IEA				P		HPO:iea	
OMIM	611131	#611131 RETINITIS PIGMENTOSA 37; RP37		HP:0008028	OMIM:611131	IEA				P		HPO:iea	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000007	PMID:17564974	PCS				I		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000107	OMIM:611134	TAS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000175	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000238	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000252	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0000568	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001162	OMIM:611134	TAS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001305	PMID:17564974	PCS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001408	OMIM:611134	TAS				P		HPO:skoehler	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001511	OMIM:611134	TAS				P		HPO:skoehler	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001629	PMID:17564974	PCS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0001631	PMID:17564974	PCS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002079	PMID:17564974	PCS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002084	OMIM:611134	TAS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002323	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002335	PMID:17564974	PCS				P		HPO:probinson	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002419	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0002435	OMIM:611134	IEA				P		HPO:skoehler	
OMIM	611134	MECKEL SYNDROME, TYPE 4; MKS4		HP:0006487	OMIM:611134	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611147	PAROXYSMAL NONKINESIGENIC DYSKINESIA 2		HP:0000006	OMIM:611147	IEA				I		HPO:iea	
OMIM	611147	PAROXYSMAL NONKINESIGENIC DYSKINESIA 2		HP:0001250	OMIM:611147	IEA				P		HPO:iea	
OMIM	611147	PAROXYSMAL NONKINESIGENIC DYSKINESIA 2		HP:0002076	OMIM:611147	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611147	PAROXYSMAL NONKINESIGENIC DYSKINESIA 2		HP:0002268	OMIM:611147	TAS				P		HPO:probinson	
OMIM	611147	PAROXYSMAL NONKINESIGENIC DYSKINESIA 2		HP:0003829	OMIM:611147	IEA				C		HPO:iea	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000007	OMIM:611174	TAS				I		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000023	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000028	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000154	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000218	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000248	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000316	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000319	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000343	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000347	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000369	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000384	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000407	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000431	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000463	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000465	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000668	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000689	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000767	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000829	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0000938	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001159	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001182	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001363	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001385	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001631	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001653	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001931	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0001935	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0002015	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0002162	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0002376	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0005338	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0009536	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0010511	OMIM:611174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0011003	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0011343	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0030084	OMIM:611174	IEA				P		HPO:skoehler	
OMIM	611174	HAMAMY SYNDROME; HMMS		HP:0200021	OMIM:611174	TAS				P		HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0000007	OMIM:611182	TAS				I	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0001137	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0001249	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0001252	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0001272	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0001298	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0002119	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0002133	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0003236	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611182	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIh; CDG2H;;CDG IIh; CDGIIh		HP:0008150	OMIM:611182	TAS				P	#611182 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIH; CDG2H;;CDG IIH; CDGIIH	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000007	OMIM:611209	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000028	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000047	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000083	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000126	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000175	OMIM:611209	IEA		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	HP:0040284
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000201	OMIM:611209	IEA		HP:0040284		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	HP:0040284
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000218	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000219	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000253	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000316	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000319	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000347	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000365	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000368	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000431	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000463	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000494	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000582	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000750	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000772	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0000938	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001252	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001263	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001272	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001511	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001531	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001762	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001773	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001873	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001903	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0001999	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0002059	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0002650	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0003160	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0003316	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0003422	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0008551	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0008897	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0008905	OMIM:611209	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:probinson	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0011800	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0012385	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0031936	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611209	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIg; CDG2G		HP:0200055	OMIM:611209	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIG; CDG2G	HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0000007	OMIM:611225	IEA				I		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0000218	OMIM:611225	TAS				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0000486	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001249	OMIM:611225	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001250	OMIM:611225	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001258	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001288	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001344	OMIM:611225	TAS				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001347	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0001761	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0002079	OMIM:611225	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0002650	OMIM:611225	TAS				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0002808	OMIM:611225	TAS				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0003202	OMIM:611225	TAS				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0003487	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0003676	OMIM:611225	TAS				C		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0003677	OMIM:611225	TAS				C		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0006986	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0007340	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611225	SPASTIC PARAPLEGIA 18, AUTOSOMAL RECESSIVE; SPG18		HP:0031936	OMIM:611225	IEA				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0000007	PMID:17572665	PCS				I		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0000762	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0001265	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0001270	OMIM:611228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0001284	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0001288	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0002359	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0002460	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0002936	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0003383	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0003431	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0003447	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0003676	OMIM:611228	TAS				C		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0003828	OMIM:611228	TAS				C		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0005684	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0006466	OMIM:611228	TAS				P		HPO:skoehler	
OMIM	611228	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J		HP:0007182	PMID:17572665	PCS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0000007	OMIM:611252	TAS				I		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0001256	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0001258	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0001272	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0001761	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0002059	OMIM:611252	TAS				P		HPO:skoehler	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0002064	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0002079	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0002355	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0003487	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0003677	OMIM:611252	TAS				C		HPO:skoehler	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0007340	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0011448	OMIM:611252	TAS				P		HPO:probinson	
OMIM	611252	%611252 SPASTIC PARAPLEGIA 32, AUTOSOMAL RECESSIVE; SPG32		HP:0011463	OMIM:611252	TAS				C		HPO:probinson	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0000007	OMIM:611263	IEA				I		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0000774	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0001156	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0001162	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0001169	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0001773	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0003027	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0008905	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611263	ASPHYXIATING THORACIC DYSTROPHY 2; ATD2		HP:0010049	OMIM:611263	IEA				P		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0000006	OMIM:611277	TAS				I		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0002069	OMIM:611277	TAS				P		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0002121	OMIM:611277	TAS				P		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0002373	OMIM:611277	TAS				P		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0003828	OMIM:611277	TAS				C		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0007359	OMIM:611277	TAS				P		HPO:skoehler	
OMIM	611277	#611277 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3; GEFSP3;;GEFS+, TYPE 3; GEFS+3FEBRILE SEIZURES, FAMILIAL, 8, INCLUDED; FEB8, INCLUDED		HP:0010819	OMIM:611277	TAS				P		HPO:skoehler	
OMIM	611283	#611283 ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY		HP:0000007	OMIM:611283	TAS				I	#611283 ISOBUTYRYL-COA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-COA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY	HPO:probinson	
OMIM	611283	#611283 ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY		HP:0001252	OMIM:611283	TAS				P	#611283 ISOBUTYRYL-COA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-COA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY	HPO:probinson	
OMIM	611283	#611283 ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY		HP:0001644	OMIM:611283	TAS				P	#611283 ISOBUTYRYL-COA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-COA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY	HPO:probinson	
OMIM	611283	#611283 ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY		HP:0001903	OMIM:611283	TAS				P	#611283 ISOBUTYRYL-COA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-COA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY	HPO:probinson	
OMIM	611283	#611283 ISOBUTYRYL-CoA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-CoA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY		HP:0003234	OMIM:611283	TAS				P	#611283 ISOBUTYRYL-COA DEHYDROGENASE DEFICIENCY;;IBD DEFICIENCY;;ACYL-COA DEHYDROGENASE FAMILY, MEMBER 8, DEFICIENCY OF;;ACAD8 DEFICIENCY	HPO:probinson	
OMIM	611284	DYSTONIA, FOCAL, TASK-SPECIFIC; FTSD		HP:0000006	OMIM:611284	IEA				I		HPO:skoehler	
OMIM	611284	DYSTONIA, FOCAL, TASK-SPECIFIC; FTSD		HP:0002356	OMIM:611284	IEA				P		HPO:skoehler	
OMIM	611284	DYSTONIA, FOCAL, TASK-SPECIFIC; FTSD		HP:0003581	OMIM:611284	IEA				C		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0000007	OMIM:611302	IEA				I		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0000666	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0001257	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0001260	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0001272	OMIM:611302	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0001310	OMIM:611302	TAS				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0001347	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0002066	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0002359	OMIM:611302	TAS				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0002380	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0002497	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0002599	OMIM:611302	TAS				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0003487	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0003676	OMIM:611302	IEA				C		HPO:skoehler	
OMIM	611302	#611302 SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE; SPAX2		HP:0003693	OMIM:611302	IEA				P		HPO:skoehler	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0000007	OMIM:611307	IEA				I		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003236	OMIM:611307	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003326	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003458	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003547	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003560	OMIM:611307	IEA				P		HPO:skoehler	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003560	OMIM:611307	TAS				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003676	OMIM:611307	IEA				C		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003701	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003749	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0003828	OMIM:611307	IEA				C		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0008981	OMIM:611307	IEA				P		HPO:iea	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0009025	OMIM:611307	IEA				P		HPO:skoehler	
OMIM	611307	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2L; LGMD2L		HP:0010628	OMIM:611307	IEA				P		HPO:iea	
OMIM	611363	#611363 ATRIAL SEPTAL DEFECT 4; ASD4		HP:0000006	PMID:17668378	PCS				I		HPO:probinson	
OMIM	611363	#611363 ATRIAL SEPTAL DEFECT 4; ASD4		HP:0001655	PMID:17668378	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611363	#611363 ATRIAL SEPTAL DEFECT 4; ASD4		HP:0001680	PMID:17668378	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611364	MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4; EJM4		HP:0000006	PMID:17431681	PCS				I		HPO:skoehler	
OMIM	611364	MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4; EJM4		HP:0002069	PMID:17431681	PCS		HP:0040284		P		HPO:skoehler	7/9
OMIM	611364	MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4; EJM4		HP:0002123	PMID:17431681	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	611364	MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 4; EJM4		HP:0002392	PMID:17431681	PCS		HP:0040284		P		HPO:lccarmody	6/8
OMIM	611369	#611369 LETHAL CONGENITAL CONTRACTURE SYNDROME 3; LCCS3;;MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B		HP:0000007	PMID:17701898	PCS				I		HPO:probinson	
OMIM	611369	#611369 LETHAL CONGENITAL CONTRACTURE SYNDROME 3; LCCS3;;MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B		HP:0002093	PMID:17701898	PCS				P		HPO:probinson	
OMIM	611369	#611369 LETHAL CONGENITAL CONTRACTURE SYNDROME 3; LCCS3;;MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B		HP:0002804	PMID:17701898	PCS				P		HPO:probinson	
OMIM	611369	#611369 LETHAL CONGENITAL CONTRACTURE SYNDROME 3; LCCS3;;MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B		HP:0003202	PMID:17701898	PCS				P		HPO:probinson	
OMIM	611369	#611369 LETHAL CONGENITAL CONTRACTURE SYNDROME 3; LCCS3;;MULTIPLE CONTRACTURE SYNDROME, ISRAELI BEDOUIN TYPE B		HP:0003811	PMID:17701898	PCS				M		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0000007	OMIM:611376	TAS				I		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0000076	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0000089	OMIM:611376	IEA				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0001488	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0001642	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0002270	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0004389	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0005180	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0011682	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0030996	OMIM:611376	TAS				P		HPO:skoehler	
OMIM	611376	MUNGAN SYNDROME		HP:0100580	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611376	MUNGAN SYNDROME		HP:0100771	OMIM:611376	TAS				P		HPO:probinson	
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0000006	OMIM:611377;PMID:17668388	PCS				I		HPO:iea	
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0000407	OMIM:611377;PMID:17668388	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0000540	OMIM:611377;PMID:17668388	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0001204	OMIM:611377;PMID:17668388	PCS		HP:0040284		P		HPO:iea	5/5
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0006109	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0006152	OMIM:611377;PMID:17668388	PCS		HP:0040284		P		HPO:iea	16/16
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0008368	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0008386	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0009623	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0009702	OMIM:611377;PMID:17668388	PCS		HP:0040284		P		HPO:iea	10/10
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0009835	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0009843	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0009882	OMIM:611377	TAS				P		HPO:skoehler	
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0010034	OMIM:611377;PMID:17668388	PCS		HP:0040284		P		HPO:iea	7/10
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0010185	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0010194	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0010554	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611377	BRACHYDACTYLY, TYPE B2		HP:0010621	OMIM:611377;PMID:17668388	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611383	USHER SYNDROME, TYPE IID; USH2D		HP:0000007	OMIM:611383	TAS				I		HPO:probinson	
OMIM	611383	USHER SYNDROME, TYPE IID; USH2D		HP:0000365	OMIM:611383	TAS	HP:0003577			P		HPO:probinson	
OMIM	611383	USHER SYNDROME, TYPE IID; USH2D		HP:0000510	OMIM:611383	TAS				P		HPO:probinson	
OMIM	611383	USHER SYNDROME, TYPE IID; USH2D		HP:0000618	OMIM:611383	IEA				P		HPO:skoehler	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0000007	OMIM:611390	IEA				I		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0000012	OMIM:611390	IEA		HP:0040284		P		HPO:iea	57%
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL	HP:0012825	HP:0000666	OMIM:611390	TAS				P		HPO:skoehler	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001257	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001260	OMIM:611390	IEA		HP:0040284		P		HPO:probinson	74%
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001272	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001310	OMIM:611390	TAS				P		HPO:skoehler	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001332	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0001347	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0002066	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0002120	OMIM:611390	IEA				P		HPO:iea	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0002352	OMIM:611390	IEA		HP:0040284		P		HPO:skoehler	52%
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0002497	OMIM:611390	IEA				P		HPO:skoehler	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0002650	OMIM:611390	IEA		HP:0040284		P		HPO:iea	35%
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0012712	OMIM:611390	TAS				P		HPO:skoehler	
OMIM	611390	#611390 SPASTIC ATAXIA 3, AUTOSOMAL RECESSIVE; SPAX3;;AUTOSOMAL RECESSIVE SPASTIC ATAXIA WITH LEUKOENCEPHALOPATHY; ARSAL		HP:0100543	OMIM:611390	IEA				P		HPO:iea	
OMIM	611391	CATARACT 33, MULTIPLE TYPES; CTRCT33		HP:0000006	OMIM:611391	TAS				I		HPO:skoehler	
OMIM	611391	CATARACT 33, MULTIPLE TYPES; CTRCT33		HP:0000007	OMIM:611391	TAS				I		HPO:probinson	
OMIM	611391	CATARACT 33, MULTIPLE TYPES; CTRCT33		HP:0007971	OMIM:611391	IEA				P		HPO:skoehler	
OMIM	611391	CATARACT 33, MULTIPLE TYPES; CTRCT33		HP:0100018	OMIM:611391	TAS				P		HPO:skoehler	
OMIM	611391	CATARACT 33, MULTIPLE TYPES; CTRCT33		HP:0100019	OMIM:611391	TAS	HP:0003621			P		HPO:probinson	
OMIM	611407	#611407 CARDIOMYOPATHY, DILATED, 1W; CMD1W		HP:0000006	PMID:11815424	IEA				I		HPO:probinson	
OMIM	611407	#611407 CARDIOMYOPATHY, DILATED, 1W; CMD1W		HP:0001644	PMID:11815424	IEA				P		HPO:probinson	
OMIM	611426	611426 TENTED EYEBROWS		HP:0000006	OMIM:611426	IEA				I		HPO:iea	
OMIM	611426	611426 TENTED EYEBROWS		HP:0000478	OMIM:611426	IEA				P		HPO:iea	
OMIM	611426	611426 TENTED EYEBROWS		HP:0001595	OMIM:611426	IEA				P		HPO:iea	
OMIM	611431	LEGIUS SYNDROME		HP:0000006	OMIM:611431	IEA				I		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000218	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000256	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000286	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000316	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000325	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000347	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000368	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000470	OMIM:611431	TAS				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000494	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000508	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000766	OMIM:611431	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611431	LEGIUS SYNDROME		HP:0000957	PMID:21649642	PCS				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0000997	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0001012	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0001067	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0001290	OMIM:611431	TAS				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0001328	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0002162	OMIM:611431	TAS				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0002705	OMIM:611431	TAS				P		HPO:skoehler	
OMIM	611431	LEGIUS SYNDROME		HP:0007018	OMIM:611431	IEA				P		HPO:skoehler	
OMIM	611451	DEAFNESS, AUTOSOMAL RECESSIVE 63		HP:0000007	PMID:18794526	PCS				I		HPO:probinson	
OMIM	611451	DEAFNESS, AUTOSOMAL RECESSIVE 63		HP:0003577	OMIM:611451	TAS				C		HPO:skoehler	
OMIM	611451	DEAFNESS, AUTOSOMAL RECESSIVE 63		HP:0008527	PMID:18794526	PCS	HP:0003577			P		HPO:probinson	
OMIM	611465	#611465 GALLBLADDER DISEASE 4; GBD4		HP:0001081	OMIM:611465	IEA				P		HPO:skoehler	
OMIM	611465	#611465 GALLBLADDER DISEASE 4; GBD4		HP:0010982	OMIM:611465	IEA				I		HPO:skoehler	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0000006	OMIM:611489	IEA				I		HPO:iea	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0000007	OMIM:611489	IEA				I		HPO:iea	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0000822	OMIM:611489	IEA				P		HPO:iea	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0001939	OMIM:611489	IEA				P		HPO:iea	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0002615	OMIM:611489	IEA				P		HPO:iea	
OMIM	611489	CORTICOSTEROID-BINDING GLOBULIN DEFICIENCY		HP:0003750	OMIM:611489	IEA				P		HPO:iea	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0000007	OMIM:611490	TAS				I		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0000505	OMIM:611490	IEA				P		HPO:skoehler	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0000543	OMIM:611490	IEA				P		HPO:skoehler	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0000648	OMIM:611490	IEA				P		HPO:skoehler	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0001433	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0001873	OMIM:611490	IEA				P		HPO:skoehler	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0001903	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0001923	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0002757	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0004576	OMIM:611490	IEA				P		HPO:skoehler	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0010628	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611490	OSTEOPETROSIS,  AUTOSOMAL RECESSIVE 4; OPTB4		HP:0011002	OMIM:611490	TAS				P		HPO:probinson	
OMIM	611493	#611493 ATRIAL FIBRILLATION, FAMILIAL, 4; ATFB4		HP:0000006	PMID:15368194	PCS				I		HPO:probinson	
OMIM	611493	#611493 ATRIAL FIBRILLATION, FAMILIAL, 4; ATFB4		HP:0001962	PMID:15368194	PCS		HP:0040284		P		HPO:lccarmody	9/10
OMIM	611493	#611493 ATRIAL FIBRILLATION, FAMILIAL, 4; ATFB4		HP:0004754	PMID:15368194	PCS		HP:0040284		P		HPO:lccarmody	1/10
OMIM	611493	#611493 ATRIAL FIBRILLATION, FAMILIAL, 4; ATFB4		HP:0004757	PMID:15368194	PCS		HP:0040284		P		HPO:lccarmody	3/10
OMIM	611493	#611493 ATRIAL FIBRILLATION, FAMILIAL, 4; ATFB4		HP:0006699	PMID:15368194	PCS		HP:0040284		P		HPO:lccarmody	10/10
OMIM	611494	ATRIAL FIBRILLATION, FAMILIAL, 5		HP:0005110	PMID:17603472	PCS				P		HPO:probinson	
OMIM	611494	ATRIAL FIBRILLATION, FAMILIAL, 5		HP:0010982	PMID:17603472	PCS				I		HPO:probinson	
OMIM	611497	#611497 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6; OPTB6;;OSTEOPETROSIS, AUTOSOMAL RECESSIVE, INTERMEDIATE FORM		HP:0000007	PMID:17404618	PCS				I		HPO:probinson	
OMIM	611497	#611497 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6; OPTB6;;OSTEOPETROSIS, AUTOSOMAL RECESSIVE, INTERMEDIATE FORM		HP:0004975	PMID:17404618	PCS				P		HPO:probinson	
OMIM	611497	#611497 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6; OPTB6;;OSTEOPETROSIS, AUTOSOMAL RECESSIVE, INTERMEDIATE FORM		HP:0011002	PMID:17404618	PCS				P		HPO:probinson	
OMIM	611497	#611497 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 6; OPTB6;;OSTEOPETROSIS, AUTOSOMAL RECESSIVE, INTERMEDIATE FORM		HP:0100959	PMID:17404618	PCS				P		HPO:probinson	
OMIM	611498	#611498 NEPHRONOPHTHISIS 7; NPHP7		HP:0000007	PMID:17618285	PCS				I		HPO:probinson	
OMIM	611498	#611498 NEPHRONOPHTHISIS 7; NPHP7		HP:0000090	PMID:17618285	PCS				P		HPO:probinson	
OMIM	611498	#611498 NEPHRONOPHTHISIS 7; NPHP7		HP:0000092	PMID:17618285	PCS				P		HPO:probinson	
OMIM	611498	#611498 NEPHRONOPHTHISIS 7; NPHP7		HP:0003774	PMID:17618285	PCS				P		HPO:probinson	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0000007	PMID:17088085	PCS				I	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0002205	OMIM:611521	TAS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0002721	OMIM:611521	TAS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:skoehler	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0002841	PMID:17088085	PCS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0003212	PMID:17088085	PCS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0004429	PMID:17088085	PCS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	611521	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IgE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE		HP:0011274	PMID:17088085	PCS				P	#611521 IMMUNODEFICIENCY 35; IMD35;;TYROSINE KINASE 2 DEFICIENCY;;TYK2 DEFICIENCY;;HYPER-IGE SYNDROME WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE;;HIES WITH ATYPICAL MYCOBACTERIOSIS, AUTOSOMAL RECESSIVE	HPO:probinson	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000007	OMIM:611523	TAS				I		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000189	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000253	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000341	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000426	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0000490	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001250	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001263	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001272	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001290	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001321	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001344	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001347	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0001508	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002033	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002059	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002061	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002104	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002151	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002421	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0002490	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0003577	OMIM:611523	TAS				C		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0003676	OMIM:611523	TAS				C		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0003819	OMIM:611523	TAS				M		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0003828	OMIM:611523	TAS				C		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0006986	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611523	PONTOCEREBELLAR HYPOPLASIA, TYPE 6		HP:0007366	OMIM:611523	TAS				P		HPO:skoehler	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0000006	OMIM:611528	TAS				I		HPO:probinson	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0001279	OMIM:611528	TAS				P		HPO:probinson	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0001425	OMIM:611528	TAS				I		HPO:skoehler	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0004308	OMIM:611528	TAS				P		HPO:skoehler	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0004756	OMIM:611528	TAS				P		HPO:probinson	
OMIM	611528	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12		HP:0011663	OMIM:611528	TAS				P		HPO:probinson	
OMIM	611543	CAVITARY OPTIC DISC ANOMALIES; CODA		HP:0000006	OMIM:611543	TAS				I		HPO:skoehler	
OMIM	611543	CAVITARY OPTIC DISC ANOMALIES; CODA		HP:0000662	OMIM:611543	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611543	CAVITARY OPTIC DISC ANOMALIES; CODA		HP:0001123	OMIM:611543	TAS				P		HPO:skoehler	
OMIM	611543	CAVITARY OPTIC DISC ANOMALIES; CODA		HP:0007663	OMIM:611543	TAS				P		HPO:skoehler	
OMIM	611543	CAVITARY OPTIC DISC ANOMALIES; CODA		HP:0500087	OMIM:611543	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000006	OMIM:611544	TAS				I		HPO:skoehler	
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000007	OMIM:611544	TAS				I		HPO:probinson	
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000482	OMIM:611544	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000519	OMIM:611544	IEA				P		HPO:skoehler	
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000639	OMIM:611544	TAS				P		HPO:skoehler	
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0000646	OMIM:611544	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0010693	OMIM:611544	TAS				P		HPO:skoehler	
OMIM	611544	CATARACT 17, MULTIPLE TYPES		HP:0100018	OMIM:611544	TAS	HP:0003577			P		HPO:probinson	
OMIM	611548	PREMATURE OVARIAN FAILURE 5; POF5		HP:0000006	OMIM:611548	TAS				I		HPO:skoehler	
OMIM	611548	PREMATURE OVARIAN FAILURE 5; POF5		HP:0000786	OMIM:611548	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611548	PREMATURE OVARIAN FAILURE 5; POF5		HP:0000869	OMIM:611548	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	611548	PREMATURE OVARIAN FAILURE 5; POF5		HP:0008209	OMIM:611548	IEA				P		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000006	PMID:17603482	PCS				I		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000154	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000256	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000286	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000303	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000316	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000369	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000465	PMID:17603482	PCS		HP:0040284		P		HPO:probinson	7/9
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000470	PMID:17603482	PCS				P		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000494	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000508	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0000766	PMID:17603482	PCS				P		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001249	OMIM:611553	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001263	PMID:17603482	PCS				P		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001631	PMID:17603482	PCS		HP:0040284		P		HPO:probinson	6/11
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001639	PMID:17603482	PCS		HP:0040284		P		HPO:probinson	8/11
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001642	OMIM:611553	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0001999	PMID:17603482	PCS				P		HPO:probinson	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0004322	PMID:17603482	PCS		HP:0040284		P		HPO:probinson	10/11
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0011220	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0011675	OMIM:611553	IEA				P		HPO:skoehler	
OMIM	611553	NOONAN SYNDROME 5; NS5		HP:0012471	OMIM:611553	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000006	PMID:17603483	PCS				I		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000179	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000268	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000286	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000303	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000316	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000369	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000465	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000470	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000494	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000766	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000957	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0000958	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0001003	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0001639	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0002212	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0002967	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0004322	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611554	#611554 LEOPARD SYNDROME 2		HP:0005280	PMID:17603483	PCS				P		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0000007	PMID:17928598	PCS				I		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0001297	OMIM:611556	IEA				P		HPO:skoehler	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0001638	PMID:17928598	PCS				P		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0001712	OMIM:611556	TAS				P		HPO:skoehler	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0002069	PMID:17928598	PCS				P		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0003546	PMID:17928598	PCS				P		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0012270	PMID:17928598	PCS				P		HPO:probinson	
OMIM	611556	GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B		HP:0031295	OMIM:611556	IEA				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000007	OMIM:611560	TAS				I		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000090	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000107	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000508	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000556	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000639	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0000657	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001162	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001249	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001251	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001263	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001273	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001290	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0001425	OMIM:611560	TAS				I		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002084	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002365	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002419	OMIM:611560	TAS				P		HPO:probinson	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002508	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002650	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002790	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002871	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611560	JOUBERT SYNDROME 7		HP:0002876	OMIM:611560	TAS				P		HPO:skoehler	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0000007	OMIM:611561	IEA				I		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0000079	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0000175	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0000204	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0000568	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0001162	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0001408	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0001425	OMIM:611561	IEA				I		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0001830	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0002085	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0002323	OMIM:611561	IEA				P		HPO:iea	
OMIM	611561	MECKEL SYNDROME, TYPE 5		HP:0006487	OMIM:611561	TAS				P		HPO:skoehler	
OMIM	611571	OTOSCLEROSIS 4		HP:0000006	OMIM:611571	IEA				I		HPO:iea	
OMIM	611571	OTOSCLEROSIS 4		HP:0000362	OMIM:611571	IEA				P		HPO:iea	
OMIM	611571	OTOSCLEROSIS 4		HP:0000410	OMIM:611571	TAS				P		HPO:probinson	
OMIM	611572	OTOSCLEROSIS 7		HP:0000006	PMID:16168495	PCS				I		HPO:iea	
OMIM	611572	OTOSCLEROSIS 7		HP:0000362	PMID:16168495	PCS				P		HPO:iea	
OMIM	611572	OTOSCLEROSIS 7		HP:0000405	PMID:16168495	PCS	HP:0011462			P		HPO:lccarmody	
OMIM	611572	OTOSCLEROSIS 7		HP:0001730	PMID:16168495	PCS				P		HPO:lccarmody	
OMIM	611572	OTOSCLEROSIS 7		HP:0011474	PMID:16168495	PCS	HP:0011463			P		HPO:lccarmody	
OMIM	611572	OTOSCLEROSIS 7		HP:0040121	PMID:16168495	PCS				P		HPO:lccarmody	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000006	OMIM:611584	PCS				I		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000407	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000458	OMIM:611584	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000635	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000639	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000767	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0000957	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001053	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001100	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001107	OMIM:611584	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001249	OMIM:611584	TAS				P		HPO:skoehler	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001263	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001276	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0001425	OMIM:611584	TAS				I		HPO:skoehler	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0002211	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0002216	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0002226	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0002227	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0002617	OMIM:611584	IEA				P		HPO:skoehler	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0006808	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0007676	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0007894	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0008936	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0011379	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0011381	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611584	WAARDENBURG SYNDROME, TYPE 2E; WS2E		HP:0011382	OMIM:611584	PCS				P		HPO:probinson	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0000007	OMIM:611588	IEA				I		HPO:iea	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0000767	OMIM:611588	IEA				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001252	OMIM:611588	IEA				P		HPO:iea	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001265	OMIM:611588	IEA				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001270	OMIM:611588	IEA				P		HPO:iea	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001290	OMIM:611588	TAS				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001371	OMIM:611588	TAS				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0001762	OMIM:611588	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003236	OMIM:611588	IEA				P		HPO:iea	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003307	OMIM:611588	TAS				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003391	OMIM:611588	IEA				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003560	OMIM:611588	TAS				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003593	OMIM:611588	IEA				C		HPO:iea	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003676	OMIM:611588	TAS				C		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003712	OMIM:611588	IEA				P		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0003828	OMIM:611588	TAS				C		HPO:skoehler	
OMIM	611588	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4; MDDGC4		HP:0012345	OMIM:611588	IEA				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0000007	PMID:15211439	PCS				I		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0000121	PMID:15211439	PCS				P		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0000980	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001254	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001433	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001508	PMID:15211439	PCS				P		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001878	OMIM:611590	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001923	OMIM:611590	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0001942	PMID:15211439	PCS				P		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0002039	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0002748	PMID:15211439	PCS				P		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0002900	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0004322	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0004918	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0008341	PMID:15211439	PCS				P		HPO:probinson	
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0025066	OMIM:611590	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611590	RENAL TUBULAR ACIDOSIS, DISTAL, WITH HEMOLYTIC ANEMIA		HP:0030036	OMIM:611590	TAS				P		HPO:skoehler	
OMIM	611597	CATARACT, AUTOSOMAL DOMINANT, MULTIPLE TYPES 1		HP:0000006	OMIM:611597	TAS				I		HPO:probinson	
OMIM	611597	CATARACT, AUTOSOMAL DOMINANT, MULTIPLE TYPES 1		HP:0000519	PMID:10739768	PCS				P		HPO:probinson	
OMIM	611597	CATARACT, AUTOSOMAL DOMINANT, MULTIPLE TYPES 1		HP:0000545	OMIM:611597	TAS				P		HPO:probinson	
OMIM	611597	CATARACT, AUTOSOMAL DOMINANT, MULTIPLE TYPES 1		HP:0007834	OMIM:611597	TAS				P		HPO:probinson	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0000006	OMIM:611603	IEA				I		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0000252	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001250	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001251	OMIM:611603	TAS				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001270	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001274	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001290	OMIM:611603	TAS				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001302	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0001320	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002079	OMIM:611603	TAS				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002119	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002126	OMIM:611603	TAS				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002282	OMIM:611603	IEA				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002365	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0002510	OMIM:611603	IEA				P		HPO:iea	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0010864	OMIM:611603	TAS				P		HPO:skoehler	
OMIM	611603	LISSENCEPHALY 3; LIS3		HP:0031882	OMIM:611603	IEA				P		HPO:skoehler	
OMIM	611615	CARDIOMYOPATHY, DILATED, 1X		HP:0000007	OMIM:611615	IEA				I		HPO:iea	
OMIM	611615	CARDIOMYOPATHY, DILATED, 1X		HP:0001644	OMIM:611615	IEA				P		HPO:iea	
OMIM	611615	CARDIOMYOPATHY, DILATED, 1X		HP:0003701	OMIM:611615	IEA				P		HPO:iea	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0000006	OMIM:611630	TAS				I		HPO:probinson	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0001425	OMIM:611630	TAS				I		HPO:skoehler	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0002321	OMIM:611630	TAS				P		HPO:skoehler	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0002349	OMIM:611630	TAS				P		HPO:probinson	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0002384	OMIM:611630	TAS				P		HPO:probinson	
OMIM	611630	EPILEPSY, FAMILIAL TEMPORAL LOBE, 3; ETL3		HP:0012005	OMIM:611630	TAS				P		HPO:probinson	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0000006	OMIM:611631	TAS				I		HPO:skoehler	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0002077	OMIM:611631	TAS				P		HPO:skoehler	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0002349	OMIM:611631	TAS				P		HPO:probinson	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0002384	OMIM:611631	TAS				P		HPO:skoehler	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0003829	OMIM:611631	TAS				C		HPO:skoehler	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0008765	OMIM:611631	TAS				P		HPO:skoehler	
OMIM	611631	EPILEPSY, FAMILIAL TEMPORAL LOBE, 4		HP:0011165	OMIM:611631	TAS				P		HPO:skoehler	
OMIM	611634	FEBRILE CONVULSIONS, FAMILIAL, 9		HP:0000006	OMIM:611634	IEA				I		HPO:iea	
OMIM	611634	FEBRILE CONVULSIONS, FAMILIAL, 9		HP:0002121	OMIM:611634	TAS				P		HPO:iea	
OMIM	611634	FEBRILE CONVULSIONS, FAMILIAL, 9		HP:0002373	OMIM:611634	IEA				P		HPO:iea	
OMIM	611634	FEBRILE CONVULSIONS, FAMILIAL, 9		HP:0010849	OMIM:611634	TAS				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0000006	OMIM:611637	IEA				I		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0001285	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0001347	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0002015	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0002064	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0002127	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0002464	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0003487	OMIM:611637	IEA				P		HPO:iea	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0003581	OMIM:611637	TAS				C		HPO:probinson	
OMIM	611637	PRIMARY LATERAL SCLEROSIS, ADULT		HP:0003677	OMIM:611637	IEA				C		HPO:iea	
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000006	PMID:12503095	PCS				I		HPO:iea	
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000202	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=anophthalmia-ov	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000504	PMID:12503095	PCS		HP:0040282		P		HPO:iea	HP:0040282
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000528	PMID:12503095	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000567	PMID:12503095	PCS				P		HPO:probinson	
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000568	OMIM:611638	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0000612	PMID:12503095	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0001360	http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=anophthalmia-ov	PCS		HP:0040283		P		HPO:iea	HP:0040283
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0003828	OMIM:611638	PCS				C		HPO:iea	
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0003829	OMIM:611638	PCS				C		HPO:iea	
OMIM	611638	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 5		HP:0007633	OMIM:611638	TAS				P		HPO:skoehler	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0000007	OMIM:611694	TAS				I		HPO:probinson	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0000473	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0000478	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0001260	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0001272	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0001348	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0001618	OMIM:611694	IEA				P		HPO:skoehler	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0002015	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0002073	OMIM:611694	IEA				P		HPO:iea	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0007979	OMIM:611694	TAS				P		HPO:skoehler	
OMIM	611694	%611694 DYSTONIA WITH CEREBELLAR ATROPHY; DYTCA		HP:0012179	OMIM:611694	TAS				P		HPO:probinson	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0001156	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0001591	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0002657	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0002812	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0002970	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0003016	OMIM:611702	TAS				P		HPO:probinson	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0003026	OMIM:611702	TAS				P		HPO:probinson	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0003300	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0003498	OMIM:611702	IEA				P		HPO:iea	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0003745	OMIM:611702	TAS				I		HPO:skoehler	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0005054	OMIM:611702	IEA				P		HPO:skoehler	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0006026	OMIM:611702	IEA				P		HPO:skoehler	
OMIM	611702	SPONDYLOMETAPHYSEAL DYSPLASIA, EAST AFRICAN TYPE		HP:0008873	OMIM:611702	TAS				P		HPO:probinson	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0000007	OMIM:611705	IEA				I		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0000508	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0001270	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0001371	OMIM:611705	TAS				P		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0001644	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0001699	OMIM:611705	TAS				M		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0002650	OMIM:611705	TAS				P		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003198	OMIM:611705	TAS				P		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003236	OMIM:611705	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003324	OMIM:611705	TAS				P		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003577	OMIM:611705	TAS				C		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003593	OMIM:611705	TAS				C		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0003687	OMIM:611705	IEA				P		HPO:skoehler	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0008981	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0010628	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0011675	OMIM:611705	IEA				P		HPO:iea	
OMIM	611705	SALIH MYOPATHY; SALMY		HP:0030059	OMIM:611705	IEA				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0000006	OMIM:611706	TAS				I		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0000613	OMIM:611706	TAS				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0002013	OMIM:611706	TAS				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0002018	OMIM:611706	TAS				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0002076	OMIM:611706	IEA				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0002183	OMIM:611706	TAS				P		HPO:skoehler	
OMIM	611706	MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 12; MGR12		HP:0002315	OMIM:611706	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000006	OMIM:611717	IEA				I		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000154	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000179	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000215	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000272	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000280	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000311	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000343	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000431	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000463	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000470	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000475	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000581	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000582	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0000767	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH	HP:0012825	HP:0000926	OMIM:611717	PCS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001156	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH	HP:0012825	HP:0001371	OMIM:611717	PCS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001498	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001609	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001620	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001773	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0001831	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0002091	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0002655	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0002663	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0002866	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0002967	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0003026	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0004279	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0004580	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0004634	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0005069	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0005257	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0005280	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0006108	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0006192	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0006216	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0007665	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0008551	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0008897	OMIM:611717	IEA				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0009803	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0010049	OMIM:611717	TAS				P		HPO:probinson	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0010585	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611717	SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH		HP:0011800	OMIM:611717	TAS				P		HPO:skoehler	
OMIM	611718	#611718 HYPOMAGNESEMIA 4, RENAL; HOMG4;;HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC		HP:0000007	PMID:17671655	PCS				I		HPO:probinson	
OMIM	611718	#611718 HYPOMAGNESEMIA 4, RENAL; HOMG4;;HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC		HP:0001250	PMID:17671655	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	611718	#611718 HYPOMAGNESEMIA 4, RENAL; HOMG4;;HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC		HP:0001263	PMID:17671655	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	611718	#611718 HYPOMAGNESEMIA 4, RENAL; HOMG4;;HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC		HP:0002342	PMID:17671655	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	611718	#611718 HYPOMAGNESEMIA 4, RENAL; HOMG4;;HYPOMAGNESEMIA, RENAL, NORMOCALCIURIC		HP:0002917	PMID:17671655	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000007	OMIM:611719	IEA				I		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000091	OMIM:611719	IEA				P		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000252	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000278	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000358	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000369	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0000969	OMIM:611719	TAS				P		HPO:probinson	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001250	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001252	OMIM:611719	IEA				P		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001290	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001510	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001522	OMIM:611719	TAS				M		HPO:probinson	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001541	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001560	OMIM:611719	IEA				P		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0001639	OMIM:611719	IEA				P		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5	HP:0012828	HP:0001942	OMIM:611719	TAS				P		HPO:probinson	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0002079	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0002151	OMIM:611719	IEA				P		HPO:iea	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0002352	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0002510	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0003577	OMIM:611719	TAS				C		HPO:probinson	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0005989	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0008936	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0012448	OMIM:611719	TAS				P		HPO:skoehler	
OMIM	611719	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5		HP:0030674	OMIM:611719	TAS				C		HPO:skoehler	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0000007	OMIM:611721	PCS				I		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0000648	OMIM:611721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0001290	OMIM:611721	TAS				P		HPO:skoehler	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0001336	OMIM:611721	TAS				P		HPO:skoehler	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0001522	OMIM:611721	PCS				M		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0001744	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002079	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002240	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002380	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002487	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002518	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0002529	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0003487	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0003577	OMIM:611721	PCS				C		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0004343	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0007305	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0011169	OMIM:611721	PCS				P		HPO:probinson	
OMIM	611721	COMBINED SAPOSIN DEFICIENCY		HP:0011968	OMIM:611721	TAS				P		HPO:skoehler	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0000007	OMIM:611722	IEA				I		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0001265	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0001276	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0002093	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0002283	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0002871	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0002878	OMIM:611722	TAS				P		HPO:skoehler	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0002922	OMIM:611722	IEA				P		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0003593	OMIM:611722	IEA				C		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0003819	OMIM:611722	IEA				M		HPO:iea	
OMIM	611722	#611722 KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY;;SAPOSIN A DEFICIENCY		HP:0007266	OMIM:611722	PCS				P		HPO:probinson	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0000007	OMIM:611726	IEA				I		HPO:iea	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0000252	OMIM:611726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0000572	OMIM:611726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0000648	OMIM:611726	TAS				P		HPO:skoehler	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0001249	OMIM:611726	IEA				P		HPO:iea	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0001260	OMIM:611726	IEA				P		HPO:iea	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0001272	OMIM:611726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0002059	OMIM:611726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0002078	OMIM:611726	IEA				P		HPO:iea	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0002079	OMIM:611726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0002123	OMIM:611726	TAS				P		HPO:probinson	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0003208	OMIM:611726	TAS				P		HPO:skoehler	
OMIM	611726	EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS		HP:0003676	OMIM:611726	IEA				C		HPO:iea	
OMIM	611755	#611755 LEBER CONGENITAL AMAUROSIS 10; LCA10		HP:0000007	OMIM:611755	TAS				I		HPO:probinson	
OMIM	611755	#611755 LEBER CONGENITAL AMAUROSIS 10; LCA10	HP:0012828	HP:0000505	OMIM:611755	TAS	HP:0003577			P		HPO:probinson	
OMIM	611755	#611755 LEBER CONGENITAL AMAUROSIS 10; LCA10	HP:0012828	HP:0001250	OMIM:611755	TAS	HP:0003577	HP:0040284		P		HPO:probinson	2/4
OMIM	611755	#611755 LEBER CONGENITAL AMAUROSIS 10; LCA10		HP:0004409	OMIM:611755	TAS				P		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0000006	PMID:18230725	PCS				I		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0000407	PMID:18230725	PCS				P		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0000988	OMIM:611762	TAS				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2	HP:0025303	HP:0001025	OMIM:611762	TAS				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0001369	OMIM:611762	IEA				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2	HP:0025206	HP:0001954	PMID:18230725	PCS	HP:0003593	HP:0040284		P		HP:probinson	3/3
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2	HP:0025303	HP:0002027	PMID:18230725	PCS				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2	HP:0025303	HP:0002315	OMIM:611762	TAS				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0002716	OMIM:611762	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0002829	PMID:18230725	PCS				P		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0003326	PMID:18230725	PCS				P		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0003593	OMIM:611762	TAS				C		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0003829	OMIM:611762	IEA				C		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2	HP:0025303	HP:0011107	OMIM:611762	TAS				P		HPO:skoehler	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0011227	PMID:18230725	PCS				P		HPO:probinson	
OMIM	611762	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 2; FCAS2		HP:0100827	OMIM:611762	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611771	#611771 LIPOPROTEIN GLOMERULOPATHY; LPG		HP:0000083	PMID:18077821	PCS				P		HPO:probinson	
OMIM	611771	#611771 LIPOPROTEIN GLOMERULOPATHY; LPG		HP:0000093	PMID:18077821	PCS				P		HPO:probinson	
OMIM	611771	#611771 LIPOPROTEIN GLOMERULOPATHY; LPG		HP:0012574	PMID:10432380	PCS				P		HPO:probinson	
OMIM	611771	#611771 LIPOPROTEIN GLOMERULOPATHY; LPG		HP:0100820	PMID:18077821	PCS				P		HPO:probinson	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000006	OMIM:611773	TAS				I		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000083	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000107	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000112	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000573	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0000790	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0001136	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0001297	OMIM:611773	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0002352	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0003394	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0004944	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0005115	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611773	ANGIOPATHY, HEREDITARY, WITH NEPHROPATHY, ANEURYSMS, AND MUSCLE CRAMPS		HP:0030880	OMIM:611773	TAS				P		HPO:skoehler	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0000006	PMID:17967977	PCS				I		HPO:probinson	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0001279	PMID:17967977	PCS				P		HPO:probinson	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0001645	PMID:17967977	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0001663	PMID:17967977	PCS				P		HPO:probinson	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0011705	PMID:17967977	PCS				P		HPO:probinson	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0011712	PMID:17967977	PCS				P		HPO:probinson	
OMIM	611777	#611777 BRUGADA SYNDROME 2; BRGDA2		HP:0012248	PMID:11839626	PCS		HP:0040284		P		HPO:probinson	7/12
OMIM	611783	#611783 ERYTHROCYTOSIS, FAMILIAL, 4; ECYT4		HP:0000006	OMIM:611783	TAS				I		HPO:probinson	
OMIM	611783	#611783 ERYTHROCYTOSIS, FAMILIAL, 4; ECYT4		HP:0001899	OMIM:611783	TAS				P		HPO:probinson	
OMIM	611783	#611783 ERYTHROCYTOSIS, FAMILIAL, 4; ECYT4		HP:0001900	OMIM:611783	TAS				P		HPO:probinson	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0000006	PMID:19409525	PCS				I		HPO:probinson	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0004933	PMID:19409525	PCS				P		HPO:probinson	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0004942	PMID:19409525	PCS				P		HPO:probinson	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0004970	OMIM:611788	TAS				P		HPO:skoehler	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0005181	PMID:19409525	PCS		HP:0040284		P		HPO:probinson	26/127
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0011834	PMID:19409525	PCS				P		HPO:probinson	
OMIM	611788	AORTIC ANEURYSM, FAMILIAL THORACIC 6		HP:0012727	OMIM:611788	IEA				P		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0000006	PMID:3058231	PCS				I		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0000007	OMIM:611804	IEA				I		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0000952	OMIM:611804	IEA				P		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0000980	OMIM:611804	IEA				P		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0001878	PMID:3058231	PCS				P		HPO:skoehler	
OMIM	611804	ELLIPTOCYTOSIS 1; EL1		HP:0004445	PMID:3058231	PCS				P		HPO:skoehler	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0000006	OMIM:611808	IEA				I		HPO:iea	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0000256	OMIM:611808	IEA				P		HPO:iea	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0001288	OMIM:611808	IEA				P		HPO:iea	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0002119	OMIM:611808	IEA				P		HPO:iea	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0002343	OMIM:611808	IEA				P		HPO:iea	
OMIM	611808	TREMOR, HEREDITARY ESSENTIAL, AND IDIOPATHIC NORMAL PRESSURE HYDROCEPHALUS		HP:0030186	OMIM:611808	TAS				P		HPO:skoehler	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0000007	PMID:18179881	PCS				I		HPO:probinson	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0000540	PMID:18179881	PCS				P		HPO:probinson	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0000654	PMID:18179881	PCS				P		HPO:probinson	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0007663	PMID:18179881	PCS				P		HPO:probinson	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0007722	PMID:18179881	PCS				P		HPO:probinson	
OMIM	611809	#611809 BESTROPHINOPATHY, AUTOSOMAL RECESSIVE; ARB		HP:0012045	PMID:18179881	PCS				P		HPO:probinson	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000007	OMIM:611812	TAS				I		HPO:iea	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000047	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000104	OMIM:611812	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000175	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000369	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0000776	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0001511	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0001629	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0002089	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0004415	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0005343	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0005944	OMIM:611812	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0011743	OMIM:611812	TAS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0012245	OMIM:611812	TAS				P		HPO:probinson	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0012861	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611812	46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS		HP:0410030	OMIM:611812	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000006	OMIM:611816	TAS				I		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000007	OMIM:611816	IEA				I		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000154	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000286	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000316	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000343	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0000445	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0001181	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0001250	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0001252	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0001263	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0001290	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0002058	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0002714	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0003593	OMIM:611816	TAS				C		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0004425	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0005280	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0006887	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0009693	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0009882	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0009928	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0010055	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0010864	OMIM:611816	TAS				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0011304	OMIM:611816	IEA				P		HPO:iea	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0012471	OMIM:611816	IEA				P		HPO:skoehler	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0012553	OMIM:611816	TAS				P		HPO:probinson	
OMIM	611816	TEMPLE-BARAITSER SYNDROME; TMBTS		HP:0012555	OMIM:611816	TAS				P		HPO:probinson	
OMIM	611818	LONG QT SYNDROME 9		HP:0000006	PMID:17060380	PCS				I		HPO:probinson	
OMIM	611818	LONG QT SYNDROME 9		HP:0001657	PMID:17060380	PCS				P		HPO:probinson	
OMIM	611818	LONG QT SYNDROME 9		HP:0001688	OMIM:611818	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611818	LONG QT SYNDROME 9		HP:0001695	OMIM:611818	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611818	LONG QT SYNDROME 9		HP:0004308	PMID:17060380	PCS				P		HPO:probinson	
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0000006	PMID:17592081	PCS				I		HPO:probinson	
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0001645	PMID:17592081	PCS				P		HPO:probinson	
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0001657	PMID:17592081	PCS				P		HPO:probinson	
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0001678	PMID:17592081	PCS				P		HPO:probinson	
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0005110	OMIM:611819	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611819	#611819 LONG QT SYNDROME 10; LQT10ATRIAL FIBRILLATION, FAMILIAL, 17, INCLUDED; ATFB17, INCLUDED		HP:0012266	PMID:17592081	PCS				P		HPO:probinson	
OMIM	611820	LONG QT SYNDROME 11		HP:0000006	OMIM:611820	TAS				I		HPO:skoehler	
OMIM	611820	LONG QT SYNDROME 11		HP:0001279	OMIM:611820	TAS				P		HPO:skoehler	
OMIM	611820	LONG QT SYNDROME 11		HP:0001657	OMIM:611820	IEA				P		HPO:skoehler	
OMIM	611863	MICROTIA - EYE COLOBOMA - IMPERFORATION OF THE NASOLACRIMAL DUCT		HP:0000006	OMIM:611863	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	611863	MICROTIA - EYE COLOBOMA - IMPERFORATION OF THE NASOLACRIMAL DUCT		HP:0008551	OMIM:611863	IEA				P		HPO:skoehler	
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000175	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	1/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000219	PMID:18179902	PCS		HP:0040282		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	HP:0040282
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000272	PMID:18179902	PCS		HP:0040282		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	HP:0040282
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000307	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	3/5
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000319	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	6/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000430	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	4/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000490	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	3/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0000708	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	2/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0001263	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	4/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0001511	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	5/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0001660	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	1/6
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0002553	PMID:18179902	PCS		HP:0040284		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	4/5
OMIM	611867	CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL		HP:0004322	PMID:18179902	PCS		HP:0040282		P	CHROMOSOME 22Q11.2 DELETION SYNDROME, DISTAL	HPO:iea	HP:0040282
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0000006	PMID:17224476	PCS				I		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0001279	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0001645	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0004308	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0005110	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0012232	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611875	#611875 BRUGADA SYNDROME 3; BRGDA3		HP:0012272	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611876	#611876 BRUGADA SYNDROME 4; BRGDA4		HP:0000006	PMID:17224476	PCS				I		HPO:probinson	
OMIM	611876	#611876 BRUGADA SYNDROME 4; BRGDA4		HP:0001279	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611876	#611876 BRUGADA SYNDROME 4; BRGDA4		HP:0005110	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611876	#611876 BRUGADA SYNDROME 4; BRGDA4		HP:0012232	PMID:17224476	PCS				P		HPO:probinson	
OMIM	611878	CARDIOMYOPATHY, DILATED, 1Y; CMD1Y		HP:0000006	OMIM:611878	TAS				I		HPO:probinson	
OMIM	611878	CARDIOMYOPATHY, DILATED, 1Y; CMD1Y		HP:0001635	OMIM:611878	TAS				P		HPO:probinson	
OMIM	611878	CARDIOMYOPATHY, DILATED, 1Y; CMD1Y		HP:0001644	OMIM:611878	TAS				P		HPO:probinson	
OMIM	611878	CARDIOMYOPATHY, DILATED, 1Y; CMD1Y		HP:0001653	OMIM:611878	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	611878	CARDIOMYOPATHY, DILATED, 1Y; CMD1Y		HP:0004756	OMIM:611878	TAS				P		HPO:probinson	
OMIM	611879	#611879 CARDIOMYOPATHY, DILATED, 1Z; CMD1Z		HP:0000006	PMID:15542288	TAS				I		HPO:probinson	
OMIM	611879	#611879 CARDIOMYOPATHY, DILATED, 1Z; CMD1Z		HP:0001644	PMID:15542288	TAS				P		HPO:probinson	
OMIM	611880	#611880 CARDIOMYOPATHY, DILATED, 2A; CMD2A;;CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE;;CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:611880	TAS				I		HPO:skoehler	
OMIM	611880	#611880 CARDIOMYOPATHY, DILATED, 2A; CMD2A;;CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE;;CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE		HP:0001635	OMIM:611880	TAS				P		HPO:skoehler	
OMIM	611880	#611880 CARDIOMYOPATHY, DILATED, 2A; CMD2A;;CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE;;CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE		HP:0001644	OMIM:611880	TAS				P		HPO:skoehler	
OMIM	611880	#611880 CARDIOMYOPATHY, DILATED, 2A; CMD2A;;CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE;;CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE		HP:0003621	OMIM:611880	TAS				C		HPO:probinson	
OMIM	611880	#611880 CARDIOMYOPATHY, DILATED, 2A; CMD2A;;CARDIOMYOPATHY, DILATED, AUTOSOMAL RECESSIVE;;CARDIOMYOPATHY, CONGESTIVE, AUTOSOMAL RECESSIVE		HP:0011462	OMIM:611880	TAS				C		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000007	OMIM:611881	TAS				I		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000286	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000470	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000508	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000823	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0000952	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001081	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001082	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001249	OMIM:611881	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001744	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001895	OMIM:611881	TAS				P		HPO:skoehler	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001897	OMIM:611881	TAS				P		HPO:skoehler	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0001930	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0002162	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0003198	OMIM:611881	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611881	#611881 GLYCOGEN STORAGE DISEASE XII; GSD12;;GSD XII;;ALDOLASE A DEFICIENCY;;ALDOA DEFICIENCY;;ALDOLASE DEFICIENCY, RED CELL;;RED CELL ALDOLASE DEFICIENCY		HP:0004322	OMIM:611881	TAS				P		HPO:probinson	
OMIM	611884	CILIARY DYSKINESIA, PRIMARY, 7; CILD7		HP:0000007	OMIM:611884	IEA				I		HPO:skoehler	
OMIM	611884	CILIARY DYSKINESIA, PRIMARY, 7; CILD7		HP:0001696	OMIM:611884	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611884	CILIARY DYSKINESIA, PRIMARY, 7; CILD7		HP:0002110	OMIM:611884	IEA				P		HPO:skoehler	
OMIM	611884	CILIARY DYSKINESIA, PRIMARY, 7; CILD7		HP:0002205	OMIM:611884	IEA				P		HPO:skoehler	
OMIM	611884	CILIARY DYSKINESIA, PRIMARY, 7; CILD7		HP:0012265	OMIM:611884	IEA				P		HPO:skoehler	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0000007	OMIM:611890	TAS				I		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0000369	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0000470	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0001989	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0002804	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD	HP:0012828	HP:0003202	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0003811	OMIM:611890	TAS				M		HPO:probinson	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0006802	OMIM:611890	IEA				P		HPO:skoehler	
OMIM	611890	#611890 LETHAL ARTHROGRYPOSIS WITH ANTERIOR HORN CELL DISEASE; LAAHD		HP:0007277	OMIM:611890	TAS				P		HPO:probinson	
OMIM	611895	#611895 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9		HP:0000006	PMID:17886298	PCS				I		HPO:probinson	
OMIM	611895	#611895 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9		HP:0001257	PMID:17886298	PCS				P		HPO:probinson	
OMIM	611895	#611895 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9		HP:0002460	PMID:17886298	PCS				P		HPO:probinson	
OMIM	611895	#611895 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9		HP:0003693	PMID:17886298	PCS				P		HPO:probinson	
OMIM	611895	#611895 AMYOTROPHIC LATERAL SCLEROSIS 9; ALS9		HP:0007354	OMIM:611895	IEA				P		HPO:skoehler	
OMIM	611907	EPISODIC ATAXIA, TYPE 7; EA7		HP:0000006	OMIM:611907	IEA				I		HPO:skoehler	
OMIM	611907	EPISODIC ATAXIA, TYPE 7; EA7		HP:0001260	OMIM:611907	IEA				P		HPO:skoehler	
OMIM	611907	EPISODIC ATAXIA, TYPE 7; EA7		HP:0001324	OMIM:611907	IEA				P		HPO:skoehler	
OMIM	611907	EPISODIC ATAXIA, TYPE 7; EA7		HP:0002131	OMIM:611907	IEA				P		HPO:skoehler	
OMIM	611907	EPISODIC ATAXIA, TYPE 7; EA7		HP:0002321	OMIM:611907	IEA				P		HPO:skoehler	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0000256	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0000316	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0000337	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0000347	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0000750	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0001250	PMID:19914906	PCS		HP:0040284		P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	5/16
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0001263	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0001270	PMID:19914906	PCS		HP:0040284		P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	8/16
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0001466	PMID:19914906	PCS				I	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HPO:probinson	
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0008872	PMID:19914906	PCS		HP:0040284		P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	8/16
OMIM	611913	CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB		HP:0011800	PMID:19914906	PCS				P	CHROMOSOME 16P11.2 DELETION SYNDROME, 593-KB	HP:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0000007	OMIM:611926	IEA				I		HPO:iea	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0000133	OMIM:611926	IEA				P		HPO:skoehler	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0000777	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0001684	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0002206	OMIM:611926	IEA				P		HPO:skoehler	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0002720	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0002721	OMIM:611926	IEA				P		HPO:skoehler	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0002850	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0004315	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0005407	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0005415	OMIM:611926	TAS				P		HPO:probinson	
OMIM	611926	IMMUNODEFICIENCY, OVARIAN DYSGENESIS, AND PULMONARY FIBROSIS		HP:0030813	OMIM:611926	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000006	OMIM:611929	IEA				I		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000054	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000272	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000278	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000316	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000377	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000465	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000470	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000473	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0000506	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0001245	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0001252	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0001256	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0001263	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0001290	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0002750	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0003298	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0003764	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0006109	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0009473	OMIM:611929	IEA				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0010487	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0012368	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0012385	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611929	CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III		HP:0430007	OMIM:611929	TAS				P		HPO:skoehler	
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000006	OMIM:611936	IEA				I	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000252	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	4/5
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000256	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/5
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000276	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000311	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	3/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000414	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	3/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000431	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000494	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0000581	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0001090	OMIM:611936	TAS				P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:skoehler	
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0001249	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	3/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0001263	OMIM:611936	TAS				P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:skoehler	
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0001513	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	3/5
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0001763	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	2/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0002162	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	1/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0003196	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	2/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0006114	PMID:18241066	PCS		HP:0040284		P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:iea	2/4
OMIM	611936	#611936 CHROMOSOME 3q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3q29 SYNDROME		HP:0012745	OMIM:611936	TAS				P	#611936 CHROMOSOME 3Q29 DUPLICATION SYNDROME;;MICRODUPLICATION 3Q29 SYNDROME	HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0000007	OMIM:611938	TAS				I		HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0001250	OMIM:611938	TAS				P		HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0001279	OMIM:611938	TAS				P		HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0001662	OMIM:611938	IEA				P		HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0001699	OMIM:611938	TAS				M		HPO:skoehler	
OMIM	611938	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2; CPVT2		HP:0004756	OMIM:611938	IEA				P		HPO:skoehler	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0000007	PMID:19203578	PCS				I		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0000252	OMIM:611943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0000958	OMIM:611943	TAS				P		HPO:skoehler	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0001251	OMIM:611943	TAS				P		HPO:skoehler	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0001999	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0002206	OMIM:611943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0002721	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0004315	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0004322	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0011133	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611943	#611943 RIDDLE SYNDROME;;RADIOSENSITIVITY, IMMUNODEFICIENCY, DYSMORPHIC FEATURES, AND LEARNINGDIFFICULTIES		HP:0011342	PMID:17940005	PCS				P		HPO:probinson	
OMIM	611944	LYMPHEDEMA, HEREDITARY, IB		HP:0000006	OMIM:611944	IEA				I		HPO:skoehler	
OMIM	611944	LYMPHEDEMA, HEREDITARY, IB		HP:0001004	OMIM:611944	IEA				P		HPO:skoehler	
OMIM	611944	LYMPHEDEMA, HEREDITARY, IB		HP:0003829	OMIM:611944	IEA				C		HPO:skoehler	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0000006	OMIM:611945	TAS				I		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0000012	OMIM:611945	TAS				P		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0000020	OMIM:611945	TAS				P		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0001258	OMIM:611945	IEA				P		HPO:skoehler	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0002061	OMIM:611945	TAS				P		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0002064	OMIM:611945	TAS				P		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0002166	OMIM:611945	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0002395	OMIM:611945	TAS				P		HPO:probinson	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0003487	OMIM:611945	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0003677	OMIM:611945	TAS				C		HPO:skoehler	
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0006986	OMIM:611945	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0007350	OMIM:611945	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611945	%611945 SPASTIC PARAPLEGIA 37, AUTOSOMAL DOMINANT; SPG37		HP:0011448	OMIM:611945	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	611953	#611953 MACULAR DEGENERATION, AGE-RELATED, 11; ARMD11		HP:0000608	OMIM:611953	TAS	HP:0003584			P		HP:probinson	
OMIM	611953	#611953 MACULAR DEGENERATION, AGE-RELATED, 11; ARMD11		HP:0010982	OMIM:611953	IEA				I		HPO:probinson	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000007	OMIM:611961	IEA				I		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000010	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000160	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000201	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000248	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000358	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000369	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000430	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000463	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000494	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000568	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0000589	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001249	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001250	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001263	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001321	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001385	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0001631	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002019	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002020	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002079	OMIM:611961	TAS				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002280	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002650	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0002714	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0005274	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0007110	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0009473	OMIM:611961	IEA				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0011670	OMIM:611961	TAS				P		HPO:skoehler	
OMIM	611961	611961 STEVENSON-CAREY SYNDROME		HP:0012385	OMIM:611961	TAS				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000006	OMIM:611962	IEA				I		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000023	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000047	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000219	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000219	OMIM:611962	TAS				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000239	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000248	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000270	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000272	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000322	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000341	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000348	OMIM:611962	TAS				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000405	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000407	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000472	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000508	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000545	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000581	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000582	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000768	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0000822	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001537	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001634	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001643	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001647	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001653	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001659	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0001840	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0002650	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0002656	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0002750	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0002858	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0002967	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0003088	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0004209	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0004322	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0004691	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0006824	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0009473	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0010584	OMIM:611962	IEA				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0011800	OMIM:611962	TAS				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME	HP:0003676	HP:0012385	OMIM:611962	TAS				P		HPO:skoehler	
OMIM	611962	HUNTER-MACDONALD SYNDROME		HP:0012745	OMIM:611962	TAS				P		HPO:skoehler	
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000006	OMIM:612001	TAS				I	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000316	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000377	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	6/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000486	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000664	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0000708	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	10/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001156	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001250	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	2/18
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001252	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	9/18
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001256	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	5/17
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001328	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	7/25
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0001999	PMID:19372089	PCS		HP:0040282		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	HP:0040282
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0002342	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	6/17
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0003829	PMID:19898479	PCS		HP:0040284		C	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	50%
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0004209	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	4/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0008050	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	7/19
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0010864	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/18
OMIM	612001	CHROMOSOME 15q13.3 MICRODELETION SYNDROME		HP:0030680	PMID:19372089	PCS		HP:0040284		P	CHROMOSOME 15Q13.3 MICRODELETION SYNDROME	HPO:iea	3/19
OMIM	612004	#612004 THROMBOCYTOPENIA 4; THC4;;THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 4		HP:0000006	OMIM:612004	TAS				I		HPO:probinson	
OMIM	612004	#612004 THROMBOCYTOPENIA 4; THC4;;THROMBOCYTOPENIA, AUTOSOMAL DOMINANT, 4		HP:0001873	OMIM:612004	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0000007	OMIM:612015	TAS				I		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0000252	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0000347	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0000407	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0000470	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001181	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001250	OMIM:612015	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001251	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001257	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001263	OMIM:612015	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001290	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001336	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001347	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0001508	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0002093	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0002240	OMIM:612015	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0003160	OMIM:612015	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0003186	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0003256	OMIM:612015	TAS				P		HPO:probinson	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0003593	OMIM:612015	TAS				C		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0004322	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0007663	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0008081	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0010864	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612015	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IN		HP:0011968	OMIM:612015	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0000007	OMIM:612016	TAS				I		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001249	OMIM:612016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001250	OMIM:612016	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001251	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001263	OMIM:612016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001272	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001290	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001336	OMIM:612016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001337	OMIM:612016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001347	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0001761	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0003128	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0003546	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0003701	OMIM:612016	TAS				P		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0003828	OMIM:612016	TAS				C		HPO:skoehler	
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0007256	OMIM:612016	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612016	COENZYME Q10 DEFICIENCY, PRIMARY, 4		HP:0012240	OMIM:612016	TAS				P		HPO:probinson	
OMIM	612018	#612018 CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA;;CJMG		HP:0000006	PMID:18304496	PCS				I		HPO:probinson	
OMIM	612018	#612018 CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA;;CJMG		HP:0000482	PMID:18304496	PCS				P		HPO:probinson	
OMIM	612018	#612018 CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA;;CJMG		HP:0000518	PMID:18304496	PCS	HP:0003621			P		HPO:probinson	
OMIM	612018	#612018 CATARACT, JUVENILE, WITH MICROCORNEA AND GLUCOSURIA;;CJMG		HP:0003076	PMID:18304496	PCS				P		HPO:probinson	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0000007	PMID:18313024	PCS				I		HPO:probinson	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0001251	OMIM:612020	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0001272	OMIM:612020	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0001288	OMIM:612020	TAS				P		HPO:skoehler	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0001347	OMIM:612020	TAS				P		HPO:skoehler	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0003487	OMIM:612020	TAS				P		HPO:skoehler	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0003693	PMID:18313024	PCS				P		HPO:probinson	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0006827	PMID:18313024	PCS				P		HPO:probinson	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0007020	PMID:18313024	PCS				P		HPO:probinson	
OMIM	612020	#612020 SPASTIC PARAPLEGIA 39, AUTOSOMAL RECESSIVE; SPG39;;NTE-RELATED MOTOR NEURON DISORDER; NTEMND		HP:0009053	PMID:18313024	PCS				P		HPO:probinson	
OMIM	612067	DYSTONIA 16; DYT16		HP:0000007	OMIM:612067	IEA				I		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0000750	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001260	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001270	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001288	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001300	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001347	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0001618	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002015	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002062	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002067	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002174	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002451	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0002544	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0003676	OMIM:612067	IEA				C		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0004305	OMIM:612067	TAS				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0007256	OMIM:612067	TAS				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0009763	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0012049	OMIM:612067	TAS				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0012514	OMIM:612067	TAS				P		HPO:skoehler	
OMIM	612067	DYSTONIA 16; DYT16		HP:0100543	OMIM:612067	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612067	DYSTONIA 16; DYT16		HP:0100660	OMIM:612067	IEA				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0000006	OMIM:612069	TAS				I		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0000712	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0000733	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0000734	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0000741	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0001257	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0001260	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0002015	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0002145	OMIM:612069	IEA				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0002747	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0003202	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0003487	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0003678	OMIM:612069	TAS				C		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0007354	OMIM:612069	IEA				P		HPO:skoehler	
OMIM	612069	AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS10		HP:0030223	OMIM:612069	TAS				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000007	OMIM:612073	IEA				I		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000407	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000486	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000508	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000602	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0000737	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001250	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001252	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001257	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)	HP:0012828	HP:0001263	OMIM:612073	TAS				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001265	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001290	OMIM:612073	TAS				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001332	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001349	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0001508	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002059	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002134	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002194	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002305	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002448	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002747	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0002912	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0003128	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0003236	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0003355	OMIM:612073	TAS				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0003593	OMIM:612073	IEA				C		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0006887	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0008872	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0008945	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0008972	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0009830	OMIM:612073	IEA				P		HPO:skoehler	
OMIM	612073	MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)		HP:0012120	OMIM:612073	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0000007	OMIM:612075	TAS				I		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0000114	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0000544	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0001249	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0001250	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0001290	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0001508	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0002066	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0002344	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0003128	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0003355	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0003676	OMIM:612075	TAS				C		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0004326	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612075	MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)		HP:0011968	OMIM:612075	TAS				P		HPO:skoehler	
OMIM	612076	HYPOURICEMIA, RENAL, 2; RHUC2		HP:0000006	PMID:19026395	PCS				I		HPO:probinson	
OMIM	612076	HYPOURICEMIA, RENAL, 2; RHUC2		HP:0000007	OMIM:612076	TAS				I		HPO:skoehler	
OMIM	612076	HYPOURICEMIA, RENAL, 2; RHUC2		HP:0000787	OMIM:612076	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612076	HYPOURICEMIA, RENAL, 2; RHUC2		HP:0003537	PMID:19026395	PCS				P		HPO:probinson	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000007	OMIM:612079	IEA				I		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000135	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000252	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000668	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000670	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000771	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000823	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000846	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000953	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0000995	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0001193	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0001249	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0001371	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0001596	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0002333	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0002493	OMIM:612079	TAS				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0002751	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0003202	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0003758	OMIM:612079	IEA				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0009487	OMIM:612079	TAS				P		HPO:skoehler	
OMIM	612079	ALOPECIA, NEUROLOGIC DEFECTS, AND ENDOCRINOPATHY SYNDROME; ANES		HP:0011734	OMIM:612079	TAS				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0000006	OMIM:612089	IEA				I		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0000117	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0000256	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0000843	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0000897	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0002007	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0002653	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0003072	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0003165	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0004322	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0004912	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0007099	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612089	HYPOPHOSPHATEMIC RICKETS AND HYPERPARATHYROIDISM		HP:0008208	OMIM:612089	IEA				P		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0000007	OMIM:612095	IEA				I		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0000510	OMIM:612095	TAS				P		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0000550	OMIM:612095	IEA				P		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0000608	OMIM:612095	IEA				P		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0000662	OMIM:612095	IEA				P		HPO:skoehler	
OMIM	612095	RETINITIS PIGMENTOSA 41		HP:0007994	OMIM:612095	TAS				P		HPO:skoehler	
OMIM	612096	OTOSCLEROSIS 8; OTSC8		HP:0000006	OMIM:612096	IEA				I		HPO:skoehler	
OMIM	612096	OTOSCLEROSIS 8; OTSC8		HP:0000362	OMIM:612096	IEA				P		HPO:skoehler	
OMIM	612096	OTOSCLEROSIS 8; OTSC8		HP:0000365	OMIM:612096	IEA				P		HPO:skoehler	
OMIM	612097	DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS		HP:0000006	OMIM:612097	IEA				I		HPO:skoehler	
OMIM	612097	DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS		HP:0000969	OMIM:612097	IEA				P		HPO:skoehler	
OMIM	612097	DEAFNESS, UNILATERAL, WITH DELAYED ENDOLYMPHATIC HYDROPS		HP:0009900	OMIM:612097	IEA				P		HPO:skoehler	
OMIM	612098	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11		HP:0000006	OMIM:612098	IEA				I		HPO:skoehler	
OMIM	612098	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11		HP:0001639	OMIM:612098	IEA				P		HPO:skoehler	
OMIM	612098	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11		HP:0011675	OMIM:612098	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000007	OMIM:612109	TAS				I		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000482	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000510	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000518	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000568	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000589	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000639	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0000647	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0001104	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0007700	OMIM:612109	IEA				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0007906	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612109	#612109 OCULOAURICULAR SYNDROME; OCACS;;MICROPHTHALMIA, MICROCORNEA, ANTERIOR SEGMENT DYSGENESIS, CATARACT,OCULAR COLOBOMA, RETINAL PIGMENT EPITHELIUM ABNORMALITIES, ROD-CONEDYSTROPHY, AND ANOMALIES OF THE EXTERNAL EAR;;SCHORDERET-MUNIER-FRANCESCHETTI SYNDROME		HP:0012376	OMIM:612109	TAS				P		HPO:skoehler	
OMIM	612119	TREHALASE DEFICIENCY		HP:0000007	OMIM:612119	TAS				I		HPO:probinson	
OMIM	612119	TREHALASE DEFICIENCY		HP:0002014	OMIM:612119	TAS				P		HPO:probinson	
OMIM	612119	TREHALASE DEFICIENCY		HP:0002027	OMIM:612119	IEA				P		HPO:skoehler	
OMIM	612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12		HP:0000006	OMIM:612124	TAS				I		HPO:probinson	
OMIM	612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12		HP:0001638	OMIM:612124	TAS				P		HPO:probinson	
OMIM	612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12		HP:0001645	OMIM:612124	TAS				P		HPO:probinson	
OMIM	612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12		HP:0004756	OMIM:612124	TAS				P		HPO:probinson	
OMIM	612124	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12		HP:0004757	OMIM:612124	TAS				P		HPO:probinson	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0000006	OMIM:612126	TAS				I		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0000737	OMIM:612126	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001251	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001263	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001266	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001332	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001337	OMIM:612126	IEA				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0001923	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0002059	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0002076	OMIM:612126	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0002353	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0003829	OMIM:612126	TAS				C		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0011972	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0100543	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612126	GLUT1 DEFICIENCY SYNDROME 2; GLUT1DS2		HP:0100660	OMIM:612126	TAS				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:612132	IEA				I		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0000668	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0000698	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0000966	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0000970	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0002007	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0002046	OMIM:612132	TAS				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0002205	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0003593	OMIM:612132	IEA				C		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0004798	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0007476	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0008070	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0011114	OMIM:612132	IEA				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0011120	OMIM:612132	TAS				P		HPO:skoehler	
OMIM	612132	ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMAL DOMINANT		HP:0011136	OMIM:612132	TAS				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0000007	OMIM:612138	IEA				I		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0000430	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0000490	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0001030	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0001371	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0001561	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0003577	OMIM:612138	IEA				C		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0008066	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612138	EPIDERMOLYSIS BULLOSA SIMPLEX WITH PYLORIC ATRESIA		HP:0008551	OMIM:612138	IEA				P		HPO:skoehler	
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0000006	PMID:14567970	PCS				I		HPO:probinson	
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0001644	PMID:14567970	PCS				P		HPO:probinson	
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0001678	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0001695	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0001706	PMID:14567970	PCS				P		HPO:probinson	
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0001712	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0004755	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0005110	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0006685	OMIM:612158	TAS				P		HPO:skoehler	
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0030682	OMIM:612158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612158	CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1AA		HP:0031319	OMIM:612158	IEA				P		HPO:skoehler	
OMIM	612160	#612160 HISTIOCYTOMA, ANGIOMATOID FIBROUS		HP:0001428	OMIM:612160	TAS				I		HPO:probinson	
OMIM	612160	#612160 HISTIOCYTOMA, ANGIOMATOID FIBROUS		HP:0012315	OMIM:612160	TAS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0000006	OMIM:612164	PCS				I		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0001151	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0001258	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0001290	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0001337	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0001344	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002059	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002069	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002079	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002123	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002133	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002376	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002510	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0002521	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0003623	OMIM:612164	PCS				C		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0003828	OMIM:612164	TAS				C		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0006808	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0007105	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0010818	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0010851	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0010864	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0011097	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0011344	OMIM:612164	PCS				P		HPO:probinson	
OMIM	612164	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4		HP:0200134	OMIM:612164	TAS				P		HPO:skoehler	
OMIM	612165	RETINITIS PIGMENTOSA 29; RP29		HP:0000007	OMIM:612165	TAS				I		HPO:skoehler	
OMIM	612165	RETINITIS PIGMENTOSA 29; RP29		HP:0000510	OMIM:612165	TAS				P		HPO:skoehler	
OMIM	612165	RETINITIS PIGMENTOSA 29; RP29		HP:0000618	OMIM:612165	IEA				P		HPO:skoehler	
OMIM	612165	RETINITIS PIGMENTOSA 29; RP29		HP:0007843	OMIM:612165	TAS				P		HPO:skoehler	
OMIM	612198	DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA		HP:0000006	OMIM:612198	TAS				I		HPO:probinson	
OMIM	612198	DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA		HP:0001540	OMIM:612198	TAS				P		HPO:probinson	
OMIM	612198	DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA		HP:0002019	OMIM:612198	TAS				P		HPO:probinson	
OMIM	612198	DIASTASIS RECTI AND WEAKNESS OF THE LINEA ALBA		HP:0009023	OMIM:612198	TAS				P		HPO:probinson	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000007	OMIM:612199	IEA				I		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000618	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000648	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000938	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000939	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0000963	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001250	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001251	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001257	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001260	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001268	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001332	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001337	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001511	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001873	OMIM:612199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0001903	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002062	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002071	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002164	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002301	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002352	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002415	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002514	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002584	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002650	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002659	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002745	OMIM:612199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002756	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0002857	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0003593	OMIM:612199	IEA				C		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0003676	OMIM:612199	IEA				C		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0004322	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0004979	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0005528	OMIM:612199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0007256	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0007763	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0007898	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0008070	OMIM:612199	IEA				P		HPO:iea	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0008897	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612199	#612199 CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS; CRMCC;;COATS PLUS SYNDROME		HP:0100864	OMIM:612199	TAS				P		HPO:skoehler	
OMIM	612201	ATRIAL FIBRILLATION, FAMILIAL, 6		HP:0000006	OMIM:612201	TAS				I		HPO:probinson	
OMIM	612201	ATRIAL FIBRILLATION, FAMILIAL, 6		HP:0005110	OMIM:612201	TAS				P		HPO:probinson	
OMIM	612219	#612219 EWING SARCOMA; ESNEUROEPITHELIOMA, PERIPHERAL, INCLUDED; PNE, INCLUDED;;ASKIN TUMOR, INCLUDED		HP:0001428	OMIM:612219	TAS				I		HPO:probinson	
OMIM	612219	#612219 EWING SARCOMA; ESNEUROEPITHELIOMA, PERIPHERAL, INCLUDED; PNE, INCLUDED;;ASKIN TUMOR, INCLUDED		HP:0012254	OMIM:612219	TAS				P		HPO:probinson	
OMIM	612225	#612225 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9; MODY9		HP:0000006	PMID:17426099	PCS				I		HPO:probinson	
OMIM	612225	#612225 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9; MODY9		HP:0004904	PMID:17426099	PCS				P		HPO:probinson	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0000006	OMIM:612227	TAS				I		HPO:skoehler	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0000007	OMIM:612227	IEA				I		HPO:skoehler	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0000819	OMIM:612227	IEA				P		HPO:skoehler	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0000855	OMIM:612227	TAS				P		HPO:probinson	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0001426	OMIM:612227	TAS				I		HPO:probinson	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0001993	OMIM:612227	TAS				P		HPO:probinson	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0002960	OMIM:612227	TAS				P		HPO:probinson	
OMIM	612227	DIABETES MELLITUS, KETOSIS-PRONE; KPD		HP:0006279	OMIM:612227	TAS				P		HPO:probinson	
OMIM	612229	COLORECTAL CANCER, SUSCEPTIBILITY TO, 3		HP:0001425	OMIM:612229	PCS				I		HPO:curators	
OMIM	612229	COLORECTAL CANCER, SUSCEPTIBILITY TO, 3		HP:0003003	PMID:18372901;PMID:17934461;PMID:18372905	PCS				P		HPO:curators	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0000007	OMIM:612233	IEA				I		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0000486	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0000639	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001250	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001252	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001263	OMIM:612233	TAS				P		HPO:skoehler	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001266	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001290	OMIM:612233	TAS				P		HPO:skoehler	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001347	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0001371	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0002104	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0002187	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0002191	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0002415	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0003487	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0003623	OMIM:612233	TAS				C		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0005484	OMIM:612233	IEA				P		HPO:iea	
OMIM	612233	LEUKODYSTROPHY, HYPOMYELINATING, 4		HP:0008872	OMIM:612233	IEA				P		HPO:iea	
OMIM	612237	#612237 CHONDROSARCOMA, EXTRASKELETAL MYXOID;;EMC		HP:0001428	OMIM:612237	TAS				I		HPO:probinson	
OMIM	612237	#612237 CHONDROSARCOMA, EXTRASKELETAL MYXOID;;EMC		HP:0006765	OMIM:612237	TAS				P		HPO:probinson	
OMIM	612240	#612240 ATRIAL FIBRILLATION, FAMILIAL, 7; ATFB7		HP:0000006	PMID:16772329	PCS				I		HPO:probinson	
OMIM	612240	#612240 ATRIAL FIBRILLATION, FAMILIAL, 7; ATFB7		HP:0001962	PMID:16772329	PCS				P		HPO:probinson	
OMIM	612240	#612240 ATRIAL FIBRILLATION, FAMILIAL, 7; ATFB7		HP:0004757	PMID:16772329	PCS				P		HPO:probinson	
OMIM	612240	#612240 ATRIAL FIBRILLATION, FAMILIAL, 7; ATFB7		HP:0005184	OMIM:612240	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612240	#612240 ATRIAL FIBRILLATION, FAMILIAL, 7; ATFB7		HP:0012248	OMIM:612240	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000219	PMID:21248748	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000256	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000316	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000319	PMID:21248748	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000337	PMID:21248748	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000490	PMID:21248748	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000582	PMID:21248748	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0000717	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0001166	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0001263	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0001466	OMIM:612242	TAS				I	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0002474	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0010863	PMID:20345475	PCS				P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612242	CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME		HP:0100783	PMID:21248748	PCS	HP:0003577			P	CHROMOSOME 10Q22.3-Q23.2 DELETION SYNDROME	HPO:probinson	
OMIM	612244	#612244 INFLAMMATORY BOWEL DISEASE 13; IBD13		HP:0002037	OMIM:612244	IEA				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000006	OMIM:612247	TAS				I		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000238	OMIM:612247	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000248	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000316	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000453	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000520	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000956	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0000995	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0001363	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612247	CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS		HP:0011800	OMIM:612247	TAS				P		HPO:skoehler	
OMIM	612269	#612269 EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5; ECA5		HP:0000006	OMIM:612269	IEA				I		HPO:skoehler	
OMIM	612269	#612269 EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 5; ECA5		HP:0002121	OMIM:612269	IEA	HP:0011463			P		HPO:skoehler	
OMIM	612271	#612271 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11; SHEP11;;MELANESIAN BLOND HAIR;;SKIN/HAIR/EYE PIGMENTATION 11, BLUE/NONBLUE EYES		HP:0000635	OMIM:612271	TAS				P		HPO:skoehler	
OMIM	612271	#612271 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11; SHEP11;;MELANESIAN BLOND HAIR;;SKIN/HAIR/EYE PIGMENTATION 11, BLUE/NONBLUE EYES		HP:0001000	OMIM:612271	IEA				P		HPO:skoehler	
OMIM	612271	#612271 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11; SHEP11;;MELANESIAN BLOND HAIR;;SKIN/HAIR/EYE PIGMENTATION 11, BLUE/NONBLUE EYES		HP:0008034	OMIM:612271	IEA				P		HPO:skoehler	
OMIM	612271	#612271 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11; SHEP11;;MELANESIAN BLOND HAIR;;SKIN/HAIR/EYE PIGMENTATION 11, BLUE/NONBLUE EYES		HP:0009887	OMIM:612271	IEA				P		HPO:skoehler	
OMIM	612278	#612278 INFLAMMATORY BOWEL DISEASE 19; IBD19		HP:0002037	OMIM:612278	IEA				P		HPO:skoehler	
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0000007	OMIM:612281	TAS				I		HPO:skoehler	
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0000656	OMIM:612281	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0000966	OMIM:612281	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0000982	OMIM:612281	TAS				P		HPO:skoehler	
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0001019	OMIM:612281	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0001036	OMIM:612281	TAS				P		HPO:skoehler	
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6		HP:0007479	OMIM:612281	IEA				P		HPO:skoehler	
OMIM	612281	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6	HP:0012826	HP:0025092	OMIM:612281	TAS				P		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000007	OMIM:612284	TAS				I		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000107	OMIM:612284	IEA	HP:0003577	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000175	OMIM:612284	IEA	HP:0003577	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000204	OMIM:612284	IEA	HP:0003577	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000238	OMIM:612284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0000812	OMIM:612284	IEA	HP:0003577	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0001161	OMIM:612284	IEA	HP:0003577	HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0001162	OMIM:612284	TAS				P		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0001395	OMIM:612284	TAS				P		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0001408	OMIM:612284	TAS				P		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0001762	OMIM:612284	IEA	HP:0003577	HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0002085	OMIM:612284	IEA	HP:0003577	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0002089	OMIM:612284	TAS				P		HPO:skoehler	
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0002323	OMIM:612284	IEA	HP:0003577	HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612284	MECKEL SYNDROME, TYPE 6; MKS6		HP:0006706	OMIM:612284	IEA	HP:0003577	HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0000007	OMIM:612285	IEA				I		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0000483	OMIM:612285	IEA				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0000510	OMIM:612285	IEA				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0000518	OMIM:612285	IEA				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0000639	OMIM:612285	IEA				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0001249	OMIM:612285	IEA				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0001250	OMIM:612285	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0002119	OMIM:612285	TAS				P		HPO:skoehler	
OMIM	612285	#612285 JOUBERT SYNDROME 9; JBTS9JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED		HP:0002419	OMIM:612285	TAS				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0000006	OMIM:612286	IEA				I		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0000117	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0000787	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0000938	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0000939	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0002148	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0002150	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0002659	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612286	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1		HP:0003109	OMIM:612286	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0000006	OMIM:612287	IEA				I		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0000117	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0000787	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0000938	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0000939	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0002148	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0002659	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612287	NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2		HP:0003109	OMIM:612287	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000006	PMID:29100093	PCS				I		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000046	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000054	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000160	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000219	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000232	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000238	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000248	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000252	PMID:29100093	PCS		HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000260	PMID:29100093	PCS		HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000262	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000278	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000294	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000303	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000316	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000319	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000325	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000337	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000343	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000347	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000358	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000369	PMID:29100093	PCS	HP:0003577	HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000377	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000405	PMID:29100093	PCS		HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000444	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000494	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000520	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000540	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000568	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000664	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000677	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000691	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000926	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0000998	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001159	PMID:29100093	PCS	HP:0003577	HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001290	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001320	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001321	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001324	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001508	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001511	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001537	PMID:29100093	PCS	HP:0003577			P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001545	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001582	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001627	PMID:29100093	PCS	HP:0003577	HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001631	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001643	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001647	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001712	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001792	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0001798	OMIM:612289	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002020	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002079	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002089	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002092	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002093	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002100	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002107	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002162	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002208	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002209	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002282	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002557	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002561	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002650	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002705	PMID:29100093	PCS		HP:0040284		P		HP:probinson	1/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0002750	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0003196	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0003577	PMID:29100093	PCS				C		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0003758	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0004322	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0004440	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0004942	PMID:29100093	PCS		HP:0040284		P		HP:probinson	2/3
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0005180	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0005247	PMID:29100093	PCS	HP:0003577			P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0005280	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0005807	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0006191	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0008038	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0009882	PMID:29100093	PCS		HP:0040284		P		HP:probinson	3/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0009891	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0010648	PMID:29100093	PCS		HP:0040284		P		HP:probinson	4/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0010808	PMID:29100093	PCS				P		HP:probinson	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0011800	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0011968	OMIM:612289	IEA				P		HPO:skoehler	
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0012745	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612289	FONTAINE PROGEROID SYNDROME; FPS		HP:0100678	PMID:29100093	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	612290	#612290 MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATEMICROTIA WITH OR WITHOUT HEARING IMPAIRMENT, INCLUDED		HP:0000006	OMIM:612290	TAS				I		HPO:skoehler	
OMIM	612290	#612290 MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATEMICROTIA WITH OR WITHOUT HEARING IMPAIRMENT, INCLUDED		HP:0000007	OMIM:612290	TAS				I		HPO:probinson	
OMIM	612290	#612290 MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATEMICROTIA WITH OR WITHOUT HEARING IMPAIRMENT, INCLUDED		HP:0000175	OMIM:612290	TAS				P		HPO:probinson	
OMIM	612290	#612290 MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATEMICROTIA WITH OR WITHOUT HEARING IMPAIRMENT, INCLUDED		HP:0000410	OMIM:612290	TAS				P		HPO:probinson	
OMIM	612290	#612290 MICROTIA, HEARING IMPAIRMENT, AND CLEFT PALATEMICROTIA WITH OR WITHOUT HEARING IMPAIRMENT, INCLUDED		HP:0008551	OMIM:612290	TAS				P		HPO:probinson	
OMIM	612291	JOUBERT SYNDROME 8		HP:0000007	PMID:18674751	PCS				I		HPO:probinson	
OMIM	612291	JOUBERT SYNDROME 8		HP:0000543	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0000580	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0000657	PMID:18674751	PCS				P		HPO:probinson	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001249	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001251	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001252	PMID:18674751	PCS				P		HPO:probinson	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001263	PMID:18674751	PCS				P		HPO:probinson	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001290	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0001513	OMIM:612291	TAS				P		HPO:skoehler	
OMIM	612291	JOUBERT SYNDROME 8		HP:0002085	OMIM:612291	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612291	JOUBERT SYNDROME 8		HP:0002419	PMID:18674751	PCS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000006	OMIM:612292	TAS				I		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000218	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000322	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000341	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000574	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0000960	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0001249	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0001252	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0001999	OMIM:612292	IEA				P		HPO:skoehler	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0002015	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0002553	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0008872	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0011229	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612292	#612292 BIRK-BAREL MENTAL RETARDATION DYSMORPHISM SYNDROME;;BIRK-BAREL SYNDROME;;MENTAL RETARDATION WITH HYPOTONIA AND FACIAL DYSMORPHISM		HP:0011819	OMIM:612292	TAS				P		HPO:probinson	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0000007	PMID:1382994	PCS				I		HPO:probinson	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0001271	OMIM:612300	IEA				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0001284	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0001290	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0001878	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0002922	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59	HP:0003676	HP:0003202	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0003470	OMIM:612300	IEA				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0003593	OMIM:612300	TAS				C		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0003690	OMIM:612300	TAS				P		HPO:skoehler	
OMIM	612300	HEMOLYTIC ANEMIA, CD59-MEDIATED, WITH OR WITHOUT IMMUNE-MEDIATED POLYNEUROPATHY; HACD59		HP:0004818	PMID:1699124	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000007	PMID:18606301	PCS				I		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000238	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000520	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000529	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000639	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0000648	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0001263	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0001270	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0001290	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0001873	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0001903	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0002199	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0004313	PMID:18606301	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0006532	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0006640	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0006956	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0007807	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0011002	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0025356	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0040194	OMIM:612301	IEA				P		HPO:skoehler	
OMIM	612301	OSTEOPETROSIS, AUTOSOMAL RECESSIVE 7; OPTB7		HP:0100671	PMID:18606301	PCS				P		HPO:probinson	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0000007	OMIM:612304	IEA				I		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0000979	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0001250	OMIM:612304	TAS				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0001263	OMIM:612304	TAS				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0002204	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0002625	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0002638	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0003828	OMIM:612304	TAS				C		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0005543	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0007902	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0100021	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612304	THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE; THPH4		HP:0100724	OMIM:612304	IEA				P		HPO:skoehler	
OMIM	612310	PREMATURE OVARIAN FAILURE 6		HP:0000013	OMIM:612310	TAS				P		HPO:skoehler	
OMIM	612310	PREMATURE OVARIAN FAILURE 6		HP:0001470	PMID:18499083	PCS				I		HPO:probinson	
OMIM	612310	PREMATURE OVARIAN FAILURE 6		HP:0008209	PMID:18499083	PCS				P		HPO:probinson	
OMIM	612313	GLASS SYNDROME		HP:0000006	OMIM:612313	TAS				I		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000023	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000160	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000175	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000218	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000252	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000272	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000276	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000319	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000347	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000348	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000369	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000414	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000426	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000460	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000494	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000677	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000678	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000698	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000718	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000750	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000752	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0000963	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0001166	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0001249	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0001250	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0001263	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0001762	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0002007	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0002136	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0002164	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0003189	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0004322	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0008070	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0011800	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0012385	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612313	GLASS SYNDROME		HP:0040082	OMIM:612313	TAS				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:612319	TAS				I		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000012	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000020	OMIM:612319	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000486	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000544	OMIM:612319	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:612319	TAS				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:612319	IEA				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001268	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001272	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001285	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001310	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0001332	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002061	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002079	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002180	OMIM:612319	IEA				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002313	OMIM:612319	IEA				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002355	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0002518	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:612319	TAS				C		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0006978	OMIM:612319	TAS				P		HPO:probinson	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0007366	OMIM:612319	TAS				P		HPO:skoehler	
OMIM	612319	SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE		HP:0011448	OMIM:612319	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0000006	OMIM:612335	IEA				I		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0001258	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0001347	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0001761	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0002064	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0002166	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0003392	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0003393	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0003426	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0003427	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0003487	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612335	SPASTIC PARAPLEGIA 38, AUTOSOMAL DOMINANT; SPG38		HP:0007340	OMIM:612335	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0000006	OMIM:612336	IEA				I		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0000979	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0001038	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0002204	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0002638	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0004420	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0004855	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0005305	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612336	THROMBOPHILIA, HEREDITARY, DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL		HP:0100724	OMIM:612336	IEA				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000006	OMIM:612337	TAS				I		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000219	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000252	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000286	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000311	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000316	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000319	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000347	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000369	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0000377	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001249	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001250	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001263	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001274	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001290	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0001344	OMIM:612337	IEA				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0003828	OMIM:612337	TAS				C		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0004322	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0005280	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612337	MENTAL RETARDATION, AUTOSOMAL DOMINANT 22; MRD22		HP:0011220	OMIM:612337	TAS				P		HPO:skoehler	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0000007	OMIM:612347	TAS				I		HPO:probinson	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0001279	OMIM:612347	TAS				P		HPO:probinson	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0001425	OMIM:612347	TAS				I		HPO:skoehler	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0001645	OMIM:612347	TAS				P		HPO:skoehler	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0001657	OMIM:612347	TAS				P		HPO:probinson	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0001664	OMIM:612347	TAS				P		HPO:skoehler	
OMIM	612347	JERVELL AND LANGE-NIELSEN SYNDROME 2		HP:0008527	OMIM:612347	TAS				P		HPO:skoehler	
OMIM	612348	%612348 THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR; THPH9HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR, INCLUDED		HP:0000006	OMIM:612348	TAS				I		HPO:probinson	
OMIM	612348	%612348 THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR; THPH9HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR, INCLUDED		HP:0004850	OMIM:612348	TAS				P		HPO:probinson	
OMIM	612348	%612348 THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR; THPH9HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGENACTIVATOR, INCLUDED		HP:0100724	OMIM:612348	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000007	OMIM:612350	IEA				I		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000193	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000218	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000494	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000592	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000668	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000684	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000689	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000926	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000938	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000963	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000974	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0000978	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0001015	OMIM:612350	TAS				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0001073	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0001182	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0001388	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0001763	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0002515	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0003016	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0003301	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0003370	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0003393	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0004322	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0006429	OMIM:612350	TAS				P		HPO:probinson	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0008848	OMIM:612350	TAS				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0009473	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0009803	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0010049	OMIM:612350	IEA				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0100490	OMIM:612350	TAS				P		HPO:skoehler	
OMIM	612350	SPONDYLOCHEIRODYSPLASIA, EHLERS-DANLOS SYNDROME-LIKE		HP:0100864	OMIM:612350	TAS				P		HPO:probinson	
OMIM	612353	%612353 POROKERATOSIS 6, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK6;;POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 4; DSAP4		HP:0000006	OMIM:612353	TAS				I		HPO:skoehler	
OMIM	612353	%612353 POROKERATOSIS 6, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK6;;POROKERATOSIS, DISSEMINATED SUPERFICIAL ACTINIC, 4; DSAP4		HP:0200044	OMIM:612353	TAS				P		HPO:skoehler	
OMIM	612354	INFLAMMATORY BOWEL DISEASE 21		HP:0000006	OMIM:612354	TAS				I		HPO:skoehler	
OMIM	612354	INFLAMMATORY BOWEL DISEASE 21		HP:0100279	OMIM:612354	TAS				P		HPO:skoehler	
OMIM	612356	HEPARIN COFACTOR II DEFICIENCY		HP:0000006	OMIM:612356	TAS				I		HPO:skoehler	
OMIM	612356	HEPARIN COFACTOR II DEFICIENCY		HP:0004761	OMIM:612356	TAS				P		HPO:skoehler	
OMIM	612356	HEPARIN COFACTOR II DEFICIENCY		HP:0004850	OMIM:612356	TAS				P		HPO:skoehler	
OMIM	612356	HEPARIN COFACTOR II DEFICIENCY		HP:0005521	OMIM:612356	TAS				P		HPO:skoehler	
OMIM	612359	#612359 COWDEN-LIKE SYNDROME		HP:0000006	PMID:18678321	PCS				I		HPO:probinson	
OMIM	612359	#612359 COWDEN-LIKE SYNDROME		HP:0000131	PMID:18678321	PCS				P		HPO:probinson	
OMIM	612359	#612359 COWDEN-LIKE SYNDROME		HP:0002895	PMID:18678321	PCS				P		HPO:probinson	
OMIM	612359	#612359 COWDEN-LIKE SYNDROME		HP:0003002	PMID:18678321	PCS				P		HPO:probinson	
OMIM	612359	#612359 COWDEN-LIKE SYNDROME		HP:0012114	PMID:18678321	PCS				P		HPO:probinson	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000006	PMID:18834967	PCS				I		HPO:probinson	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000028	OMIM:612370	TAS				P		HPO:skoehler	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000044	PMID:18834967	PCS				P		HPO:probinson	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000175	OMIM:612370	TAS				P		HPO:skoehler	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000407	OMIM:612370	TAS				P		HPO:skoehler	
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0000458	PMID:18834967	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	612370	HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA		HP:0410030	OMIM:612370	TAS				P		HPO:skoehler	
OMIM	612376	#612376 ACUTE PROMYELOCYTIC LEUKEMIA; APL;;LEUKEMIA, ACUTE PROMYELOCYTIC		HP:0001428	PMID:1652368	PCS				I		HPO:probinson	
OMIM	612376	#612376 ACUTE PROMYELOCYTIC LEUKEMIA; APL;;LEUKEMIA, ACUTE PROMYELOCYTIC		HP:0004836	OMIM:612376	TAS				P		HPO:skoehler	
OMIM	612376	#612376 ACUTE PROMYELOCYTIC LEUKEMIA; APL;;LEUKEMIA, ACUTE PROMYELOCYTIC		HP:0012135	OMIM:612376	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000007	OMIM:612379	IEA				I		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000248	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000316	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000369	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000572	OMIM:612379	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000589	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000639	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000962	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000964	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000973	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0000998	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001000	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001249	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001270	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001290	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001320	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001935	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0001976	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0002126	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0002910	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0003593	OMIM:612379	TAS				C		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0003642	OMIM:612379	TAS				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0005280	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612379	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IQ		HP:0008064	OMIM:612379	IEA				P		HPO:skoehler	
OMIM	612387	SARCOIDOSIS, SUSCEPTIBILITY TO, 2; SS2		HP:0006530	OMIM:612387	IEA				P		HPO:skoehler	
OMIM	612387	SARCOIDOSIS, SUSCEPTIBILITY TO, 2; SS2		HP:0010628	OMIM:612387	IEA				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0000007	OMIM:612389	TAS				I		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0000253	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0000340	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0000505	OMIM:612389	IEA				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0001250	OMIM:612389	TAS				P		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0001272	OMIM:612389	IEA				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0001290	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0001321	OMIM:612389	TAS				P		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0001332	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002059	OMIM:612389	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002072	OMIM:612389	TAS				P		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002079	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002119	OMIM:612389	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002169	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002179	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002365	OMIM:612389	TAS				P		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0002509	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0003487	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0003577	OMIM:612389	TAS				C		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0007308	OMIM:612389	TAS				P		HPO:probinson	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0008936	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0009879	OMIM:612389	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612389	PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B		HP:0011968	OMIM:612389	TAS				P		HPO:skoehler	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0000007	PMID:18711368	PCS				I		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0000252	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0000505	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0001320	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0001332	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0002072	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612390	#612390 PONTOCEREBELLAR HYPOPLASIA, TYPE 2C; PCH2C		HP:0100307	PMID:18711368	PCS				P		HPO:probinson	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000007	OMIM:612394	IEA				I		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000272	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000343	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000365	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000369	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000377	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000463	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000518	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000545	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000586	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000926	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000938	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0000978	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0001263	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0001511	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0001762	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002164	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002208	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002650	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002680	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002714	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002756	OMIM:612394	TAS				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0002987	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0003090	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0003196	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0003393	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0004944	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0006184	OMIM:612394	TAS				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0008897	OMIM:612394	TAS				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0009110	OMIM:612394	IEA				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0012368	OMIM:612394	TAS				P		HPO:skoehler	
OMIM	612394	BONE FRAGILITY WITH CONTRACTURES, ARTERIAL RUPTURE, AND DEAFNESS		HP:0025019	OMIM:612394	TAS				P		HPO:skoehler	
OMIM	612406	DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE; DYT17		HP:0000007	OMIM:612406	IEA				I		HPO:skoehler	
OMIM	612406	DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE; DYT17		HP:0000473	OMIM:612406	IEA				P		HPO:skoehler	
OMIM	612406	DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE; DYT17		HP:0001260	OMIM:612406	IEA				P		HPO:skoehler	
OMIM	612406	DYSTONIA 17, TORSION, AUTOSOMAL RECESSIVE; DYT17		HP:0001618	OMIM:612406	IEA				P		HPO:skoehler	
OMIM	612416	#612416 FACTOR XI DEFICIENCY;;F11 DEFICIENCY;;PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY;;PTA DEFICIENCY;;ROSENTHAL SYNDROME		HP:0000006	OMIM:612416	TAS				I		HPO:probinson	
OMIM	612416	#612416 FACTOR XI DEFICIENCY;;F11 DEFICIENCY;;PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY;;PTA DEFICIENCY;;ROSENTHAL SYNDROME		HP:0000007	OMIM:612416	TAS				I		HPO:probinson	
OMIM	612416	#612416 FACTOR XI DEFICIENCY;;F11 DEFICIENCY;;PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY;;PTA DEFICIENCY;;ROSENTHAL SYNDROME		HP:0001892	OMIM:612416	TAS				P		HPO:probinson	
OMIM	612416	#612416 FACTOR XI DEFICIENCY;;F11 DEFICIENCY;;PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY;;PTA DEFICIENCY;;ROSENTHAL SYNDROME		HP:0001929	OMIM:612416	TAS				P		HPO:probinson	
OMIM	612416	#612416 FACTOR XI DEFICIENCY;;F11 DEFICIENCY;;PLASMA THROMBOPLASTIN ANTECEDENT DEFICIENCY;;PTA DEFICIENCY;;ROSENTHAL SYNDROME		HP:0003645	OMIM:612416	TAS				P		HPO:probinson	
OMIM	612422	#612422 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3		HP:0000006	OMIM:612422	TAS				I		HPO:skoehler	
OMIM	612422	#612422 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3		HP:0001638	OMIM:612422	IEA				P		HPO:skoehler	
OMIM	612423	#612423 PREKALLIKREIN DEFICIENCY;;PKK DEFICIENCY;;FLETCHER FACTOR DEFICIENCY		HP:0000007	PMID:15461630	PCS				I		HPO:probinson	
OMIM	612423	#612423 PREKALLIKREIN DEFICIENCY;;PKK DEFICIENCY;;FLETCHER FACTOR DEFICIENCY		HP:0003645	PMID:15461630	PCS				P		HPO:probinson	
OMIM	612431	DEAFNESS, AUTOSOMAL DOMINANT 27		HP:0000006	PMID:18279434	PCS				I		HPO:skoehler	
OMIM	612431	DEAFNESS, AUTOSOMAL DOMINANT 27		HP:0000407	PMID:18279434	PCS	HP:0003621			P		HPO:probinson	
OMIM	612433	DEAFNESS, AUTOSOMAL RECESSIVE 45		HP:0000007	PMID:18325041	PCS				I		HPO:skoehler	
OMIM	612433	DEAFNESS, AUTOSOMAL RECESSIVE 45		HP:0000399	PMID:18325041	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0000007	OMIM:612437	IEA				I		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0001260	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0001310	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0001337	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0002123	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0003390	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0003487	OMIM:612437	IEA				P		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0003676	OMIM:612437	IEA				C		HPO:skoehler	
OMIM	612437	#612437 EPILEPSY, PROGRESSIVE MYOCLONIC 1B; EPM1B		HP:0010819	OMIM:612437	TAS				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000006	OMIM:612438	TAS				I		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000007	OMIM:612438	IEA				I		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000252	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000365	OMIM:612438	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000505	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000639	OMIM:612438	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000648	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0000750	OMIM:612438	TAS				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001249	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001250	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001251	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001257	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001260	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001266	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001270	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001272	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001328	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001332	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0001337	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0002063	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0002415	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0002465	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0003676	OMIM:612438	IEA				C		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0003745	OMIM:612438	IEA				I		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0003828	OMIM:612438	IEA				C		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0004322	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0006808	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612438	#612438 LEUKODYSTROPHY, HYPOMYELINATING, 6; HLD6;;LEUKODYSTROPHY, HYPOMYELINATING, WITH ATROPHY OF THE BASAL GANGLIAAND CEREBELLUM; HABC		HP:0008936	OMIM:612438	IEA				P		HPO:skoehler	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:612444	TAS				I		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0000403	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0002257	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0003251	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0011108	OMIM:612444	TAS				P		HPO:probinson	
OMIM	612444	#612444 CILIARY DYSKINESIA, PRIMARY, 9; CILD9;;CILIARY DYSKINESIA, PRIMARY, 9, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:612444	IEA				P		HPO:skoehler	
OMIM	612446	#612446 COMPLEMENT COMPONENT 6 DEFICIENCY; C6D;;C6 DEFICIENCYCOMPLEMENT COMPONENT 6 DEFICIENCY, SUBTOTAL, INCLUDED;;C6 DEFICIENCY, SUBTOTAL, INCLUDED		HP:0000007	OMIM:612446	TAS				I		HPO:skoehler	
OMIM	612446	#612446 COMPLEMENT COMPONENT 6 DEFICIENCY; C6D;;C6 DEFICIENCYCOMPLEMENT COMPONENT 6 DEFICIENCY, SUBTOTAL, INCLUDED;;C6 DEFICIENCY, SUBTOTAL, INCLUDED		HP:0004431	OMIM:612446	TAS				P		HPO:skoehler	
OMIM	612446	#612446 COMPLEMENT COMPONENT 6 DEFICIENCY; C6D;;C6 DEFICIENCYCOMPLEMENT COMPONENT 6 DEFICIENCY, SUBTOTAL, INCLUDED;;C6 DEFICIENCY, SUBTOTAL, INCLUDED		HP:0005381	OMIM:612446	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000007	OMIM:612447	TAS				I		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000028	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000054	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000160	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000233	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000252	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0000486	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0001249	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0002750	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0003022	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0003038	OMIM:612447	TAS				P		HPO:probinson	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0003097	OMIM:612447	TAS				P		HPO:probinson	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0004322	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0005736	OMIM:612447	TAS				P		HPO:probinson	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0005815	OMIM:612447	TAS				P		HPO:probinson	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0006501	OMIM:612447	TAS				P		HPO:probinson	
OMIM	612447	SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION		HP:0009777	OMIM:612447	TAS				P		HPO:skoehler	
OMIM	612460	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14		HP:0000007	OMIM:612460	TAS				I		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000006	OMIM:612462	IEA				I		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000135	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000293	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000311	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000470	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000518	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000639	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000684	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000821	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000852	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0000939	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0001156	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0001249	OMIM:612462	TAS				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0001250	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0001513	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0002135	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0002905	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0003165	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0003456	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0003472	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0004322	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0005280	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0006297	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0006960	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0010049	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0010743	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612462	#612462 PSEUDOHYPOPARATHYROIDISM, TYPE IC; PHP1C;;PHP IC		HP:0100543	OMIM:612462	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000006	OMIM:612463	IEA				I		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000293	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000311	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000470	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000518	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000639	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000684	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000852	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0000939	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0001156	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0001249	OMIM:612463	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0001513	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0004322	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0005280	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0006297	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0010049	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0010743	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612463	#612463 PSEUDOPSEUDOHYPOPARATHYROIDISM; PPHP;;ALBRIGHT HEREDITARY OSTEODYSTROPHY WITHOUT MULTIPLE HORMONE RESISTANCE		HP:0100543	OMIM:612463	IEA				P		HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0000006	OMIM:612474	TAS				I	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0000252	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0000414	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0000490	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0000717	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0001249	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0001643	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0001660	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0001669	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0001680	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0002007	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0003745	OMIM:612474	TAS				I	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0003829	OMIM:612474	TAS				C	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0010055	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0011304	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612474	CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB		HP:0100753	OMIM:612474	TAS				P	CHROMOSOME 1Q21.1 DELETION SYNDROME, 1.35-MB	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0000006	OMIM:612475	IEA				I	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0000256	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0000316	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0000717	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0001250	OMIM:612475	IEA		HP:0040283		P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0001256	OMIM:612475	IEA		HP:0040283		P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	HP:0040283
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0001328	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0002007	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0002079	OMIM:612475	IEA				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0003745	OMIM:612475	IEA				I	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0003829	OMIM:612475	IEA				C	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612475	#612475 CHROMOSOME 1q21.1 DUPLICATION SYNDROME		HP:0100753	OMIM:612475	TAS				P	#612475 CHROMOSOME 1Q21.1 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000028	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000054	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000126	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000135	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000218	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000219	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000232	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000248	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000252	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000278	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000286	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000341	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000343	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000358	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000369	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000400	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000407	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000431	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000486	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000494	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000506	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000508	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000581	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000609	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0000767	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001166	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001249	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001257	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001263	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001290	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001302	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001601	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001611	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001840	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0001848	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002059	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002079	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002119	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002539	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002705	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002751	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0002788	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0003745	OMIM:612513	IEA				I		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0004322	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0005274	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0005280	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0006610	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0007018	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0008734	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0008872	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0009473	OMIM:612513	IEA				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0012110	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0012385	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612513	CHROMOSOME 2P16.1-P15 DELETION SYNDROME		HP:0012745	OMIM:612513	TAS				P		HPO:skoehler	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0000007	OMIM:612518	TAS				I		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0000389	OMIM:612518	TAS				P		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0001696	OMIM:612518	TAS				P		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0005938	OMIM:612518	TAS				P		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0011108	OMIM:612518	TAS				P		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0011109	OMIM:612518	TAS				P		HPO:probinson	
OMIM	612518	#612518 CILIARY DYSKINESIA, PRIMARY, 10; CILD10		HP:0012265	OMIM:612518	IEA				P		HPO:skoehler	
OMIM	612520	#612520 DIABETES MELLITUS, INSULIN-DEPENDENT, 20; IDDM20		HP:0100651	PMID:9313763	IEA				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0000007	PMID:18211975	PCS				I		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0000819	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0000855	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0000956	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0001007	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0001397	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0001433	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0002155	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0002901	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0003124	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0003758	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0004322	PMID:18211975	PCS				P		HPO:probinson	
OMIM	612526	#612526 LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3; CGL3;;BERARDINELLI-SEIP CONGENITAL LIPODYSTROPHY, TYPE 3; BSCL3;;LIPODYSTROPHY, BERARDINELLI-SEIP CONGENITAL, TYPE 3		HP:0009125	OMIM:612526	IEA				P		HPO:skoehler	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0000006	PMID:20378560	PCS				I		HPO:probinson	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0001631	OMIM:612527	TAS				P		HPO:skoehler	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0001875	OMIM:612527	TAS				P		HPO:skoehler	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0001896	PMID:20378560	PCS				P		HPO:probinson	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0001972	PMID:20378560	PCS				P		HPO:probinson	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0001999	OMIM:612527	TAS				P		HPO:skoehler	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0004322	OMIM:612527	TAS				P		HPO:skoehler	
OMIM	612527	DIAMOND-BLACKFAN ANEMIA 4		HP:0012133	PMID:20378560	PCS				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0000006	OMIM:612528	TAS				I		HPO:skoehler	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0000047	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0000316	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0000369	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0001263	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0001629	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0001882	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0001896	OMIM:612528	TAS				P		HPO:skoehler	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0001972	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0003593	OMIM:612528	TAS				C		HPO:skoehler	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0004322	OMIM:612528	TAS				P		HPO:skoehler	
OMIM	612528	DIAMOND-BLACKFAN ANEMIA 5		HP:0012133	PMID:18535205	IEA				P		HPO:probinson	
OMIM	612529	#612529 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2;;AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 2		HP:0000007	OMIM:612529	TAS				I		HPO:probinson	
OMIM	612529	#612529 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2;;AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 2		HP:0000705	OMIM:612529	TAS				P		HPO:probinson	
OMIM	612529	#612529 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2; AI2A2;;AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 2		HP:0200095	OMIM:612529	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000006	OMIM:612530	IEA				I	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000028	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000175	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000204	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000252	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000280	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000384	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000463	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000490	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000568	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000582	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000601	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0000776	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0001249	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0001250	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0001263	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0001360	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0001762	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0002007	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0003422	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0003745	OMIM:612530	TAS				I	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0004322	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0005280	OMIM:612530	TAS				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612530	CHROMOSOME 1q41-q42 DELETION SYNDROME		HP:0008551	OMIM:612530	IEA				P	CHROMOSOME 1Q41-Q42 DELETION SYNDROME	HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0000006	OMIM:612539	IEA				I		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0001258	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0001324	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0001761	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0002064	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0002395	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0003202	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612539	SPASTIC PARAPLEGIA 42, AUTOSOMAL DOMINANT; SPG42		HP:0003487	OMIM:612539	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0000007	OMIM:612540	IEA				I		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0000218	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0000268	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0000300	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0000316	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001166	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001284	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001319	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001518	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001522	OMIM:612540	IEA				M		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001558	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001561	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0001989	OMIM:612540	TAS				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0002033	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0002304	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0002705	OMIM:612540	TAS				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0002747	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0009473	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0010557	OMIM:612540	IEA				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0012385	OMIM:612540	TAS				P		HPO:skoehler	
OMIM	612540	MYOPATHY, CONGENITAL, COMPTON-NORTH		HP:0030799	OMIM:612540	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000007	OMIM:612541	IEA				I		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000028	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000126	OMIM:612541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000175	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000218	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000252	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000365	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000431	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000768	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000778	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0000954	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001263	OMIM:612541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001508	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001510	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001631	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001642	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001643	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001653	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001744	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001873	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001875	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001888	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0001903	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002092	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002093	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002205	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002240	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002619	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0002718	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0010774	OMIM:612541	IEA				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0011304	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0012133	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0012311	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0030084	OMIM:612541	TAS				P		HPO:skoehler	
OMIM	612541	NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4		HP:0100806	OMIM:612541	TAS	HP:0003623			P		HPO:skoehler	
OMIM	612551	#612551 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO; FSGS4;;END-STAGE RENAL DISEASE, NONDIABETIC, SUSCEPTIBILITY TO, INCLUDED		HP:0000097	OMIM:612551	IEA				P		HPO:skoehler	
OMIM	612551	#612551 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO; FSGS4;;END-STAGE RENAL DISEASE, NONDIABETIC, SUSCEPTIBILITY TO, INCLUDED		HP:0003774	OMIM:612551	TAS				P		HPO:skoehler	
OMIM	612551	#612551 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO; FSGS4;;END-STAGE RENAL DISEASE, NONDIABETIC, SUSCEPTIBILITY TO, INCLUDED		HP:0010982	OMIM:612551	IEA				I		HPO:skoehler	
OMIM	612555	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2		HP:0000006	OMIM:612555	IEA				I		HPO:skoehler	
OMIM	612555	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2		HP:0001426	OMIM:612555	IEA				I		HPO:skoehler	
OMIM	612555	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2		HP:0003002	OMIM:612555	IEA				P		HPO:skoehler	
OMIM	612555	BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2		HP:0100615	OMIM:612555	IEA				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000006	PMID:19061985	PCS				I		HPO:probinson	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000175	PMID:19061985	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000193	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000204	PMID:19061985	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000278	OMIM:612561	IEA				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000316	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0000347	PMID:19061985	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001199	PMID:19061985	PCS		HP:0040284		P		HPO:probinson	8/20
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001508	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001510	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001629	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001631	PMID:19061985	PCS		HP:0040284		P		HPO:probinson	3/20
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001634	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001636	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001643	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001653	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001714	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0001972	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0002779	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0005518	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0009778	OMIM:612561	TAS				P		HPO:skoehler	
OMIM	612561	DIAMOND-BLACKFAN ANEMIA 6; DBA6		HP:0011904	PMID:19061985	PCS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000006	PMID:19061985	PCS				I		HPO:probinson	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000076	PMID:19061985	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000085	PMID:19061985	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000175	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000365	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000403	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000413	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000453	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000912	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000938	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0000939	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001199	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001511	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001561	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001629	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001636	PMID:19061985	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001643	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001684	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001875	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0001972	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0002650	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0005518	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0009778	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0010487	PMID:19061985	PCS				P		HPO:probinson	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0025116	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0100512	OMIM:612562	TAS				P		HPO:skoehler	
OMIM	612562	DIAMOND-BLACKFAN ANEMIA 7; DBA7		HP:0100633	OMIM:612562	IEA				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0000006	PMID:19061985	PCS		HP:0040284		I		HPO:probinson	1/1
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0000215	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0000316	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0000431	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0001875	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0001972	PMID:19061985	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0003196	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0004322	OMIM:612563	TAS				P		HPO:skoehler	
OMIM	612563	DIAMOND-BLACKFAN ANEMIA 8		HP:0005518	PMID:19061985	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0000007	OMIM:612567	TAS				I		HPO:probinson	
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0000143	OMIM:612567	TAS				P		HPO:probinson	
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0004387	PMID:19890111	PCS				P		HPO:probinson	
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0005224	OMIM:612567	TAS				P		HPO:probinson	
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0009789	OMIM:612567	TAS				P		HPO:skoehler	
OMIM	612567	INFLAMMATORY BOWEL DISEASE 25, AUTOSOMAL RECESSIVE; IBD25		HP:0025084	OMIM:612567	IEA				P		HPO:skoehler	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0000007	OMIM:612572	TAS				I		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0000510	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0000543	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0000654	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0001133	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0007703	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612572	#612572 RETINITIS PIGMENTOSA 46; RP46;;RETINITIS PIGMENTOSA, AUTOSOMAL RECESSIVE, IDH3B-RELATED		HP:0007843	OMIM:612572	TAS				P		HPO:probinson	
OMIM	612576	#612576 CHROMOSOME 17P13.3, TELOMERIC, DUPLICATION SYNDROME;;SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3; SHFLD3		HP:0000006	OMIM:612576	TAS				I		HPO:skoehler	
OMIM	612576	#612576 CHROMOSOME 17P13.3, TELOMERIC, DUPLICATION SYNDROME;;SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3; SHFLD3		HP:0001156	OMIM:612576	TAS				P		HPO:skoehler	
OMIM	612576	#612576 CHROMOSOME 17P13.3, TELOMERIC, DUPLICATION SYNDROME;;SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3; SHFLD3		HP:0001171	OMIM:612576	TAS				P		HPO:skoehler	
OMIM	612576	#612576 CHROMOSOME 17P13.3, TELOMERIC, DUPLICATION SYNDROME;;SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3; SHFLD3		HP:0001762	OMIM:612576	TAS				P		HPO:skoehler	
OMIM	612576	#612576 CHROMOSOME 17P13.3, TELOMERIC, DUPLICATION SYNDROME;;SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 3; SHFLD3		HP:0012165	OMIM:612576	TAS				P		HPO:skoehler	
OMIM	612577	AMYOTROPHIC LATERAL SCLEROSIS 11		HP:0000006	PMID:19118816	PCS				I		HPO:probinson	
OMIM	612577	AMYOTROPHIC LATERAL SCLEROSIS 11		HP:0002483	OMIM:612577	TAS				P		HPO:skoehler	
OMIM	612577	AMYOTROPHIC LATERAL SCLEROSIS 11		HP:0002493	PMID:19118816	PCS				P		HPO:probinson	
OMIM	612577	AMYOTROPHIC LATERAL SCLEROSIS 11		HP:0003202	PMID:19118816	PCS				P		HPO:probinson	
OMIM	612577	AMYOTROPHIC LATERAL SCLEROSIS 11		HP:0007354	PMID:19118816	PCS				P		HPO:probinson	
OMIM	612580	#612580 MENTAL RETARDATION, AUTOSOMAL DOMINANT 3; MRD3		HP:0000006	PMID:19012874	PCS				I		HPO:probinson	
OMIM	612580	#612580 MENTAL RETARDATION, AUTOSOMAL DOMINANT 3; MRD3		HP:0000729	PMID:19012874	PCS		HP:0040284		P		HPO:probinson	1/5
OMIM	612580	#612580 MENTAL RETARDATION, AUTOSOMAL DOMINANT 3; MRD3		HP:0001249	PMID:19012874	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	612580	#612580 MENTAL RETARDATION, AUTOSOMAL DOMINANT 3; MRD3		HP:0001250	PMID:19012874	PCS		HP:0040284		P		HPO:probinson	1/5
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0000006	PMID:19012874	TAS				I		HPO:probinson	
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0000331	OMIM:612581	IEA				P		HPO:skoehler	
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0001159	OMIM:612581	IEA				P		HPO:skoehler	
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0001249	PMID:19012874	TAS				P		HPO:probinson	
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0001831	OMIM:612581	IEA				P		HPO:skoehler	
OMIM	612581	MENTAL RETARDATION, AUTOSOMAL DOMINANT 4; MRD4		HP:0011800	OMIM:612581	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000204	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000218	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000248	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000272	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000286	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000316	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000337	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000358	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000369	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000407	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000470	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000494	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000540	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000577	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000627	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000678	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0000750	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001249	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001250	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001252	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001263	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001270	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001290	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001305	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001328	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001385	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001492	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001636	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001643	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001655	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0001838	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0002007	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0003745	OMIM:612582	IEA				I		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0005280	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0006482	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0007759	OMIM:612582	IEA				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0010804	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612582	CHROMOSOME 6PTER-P24 DELETION SYNDROME		HP:0011800	OMIM:612582	TAS				P		HPO:skoehler	
OMIM	612591	COLORECTAL CANCER, SUSCEPTIBILITY TO, 10; CRCS10		HP:0000006	OMIM:612591	TAS				I		HPO:skoehler	
OMIM	612591	COLORECTAL CANCER, SUSCEPTIBILITY TO, 10; CRCS10		HP:0012114	OMIM:612591	TAS				P		HPO:skoehler	
OMIM	612591	COLORECTAL CANCER, SUSCEPTIBILITY TO, 10; CRCS10		HP:0030731	OMIM:612591	IEA				P		HPO:skoehler	
OMIM	612591	COLORECTAL CANCER, SUSCEPTIBILITY TO, 10; CRCS10		HP:0200063	OMIM:612591	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0000006	OMIM:612621	TAS				I		HPO:probinson	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0000252	OMIM:612621	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0000473	OMIM:612621	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0000729	OMIM:612621	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0001249	OMIM:612621	TAS				P		HPO:probinson	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0001250	OMIM:612621	TAS		HP:0040284		P		HPO:probinson	2/3
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0001263	OMIM:612621	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0001270	OMIM:612621	TAS				P		HPO:probinson	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0001290	OMIM:612621	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0002353	OMIM:612621	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0002376	OMIM:612621	TAS				P		HPO:skoehler	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0002463	OMIM:612621	TAS				P		HPO:probinson	
OMIM	612621	MENTAL RETARDATION, AUTOSOMAL DOMINANT 5		HP:0200134	OMIM:612621	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000028	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000047	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000054	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000252	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000325	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000347	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000369	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000431	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000486	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0000581	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001156	OMIM:612626	TAS				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001249	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001263	OMIM:612626	TAS				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001508	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001511	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001518	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001671	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0001762	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0003577	OMIM:612626	IEA				C	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0003745	OMIM:612626	IEA				I	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0004322	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612626	#612626 CHROMOSOME 15q26-qter DELETION SYNDROME;;DRAYER SYNDROME		HP:0005819	OMIM:612626	IEA				P	#612626 CHROMOSOME 15Q26-QTER DELETION SYNDROME;;DRAYER SYNDROME	HPO:skoehler	
OMIM	612631	#612631 ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO		HP:0000007	OMIM:612631	TAS				I		HPO:skoehler	
OMIM	612631	#612631 ADENYLATE KINASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO		HP:0001878	OMIM:612631	TAS				P		HPO:skoehler	
OMIM	612642	DEAFNESS, AUTOSOMAL DOMINANT 59		HP:0000006	PMID:19030898	PCS				I		HPO:skoehler	
OMIM	612642	DEAFNESS, AUTOSOMAL DOMINANT 59	HP:0012828	HP:0000407	PMID:19030898	PCS	HP:0003577			P		HPO:probinson	
OMIM	612643	#612643 DEAFNESS, AUTOSOMAL DOMINANT 3B; DFNA3B		HP:0000006	OMIM:612643	TAS				I		HPO:probinson	
OMIM	612643	#612643 DEAFNESS, AUTOSOMAL DOMINANT 3B; DFNA3B		HP:0008615	OMIM:612643	TAS				P		HPO:probinson	
OMIM	612644	#612644 DEAFNESS, AUTOSOMAL DOMINANT 2B; DFNA2B		HP:0000006	OMIM:612644	TAS				I		HPO:probinson	
OMIM	612644	#612644 DEAFNESS, AUTOSOMAL DOMINANT 2B; DFNA2B		HP:0005101	OMIM:612644	TAS				P		HPO:probinson	
OMIM	612645	#612645 DEAFNESS, AUTOSOMAL RECESSIVE 1B; DFNB1B		HP:0000007	OMIM:612645	TAS				I		HPO:skoehler	
OMIM	612645	#612645 DEAFNESS, AUTOSOMAL RECESSIVE 1B; DFNB1B		HP:0000365	OMIM:612645	IEA				P		HPO:skoehler	
OMIM	612645	#612645 DEAFNESS, AUTOSOMAL RECESSIVE 1B; DFNB1B		HP:0001751	OMIM:612645	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0000007	OMIM:612649	TAS				I		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0002110	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0002257	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0003546	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0004322	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0011108	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0012260	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0012262	OMIM:612649	TAS				P		HPO:probinson	
OMIM	612649	#612649 CILIARY DYSKINESIA, PRIMARY, 11; CILD11		HP:0012265	OMIM:612649	IEA				P		HPO:skoehler	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0000007	PMID:19200523	PCS				I		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0002110	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0002205	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0002257	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0003546	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0004322	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0011109	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0012208	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0012260	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612650	#612650 CILIARY DYSKINESIA, PRIMARY, 12; CILD12		HP:0012265	PMID:19200523	PCS				P		HPO:probinson	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000007	OMIM:612651	IEA				I		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000028	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000046	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000047	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000054	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000062	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000175	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000204	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000238	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000272	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000347	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000369	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000377	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000431	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000437	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000835	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0000914	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001156	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001159	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001193	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001360	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001552	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0001852	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0002119	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0002983	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0006610	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0007370	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0009487	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0010442	OMIM:612651	IEA				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0011800	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0030260	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612651	ENDOCRINE-CEREBROOSTEODYSPLASIA; ECO		HP:0100259	OMIM:612651	TAS				P		HPO:skoehler	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0000006	OMIM:612653	TAS				I		HPO:probinson	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0000952	OMIM:612653	TAS				P		HPO:skoehler	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0001744	OMIM:612653	TAS				P		HPO:skoehler	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0001878	OMIM:612653	TAS				P		HPO:probinson	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0001923	OMIM:612653	TAS				P		HPO:probinson	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0002904	OMIM:612653	TAS				P		HPO:skoehler	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0004444	OMIM:612653	TAS				P		HPO:probinson	
OMIM	612653	#612653 SPHEROCYTOSIS, TYPE 4; SPH4;;SPHEROCYTOSIS, HEREDITARY, 4; HS4		HP:0005502	OMIM:612653	TAS				P		HPO:probinson	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0000006	OMIM:612656	TAS				I		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0000571	OMIM:612656	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0000613	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0000639	OMIM:612656	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0000651	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001250	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001260	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001269	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001270	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001290	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001321	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0001350	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002013	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002018	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002076	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002078	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002131	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002183	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002301	OMIM:612656	IEA				P		HPO:skoehler	
OMIM	612656	EPISODIC ATAXIA, TYPE 6		HP:0002321	OMIM:612656	TAS				P		HPO:skoehler	
OMIM	612657	#612657 CONE-ROD DYSTROPHY 12; CORD12		HP:0000006	PMID:18654668	PCS				I		HPO:probinson	
OMIM	612657	#612657 CONE-ROD DYSTROPHY 12; CORD12		HP:0000548	PMID:18654668	PCS				P		HPO:probinson	
OMIM	612657	#612657 CONE-ROD DYSTROPHY 12; CORD12		HP:0007663	PMID:18654668	PCS				P		HPO:probinson	
OMIM	612671	#612671 URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4; UAQTL4;;GOUT SUSCEPTIBILITY 4; GOUT4		HP:0000006	OMIM:612671	TAS				I		HPO:skoehler	
OMIM	612671	#612671 URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4; UAQTL4;;GOUT SUSCEPTIBILITY 4; GOUT4		HP:0001997	OMIM:612671	TAS				P		HPO:skoehler	
OMIM	612671	#612671 URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4; UAQTL4;;GOUT SUSCEPTIBILITY 4; GOUT4		HP:0002149	OMIM:612671	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000007	OMIM:612674	IEA				I		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000407	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000510	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000523	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000639	OMIM:612674	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000648	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0000762	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001251	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001257	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001260	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001265	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001271	OMIM:612674	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001272	OMIM:612674	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001310	OMIM:612674	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001347	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001761	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0001771	OMIM:612674	TAS				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0002080	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0002936	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0003487	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0003674	OMIM:612674	IEA				C		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0003677	OMIM:612674	IEA				C		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0003693	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612674	#612674 POLYNEUROPATHY, HEARING LOSS, ATAXIA, RETINITIS PIGMENTOSA, AND CATARACT;PHARC		HP:0007141	OMIM:612674	IEA				P		HPO:skoehler	
OMIM	612690	#612690 SPHEROCYTOSIS, TYPE 5; SPH5;;SPHEROCYTOSIS, HEREDITARY, 5; HS5		HP:0000007	OMIM:612690	TAS				I		HPO:probinson	
OMIM	612690	#612690 SPHEROCYTOSIS, TYPE 5; SPH5;;SPHEROCYTOSIS, HEREDITARY, 5; HS5		HP:0001878	OMIM:612690	TAS				P		HPO:probinson	
OMIM	612690	#612690 SPHEROCYTOSIS, TYPE 5; SPH5;;SPHEROCYTOSIS, HEREDITARY, 5; HS5		HP:0004444	OMIM:612690	TAS				P		HPO:probinson	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0000007	OMIM:612691	TAS				I		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0000718	OMIM:612691	TAS				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0002119	OMIM:612691	TAS				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0002126	OMIM:612691	IEA				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0002133	OMIM:612691	TAS				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0002367	OMIM:612691	TAS				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0002384	OMIM:612691	TAS				P		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0003828	OMIM:612691	TAS				C		HPO:skoehler	
OMIM	612691	POLYMICROGYRIA, BILATERAL TEMPOROOCCIPITAL; BTOP		HP:0031258	OMIM:612691	IEA				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0000007	OMIM:612692	TAS				I		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0000403	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0000509	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0002014	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0002718	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0002837	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0003593	OMIM:612692	TAS				C		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0004432	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0006532	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612692	#612692 AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE; AGM6;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79B DEFECT		HP:0011109	OMIM:612692	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000006	OMIM:612702	TAS				I		HPO:probinson	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000028	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000044	OMIM:612702	TAS				P		HPO:probinson	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000054	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000218	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000458	OMIM:612702	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0000786	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0002750	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0004409	OMIM:612702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0012506	OMIM:612702	TAS				P		HPO:skoehler	
OMIM	612702	HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA; HH6		HP:0410030	OMIM:612702	IEA				P		HPO:skoehler	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:612703	TAS				I		HPO:probinson	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:612703	TAS				P		HPO:probinson	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000340	OMIM:612703	TAS				P		HPO:skoehler	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:612703	TAS				P		HPO:probinson	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:612703	TAS				C		HPO:skoehler	
OMIM	612703	MICROCEPHALY 7, PRIMARY, AUTOSOMAL RECESSIVE		HP:0009879	OMIM:612703	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612712	LEBER CONGENITAL AMAUROSIS 13; LCA13		HP:0000006	OMIM:612712	IEA				I		HPO:skoehler	
OMIM	612712	LEBER CONGENITAL AMAUROSIS 13; LCA13		HP:0000007	OMIM:612712	TAS				I		HPO:skoehler	
OMIM	612712	LEBER CONGENITAL AMAUROSIS 13; LCA13		HP:0000556	OMIM:612712	TAS				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:612713	IEA				I		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000179	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000414	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000431	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000518	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0000612	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0001270	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0002942	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0002987	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0005306	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0006380	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0006887	OMIM:612713	IEA				P		HPO:skoehler	
OMIM	612713	#612713 KAHRIZI SYNDROME; KHRZ;;MENTAL RETARDATION, CATARACT, COLOBOMA, AND KYPHOSIS, AUTOSOMAL RECESSIVE		HP:0010864	OMIM:612713	TAS				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0000007	OMIM:612714	IEA				I		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0000670	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0000938	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0000952	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0000988	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0001263	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0001508	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0001738	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0001744	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0001903	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0002099	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0002240	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0002570	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0002750	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0003193	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0003593	OMIM:612714	IEA				C		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0004395	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0004490	OMIM:612714	IEA				P		HPO:skoehler	
OMIM	612714	#612714 EXOCRINE PANCREATIC INSUFFICIENCY, DYSERYTHROPOIETIC ANEMIA, AND CALVARIALHYPEROSTOSIS		HP:0010972	OMIM:612714	TAS				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000006	OMIM:612716	IEA				I		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000007	OMIM:612716	IEA				I		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000252	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000657	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000718	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0000752	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001249	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001250	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001251	OMIM:612716	TAS				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001257	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001260	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001263	OMIM:612716	TAS				P		HPO:probinson	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001266	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001332	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001337	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0001510	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0002360	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0003593	OMIM:612716	IEA				C		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0003828	OMIM:612716	TAS				C		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0008297	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612716	#612716 DYSTONIA, DOPA-RESPONSIVE, DUE TO SEPIAPTERIN REDUCTASE DEFICIENCY;;SEPIAPTERIN REDUCTASE DEFICIENCY;;SPR DEFICIENCY		HP:0008936	OMIM:612716	IEA				P		HPO:skoehler	
OMIM	612717	MYOPIA 15; MYP15		HP:0000006	OMIM:612717	IEA				I		HPO:skoehler	
OMIM	612717	MYOPIA 15; MYP15		HP:0000545	OMIM:612717	IEA				P		HPO:skoehler	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0000007	OMIM:612718	TAS				I	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:probinson	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0000717	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:probinson	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0000750	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:probinson	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0001249	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:skoehler	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0001263	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:probinson	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0001508	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:skoehler	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0001992	OMIM:612718	TAS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:skoehler	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0003391	OMIM:612718	TAS		HP:0040283		P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:skoehler	HP:0040283
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0003593	OMIM:612718	TAS				C	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HPO:skoehler	
OMIM	612718	Cerebral creatine deficiency syndrome 3		HP:0025051	PMID:20682460	PCS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 3	HP:probinson	
OMIM	612726	HARDIKAR SYNDROME		HP:0000010	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000071	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000072	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000076	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000126	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000148	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000175	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000204	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000365	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000580	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000581	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000952	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0000989	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001070	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001409	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001508	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001510	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001629	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001643	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001655	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001680	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0001744	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0002240	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0002566	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0002904	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0002910	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0003577	OMIM:612726	IEA				C		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0003745	OMIM:612726	IEA				I		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0004415	OMIM:612726	IEA				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0030151	OMIM:612726	TAS				P		HPO:skoehler	
OMIM	612726	HARDIKAR SYNDROME		HP:0200065	OMIM:612726	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000007	OMIM:612731	IEA				I		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000154	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000252	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000343	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000347	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000463	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000506	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000508	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000577	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000689	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000774	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0000938	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0001249	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0001520	OMIM:612731	TAS				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0002753	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0003100	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0004634	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0005280	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0008839	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0010442	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0010764	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0011565	OMIM:612731	TAS				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0200000	OMIM:612731	IEA				P		HPO:skoehler	
OMIM	612731	FACIOCARDIOMELIC SYNDROME		HP:0430028	OMIM:612731	TAS				P		HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0000007	OMIM:612736	IEA				I	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0000750	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:probinson	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001249	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001250	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001251	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001263	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001276	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001336	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0001347	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0007153	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0008947	OMIM:612736	IEA				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HPO:skoehler	
OMIM	612736	Cerebral creatine deficiency syndrome 2		HP:0025051	PMID:7808840	PCS				P	CEREBRAL CREATINE DEFICIENCY SYNDROME 2	HP:probinson	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0000007	OMIM:612740	IEA				I		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0001252	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0001290	OMIM:612740	TAS				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0001508	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0001878	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0002013	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0002203	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0003163	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0003401	OMIM:612740	IEA				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0011848	OMIM:612740	TAS				P		HPO:skoehler	
OMIM	612740	PORPHYRIA, ACUTE HEPATIC		HP:0040284	OMIM:612740	IEA						HPO:skoehler	
OMIM	612775	#612775 CONE-ROD DYSTROPHY 9; CORD9		HP:0000007	OMIM:612775	TAS				I		HPO:probinson	
OMIM	612775	#612775 CONE-ROD DYSTROPHY 9; CORD9		HP:0000505	OMIM:612775	TAS	HP:0011463			P		HPO:probinson	
OMIM	612775	#612775 CONE-ROD DYSTROPHY 9; CORD9		HP:0000548	OMIM:612775	TAS				P		HPO:probinson	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000160	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000171	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000218	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000347	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000369	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000668	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0000750	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0001696	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0001746	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0001748	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0002098	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0002781	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0003577	OMIM:612776	IEA				C		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0003745	OMIM:612776	IEA				I		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0004395	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612776	HYPOGLOSSIA WITH SITUS INVERSUS		HP:0008872	OMIM:612776	IEA				P		HPO:skoehler	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000007	OMIM:612780	PCS				I		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000103	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000127	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000128	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000407	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000750	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000805	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000848	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0000859	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001249	OMIM:612780	TAS				P		HPO:skoehler	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001250	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001252	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001263	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001272	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001290	OMIM:612780	TAS				P		HPO:skoehler	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001959	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0001960	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0002075	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0002080	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0002900	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0002917	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0003127	OMIM:612780	PCS				P		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0003593	OMIM:612780	PCS				C		HPO:probinson	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0004322	OMIM:612780	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0007182	OMIM:612780	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0007267	OMIM:612780	PCS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0012606	OMIM:612780	TAS				P		HPO:skoehler	
OMIM	612780	SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE		HP:0030083	OMIM:612780	TAS				P		HPO:skoehler	
OMIM	612781	#612781 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB; IGHD1B;;IGHD IB;;DWARFISM OF SINDH		HP:0000007	OMIM:612781	TAS				I		HPO:probinson	
OMIM	612781	#612781 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB; IGHD1B;;IGHD IB;;DWARFISM OF SINDH		HP:0000824	OMIM:612781	TAS				P		HPO:probinson	
OMIM	612781	#612781 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB; IGHD1B;;IGHD IB;;DWARFISM OF SINDH		HP:0002750	OMIM:612781	TAS				P		HPO:probinson	
OMIM	612781	#612781 ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IB; IGHD1B;;IGHD IB;;DWARFISM OF SINDH		HP:0004322	OMIM:612781	TAS				P		HPO:probinson	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0000007	OMIM:612782	IEA				I		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0000705	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0000968	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0001252	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0001508	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0001954	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0002046	OMIM:612782	TAS				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0002355	OMIM:612782	TAS				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0002719	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0002721	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0002747	OMIM:612782	TAS				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0003198	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0003391	OMIM:612782	TAS				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0010280	OMIM:612782	IEA				P		HPO:skoehler	
OMIM	612782	IMMUNODEFICIENCY 9; IMD9		HP:0011107	OMIM:612782	TAS				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0000007	OMIM:612783	IEA				I		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0000705	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0000966	OMIM:612783	TAS				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0001252	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0001873	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0001890	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0001954	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0002164	OMIM:612783	TAS				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0002716	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0002718	OMIM:612783	TAS				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0002719	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0002721	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0003198	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0003828	OMIM:612783	TAS				C		HPO:skoehler	
OMIM	612783	IMMUNODEFICIENCY 10; IMD10		HP:0007676	OMIM:612783	IEA				P		HPO:skoehler	
OMIM	612789	DEAFNESS, AUTOSOMAL RECESSIVE 71		HP:0000007	PMID:19229252	PCS				I		HPO:probinson	
OMIM	612789	DEAFNESS, AUTOSOMAL RECESSIVE 71		HP:0000399	PMID:19229252	PCS				P		HPO:probinson	
OMIM	612794	ATRIAL SEPTAL DEFECT 5		HP:0000006	OMIM:612794	TAS				I		HPO:skoehler	
OMIM	612794	ATRIAL SEPTAL DEFECT 5		HP:0001631	OMIM:612794	IEA				P		HPO:skoehler	
OMIM	612798	#612798 QUESTION MARK EARS, ISOLATED; QME;;EARS, PROMINENT AND CONSTRICTED;;COSMAN DEFORMITY OF THE AURICLE;;AURICULAR CLEFT, CONGENITAL		HP:0000006	OMIM:612798	IEA				I		HPO:skoehler	
OMIM	612798	#612798 QUESTION MARK EARS, ISOLATED; QME;;EARS, PROMINENT AND CONSTRICTED;;COSMAN DEFORMITY OF THE AURICLE;;AURICULAR CLEFT, CONGENITAL		HP:0030022	OMIM:612798	TAS				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0000007	PMID:19110214	IEA				I		HPO:probinson	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0000272	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0000303	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG	HP:0012825	HP:0000358	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG	HP:0012825	HP:0000369	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0000470	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0000926	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0001156	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0001388	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0001552	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0001609	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	2/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0002651	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0002938	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0003016	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0003027	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0004482	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0005285	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0008905	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0009381	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0010582	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0011304	PMID:19110214	IEA		HP:0040284		P		HPO:probinson	3/3
OMIM	612813	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, AGGRECAN TYPE; SEMDAG		HP:0011800	OMIM:612813	IEA				P		HPO:skoehler	
OMIM	612838	#612838 BRUGADA SYNDROME 5; BRGDA5CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED		HP:0000006	PMID:18464934	TAS				I		HPO:probinson	
OMIM	612838	#612838 BRUGADA SYNDROME 5; BRGDA5CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED		HP:0001663	PMID:18464934	TAS				P		HPO:probinson	
OMIM	612838	#612838 BRUGADA SYNDROME 5; BRGDA5CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED		HP:0011710	PMID:18464934	TAS				P		HPO:probinson	
OMIM	612838	#612838 BRUGADA SYNDROME 5; BRGDA5CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED		HP:0012251	PMID:18464934	TAS				P		HPO:probinson	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0000007	OMIM:612840	TAS				I		HPO:skoehler	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0000421	PMID:17185466	PCS		HP:0040283		P		HPO:lccarmody	HP:0040283
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0000967	OMIM:612840	IEA				P		HPO:skoehler	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001433	PMID:17185466	PCS		HP:0040282		P		HPO:lccarmody	HP:0040282
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001482	PMID:17185466	PCS				P		HPO:lccarmody	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001581	PMID:17185466	PCS				P		HPO:lccarmody	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001744	PMID:17185466	PCS		HP:0040282		P		HPO:lccarmody	HP:0040282
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001872	PMID:17185466	PCS		HP:0040282		P		HPO:lccarmody	HP:0040282
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001903	OMIM:612840	IEA				P		HPO:skoehler	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001974	PMID:9312170	PCS				P		HPO:lccarmody	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0001978	PMID:17185466	PCS		HP:0040284		P		HPO:lccarmody	HP:0040284
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0002240	OMIM:612840	TAS				P		HPO:skoehler	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0002718	PMID:9312170	PCS	HP:0003593	HP:0040282		P		HPO:lccarmody	HP:0040282
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0002733	PMID:17185466	PCS				P		HPO:lccarmody	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0003593	OMIM:612840	TAS				C		HPO:skoehler	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0011002	OMIM:612840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0012531	PMID:17185466	PCS				P		HPO:lccarmody	
OMIM	612840	LEUKOCYTE ADHESION DEFICIENCY, TYPE III		HP:0100806	PMID:17185466	PCS				P		HPO:lccarmody	
OMIM	612841	HYPOTRICHOSIS 5; HYPT5		HP:0000653	OMIM:612841	IEA				P		HPO:skoehler	
OMIM	612841	HYPOTRICHOSIS 5; HYPT5		HP:0001596	OMIM:612841	IEA				P		HPO:skoehler	
OMIM	612841	HYPOTRICHOSIS 5; HYPT5		HP:0002221	OMIM:612841	IEA				P		HPO:skoehler	
OMIM	612841	HYPOTRICHOSIS 5; HYPT5		HP:0002555	OMIM:612841	IEA				P		HPO:skoehler	
OMIM	612841	HYPOTRICHOSIS 5; HYPT5		HP:0045074	OMIM:612841	IEA				P		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000006	PMID:18984066	PCS				I		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000491	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	19/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000498	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	17/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000509	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	17/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000518	PMID:18984066	PCS		HP:0040284		P		HP:probinson	3/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000535	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	7/8
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000613	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	26/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000653	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	42/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000670	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	9/46
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0000982	PMID:18984066	PCS		HP:0040284		P		HP:probinson	8/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0001041	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	21/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0001425	OMIM:612843	IEA				I		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0001596	OMIM:612843	IEA				P		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0002164	OMIM:612843	IEA				P		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0004552	PMID:18984066	PCS		HP:0040284		P		HP:probinson	39/46
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0006297	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	9/46
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0008404	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	15/46
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0025084	PMID:18984066	PCS		HP:0040284		P		HPO:skoehler	17/47
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0030054	OMIM:612843	TAS				P		HPO:skoehler	
OMIM	612843	KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT; KFSD		HP:0032152	PMID:18984066	PCS		HP:0040284		P		HP:probinson	45/47
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0000007	OMIM:612847	TAS				I		HPO:probinson	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0000869	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0000926	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0001007	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0001061	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4	HP:0012825	HP:0001156	OMIM:612847	TAS				P		HPO:probinson	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0002651	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0002751	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0002979	OMIM:612847	TAS				P		HPO:probinson	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0003301	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0004322	OMIM:612847	TAS				P		HPO:probinson	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0004626	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0009816	OMIM:612847	TAS				P		HPO:probinson	
OMIM	612847	BRACHYOLMIA TYPE 4 WITH MILD EPIPHYSEAL AND METAPHYSEAL CHANGES; BCYM4		HP:0012411	OMIM:612847	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0000007	OMIM:612852	TAS				I		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0000962	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0001386	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0001744	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002098	OMIM:612852	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002240	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002754	OMIM:612852	IEA				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002797	OMIM:612852	IEA				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002829	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0002949	OMIM:612852	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0006530	OMIM:612852	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0010280	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0025092	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0025116	OMIM:612852	TAS				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0040165	OMIM:612852	IEA				P		HPO:skoehler	
OMIM	612852	OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS; OMPP		HP:0200039	OMIM:612852	IEA				P		HPO:skoehler	
OMIM	612867	612867 CORNEAL DYSTROPHY, SUBEPITHELIAL MUCINOUS; SMCD;;SUBEPITHELIAL MUCINOUS CORNEAL DYSTROPHY		HP:0000006	OMIM:612867	TAS				I		HPO:skoehler	
OMIM	612867	612867 CORNEAL DYSTROPHY, SUBEPITHELIAL MUCINOUS; SMCD;;SUBEPITHELIAL MUCINOUS CORNEAL DYSTROPHY		HP:0000529	OMIM:612867	TAS				P		HPO:skoehler	
OMIM	612867	612867 CORNEAL DYSTROPHY, SUBEPITHELIAL MUCINOUS; SMCD;;SUBEPITHELIAL MUCINOUS CORNEAL DYSTROPHY		HP:0001131	OMIM:612867	IEA				P		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0000006	OMIM:612868	TAS				I		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0000540	OMIM:612868	TAS				P		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0000612	OMIM:612868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0001131	OMIM:612868	IEA				P		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0003593	OMIM:612868	TAS				C		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0003680	OMIM:612868	TAS				C		HPO:skoehler	
OMIM	612868	CORNEAL DYSTROPHY, POSTERIOR AMORPHOUS		HP:0009918	OMIM:612868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612874	ERYTHROCYTE AMP DEAMINASE DEFICIENCY		HP:0000007	OMIM:612874	TAS				I		HPO:skoehler	
OMIM	612877	#612877 CARDIOMYOPATHY, DILATED, 1BB; CMD1BB		HP:0001644	PMID:18678517	IEA				P		HPO:probinson	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0000007	PMID:25437880	PCS				I		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0000027	OMIM:612885	TAS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0000786	PMID:25437880	PCS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0000821	PMID:25437880	PCS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0008209	PMID:25437880	PCS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0008232	PMID:25437880	PCS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0008724	PMID:25437880	PCS				P		HPO:probinson	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0008734	OMIM:612885	TAS				P		HPO:skoehler	
OMIM	612885	#612885 PREMATURE OVARIAN FAILURE 10; POF10MENOPAUSE, NATURAL, AGE AT, QUANTITATIVE TRAIT LOCUS 3, INCLUDED;MENOQ3, INCLUDED		HP:0011969	OMIM:612885	TAS				P		HPO:skoehler	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0001249	OMIM:612900	IEA				P		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0001252	OMIM:612900	IEA	HP:0003577			P		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0002059	OMIM:612900	IEA				P		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0002119	OMIM:612900	IEA				P		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0002510	OMIM:612900	IEA				P		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0012275	PMID:16301218	PCS				I		HPO:probinson	
OMIM	612900	#612900 CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 2; CPSQ2		HP:0100021	OMIM:612900	IEA				P		HPO:skoehler	
OMIM	612908	KERATOSIS PALMOPLANTARIS STRIATA II; PPKS2		HP:0000006	OMIM:612908	TAS				I		HPO:probinson	
OMIM	612908	KERATOSIS PALMOPLANTARIS STRIATA II; PPKS2		HP:0000982	OMIM:612908	TAS				P		HPO:probinson	
OMIM	612908	KERATOSIS PALMOPLANTARIS STRIATA II; PPKS2		HP:0025092	OMIM:612908	IEA				P		HPO:skoehler	
OMIM	612913	OROFACIODIGITAL SYNDROME XI; OFD11		HP:0000175	OMIM:612913	IEA				P		HPO:skoehler	
OMIM	612913	OROFACIODIGITAL SYNDROME XI; OFD11		HP:0001249	OMIM:612913	IEA				P		HPO:skoehler	
OMIM	612913	OROFACIODIGITAL SYNDROME XI; OFD11		HP:0002751	OMIM:612913	IEA				P		HPO:skoehler	
OMIM	612913	OROFACIODIGITAL SYNDROME XI; OFD11		HP:0003310	OMIM:612913	IEA				P		HPO:skoehler	
OMIM	612913	OROFACIODIGITAL SYNDROME XI; OFD11		HP:0003745	OMIM:612913	IEA				I		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000007	OMIM:612916	TAS				I		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000175	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000204	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000272	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000402	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000430	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000431	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000445	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000581	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0000677	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001249	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001320	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001792	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001833	OMIM:612916	IEA				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001852	OMIM:612916	IEA				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0001999	OMIM:612916	IEA				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0009882	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0010743	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0011220	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0011800	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0011815	OMIM:612916	IEA				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0012745	OMIM:612916	TAS				P		HPO:skoehler	
OMIM	612916	ZECHI-CEIDE SYNDROME		HP:0045025	OMIM:612916	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0000006	OMIM:612917	IEA				I		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0000098	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0000276	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0000348	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0000601	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0001328	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0001833	OMIM:612917	TAS				P		HPO:skoehler	
OMIM	612917	612917 GIACHETI SYNDROME;;MARFANOID HABITUS AND SPECIFIC LANGUAGE AND LEARNING DISABILITIES		HP:0002167	OMIM:612917	IEA				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0000324	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0001528	OMIM:612918	TAS		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0001548	OMIM:612918	TAS	HP:0003577			P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0001744	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0001852	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0002144	OMIM:612918	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0002650	OMIM:612918	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0003745	OMIM:612918	TAS				I		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0004099	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0004437	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0008678	OMIM:612918	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0010301	OMIM:612918	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0012032	OMIM:612918	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0012721	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0025104	OMIM:612918	TAS				P		HPO:skoehler	
OMIM	612918	CONGENITAL LIPOMATOUS OVERGROWTH, VASCULAR MALFORMATIONS, AND EPIDERMAL NEVI		HP:0100559	OMIM:612918	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000007	OMIM:612921	TAS				I		HPO:probinson	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000218	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000268	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000272	OMIM:612921	TAS				P		HPO:probinson	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000307	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000325	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000343	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000411	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000463	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	8/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000470	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000684	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000689	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000766	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0000883	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0002007	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	8/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0003100	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	4/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0003307	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0003691	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0004322	OMIM:612921	TAS				P		HPO:probinson	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0004482	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0005274	OMIM:612921	TAS				P		HPO:probinson	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0005280	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0009237	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0010306	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0011800	OMIM:612921	IEA				P		HPO:skoehler	
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0012428	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	8/8
OMIM	612921	THREE M SYNDROME 2; 3M2		HP:0012471	PMID:19481195	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0000006	OMIM:612922	TAS				I		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0000007	OMIM:612922	TAS				I		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0000093	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0000790	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0000822	OMIM:612922	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0001873	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0001919	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0001937	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0003138	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0003259	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0005575	OMIM:612922	IEA				P		HPO:skoehler	
OMIM	612922	#612922 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 2; AHUS2;;AHUS, SUSCEPTIBILITY TO, 2		HP:0100519	OMIM:612922	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0000006	OMIM:612923	TAS				I		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0000093	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0000790	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0000822	OMIM:612923	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0001873	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0001919	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0001937	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0003138	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0003259	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0005575	OMIM:612923	IEA				P		HPO:skoehler	
OMIM	612923	#612923 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 3; AHUS3;;AHUS, SUSCEPTIBILITY TO, 3		HP:0100519	OMIM:612923	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0000006	OMIM:612924	TAS				I		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0000093	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0000790	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0000822	OMIM:612924	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0001873	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0001919	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0001937	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0003138	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0003259	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0005575	OMIM:612924	IEA				P		HPO:skoehler	
OMIM	612924	#612924 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 4; AHUS4;;AHUS, SUSCEPTIBILITY TO, 4		HP:0100519	OMIM:612924	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0000006	OMIM:612925	TAS				I		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0000093	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0000790	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0000822	OMIM:612925	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0001873	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0001919	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0001937	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0003138	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0003259	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0005575	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612925	#612925 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 5; AHUS5;;AHUS, SUSCEPTIBILITY TO, 5		HP:0100519	OMIM:612925	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0000006	OMIM:612926	TAS				I		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0000093	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0000790	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0000822	OMIM:612926	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0001873	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0001919	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0001937	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0003138	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0003259	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0005575	OMIM:612926	IEA				P		HPO:skoehler	
OMIM	612926	#612926 HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 6; AHUS6;;AHUS, SUSCEPTIBILITY TO, 6		HP:0100519	OMIM:612926	TAS				P		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0000007	OMIM:612932	TAS				I		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0003236	OMIM:612932	TAS				P		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0003326	OMIM:612932	TAS				P		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0003546	OMIM:612932	TAS				P		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0003581	OMIM:612932	TAS				C		HPO:skoehler	
OMIM	612932	GLYCOGEN STORAGE DISEASE XIII; GSD13		HP:0009051	OMIM:612932	TAS				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0000007	OMIM:612933	IEA				I		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0000083	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0002063	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0002151	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0002913	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003201	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003236	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003326	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003394	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003542	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003546	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003552	OMIM:612933	IEA				P		HPO:skoehler	
OMIM	612933	GLYCOGEN STORAGE DISEASE XI; GSD11		HP:0003621	OMIM:612933	IEA				C		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000007	OMIM:612936	IEA				I		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000154	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000218	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000252	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000280	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000303	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000322	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000341	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000414	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0000486	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001181	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001250	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001258	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001263	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001272	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001319	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001347	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0001762	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002079	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002119	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002171	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002200	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002307	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0002510	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0003487	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0003577	OMIM:612936	IEA				C		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0006887	OMIM:612936	IEA				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0010864	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0012811	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612936	#612936 SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3, FORMERLY; CPSQ3, FORMERLY		HP:0100021	OMIM:612936	TAS				P		HPO:skoehler	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0000007	PMID:19576565	PCS				I		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0001324	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0001644	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0002317	OMIM:612937	IEA				P		HPO:skoehler	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0002515	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0002910	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003236	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003391	OMIM:612937	IEA				P		HPO:skoehler	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003557	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003560	OMIM:612937	IEA				P		HPO:skoehler	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003581	OMIM:612937	IEA				C		HPO:skoehler	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003642	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612937	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 15; MDDGC15		HP:0003805	PMID:19576565	PCS				P		HPO:probinson	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000007	OMIM:612938	IEA				I		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000028	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000158	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000175	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000193	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000238	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000252	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000278	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000280	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000407	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000463	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000470	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0000965	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001156	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001250	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001263	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001276	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001305	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001339	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001508	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001511	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001513	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001537	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001629	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001639	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001643	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0001792	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0002678	OMIM:612938	IEA				P		HPO:skoehler	
OMIM	612938	#612938 GROWTH RETARDATION, DEVELOPMENTAL DELAY, COARSE FACIES, AND EARLYDEATH; GDFD		HP:0010808	OMIM:612938	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000007	OMIM:612940	IEA				I		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000238	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000239	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000252	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000272	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000316	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000325	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000337	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000411	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000418	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000490	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000494	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000592	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000601	OMIM:612940	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0000938	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001015	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001263	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001274	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001374	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001382	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001508	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001511	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0001582	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0002007	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0002020	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0002650	OMIM:612940	IEA				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0006487	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0011220	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612940	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIB		HP:0011800	OMIM:612940	TAS				P		HPO:skoehler	
OMIM	612943	#612943 RETINITIS PIGMENTOSA 42; RP42		HP:0000006	OMIM:612943	TAS				I		HPO:skoehler	
OMIM	612943	#612943 RETINITIS PIGMENTOSA 42; RP42		HP:0000510	OMIM:612943	TAS				P		HPO:skoehler	
OMIM	612943	#612943 RETINITIS PIGMENTOSA 42; RP42		HP:0000980	OMIM:612943	TAS				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000007	OMIM:612946	IEA				I		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000089	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000179	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000218	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000252	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000286	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000294	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000358	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000369	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000426	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000463	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000486	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000508	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0000601	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001249	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001252	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001263	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001290	OMIM:612946	TAS				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001321	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001344	OMIM:612946	TAS				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001508	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001620	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001629	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001631	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001636	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0001714	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0002023	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0002079	OMIM:612946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0002750	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0004322	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0004935	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612946	HADZISELIMOVIC SYNDROME		HP:0010806	OMIM:612946	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000007	OMIM:612947	IEA				I		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000028	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000252	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000278	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000286	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000365	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000414	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000455	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000518	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000958	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000964	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0000969	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0001250	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0001263	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0001831	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0002283	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0002750	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0003241	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0004279	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0004322	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0004325	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0008897	OMIM:612947	TAS				P		HPO:skoehler	
OMIM	612947	MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUAL APPEARANCE		HP:0012393	OMIM:612947	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000007	OMIM:612948	IEA				I		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000218	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000219	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000219	OMIM:612948	TAS				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000293	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000307	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000319	OMIM:612948	TAS				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000407	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000455	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000486	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000582	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000608	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000678	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0000817	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0001249	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0001263	OMIM:612948	TAS				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0001274	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0001763	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0002079	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0004209	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0009748	OMIM:612948	IEA				P		HPO:skoehler	
OMIM	612948	612948 STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES		HP:0011229	OMIM:612948	TAS				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0000007	OMIM:612949	IEA				I		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0000817	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0001250	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0001257	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0001263	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0001344	OMIM:612949	TAS				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0001347	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0003593	OMIM:612949	IEA				C		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0006808	OMIM:612949	TAS				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0006829	OMIM:612949	IEA				P		HPO:skoehler	
OMIM	612949	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 39		HP:0200134	OMIM:612949	TAS				P		HPO:skoehler	
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000007	OMIM:612951	IEA				I		HPO:probinson	
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000252	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000295	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000407	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000639	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0000750	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0001250	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0001251	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0001257	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0001332	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0002119	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0002305	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0002352	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0002465	OMIM:612951	TAS				P		HPO:skoehler	
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0002514	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0003593	OMIM:612951	IEA		HP:0040283		C		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0003677	OMIM:612951	TAS				C		HPO:skoehler	
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0007042	OMIM:612951	TAS				P		HPO:skoehler	
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0011344	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612951	#612951 LEUKOENCEPHALOPATHY, CYSTIC, WITHOUT MEGALENCEPHALY		HP:0011400	OMIM:612951	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0000007	OMIM:612952	TAS				I		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0000252	OMIM:612952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0000737	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0000958	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0001257	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0001263	OMIM:612952	TAS				P		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0001371	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0001873	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0002135	OMIM:612952	TAS				P		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0002352	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0002415	OMIM:612952	TAS				P		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0003040	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0003828	OMIM:612952	TAS				C		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0007321	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0008872	OMIM:612952	TAS				P		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0008936	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0009710	OMIM:612952	TAS				P		HPO:probinson	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0040189	OMIM:612952	TAS				P		HPO:skoehler	
OMIM	612952	AICARDI-GOUTIERES SYNDROME 5		HP:0200149	OMIM:612952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0000007	OMIM:612953	TAS				I		HPO:probinson	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0000605	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0000716	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0000718	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0000751	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001257	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001260	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001300	OMIM:612953	TAS				P		HPO:probinson	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001332	OMIM:612953	TAS				P		HPO:probinson	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001337	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0001347	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002063	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002067	OMIM:612953	TAS				P		HPO:probinson	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002145	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002172	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002186	OMIM:612953	IEA				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002283	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0002312	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0003236	OMIM:612953	TAS				P		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0003678	OMIM:612953	TAS				C		HPO:skoehler	
OMIM	612953	PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE; PARK14		HP:0006892	OMIM:612953	TAS				P		HPO:probinson	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0000006	OMIM:612954	IEA				I		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0001265	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0001611	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0001639	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0001761	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0002093	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0002650	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0002936	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003236	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003306	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003388	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003447	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003458	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003560	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003678	OMIM:612954	IEA				C		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003700	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0003715	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0006380	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0006597	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0007108	OMIM:612954	IEA				P		HPO:skoehler	
OMIM	612954	#612954 MYOPATHY, MYOFIBRILLAR, 6; MFM6;;MYOPATHY, MYOFIBRILLAR, BAG3-RELATED		HP:0010628	OMIM:612954	TAS				P		HPO:skoehler	
OMIM	612955	#612955 LONG QT SYNDROME 12; LQT12		HP:0000006	PMID:18591664	PCS				I		HPO:probinson	
OMIM	612955	#612955 LONG QT SYNDROME 12; LQT12		HP:0001279	PMID:18591664	PCS				P		HPO:probinson	
OMIM	612955	#612955 LONG QT SYNDROME 12; LQT12		HP:0001663	OMIM:612955	TAS				P		HPO:skoehler	
OMIM	612955	#612955 LONG QT SYNDROME 12; LQT12		HP:0001664	PMID:10220144	PCS				P		HPO:probinson	
OMIM	612955	#612955 LONG QT SYNDROME 12; LQT12		HP:0005184	PMID:18591664	PCS				P		HPO:probinson	
OMIM	612956	VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2; VF2		HP:0000006	OMIM:612956	TAS				I		HPO:skoehler	
OMIM	612956	VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2; VF2		HP:0001645	OMIM:612956	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612956	VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2; VF2		HP:0001663	OMIM:612956	TAS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0000006	PMID:19589401	PCS				I		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0001440	PMID:19589401	PCS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0002967	PMID:19589401	PCS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0003041	PMID:19589401	PCS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0006064	PMID:19589401	PCS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0008080	OMIM:612961	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0009701	PMID:19589401	PCS				P		HPO:probinson	
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0010055	OMIM:612961	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0010621	OMIM:612961	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	612961	MULTIPLE SYNOSTOSES SYNDROME 3; SYNS3		HP:0011304	OMIM:612961	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0000013	OMIM:612964	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0000786	OMIM:612964	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0000869	OMIM:612964	TAS				P		HPO:skoehler	
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0001470	PMID:19246354	PCS				I		HPO:probinson	
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0002555	OMIM:612964	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0008209	PMID:19246354	PCS				P		HPO:probinson	
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0008232	OMIM:612964	TAS				P		HPO:skoehler	
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0008665	OMIM:612964	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612964	PREMATURE OVARIAN FAILURE 7		HP:0011969	OMIM:612964	TAS				P		HPO:skoehler	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0000013	OMIM:612965	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612965	46,XY SEX REVERSAL 3		HP:0000062	OMIM:612965	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612965	46,XY SEX REVERSAL 3		HP:0000133	OMIM:612965	TAS				P		HPO:probinson	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0000808	OMIM:612965	TAS				P		HPO:skoehler	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0001470	OMIM:612965	TAS				I		HPO:probinson	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0005092	OMIM:612965	TAS				P		HPO:probinson	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0008232	OMIM:612965	TAS				P		HPO:skoehler	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0008665	OMIM:612965	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612965	46,XY SEX REVERSAL 3		HP:0011969	OMIM:612965	TAS				P		HPO:skoehler	
OMIM	612965	46,XY SEX REVERSAL 3		HP:0012245	OMIM:612965	TAS				P		HPO:skoehler	
OMIM	612975	SHORT SLEEPER		HP:0000006	OMIM:612975	IEA				I		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000007	PMID:19327736	PCS				I		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000407	OMIM:612989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000486	OMIM:612989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000543	PMID:19327736	PCS				P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000603	PMID:19327736	PCS	HP:0011463			P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000648	OMIM:612989	TAS				P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000666	OMIM:612989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0000980	OMIM:612989	IEA				P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0001133	OMIM:612989	TAS				P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0001639	OMIM:612989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0003828	OMIM:612989	TAS				C		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7		HP:0007641	OMIM:612989	TAS				P		HPO:skoehler	
OMIM	612989	OPTIC ATROPHY 7 WITH OR WITHOUT AUDITORY NEUROPATHY; OPA7	HP:0012832	HP:0007663	OMIM:612989	TAS				P		HPO:skoehler	
OMIM	612997	#612997 SPERMATOGENIC FAILURE 7; SPGF7;;MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE; MIAR		HP:0000007	OMIM:612997	TAS				I		HPO:probinson	
OMIM	612997	#612997 SPERMATOGENIC FAILURE 7; SPGF7;;MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE; MIAR		HP:0000798	OMIM:612997	TAS				P		HPO:probinson	
OMIM	612997	#612997 SPERMATOGENIC FAILURE 7; SPGF7;;MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE; MIAR		HP:0003251	OMIM:612997	TAS				P		HPO:probinson	
OMIM	612997	#612997 SPERMATOGENIC FAILURE 7; SPGF7;;MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE; MIAR		HP:0012207	OMIM:612997	TAS				P		HPO:probinson	
OMIM	612997	#612997 SPERMATOGENIC FAILURE 7; SPGF7;;MALE INFERTILITY, NONSYNDROMIC, AUTOSOMAL RECESSIVE; MIAR		HP:0012208	OMIM:612997	TAS				P		HPO:skoehler	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0000006	OMIM:612998	TAS				I		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0000467	OMIM:612998	TAS				P		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0003236	OMIM:612998	TAS				P		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0003560	OMIM:612998	IEA				P		HPO:skoehler	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0003701	OMIM:612998	TAS				P		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0005144	OMIM:612998	TAS				P		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0007126	OMIM:612998	TAS				P		HPO:probinson	
OMIM	612998	#612998 EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT; EDMD4;;EMERY-DREIFUSS MUSCULAR DYSTROPHY 4 WITH VARIABLE FEATURES		HP:0011463	OMIM:612998	TAS				C		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0000006	OMIM:612999	TAS				I		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0001638	OMIM:612999	TAS				P		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0002093	OMIM:612999	TAS				P		HPO:skoehler	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0003236	OMIM:612999	TAS				P		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0003560	OMIM:612999	TAS				P		HPO:skoehler	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0003701	OMIM:612999	TAS				P		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0007126	OMIM:612999	TAS				P		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0011463	OMIM:612999	TAS				C		HPO:probinson	
OMIM	612999	#612999 EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT; EDMD5		HP:0011675	OMIM:612999	TAS				P		HPO:probinson	
OMIM	613000	#613000 PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL; FNEPPK;;FOCAL NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA;;KERATODERMA, FOCAL NONEPIDERMOLYTIC PALMOPLANTAR		HP:0000006	OMIM:613000	TAS				I		HPO:probinson	
OMIM	613000	#613000 PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL; FNEPPK;;FOCAL NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA;;KERATODERMA, FOCAL NONEPIDERMOLYTIC PALMOPLANTAR		HP:0000982	OMIM:613000	TAS				P		HPO:probinson	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000028	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000125	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000126	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000238	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000568	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000593	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000625	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0000647	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001031	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001140	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001250	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001263	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001274	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001305	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001321	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001442	OMIM:613001	TAS				I		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001596	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001629	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001631	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0001682	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0002079	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0002132	OMIM:613001	IEA				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0002539	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0003745	OMIM:613001	TAS				I		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0004969	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0007546	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0007676	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0012032	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0025356	OMIM:613001	IEA				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0100251	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613001	ENCEPHALOCRANIOCUTANEOUS LIPOMATOSIS; ECCL		HP:0100702	OMIM:613001	TAS				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0000006	OMIM:613002	IEA				I		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0000007	OMIM:613002	IEA				I		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001249	OMIM:613002	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001250	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001254	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001268	OMIM:613002	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001269	OMIM:613002	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001287	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0001289	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0002171	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0002353	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0003829	OMIM:613002	IEA				C		HPO:skoehler	
OMIM	613002	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 2; IIAE2		HP:0012302	OMIM:613002	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0000006	OMIM:613005	IEA				I		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0001156	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0001159	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0001762	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0001798	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0001840	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0002857	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0004322	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0010442	OMIM:613005	IEA				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0012165	OMIM:613005	TAS				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0100258	OMIM:613005	TAS				P		HPO:skoehler	
OMIM	613005	613005 SANTOS SYNDROME;;FIBULAR AGENESIS/HYPOPLASIA, OLIGODACTYLOUS CLUBFEET, AND ANONYCHIA/NAILHYPOPLASIA SYNDROME		HP:0100259	OMIM:613005	TAS				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0000007	OMIM:613011	IEA				I		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0001744	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0001873	OMIM:613011	TAS				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0001876	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0001903	OMIM:613011	TAS				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0002240	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0002665	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0002716	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0002719	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0002960	OMIM:613011	TAS				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0003565	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0003621	OMIM:613011	IEA				C		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0004315	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0010280	OMIM:613011	IEA				P		HPO:skoehler	
OMIM	613011	#613011 LYMPHOPROLIFERATIVE SYNDROME 1; LPFS1		HP:0011107	OMIM:613011	TAS				P		HPO:skoehler	
OMIM	613013	#613013 NEUROBLASTOMA, SUSCEPTIBILITY TO, 2; NBLST2NEUROBLASTOMA WITH HIRSCHSPRUNG DISEASE, INCLUDED		HP:0000006	OMIM:613013	TAS				I		HPO:probinson	
OMIM	613013	#613013 NEUROBLASTOMA, SUSCEPTIBILITY TO, 2; NBLST2NEUROBLASTOMA WITH HIRSCHSPRUNG DISEASE, INCLUDED		HP:0002251	OMIM:613013	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	613013	#613013 NEUROBLASTOMA, SUSCEPTIBILITY TO, 2; NBLST2NEUROBLASTOMA WITH HIRSCHSPRUNG DISEASE, INCLUDED		HP:0003005	OMIM:613013	TAS		HP:0040284		P		HPO:probinson	5%
OMIM	613013	#613013 NEUROBLASTOMA, SUSCEPTIBILITY TO, 2; NBLST2NEUROBLASTOMA WITH HIRSCHSPRUNG DISEASE, INCLUDED		HP:0006747	OMIM:613013	TAS		HP:0040284		P		HPO:probinson	5%
OMIM	613021	#613021 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2; BESC2;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0000006	OMIM:613021	IEA				I		HPO:skoehler	
OMIM	613021	#613021 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2; BESC2;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0002110	OMIM:613021	IEA				P		HPO:skoehler	
OMIM	613021	#613021 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2; BESC2;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0004469	OMIM:613021	IEA				P		HPO:skoehler	
OMIM	613021	#613021 BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 2; BESC2;;CYSTIC FIBROSIS-LIKE SYNDROME		HP:0012236	OMIM:613021	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613024	FOLLICULAR LYMPHOMA		HP:0002665	OMIM:613024	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000006	OMIM:613026	TAS				I		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000023	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000028	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000047	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000048	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000233	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000252	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000276	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000278	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000322	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000347	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000348	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000369	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000400	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000430	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000431	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000463	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000483	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000508	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000535	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000581	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000637	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000653	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000668	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000670	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0000958	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001195	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001249	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001263	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001508	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001511	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001671	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0001845	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0002164	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0002373	OMIM:613026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0002719	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0003196	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0003745	OMIM:613026	IEA				I		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0003758	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0004209	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0004322	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0006610	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0008872	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0008897	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0010554	OMIM:613026	IEA				P		HPO:skoehler	
OMIM	613026	CHROMOSOME 19Q13.11 DELETION SYNDROME, DISTAL		HP:0012745	OMIM:613026	TAS				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0000007	OMIM:613027	IEA				I		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001252	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001270	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001290	OMIM:613027	TAS				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001394	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001408	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001510	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001744	OMIM:613027	TAS				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0001946	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0002155	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0002240	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0002910	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0003128	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0003162	OMIM:613027	IEA				P		HPO:skoehler	
OMIM	613027	GLYCOGEN STORAGE DISEASE IXC		HP:0003593	OMIM:613027	IEA				C		HPO:skoehler	
OMIM	613029	GLIOMA SUSCEPTIBILITY 3		HP:0000007	OMIM:613029	TAS				I		HPO:skoehler	
OMIM	613029	GLIOMA SUSCEPTIBILITY 3		HP:0002885	OMIM:613029	TAS				P		HPO:skoehler	
OMIM	613029	GLIOMA SUSCEPTIBILITY 3		HP:0009592	OMIM:613029	TAS				P		HPO:skoehler	
OMIM	613029	GLIOMA SUSCEPTIBILITY 3		HP:0012174	OMIM:613029	TAS				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000006	OMIM:613038	TAS				I		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000007	OMIM:613038	TAS				I		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000158	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000270	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000272	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000463	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000490	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000821	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0000952	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0001249	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0001252	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0001290	OMIM:613038	TAS				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0002007	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0003196	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0004322	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0005280	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0006579	OMIM:613038	TAS				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0008850	OMIM:613038	IEA				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0011220	OMIM:613038	TAS				P		HPO:skoehler	
OMIM	613038	PITUITARY HORMONE DEFICIENCY, COMBINED, 1		HP:0011800	OMIM:613038	TAS				P		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0000006	OMIM:613060	TAS				I		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0002069	OMIM:613060	TAS				P		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0002121	OMIM:613060	TAS				P		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0002123	OMIM:613060	TAS				P		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0002373	OMIM:613060	TAS				P		HPO:skoehler	
OMIM	613060	#613060 EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 10; EIG10GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 5, SUSCEPTIBILITYTO, INCLUDED; GEFS5, INCLUDED;;GEFS+, TYPE 5, SUSCEPTIBILITY TO, INCLUDED;;GEFS+5, SUSCEPTIBILITY TO, INCLUDED;;GEFSP5, SUSCEPTIBILITY TO, INCLUDED;;EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 7, INCLUDED; EJM7,INCLUDED		HP:0007359	OMIM:613060	TAS				P		HPO:skoehler	
OMIM	613065	%613065 LEUKEMIA, ACUTE LYMPHOBLASTIC; ALLLEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1, INCLUDED;;ALL1, INCLUDED;;LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1, INCLUDED;;LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, INCLUDED;;LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, INCLUDED;;LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO,INCLUDED		HP:0006721	OMIM:613065	TAS				P		HPO:probinson	
OMIM	613065	%613065 LEUKEMIA, ACUTE LYMPHOBLASTIC; ALLLEUKEMIA, ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, 1, INCLUDED;;ALL1, INCLUDED;;LEUKEMIA, ACUTE LYMPHOCYTIC, SUSCEPTIBILITY TO, 1, INCLUDED;;LEUKEMIA, B-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, INCLUDED;;LEUKEMIA, T-CELL ACUTE LYMPHOBLASTIC, SUSCEPTIBILITY TO, INCLUDED;;LEUKEMIA, ACUTE LYMPHOBLASTIC, B-HYPERDIPLOID, SUSCEPTIBILITY TO,INCLUDED		HP:0010982	OMIM:613065	TAS				I		HPO:probinson	
OMIM	613068	NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY		HP:0000007	OMIM:613068	IEA				I		HPO:skoehler	
OMIM	613068	NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY		HP:0001249	OMIM:613068	IEA				P		HPO:skoehler	
OMIM	613068	NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY		HP:0001250	OMIM:613068	IEA				P		HPO:skoehler	
OMIM	613068	NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY		HP:0002180	OMIM:613068	IEA				P		HPO:skoehler	
OMIM	613068	NEURODEGENERATION DUE TO CEREBRAL FOLATE TRANSPORT DEFICIENCY		HP:0002376	OMIM:613068	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0000007	OMIM:613070	IEA				I		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0000952	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0001290	OMIM:613070	TAS				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0001403	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0001414	OMIM:613070	TAS				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0002013	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0002151	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0002240	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0002904	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0002910	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0003128	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0003256	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0003270	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0006554	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0008872	OMIM:613070	IEA				P		HPO:skoehler	
OMIM	613070	LIVER FAILURE, INFANTILE, TRANSIENT		HP:0200125	OMIM:613070	TAS				P		HPO:skoehler	
OMIM	613071	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3		HP:0000006	OMIM:613071	IEA				I		HPO:skoehler	
OMIM	613071	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3		HP:0002110	OMIM:613071	IEA				P		HPO:skoehler	
OMIM	613071	BRONCHIECTASIS WITH OR WITHOUT ELEVATED SWEAT CHLORIDE 3; BESC3		HP:0004469	OMIM:613071	IEA				P		HPO:skoehler	
OMIM	613073	#613073 METAPHYSEAL ANADYSPLASIA 2; MANDP2		HP:0000007	PMID:19615667	PCS				I		HPO:probinson	
OMIM	613073	#613073 METAPHYSEAL ANADYSPLASIA 2; MANDP2		HP:0002979	PMID:19615667	PCS				P		HPO:probinson	
OMIM	613073	#613073 METAPHYSEAL ANADYSPLASIA 2; MANDP2		HP:0003016	PMID:19615667	PCS				P		HPO:probinson	
OMIM	613073	#613073 METAPHYSEAL ANADYSPLASIA 2; MANDP2		HP:0003025	PMID:19615667	PCS				P		HPO:probinson	
OMIM	613073	#613073 METAPHYSEAL ANADYSPLASIA 2; MANDP2		HP:0100864	PMID:19615667	PCS				P		HPO:probinson	
OMIM	613074	DEAFNESS, AUTOSOMAL DOMINANT 50		HP:0000006	PMID:19363479	PCS				I		HPO:probinson	
OMIM	613074	DEAFNESS, AUTOSOMAL DOMINANT 50		HP:0000360	OMIM:613074	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613074	DEAFNESS, AUTOSOMAL DOMINANT 50		HP:0000407	PMID:19363479	PCS				P		HPO:probinson	
OMIM	613074	DEAFNESS, AUTOSOMAL DOMINANT 50		HP:0000408	OMIM:613074	TAS				P		HPO:skoehler	
OMIM	613074	DEAFNESS, AUTOSOMAL DOMINANT 50		HP:0001730	PMID:19363479	PCS				P		HPO:probinson	
OMIM	613075	MACS SYNDROME		HP:0000007	OMIM:613075	TAS				I		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000028	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0000179	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000212	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000218	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0000280	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000494	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000535	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000766	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000815	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0000939	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0000954	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0000974	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0000978	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001156	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0001252	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001382	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001537	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0001582	OMIM:613075	IEA				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001596	OMIM:613075	IEA				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001620	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0001763	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0002110	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0002650	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0003010	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0004322	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0004325	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0008064	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0008070	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0008661	OMIM:613075	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613075	MACS SYNDROME		HP:0012472	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0040079	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613075	MACS SYNDROME		HP:0100540	OMIM:613075	TAS				P		HPO:skoehler	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0000007	PMID:19409522	PCS				I		HPO:probinson	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0000407	PMID:19409522	PCS				P		HPO:probinson	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0000518	PMID:19409522	PCS				P		HPO:probinson	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0000519	OMIM:613076	IEA				P		HPO:skoehler	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0001263	PMID:19409522	PCS				P		HPO:probinson	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0003198	PMID:19409522	PCS				P		HPO:probinson	
OMIM	613076	#613076 MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARINGLOSS, AND DEVELOPMENTAL DELAY;;MYOPATHY WITH CATARACT AND COMBINED RESPIRATORY CHAIN DEFICIENCY;;MITOCHONDRIAL COMPLEX DEFICIENCY, COMBINED		HP:0008972	PMID:19409522	PCS				P		HPO:probinson	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000006	OMIM:613077	TAS				I		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000365	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000501	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000508	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000590	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000716	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0000739	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0001260	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0001265	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0002015	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0002066	OMIM:613077	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0003198	OMIM:613077	IEA				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0003546	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0003689	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613077	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 5; PEOA5		HP:0003750	OMIM:613077	TAS				P		HPO:skoehler	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY		HP:0000007	OMIM:613078	TAS				I		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY		HP:0000252	OMIM:613078	TAS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY	HP:0012828	HP:0000540	OMIM:613078	TAS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY		HP:0001249	PMID:19409520	PCS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY	HP:0012825	HP:0001251	OMIM:613078	TAS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY	HP:0012825	HP:0001257	OMIM:613078	TAS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY		HP:0004322	PMID:19409520	PCS				P		HPO:probinson	
OMIM	613078	#613078 NIJMEGEN BREAKAGE SYNDROME-LIKE DISORDER; NBSLD;;NBS-LIKE DISORDER;;RAD50 DEFICIENCY;;MICROCEPHALY AND SPONTANEOUS CHROMOSOME INSTABILITY WITHOUT IMMUNODEFICIENCY		HP:0010997	OMIM:613078	TAS				P		HPO:probinson	
OMIM	613079	DEAFNESS, AUTOSOMAL RECESSIVE 77; DFNB77		HP:0000007	OMIM:613079	TAS				I		HPO:probinson	
OMIM	613079	DEAFNESS, AUTOSOMAL RECESSIVE 77; DFNB77		HP:0008619	OMIM:613079	TAS				P		HPO:skoehler	
OMIM	613080	46,XY SEX REVERSAL 5		HP:0000006	OMIM:613080	TAS				I		HPO:probinson	
OMIM	613080	46,XY SEX REVERSAL 5		HP:0000007	OMIM:613080	TAS				I		HPO:skoehler	
OMIM	613080	46,XY SEX REVERSAL 5		HP:0008232	OMIM:613080	TAS				P		HPO:probinson	
OMIM	613080	46,XY SEX REVERSAL 5		HP:0012245	OMIM:613080	TAS				P		HPO:probinson	
OMIM	613086	#613086 GLAUCOMA 3, PRIMARY CONGENITAL, D; GLC3D		HP:0000007	OMIM:613086	TAS				I		HPO:probinson	
OMIM	613086	#613086 GLAUCOMA 3, PRIMARY CONGENITAL, D; GLC3D		HP:0000613	OMIM:613086	TAS				P		HPO:probinson	
OMIM	613086	#613086 GLAUCOMA 3, PRIMARY CONGENITAL, D; GLC3D		HP:0001083	OMIM:613086	TAS		HP:0040284		P		HPO:probinson	1/8
OMIM	613086	#613086 GLAUCOMA 3, PRIMARY CONGENITAL, D; GLC3D		HP:0007957	OMIM:613086	TAS				P		HPO:probinson	
OMIM	613086	#613086 GLAUCOMA 3, PRIMARY CONGENITAL, D; GLC3D		HP:0008007	OMIM:613086	TAS				P		HPO:probinson	
OMIM	613087	#613087 ATRIAL SEPTAL DEFECT 6; ASD6		HP:0000006	OMIM:613087	TAS				I		HPO:probinson	
OMIM	613087	#613087 ATRIAL SEPTAL DEFECT 6; ASD6		HP:0001631	OMIM:613087	TAS				P		HPO:probinson	
OMIM	613087	#613087 ATRIAL SEPTAL DEFECT 6; ASD6		HP:0001662	OMIM:613087	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613087	#613087 ATRIAL SEPTAL DEFECT 6; ASD6		HP:0005110	OMIM:613087	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613089	CAPILLARY MALFORMATION OF THE LOWER LIP, LYMPHATIC MALFORMATION OF FACE AND NECK, ASYMMETRY OF FACE AND LIMBS, AND PARTIAL/GENERALIZED OVERGROWTH		HP:0001004	OMIM:613089	IEA				P		HPO:skoehler	
OMIM	613089	CAPILLARY MALFORMATION OF THE LOWER LIP, LYMPHATIC MALFORMATION OF FACE AND NECK, ASYMMETRY OF FACE AND LIMBS, AND PARTIAL/GENERALIZED OVERGROWTH		HP:0002619	OMIM:613089	IEA				P		HPO:skoehler	
OMIM	613089	CAPILLARY MALFORMATION OF THE LOWER LIP, LYMPHATIC MALFORMATION OF FACE AND NECK, ASYMMETRY OF FACE AND LIMBS, AND PARTIAL/GENERALIZED OVERGROWTH		HP:0012721	OMIM:613089	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000083	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000103	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000127	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000407	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000859	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0000969	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001249	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001252	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001265	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001270	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001290	OMIM:613090	TAS				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001425	OMIM:613090	IEA				I		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001508	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001561	OMIM:613090	TAS				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001563	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0001622	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002900	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002902	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0002914	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003081	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003113	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0003577	OMIM:613090	IEA				C		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0004909	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0012213	OMIM:613090	TAS				P		HPO:skoehler	
OMIM	613090	BARTTER SYNDROME, TYPE 4B, NEONATAL, WITH SENSORINEURAL DEAFNESS		HP:0012605	OMIM:613090	IEA				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000007	OMIM:613091	TAS				I		HPO:probinson	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000054	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000062	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000105	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000110	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000113	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000175	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000204	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000773	OMIM:613091	TAS				P		HPO:probinson	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000888	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000895	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0000895	PMID:23456818	PCS				P		HPO:lccarmody	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0001156	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0001274	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0001762	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0002023	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0002350	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0002566	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0002650	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0002980	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0003016	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0003022	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0003038	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0004322	OMIM:613091	TAS				P		HPO:probinson	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0005054	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0005257	OMIM:613091	TAS				P		HPO:probinson	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0009556	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0010297	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0010454	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0010579	OMIM:613091	TAS				P		HPO:skoehler	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0010984	OMIM:613091	TAS				I		HPO:probinson	
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0011802	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0100258	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613091	#613091 ASPHYXIATING THORACIC DYSTROPHY 3; ATD3		HP:0100259	OMIM:613091	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0000006	OMIM:613092	TAS				I		HPO:skoehler	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0000089	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE	HP:0030650	HP:0000092	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0000097	OMIM:613092	TAS				P		HPO:skoehler	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE	HP:0012825	HP:0001903	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0002149	OMIM:613092	TAS				P		HPO:skoehler	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0004719	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0005576	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613092	#613092 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2; HNFJ2;;EARLY-ONSET HYPERURICEMIA, ANEMIA, AND PROGRESSIVE KIDNEY FAILURE		HP:0012622	OMIM:613092	TAS				P		HPO:probinson	
OMIM	613093	CONE DYSTROPHY 4		HP:0000007	OMIM:613093	IEA				I		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0000505	OMIM:613093	IEA				P		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0000548	OMIM:613093	IEA				P		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0000613	OMIM:613093	IEA				P		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0000639	OMIM:613093	IEA				P		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0007641	OMIM:613093	TAS				P		HPO:skoehler	
OMIM	613093	CONE DYSTROPHY 4		HP:0007663	OMIM:613093	TAS				P		HPO:skoehler	
OMIM	613094	MICROPHTHALMIA, ISOLATED 4		HP:0000006	PMID:19129173	PCS				I		HPO:iea	
OMIM	613094	MICROPHTHALMIA, ISOLATED 4		HP:0000568	PMID:19129173	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	613094	MICROPHTHALMIA, ISOLATED 4		HP:0000589	PMID:19129173	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	613094	MICROPHTHALMIA, ISOLATED 4		HP:0010469	PMID:19129173	PCS				P		HPO:iea	
OMIM	613094	MICROPHTHALMIA, ISOLATED 4		HP:0100259	PMID:19129173	PCS		HP:0040284		P		HPO:iea	1/3
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0000006	OMIM:613095	TAS				I		HPO:probinson	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0000010	OMIM:613095	TAS				P		HPO:skoehler	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0000113	OMIM:613095	TAS				P		HPO:probinson	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0000324	OMIM:613095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0000822	OMIM:613095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0001407	OMIM:613095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0001696	OMIM:613095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0003259	OMIM:613095	TAS				P		HPO:skoehler	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0003676	OMIM:613095	TAS				C		HPO:skoehler	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0003774	OMIM:613095	TAS				P		HPO:skoehler	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0003829	OMIM:613095	TAS				C		HPO:skoehler	
OMIM	613095	POLYCYSTIC KIDNEY DISEASE 2		HP:0011800	OMIM:613095	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0000006	OMIM:613096	IEA				I		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0000012	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0000020	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0000763	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0001258	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0001347	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0001761	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0002064	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0002166	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0003487	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0003676	OMIM:613096	IEA				C		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0007220	OMIM:613096	TAS				P		HPO:probinson	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0007340	OMIM:613096	IEA				P		HPO:skoehler	
OMIM	613096	SPASTIC PARAPLEGIA 36, AUTOSOMAL DOMINANT; SPG36		HP:0011402	OMIM:613096	TAS				P		HPO:probinson	
OMIM	613100	#613100 GLAUCOMA 1, OPEN ANGLE, O; GLC1O		HP:0012108	OMIM:613100	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0000007	PMID:19804848	TAS				I		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0001433	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0001954	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0002155	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0003281	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0012156	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613101	#613101 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5; FHL5		HP:0012177	PMID:19804848	TAS				P		HPO:probinson	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0000007	OMIM:613102	TAS				I		HPO:probinson	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0001006	OMIM:613102	TAS				P		HPO:probinson	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0002209	OMIM:613102	TAS				P		HPO:skoehler	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0002215	OMIM:613102	TAS				P		HPO:skoehler	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0100840	OMIM:613102	TAS				P		HPO:skoehler	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0200037	OMIM:613102	TAS				P		HPO:probinson	
OMIM	613102	#613102 HYPOTRICHOSIS AND RECURRENT SKIN VESICLES		HP:0200102	OMIM:613102	TAS				P		HPO:skoehler	
OMIM	613105	CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2; CACD2		HP:0000006	OMIM:613105	IEA				I		HPO:skoehler	
OMIM	613105	CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2; CACD2		HP:0000533	PMID:14557183	PCS				P		HPO:probinson	
OMIM	613105	CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 2; CACD2		HP:0000613	OMIM:613105	IEA				P		HPO:skoehler	
OMIM	613107	#613107 NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2		HP:0000006	OMIM:613107	TAS				I		HPO:probinson	
OMIM	613107	#613107 NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2		HP:0001875	OMIM:613107	TAS				P		HPO:probinson	
OMIM	613107	#613107 NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2		HP:0010976	OMIM:613107	TAS				P		HPO:probinson	
OMIM	613107	#613107 NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT; SCN2		HP:0012311	OMIM:613107	TAS				P		HPO:probinson	
OMIM	613108	#613108 CANDIDIASIS, FAMILIAL, 4; CANDF4;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS		HP:0000007	PMID:19864674	PCS				I		HPO:probinson	
OMIM	613108	#613108 CANDIDIASIS, FAMILIAL, 4; CANDF4;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS		HP:0012203	PMID:19864674	PCS				P		HPO:probinson	
OMIM	613108	#613108 CANDIDIASIS, FAMILIAL, 4; CANDF4;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS		HP:0012204	PMID:19864674	PCS				P		HPO:probinson	
OMIM	613112	#613112 MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED		HP:0000006	OMIM:613112	IEA				I		HPO:skoehler	
OMIM	613112	#613112 MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED		HP:0040185	OMIM:613112	TAS				P		HPO:skoehler	
OMIM	613112	#613112 MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, TUBB1-RELATED		HP:0040185	OMIM:613112	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0000007	OMIM:613115	IEA				I		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0000020	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0001069	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0001257	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0001265	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0001284	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0002754	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0003477	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0003621	OMIM:613115	IEA				C		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0003676	OMIM:613115	IEA				C		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0006121	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0007460	OMIM:613115	TAS				P		HP:probinson	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0009771	OMIM:613115	IEA				P		HPO:skoehler	
OMIM	613115	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB; HSAN2B		HP:0009771	OMIM:613115	TAS				P		HP:probinson	
OMIM	613116	THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY		HP:0000006	OMIM:613116	TAS				I		HPO:probinson	
OMIM	613116	THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY		HP:0004831	OMIM:613116	TAS				P		HPO:skoehler	
OMIM	613116	THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY		HP:0100724	OMIM:613116	TAS				P		HPO:probinson	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0000006	OMIM:613118	TAS				I		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0000007	OMIM:613118	TAS				I		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0001976	OMIM:613118	TAS				P		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0002204	OMIM:613118	TAS				P		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0002625	OMIM:613118	TAS				P		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0004419	OMIM:613118	TAS				P		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0005305	OMIM:613118	TAS				P		HPO:skoehler	
OMIM	613118	ANTITHROMBIN III DEFICIENCY; AT3D		HP:0025324	OMIM:613118	IEA				P		HPO:skoehler	
OMIM	613119	#613119 BRUGADA SYNDROME 6; BRGDA6		HP:0000006	OMIM:613119	TAS				I		HPO:probinson	
OMIM	613119	#613119 BRUGADA SYNDROME 6; BRGDA6		HP:0001663	OMIM:613119	TAS				P		HPO:probinson	
OMIM	613119	#613119 BRUGADA SYNDROME 6; BRGDA6		HP:0001695	OMIM:613119	TAS				P		HPO:probinson	
OMIM	613119	#613119 BRUGADA SYNDROME 6; BRGDA6		HP:0012251	OMIM:613119	TAS				P		HPO:probinson	
OMIM	613120	BRUGADA SYNDROME 7; BRGDA7		HP:0000006	OMIM:613120	TAS				I		HPO:skoehler	
OMIM	613120	BRUGADA SYNDROME 7; BRGDA7		HP:0004749	OMIM:613120	TAS				P		HPO:probinson	
OMIM	613120	BRUGADA SYNDROME 7; BRGDA7		HP:0012251	OMIM:613120	TAS				P		HPO:probinson	
OMIM	613122	CARDIOMYOPATHY, DILATED, 1CC		HP:0000006	OMIM:613122	TAS				I		HPO:skoehler	
OMIM	613122	CARDIOMYOPATHY, DILATED, 1CC		HP:0001644	OMIM:613122	IEA	HP:0003581			P		HPO:skoehler	
OMIM	613123	#613123 BRUGADA SYNDROME 8; BRGDA8		HP:0004756	OMIM:613123	TAS				P		HPO:probinson	
OMIM	613123	#613123 BRUGADA SYNDROME 8; BRGDA8		HP:0012251	OMIM:613123	TAS				P		HPO:probinson	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0000007	OMIM:613124	IEA				I		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0000463	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0000835	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0001561	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0001790	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0002089	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0005257	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613124	HYDROPS FETALIS, NONIMMUNE, WITH GRACILE BONES AND DYSMORPHIC FEATURES		HP:0009824	OMIM:613124	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0000007	OMIM:613135	IEA				I		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0001263	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0001276	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0001300	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0001337	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002019	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002020	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002062	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002063	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002067	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002072	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002194	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0002451	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0003593	OMIM:613135	IEA				C		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0003676	OMIM:613135	IEA				C		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0007256	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0008936	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0011968	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0031931	OMIM:613135	IEA				P		HPO:skoehler	
OMIM	613135	PARKINSONISM-DYSTONIA, INFANTILE, 1; PKDYS1		HP:0100660	OMIM:613135	TAS				P		HPO:skoehler	
OMIM	613144	%613144 CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 3; CACD3;;CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, WITH OR WITHOUT DRUSEN		HP:0000006	OMIM:613144	IEA				I		HPO:skoehler	
OMIM	613144	%613144 CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 3; CACD3;;CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, WITH OR WITHOUT DRUSEN		HP:0000533	PMID:19696794	IEA				P		HPO:skoehler	
OMIM	613144	%613144 CHOROIDAL DYSTROPHY, CENTRAL AREOLAR 3; CACD3;;CHOROIDAL DYSTROPHY, CENTRAL AREOLAR, WITH OR WITHOUT DRUSEN		HP:0011510	PMID:19696794	PCS		HP:0040284		P		HPO:skoehler	6/21
OMIM	613148	#613148 INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE; IBD28;;INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:613148	TAS				I		HPO:probinson	
OMIM	613148	#613148 INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE; IBD28;;INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE		HP:0000999	OMIM:613148	TAS				P		HPO:probinson	
OMIM	613148	#613148 INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE; IBD28;;INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE		HP:0002573	OMIM:613148	TAS				P		HPO:probinson	
OMIM	613148	#613148 INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE; IBD28;;INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE		HP:0004387	OMIM:613148	TAS				P		HPO:probinson	
OMIM	613148	#613148 INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE; IBD28;;INFLAMMATORY BOWEL DISEASE, EARLY-ONSET, AUTOSOMAL RECESSIVE		HP:0009789	OMIM:613148	TAS				P		HPO:probinson	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000007	OMIM:613150	TAS				I		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000158	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000175	OMIM:613150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000204	OMIM:613150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000238	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000252	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000518	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000540	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000545	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000557	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000568	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0000659	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0001250	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0001302	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0001321	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0001425	OMIM:613150	TAS				I		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002084	OMIM:613150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002119	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002126	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002187	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002350	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002365	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002650	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0002803	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0003236	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0003306	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0003560	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0006829	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0007033	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0007260	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0007370	OMIM:613150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0009917	OMIM:613150	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613150	#613150 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2; MDDGA2;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, POMT2-RELATED		HP:0010864	OMIM:613150	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0000007	OMIM:613151	TAS				I		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0000252	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0000486	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0000545	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0000648	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0001249	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0001270	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0001321	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0002119	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0002350	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0003236	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0003560	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0003577	OMIM:613151	TAS				C		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0003741	OMIM:613151	IEA				P		HPO:skoehler	
OMIM	613151	#613151 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3; MDDGB3;;MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATED		HP:0012110	OMIM:613151	TAS				P		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0000007	OMIM:613152	TAS				I		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0001270	OMIM:613152	TAS				P		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0001290	OMIM:613152	TAS				P		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0003236	OMIM:613152	TAS				P		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0003560	OMIM:613152	TAS				P		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0003593	OMIM:613152	TAS				C		HPO:skoehler	
OMIM	613152	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4		HP:0003741	OMIM:613152	IEA				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000007	OMIM:613153	TAS				I		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000238	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000518	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000541	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000545	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000568	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0000589	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0001265	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5	HP:0012828	HP:0001270	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0001302	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0001305	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0001321	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0001712	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0002093	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0002187	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0002365	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0002500	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0003236	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0003560	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0003577	OMIM:613153	TAS				C		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0003819	OMIM:613153	TAS				M		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0006829	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0007033	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0007260	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0007957	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0012110	OMIM:613153	TAS				P		HPO:skoehler	
OMIM	613153	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5; MDDGA5		HP:0031882	OMIM:613153	IEA				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0000007	OMIM:613154	TAS				I		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0000238	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0000518	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0000648	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0001249	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0001284	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0001305	OMIM:613154	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0001371	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0003236	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0003560	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0006829	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0007260	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0007973	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613154	#613154 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6; MDDGA6;;WALKER-WARBURG SYNDROME OR MUSCLE-EYE-BRAIN DISEASE, LARGE-RELATED		HP:0012110	OMIM:613154	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000007	OMIM:613155	TAS				I		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000158	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000252	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000519	OMIM:613155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000545	OMIM:613155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0000556	OMIM:613155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0001263	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0001321	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0001344	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0001371	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0001638	OMIM:613155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0002079	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0002280	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0002540	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0003236	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0003560	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0003593	OMIM:613155	TAS				C		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0003741	OMIM:613155	IEA				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0005162	OMIM:613155	IEA				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0007033	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0010628	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613155	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1; MDDGB1		HP:0010864	OMIM:613155	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000007	OMIM:613156	TAS				I		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000028	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000054	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000158	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000194	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000252	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000486	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000545	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0000580	OMIM:613156	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001249	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001265	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001270	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001284	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001290	OMIM:613156	TAS	HP:0003577			P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001321	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001371	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0001712	OMIM:613156	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002079	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002093	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002119	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002120	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002650	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0002827	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003236	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003307	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003324	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003560	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003701	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0003741	OMIM:613156	IEA				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0010628	OMIM:613156	TAS				P		HPO:skoehler	
OMIM	613156	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2		HP:0025169	OMIM:613156	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0000007	OMIM:613157	TAS				I		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0000545	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0001270	OMIM:613157	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003236	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003307	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003391	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003551	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003560	OMIM:613157	IEA				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003676	OMIM:613157	TAS				C		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0003712	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613157	#613157 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 3; MDDGC3;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2O; LGMD2O;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMGNT1-RELATED		HP:0012378	OMIM:613157	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0000007	OMIM:613158	TAS				I		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0001270	OMIM:613158	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0003236	OMIM:613158	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0003560	OMIM:613158	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0003593	OMIM:613158	TAS				C		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED	HP:0012825	HP:0003701	OMIM:613158	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0003712	OMIM:613158	TAS				P		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0003828	OMIM:613158	TAS				C		HPO:skoehler	
OMIM	613158	#613158 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 2; MDDGC2;;MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2N; LGMD2N;;MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY, LIMB-GIRDLE, POMT2-RELATED		HP:0011712	OMIM:613158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000007	OMIM:613159	TAS				I		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000090	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000092	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000108	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000407	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0000822	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0001249	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0001250	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0001737	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0003774	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0005583	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0006280	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0030186	OMIM:613159	TAS				P		HPO:skoehler	
OMIM	613159	NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1		HP:0100702	OMIM:613159	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0000007	OMIM:613161	IEA				I		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0000048	OMIM:613161	IEA		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0000252	OMIM:613161	TAS		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0001249	OMIM:613161	IEA		HP:0040284		P		HPO:skoehler	2/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0001263	OMIM:613161	TAS				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0001319	OMIM:613161	TAS				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0001332	OMIM:613161	IEA				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002023	OMIM:613161	IEA		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002133	OMIM:613161	IEA		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002167	OMIM:613161	IEA				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002188	OMIM:613161	IEA				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002521	OMIM:613161	TAS		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002650	OMIM:613161	IEA		HP:0040284		P		HPO:skoehler	1/6
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0002836	OMIM:613161	IEA				P		HPO:skoehler	
OMIM	613161	BETA-UREIDOPROPIONASE DEFICIENCY		HP:0003593	OMIM:613161	IEA				C		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0000007	OMIM:613162	IEA				I		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0000545	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0000639	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0000648	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001249	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001258	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001270	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001347	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001371	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0001762	OMIM:613162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0002064	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0002079	OMIM:613162	TAS				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0003487	OMIM:613162	IEA				P		HPO:skoehler	
OMIM	613162	#613162 SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE; SPG45		HP:0006989	OMIM:613162	TAS				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0000007	OMIM:613163	IEA				I		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0000098	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0000278	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0000494	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001250	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001254	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001263	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001274	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001321	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0001347	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0002415	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0003819	OMIM:613163	IEA				M		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0006829	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0007291	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0025356	OMIM:613163	IEA				P		HPO:skoehler	
OMIM	613163	GABA-TRANSAMINASE DEFICIENCY		HP:0025430	OMIM:613163	TAS				P		HPO:skoehler	
OMIM	613172	#613172 CARDIOMYOPATHY, DILATED, 1DD; CMD1DD		HP:0000006	OMIM:613172	TAS				I		HPO:probinson	
OMIM	613172	#613172 CARDIOMYOPATHY, DILATED, 1DD; CMD1DD		HP:0001635	OMIM:613172	TAS				P		HPO:skoehler	
OMIM	613172	#613172 CARDIOMYOPATHY, DILATED, 1DD; CMD1DD		HP:0001644	OMIM:613172	TAS				P		HPO:probinson	
OMIM	613172	#613172 CARDIOMYOPATHY, DILATED, 1DD; CMD1DD		HP:0001645	OMIM:613172	TAS				P		HPO:probinson	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000218	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000248	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000256	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000262	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000286	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000316	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000322	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000337	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000341	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000369	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000414	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000431	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000483	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000520	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000577	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000581	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000582	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000601	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000722	OMIM:613174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0000733	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001176	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001249	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001250	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001252	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001263	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001274	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001290	OMIM:613174	TAS				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001363	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001518	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0001833	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0002007	OMIM:613174	TAS				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0002162	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0002360	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0002650	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0003745	OMIM:613174	IEA				I		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0008070	OMIM:613174	IEA				P		HPO:skoehler	
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0012745	OMIM:613174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613174	CHROMOSOME 5P13 DUPLICATION SYNDROME		HP:0100807	OMIM:613174	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000007	OMIM:613177	TAS				I		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000015	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000023	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000126	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000272	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000278	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000316	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000340	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000343	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000347	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000431	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0000973	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001290	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001388	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001537	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001601	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001655	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0001852	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002020	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002021	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002035	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002089	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002097	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002617	OMIM:613177	IEA				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002779	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0002780	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0004415	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0011800	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613177	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IC; ARCL1C		HP:0100539	OMIM:613177	TAS				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0000007	OMIM:613179	IEA				I		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0000010	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0000246	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0000388	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0000708	OMIM:613179	TAS				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001249	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001251	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001252	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001264	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001270	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001290	OMIM:613179	TAS				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001337	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001508	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001744	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001888	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001890	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001904	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0001973	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002090	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002273	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002665	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002718	OMIM:613179	TAS				P		HPO:probinson	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002732	OMIM:613179	TAS				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002783	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0002788	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0003537	OMIM:613179	TAS				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0004429	OMIM:613179	TAS				P		HPO:probinson	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0005318	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0005372	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY		HP:0005390	OMIM:613179	IEA				P		HPO:skoehler	
OMIM	613179	PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY	HP:0012828	HP:0005435	OMIM:613179	TAS				P		HPO:probinson	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0000007	OMIM:613180	IEA				I		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0000252	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0000609	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0001250	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0001263	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0001265	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0001319	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0002126	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0002187	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0002365	OMIM:613180	IEA				P		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0003577	OMIM:613180	IEA				C		HPO:skoehler	
OMIM	613180	#613180 POLYMICROGYRIA WITH OPTIC NERVE HYPOPLASIA		HP:0030048	OMIM:613180	TAS				P		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000007	OMIM:613192	TAS				I		HPO:probinson	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000204	OMIM:613192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000316	OMIM:613192	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000319	OMIM:613192	TAS				P		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000322	OMIM:613192	TAS				P		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000431	OMIM:613192	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000470	OMIM:613192	TAS				P		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000601	OMIM:613192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000664	OMIM:613192	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0000752	OMIM:613192	TAS				P		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0001249	OMIM:613192	TAS				P		HPO:probinson	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0001250	OMIM:613192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0001956	OMIM:613192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0002079	OMIM:613192	TAS				P		HPO:probinson	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0002334	OMIM:613192	TAS				P		HPO:probinson	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0002714	OMIM:613192	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0003593	OMIM:613192	TAS				C		HPO:skoehler	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0005484	OMIM:613192	TAS				P		HPO:probinson	
OMIM	613192	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13; MRT13		HP:0031936	OMIM:613192	IEA				P		HPO:skoehler	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:613193	TAS				I		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0000246	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0000403	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0000789	OMIM:613193	TAS				P		HPO:skoehler	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0002837	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0012256	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0012257	OMIM:613193	TAS				P		HPO:probinson	
OMIM	613193	#613193 CILIARY DYSKINESIA, PRIMARY, 13; CILD13;;CILIARY DYSKINESIA, PRIMARY, 13, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:613193	IEA				P		HPO:skoehler	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000006	PMID:19853238	PCS				I		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000510	OMIM:613194	IEA				P		HPO:skoehler	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000512	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000541	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000543	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0000662	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0007663	PMID:19853238	PCS	HP:0003621			P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0007843	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613194	#613194 RETINITIS PIGMENTOSA 50; RP50RETINITIS PIGMENTOSA, CONCENTRIC, INCLUDED		HP:0012045	PMID:19853238	PCS				P		HPO:probinson	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0000007	OMIM:613195	TAS				I		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0000501	OMIM:613195	TAS				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0000545	OMIM:613195	IEA				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0001083	OMIM:613195	TAS				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0004322	OMIM:613195	TAS				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0007906	OMIM:613195	IEA				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0012629	OMIM:613195	IEA				P		HPO:skoehler	
OMIM	613195	WEILL-MARCHESANI SYNDROME 4; WMS4		HP:0100693	OMIM:613195	IEA				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0000007	OMIM:613204	TAS				I		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0001249	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0001270	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0001319	OMIM:613204	TAS				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0001324	OMIM:613204	IEA				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0002650	OMIM:613204	TAS				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0003198	OMIM:613204	TAS	HP:0003577			P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0003202	OMIM:613204	TAS				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY	HP:0012825	HP:0003236	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0003557	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0003593	OMIM:613204	TAS				C		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0003741	OMIM:613204	IEA				P		HPO:skoehler	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0008947	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0012548	OMIM:613204	TAS				P		HPO:probinson	
OMIM	613204	MUSCULAR DYSTROPHY, CONGENITAL, DUE TO INTEGRIN ALPHA-7 DEFICIENCY		HP:0100543	OMIM:613204	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0000006	OMIM:613205	TAS				I		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0000467	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0001270	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0001371	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0001508	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0001558	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0001883	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0002747	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003236	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003306	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003676	OMIM:613205	TAS				C		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003700	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003741	OMIM:613205	IEA				P		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0003828	OMIM:613205	TAS				C		HPO:skoehler	
OMIM	613205	#613205 MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED;;MDCL		HP:0006829	OMIM:613205	TAS				P		HPO:skoehler	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0000007	OMIM:613206	TAS				I		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0000020	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0000407	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0000514	OMIM:613206	TAS				P		HPO:skoehler	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001250	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001258	OMIM:613206	IEA				P		HPO:skoehler	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001260	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001310	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001347	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0001761	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002019	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002061	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002064	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002079	OMIM:613206	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002080	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002352	OMIM:613206	IEA				P		HPO:skoehler	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002650	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0002936	OMIM:613206	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0003487	OMIM:613206	TAS				P		HPO:probinson	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0006986	OMIM:613206	TAS				P		HPO:skoehler	
OMIM	613206	SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44		HP:0100543	OMIM:613206	TAS				P		HPO:skoehler	
OMIM	613211	#613211 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3; AI2A3		HP:0000007	OMIM:613211	TAS				I		HPO:probinson	
OMIM	613211	#613211 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3; AI2A3		HP:0000705	OMIM:613211	TAS				P		HPO:probinson	
OMIM	613211	#613211 AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA3; AI2A3		HP:0011085	OMIM:613211	TAS				P		HPO:probinson	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:613216	IEA				I		HPO:nvasilevsky	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000486	PMID:19896113	PCS				P		HPO:nvasilevsky	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000512	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000545	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000958	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0000964	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0007642	OMIM:613216	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613216	#613216 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C;;CSNB, COMPLETE, AUTOSOMAL RECESSIVE		HP:0007663	OMIM:613216	IEA				P		HPO:skoehler	
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0000007	OMIM:613217	IEA				I		HPO:skoehler	
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0001369	OMIM:613217	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0001508	OMIM:613217	IEA				P		HPO:skoehler	
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0001518	OMIM:613217	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0002041	OMIM:613217	IEA				P		HPO:skoehler	
OMIM	613217	#613217 DIARRHEA 5, WITH TUFTING ENTEROPATHY, CONGENITAL; DIAR5;;ENTEROPATHY, CONGENITAL TUFTING; CTE;;INTESTINAL EPITHELIAL CELL DYSPLASIA		HP:0011473	OMIM:613217	TAS				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000028	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000256	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	3/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000286	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000316	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000369	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000407	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000431	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000465	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000494	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000545	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	2/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000750	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	1/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000957	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000962	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0000969	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001256	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	2/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001263	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001270	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001290	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001555	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001639	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	3/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0001642	OMIM:613224	IEA		HP:0040284		P		HPO:skoehler	3/4
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0002212	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0004322	OMIM:613224	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0004523	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0005280	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0008070	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613224	NOONAN SYNDROME 6; NS6		HP:0032152	OMIM:613224	IEA				P		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0000007	OMIM:613225	TAS				I		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0000421	OMIM:613225	TAS				P		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0000978	OMIM:613225	TAS				P		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0002170	OMIM:613225	TAS				P		HPO:probinson	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0003577	OMIM:613225	TAS				C		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0005261	OMIM:613225	TAS				P		HPO:skoehler	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0007420	OMIM:613225	TAS				P		HPO:probinson	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0008357	OMIM:613225	TAS				P		HPO:probinson	
OMIM	613225	FACTOR XIII, A SUBUNIT, DEFICIENCY OF		HP:0031364	OMIM:613225	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0000007	OMIM:613227	IEA				I		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0000486	OMIM:613227	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0001251	OMIM:613227	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0001256	OMIM:613227	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0001260	OMIM:613227	TAS				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0001337	OMIM:613227	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0001350	OMIM:613227	IEA				P		HPO:skoehler	
OMIM	613227	#613227 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME3; CAMRQ3;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 3		HP:0003577	OMIM:613227	TAS				C		HPO:skoehler	
OMIM	613229	TRICHOTILLOMANIA; TTM		HP:0000006	OMIM:613229	IEA				I		HPO:skoehler	
OMIM	613229	TRICHOTILLOMANIA; TTM		HP:0000722	OMIM:613229	IEA				P		HPO:skoehler	
OMIM	613229	TRICHOTILLOMANIA; TTM		HP:0001426	OMIM:613229	IEA				I		HPO:skoehler	
OMIM	613229	TRICHOTILLOMANIA; TTM		HP:0001596	OMIM:613229	IEA				P		HPO:skoehler	
OMIM	613229	TRICHOTILLOMANIA; TTM		HP:0012167	OMIM:613229	IEA				P		HPO:skoehler	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0000007	OMIM:613235	TAS				I		HPO:skoehler	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0000978	OMIM:613235	TAS				P		HPO:skoehler	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0003577	OMIM:613235	TAS				C		HPO:skoehler	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0004846	OMIM:613235	TAS				P		HPO:probinson	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0008357	OMIM:613235	TAS				P		HPO:probinson	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0011884	OMIM:613235	TAS				P		HPO:probinson	
OMIM	613235	FACTOR XIII, B SUBUNIT, DEFICIENCY OF		HP:0031364	OMIM:613235	IEA				P		HPO:skoehler	
OMIM	613237	#613237 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5; FSGS5;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 5		HP:0000006	OMIM:613237	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	613237	#613237 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5; FSGS5;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 5		HP:0000097	OMIM:613237	IEA				P		HPO:skoehler	
OMIM	613237	#613237 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5; FSGS5;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 5		HP:0000100	OMIM:613237	IEA				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0000836	OMIM:613239	TAS				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0000853	OMIM:613239	TAS				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2	HP:0025303	HP:0001324	OMIM:613239	TAS				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0001425	OMIM:613239	TAS				I		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0001649	OMIM:613239	IEA				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0001962	OMIM:613239	TAS				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0002900	OMIM:613239	IEA				P		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0003745	OMIM:613239	TAS				I		HPO:skoehler	
OMIM	613239	THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2; TTPP2		HP:0003768	OMIM:613239	IEA				P		HPO:skoehler	
OMIM	613241	613241 PSEUDOPILI ANNULATI		HP:0003593	OMIM:613241	TAS				C		HPO:skoehler	
OMIM	613241	613241 PSEUDOPILI ANNULATI		HP:0003745	OMIM:613241	TAS				I		HPO:skoehler	
OMIM	613241	613241 PSEUDOPILI ANNULATI		HP:0010719	OMIM:613241	TAS				P		HPO:skoehler	
OMIM	613241	613241 PSEUDOPILI ANNULATI		HP:0100037	OMIM:613241	TAS				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0000006	OMIM:613243	TAS				I		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0001279	OMIM:613243	IEA				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0001639	OMIM:613243	IEA				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0001663	OMIM:613243	TAS				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0002094	OMIM:613243	IEA				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0005110	OMIM:613243	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0011711	OMIM:613243	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0011712	OMIM:613243	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0012250	OMIM:613243	IEA				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0100749	OMIM:613243	TAS				P		HPO:skoehler	
OMIM	613243	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13; CMH13		HP:0200128	OMIM:613243	IEA				P		HPO:skoehler	
OMIM	613244	#613244 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8; HNPCC8		HP:0006716	OMIM:613244	IEA				P		HPO:skoehler	
OMIM	613251	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14		HP:0000006	OMIM:613251	TAS				I		HPO:skoehler	
OMIM	613251	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14		HP:0001639	OMIM:613251	IEA				P		HPO:skoehler	
OMIM	613252	#613252 CARDIOMYOPATHY, DILATED, 1EE; CMD1EE		HP:0001644	OMIM:613252	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000006	OMIM:613254	IEA				I		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000107	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000169	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000717	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000821	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000826	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0000957	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001249	OMIM:613254	TAS		HP:0040284		P		HPO:skoehler	30%
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001250	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001328	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001425	OMIM:613254	TAS				I		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001482	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0001716	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0002514	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0002888	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0005584	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0006772	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0007018	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009592	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009716	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009717	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009720	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009721	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009724	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009727	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009729	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0009734	OMIM:613254	IEA				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0010762	OMIM:613254	TAS				P		HPO:skoehler	
OMIM	613254	TUBEROUS SCLEROSIS 2; TSC2		HP:0012469	OMIM:613254	TAS				P		HPO:skoehler	
OMIM	613255	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15		HP:0000006	OMIM:613255	TAS				I		HPO:skoehler	
OMIM	613255	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15		HP:0001635	OMIM:613255	TAS				P		HPO:skoehler	
OMIM	613255	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15		HP:0001639	OMIM:613255	IEA				P		HPO:skoehler	
OMIM	613255	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15		HP:0002094	OMIM:613255	IEA				P		HPO:skoehler	
OMIM	613255	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15		HP:0006685	OMIM:613255	TAS				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0000006	OMIM:613265	IEA				I		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0000007	OMIM:613265	IEA				I		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0000407	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0000635	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0001053	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0001100	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0001425	OMIM:613265	IEA				I		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0002211	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0002216	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0002226	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0002227	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613265	WAARDENBURG SYNDROME, TYPE 4B; WS4B		HP:0002251	OMIM:613265	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000006	OMIM:613266	IEA				I		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000028	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000135	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000407	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000458	OMIM:613266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0000635	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0001053	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0001100	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0001425	OMIM:613266	IEA				I		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0002211	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0002216	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0002226	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0002227	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0002251	OMIM:613266	IEA				P		HPO:skoehler	
OMIM	613266	#613266 WAARDENBURG SYNDROME, TYPE 4C; WS4C;;WAARDENBURG SYNDROME WITH HIRSCHSPRUNG DISEASE, TYPE 4C;;WAARDENBURG SYNDROME, TYPE IVC		HP:0007732	OMIM:613266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613267	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3; FECD3		HP:0000006	OMIM:613267	TAS				I		HPO:skoehler	
OMIM	613267	CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 3; FECD3		HP:0000969	OMIM:613267	IEA				P		HPO:skoehler	
OMIM	613268	#613268 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4; FECD4;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0000006	PMID:18024964	PCS				I		HP:probinson	
OMIM	613268	#613268 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4; FECD4;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0000505	PMID:25007886	PCS	HP:0003584			P		HP:probinson	
OMIM	613268	#613268 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4; FECD4;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0001131	PMID:18024964	PCS				P		HPO:skoehler	
OMIM	613268	#613268 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4; FECD4;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0012038	PMID:25007886	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	613270	#613270 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0000491	PMID:24094747	PCS				P		HPO:lccarmody	
OMIM	613270	#613270 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0001131	OMIM:613270	IEA				P		HPO:skoehler	
OMIM	613270	#613270 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0007663	PMID:24094747	PCS				P		HPO:lccarmody	
OMIM	613270	#613270 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0012038	PMID:24094747	PCS				P		HPO:lccarmody	
OMIM	613270	#613270 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6; FECD6;;CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, LATE-ONSET		HP:0012040	PMID:24094747	PCS				P		HPO:lccarmody	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0000007	OMIM:613280	TAS				I		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001260	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001300	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001332	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001337	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001394	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001410	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0001901	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002063	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002067	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002172	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002240	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002313	OMIM:613280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002904	OMIM:613280	IEA				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0002910	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0003376	OMIM:613280	IEA				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0003828	OMIM:613280	TAS				C		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0007010	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0007141	OMIM:613280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613280	HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1		HP:0025196	OMIM:613280	TAS				P		HPO:skoehler	
OMIM	613282	%613282 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1; NAFLD1LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1, INCLUDED		HP:0001397	OMIM:613282	TAS				P		HPO:skoehler	
OMIM	613282	%613282 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1; NAFLD1LIVER DISEASE, ALCOHOLIC, SUSCEPTIBILITY TO, 1, INCLUDED		HP:0001425	OMIM:613282	TAS				I		HPO:skoehler	
OMIM	613285	#613285 DEAFNESS, AUTOSOMAL RECESSIVE 25; DFNB25		HP:0000007	OMIM:613285	IEA				I		HPO:skoehler	
OMIM	613285	#613285 DEAFNESS, AUTOSOMAL RECESSIVE 25; DFNB25		HP:0000408	PMID:20137778	TAS	HP:0011463			P		HPO:skoehler	
OMIM	613286	#613286 CARDIOMYOPATHY, DILATED, 1FF; CMD1FF		HP:0001644	OMIM:613286	IEA				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0000006	OMIM:613287	TAS				I		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0000407	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0001284	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0001761	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0001765	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0002460	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0002936	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0003202	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0003431	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0003477	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0003828	OMIM:613287	TAS				C		HPO:skoehler	
OMIM	613287	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2N		HP:0009027	OMIM:613287	TAS				P		HPO:skoehler	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0000007	OMIM:613291	TAS				I		HPO:probinson	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0001508	OMIM:613291	TAS				P		HPO:skoehler	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0001510	OMIM:613291	TAS				P		HPO:skoehler	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0002028	OMIM:613291	TAS				P		HPO:probinson	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0002570	OMIM:613291	TAS				P		HPO:skoehler	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0003593	OMIM:613291	TAS				C		HPO:skoehler	
OMIM	613291	#613291 BILE ACID MALABSORPTION, PRIMARY; PBAM		HP:0003828	OMIM:613291	TAS				C		HPO:skoehler	
OMIM	613307	DEAFNESS, AUTOSOMAL RECESSIVE 79; DFNB79		HP:0000007	OMIM:613307	TAS				I		HPO:skoehler	
OMIM	613307	DEAFNESS, AUTOSOMAL RECESSIVE 79; DFNB79		HP:0000407	OMIM:613307	IEA	HP:0011463			P		HPO:skoehler	
OMIM	613307	DEAFNESS, AUTOSOMAL RECESSIVE 79; DFNB79		HP:0000408	OMIM:613307	TAS				P		HPO:skoehler	
OMIM	613307	DEAFNESS, AUTOSOMAL RECESSIVE 79; DFNB79		HP:0000750	OMIM:613307	IEA	HP:0011463			P		HPO:skoehler	
OMIM	613308	DIAMOND-BLACKFAN ANEMIA 9		HP:0000006	OMIM:613308	TAS				I		HPO:skoehler	
OMIM	613308	DIAMOND-BLACKFAN ANEMIA 9		HP:0000465	OMIM:613308	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613308	DIAMOND-BLACKFAN ANEMIA 9		HP:0001510	OMIM:613308	TAS				P		HPO:skoehler	
OMIM	613308	DIAMOND-BLACKFAN ANEMIA 9		HP:0001903	OMIM:613308	IEA				P		HPO:skoehler	
OMIM	613308	DIAMOND-BLACKFAN ANEMIA 9		HP:0100512	OMIM:613308	TAS				P		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000006	OMIM:613309	TAS				I		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000086	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000175	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000272	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000347	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000358	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000369	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000405	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000413	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000453	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000475	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0000776	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0001629	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0001643	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0001896	OMIM:613309	TAS				P		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0001903	OMIM:613309	IEA				P		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0001972	OMIM:613309	TAS				P		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0002098	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0003593	OMIM:613309	TAS				C		HPO:skoehler	
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0004322	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0005321	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613309	DIAMOND-BLACKFAN ANEMIA 10		HP:0008551	OMIM:613309	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0000006	OMIM:613310	TAS				I		HPO:skoehler	
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0000594	OMIM:613310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0001147	OMIM:613310	IEA				P		HPO:skoehler	
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0007663	OMIM:613310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0007917	OMIM:613310	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613310	EXUDATIVE VITREORETINOPATHY 5; EVR5		HP:0030490	OMIM:613310	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0000007	OMIM:613312	IEA				I		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0000670	OMIM:613312	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0000685	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0001642	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0002857	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0002970	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0003109	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613312	HYPOPHOSPHATEMIC RICKETS, AUTOSOMAL RECESSIVE, 2; ARHR2		HP:0004912	OMIM:613312	IEA				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0000007	OMIM:613313	TAS				I		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0000135	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0001394	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0001635	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0001638	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0001744	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0001903	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0002240	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0002910	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0003281	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0003452	OMIM:613313	TAS				P		HPO:skoehler	
OMIM	613313	HEMOCHROMATOSIS, TYPE 2B		HP:0011031	OMIM:613313	IEA	HP:0003621			P		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0000007	OMIM:613319	TAS				I		HPO:probinson	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0002460	OMIM:613319	TAS				P		HPO:probinson	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0003236	OMIM:613319	TAS				P		HPO:probinson	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0003551	OMIM:613319	TAS				P		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0003560	OMIM:613319	IEA				P		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0003581	OMIM:613319	TAS				C		HPO:probinson	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0003828	OMIM:613319	TAS				C		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0008981	OMIM:613319	TAS				P		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0009046	OMIM:613319	TAS				P		HPO:skoehler	
OMIM	613319	MIYOSHI MUSCULAR DYSTROPHY 3; MMD3		HP:0009050	OMIM:613319	TAS				P		HPO:probinson	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000007	OMIM:613320	IEA				I		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000239	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000311	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000369	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000445	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000463	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000470	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000773	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000774	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0000822	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0001263	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0001518	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0001591	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0001640	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002002	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002007	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002092	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002375	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002617	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002645	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002657	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002750	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002789	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0002983	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0003021	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0003026	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0003175	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0003177	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0003196	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0004322	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0004565	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0005280	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0008455	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0008551	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0008786	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0008936	OMIM:613320	IEA				P		HPO:skoehler	
OMIM	613320	SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE; SMDMDM		HP:0011220	OMIM:613320	TAS				P		HPO:skoehler	
OMIM	613325	RHABDOID TUMOR PREDISPOSITION SYNDROME 2; RTPS2		HP:0000006	OMIM:613325	TAS				I		HPO:skoehler	
OMIM	613325	RHABDOID TUMOR PREDISPOSITION SYNDROME 2; RTPS2		HP:0030731	OMIM:613325	IEA				P		HPO:skoehler	
OMIM	613325	RHABDOID TUMOR PREDISPOSITION SYNDROME 2; RTPS2		HP:0100006	OMIM:614255	TAS				P		HPO:probinson	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000007	OMIM:613327	IEA				I		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000842	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000855	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000938	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000939	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0000956	OMIM:613327	TAS				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001007	OMIM:613327	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001371	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001397	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001508	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001544	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001649	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001657	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001662	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0001744	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002015	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002019	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002021	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002155	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002240	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002595	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002617	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002650	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002719	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002720	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0002910	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003236	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003306	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003307	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003324	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003326	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003546	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003552	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003560	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003593	OMIM:613327	IEA				C		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003701	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003712	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0003719	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0005110	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0009125	OMIM:613327	IEA				P		HPO:skoehler	
OMIM	613327	LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 4; CGL4		HP:0011968	OMIM:613327	TAS				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000007	OMIM:613328	IEA				I		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000086	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000316	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000431	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000470	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000648	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0000938	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0001369	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0001537	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0001999	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0002090	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0002119	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0002123	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0005280	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0007678	OMIM:613328	TAS				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0009891	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0010049	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0010282	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0010579	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613328	613328 ROIFMAN-CHITAYAT SYNDROME;;COMBINED IMMUNODEFICIENCY, FACIAL DYSMORPHISM, OPTIC NERVE ATROPHY,SKELETAL ANOMALIES, AND DEVELOPMENTAL DELAY		HP:0010743	OMIM:613328	IEA				P		HPO:skoehler	
OMIM	613329	PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY		HP:0000006	OMIM:613329	TAS				I		HPO:probinson	
OMIM	613329	PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY		HP:0000007	OMIM:613329	TAS				I		HPO:probinson	
OMIM	613329	PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY		HP:0000132	OMIM:613329	TAS				P		HPO:probinson	
OMIM	613329	PLASMINOGEN ACTIVATOR INHIBITOR-1 DEFICIENCY		HP:0003577	OMIM:613329	TAS				C		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000007	OMIM:613330	TAS				I		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000256	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000316	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000470	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000773	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0000946	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0001371	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0001538	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0002812	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0002857	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0002970	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0003025	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0003521	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0004288	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0008788	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0009714	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0010580	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0100255	OMIM:613330	TAS				P		HPO:skoehler	
OMIM	613330	SPONDYLO-MEGAEPIPHYSEAL-METAPHYSEAL DYSPLASIA; SMMD		HP:0100569	OMIM:613330	TAS				P		HPO:probinson	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0000006	OMIM:613339	IEA				I		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0001252	OMIM:613339	IEA				P		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0001290	OMIM:613339	TAS				P		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0001425	OMIM:613339	IEA				I		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0002329	OMIM:613339	IEA				P		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0002373	OMIM:613339	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0003621	OMIM:613339	IEA				C		HPO:skoehler	
OMIM	613339	EPILEPSY, HOT WATER, 1		HP:0003829	OMIM:613339	IEA				C		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000007	OMIM:613341	IEA				I		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000510	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000543	OMIM:613341	TAS				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000550	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000613	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000639	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000654	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000662	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0000980	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0002527	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0007663	OMIM:613341	TAS				P		HPO:skoehler	
OMIM	613341	#613341 LEBER CONGENITAL AMAUROSIS 14; LCA14RETINAL DYSTROPHY, EARLY-ONSET SEVERE, LRAT-RELATED, INCLUDED;;RETINITIS PIGMENTOSA, JUVENILE, LRAT-RELATED, INCLUDED		HP:0007875	OMIM:613341	IEA				P		HPO:skoehler	
OMIM	613342	BRACHYDACTYLOUS DWARFISM, MSELENI TYPE		HP:0003510	OMIM:613342	IEA				P		HPO:skoehler	
OMIM	613345	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2		HP:0000006	OMIM:613345	IEA				I		HPO:skoehler	
OMIM	613345	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2		HP:0002900	OMIM:613345	IEA				P		HPO:skoehler	
OMIM	613345	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2		HP:0003198	OMIM:613345	IEA				P		HPO:skoehler	
OMIM	613345	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2		HP:0003752	OMIM:613345	IEA				P		HPO:skoehler	
OMIM	613345	HYPOKALEMIC PERIODIC PARALYSIS, TYPE 2; HOKPP2		HP:0003768	OMIM:613345	IEA				P		HPO:skoehler	
OMIM	613347	#613347 PANCREATIC CANCER, SUSCEPTIBILITY TO, 2;;PNCA2		HP:0002894	OMIM:613347	TAS				P		HPO:probinson	
OMIM	613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD		HP:0000006	OMIM:613353	IEA				I		HPO:skoehler	
OMIM	613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD		HP:0001271	OMIM:613353	IEA				P		HPO:skoehler	
OMIM	613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD		HP:0003477	OMIM:613353	IEA				P		HPO:skoehler	
OMIM	613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD		HP:0009831	OMIM:613353	IEA				P		HPO:skoehler	
OMIM	613353	MONONEUROPATHY OF THE MEDIAN NERVE, MILD		HP:0012185	OMIM:613353	TAS				P		HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0000252	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0000365	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0000718	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0000822	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001238	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001256	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001263	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001518	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001631	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001643	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001647	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001762	OMIM:613355	TAS				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0001999	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0002092	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0003745	OMIM:613355	IEA				I	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0008897	OMIM:613355	TAS				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0010511	OMIM:613355	IEA				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613355	CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME		HP:0100807	OMIM:613355	TAS				P	CHROMOSOME 17Q23.1-Q23.2 DELETION SYNDROME	HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41		HP:0000006	OMIM:613364	TAS				I		HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41		HP:0000012	OMIM:613364	TAS				P		HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41		HP:0001258	OMIM:613364	TAS				P		HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41		HP:0001347	OMIM:613364	TAS				P		HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41		HP:0002064	OMIM:613364	TAS				P		HPO:skoehler	
OMIM	613364	%613364 SPASTIC PARAPLEGIA 41, AUTOSOMAL DOMINANT; SPG41	HP:0012840	HP:0007340	OMIM:613364	TAS				P		HPO:skoehler	
OMIM	613370	#613370 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10		HP:0000006	PMID:18162506	PCS				I		HPO:skoehler	
OMIM	613370	#613370 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10		HP:0001511	PMID:18162506	PCS	HP:0030674			P		HPO:lccarmody	
OMIM	613370	#613370 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10		HP:0001953	PMID:18162506	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	613370	#613370 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10		HP:0003074	PMID:18162506	PCS	HP:0003593			P		HPO:lccarmody	
OMIM	613370	#613370 MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10		HP:0004904	PMID:18162506	PCS	HP:0003593			P		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0000006	OMIM:613371	TAS				I		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0000640	OMIM:613371	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0001251	OMIM:613371	IEA				P		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0001260	OMIM:613371	TAS				P		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0001272	OMIM:613371	TAS				P		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0003581	OMIM:613371	TAS				C		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0003587	OMIM:613371	TAS				C		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0003677	OMIM:613371	TAS				C		HPO:skoehler	
OMIM	613371	SPINOCEREBELLAR ATAXIA 30; SCA30		HP:0007338	OMIM:613371	TAS				P		HPO:skoehler	
OMIM	613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11		HP:0000006	OMIM:613375	TAS				I		HPO:skoehler	
OMIM	613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11		HP:0000819	OMIM:613375	TAS				P		HPO:skoehler	
OMIM	613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11		HP:0001513	OMIM:613375	TAS				P		HPO:skoehler	
OMIM	613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11		HP:0004904	OMIM:613375	IEA				P		HPO:skoehler	
OMIM	613375	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 11		HP:0025502	OMIM:613375	TAS				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0000006	OMIM:613376	IEA				I		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0002355	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0002522	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0002600	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0003202	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0003376	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0003445	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0003677	OMIM:613376	IEA				C		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0007340	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0008959	OMIM:613376	TAS				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0009053	OMIM:613376	TAS				P		HPO:skoehler	
OMIM	613376	#613376 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC; HMN2C;;HMN IIC;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC;;DHMN2C		HP:0009830	OMIM:613376	IEA				P		HPO:skoehler	
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0000006	OMIM:613382	IEA				I		HPO:skoehler	
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0000677	OMIM:613382	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0000684	OMIM:613382	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0001156	OMIM:613382	IEA				P		HPO:skoehler	
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0004322	OMIM:613382	IEA				P		HPO:skoehler	
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0010049	OMIM:613382	IEA				P		HPO:skoehler	
OMIM	613382	BRACHYDACTYLY, TYPE E2; BDE2		HP:0010743	OMIM:613382	IEA				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000007	OMIM:613385	TAS				I		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000268	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000269	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000331	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000358	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000369	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0000520	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0001263	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0001744	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0001999	OMIM:613385	IEA				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0002007	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0002028	OMIM:613385	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0002240	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0002960	OMIM:613385	IEA				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0004482	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0006528	OMIM:613385	IEA				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0012385	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613385	AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM; ADMFD		HP:0030084	OMIM:613385	TAS				P		HPO:skoehler	
OMIM	613387	%613387 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2; NAFLD2		HP:0001397	OMIM:613387	TAS				P		HPO:skoehler	
OMIM	613387	%613387 FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2; NAFLD2		HP:0001425	OMIM:613387	TAS				I		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0000007	OMIM:613388	TAS				I		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0000083	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0000114	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0000938	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0001324	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0002148	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0002150	OMIM:613388	TAS	HP:0011463			P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0002748	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0002909	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0003076	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0004322	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613388	#613388 FANCONI RENOTUBULAR SYNDROME 2; FRTS2		HP:0010639	OMIM:613388	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0000007	OMIM:613390	TAS				I		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0000028	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0000107	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0000126	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0001627	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0002023	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0002984	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0003241	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0003774	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0004322	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0009777	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0009778	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613390	FANCONI ANEMIA, COMPLEMENTATION GROUP O		HP:0025023	OMIM:613390	TAS				P		HPO:skoehler	
OMIM	613391	DEAFNESS, AUTOSOMAL RECESSIVE 84; DFNB84		HP:0000007	OMIM:613391	IEA				I		HPO:skoehler	
OMIM	613391	DEAFNESS, AUTOSOMAL RECESSIVE 84; DFNB84		HP:0000365	OMIM:613391	IEA				P		HPO:skoehler	
OMIM	613391	DEAFNESS, AUTOSOMAL RECESSIVE 84; DFNB84		HP:0001270	OMIM:613391	IEA				P		HPO:skoehler	
OMIM	613391	DEAFNESS, AUTOSOMAL RECESSIVE 84; DFNB84		HP:0001751	OMIM:613391	IEA				P		HPO:skoehler	
OMIM	613391	DEAFNESS, AUTOSOMAL RECESSIVE 84; DFNB84		HP:0003593	OMIM:613391	IEA				C		HPO:skoehler	
OMIM	613392	DEAFNESS, AUTOSOMAL RECESSIVE 85		HP:0000007	PMID:19888295	PCS				I		HPO:skoehler	
OMIM	613392	DEAFNESS, AUTOSOMAL RECESSIVE 85		HP:0000365	PMID:19888295	IEA				P		HPO:probinson	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000007	OMIM:613398	TAS				I		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000154	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000218	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000252	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000274	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000286	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000340	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000365	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000378	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000588	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000954	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0000965	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001249	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001263	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001290	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001511	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001629	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0001636	OMIM:613398	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0004691	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0008586	OMIM:613398	TAS				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0025356	OMIM:613398	IEA				P		HPO:skoehler	
OMIM	613398	WARSAW BREAKAGE SYNDROME; WABS		HP:0030084	OMIM:613398	IEA				P		HPO:skoehler	
OMIM	613399	Familial breast-ovarian cancer-1		HP:0003002	PMID:20400964	PCS	HP:0003596			P	FAMILIAL BREAST-OVARIAN CANCER-1	HPO:probinson	
OMIM	613399	Familial breast-ovarian cancer-1		HP:0025318	PMID:22538716	PCS	HP:0003596			P	FAMILIAL BREAST-OVARIAN CANCER-1	HPO:probinson	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0000007	OMIM:613402	TAS				I		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0000253	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0000752	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0001250	OMIM:613402	IEA				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0001251	OMIM:613402	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0001265	OMIM:613402	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0001270	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0001290	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0002079	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0002119	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0003202	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0009879	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0010864	OMIM:613402	TAS				P		HPO:skoehler	
OMIM	613402	MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY		HP:0200134	OMIM:613402	IEA				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000007	OMIM:613404	TAS				I		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000112	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000121	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000252	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000340	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000369	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0000952	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001263	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001290	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001339	OMIM:613404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001385	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001508	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001629	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001667	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001884	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001942	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0001947	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0002611	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0002804	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0002908	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0002910	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0008064	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0009806	OMIM:613404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613404	ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2		HP:0200084	OMIM:613404	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000006	OMIM:613406	TAS				I		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000023	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000028	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000047	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000054	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000160	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000179	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000194	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000218	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000233	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000252	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000275	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000276	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000286	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000308	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000316	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000319	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000324	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000343	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000348	PMID:19921647	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000356	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000365	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000378	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000400	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000426	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000430	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000431	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000445	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000454	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000463	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000486	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000490	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000494	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000540	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000568	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000582	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000612	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000639	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000687	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000717	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000718	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000750	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000752	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000765	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000776	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000824	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000954	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0000957	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001156	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001166	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001249	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001250	OMIM:613406	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001252	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001256	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001263	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001290	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001388	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001510	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001511	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001513	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001518	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001561	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001608	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0001770	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002079	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002119	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002213	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002360	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002376	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002589	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002650	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002705	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0002719	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0003196	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0003745	PMID:20678247	PCS				I		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0004279	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0004322	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0005280	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0006989	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0007018	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0008872	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0009466	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0009623	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0009778	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0009890	PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0009916	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0010747	PMID:19921647;PMID:20678247	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0030084	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0030260	OMIM:613406	TAS				P		HPO:skoehler	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0030680	PMID:19921647	PCS				P		HPO:iea	
OMIM	613406	WITTEVEEN-KOLK SYNDROME		HP:0100024	PMID:20678247	PCS				P		HPO:iea	
OMIM	613411	#613411 OGUCHI DISEASE 2;;NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 2		HP:0000007	OMIM:613411	IEA				I		HPO:skoehler	
OMIM	613411	#613411 OGUCHI DISEASE 2;;NIGHT BLINDNESS, CONGENITAL STATIONARY, OGUCHI TYPE 2		HP:0007642	OMIM:613411	IEA				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0001508	OMIM:613412	TAS				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0001880	OMIM:613412	IEA				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0002013	OMIM:613412	TAS				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0002015	OMIM:613412	TAS				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0100633	OMIM:613412	TAS				P		HPO:skoehler	
OMIM	613412	ESOPHAGITIS, EOSINOPHILIC, 2; EOE2		HP:0410019	OMIM:613412	TAS				P		HPO:skoehler	
OMIM	613418	#613418 BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15; BMND15;;OSTEOPOROSIS, SUSCEPTIBILITY TO;;METAPHYSEAL FRACTURE, SUSCEPTIBILITY TO;;COMPRESSION FRACTURE, SUSCEPTIBILITY TO		HP:0000006	OMIM:613418	TAS				I		HPO:skoehler	
OMIM	613418	#613418 BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15; BMND15;;OSTEOPOROSIS, SUSCEPTIBILITY TO;;METAPHYSEAL FRACTURE, SUSCEPTIBILITY TO;;COMPRESSION FRACTURE, SUSCEPTIBILITY TO		HP:0000007	OMIM:613418	TAS				I		HPO:skoehler	
OMIM	613418	#613418 BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15; BMND15;;OSTEOPOROSIS, SUSCEPTIBILITY TO;;METAPHYSEAL FRACTURE, SUSCEPTIBILITY TO;;COMPRESSION FRACTURE, SUSCEPTIBILITY TO		HP:0000939	OMIM:613418	TAS				P		HPO:skoehler	
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0000006	OMIM:613424	IEA				I		HPO:skoehler	
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0001635	OMIM:613424	IEA				P		HPO:skoehler	
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0001644	OMIM:613424	IEA				P		HPO:skoehler	
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0001712	OMIM:613424	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0001723	OMIM:613424	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0004308	OMIM:613424	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613424	#613424 CARDIOMYOPATHY, DILATED, 1R; CMD1RLEFT VENTRICULAR NONCOMPACTION 4, INCLUDED; LVNC4, INCLUDED		HP:0030682	OMIM:613424	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0000006	OMIM:613426	TAS				I		HPO:skoehler	
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0001635	OMIM:613426	TAS				P		HPO:skoehler	
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0001644	OMIM:613426	IEA				P		HPO:skoehler	
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0001647	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0001680	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0004308	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0004971	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0005180	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613426	#613426 CARDIOMYOPATHY, DILATED, 1S; CMD1SLEFT VENTRICULAR NONCOMPACTION 5, INCLUDED; LVNC5, INCLUDED		HP:0030682	OMIM:613426	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0000007	OMIM:613428	TAS				I		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0000505	PMID:20398884	PCS				P		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0000510	OMIM:613428	IEA				P		HPO:skoehler	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0000512	OMIM:613428	TAS				P		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0000662	OMIM:613428	TAS				P		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0001099	PMID:20398884	PCS				P		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0007737	OMIM:613428	TAS				P		HPO:probinson	
OMIM	613428	#613428 RETINITIS PIGMENTOSA 54; RP54		HP:0007843	OMIM:613428	TAS				P		HPO:probinson	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0000006	PMID:20428114	TAS				I		HPO:nvasilevsky	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0000007	PMID:20428114	TAS				I		HPO:nvasilevsky	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0001260	OMIM:613435	TAS				P		HPO:probinson	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0001308	OMIM:613435	TAS				P		HPO:probinson	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0001324	OMIM:613435	TAS				P		HPO:probinson	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0002015	OMIM:613435	TAS				P		HPO:probinson	
OMIM	613435	#613435 AMYOTROPHIC LATERAL SCLEROSIS 12; ALS12		HP:0007354	OMIM:613435	IEA				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000006	OMIM:613443	TAS				I		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000316	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000322	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000331	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000337	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000369	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000463	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000582	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0000817	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0001250	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0001270	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0001290	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0002119	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0002518	OMIM:613443	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0002540	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0002714	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0003196	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0003745	OMIM:613443	TAS				I		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0005280	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0010864	OMIM:613443	TAS				P		HPO:skoehler	
OMIM	613443	MENTAL RETARDATION, AUTOSOMAL DOMINANT 20		HP:0200134	OMIM:613443	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000007	OMIM:613451	TAS				I		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000252	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000316	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000431	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000456	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000457	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000535	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000582	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000633	OMIM:613451	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000653	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0000966	OMIM:613451	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0001249	OMIM:613451	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0001320	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0001363	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0001596	OMIM:613451	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0002079	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0002084	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0002697	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0003828	OMIM:613451	TAS				C		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0005280	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0010761	OMIM:613451	IEA				P		HPO:skoehler	
OMIM	613451	FRONTONASAL DYSPLASIA 2; FND2		HP:0012745	OMIM:613451	TAS				P		HPO:skoehler	
OMIM	613453	#613453 DEAFNESS, AUTOSOMAL RECESSIVE 91; DFNB91		HP:0000007	OMIM:613453	TAS				I		HPO:probinson	
OMIM	613453	#613453 DEAFNESS, AUTOSOMAL RECESSIVE 91; DFNB91		HP:0001730	OMIM:613453	TAS				P		HPO:probinson	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0000006	OMIM:613454	TAS				I		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0000253	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0000737	OMIM:613454	IEA				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0000817	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001250	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001257	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001270	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001302	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001319	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001332	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001762	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0001763	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002019	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002020	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002072	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002079	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002186	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002305	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002307	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002353	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002376	OMIM:613454	IEA				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002650	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0002808	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0003745	OMIM:613454	TAS				I		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0003763	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0009879	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0010864	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0012448	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0100660	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613454	RETT SYNDROME, CONGENITAL VARIANT		HP:0100703	OMIM:613454	TAS				P		HPO:skoehler	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000007	OMIM:613456	TAS				I		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000175	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000248	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000316	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000368	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000430	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000431	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000568	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000636	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0000653	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0001249	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0002006	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0002057	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613456	#613456 FRONTONASAL DYSPLASIA 3; FND3		HP:0002223	OMIM:613456	TAS				P		HPO:probinson	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000028	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000160	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000218	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000252	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000286	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000325	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000343	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000347	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000369	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000377	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000445	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000490	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000581	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000648	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0000817	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001250	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001257	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001263	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001319	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001347	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001357	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001508	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001510	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001629	OMIM:613457	TAS		HP:0040283		P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001643	OMIM:613457	TAS		HP:0040283		P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0001655	OMIM:613457	TAS		HP:0040283		P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0002079	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0002421	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0002540	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0003196	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0003745	OMIM:613457	TAS				I	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0005280	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0010864	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0011400	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0012745	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613457	CHROMOSOME 14q11-q22 DELETION SYNDROME		HP:0100704	OMIM:613457	TAS				P	CHROMOSOME 14Q11-Q22 DELETION SYNDROME	HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000006	OMIM:613458	TAS				I		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000272	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000276	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000369	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000411	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000414	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000508	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000582	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000729	OMIM:613458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0000767	OMIM:613458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001182	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001256	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001263	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001629	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001631	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001761	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0001831	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0002827	OMIM:613458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0003196	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0003745	OMIM:613458	TAS				I		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0009623	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0009803	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0011800	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613458	CHROMOSOME 16P13.3 DUPLICATION SYNDROME		HP:0012385	OMIM:613458	TAS				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000007	OMIM:613464	TAS				I		HPO:probinson	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000510	OMIM:613464	IEA				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000608	OMIM:613464	TAS				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000613	OMIM:613464	TAS				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000662	OMIM:613464	TAS				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0000980	OMIM:613464	IEA				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0007663	OMIM:613464	TAS				P		HPO:skoehler	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0007737	OMIM:613464	TAS				P		HPO:probinson	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0007843	OMIM:613464	TAS				P		HPO:probinson	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0008323	OMIM:613464	TAS				P		HPO:probinson	
OMIM	613464	RETINITIS PIGMENTOSA 51; RP51		HP:0011003	OMIM:613464	TAS				P		HPO:skoehler	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0000007	OMIM:613470	TAS				I		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0000952	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001082	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001249	OMIM:613470	TAS				P		HPO:skoehler	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001251	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001324	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001744	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0001930	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0003568	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0005525	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0010871	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0011981	OMIM:613470	TAS				P		HPO:probinson	
OMIM	613470	#613470 HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASEDEFICIENCY		HP:0011993	PMID:4076245	PCS				P		HPO:probinson	
OMIM	613471	REYNOLDS SYNDROME		HP:0000006	OMIM:613471	TAS				I		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0000214	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0000952	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0000989	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0001744	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002239	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002240	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002570	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002613	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002904	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0002910	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0003155	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0003761	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0011838	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0025520	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0030880	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0100324	OMIM:613471	IEA				P		HPO:skoehler	
OMIM	613471	REYNOLDS SYNDROME		HP:0100869	OMIM:613471	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0000006	OMIM:613477	TAS				I		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0000253	OMIM:613477	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0001250	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0001272	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0001290	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0001347	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0002059	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0002079	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0002187	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0002510	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0002521	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0003429	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0003593	OMIM:613477	TAS				C		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0003828	OMIM:613477	TAS				C		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0007366	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0010864	OMIM:613477	TAS				P		HPO:skoehler	
OMIM	613477	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5		HP:0200134	OMIM:613477	IEA				P		HPO:skoehler	
OMIM	613480	#613480 LYMPHEDEMA, HEREDITARY, IC;;LMPH1C		HP:0000006	OMIM:613480	TAS				I		HPO:skoehler	
OMIM	613480	#613480 LYMPHEDEMA, HEREDITARY, IC;;LMPH1C		HP:0001004	OMIM:613480	TAS				P		HPO:skoehler	
OMIM	613480	#613480 LYMPHEDEMA, HEREDITARY, IC;;LMPH1C		HP:0001581	OMIM:613480	TAS				P		HPO:skoehler	
OMIM	613480	#613480 LYMPHEDEMA, HEREDITARY, IC;;LMPH1C		HP:0003829	OMIM:613480	TAS				C		HPO:skoehler	
OMIM	613480	#613480 LYMPHEDEMA, HEREDITARY, IC;;LMPH1C		HP:0100658	OMIM:613480	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0000006	OMIM:613485	IEA				I		HPO:probinson	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0000822	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001279	OMIM:613485	IEA				P		HPO:probinson	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001635	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001649	OMIM:613485	IEA				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001657	OMIM:613485	IEA				P		HPO:probinson	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001677	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001678	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0001695	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0002204	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0004757	OMIM:613485	TAS				P		HPO:skoehler	
OMIM	613485	LONG QT SYNDROME 13; LQT13		HP:0005110	OMIM:613485	IEA				P		HPO:probinson	
OMIM	613488	#613488 MYXOID LIPOSARCOMA		HP:0001428	OMIM:613488	IEA				I		HPO:probinson	
OMIM	613488	#613488 MYXOID LIPOSARCOMA		HP:0012268	OMIM:613488	TAS				P		HPO:probinson	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0000007	OMIM:613489	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0000252	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0000639	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0000737	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001250	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001251	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001276	OMIM:613489	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001290	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001344	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001394	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001399	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001508	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001744	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0001999	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002028	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002059	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002079	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002205	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002240	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0002910	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0003155	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0004798	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0008936	OMIM:613489	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0011968	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613489	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj; CDG2J		HP:0100874	OMIM:613489	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIJ; CDG2J	HPO:skoehler	HP:0040283
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0000007	OMIM:613490	TAS				I		HPO:skoehler	
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0001394	OMIM:613490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0001402	OMIM:613490	TAS				P		HPO:skoehler	
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0002094	OMIM:613490	TAS				P		HPO:skoehler	
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0002097	OMIM:613490	IEA				P		HPO:skoehler	
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0002910	OMIM:613490	TAS				P		HPO:skoehler	
OMIM	613490	ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD		HP:0006510	OMIM:613490	TAS				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0000007	OMIM:613493	TAS				I		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0000403	OMIM:613493	TAS				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0000509	OMIM:613493	TAS				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0002718	OMIM:613493	TAS				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0002721	OMIM:613493	IEA				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0004313	OMIM:613493	TAS				P		HPO:skoehler	
OMIM	613493	#613493 IMMUNODEFICIENCY, COMMON VARIABLE, 3; CVID3;;ANTIBODY DEFICIENCY DUE TO CD19 DEFECT		HP:0011108	OMIM:613493	TAS				P		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0000007	OMIM:613494	TAS				I		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0002718	OMIM:613494	TAS				P		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0002721	OMIM:613494	TAS				P		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0003581	OMIM:613494	TAS				C		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0004315	OMIM:613494	TAS				P		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0006532	OMIM:613494	TAS				P		HPO:skoehler	
OMIM	613494	#613494 IMMUNODEFICIENCY, COMMON VARIABLE, 4; CVID4;;ANTIBODY DEFICIENCY DUE TO BAFFR DEFECT		HP:0011108	OMIM:613494	TAS				P		HPO:skoehler	
OMIM	613495	#613495 IMMUNODEFICIENCY, COMMON VARIABLE, 5; CVID5;;ANTIBODY DEFICIENCY DUE TO CD20 DEFECT		HP:0000007	OMIM:613495	TAS				I		HPO:skoehler	
OMIM	613495	#613495 IMMUNODEFICIENCY, COMMON VARIABLE, 5; CVID5;;ANTIBODY DEFICIENCY DUE TO CD20 DEFECT		HP:0002205	OMIM:613495	TAS				P		HPO:skoehler	
OMIM	613495	#613495 IMMUNODEFICIENCY, COMMON VARIABLE, 5; CVID5;;ANTIBODY DEFICIENCY DUE TO CD20 DEFECT		HP:0002718	OMIM:613495	TAS				P		HPO:skoehler	
OMIM	613495	#613495 IMMUNODEFICIENCY, COMMON VARIABLE, 5; CVID5;;ANTIBODY DEFICIENCY DUE TO CD20 DEFECT		HP:0002721	OMIM:613495	TAS				P		HPO:skoehler	
OMIM	613495	#613495 IMMUNODEFICIENCY, COMMON VARIABLE, 5; CVID5;;ANTIBODY DEFICIENCY DUE TO CD20 DEFECT		HP:0004313	OMIM:613495	TAS				P		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0000007	OMIM:613496	TAS				I		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0000979	OMIM:613496	TAS				P		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0002205	OMIM:613496	TAS				P		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0002718	OMIM:613496	TAS				P		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0002721	OMIM:613496	IEA				P		HPO:skoehler	
OMIM	613496	#613496 IMMUNODEFICIENCY, COMMON VARIABLE, 6; CVID6;;ANTIBODY DEFICIENCY DUE TO CD81 DEFECT		HP:0004313	OMIM:613496	TAS				P		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0000007	OMIM:613500	TAS				I		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0001287	OMIM:613500	TAS				P		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0002718	OMIM:613500	TAS				P		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0003593	OMIM:613500	TAS				C		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0004432	OMIM:613500	TAS				P		HPO:skoehler	
OMIM	613500	#613500 AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO IGLL1 DEFECT		HP:0006532	OMIM:613500	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0000007	OMIM:613501	TAS				I		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0000403	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0001508	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0001875	OMIM:613501	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0002014	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0002718	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0002837	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613501	#613501 AGAMMAGLOBULINEMIA 3, AUTOSOMAL RECESSIVE; AGM3;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO CD79A DEFECT		HP:0004432	OMIM:613501	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0000007	OMIM:613502	TAS				I		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0000403	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0001875	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0002014	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0002718	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0003593	OMIM:613502	TAS				C		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0004432	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0006532	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613502	#613502 AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE; AGM4;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO BLNK DEFECT		HP:0011109	OMIM:613502	TAS				P		HPO:skoehler	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT		HP:0000006	OMIM:613506	TAS				I		HPO:probinson	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT		HP:0000218	OMIM:613506	TAS				P		HPO:probinson	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT		HP:0000286	OMIM:613506	TAS				P		HPO:probinson	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT	HP:0012825	HP:0000316	OMIM:613506	TAS				P		HPO:probinson	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT		HP:0000369	OMIM:613506	TAS				P		HPO:probinson	
OMIM	613506	#613506 AGAMMAGLOBULINEMIA 5, AUTOSOMAL DOMINANT; AGM5;;AGAMMAGLOBULINEMIA, AUTOSOMAL DOMINANT, DUE TO LRRC8A DEFECT		HP:0004432	OMIM:613506	TAS				P		HPO:probinson	
OMIM	613507	#613507 GLYCOGEN STORAGE DISEASE XV; GSD15;;GSD XV;;GLYCOGENIN DEFICIENCY;;GYG1 DEFICIENCY		HP:0000007	OMIM:613507	TAS				I		HPO:skoehler	
OMIM	613507	#613507 GLYCOGEN STORAGE DISEASE XV; GSD15;;GSD XV;;GLYCOGENIN DEFICIENCY;;GYG1 DEFICIENCY		HP:0001324	OMIM:613507	TAS				P		HPO:skoehler	
OMIM	613507	#613507 GLYCOGEN STORAGE DISEASE XV; GSD15;;GSD XV;;GLYCOGENIN DEFICIENCY;;GYG1 DEFICIENCY		HP:0004308	OMIM:613507	TAS				P		HPO:skoehler	
OMIM	613507	#613507 GLYCOGEN STORAGE DISEASE XV; GSD15;;GSD XV;;GLYCOGENIN DEFICIENCY;;GYG1 DEFICIENCY		HP:0011712	OMIM:613507	TAS				P		HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0000316	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0000322	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0000337	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0001263	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0001290	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0002007	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0002714	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0003745	OMIM:613509	TAS				I	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0006872	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME	HP:0012828	HP:0008897	OMIM:613509	TAS				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613509	CHROMOSOME 4q21 DELETION SYNDROME		HP:0025356	OMIM:613509	IEA				P	CHROMOSOME 4Q21 DELETION SYNDROME	HPO:skoehler	
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0000007	OMIM:613517	TAS				I		HPO:skoehler	
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0000482	OMIM:613517	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0000568	OMIM:613517	IEA				P		HPO:skoehler	
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0007906	OMIM:613517	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0008052	OMIM:613517	IEA				P		HPO:skoehler	
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0008499	OMIM:613517	IEA				P		HPO:skoehler	
OMIM	613517	MICROPHTHALMIA, ISOLATED 6; MCOP6		HP:0030823	OMIM:613517	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0000006	OMIM:613530	TAS				I		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0001265	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0001324	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003236	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003560	OMIM:613530	IEA				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003677	OMIM:613530	TAS				C		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003687	OMIM:613530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003701	OMIM:613530	IEA				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003724	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003828	OMIM:613530	TAS				C		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0003829	OMIM:613530	TAS				C		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0008981	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613530	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1H; LGMD1H		HP:0009025	OMIM:613530	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000023	OMIM:613544	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000218	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000219	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000286	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000316	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000343	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000369	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000377	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000455	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000470	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000582	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000601	OMIM:613544	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0000954	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0001263	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0001290	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0001537	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0003196	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0003745	OMIM:613544	TAS				I		HPO:skoehler	
OMIM	613544	CHROMOSOME 6Q11-Q14 DELETION SYNDROME		HP:0004322	OMIM:613544	TAS				P		HPO:skoehler	
OMIM	613546	AROMATASE DEFICIENCY		HP:0000007	OMIM:613546	TAS				I		HPO:probinson	
OMIM	613546	AROMATASE DEFICIENCY		HP:0000138	OMIM:613546	TAS				P		HPO:probinson	
OMIM	613546	AROMATASE DEFICIENCY		HP:0000786	OMIM:613546	TAS				P		HPO:probinson	
OMIM	613546	AROMATASE DEFICIENCY		HP:0000815	OMIM:613546	TAS				P		HPO:probinson	
OMIM	613546	AROMATASE DEFICIENCY		HP:0002750	OMIM:613546	TAS				P		HPO:probinson	
OMIM	613546	AROMATASE DEFICIENCY		HP:0010458	OMIM:613546	TAS				P		HPO:probinson	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000007	OMIM:613550	TAS				I		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000090	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000092	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000103	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000108	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000486	OMIM:613550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000546	OMIM:613550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0000639	OMIM:613550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0001263	OMIM:613550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0001395	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0001510	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0001903	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0001959	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0003774	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0005583	OMIM:613550	TAS				P		HPO:skoehler	
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0009916	OMIM:613550	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613550	NEPHRONOPHTHISIS 11; NPHP11		HP:0025356	OMIM:613550	IEA				P		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0000006	OMIM:613554	TAS				I		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0000007	OMIM:613554	TAS				I		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0000132	OMIM:613554	TAS				P		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0000421	OMIM:613554	TAS				P		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0000978	OMIM:613554	TAS				P		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0001873	OMIM:613554	IEA				P		HPO:skoehler	
OMIM	613554	VON WILLEBRAND DISEASE, TYPE 2; VWD2		HP:0003828	OMIM:613554	TAS				C		HPO:skoehler	
OMIM	613558	#613558 DEAFNESS, AUTOSOMAL DOMINANT 51; DFNA51;;CHROMOSOME 9Q21.11 DUPLICATION SYNDROME		HP:0000006	OMIM:613558	TAS				I		HPO:skoehler	
OMIM	613558	#613558 DEAFNESS, AUTOSOMAL DOMINANT 51; DFNA51;;CHROMOSOME 9Q21.11 DUPLICATION SYNDROME		HP:0000365	OMIM:613558	IEA				P		HPO:skoehler	
OMIM	613558	#613558 DEAFNESS, AUTOSOMAL DOMINANT 51; DFNA51;;CHROMOSOME 9Q21.11 DUPLICATION SYNDROME		HP:0003676	OMIM:613558	TAS				C		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000007	OMIM:613559	TAS				I		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000505	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000508	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000602	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000639	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0000648	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001251	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001260	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001263	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001271	OMIM:613559	IEA				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001284	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001290	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001349	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0001508	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0002151	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0002376	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0002490	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0002590	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0002936	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0003202	OMIM:613559	TAS				P		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0003676	OMIM:613559	TAS				C		HPO:skoehler	
OMIM	613559	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7		HP:0025356	OMIM:613559	IEA				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0000007	OMIM:613561	TAS				I		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0000486	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0000508	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0000639	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0001508	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0001510	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0001639	OMIM:613561	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0001924	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0002015	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0002151	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0002240	OMIM:613561	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0002747	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0002910	OMIM:613561	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0003128	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0003323	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0003546	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0003676	OMIM:613561	TAS				C		HPO:skoehler	
OMIM	613561	#613561 MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2		HP:0003700	OMIM:613561	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000006	OMIM:613563	TAS				I		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000028	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000286	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000316	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000325	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000343	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000358	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000369	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000400	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000465	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000470	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000494	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000508	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000750	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000767	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0000957	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001004	OMIM:613563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001263	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001290	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001382	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001388	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001561	OMIM:613563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001647	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001650	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0001653	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0002002	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0002007	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0002213	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0002967	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0004322	OMIM:613563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0005280	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0006610	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0008070	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0010310	OMIM:613563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0012209	OMIM:613563	TAS				P		HPO:probinson	
OMIM	613563	NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA		HP:0012471	OMIM:613563	TAS				P		HPO:skoehler	
OMIM	613571	#613571 DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY;;ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASEDEFICIENCY;;DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY		HP:0000007	OMIM:613571	IEA				I		HPO:skoehler	
OMIM	613571	#613571 DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY;;ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASEDEFICIENCY;;DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY		HP:0000062	OMIM:613571	IEA				P		HPO:skoehler	
OMIM	613571	#613571 DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY;;ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASEDEFICIENCY;;DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY		HP:0003154	OMIM:613571	IEA				P		HPO:skoehler	
OMIM	613571	#613571 DISORDERED STEROIDOGENESIS DUE TO CYTOCHROME P450 OXIDOREDUCTASE DEFICIENCY;;ADRENAL HYPERPLASIA, CONGENITAL, DUE TO CYTOCHROME P450 OXIDOREDUCTASEDEFICIENCY;;DISORDERED STEROIDOGENESIS DUE TO POR DEFICIENCY		HP:0008258	OMIM:613571	IEA				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000007	OMIM:613573	TAS				I		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000535	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000653	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000687	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000698	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0000968	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0001800	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0002046	OMIM:613573	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0002208	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0002209	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0002232	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0002550	OMIM:613573	TAS				P		HPO:skoehler	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0003777	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0005709	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0006297	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0010554	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613573	ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1		HP:0010765	OMIM:613573	TAS				P		HPO:probinson	
OMIM	613575	#613575 RETINITIS PIGMENTOSA 55; RP55		HP:0000007	PMID:19956407	PCS				I		HPO:probinson	
OMIM	613575	#613575 RETINITIS PIGMENTOSA 55; RP55		HP:0000510	PMID:19956407	PCS				P		HPO:probinson	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000007	OMIM:613576	TAS				I		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000219	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000400	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000968	OMIM:613576	IEA				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000975	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0000982	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0001006	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0001159	OMIM:613576	IEA				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0001640	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0006297	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2	HP:0012825	HP:0007475	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613576	%613576 ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2; EDSS2		HP:0007502	OMIM:613576	TAS				P		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0000007	OMIM:613581	TAS				I		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0000510	OMIM:613581	IEA				P		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0000580	OMIM:613581	IEA				P		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0000662	OMIM:613581	TAS				P		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0007663	OMIM:613581	TAS				P		HPO:skoehler	
OMIM	613581	RETINITIS PIGMENTOSA 56; RP56		HP:0007787	OMIM:613581	TAS				P		HPO:skoehler	
OMIM	613582	#613582 RETINITIS PIGMENTOSA 57; RP57		HP:0000007	OMIM:613582	TAS				I		HPO:skoehler	
OMIM	613582	#613582 RETINITIS PIGMENTOSA 57; RP57		HP:0000510	OMIM:613582	IEA				P		HPO:skoehler	
OMIM	613582	#613582 RETINITIS PIGMENTOSA 57; RP57		HP:0000543	OMIM:613582	TAS				P		HPO:skoehler	
OMIM	613582	#613582 RETINITIS PIGMENTOSA 57; RP57		HP:0007843	OMIM:613582	TAS				P		HPO:skoehler	
OMIM	613582	#613582 RETINITIS PIGMENTOSA 57; RP57		HP:0011505	OMIM:613582	TAS				P		HPO:skoehler	
OMIM	613587	#613587 OCCULT MACULAR DYSTROPHY; OCMD;;OMD		HP:0000006	PMID:20826268	PCS				I		HPO:probinson	
OMIM	613587	#613587 OCCULT MACULAR DYSTROPHY; OCMD;;OMD	HP:0003831	HP:0007754	PMID:20826268	PCS		HP:0040281		P		HPO:probinson	HP:0040281
OMIM	613587	#613587 OCCULT MACULAR DYSTROPHY; OCMD;;OMD		HP:0007924	PMID:20826268	PCS				P		HPO:skoehler	
OMIM	613587	#613587 OCCULT MACULAR DYSTROPHY; OCMD;;OMD		HP:0030468	PMID:20826268	PCS				P		HPO:probinson	
OMIM	613589	LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6		HP:0000006	OMIM:613589	TAS				I		HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000006	OMIM:613603	TAS				I	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000238	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000256	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000286	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000308	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000322	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000369	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000431	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000494	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0000508	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0001263	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0002007	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0002019	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0002251	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0003196	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0008551	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613603	#613603 CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME		HP:0045025	OMIM:613603	TAS				P	#613603 CHROMOSOME 4Q32.1-Q32.2 TRIPLICATION SYNDROME	HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000194	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000218	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000219	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000276	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000286	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000347	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000348	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000358	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000365	OMIM:613604	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000369	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000414	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000490	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0000494	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0001156	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0001249	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0001263	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0001290	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0001511	OMIM:613604	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0002007	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0003196	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0003745	OMIM:613604	TAS				I		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0004322	OMIM:613604	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0011968	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0012368	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0012385	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0030084	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0045025	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613604	CHROMOSOME 16P12.2-P11.2 DELETION SYNDROME, 7.1- TO 8.7-MB		HP:0410018	OMIM:613604	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000007	OMIM:613606	TAS				I		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000252	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000369	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000400	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000426	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000490	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000750	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0000939	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0001263	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0001873	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0002007	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0002750	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0004322	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613606	%613606 FORSYTHE-WAKELING SYNDROME; FWS;;MICROCEPHALY AND GROWTH RETARDATION WITH CHILDHOOD-ONSET NEPHROTICSYNDROME AND THROMBOCYTOPENIA		HP:0004325	OMIM:613606	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0000006	OMIM:613608	TAS				I		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0001312	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0001336	OMIM:613608	TAS	HP:0003581			P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0001337	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0001340	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0001351	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0002069	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0002355	OMIM:613608	TAS	HP:0003581			P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0003581	OMIM:613608	TAS				C		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0003680	OMIM:613608	TAS				C		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0007359	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0010852	OMIM:613608	TAS				P		HPO:skoehler	
OMIM	613608	%613608 EPILEPSY, FAMILIAL ADULT MYOCLONIC, 3; FAME3;;CORTICAL MYOCLONIC TREMOR WITH EPILEPSY, FAMILIAL, 3; FCMTE3		HP:0011463	OMIM:613608	TAS				C		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000007	OMIM:613610	TAS				I		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000023	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000083	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000107	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000175	OMIM:613610	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000218	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000232	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000268	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000278	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000286	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000289	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000293	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000316	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000319	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000341	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000347	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000348	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000369	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000377	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000431	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000470	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000476	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000506	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000581	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000582	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000653	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000687	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000691	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000767	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000773	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000774	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000888	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000968	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0000973	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001156	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001159	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001162	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001357	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001363	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001388	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001396	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001408	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001561	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001643	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001655	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001712	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001744	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001748	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001789	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0001941	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002007	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002240	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002613	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002676	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002904	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0002910	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0003027	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0005280	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0006580	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0008070	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0008905	OMIM:613610	TAS				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0011330	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0011800	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0030084	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0030151	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0045025	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613610	CRANIOECTODERMAL DYSPLASIA 2; CED2		HP:0045075	OMIM:613610	IEA				P		HPO:skoehler	
OMIM	613611	#613611 CHOANAL ATRESIA AND LYMPHEDEMA		HP:0000007	OMIM:613611	TAS				I		HPO:skoehler	
OMIM	613611	#613611 CHOANAL ATRESIA AND LYMPHEDEMA		HP:0000218	OMIM:613611	TAS				P		HPO:skoehler	
OMIM	613611	#613611 CHOANAL ATRESIA AND LYMPHEDEMA		HP:0000453	OMIM:613611	TAS				P		HPO:skoehler	
OMIM	613611	#613611 CHOANAL ATRESIA AND LYMPHEDEMA		HP:0001004	OMIM:613611	IEA				P		HPO:skoehler	
OMIM	613611	#613611 CHOANAL ATRESIA AND LYMPHEDEMA		HP:0001698	OMIM:613611	TAS				P		HPO:skoehler	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0000007	OMIM:613612	TAS				I	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0001249	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0001252	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0001272	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0002078	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0003642	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613612	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; CDG2I;;CDG IIi; CDGIIi		HP:0007366	OMIM:613612	TAS				P	#613612 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE III; CDG2I;;CDG III; CDGIII	HPO:probinson	
OMIM	613615	#613615 SENIOR-LOKEN SYNDROME 7; SLSN7		HP:0000007	OMIM:613615	TAS				I		HPO:probinson	
OMIM	613615	#613615 SENIOR-LOKEN SYNDROME 7; SLSN7		HP:0000090	OMIM:613615	TAS				P		HPO:probinson	
OMIM	613615	#613615 SENIOR-LOKEN SYNDROME 7; SLSN7		HP:0000546	OMIM:613615	TAS				P		HPO:probinson	
OMIM	613616	#613616 HYPEROXALURIA, PRIMARY, TYPE III; HP3		HP:0000007	PMID:20797690	TAS				I		HPO:probinson	
OMIM	613616	#613616 HYPEROXALURIA, PRIMARY, TYPE III; HP3		HP:0003159	PMID:20797690	TAS				P		HPO:probinson	
OMIM	613616	#613616 HYPEROXALURIA, PRIMARY, TYPE III; HP3		HP:0008672	PMID:20797690	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0000007	OMIM:613617	TAS				I		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0000510	OMIM:613617	IEA				P		HPO:skoehler	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0000543	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0000662	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0001141	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0007737	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0007843	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0007994	OMIM:613617	TAS				P		HPO:skoehler	
OMIM	613617	RETINITIS PIGMENTOSA 58		HP:0008323	OMIM:613617	TAS				P		HPO:probinson	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0000006	OMIM:613618	TAS				I	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0001385	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0001762	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0001792	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0002673	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0002857	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613618	#613618 CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME		HP:0008807	OMIM:613618	TAS				P	#613618 CHROMOSOME 17Q23.1-Q23.2 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000007	OMIM:613623	TAS				I		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000218	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000219	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000260	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000268	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000286	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000343	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000358	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000369	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000463	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000822	OMIM:613623	IEA				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0000960	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001004	OMIM:613623	IEA				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001263	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001274	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001290	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001511	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001562	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001622	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001643	OMIM:613623	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0001667	OMIM:613623	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0002020	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0002092	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613623	AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA		HP:0006799	OMIM:613623	TAS				P		HPO:skoehler	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0000007	OMIM:613625	TAS				I		HPO:probinson	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0000132	OMIM:613625	TAS				P		HPO:probinson	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0000421	OMIM:613625	TAS				P		HPO:probinson	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0001934	OMIM:613625	TAS				P		HPO:probinson	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0003125	OMIM:613625	TAS				P		HPO:probinson	
OMIM	613625	#613625 FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF, 2; F5F8D2		HP:0003225	OMIM:613625	TAS				P		HPO:probinson	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000007	OMIM:613627	TAS				I		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000252	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000286	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000389	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000410	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000414	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000508	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0000582	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0001156	OMIM:613627	IEA				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0001249	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0001792	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0001991	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0002650	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0004322	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0005819	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0010241	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613627	613627 BRACHYDACTYLY, TYPE A1, WITH SHORT STATURE, SCOLIOSIS, MICROCEPHALY,PTOSIS, HEARING LOSS, AND MENTAL RETARDATION;;TSUKAHARA SYNDROME		HP:0010743	OMIM:613627	TAS				P		HPO:skoehler	
OMIM	613628	%613628 ODONTOID HYPOPLASIA		HP:0000006	OMIM:613628	TAS				I		HPO:skoehler	
OMIM	613628	%613628 ODONTOID HYPOPLASIA		HP:0003311	OMIM:613628	TAS				P		HPO:skoehler	
OMIM	613628	%613628 ODONTOID HYPOPLASIA		HP:0003467	OMIM:613628	TAS				P		HPO:skoehler	
OMIM	613628	%613628 ODONTOID HYPOPLASIA		HP:0008462	OMIM:613628	TAS				P		HPO:skoehler	
OMIM	613628	%613628 ODONTOID HYPOPLASIA		HP:0040143	OMIM:613628	TAS				P		HPO:skoehler	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0000007	OMIM:613630	IEA				I		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0000042	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0000252	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0000963	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0001539	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0009816	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0009824	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0009892	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0009939	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0010808	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613630	#613630 COCOON SYNDROME;;FETAL ENCASEMENT SYNDROME		HP:0011136	OMIM:613630	IEA				P		HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000252	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000256	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000340	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000486	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000494	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000609	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000639	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000648	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0000750	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0001250	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0001263	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0001548	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002007	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002013	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002014	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002019	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002027	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0002119	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0003186	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0007099	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0010864	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0011968	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613638	CHROMOSOME 19p13.13 DELETION SYNDROME		HP:0100716	PMID:20613546	PCS				P	CHROMOSOME 19P13.13 DELETION SYNDROME	HPO:probinson	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0000006	OMIM:613640	TAS				I		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0000970	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0001218	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0001760	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0002460	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0002754	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0002936	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0006984	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0007141	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0012534	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613640	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC; HSAN1C		HP:0200042	OMIM:613640	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0000007	OMIM:613641	TAS				I		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0001263	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0001265	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0001284	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0001761	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0002936	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0003376	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0009027	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613641	#613641 CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE B; CMTRIB;;CHARCOT-MARIE-TOOTH NEUROPATHY, RECESSIVE INTERMEDIATE B; RI-CMTB		HP:0009588	OMIM:613641	TAS				P		HPO:skoehler	
OMIM	613642	#613642 CARDIOMYOPATHY, DILATED, 1GG; CMD1GG		HP:0000007	OMIM:613642	TAS				I		HPO:probinson	
OMIM	613642	#613642 CARDIOMYOPATHY, DILATED, 1GG; CMD1GG		HP:0001644	OMIM:613642	TAS	HP:0003623			P		HPO:probinson	
OMIM	613646	#613646 METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT;;METHYLMALONIC ACIDEMIA, TCblR TYPE		HP:0000007	OMIM:613646	TAS				I	#613646 METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT;;METHYLMALONIC ACIDEMIA, TCBLR TYPE	HPO:probinson	
OMIM	613646	#613646 METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT;;METHYLMALONIC ACIDEMIA, TCblR TYPE		HP:0012120	OMIM:613646	TAS				P	#613646 METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT;;METHYLMALONIC ACIDEMIA, TCBLR TYPE	HPO:probinson	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0000007	OMIM:613647	TAS				I		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0000020	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0000488	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001249	OMIM:613647	IEA				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001258	OMIM:613647	IEA				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001263	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001268	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001300	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0001310	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0002061	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0002064	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0002079	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0002136	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0002518	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0003676	OMIM:613647	TAS				C		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0007340	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613647	SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE; SPG48		HP:0009830	OMIM:613647	TAS				P		HPO:skoehler	
OMIM	613652	#613652 C1q DEFICIENCY; C1QD		HP:0000007	OMIM:613652	TAS				I	#613652 C1Q DEFICIENCY; C1QD	HPO:skoehler	
OMIM	613652	#613652 C1q DEFICIENCY; C1QD		HP:0000793	OMIM:613652	TAS		HP:0040283		P	#613652 C1Q DEFICIENCY; C1QD	HPO:probinson	HP:0040283
OMIM	613652	#613652 C1q DEFICIENCY; C1QD		HP:0002719	OMIM:613652	TAS				P	#613652 C1Q DEFICIENCY; C1QD	HPO:probinson	
OMIM	613652	#613652 C1q DEFICIENCY; C1QD		HP:0002725	OMIM:613652	TAS		HP:0040283		P	#613652 C1Q DEFICIENCY; C1QD	HPO:probinson	HP:0040283
OMIM	613652	#613652 C1q DEFICIENCY; C1QD		HP:0005356	OMIM:613652	TAS				P	#613652 C1Q DEFICIENCY; C1QD	HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0000006	OMIM:613657	TAS				I		HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0001250	OMIM:613657	TAS				P		HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0001252	OMIM:613657	TAS				P		HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0001263	OMIM:613657	TAS				P		HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0001638	OMIM:613657	TAS				P		HPO:probinson	
OMIM	613657	#613657 D-2-@HYDROXYGLUTARIC ACIDURIA 2;;D2HGA2		HP:0012321	OMIM:613657	TAS				P		HPO:probinson	
OMIM	613658	Rajab syndrome		HP:0000007	PMID:29979980	PCS				I	RAJAB SYNDROME	HPO:skoehler	
OMIM	613658	Rajab syndrome		HP:0000252	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HPO:skoehler	8/8
OMIM	613658	Rajab syndrome		HP:0000601	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0000767	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0001252	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	5/5
OMIM	613658	Rajab syndrome		HP:0001328	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	7/7
OMIM	613658	Rajab syndrome		HP:0001394	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0001903	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	7/7
OMIM	613658	Rajab syndrome		HP:0002315	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	7/7
OMIM	613658	Rajab syndrome		HP:0002514	PMID:29979980,PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	3/4
OMIM	613658	Rajab syndrome		HP:0002566	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0002650	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0002750	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	7/7
OMIM	613658	Rajab syndrome		HP:0002753	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	7/7
OMIM	613658	Rajab syndrome		HP:0002910	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0003546	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	8/8
OMIM	613658	Rajab syndrome		HP:0004322	PMID:19161147	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	8/8
OMIM	613658	Rajab syndrome		HP:0004349	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613658	Rajab syndrome		HP:0004944	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/2
OMIM	613658	Rajab syndrome		HP:0006530	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	5/5
OMIM	613658	Rajab syndrome		HP:0011220	PMID:29979980	PCS		HP:0040284		P	RAJAB SYNDROME	HP:probinson	2/5
OMIM	613659	#613659 GASTRIC CANCERGASTRIC CANCER, INTESTINAL, INCLUDED		HP:0001428	OMIM:613659	TAS				I		HPO:skoehler	
OMIM	613659	#613659 GASTRIC CANCERGASTRIC CANCER, INTESTINAL, INCLUDED		HP:0012126	OMIM:613659	TAS				P		HPO:skoehler	
OMIM	613659	#613659 GASTRIC CANCERGASTRIC CANCER, INTESTINAL, INCLUDED		HP:0410067	PMID:2311216	PCS				P		HPO:NicoleVasilevsky	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000007	OMIM:613660	TAS				I		HPO:skoehler	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000510	OMIM:613660	IEA				P		HPO:skoehler	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000529	OMIM:613660	TAS				P		HPO:skoehler	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000548	OMIM:613660	IEA				P		HPO:skoehler	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000551	OMIM:613660	TAS				P		HPO:skoehler	
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000613	OMIM:613660	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613660	#613660 CONE-ROD DYSTROPHY 15; CORD15RETINITIS PIGMENTOSA 65, INCLUDED; RP65, INCLUDED		HP:0000662	OMIM:613660	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0000007	OMIM:613661	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0000252	OMIM:613661	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	HP:0040283
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0000348	OMIM:613661	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	HP:0040283
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0000407	OMIM:613661	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	HP:0040283
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0000486	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0001250	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0001263	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0001319	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0001344	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P	HP:0031796	HP:0002013	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0002179	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0003186	OMIM:613661	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	HP:0040283
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0003593	OMIM:613661	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0003642	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0005968	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0011968	OMIM:613661	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613661	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip; CDG1P		HP:0025356	OMIM:613661	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IP; CDG1P	HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0000007	OMIM:613662	TAS				I		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0000365	OMIM:613662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0000590	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0001250	OMIM:613662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0001251	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0001263	OMIM:613662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0001290	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0001533	OMIM:613662	IEA				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0002019	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0002024	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0002027	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0002500	OMIM:613662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0002579	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003270	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003324	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003434	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003593	OMIM:613662	TAS				C		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003676	OMIM:613662	TAS				C		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003737	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0003828	OMIM:613662	TAS				C		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0004326	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613662	MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE); MTDPS4B		HP:0004395	OMIM:613662	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0000007	OMIM:613668	TAS				I		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0000253	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0001250	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0001257	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY	HP:0012828	HP:0001263	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0001508	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0002015	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0002169	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY	HP:0012828	HP:0002506	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0002521	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0003676	OMIM:613668	TAS				C		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0005484	OMIM:613668	IEA				P		HPO:skoehler	
OMIM	613668	#613668 MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY		HP:0011968	OMIM:613668	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000006	OMIM:613670	TAS				I		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000194	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000256	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000278	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000316	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000455	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000486	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000494	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000639	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000718	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000733	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES	HP:0012828	HP:0000750	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0000752	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0001249	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0001290	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0001513	OMIM:613670	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0002186	OMIM:613670	IEA				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0002194	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0003196	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0011220	OMIM:613670	TAS				P		HPO:skoehler	
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0012448	OMIM:613670	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613670	MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES		HP:0031936	OMIM:613670	IEA				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000007	OMIM:613671	TAS				I		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000540	OMIM:613671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000565	OMIM:613671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000646	OMIM:613671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000709	OMIM:613671	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000736	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0000750	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0001263	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0002465	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0010807	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613671	#613671 MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS;MRAMS		HP:0010864	OMIM:613671	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0000007	OMIM:613672	TAS				I		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0000639	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0000648	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0000712	OMIM:613672	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0000750	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0001260	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0001265	OMIM:613672	TAS	HP:0003584			P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0001347	OMIM:613672	IEA				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0002313	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0002497	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0003487	OMIM:613672	TAS				P		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0003677	OMIM:613672	TAS				C		HPO:skoehler	
OMIM	613672	SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE; SPAX4		HP:0031936	OMIM:613672	IEA				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0000006	OMIM:613673	TAS				I		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0001639	OMIM:613673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0001744	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0001789	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0001923	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0002240	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0002904	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0003577	OMIM:613673	TAS				C		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0004322	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0010972	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613673	#613673 ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV; CDAN4		HP:0012132	OMIM:613673	TAS				P		HPO:skoehler	
OMIM	613674	#613674 VESICOURETERAL REFLUX 3; VUR3		HP:0000006	OMIM:613674	TAS				I		HPO:skoehler	
OMIM	613674	#613674 VESICOURETERAL REFLUX 3; VUR3		HP:0000072	OMIM:613674	TAS				P		HPO:skoehler	
OMIM	613674	#613674 VESICOURETERAL REFLUX 3; VUR3		HP:0000076	OMIM:613674	TAS				P		HPO:skoehler	
OMIM	613674	#613674 VESICOURETERAL REFLUX 3; VUR3		HP:0000126	OMIM:613674	TAS				P		HPO:skoehler	
OMIM	613674	#613674 VESICOURETERAL REFLUX 3; VUR3		HP:0001561	OMIM:613674	TAS				P		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000006	OMIM:613675	TAS				I		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000098	PMID:20543202	PCS		HP:0040284		P		HPO:iea	13/28
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000256	PMID:20543202	PCS		HP:0040284		P		HPO:iea	9/23
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000280	PMID:20543202	PCS		HP:0040284		P		HPO:iea	17/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000316	PMID:20543202	PCS		HP:0040284		P		HPO:iea	25/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000324	PMID:20543202	PCS		HP:0040284		P		HPO:iea	8/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000365	PMID:20543202	PCS		HP:0040284		P		HPO:iea	3/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000369	PMID:20543202	PCS		HP:0040284		P		HPO:iea	4/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000475	PMID:20543202	PCS		HP:0040284		P		HPO:iea	9/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000486	PMID:20543202	PCS		HP:0040284		P		HPO:iea	4/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000750	PMID:20543202	PCS		HP:0040284		P		HPO:iea	14/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000767	PMID:20543202	PCS		HP:0040284		P		HPO:iea	9/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000957	PMID:20543202	PCS		HP:0040284		P		HPO:iea	27/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0000997	PMID:20543202	PCS		HP:0040284		P		HPO:iea	28/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001176	PMID:20543202	PCS		HP:0040284		P		HPO:iea	13/28
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001249	OMIM:613675	TAS		HP:0040284		P		HPO:skoehler	38%
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001250	PMID:20543202	PCS		HP:0040284		P		HPO:iea	2/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001252	PMID:20543202	PCS		HP:0040284		P		HPO:iea	13/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001263	PMID:20543202	PCS		HP:0040284		P		HPO:iea	14/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001290	OMIM:613675	TAS				P		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001328	PMID:20543202	PCS		HP:0040284		P		HPO:iea	13/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001382	PMID:20543202	PCS		HP:0040284		P		HPO:iea	21/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001548	OMIM:613675	TAS				P		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001627	OMIM:613675	TAS				P		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001761	PMID:20543202	PCS		HP:0040284		P		HPO:iea	5/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0001833	OMIM:613675	TAS		HP:0040284		P		HPO:skoehler	46%
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0002650	PMID:20543202	PCS		HP:0040284		P		HPO:iea	12/28
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0003745	OMIM:613675	PCS				I		HPO:iea	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0007018	PMID:20543202	PCS		HP:0040284		P		HPO:iea	8/24
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0007183	PMID:20543202	PCS		HP:0040284		P		HPO:iea	13/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0009732	PMID:20543202	PCS		HP:0040284		P		HPO:iea	22/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0009734	PMID:20543202	PCS		HP:0040284		P		HPO:iea	5/27
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0009735	PMID:20543202	PCS		HP:0040284		P		HPO:iea	9/14
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0009737	PMID:20543202	PCS		HP:0040284		P		HPO:iea	27/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0012062	PMID:20543202	PCS		HP:0040284		P		HPO:iea	8/16
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0030052	OMIM:613675	TAS				P		HPO:skoehler	
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0030680	PMID:20543202	PCS		HP:0040284		P		HPO:iea	8/28
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0100543	PMID:20543202	PCS		HP:0040284		P		HPO:iea	27/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0100697	PMID:20543202	PCS		HP:0040284		P		HPO:iea	6/29
OMIM	613675	CHROMOSOME 17Q11.2 DELETION SYNDROME, 1.4-MB		HP:0100698	PMID:20543202	PCS		HP:0040284		P		HPO:iea	22/29
OMIM	613676	SECKEL SYNDROME 4		HP:0000007	OMIM:613676	TAS				I		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000252	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000278	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000348	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000369	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000430	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0000878	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0001511	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0004322	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0004325	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0010455	OMIM:613676	TAS				P		HPO:skoehler	
OMIM	613676	SECKEL SYNDROME 4		HP:0100543	OMIM:613676	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0000006	OMIM:613677	TAS				I		HPO:probinson	
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0000103	OMIM:613677	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0000822	OMIM:613677	TAS				P		HPO:probinson	
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0000859	OMIM:613677	TAS				P		HPO:probinson	
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0001942	OMIM:613677	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0001959	OMIM:613677	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0002150	OMIM:613677	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0002900	OMIM:613677	TAS				P		HPO:skoehler	
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0003351	OMIM:613677	TAS				P		HPO:probinson	
OMIM	613677	#613677 HYPERALDOSTERONISM, FAMILIAL, TYPE III;;FH III		HP:0008221	OMIM:613677	TAS				P		HPO:probinson	
OMIM	613678	%613678 BRACHYOLMIA TYPE 2;;BRACHYOLMIA, MAROTEAUX TYPE		HP:0000007	OMIM:613678	TAS				I		HPO:skoehler	
OMIM	613678	%613678 BRACHYOLMIA TYPE 2;;BRACHYOLMIA, MAROTEAUX TYPE		HP:0000926	OMIM:613678	TAS				P		HPO:skoehler	
OMIM	613678	%613678 BRACHYOLMIA TYPE 2;;BRACHYOLMIA, MAROTEAUX TYPE		HP:0004322	OMIM:613678	TAS				P		HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0000007	PMID:7740448	PCS				I	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0000132	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0000225	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0000421	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0000978	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0002239	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0003010	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0003577	OMIM:613679	TAS				C	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0003645	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0003828	OMIM:613679	TAS				C	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0005261	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0008151	OMIM:613679	TAS				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613679	Congenital prothrombin deficiency		HP:0031364	OMIM:613679	IEA				P	CONGENITAL PROTHROMBIN DEFICIENCY	HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000007	OMIM:613680	TAS				I		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000010	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000085	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000104	OMIM:613680	IEA				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000252	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000348	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000490	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000545	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000581	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000582	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000670	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0000689	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0001249	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0001263	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0001643	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0001999	OMIM:613680	IEA				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0003189	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0009765	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0009890	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0012745	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613680	BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS		HP:0030127	OMIM:613680	TAS				P		HPO:skoehler	
OMIM	613681	CHROMOSOME 2Q31.1 DUPLICATION SYNDROME		HP:0000006	OMIM:613681	TAS				I		HPO:skoehler	
OMIM	613681	CHROMOSOME 2Q31.1 DUPLICATION SYNDROME		HP:0001762	OMIM:613681	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613681	CHROMOSOME 2Q31.1 DUPLICATION SYNDROME		HP:0004322	OMIM:613681	TAS				P		HPO:skoehler	
OMIM	613681	CHROMOSOME 2Q31.1 DUPLICATION SYNDROME		HP:0012043	OMIM:613681	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613681	CHROMOSOME 2Q31.1 DUPLICATION SYNDROME		HP:0012725	OMIM:613681	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000006	OMIM:613684	TAS				I		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000189	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000218	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000252	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000278	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000347	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000444	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000448	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000494	OMIM:613684	IEA				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000527	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000670	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000689	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000729	OMIM:613684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000750	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0000752	OMIM:613684	IEA				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0001159	OMIM:613684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0001256	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0001263	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0001290	OMIM:613684	IEA				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0002194	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0002566	OMIM:613684	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0003577	OMIM:613684	TAS				C		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0003745	OMIM:613684	TAS				I		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0008523	OMIM:613684	TAS				P		HPO:probinson	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0010055	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0011094	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0011304	OMIM:613684	TAS				P		HPO:skoehler	
OMIM	613684	RUBINSTEIN-TAYBI SYNDROME 2; RSTS2		HP:0100602	OMIM:613684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613685	DEAFNESS, AUTOSOMAL RECESSIVE 83		HP:0000007	PMID:19888295	PCS				I		HPO:skoehler	
OMIM	613685	DEAFNESS, AUTOSOMAL RECESSIVE 83		HP:0000399	PMID:19888295	PCS				P		HP:probinson	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0000007	OMIM:613686	TAS				I		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0000902	OMIM:613686	TAS				P		HPO:probinson	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0000921	OMIM:613686	TAS				P		HPO:probinson	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0001696	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0002111	OMIM:613686	TAS				P		HPO:probinson	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0002475	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0002937	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0003298	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0003305	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0003310	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0004322	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0010306	OMIM:613686	TAS				P		HPO:skoehler	
OMIM	613686	SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE; SCDO4		HP:0030323	OMIM:613686	TAS				P		HPO:probinson	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0000006	OMIM:613688	TAS				I		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001279	OMIM:613688	TAS				P		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001425	OMIM:613688	TAS				I		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001645	OMIM:613688	TAS				P		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001657	OMIM:613688	TAS				P		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001663	OMIM:613688	TAS				P		HPO:skoehler	
OMIM	613688	LONG QT SYNDROME 2; LQT2		HP:0001664	OMIM:613688	TAS				P		HPO:skoehler	
OMIM	613689	%613689 MAMMARY-DIGITAL-NAIL SYNDROME; MDNS		HP:0000006	OMIM:613689	TAS				I		HPO:skoehler	
OMIM	613689	%613689 MAMMARY-DIGITAL-NAIL SYNDROME; MDNS		HP:0001798	OMIM:613689	TAS				P		HPO:skoehler	
OMIM	613689	%613689 MAMMARY-DIGITAL-NAIL SYNDROME; MDNS		HP:0002164	OMIM:613689	TAS				P		HPO:skoehler	
OMIM	613689	%613689 MAMMARY-DIGITAL-NAIL SYNDROME; MDNS		HP:0008404	OMIM:613689	TAS				P		HPO:skoehler	
OMIM	613689	%613689 MAMMARY-DIGITAL-NAIL SYNDROME; MDNS		HP:0010313	OMIM:613689	TAS				P		HPO:skoehler	
OMIM	613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7		HP:0000006	OMIM:613690	TAS				I		HPO:skoehler	
OMIM	613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7		HP:0001425	OMIM:613690	TAS				I		HPO:skoehler	
OMIM	613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7		HP:0001638	OMIM:613690	IEA				P		HPO:skoehler	
OMIM	613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7		HP:0001714	OMIM:613690	TAS				P		HPO:skoehler	
OMIM	613690	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7; CMH7		HP:0005110	OMIM:613690	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0000006	OMIM:613693	TAS				I		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001279	OMIM:613693	TAS				P		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001425	OMIM:613693	TAS				I		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001645	OMIM:613693	TAS				P		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001657	OMIM:613693	TAS				P		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001663	OMIM:613693	TAS				P		HPO:skoehler	
OMIM	613693	LONG QT SYNDROME 6; LQT6		HP:0001664	OMIM:613693	TAS				P		HPO:skoehler	
OMIM	613694	#613694 CARDIOMYOPATHY, DILATED, 1U; CMD1U		HP:0000006	OMIM:613694	TAS				I		HPO:skoehler	
OMIM	613694	#613694 CARDIOMYOPATHY, DILATED, 1U; CMD1U		HP:0001279	OMIM:613694	TAS				P		HPO:skoehler	
OMIM	613694	#613694 CARDIOMYOPATHY, DILATED, 1U; CMD1U		HP:0001635	OMIM:613694	TAS				P		HPO:skoehler	
OMIM	613694	#613694 CARDIOMYOPATHY, DILATED, 1U; CMD1U		HP:0001644	OMIM:613694	TAS				P		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0000006	OMIM:613695	TAS				I		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001279	OMIM:613695	TAS				P		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001425	OMIM:613695	TAS				I		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001645	OMIM:613695	TAS				P		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001657	OMIM:613695	TAS				P		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001663	OMIM:613695	TAS				P		HPO:skoehler	
OMIM	613695	LONG QT SYNDROME 5; LQT5		HP:0001664	OMIM:613695	TAS				P		HPO:skoehler	
OMIM	613697	CARDIOMYOPATHY, DILATED, 1V		HP:0000006	OMIM:613697	TAS				I		HPO:probinson	
OMIM	613697	CARDIOMYOPATHY, DILATED, 1V		HP:0001279	OMIM:613697	TAS				P		HPO:probinson	
OMIM	613697	CARDIOMYOPATHY, DILATED, 1V		HP:0001635	OMIM:613697	TAS				P		HPO:probinson	
OMIM	613697	CARDIOMYOPATHY, DILATED, 1V		HP:0001644	OMIM:613697	TAS				P		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0000006	PMID:19864492	PCS				I		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0000567	PMID:19864492	PCS				P		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0000612	PMID:19864492	PCS				P		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0002943	PMID:19864492	PCS				P		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0004635	OMIM:613702	TAS				P		HPO:probinson	
OMIM	613702	#613702 KLIPPEL-FEIL SYNDROME 3, AUTOSOMAL DOMINANT; KFS3		HP:0030281	PMID:19864492	PCS				P		HPO:probinson	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0000006	PMID:19864492	PCS				I		HPO:iea	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0000505	PMID:19864492	TAS				P		HPO:iea	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0000589	PMID:19864492	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0000639	PMID:19864492	PCS				P		HPO:iea	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0007633	PMID:19864492	PCS		HP:0040281		P		HPO:iea	HP:0040281
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0007750	PMID:19864492	PCS				P		HPO:iea	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0007766	PMID:19864492	PCS				P		HPO:iea	
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0009911	PMID:19864492	PCS		HP:0040284		P		HPO:iea	1/2
OMIM	613703	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 6		HP:0010984	PMID:19864492	PCS				I		HPO:iea	
OMIM	613704	#613704 MICROPHTHALMIA, ISOLATED 7; MCOP7		HP:0000568	OMIM:613704	TAS				P		HPO:probinson	
OMIM	613705	#613705 OROFACIAL CLEFT 10; OFC10;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 10		HP:0100333	OMIM:613705	IEA				P		HPO:probinson	
OMIM	613705	#613705 OROFACIAL CLEFT 10; OFC10;;CLEFT LIP WITH OR WITHOUT CLEFT PALATE, NONSYNDROMIC, 10		HP:0100334	OMIM:613705	IEA				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000006	OMIM:613706	TAS				I		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000268	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000316	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000341	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000369	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000391	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000465	OMIM:613706	IEA				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000470	OMIM:613706	IEA				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000768	OMIM:613706	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000768	OMIM:613706	IEA				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0000953	OMIM:613706	TAS		HP:0040284		P		HPO:probinson	3/5
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0001249	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0001290	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0001631	OMIM:613706	TAS		HP:0040284		P		HPO:probinson	2/5
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0001642	OMIM:613706	TAS		HP:0040284		P		HPO:probinson	2/5
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0002015	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0002033	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0002650	OMIM:613706	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0004322	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0005280	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0011220	OMIM:613706	TAS				P		HPO:probinson	
OMIM	613706	NOONAN SYNDROME 7; NS7		HP:0100543	OMIM:613706	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000006	OMIM:613707	TAS				I		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000316	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000358	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000369	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000407	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000465	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000470	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000914	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0000962	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001003	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001054	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001249	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001250	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001319	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001633	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001636	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0001646	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0002212	OMIM:613707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0002750	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0004322	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0005280	OMIM:613707	TAS				P		HPO:skoehler	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0007565	OMIM:613707	TAS				P		HPO:probinson	
OMIM	613707	#613707 LEOPARD SYNDROME 3; LPRD3		HP:0100543	OMIM:613707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0000006	OMIM:613708	TAS				I		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0001218	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0001347	OMIM:613708	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0001761	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0002164	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0002754	OMIM:613708	IEA				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0002936	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0003401	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0003477	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0003581	OMIM:613708	TAS				C		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0003676	OMIM:613708	TAS				C		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0003693	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0006984	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613708	NEUROPATHY, HEREDITARY SENSORY, TYPE ID; HSN1D		HP:0008404	OMIM:613708	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0000007	OMIM:613710	TAS				I		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0001254	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0001265	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0001271	OMIM:613710	TAS	HP:0011463			P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0001324	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0001762	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0002355	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0002490	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0003202	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0003470	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0003477	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613710	#613710 THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATIONAND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4;;BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY;;STRIATAL NECROSIS, BILATERAL, AND PROGRESSIVE POLYNEUROPATHY		HP:0005750	OMIM:613710	TAS				P		HPO:skoehler	
OMIM	613711	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3; HSCR3		HP:0002251	OMIM:613711	IEA				P		HPO:skoehler	
OMIM	613712	HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 4; HSCR4		HP:0002251	OMIM:613712	IEA				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000006	OMIM:613717	TAS				I		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000007	OMIM:613717	IEA				I		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000175	OMIM:613717	TAS				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000347	OMIM:613717	TAS				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000405	OMIM:613717	IEA				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000452	OMIM:613717	TAS				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000453	OMIM:613717	TAS				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000494	OMIM:613717	TAS				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0000589	OMIM:613717	IEA				P		HPO:skoehler	
OMIM	613717	TREACHER COLLINS SYNDROME 2; TCS2		HP:0008551	OMIM:613717	IEA				P		HPO:skoehler	
OMIM	613718	#613718 DEAFNESS, AUTOSOMAL RECESSIVE 74; DFNB74		HP:0000007	OMIM:613718	TAS				I		HPO:skoehler	
OMIM	613718	#613718 DEAFNESS, AUTOSOMAL RECESSIVE 74; DFNB74		HP:0000365	OMIM:613718	IEA				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0000006	OMIM:613720	TAS				I		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001249	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001250	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001263	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001285	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001290	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0001332	OMIM:613720	TAS				P		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0002079	OMIM:613720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0003593	OMIM:613720	TAS				C		HPO:skoehler	
OMIM	613720	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 7		HP:0200134	OMIM:613720	IEA				P		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0000006	OMIM:613721	TAS				I		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0001263	OMIM:613721	TAS				P		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0002069	OMIM:613721	TAS				P		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0002133	OMIM:613721	TAS				P		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0002510	OMIM:613721	TAS				P		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0003593	OMIM:613721	TAS				C		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0003828	OMIM:613721	TAS				C		HPO:skoehler	
OMIM	613721	#613721 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11; EIEE11		HP:0200134	OMIM:613721	IEA				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0000007	OMIM:613722	TAS				I		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0001257	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0001347	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0002197	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0002521	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0007359	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0008936	OMIM:613722	TAS				P		HPO:skoehler	
OMIM	613722	#613722 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 12; EIEE12		HP:0200134	OMIM:613722	IEA				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0000007	OMIM:613723	TAS				I		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0001270	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0001371	OMIM:613723	TAS	HP:0003584			P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0002938	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003202	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003236	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003324	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003391	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003551	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003560	OMIM:613723	TAS				P		HPO:skoehler	
OMIM	613723	#613723 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Q; LGMD2Q		HP:0003678	OMIM:613723	TAS				C		HPO:skoehler	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0000007	OMIM:613724	TAS				I		HPO:skoehler	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0000027	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0000473	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0000570	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0000815	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0002080	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0002346	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0002352	OMIM:613724	IEA				P		HPO:skoehler	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0002450	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0004409	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0009830	OMIM:613724	IEA				P		HPO:skoehler	
OMIM	613724	LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY		HP:0010663	OMIM:613724	TAS				P		HPO:probinson	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0000007	OMIM:613728	TAS				I		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0000639	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0001249	OMIM:613728	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0001260	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10	HP:0012828	HP:0001272	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0001310	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0001347	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0001761	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0002066	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0002070	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0002078	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0002080	OMIM:613728	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0002380	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613728	#613728 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 10; SCAR10		HP:0007338	OMIM:613728	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0000007	OMIM:613730	TAS				I		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0000028	OMIM:613730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0000086	OMIM:613730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0000518	OMIM:613730	TAS	HP:0003577			P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0000800	OMIM:613730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0001250	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0001257	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC	HP:0012829	HP:0001263	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0001321	OMIM:613730	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0001347	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0002119	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0002240	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0003577	OMIM:613730	TAS				C		HPO:skoehler	
OMIM	613730	#613730 HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION,AND CATARACTS; HDBSCC		HP:0005484	OMIM:613730	TAS				P		HPO:skoehler	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000006	OMIM:613731	IEA				I		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000007	OMIM:613731	IEA				I		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000510	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000512	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000518	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000580	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000618	OMIM:613731	IEA				P		HPO:skoehler	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0000662	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613731	RETINITIS PIGMENTOSA 4; RP4		HP:0001123	OMIM:613731	IEA				P		HPO:probinson	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000023	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000076	OMIM:613735	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000089	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000126	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000160	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000219	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000256	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000283	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000331	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000337	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000369	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000463	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0000965	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0001249	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0001250	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0001263	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0001274	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0001290	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0002079	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0002119	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0003196	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0003396	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0003745	OMIM:613735	TAS				I		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0007099	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613735	BRAIN MALFORMATIONS AND URINARY TRACT DEFECTS		HP:0100543	OMIM:613735	TAS				P		HPO:skoehler	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0000006	OMIM:613736	TAS				I		HPO:skoehler	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0007502	OMIM:613736	IEA				P		HPO:skoehler	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0011132	OMIM:613736	IEA				P		HPO:probinson	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0012322	OMIM:613736	IEA				P		HPO:probinson	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0040154	OMIM:613736	IEA				P		HPO:skoehler	
OMIM	613736	ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE; ACNINV2		HP:0100838	OMIM:613736	IEA				P		HPO:probinson	
OMIM	613737	ACNE INVERSA, FAMILIAL, 3; ACNINV3		HP:0000006	PMID:20929727	PCS				I		HPO:skoehler	
OMIM	613737	ACNE INVERSA, FAMILIAL, 3; ACNINV3		HP:0011132	OMIM:613737	TAS				P		HPO:probinson	
OMIM	613737	ACNE INVERSA, FAMILIAL, 3; ACNINV3		HP:0012322	OMIM:613737	TAS				P		HPO:probinson	
OMIM	613737	ACNE INVERSA, FAMILIAL, 3; ACNINV3		HP:0040154	PMID:20929727	PCS				P		HPO:skoehler	
OMIM	613737	ACNE INVERSA, FAMILIAL, 3; ACNINV3		HP:0100838	PMID:20929727	PCS				P		HPO:probinson	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0000127	OMIM:613743	TAS				P		HPO:probinson	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0000846	OMIM:613743	IEA				P		HPO:skoehler	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0000859	OMIM:613743	TAS				P		HPO:probinson	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0000953	OMIM:613743	TAS				P		HPO:probinson	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0011749	OMIM:613743	TAS				P		HPO:probinson	
OMIM	613743	#613743 ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIALOR COMPLETE;;P450SCC DEFICIENCY		HP:0012245	OMIM:613743	TAS				P		HPO:probinson	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000007	OMIM:613744	TAS				I		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000154	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000252	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000275	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000280	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000297	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000307	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000322	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000341	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000395	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000414	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000431	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000494	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0000639	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001250	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001258	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001263	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001272	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001319	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001347	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001371	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0001762	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0002119	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0002120	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0002307	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0002510	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0003189	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0003199	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0003487	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0003577	OMIM:613744	TAS				C		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0004322	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613744	#613744 SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE; SPG51;;CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 4, FORMERLY; CPSQ4, FORMERLY		HP:0010864	OMIM:613744	TAS				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000006	OMIM:613750	TAS				I		HPO:probinson	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000505	OMIM:613750	TAS				P		HPO:probinson	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000510	OMIM:613750	IEA				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000550	OMIM:613750	TAS				P		HPO:probinson	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000618	OMIM:613750	IEA				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000662	OMIM:613750	TAS				P		HPO:probinson	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0000980	OMIM:613750	IEA				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0007401	OMIM:613750	IEA				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27	HP:0003676	HP:0007950	OMIM:613750	TAS				P		HPO:skoehler	
OMIM	613750	RETINITIS PIGMENTOSA 27; RP27		HP:0040049	OMIM:613750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0000006	OMIM:613751	TAS				I		HPO:probinson	
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0001629	OMIM:613751	TAS				P		HPO:probinson	
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0001651	OMIM:613751	TAS				P		HPO:probinson	
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0006695	OMIM:613751	TAS				P		HPO:probinson	
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0010452	OMIM:613751	TAS				P		HPO:probinson	
OMIM	613751	#613751 HETEROTAXY, VISCERAL, 4, AUTOSOMAL; HTX4		HP:0012020	OMIM:613751	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0000007	OMIM:613752	TAS				I		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0000164	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001249	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001263	OMIM:613752	TAS				P		HPO:skoehler	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001270	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001508	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001638	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0001999	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613752	#613752 HYPERMETHIONINEMIA WITH S-ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY		HP:0003235	OMIM:613752	TAS				P		HPO:probinson	
OMIM	613756	#613756 RETINITIS PIGMENTOSA 49; RP49		HP:0000007	PMID:7479749	PCS				I		HPO:probinson	
OMIM	613756	#613756 RETINITIS PIGMENTOSA 49; RP49		HP:0000510	PMID:7479749	PCS				P		HPO:probinson	
OMIM	613757	#613757 MACULAR DEGENERATION, AGE-RELATED, 6; ARMD6		HP:0000608	OMIM:613757	TAS				P		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000007	PMID:9565049	PCS				I		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000505	PMID:9565049	PCS				P		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000510	PMID:9565049	PCS				P		HPO:skoehler	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000533	PMID:9565049	PCS				P		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000580	PMID:9565049	PCS				P		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000654	PMID:9565049	PCS				P		HPO:probinson	
OMIM	613758	#613758 RETINITIS PIGMENTOSA 47; RP47		HP:0000662	PMID:9565049	PCS				P		HPO:probinson	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0000007	OMIM:613759	TAS				I		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0001250	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0001298	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0001410	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0001629	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0002059	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0002719	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613759	#613759 INFECTIONS, RECURRENT, WITH ENCEPHALOPATHY, HEPATIC DYSFUNCTION, ANDCARDIOVASCULAR MALFORMATIONS;;FADD DEFICIENCY		HP:0004935	OMIM:613759	TAS				P		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0000006	OMIM:613762	TAS				I		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0000041	OMIM:613762	TAS				P		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0000047	OMIM:613762	IEA				P		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0000150	OMIM:613762	TAS				P		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0001007	OMIM:613762	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0002215	OMIM:613762	TAS				P		HPO:skoehler	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0008665	OMIM:613762	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0012245	OMIM:613762	TAS				P		HPO:probinson	
OMIM	613762	46,XY SEX REVERSAL 6; SRXY6		HP:0100621	OMIM:613762	TAS				P		HPO:skoehler	
OMIM	613763	#613763 CATARACT, POSTERIOR POLAR, 2; CTPP2CATARACT, CONGENITAL LAMELLAR, INCLUDED;;CATARACT, JUVENILE, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000006	OMIM:613763	TAS				I		HPO:probinson	
OMIM	613763	#613763 CATARACT, POSTERIOR POLAR, 2; CTPP2CATARACT, CONGENITAL LAMELLAR, INCLUDED;;CATARACT, JUVENILE, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000007	OMIM:613763	TAS				I		HPO:skoehler	
OMIM	613763	#613763 CATARACT, POSTERIOR POLAR, 2; CTPP2CATARACT, CONGENITAL LAMELLAR, INCLUDED;;CATARACT, JUVENILE, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000519	OMIM:613763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613763	#613763 CATARACT, POSTERIOR POLAR, 2; CTPP2CATARACT, CONGENITAL LAMELLAR, INCLUDED;;CATARACT, JUVENILE, AUTOSOMAL RECESSIVE, INCLUDED		HP:0000556	OMIM:613763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613763	#613763 CATARACT, POSTERIOR POLAR, 2; CTPP2CATARACT, CONGENITAL LAMELLAR, INCLUDED;;CATARACT, JUVENILE, AUTOSOMAL RECESSIVE, INCLUDED		HP:0001115	OMIM:613763	TAS				P		HPO:probinson	
OMIM	613765	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9		HP:0000006	PMID:22335739	PCS				I		HPO:probinson	
OMIM	613765	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9		HP:0001639	OMIM:613765	TAS				P		HPO:skoehler	
OMIM	613765	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9		HP:0001644	PMID:22335739	PCS				P		HPO:probinson	
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0000007	OMIM:613767	TAS				I		HPO:probinson	
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0000510	OMIM:613767	TAS				P		HPO:probinson	
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0000608	OMIM:613767	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0000662	OMIM:613767	TAS				P		HPO:probinson	
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0007737	OMIM:613767	TAS				P		HPO:probinson	
OMIM	613767	#613767 RETINITIS PIGMENTOSA 45; RP45		HP:0007994	OMIM:613767	TAS				P		HPO:probinson	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0000006	OMIM:613769	TAS				I		HPO:probinson	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0000510	OMIM:613769	IEA				P		HPO:skoehler	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0000654	OMIM:613769	TAS				P		HPO:probinson	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0001133	OMIM:613769	TAS				P		HPO:probinson	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0007722	OMIM:613769	TAS				P		HPO:probinson	
OMIM	613769	#613769 RETINITIS PIGMENTOSA 44; RP44		HP:0007843	OMIM:613769	TAS				P		HPO:probinson	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000006	OMIM:613776	TAS				I		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000218	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000238	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000286	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000331	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000348	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000426	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000463	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000465	OMIM:613776	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000470	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000486	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0000494	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001263	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001290	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001388	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001466	OMIM:613776	TAS				I		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001773	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0001847	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0002360	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0002553	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0002987	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0003186	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0004279	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0006380	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0006801	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0009623	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0010055	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0011448	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613776	CHROMOSOME 17P13.1 DELETION SYNDROME		HP:0011968	OMIM:613776	TAS				P		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0000007	OMIM:613779	TAS				I		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0000083	OMIM:613779	TAS				P		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0000100	OMIM:613779	TAS				P		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0000793	OMIM:613779	TAS		HP:0040284		P		HPO:skoehler	26%
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0002718	OMIM:613779	TAS				P		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0002725	OMIM:613779	IEA				P		HPO:skoehler	
OMIM	613779	COMPLEMENT COMPONENT 3 DEFICIENCY, AUTOSOMAL RECESSIVE; C3D		HP:0005421	OMIM:613779	TAS				P		HPO:probinson	
OMIM	613780	#613780 AORTIC ANEURYSM, FAMILIAL THORACIC 7; AAT7;;AORTIC DISSECTION, FAMILIAL, WITH OR WITHOUT AORTIC ANEURYSM		HP:0000006	OMIM:613780	TAS				I		HPO:skoehler	
OMIM	613780	#613780 AORTIC ANEURYSM, FAMILIAL THORACIC 7; AAT7;;AORTIC DISSECTION, FAMILIAL, WITH OR WITHOUT AORTIC ANEURYSM		HP:0002647	OMIM:613780	TAS				P		HPO:skoehler	
OMIM	613780	#613780 AORTIC ANEURYSM, FAMILIAL THORACIC 7; AAT7;;AORTIC DISSECTION, FAMILIAL, WITH OR WITHOUT AORTIC ANEURYSM		HP:0004942	OMIM:613780	TAS				P		HPO:skoehler	
OMIM	613783	#613783 COMPLEMENT COMPONENT C1s DEFICIENCY; C1SD;;C1s DEFICIENCY		HP:0000872	OMIM:613783	TAS				P	#613783 COMPLEMENT COMPONENT C1S DEFICIENCY; C1SD;;C1S DEFICIENCY	HPO:probinson	
OMIM	613783	#613783 COMPLEMENT COMPONENT C1s DEFICIENCY; C1SD;;C1s DEFICIENCY		HP:0002725	OMIM:613783	TAS				P	#613783 COMPLEMENT COMPONENT C1S DEFICIENCY; C1SD;;C1S DEFICIENCY	HPO:probinson	
OMIM	613783	#613783 COMPLEMENT COMPONENT C1s DEFICIENCY; C1SD;;C1s DEFICIENCY		HP:0005339	OMIM:613783	TAS				P	#613783 COMPLEMENT COMPONENT C1S DEFICIENCY; C1SD;;C1S DEFICIENCY	HPO:probinson	
OMIM	613783	#613783 COMPLEMENT COMPONENT C1s DEFICIENCY; C1SD;;C1s DEFICIENCY		HP:0012115	OMIM:613783	TAS				P	#613783 COMPLEMENT COMPONENT C1S DEFICIENCY; C1SD;;C1S DEFICIENCY	HPO:probinson	
OMIM	613789	#613789 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2;;C8 DEFICIENCY, TYPE II;;COMPLEMENT COMPONENT 8B DEFICIENCY;;C8 BETA DEFICIENCY;;C8B DEFICIENCY		HP:0000007	OMIM:613789	TAS				I		HPO:skoehler	
OMIM	613789	#613789 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2;;C8 DEFICIENCY, TYPE II;;COMPLEMENT COMPONENT 8B DEFICIENCY;;C8 BETA DEFICIENCY;;C8B DEFICIENCY		HP:0001287	OMIM:613789	TAS				P		HPO:skoehler	
OMIM	613789	#613789 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2;;C8 DEFICIENCY, TYPE II;;COMPLEMENT COMPONENT 8B DEFICIENCY;;C8 BETA DEFICIENCY;;C8B DEFICIENCY		HP:0004434	OMIM:613789	TAS				P		HPO:skoehler	
OMIM	613789	#613789 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II; C8D2;;C8 DEFICIENCY, TYPE II;;COMPLEMENT COMPONENT 8B DEFICIENCY;;C8 BETA DEFICIENCY;;C8B DEFICIENCY		HP:0005430	OMIM:613789	TAS				P		HPO:skoehler	
OMIM	613790	#613790 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I; C8D1;;C8 DEFICIENCY, TYPE I;;C8 ALPHA-GAMMA DEFICIENCY;;C8AG DEFICIENCY		HP:0000007	OMIM:613790	TAS				I		HPO:skoehler	
OMIM	613790	#613790 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I; C8D1;;C8 DEFICIENCY, TYPE I;;C8 ALPHA-GAMMA DEFICIENCY;;C8AG DEFICIENCY		HP:0001287	OMIM:613790	TAS				P		HPO:skoehler	
OMIM	613790	#613790 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I; C8D1;;C8 DEFICIENCY, TYPE I;;C8 ALPHA-GAMMA DEFICIENCY;;C8AG DEFICIENCY		HP:0002725	OMIM:613790	TAS				P		HPO:skoehler	
OMIM	613790	#613790 COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I; C8D1;;C8 DEFICIENCY, TYPE I;;C8 ALPHA-GAMMA DEFICIENCY;;C8AG DEFICIENCY		HP:0004434	OMIM:613790	TAS				P		HPO:skoehler	
OMIM	613791	MASP2 DEFICIENCY		HP:0000006	PMID:12904520	PCS				I		HPO:probinson	
OMIM	613791	MASP2 DEFICIENCY		HP:0000007	OMIM:613791	TAS				I		HPO:skoehler	
OMIM	613791	MASP2 DEFICIENCY		HP:0002725	PMID:12904520	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	613791	MASP2 DEFICIENCY		HP:0004431	PMID:12904520	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	613791	MASP2 DEFICIENCY		HP:0006532	PMID:12904520	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	613791	MASP2 DEFICIENCY		HP:0100279	PMID:12904520	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000006	OMIM:613792	TAS				I	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000028	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000218	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000233	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000243	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000248	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000252	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000278	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000286	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000316	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000325	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000343	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000347	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000365	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000369	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000426	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000431	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000455	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000486	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000508	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000581	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000582	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000629	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000664	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0000960	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001104	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001182	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001250	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001252	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001257	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001263	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001344	OMIM:613792	IEA				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0001518	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0002553	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0002714	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0004322	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0004467	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0005280	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0005469	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0005487	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0006695	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0008897	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0009765	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0011968	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0012210	OMIM:613792	TAS		HP:0040283		P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0025356	OMIM:613792	IEA				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613792	CHROMOSOME 3pter-p25 DELETION SYNDROME		HP:0100259	OMIM:613792	TAS				P	CHROMOSOME 3PTER-P25 DELETION SYNDROME	HPO:skoehler	
OMIM	613793	BLOOD GROUP, CROMER SYSTEM; CROM		HP:0002243	OMIM:613793	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0000007	OMIM:613794	IEA				I		HPO:probinson	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0000505	OMIM:613794	IEA				P		HPO:probinson	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0000510	OMIM:613794	IEA				P		HPO:skoehler	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0000639	OMIM:613794	TAS				P		HPO:skoehler	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0000662	OMIM:613794	IEA				P		HPO:probinson	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0001141	OMIM:613794	TAS				P		HPO:skoehler	
OMIM	613794	RETINITIS PIGMENTOSA 20		HP:0007843	OMIM:613794	IEA				P		HPO:probinson	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000006	PMID:21217753	PCS				I		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000023	PMID:21217753	PCS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000139	PMID:21217753	PCS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000175	OMIM:613795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000193	PMID:21217753	PCS				P		HP:probinson	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000218	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000268	PMID:29392890	PCS		HP:0040284		P		HP:probinson	9/28
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000272	PMID:29392890	PCS		HP:0040284		P		HP:probinson	14/41
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000276	PMID:21217753	PCS				P		HP:probinson	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000278	PMID:29392890	PCS		HP:0040284		P		HP:probinson	6/29
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000316	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	13/55
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000518	PMID:29392890	PCS		HP:0040284		P		HP:probinson	4/19
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000520	PMID:29392890	PCS		HP:0040284		P		HP:probinson	2/29
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000577	PMID:29392890	PCS				P		HP:probinson	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000689	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	8/23
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000766	PMID:21217753	PCS		HP:0040284		P		HPO:skoehler	3/19
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000939	OMIM:613795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000977	PMID:29392890	PCS		HP:0040284		P		HP:probinson	19/45
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0000978	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	14/42
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001065	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	27/83
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001075	PMID:29392890	PCS		HP:0040284		P		HP:probinson	8/36
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001166	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	22/74
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001363	PMID:29392890	PCS		HP:0040284		P		HP:probinson	1/31
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001388	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	14/72
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001537	PMID:21217753	PCS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001634	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001642	OMIM:613795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001643	OMIM:613795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001653	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001659	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001699	PMID:29392890	PCS		HP:0040284		M		HP:probinson	16/57
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001712	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	7/34
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001762	PMID:29392890	PCS		HP:0040284		P		HP:probinson	4/31
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0001763	PMID:29392890	TAS		HP:0040284		P		HPO:skoehler	62/81
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0002107	PMID:29392890	PCS		HP:0040284		P		HP:probinson	1/29
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0002138	PMID:29392890	PCS		HP:0040284		P		HP:probinson	4/42
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0002619	PMID:21282188	PCS		HP:0040284		P		HP:probinson	19/38
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0002647	PMID:21217753	PCS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0002650	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	60/112
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0003179	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	7/20
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0003302	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	19/61
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0005086	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0005110	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	8/33
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0005112	PMID:29392890	PCS		HP:0040284		P		HP:probinson	7/76
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0005116	PMID:21217753	PCS		HP:0040284		P		HPO:skoehler	9/17
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0006687	PMID:29392890	PCS		HP:0040284		P		HP:probinson	14/34
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0008419	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	42/71
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0008843	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0010646	PMID:29392890	PCS		HP:0040284		P		HP:probinson	1/22
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0010648	PMID:29392890	PCS		HP:0040284		P		HP:probinson	10/40
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0010886	OMIM:613795	TAS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0012385	PMID:29392890	PCS		HP:0040284		P		HPO:skoehler	8/68
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0012432	PMID:29392890	PCS		HP:0040284		P		HP:probinson	11/28
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0100775	PMID:29392890	PCS				P		HPO:skoehler	
OMIM	613795	#613795 LOEYS-DIETZ SYNDROME, TYPE 3; LDS3;;ANEURYSMS-OSTEOARTHRITIS SYNDROME;;LOEYS-DIETZ SYNDROME WITH OSTEOARTHRITIS;;LOEYS-DIETZ SYNDROME, TYPE 1C, FORMERLY; LDS1C, FORMERLY		HP:0410151	PMID:23608731	PCS				P		HPO:lccarmody	
OMIM	613796	#613796 MYCOBACTERIAL AND VIRAL INFECTIONS, SUSCEPTIBILITY TO, AUTOSOMAL RECESSIVE;;STAT1 DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:613796	TAS				I		HPO:probinson	
OMIM	613796	#613796 MYCOBACTERIAL AND VIRAL INFECTIONS, SUSCEPTIBILITY TO, AUTOSOMAL RECESSIVE;;STAT1 DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0004429	OMIM:613796	TAS				P		HPO:probinson	
OMIM	613796	#613796 MYCOBACTERIAL AND VIRAL INFECTIONS, SUSCEPTIBILITY TO, AUTOSOMAL RECESSIVE;;STAT1 DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0011274	OMIM:613796	TAS				P		HPO:probinson	
OMIM	613796	#613796 MYCOBACTERIAL AND VIRAL INFECTIONS, SUSCEPTIBILITY TO, AUTOSOMAL RECESSIVE;;STAT1 DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0012302	OMIM:613796	TAS				P		HPO:probinson	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000007	OMIM:613800	TAS				I		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2	HP:0012825	HP:0000059	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000160	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000252	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000268	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000319	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000347	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0000430	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0001382	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0001508	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0001511	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0001620	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0002020	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0002750	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0002779	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0002780	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0003100	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0003187	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0003561	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0006498	OMIM:613800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0008551	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0008665	OMIM:613800	TAS				P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0011968	OMIM:613800	TAS	HP:0003593			P		HPO:skoehler	
OMIM	613800	MEIER-GORLIN SYNDROME 2; MGORS2		HP:0012385	OMIM:613800	IEA				P		HPO:skoehler	
OMIM	613801	#613801 RETINITIS PIGMENTOSA 40; RP40		HP:0000007	OMIM:613801	TAS				I		HPO:skoehler	
OMIM	613801	#613801 RETINITIS PIGMENTOSA 40; RP40		HP:0000510	OMIM:613801	TAS				P		HPO:skoehler	
OMIM	613801	#613801 RETINITIS PIGMENTOSA 40; RP40		HP:0008323	OMIM:613801	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000007	OMIM:613803	TAS				I		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000028	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000046	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000047	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000054	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000064	OMIM:613803	IEA				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000160	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000179	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000252	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000308	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000325	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000327	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000358	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000369	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000426	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000494	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000750	OMIM:613803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000773	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0000774	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0001270	OMIM:613803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0001508	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0001511	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0001601	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0001762	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002020	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002094	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002215	OMIM:613803	IEA				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002225	OMIM:613803	IEA				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002750	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002779	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002780	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002812	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0002970	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0003100	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0003187	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0003561	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0006498	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0006532	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0006628	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0008551	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0008665	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0010306	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613803	MEIER-GORLIN SYNDROME 3; MGORS3		HP:0011968	OMIM:613803	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000007	OMIM:613804	TAS				I		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000028	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000160	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000179	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000252	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000327	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000347	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000369	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0000895	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0001508	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0001511	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0002097	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0002750	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0002816	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0003100	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0003187	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0003561	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0006443	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0008551	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613804	#613804 MEIER-GORLIN SYNDROME 4; MGORS4		HP:0011968	OMIM:613804	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000007	OMIM:613805	TAS				I		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000028	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000054	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000252	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000325	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000327	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000343	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000347	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000369	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0000385	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0001270	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0001508	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0001511	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0002020	OMIM:613805	TAS	HP:0003593			P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0002750	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0003042	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0003090	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0003100	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0003561	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0005487	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0006361	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0006443	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0008551	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0011342	OMIM:613805	TAS				P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0011968	OMIM:613805	TAS	HP:0003593			P		HPO:skoehler	
OMIM	613805	MEIER-GORLIN SYNDROME 5; MGORS5		HP:0030084	OMIM:613805	IEA				P		HPO:skoehler	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:613807	TAS				I		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0000388	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0000789	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:613807	TAS		HP:0040284		P		HPO:probinson	10/19
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0001748	OMIM:613807	TAS		HP:0040284		P		HPO:probinson	2/19
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0002205	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0011109	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0012257	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0012258	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0012262	OMIM:613807	TAS				P		HPO:probinson	
OMIM	613807	#613807 CILIARY DYSKINESIA, PRIMARY, 14; CILD14;;CILIARY DYSKINESIA, PRIMARY, 14, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:613807	IEA				P		HPO:skoehler	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:613808	TAS				I		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0000246	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0000403	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0000789	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:613808	TAS		HP:0040284		P		HPO:probinson	11/16
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0002205	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0012258	OMIM:613808	TAS				P		HPO:probinson	
OMIM	613808	#613808 CILIARY DYSKINESIA, PRIMARY, 15; CILD15;;CILIARY DYSKINESIA, PRIMARY, 15, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:613808	IEA				P		HPO:skoehler	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0000007	OMIM:613809	TAS				I		HPO:probinson	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0000510	OMIM:613809	IEA				P		HPO:skoehler	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0000512	OMIM:613809	TAS				P		HPO:probinson	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0001123	OMIM:613809	TAS				P		HPO:probinson	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0007737	OMIM:613809	TAS				P		HPO:probinson	
OMIM	613809	#613809 RETINITIS PIGMENTOSA 39; RP39		HP:0007843	OMIM:613809	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000007	OMIM:613810	TAS				I		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000510	OMIM:613810	IEA				P		HPO:skoehler	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000512	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000543	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000580	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0000662	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0007843	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613810	#613810 RETINITIS PIGMENTOSA 43; RP43		HP:0007994	OMIM:613810	TAS				P		HPO:probinson	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0000007	OMIM:613811	TAS				I		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0000253	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0000737	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0001250	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0001263	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0001272	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002059	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002072	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002079	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002169	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002187	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002360	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002510	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0002518	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0003121	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0003593	OMIM:613811	TAS				C		HPO:skoehler	
OMIM	613811	PONTOCEREBELLAR HYPOPLASIA, TYPE 2D		HP:0012448	OMIM:613811	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0000007	OMIM:613812	TAS				I		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0000952	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0001394	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0001399	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0001406	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0001508	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0001744	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0002014	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0002240	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0002570	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0002910	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0003155	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0003256	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0003623	OMIM:613812	TAS				C		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0011985	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613812	#613812 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3; CBAS3		HP:0012115	OMIM:613812	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0000007	OMIM:613818	TAS				I		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0000750	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0001249	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0001263	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0002355	OMIM:613818	IEA				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0002938	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0003236	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0003325	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0003391	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0003560	OMIM:613818	IEA				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0006466	OMIM:613818	TAS				P		HPO:skoehler	
OMIM	613818	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 9; MDDGC9		HP:0030046	OMIM:613818	IEA				P		HPO:skoehler	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0000007	OMIM:613819	IEA				I		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0000546	OMIM:613819	IEA				P		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0000773	OMIM:613819	IEA				P		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0000774	OMIM:613819	IEA				P		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0001156	OMIM:613819	IEA				P		HPO:skoehler	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0003026	OMIM:613819	IEA				P		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0004322	OMIM:613819	IEA				P		HPO:probinson	
OMIM	613819	SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4		HP:0010442	OMIM:613819	IEA				P		HPO:skoehler	
OMIM	613820	NEPHRONOPHTHISIS 12		HP:0000006	OMIM:613820	TAS				I		HPO:skoehler	
OMIM	613820	NEPHRONOPHTHISIS 12		HP:0000007	PMID:21258341	PCS				I		HPO:probinson	
OMIM	613820	NEPHRONOPHTHISIS 12		HP:0000090	PMID:21258341	PCS				P		HPO:probinson	
OMIM	613820	NEPHRONOPHTHISIS 12		HP:0003774	PMID:21258341	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000007	PMID:21131973	PCS				I		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000028	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000218	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000252	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000278	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000340	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000347	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000426	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000444	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000486	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000494	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000581	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000668	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000677	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0000878	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0001249	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0001592	OMIM:613823	IEA				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0001763	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0002536	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0002750	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0003683	PMID:21131973	PCS				P		HPO:probinson	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0004209	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0004322	OMIM:613823	TAS				P		HPO:skoehler	
OMIM	613823	SECKEL SYNDROME 5; SCKL5		HP:0008665	OMIM:613823	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613824	#613824 NEPHRONOPHTHISIS 9; NPHP9		HP:0000007	OMIM:613824	TAS				I		HPO:probinson	
OMIM	613824	#613824 NEPHRONOPHTHISIS 9; NPHP9		HP:0000090	OMIM:613824	TAS				P		HPO:probinson	
OMIM	613824	#613824 NEPHRONOPHTHISIS 9; NPHP9		HP:0003774	OMIM:613824	TAS				P		HPO:probinson	
OMIM	613824	#613824 NEPHRONOPHTHISIS 9; NPHP9		HP:0004734	OMIM:613824	TAS				P		HPO:probinson	
OMIM	613825	#613825 COMPLEMENT COMPONENT 9 DEFICIENCY; C9D;;C9 DEFICIENCY		HP:0012308	OMIM:613825	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0000007	OMIM:613826	TAS				I		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0000518	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0000550	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0000563	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6	HP:0012828	HP:0000613	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0001141	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0007843	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0008499	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613826	#613826 LEBER CONGENITAL AMAUROSIS 6; LCA6		HP:0012043	OMIM:613826	TAS				P		HPO:probinson	
OMIM	613827	#613827 RETINITIS PIGMENTOSA 48; RP48		HP:0000006	OMIM:613827	IEA				I		HPO:probinson	
OMIM	613827	#613827 RETINITIS PIGMENTOSA 48; RP48		HP:0000505	OMIM:613827	IEA				P		HPO:probinson	
OMIM	613827	#613827 RETINITIS PIGMENTOSA 48; RP48		HP:0000510	OMIM:613827	IEA				P		HPO:skoehler	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0000007	OMIM:613829	IEA				I		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0000505	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0000518	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0000550	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0000563	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7	HP:0012828	HP:0000613	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613829	#613829 LEBER CONGENITAL AMAUROSIS 7; LCA7		HP:0012043	OMIM:613829	IEA				P		HPO:probinson	
OMIM	613830	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D		HP:0000007	OMIM:613830	TAS				I		HPO:skoehler	
OMIM	613830	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D		HP:0000618	OMIM:613830	IEA				P		HPO:skoehler	
OMIM	613830	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D		HP:0007642	OMIM:613830	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0000006	OMIM:613834	TAS				I		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0000028	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0000822	OMIM:613834	IEA				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0001643	OMIM:613834	IEA				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0002092	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0002566	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0002789	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0004944	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0007866	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0011499	OMIM:613834	TAS	HP:0003577			P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0012727	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0030891	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613834	MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME		HP:0100770	OMIM:613834	TAS				P		HPO:skoehler	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0000007	OMIM:613835	TAS				I		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8	HP:0012828	HP:0000505	OMIM:613835	TAS	HP:0011463			P		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0000518	OMIM:613835	TAS				P		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0000550	OMIM:613835	TAS				P		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0000563	OMIM:613835	TAS				P		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0008499	OMIM:613835	TAS				P		HPO:probinson	
OMIM	613835	#613835 LEBER CONGENITAL AMAUROSIS 8; LCA8		HP:0012043	OMIM:613835	TAS	HP:0011463			P		HPO:probinson	
OMIM	613837	LEBER CONGENITAL AMAUROSIS 11; LCA11		HP:0000006	PMID:16384941	PCS				I		HPO:probinson	
OMIM	613837	LEBER CONGENITAL AMAUROSIS 11; LCA11		HP:0000505	PMID:16384941	PCS				P		HPO:probinson	
OMIM	613837	LEBER CONGENITAL AMAUROSIS 11; LCA11		HP:0000639	PMID:16384941	PCS				P		HPO:probinson	
OMIM	613837	LEBER CONGENITAL AMAUROSIS 11; LCA11		HP:0007663	OMIM:613837	IEA				P		HPO:skoehler	
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0000006	OMIM:613838	TAS				I		HPO:skoehler	
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0001670	OMIM:613838	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0001712	OMIM:613838	TAS				P		HPO:skoehler	
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0004756	OMIM:613838	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0005110	OMIM:613838	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613838	#613838 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16		HP:0011713	OMIM:613838	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0000007	OMIM:613839	TAS				I		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0000952	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0000980	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001251	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001263	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001290	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001321	OMIM:613839	IEA				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001873	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001876	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0001889	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0002059	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0002121	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0002240	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0002421	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0003828	OMIM:613839	TAS				C		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0005484	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0011968	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0012448	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613839	MEGALOBLASTIC ANEMIA DUE TO DIHYDROFOLATE REDUCTASE DEFICIENCY		HP:0025097	OMIM:613839	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000007	OMIM:613843	TAS				I		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000488	OMIM:613843	IEA				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000510	OMIM:613843	IEA				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000540	OMIM:613843	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000543	OMIM:613843	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000545	OMIM:613843	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000546	OMIM:613843	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000551	OMIM:613843	TAS				P		HPO:probinson	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000580	OMIM:613843	TAS				P		HPO:probinson	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0000662	OMIM:613843	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0001133	OMIM:613843	TAS				P		HPO:probinson	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0006934	OMIM:613843	TAS				P		HPO:skoehler	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0007772	OMIM:613843	TAS				P		HPO:probinson	
OMIM	613843	LEBER CONGENITAL AMAUROSIS 15; LCA15		HP:0030211	OMIM:613843	TAS				P		HPO:probinson	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0000007	OMIM:613845	TAS				I		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0000093	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0000103	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0000127	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0000819	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001290	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001508	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001622	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001873	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001882	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0001903	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0002092	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0002149	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0002878	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0002902	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0002917	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0003554	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0003593	OMIM:613845	TAS				C		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0004719	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0005977	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0011968	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613845	HYPERURICEMIA, PULMONARY HYPERTENSION, RENAL FAILURE, AND ALKALOSIS SYNDROME		HP:0012622	OMIM:613845	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000007	OMIM:613848	TAS				I		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000023	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000272	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000325	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000341	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000347	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000348	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000586	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000592	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000703	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000774	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000787	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000883	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000885	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000926	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0000938	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0001290	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X	HP:0012837	HP:0001388	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0001620	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002021	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002650	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002761	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002857	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002953	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0002983	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0004322	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0004482	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0006528	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0011220	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613848	OSTEOGENESIS IMPERFECTA, TYPE X		HP:0011800	OMIM:613848	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000007	OMIM:613849	TAS				I		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000160	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000218	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000272	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000324	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000336	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000347	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000684	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0000768	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0001270	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0002645	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0002650	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0004322	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0005280	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0011220	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0011800	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0030680	OMIM:613849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613849	#613849 OSTEOGENESIS IMPERFECTA, TYPE XII; OI12;;OI, TYPE XII		HP:0040160	OMIM:613849	TAS				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0000006	PMID:17924340	PCS				I		HPO:probinson	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001629	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001636	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001642	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001669	PMID:17924340	PCS				P		HPO:probinson	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001674	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001680	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001684	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001719	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0001750	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0004935	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0005160	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0005304	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0012020	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613854	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 6; CHTD6		HP:0032092	OMIM:613854	IEA				P		HPO:skoehler	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0000006	OMIM:613855	IEA				I		HPO:probinson	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0000640	OMIM:613855	IEA				P		HPO:probinson	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0001260	OMIM:613855	IEA				P		HPO:probinson	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0002131	OMIM:613855	IEA				P		HPO:probinson	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0002321	OMIM:613855	TAS				P		HPO:skoehler	
OMIM	613855	EPISODIC ATAXIA, TYPE 5		HP:0003829	OMIM:613855	TAS				C		HPO:skoehler	
OMIM	613856	#613856 ACHROMATOPSIA 4; ACHM4		HP:0000007	OMIM:613856	IEA				I		HPO:probinson	
OMIM	613856	#613856 ACHROMATOPSIA 4; ACHM4		HP:0000505	OMIM:613856	IEA				P		HPO:probinson	
OMIM	613856	#613856 ACHROMATOPSIA 4; ACHM4		HP:0000613	OMIM:613856	IEA				P		HPO:probinson	
OMIM	613856	#613856 ACHROMATOPSIA 4; ACHM4		HP:0000639	OMIM:613856	IEA				P		HPO:probinson	
OMIM	613856	#613856 ACHROMATOPSIA 4; ACHM4		HP:0011516	OMIM:613856	IEA				P		HPO:probinson	
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000006	PMID:21295280	PCS				I		HPO:skoehler	
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000185	PMID:21295280	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000272	PMID:21295280	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000278	PMID:21295280	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000347	PMID:21295280	PCS		HP:0040284		P		HP:probinson	3/3
OMIM	613857	%613857 OROFACIAL CLEFT 13; OFC13		HP:0000677	PMID:21295280	PCS				P		HP:probinson	
OMIM	613860	#613860 IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY;;FICOLIN 3 DEFICIENCY;;FCN3 DEFICIENCY		HP:0000007	PMID:19535802	PCS				I		HPO:probinson	
OMIM	613860	#613860 IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY;;FICOLIN 3 DEFICIENCY;;FCN3 DEFICIENCY		HP:0002721	OMIM:613860	TAS				P		HPO:skoehler	
OMIM	613860	#613860 IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY;;FICOLIN 3 DEFICIENCY;;FCN3 DEFICIENCY		HP:0002722	PMID:19535802	PCS				P		HPO:probinson	
OMIM	613860	#613860 IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY;;FICOLIN 3 DEFICIENCY;;FCN3 DEFICIENCY		HP:0002783	PMID:19535802	PCS				P		HPO:probinson	
OMIM	613860	#613860 IMMUNODEFICIENCY DUE TO FICOLIN 3 DEFICIENCY;;FICOLIN 3 DEFICIENCY;;FCN3 DEFICIENCY		HP:0200043	PMID:19535802	PCS				P		HPO:probinson	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0000007	OMIM:613861	TAS				I		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0000028	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0000054	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0000510	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0001250	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0001257	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0001508	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0001511	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0002240	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0002910	OMIM:613861	IEA				P		HPO:skoehler	
OMIM	613861	RETINITIS PIGMENTOSA 59; RP59		HP:0011505	OMIM:613861	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0000007	OMIM:613862	TAS				I		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0000510	OMIM:613862	IEA				P		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0000529	OMIM:613862	TAS				P		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0000543	OMIM:613862	TAS				P		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0000662	OMIM:613862	TAS				P		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0007401	OMIM:613862	TAS				P		HPO:skoehler	
OMIM	613862	#613862 RETINITIS PIGMENTOSA 38; RP38;;ROD-CONE DYSTROPHY, CHILDHOOD-ONSET		HP:0200070	OMIM:613862	TAS				P		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0000006	OMIM:613863	TAS				I		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0002069	OMIM:613863	TAS				P		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0002121	OMIM:613863	TAS				P		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0002373	OMIM:613863	TAS				P		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0003828	OMIM:613863	TAS				C		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0007359	OMIM:613863	TAS				P		HPO:skoehler	
OMIM	613863	#613863 GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 7; GEFSP7;;GEFS+, TYPE 7; GEFS+7FEBRILE SEIZURES, FAMILIAL, 3B, INCLUDED; FEB3B, INCLUDED		HP:0010819	OMIM:613863	TAS				P		HPO:skoehler	
OMIM	613865	#613865 DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61		HP:0000007	PMID:12719379	PCS				I		HPO:probinson	
OMIM	613865	#613865 DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61		HP:0000407	PMID:12719379	PCS	HP:0003577			P		HPO:probinson	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0000007	OMIM:613869	TAS				I		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0001371	OMIM:613869	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0001612	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0002063	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0002104	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0002878	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0003236	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0003560	OMIM:613869	TAS				P		HPO:skoehler	
OMIM	613869	#613869 MYOPATHY, MYOFIBRILLAR, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED;;MFM, FATAL INFANTILE HYPERTONIC, ALPHA-B CRYSTALLIN-RELATED		HP:0003678	OMIM:613869	TAS				C		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000006	OMIM:613870	TAS				I		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000054	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000358	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000378	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000414	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000426	OMIM:613870	TAS				P		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000713	OMIM:613870	TAS				P		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0000822	OMIM:613870	TAS				P		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001182	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001629	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001631	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001643	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001649	OMIM:613870	TAS				P		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0001795	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0002133	OMIM:613870	TAS				P		HPO:skoehler	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0002251	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0003196	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0009626	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613870	HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION		HP:0012332	OMIM:613870	TAS				P		HPO:probinson	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0000006	OMIM:613873	TAS				I		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0001638	OMIM:613873	IEA				P		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0001685	OMIM:613873	IEA				P		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0001712	OMIM:613873	TAS				P		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0001962	OMIM:613873	TAS				P		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0002094	OMIM:613873	TAS				P		HPO:skoehler	
OMIM	613873	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17; CMH17		HP:0004756	OMIM:613873	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613874	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18		HP:0000006	OMIM:613874	TAS				I		HPO:skoehler	
OMIM	613874	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18		HP:0001638	OMIM:613874	IEA				P		HPO:skoehler	
OMIM	613874	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18		HP:0001712	OMIM:613874	TAS				P		HPO:skoehler	
OMIM	613874	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18		HP:0005110	OMIM:613874	TAS				P		HPO:skoehler	
OMIM	613874	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18; CMH18		HP:0100749	OMIM:613874	IEA				P		HPO:skoehler	
OMIM	613875	#613875 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 19; CMH19		HP:0000006	OMIM:613875	TAS				I		HPO:skoehler	
OMIM	613875	#613875 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 19; CMH19		HP:0001670	OMIM:613875	TAS				P		HPO:skoehler	
OMIM	613876	#613876 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20		HP:0000006	OMIM:613876	TAS				I		HPO:skoehler	
OMIM	613876	#613876 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20		HP:0001638	OMIM:613876	IEA				P		HPO:skoehler	
OMIM	613876	#613876 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20		HP:0001712	OMIM:613876	TAS				P		HPO:skoehler	
OMIM	613876	#613876 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20; CMH20		HP:0005110	OMIM:613876	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0000006	OMIM:613877	TAS				I		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0000819	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0000822	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0000876	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0000956	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0001397	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0002155	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0003712	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613877	#613877 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 4; FPLD4;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PLIN1 MUTATIONS		HP:0100578	OMIM:613877	TAS				P		HPO:skoehler	
OMIM	613881	#613881 CARDIOMYOPATHY, DILATED, 1HH; CMD1HH		HP:0000006	OMIM:613881	TAS				I		HPO:skoehler	
OMIM	613881	#613881 CARDIOMYOPATHY, DILATED, 1HH; CMD1HH		HP:0001635	OMIM:613881	TAS				P		HPO:skoehler	
OMIM	613881	#613881 CARDIOMYOPATHY, DILATED, 1HH; CMD1HH		HP:0001644	OMIM:613881	TAS				P		HPO:skoehler	
OMIM	613882	#613882 HYPOMAGNESEMIA 6, RENAL; HOMG6		HP:0000006	OMIM:613882	TAS				I		HPO:skoehler	
OMIM	613882	#613882 HYPOMAGNESEMIA 6, RENAL; HOMG6		HP:0001324	OMIM:613882	TAS				P		HPO:skoehler	
OMIM	613882	#613882 HYPOMAGNESEMIA 6, RENAL; HOMG6		HP:0002315	OMIM:613882	TAS				P		HPO:skoehler	
OMIM	613882	#613882 HYPOMAGNESEMIA 6, RENAL; HOMG6		HP:0002321	OMIM:613882	TAS				P		HPO:skoehler	
OMIM	613882	#613882 HYPOMAGNESEMIA 6, RENAL; HOMG6		HP:0002917	OMIM:613882	IEA				P		HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000006	OMIM:613884	TAS				I	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000219	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000232	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000268	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000286	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000337	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000414	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000601	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0000750	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0001249	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0002002	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0002007	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0002079	OMIM:613884	TAS		HP:0040283		P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0003745	OMIM:613884	TAS				I	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0008936	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0009919	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613884	CHROMOSOME 13q14 DELETION SYNDROME		HP:0040080	OMIM:613884	TAS				P	CHROMOSOME 13Q14 DELETION SYNDROME	HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000007	OMIM:613885	TAS				I		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000175	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000204	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000252	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000337	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000369	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000457	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000470	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000528	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0000568	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0001162	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0001762	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0002084	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0003196	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0003270	OMIM:613885	TAS				P		HPO:skoehler	
OMIM	613885	#613885 MECKEL SYNDROME, TYPE 8; MKS8		HP:0004719	OMIM:613885	TAS				P		HPO:probinson	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0000006	OMIM:613886	TAS				I		HPO:probinson	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0000324	OMIM:613886	TAS				P		HPO:skoehler	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0000729	OMIM:613886	IEA				P		HPO:skoehler	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0000733	OMIM:613886	TAS				P		HPO:skoehler	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0001249	OMIM:613886	IEA				P		HPO:skoehler	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0001250	OMIM:613886	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0001513	OMIM:613886	TAS				P		HPO:probinson	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0002591	OMIM:613886	TAS				P		HPO:probinson	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0011344	OMIM:613886	TAS				P		HPO:probinson	
OMIM	613886	OBESITY, HYPERPHAGIA, AND DEVELOPMENTAL DELAY; OBHD		HP:0012448	OMIM:613886	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613887	#613887 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 4; CATC4		HP:0000007	OMIM:613887	TAS				I		HPO:probinson	
OMIM	613887	#613887 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 4; CATC4		HP:0000518	OMIM:613887	TAS	HP:0003577			P		HPO:probinson	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0000006	OMIM:613908	TAS				I		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0000315	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0000467	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0000473	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0001260	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0001272	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0001310	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0001347	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0002080	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0002311	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0002355	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0003487	OMIM:613908	TAS				P		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0003581	OMIM:613908	TAS				C		HPO:skoehler	
OMIM	613908	#613908 SPINOCEREBELLAR ATAXIA 35; SCA35		HP:0003677	OMIM:613908	TAS				C		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0000006	OMIM:613909	TAS				I		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0000027	OMIM:613909	TAS				P		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0000029	OMIM:613909	TAS				P		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0000789	OMIM:613909	TAS				P		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0001251	OMIM:613909	TAS				P		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0001272	OMIM:613909	TAS				P		HPO:skoehler	
OMIM	613909	SPINOCEREBELLAR ATAXIA 32; SCA32		HP:0100543	OMIM:613909	IEA				P		HPO:skoehler	
OMIM	613912	#613912 COMPLEMENT FACTOR D DEFICIENCY; CFDD;;FACTOR D DEFICIENCY		HP:0000007	OMIM:613912	TAS				I		HPO:skoehler	
OMIM	613912	#613912 COMPLEMENT FACTOR D DEFICIENCY; CFDD;;FACTOR D DEFICIENCY		HP:0002718	OMIM:613912	TAS				P		HPO:skoehler	
OMIM	613912	#613912 COMPLEMENT FACTOR D DEFICIENCY; CFDD;;FACTOR D DEFICIENCY		HP:0003828	OMIM:613912	TAS				C		HPO:skoehler	
OMIM	613912	#613912 COMPLEMENT FACTOR D DEFICIENCY; CFDD;;FACTOR D DEFICIENCY		HP:0004431	OMIM:613912	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0000093	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0000100	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0000790	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0000793	OMIM:613913	TAS		HP:0040284		P		HPO:skoehler	26%
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0002719	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0003745	OMIM:613913	TAS				I		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0005421	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0009019	OMIM:613913	TAS				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0009056	OMIM:613913	IEA				P		HPO:skoehler	
OMIM	613913	LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3, WITH OR WITHOUT GLOMERULONEPHRITIS; APLDC3		HP:0009125	OMIM:613913	IEA				P		HPO:skoehler	
OMIM	613916	%613916 DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89		HP:0000007	OMIM:613916	TAS				I		HPO:skoehler	
OMIM	613916	%613916 DEAFNESS, AUTOSOMAL RECESSIVE 89; DFNB89		HP:0000365	OMIM:613916	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0000007	OMIM:613925	TAS				I		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0000256	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001249	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001250	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001251	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001257	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001260	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001270	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001272	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0001355	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0002059	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0002119	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0002344	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0003677	OMIM:613925	TAS				C		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0007204	OMIM:613925	IEA				P		HPO:skoehler	
OMIM	613925	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2A; MLC2A		HP:0007341	OMIM:613925	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0000006	OMIM:613926	TAS				I		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0000256	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0001249	OMIM:613926	TAS		HP:0040284		P		HPO:skoehler	40%
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0001270	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0001290	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0001355	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B	HP:0012825	HP:0002312	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0007204	OMIM:613926	IEA				P		HPO:skoehler	
OMIM	613926	MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS 2B, REMITTING, WITH OR WITHOUT MENTAL RETARDATION; MLC2B		HP:0007341	OMIM:613926	TAS				P		HPO:skoehler	
OMIM	613930	%613930 ALOPECIA-MENTAL RETARDATION SYNDROME 3; APMR3		HP:0000007	OMIM:613930	TAS				I		HPO:skoehler	
OMIM	613930	%613930 ALOPECIA-MENTAL RETARDATION SYNDROME 3; APMR3		HP:0002289	OMIM:613930	TAS				P		HPO:skoehler	
OMIM	613930	%613930 ALOPECIA-MENTAL RETARDATION SYNDROME 3; APMR3		HP:0003577	OMIM:613930	TAS				C		HPO:skoehler	
OMIM	613930	%613930 ALOPECIA-MENTAL RETARDATION SYNDROME 3; APMR3		HP:0010864	OMIM:613930	TAS				P		HPO:skoehler	
OMIM	613933	ACETYL-COA CARBOXYLASE DEFICIENCY		HP:0000007	OMIM:613933	TAS				I		HPO:skoehler	
OMIM	613933	ACETYL-COA CARBOXYLASE DEFICIENCY		HP:0001290	OMIM:613933	TAS				P		HPO:skoehler	
OMIM	613933	ACETYL-COA CARBOXYLASE DEFICIENCY		HP:0001510	OMIM:613933	TAS				P		HPO:skoehler	
OMIM	613933	ACETYL-COA CARBOXYLASE DEFICIENCY		HP:0003198	OMIM:613933	TAS				P		HPO:skoehler	
OMIM	613938	%613938 PARASOMNIA, SLEEPWALKING TYPE; PSMNSWPARASOMNIA, SLEEP TERRORS TYPE, INCLUDED; PSMNST, INCLUDED		HP:0000006	OMIM:613938	TAS				I		HPO:skoehler	
OMIM	613938	%613938 PARASOMNIA, SLEEPWALKING TYPE; PSMNSWPARASOMNIA, SLEEP TERRORS TYPE, INCLUDED; PSMNST, INCLUDED		HP:0030765	OMIM:613938	TAS				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0000007	OMIM:613943	TAS				I		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0000962	OMIM:613943	TAS				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0007431	OMIM:613943	IEA				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0010783	OMIM:613943	IEA				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0025092	OMIM:613943	TAS				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0025114	OMIM:613943	TAS				P		HPO:skoehler	
OMIM	613943	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 8; ARCI8		HP:0040162	OMIM:613943	TAS				P		HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0000093	OMIM:613944	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0000123	OMIM:613944	IEA				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0000790	OMIM:613944	IEA				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0000794	OMIM:613944	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0000822	OMIM:613944	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0002829	OMIM:613944	TAS		HP:0040283		P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	HP:0040283
OMIM	613944	IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2		HP:0003774	OMIM:613944	TAS				P	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 2; IGAN2	HPO:skoehler	
OMIM	613949	#613949 OKT4 EPITOPE DEFICIENCY ;;T4 EPITOPE DEFICIENCY		HP:0002843	OMIM:613949	IEA				P		HPO:skoehler	
OMIM	613950	#613950 SCHIZOPHRENIA 15; SCZD15;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22q13-RELATED		HP:0010982	OMIM:613950	IEA				I	#613950 SCHIZOPHRENIA 15; SCZD15;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22Q13-RELATED	HPO:skoehler	
OMIM	613950	#613950 SCHIZOPHRENIA 15; SCZD15;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22q13-RELATED		HP:0100753	OMIM:613950	IEA				P	#613950 SCHIZOPHRENIA 15; SCZD15;;SCHIZOPHRENIA SUSCEPTIBILITY LOCUS, CHROMOSOME 22Q13-RELATED	HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000007	OMIM:613951	TAS				I		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000028	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000085	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000125	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000252	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000347	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000365	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000414	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000581	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0000957	OMIM:613951	TAS				P		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0001045	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0001876	OMIM:613951	TAS				P		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0001903	OMIM:613951	TAS				P		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0002860	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0002984	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0003828	OMIM:613951	TAS				C		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0004322	OMIM:613951	TAS				P		HPO:skoehler	
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0009777	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0009778	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613951	FANCONI ANEMIA, COMPLEMENTATION GROUP P; FANCP		HP:0012745	OMIM:613951	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0000007	PMID:21350122	PCS				I		HPO:probinson	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0000403	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0002205	OMIM:613953	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0002726	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0002728	PMID:21350122	PCS				P		HPO:probinson	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0002837	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0011108	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0011132	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0025084	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0031292	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613953	#613953 CANDIDIASIS, FAMILIAL, 5; CANDF5;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0200039	PMID:21350122	PCS				P		HPO:lccarmody	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0000006	OMIM:613954	IEA				I		HPO:probinson	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0001260	OMIM:613954	IEA				P		HPO:probinson	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0001324	OMIM:613954	IEA				P		HPO:probinson	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0002380	OMIM:613954	IEA				P		HPO:probinson	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0003202	OMIM:613954	IEA				P		HPO:probinson	
OMIM	613954	#613954 AMYOTROPHIC LATERAL SCLEROSIS 14, WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA;ALS14		HP:0007354	OMIM:613954	IEA				P		HPO:skoehler	
OMIM	613955	#613955 AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2; PLCA2		HP:0000006	OMIM:613955	TAS				I		HPO:probinson	
OMIM	613955	#613955 AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2; PLCA2		HP:0000989	OMIM:613955	TAS				P		HPO:probinson	
OMIM	613955	#613955 AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 2; PLCA2		HP:0012309	OMIM:613955	TAS				P		HPO:probinson	
OMIM	613956	#613956 CANDIDIASIS, FAMILIAL, 6; CANDF6;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000006	PMID:21350122	PCS				I		HPO:probinson	
OMIM	613956	#613956 CANDIDIASIS, FAMILIAL, 6; CANDF6;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002728	PMID:21350122	PCS				P		HPO:probinson	
OMIM	613957	SPERMATOGENIC FAILURE 8		HP:0000007	OMIM:613957	TAS				I		HPO:skoehler	
OMIM	613957	SPERMATOGENIC FAILURE 8		HP:0000027	OMIM:613957	TAS				P		HPO:skoehler	
OMIM	613957	SPERMATOGENIC FAILURE 8		HP:0030974	OMIM:613957	TAS				P		HPO:skoehler	
OMIM	613958	#613958 SPERMATOGENIC FAILURE 9; SPGF9;;GLOBOZOOSPERMIA, COMPLETE;;GLOBOZOOSPERMIA, TOTAL		HP:0000007	OMIM:613958	TAS				I		HPO:skoehler	
OMIM	613958	#613958 SPERMATOGENIC FAILURE 9; SPGF9;;GLOBOZOOSPERMIA, COMPLETE;;GLOBOZOOSPERMIA, TOTAL		HP:0012205	OMIM:613958	TAS				P		HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0000007	OMIM:613960	TAS				I	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0002014	OMIM:613960	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0002583	OMIM:613960	IEA				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0011107	OMIM:613960	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0011108	OMIM:613960	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613960	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE, TYPE III; CDG3		HP:0011127	OMIM:613960	TAS				P	GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME B-POSITIVE, TYPE III; CDG3	HPO:skoehler	
OMIM	613969	%613969 MYOPIA 19, AUTOSOMAL DOMINANT; MYP19		HP:0000006	OMIM:613969	TAS				I		HPO:skoehler	
OMIM	613969	%613969 MYOPIA 19, AUTOSOMAL DOMINANT; MYP19		HP:0011003	OMIM:613969	TAS				P		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0000006	OMIM:613970	TAS				I		HPO:probinson	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0000708	OMIM:613970	TAS				P		HPO:probinson	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0001249	OMIM:613970	TAS				P		HPO:probinson	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0001250	OMIM:613970	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0001257	OMIM:613970	IEA				P		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0001263	OMIM:613970	IEA				P		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0001332	OMIM:613970	IEA				P		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0002072	OMIM:613970	IEA				P		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0002353	OMIM:613970	TAS				P		HPO:probinson	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0003828	OMIM:613970	IEA				C		HPO:skoehler	
OMIM	613970	MENTAL RETARDATION, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6		HP:0100660	OMIM:613970	IEA				P		HPO:skoehler	
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0000006	OMIM:613977	TAS				I		HPO:skoehler	
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0000952	OMIM:613977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0000961	OMIM:613977	TAS				P		HPO:skoehler	
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0001903	OMIM:613977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0001923	OMIM:613977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0002240	OMIM:613977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0003577	OMIM:613977	TAS				C		HPO:skoehler	
OMIM	613977	#613977 CYANOSIS, TRANSIENT NEONATAL; TNCY		HP:0012119	OMIM:613977	TAS				P		HPO:skoehler	
OMIM	613978	#613978 HEMOGLOBIN H DISEASE; HBH;;ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE;;HEMOGLOBIN H DISEASE, DELETIONALHEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED		HP:0001744	OMIM:613978	TAS				P		HPO:probinson	
OMIM	613978	#613978 HEMOGLOBIN H DISEASE; HBH;;ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE;;HEMOGLOBIN H DISEASE, DELETIONALHEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED		HP:0001878	OMIM:613978	TAS				P		HPO:probinson	
OMIM	613978	#613978 HEMOGLOBIN H DISEASE; HBH;;ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE;;HEMOGLOBIN H DISEASE, DELETIONALHEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED		HP:0002240	OMIM:613978	TAS				P		HPO:probinson	
OMIM	613978	#613978 HEMOGLOBIN H DISEASE; HBH;;ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE;;HEMOGLOBIN H DISEASE, DELETIONALHEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED		HP:0011903	OMIM:613978	IEA				P		HPO:skoehler	
OMIM	613978	#613978 HEMOGLOBIN H DISEASE; HBH;;ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE;;HEMOGLOBIN H DISEASE, DELETIONALHEMOGLOBIN H DISEASE, NONDELETIONAL, INCLUDED		HP:0011907	OMIM:613978	TAS				P		HPO:probinson	
OMIM	613980	#613980 ATRIAL FIBRILLATION, FAMILIAL, 9; ATFB9		HP:0000006	OMIM:613980	TAS				I		HPO:skoehler	
OMIM	613980	#613980 ATRIAL FIBRILLATION, FAMILIAL, 9; ATFB9		HP:0004757	OMIM:613980	TAS				P		HPO:skoehler	
OMIM	613981	HYPOTRICHOSIS 3; HYPT3		HP:0000006	OMIM:613981	TAS				I		HPO:probinson	
OMIM	613981	HYPOTRICHOSIS 3; HYPT3		HP:0002209	OMIM:613981	IEA				P		HPO:skoehler	
OMIM	613981	HYPOTRICHOSIS 3; HYPT3		HP:0004782	OMIM:613981	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0000007	OMIM:613982	TAS				I		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0001388	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0002659	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0002812	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0002953	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0003179	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0004568	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613982	#613982 OSTEOGENESIS IMPERFECTA, TYPE VI; OI6		HP:0004586	OMIM:613982	TAS				P		HPO:probinson	
OMIM	613983	RETINITIS PIGMENTOSA 60; RP60		HP:0000006	OMIM:613983	TAS				I		HPO:skoehler	
OMIM	613983	RETINITIS PIGMENTOSA 60; RP60		HP:0000510	OMIM:613983	IEA				P		HPO:skoehler	
OMIM	613983	RETINITIS PIGMENTOSA 60; RP60		HP:0000980	OMIM:613983	IEA				P		HPO:skoehler	
OMIM	613983	RETINITIS PIGMENTOSA 60; RP60		HP:0007663	OMIM:613983	TAS				P		HPO:skoehler	
OMIM	613985	BETA-THALASSEMIA		HP:0004840	OMIM:613985	TAS				P		HPO:probinson	
OMIM	613985	BETA-THALASSEMIA		HP:0011906	OMIM:613985	TAS				P		HPO:probinson	
OMIM	613986	#613986 PITUITARY HORMONE DEFICIENCY, COMBINED, 6; CPHD6		HP:0000006	OMIM:613986	TAS				I		HPO:skoehler	
OMIM	613986	#613986 PITUITARY HORMONE DEFICIENCY, COMBINED, 6; CPHD6		HP:0004322	OMIM:613986	TAS				P		HPO:skoehler	
OMIM	613986	#613986 PITUITARY HORMONE DEFICIENCY, COMBINED, 6; CPHD6		HP:0011755	OMIM:613986	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0000007	OMIM:613987	TAS				I		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0000029	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0001249	OMIM:613987	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0001394	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0001510	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0001873	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0001876	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0002164	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0002514	OMIM:613987	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0005528	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0007427	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613987	#613987 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 2; DKCB2		HP:0008404	OMIM:613987	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0000007	OMIM:613988	TAS				I		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0001000	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0001876	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0002164	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0002860	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0005528	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613988	#613988 DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 3; DKCB3		HP:0008404	OMIM:613988	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000006	OMIM:613989	TAS				I		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000007	OMIM:613989	TAS				I		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000164	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000252	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000939	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0000972	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001263	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001321	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001508	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001644	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001873	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001882	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0001915	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0002028	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0002043	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0002164	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0002206	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0002216	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0003743	OMIM:613989	TAS				I		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0004322	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0005528	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0007427	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0008404	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0010885	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613989	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 2; DKCA2		HP:0012227	OMIM:613989	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000006	OMIM:613990	TAS				I		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000028	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000252	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000365	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000488	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000750	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000939	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0000958	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001251	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001321	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001511	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001596	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001873	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001882	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0001915	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002164	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002206	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002213	OMIM:613990	IEA				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002216	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002514	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0002745	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0004322	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0005528	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0007427	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	613990	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 3; DKCA3		HP:0009926	OMIM:613990	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000007	OMIM:614008	TAS				I		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000272	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000347	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000444	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000520	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000535	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000653	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000678	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000772	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000822	OMIM:614008	IEA				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000905	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0000939	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0001371	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0001387	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0001476	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0001508	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0002092	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0002621	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0002650	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0002973	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0004322	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0005585	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0009839	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0010537	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0011703	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0011712	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0011800	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614008	NESTOR-GUILLERMO PROGERIA SYNDROME; NGPS		HP:0100578	OMIM:614008	TAS				P		HPO:skoehler	
OMIM	614009	#614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO; BDPLT13;;BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANEA2 RECEPTOR		HP:0000006	PMID:7929844	PCS				I		HPO:skoehler	
OMIM	614009	#614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO; BDPLT13;;BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANEA2 RECEPTOR		HP:0000421	PMID:19828703	PCS				P		HPO:skoehler	
OMIM	614009	#614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO; BDPLT13;;BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANEA2 RECEPTOR		HP:0000978	PMID:19828703	PCS				P		HPO:skoehler	
OMIM	614009	#614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO; BDPLT13;;BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANEA2 RECEPTOR		HP:0011894	PMID:7929844	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	614009	#614009 BLEEDING DISORDER, PLATELET-TYPE, 13, SUSCEPTIBILITY TO; BDPLT13;;BLEEDING DISORDER, SUSCEPTIBILITY TO, DUE TO DEFECTIVE PLATELET THROMBOXANEA2 RECEPTOR		HP:0031364	PMID:19828703	PCS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:614017	TAS				I		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0000389	OMIM:614017	TAS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:614017	TAS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0002110	OMIM:614017	TAS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0002257	OMIM:614017	TAS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0003577	OMIM:614017	TAS				C		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0011109	OMIM:614017	TAS				P		HPO:skoehler	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0012256	OMIM:614017	TAS				P		HPO:probinson	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0012262	OMIM:614017	TAS				P		HPO:probinson	
OMIM	614017	#614017 CILIARY DYSKINESIA, PRIMARY, 16; CILD16;;CILIARY DYSKINESIA, PRIMARY, 16, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:614017	IEA				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0000007	OMIM:614018	TAS				I		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0001251	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0001260	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0001284	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0001336	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0001337	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0002121	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0002355	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0002650	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0003236	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0003676	OMIM:614018	TAS				C		HPO:skoehler	
OMIM	614018	#614018 EPILEPSY, PROGRESSIVE MYOCLONIC, 6; EPM6		HP:0010819	OMIM:614018	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0000007	OMIM:614019	TAS				I		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4	HP:0012828	HP:0000252	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0001250	OMIM:614019	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614019	LISSENCEPHALY 4		HP:0001263	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0001274	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0001276	OMIM:614019	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614019	LISSENCEPHALY 4		HP:0001321	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0001339	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0002187	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0003577	OMIM:614019	TAS				C		HPO:skoehler	
OMIM	614019	LISSENCEPHALY 4		HP:0004322	OMIM:614019	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614019	LISSENCEPHALY 4		HP:0009879	OMIM:614019	TAS				P		HPO:skoehler	
OMIM	614020	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14		HP:0000007	OMIM:614020	TAS				I		HPO:probinson	
OMIM	614020	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14		HP:0000189	OMIM:614020	TAS				P		HPO:skoehler	
OMIM	614020	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14		HP:0000750	OMIM:614020	TAS				P		HPO:skoehler	
OMIM	614020	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14		HP:0001249	OMIM:614020	TAS				P		HPO:probinson	
OMIM	614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3; CPVT3		HP:0000007	OMIM:614021	TAS				I		HPO:skoehler	
OMIM	614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3; CPVT3		HP:0001279	OMIM:614021	TAS				P		HPO:skoehler	
OMIM	614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3; CPVT3		HP:0001657	OMIM:614021	IEA				P		HPO:skoehler	
OMIM	614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3; CPVT3		HP:0001699	OMIM:614021	TAS				M		HPO:skoehler	
OMIM	614021	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3; CPVT3		HP:0004756	OMIM:614021	IEA				P		HPO:skoehler	
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0000006	OMIM:614022	TAS				I		HPO:skoehler	
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0001712	OMIM:614022	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0004749	OMIM:614022	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0004757	OMIM:614022	TAS				P		HPO:probinson	
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0005180	OMIM:614022	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0006671	OMIM:614022	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614022	ATRIAL FIBRILLATION, FAMILIAL, 10; ATFB10		HP:0031295	OMIM:614022	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0000007	OMIM:614023	TAS				I		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0000252	OMIM:614023	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0001249	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0001250	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0001263	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0001276	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0001511	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0002059	OMIM:614023	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0003593	OMIM:614023	TAS				C		HPO:skoehler	
OMIM	614023	PHOSPHOSERINE PHOSPHATASE DEFICIENCY; PSPHD		HP:0008897	OMIM:614023	TAS				P		HPO:skoehler	
OMIM	614025	#614025 HEPATIC LIPASE DEFICIENCY;;LIPC DEFICIENCY;;HL DEFICIENCY		HP:0000007	OMIM:614025	TAS				I		HPO:skoehler	
OMIM	614025	#614025 HEPATIC LIPASE DEFICIENCY;;LIPC DEFICIENCY;;HL DEFICIENCY		HP:0001013	OMIM:614025	TAS				P		HPO:skoehler	
OMIM	614025	#614025 HEPATIC LIPASE DEFICIENCY;;LIPC DEFICIENCY;;HL DEFICIENCY		HP:0001681	OMIM:614025	TAS				P		HPO:skoehler	
OMIM	614028	#614028 HYPERALPHALIPOPROTEINEMIA 2; HALP2;;APOLIPOPROTEIN C-III DEFICIENCY		HP:0003563	PMID:19074352	IEA				P		HPO:probinson	
OMIM	614028	#614028 HYPERALPHALIPOPROTEINEMIA 2; HALP2;;APOLIPOPROTEIN C-III DEFICIENCY		HP:0012153	PMID:19074352	IEA				P		HPO:probinson	
OMIM	614028	#614028 HYPERALPHALIPOPROTEINEMIA 2; HALP2;;APOLIPOPROTEIN C-III DEFICIENCY		HP:0012184	PMID:19074352	IEA				P		HPO:probinson	
OMIM	614033	HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY		HP:0000006	OMIM:614033	TAS				I		HPO:skoehler	
OMIM	614033	HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY		HP:0003258	OMIM:614033	TAS				P		HPO:skoehler	
OMIM	614033	HYDROXYACYL GLUTATHIONE HYDROLASE DEFICIENCY		HP:0004445	OMIM:614033	TAS				P		HPO:skoehler	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0000007	OMIM:614034	TAS				I		HPO:probinson	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0000093	OMIM:614034	TAS				P		HPO:probinson	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0000790	OMIM:614034	TAS				P		HPO:probinson	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0001510	OMIM:614034	TAS				P		HPO:probinson	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0001878	OMIM:614034	TAS				P		HPO:probinson	
OMIM	614034	#614034 HEME OXYGENASE 1 DEFICIENCY; HMOX1D		HP:0002240	OMIM:614034	TAS				P		HPO:probinson	
OMIM	614035	DEAFNESS, AUTOSOMAL RECESSIVE 29		HP:0000007	PMID:11163249	PCS				I		HPO:probinson	
OMIM	614035	DEAFNESS, AUTOSOMAL RECESSIVE 29		HP:0000365	PMID:11163249	PCS				P		HPO:probinson	
OMIM	614035	DEAFNESS, AUTOSOMAL RECESSIVE 29		HP:0000407	OMIM:614035	TAS				P		HPO:skoehler	
OMIM	614035	DEAFNESS, AUTOSOMAL RECESSIVE 29		HP:0003680	OMIM:614035	TAS				C		HPO:skoehler	
OMIM	614036	614036 ALPHA-2-MACROGLOBULIN DEFICIENCY; A2MD		HP:0000006	OMIM:614036	TAS				I		HPO:skoehler	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0000007	PMID:9820300	PCS				I	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:skoehler	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0000252	PMID:9820300	PCS				P	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:probinson	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0001252	PMID:9820300	PCS				P	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:probinson	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0001263	PMID:9820300	PCS				P	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:probinson	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0001522	PMID:9820300	PCS				M	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:probinson	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0001531	PMID:9820300	PCS				P	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HPO:probinson	
OMIM	614037	Leukotriene C4 synthase deficiency		HP:0030390	PMID:9820300	PCS				P	LEUKOTRIENE C4 SYNTHASE DEFICIENCY	HP:probinson	
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0000006	OMIM:614038	TAS				I		HPO:skoehler	
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0000286	OMIM:614038	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0000465	OMIM:614038	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0000601	OMIM:614038	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0001004	OMIM:614038	TAS				P		HPO:skoehler	
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0001182	OMIM:614038	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0001876	OMIM:614038	TAS				P		HPO:skoehler	
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME		HP:0002863	OMIM:614038	TAS				P		HPO:skoehler	
OMIM	614038	#614038 LYMPHEDEMA, PRIMARY, WITH MYELODYSPLASIA;;EMBERGER SYNDROME	HP:0031796	HP:0100658	OMIM:614038	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0000006	OMIM:614039	TAS				I		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0000252	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0000486	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0000639	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0001250	OMIM:614039	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0001257	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0001263	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0001274	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0001339	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0002079	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0002126	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0002342	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0002365	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0002539	OMIM:614039	IEA				P		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0003577	OMIM:614039	TAS				C		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0003828	OMIM:614039	TAS				C		HPO:skoehler	
OMIM	614039	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1		HP:0008936	OMIM:614039	TAS				P		HPO:skoehler	
OMIM	614042	#614042 MOYAMOYA DISEASE 5; MYMY5		HP:0000006	OMIM:614042	TAS				I		HPO:probinson	
OMIM	614042	#614042 MOYAMOYA DISEASE 5; MYMY5		HP:0004970	OMIM:614042	TAS				P		HPO:probinson	
OMIM	614042	#614042 MOYAMOYA DISEASE 5; MYMY5		HP:0011834	OMIM:614042	TAS				P		HPO:probinson	
OMIM	614044	614044 TRYPSINOGEN DEFICIENCY		HP:0000007	OMIM:614044	TAS				I		HPO:skoehler	
OMIM	614044	614044 TRYPSINOGEN DEFICIENCY		HP:0001508	OMIM:614044	TAS				P		HPO:skoehler	
OMIM	614044	614044 TRYPSINOGEN DEFICIENCY		HP:0002023	OMIM:614044	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614044	614044 TRYPSINOGEN DEFICIENCY		HP:0003075	OMIM:614044	TAS				P		HPO:skoehler	
OMIM	614049	#614049 ATRIAL FIBRILLATION, FAMILIAL, 11; ATFB11		HP:0000006	OMIM:614049	TAS				I		HPO:skoehler	
OMIM	614049	#614049 ATRIAL FIBRILLATION, FAMILIAL, 11; ATFB11		HP:0005110	OMIM:614049	TAS				P		HPO:skoehler	
OMIM	614050	#614050 ATRIAL FIBRILLATION, FAMILIAL, 12; ATFB12		HP:0000006	OMIM:614050	TAS				I		HPO:skoehler	
OMIM	614050	#614050 ATRIAL FIBRILLATION, FAMILIAL, 12; ATFB12		HP:0004757	OMIM:614050	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000007	OMIM:614052	TAS				I		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000023	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000028	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000047	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000308	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000343	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000369	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000431	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000463	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000518	OMIM:614052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0000822	OMIM:614052	IEA				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001250	OMIM:614052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001251	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001263	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001290	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001298	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001337	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001508	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001511	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001518	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001537	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001562	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001622	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001639	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0001987	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0002080	OMIM:614052	IEA				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0002093	OMIM:614052	TAS	HP:0003623			P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0002151	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0002352	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0002578	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0003128	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0003348	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0003535	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0003577	OMIM:614052	TAS				C		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0005469	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0011675	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0012368	OMIM:614052	TAS				P		HPO:skoehler	
OMIM	614052	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2		HP:0025356	OMIM:614052	IEA				P		HPO:skoehler	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0000007	OMIM:614053	TAS				I		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0001249	OMIM:614053	TAS				P		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0001639	OMIM:614053	TAS				P		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0003128	OMIM:614053	TAS	HP:0003623			P		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0003535	OMIM:614053	TAS				P		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0009830	OMIM:614053	TAS				P		HPO:probinson	
OMIM	614053	#614053 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3;MC5DN3;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATP5E TYPE		HP:0011925	PMID:20566710	PCS				P		HPO:probinson	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0001263	OMIM:614055	TAS				P		HPO:skoehler	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0001290	OMIM:614055	TAS				P		HPO:skoehler	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0002072	OMIM:614055	TAS				P		HPO:skoehler	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0002151	OMIM:614055	TAS				P		HPO:skoehler	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0003542	OMIM:614055	TAS				P		HPO:skoehler	
OMIM	614055	ACETYL-COA ACETYLTRANSFERASE-2 DEFICIENCY		HP:0003745	OMIM:614055	TAS				I		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000007	OMIM:614063	TAS				I		HPO:probinson	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000023	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000252	OMIM:614063	TAS				P		HPO:probinson	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000733	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000736	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0000742	OMIM:614063	IEA				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0001250	OMIM:614063	TAS				P		HPO:probinson	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0001263	OMIM:614063	TAS				P		HPO:probinson	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0001290	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0002078	OMIM:614063	TAS				P		HPO:probinson	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0002317	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0004322	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614063	N-ACETYLASPARTATE DEFICIENCY; NACED		HP:0004325	OMIM:614063	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0000006	OMIM:614065	TAS				I		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0001265	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0001324	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0001430	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0001638	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0003198	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0003677	OMIM:614065	TAS				C		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0003701	OMIM:614065	IEA				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0007149	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0008180	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614065	MYOPATHY, DISTAL, 4; MPD4		HP:0008944	OMIM:614065	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000007	OMIM:614066	TAS				I		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000154	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000218	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000252	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000280	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000322	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000341	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000414	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000431	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0000750	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001250	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001257	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001258	OMIM:614066	IEA				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001260	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001263	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001319	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001332	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001347	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001371	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001762	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0001763	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002079	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002119	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002515	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002518	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002540	OMIM:614066	IEA				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0002816	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0003487	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0003577	OMIM:614066	TAS				C		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0003677	OMIM:614066	TAS				C		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0004322	OMIM:614066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0008807	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614066	SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47		HP:0010864	OMIM:614066	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:614067	TAS				I		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000154	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000218	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000280	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000297	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000316	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000322	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000414	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000431	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0000448	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001257	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:614067	IEA				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001371	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0001762	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0002373	OMIM:614067	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:614067	TAS				C		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0006957	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0007359	OMIM:614067	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0008936	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0010864	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0012471	OMIM:614067	TAS				P		HPO:skoehler	
OMIM	614067	SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE		HP:0100021	OMIM:614067	IEA				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000007	OMIM:614069	TAS				I		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000218	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000278	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000286	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000311	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000316	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000331	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000369	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0000463	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0001249	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0001270	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0001510	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0002090	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0002719	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0002721	OMIM:614069	IEA				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0003196	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0003577	OMIM:614069	TAS				C		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0004313	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0004469	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614069	#614069 IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2; ICF2		HP:0005280	OMIM:614069	TAS				P		HPO:skoehler	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0000007	OMIM:614072	TAS				I		HPO:probinson	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0000505	OMIM:614072	TAS				P		HPO:probinson	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0000639	OMIM:614072	TAS				P		HPO:probinson	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0000666	OMIM:614072	IEA				P		HPO:skoehler	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0000978	OMIM:614072	IEA				P		HPO:skoehler	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0001892	OMIM:614072	TAS				P		HPO:probinson	
OMIM	614072	HERMANSKY-PUDLAK SYNDROME 3; HPS3		HP:0011883	OMIM:614072	TAS				P		HPO:probinson	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0000007	OMIM:614073	IEA				I		HPO:probinson	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0000666	OMIM:614073	IEA				P		HPO:skoehler	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0000978	OMIM:614073	IEA				P		HPO:skoehler	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0001022	OMIM:614073	IEA				P		HPO:probinson	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0001107	OMIM:614073	IEA				P		HPO:probinson	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0002091	OMIM:614073	IEA				P		HPO:skoehler	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0002206	OMIM:614073	IEA				P		HPO:probinson	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0007663	OMIM:614073	IEA				P		HPO:skoehler	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0007750	OMIM:614073	IEA				P		HPO:skoehler	
OMIM	614073	HERMANSKY-PUDLAK SYNDROME 4; HPS4		HP:0011883	OMIM:614073	IEA				P		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0000007	OMIM:614074	TAS				I		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0000486	OMIM:614074	IEA				P		HPO:skoehler	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0000666	OMIM:614074	IEA				P		HPO:skoehler	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0000978	OMIM:614074	TAS				P		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0001022	OMIM:614074	TAS				P		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0001107	OMIM:614074	TAS				P		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5	HP:0012825	HP:0001873	OMIM:614074	TAS				P		HPO:probinson	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5	HP:0012826	HP:0003010	OMIM:614074	IEA				P		HPO:skoehler	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0007663	OMIM:614074	IEA				P		HPO:skoehler	
OMIM	614074	HERMANSKY-PUDLAK SYNDROME 5; HPS5		HP:0007750	OMIM:614074	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000007	OMIM:614075	IEA				I		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000421	OMIM:614075	IEA				P		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000486	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000613	OMIM:614075	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000639	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0000978	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0001022	OMIM:614075	IEA				P		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0001104	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0001107	OMIM:614075	IEA				P		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0002788	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0003010	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0004866	OMIM:614075	IEA				P		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0007663	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0011883	OMIM:614075	IEA				P		HPO:probinson	
OMIM	614075	HERMANSKY-PUDLAK SYNDROME 6; HPS6		HP:0030825	OMIM:614075	IEA				P		HPO:skoehler	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0000007	OMIM:614076	IEA				I		HPO:probinson	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0000421	OMIM:614076	TAS				P		HPO:skoehler	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0000639	OMIM:614076	TAS				P		HPO:skoehler	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0000978	OMIM:614076	IEA				P		HPO:probinson	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0001022	OMIM:614076	IEA				P		HPO:probinson	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0001107	OMIM:614076	IEA				P		HPO:probinson	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0003540	OMIM:614076	IEA				P		HPO:probinson	
OMIM	614076	#614076 HERMANSKY-PUDLAK SYNDROME 7; HPS7		HP:0007663	OMIM:614076	TAS				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000007	OMIM:614077	TAS				I		HPO:probinson	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000483	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000505	OMIM:614077	TAS				P		HPO:probinson	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000540	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000543	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000545	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000565	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000577	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000666	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0000978	OMIM:614077	TAS				P		HPO:probinson	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0001022	OMIM:614077	TAS				P		HPO:probinson	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0001107	OMIM:614077	TAS				P		HPO:probinson	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0003540	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0007663	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614077	HERMANSKY-PUDLAK SYNDROME 8; HPS8		HP:0007750	OMIM:614077	IEA				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000007	OMIM:614078	TAS				I		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000160	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000175	OMIM:614078	IEA				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000347	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000348	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000365	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000431	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0000520	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0001156	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0001773	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0001831	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0002857	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0002999	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0003196	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0004322	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0004440	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0010049	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614078	CHONDRODYSPLASIA WITH JOINT DISLOCATIONS, GPAPP TYPE		HP:0012368	OMIM:614078	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000007	OMIM:614080	TAS				I		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000034	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000073	OMIM:614080	TAS				P		HPO:nvasilevsky	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000076	OMIM:614080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000110	OMIM:614080	TAS				P		HPO:nvasilevsky	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000126	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000175	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000194	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000218	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000233	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000256	OMIM:614080	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000280	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000286	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000316	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000341	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000343	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000347	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000358	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000369	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000378	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000396	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000463	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000639	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000646	PMID:21493957	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0000776	OMIM:614080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001249	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001250	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001257	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001263	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001265	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001266	OMIM:614080	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001272	OMIM:614080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001290	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001337	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001344	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001347	OMIM:614080	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001520	PMID:21493957	TAS				P		HPO:nvasilevsky	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001561	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001631	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001643	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0001869	OMIM:614080	TAS				P		HPO:nvasilevsky	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002007	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002020	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002023	PMID:21493957	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002025	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002059	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002089	OMIM:614080	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002265	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0002867	OMIM:614080	TAS				P		HPO:nvasilevsky	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0003196	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0003577	OMIM:614080	TAS				C		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0003828	OMIM:614080	TAS				C		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0005280	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614080	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 1		HP:0009882	OMIM:614080	TAS				P		HPO:skoehler	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0000252	PMID:11093276	PCS		HP:0040284		P		HPO:probinson	14/22
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0000568	PMID:11093276	PCS		HP:0040284		P		HPO:probinson	8/22
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001172	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001510	PMID:11093276	PCS		HP:0040284		P		HPO:probinson	19/23
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001873	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001875	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001903	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0001909	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0002863	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0003220	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614082	#614082 FANCONI ANEMIA, COMPLEMENTATION GROUP G; FANCG		HP:0007565	PMID:11093276	PCS				P		HPO:probinson	
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000007	OMIM:614083	TAS				I		HPO:probinson	
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000054	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000089	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000175	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000238	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000316	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000431	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000470	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000568	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0000957	OMIM:614083	TAS				P		HPO:probinson	
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0001263	OMIM:614083	TAS				P		HPO:probinson	
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0001511	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0001903	OMIM:614083	TAS				P		HPO:probinson	
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0001999	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0002023	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0002032	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0002575	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0005280	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0005528	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0008551	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0009777	OMIM:614083	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614083	FANCONI ANEMIA, COMPLEMENTATION GROUP L		HP:0040012	OMIM:614083	TAS				P		HPO:skoehler	
OMIM	614089	#614089 ATRIAL SEPTAL DEFECT 3; ASD3		HP:0000006	PMID:15735645	PCS				I		HPO:probinson	
OMIM	614089	#614089 ATRIAL SEPTAL DEFECT 3; ASD3		HP:0001684	PMID:15735645	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000007	PMID:21473986	PCS				I		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7	HP:0012825	HP:0000047	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000089	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000107	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000113	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000175	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000200	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000218	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000268	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000286	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000476	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000691	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000773	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000774	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0000882	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0001156	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0001159	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0001789	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0002089	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0002213	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0002983	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0003026	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0003027	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0006349	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0006487	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0006644	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0008070	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0009882	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0010442	PMID:21473986	PCS				P		HPO:probinson	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0010812	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0011090	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0100259	OMIM:614091	TAS				P		HPO:skoehler	
OMIM	614091	SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY; SRTD7		HP:0100840	OMIM:614091	IEA				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0000007	OMIM:614096	TAS				I		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0001508	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0001522	OMIM:614096	TAS				M		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0001639	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE	HP:0012825	HP:0002089	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0002151	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0002353	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0003128	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614096	#614096 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8;;CARDIOMYOPATHY, HYPERTROPHIC MITOCHONDRIAL, FATAL INFANTILE		HP:0003324	OMIM:614096	TAS				P		HPO:skoehler	
OMIM	614097	#614097 ACATALASEMIA;;ACATALASIA;;CATALASE DEFICIENCY		HP:0000007	OMIM:614097	TAS				I		HPO:probinson	
OMIM	614097	#614097 ACATALASEMIA;;ACATALASIA;;CATALASE DEFICIENCY		HP:0000155	OMIM:614097	TAS				P		HPO:probinson	
OMIM	614097	#614097 ACATALASEMIA;;ACATALASIA;;CATALASE DEFICIENCY		HP:0012517	OMIM:614097	TAS				P		HPO:probinson	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000006	OMIM:614098	TAS				I		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000194	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000252	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000322	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000347	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000430	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0000520	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0001090	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0001285	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0001347	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0001371	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0001508	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0002373	OMIM:614098	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0002650	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0002705	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0005328	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0007485	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0009064	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0010804	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614098	KEPPEN-LUBINSKY SYNDROME; KPLBS		HP:0010864	OMIM:614098	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000007	OMIM:614099	TAS				I		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000090	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000232	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000256	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000347	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000506	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000685	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000687	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000774	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000958	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000968	OMIM:614099	IEA				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0000973	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001156	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001159	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001388	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001394	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001799	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001821	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0001852	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0002007	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0002213	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0003774	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0004322	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0004442	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0004969	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0008070	OMIM:614099	TAS				P		HPO:skoehler	
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0030799	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614099	CRANIOECTODERMAL DYSPLASIA 3		HP:0100259	OMIM:614099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0000006	OMIM:614100	TAS				I		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0000776	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0000973	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0001166	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0001627	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0002097	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614100	%614100 CUTIS LAXA, NEONATAL, WITH MARFANOID PHENOTYPE;;CUTIS LAXA-MARFANOID SYNDROME		HP:0002827	OMIM:614100	TAS				P		HPO:skoehler	
OMIM	614101	PLASMA FIBRONECTIN DEFICIENCY		HP:0000006	OMIM:614101	TAS				I		HPO:skoehler	
OMIM	614102	#614102 IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY; IGKCD;;KAPPA CHAIN DEFICIENCY		HP:0000007	OMIM:614102	TAS				I		HPO:skoehler	
OMIM	614102	#614102 IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY; IGKCD;;KAPPA CHAIN DEFICIENCY		HP:0002014	OMIM:614102	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614102	#614102 IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY; IGKCD;;KAPPA CHAIN DEFICIENCY		HP:0002719	OMIM:614102	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614102	#614102 IMMUNOGLOBULIN KAPPA LIGHT CHAIN DEFICIENCY; IGKCD;;KAPPA CHAIN DEFICIENCY		HP:0010701	OMIM:614102	TAS				P		HPO:probinson	
OMIM	614103	LIPEDEMA		HP:0000006	OMIM:614103	TAS				I		HPO:skoehler	
OMIM	614103	LIPEDEMA		HP:0000969	OMIM:614103	IEA				P		HPO:skoehler	
OMIM	614103	LIPEDEMA		HP:0100695	OMIM:614103	IEA				P		HPO:skoehler	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000006	PMID:25920557	PCS				I		HPO:probinson	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000179	PMID:23099646	PCS		HP:0040284		P		HP:probinson	3/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000219	PMID:25920557	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000252	PMID:23099646,PMID:25167861,PMID:25920557	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000319	PMID:25920557	PCS		HP:0040284		P		HP:probinson	5/10
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000341	OMIM:614104	TAS				P		HPO:probinson	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000347	OMIM:614104,PMID:25920557	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000377	OMIM:614104	TAS				P		HPO:skoehler	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000391	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000400	PMID:23099646,PMID:25920557	PCS		HP:0040284		P		HPO:skoehler	5/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000414	PMID:23099646	TAS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000490	PMID:23099646,PMID:25920557	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000601	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000717	PMID:25920557	PCS		HP:0040284		P		HPO:probinson	4/10
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000748	PMID:23099646	PCS		HP:0040284		P		HP:probinson	1/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000750	PMID:23099646,PMID:25920557	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000752	PMID:23099646,PMID:25167861	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0000767	PMID:25167861	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001250	PMID:23099646,PMID:25920557	PCS		HP:0040284		P		HP:probinson	6/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001251	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001288	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001290	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001511	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001518	PMID:23099646	PCS		HP:0040284		P		HP:probinson	5/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001531	OMIM:614104	TAS				P		HPO:probinson	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0001822	OMIM:614104	TAS				P		HPO:probinson	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0002120	PMID:23099646	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0002311	PMID:25920557	PCS		HP:0040284		P		HP:probinson	6/9
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0002373	OMIM:614104	TAS				P		HPO:probinson	
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0002719	PMID:25920557	PCS		HP:0040284		P		HP:probinson	4/9
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0003561	PMID:23099646	PCS		HP:0040284		P		HP:probinson	5/5
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0008872	PMID:23099646,PMID:25920557	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0010864	PMID:23099646	PCS		HP:0040284		P		HPO:skoehler	1/1
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0011344	PMID:23099646,PMID:25167861	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0012171	PMID:23099646	PCS		HP:0040284		P		HP:probinson	2/3
OMIM	614104	MENTAL RETARDATION, AUTOSOMAL DOMINANT 7		HP:0040082	PMID:23099646	PCS		HP:0040284		P		HP:probinson	1/6
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000007	OMIM:614105	TAS				I		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000218	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000252	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000286	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000316	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000343	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000348	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000414	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000494	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000518	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0000568	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0001263	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0001290	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0001332	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0001942	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0001999	OMIM:614105	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0002007	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0002079	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0003196	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0005280	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0010804	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0011968	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614105	METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE DEFICIENCY		HP:0012448	OMIM:614105	TAS				P		HPO:skoehler	
OMIM	614111	#614111 PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY; PDHBD		HP:0000007	OMIM:614111	TAS				I		HPO:probinson	
OMIM	614111	#614111 PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY; PDHBD		HP:0001290	OMIM:614111	TAS				P		HPO:probinson	
OMIM	614111	#614111 PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY; PDHBD		HP:0003128	OMIM:614111	TAS				P		HPO:probinson	
OMIM	614113	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2		HP:0000006	OMIM:614113	TAS				I		HPO:probinson	
OMIM	614113	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2		HP:0000750	OMIM:614113	TAS				P		HPO:skoehler	
OMIM	614113	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2		HP:0001249	OMIM:614113	TAS				P		HPO:probinson	
OMIM	614113	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2		HP:0001250	OMIM:614113	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614113	MENTAL RETARDATION, AUTOSOMAL DOMINANT 2		HP:0001263	OMIM:614113	TAS				P		HPO:probinson	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000007	OMIM:614114	TAS				I		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000252	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000268	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000276	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000286	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	3/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000325	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000347	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000365	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000369	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000490	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000494	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000581	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000821	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000824	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0000957	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001256	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001290	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001511	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001518	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001629	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001631	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001659	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001680	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0001682	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0002007	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0002101	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0002247	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0002750	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0003196	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0004322	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0005280	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	2/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0010535	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0012745	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0030084	OMIM:614114	TAS				P		HPO:skoehler	
OMIM	614114	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2		HP:0200040	OMIM:614114	TAS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0000007	OMIM:614115	TAS				I		HPO:skoehler	
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM	HP:0025303	HP:0000572	OMIM:614115	TAS				P		HPO:skoehler	
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0001263	OMIM:614115	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0001302	OMIM:614115	IEA				P		HPO:skoehler	
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0002069	OMIM:614115	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0002126	OMIM:614115	IEA				P		HPO:skoehler	
OMIM	614115	CORTICAL MALFORMATIONS, OCCIPITAL; OCCM		HP:0002353	OMIM:614115	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000006	OMIM:614116	TAS				I		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000407	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000726	OMIM:614116	TAS	HP:0003581			P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000737	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000741	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0000763	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0001262	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0001265	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0002059	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0002354	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0002754	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0003380	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0003676	OMIM:614116	TAS				C		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0031258	OMIM:614116	IEA				P		HPO:skoehler	
OMIM	614116	NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E		HP:0100710	OMIM:614116	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0000007	OMIM:614120	TAS				I		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0000175	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0000238	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0000347	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0001274	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0002119	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0002323	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0002419	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0100258	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614120	#614120 HYDROLETHALUS SYNDROME 2; HLS2		HP:0100259	OMIM:614120	TAS				P		HPO:skoehler	
OMIM	614122	CHITOTRIOSIDASE DEFICIENCY		HP:0000007	OMIM:614122	TAS				I		HPO:skoehler	
OMIM	614128	#614128 LACTATE DEHYDROGENASE B DEFICIENCY; LDHBD		HP:0045041	OMIM:614128	IEA				P		HPO:skoehler	
OMIM	614129	PERRAULT SYNDROME 3		HP:0000007	OMIM:614129	TAS				I		HPO:probinson	
OMIM	614129	PERRAULT SYNDROME 3		HP:0000013	OMIM:614129	TAS				P		HPO:skoehler	
OMIM	614129	PERRAULT SYNDROME 3		HP:0000252	OMIM:614129	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614129	PERRAULT SYNDROME 3		HP:0000786	OMIM:614129	TAS				P		HPO:probinson	
OMIM	614129	PERRAULT SYNDROME 3		HP:0000815	OMIM:614129	TAS				P		HPO:probinson	
OMIM	614129	PERRAULT SYNDROME 3		HP:0001250	OMIM:614129	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614129	PERRAULT SYNDROME 3		HP:0004322	OMIM:614129	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614129	PERRAULT SYNDROME 3		HP:0008527	OMIM:614129	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000007	OMIM:614131	TAS				I		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000092	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000093	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000097	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000100	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000790	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0000969	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0003073	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0003676	OMIM:614131	TAS				C		HPO:skoehler	
OMIM	614131	#614131 FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6;;GLOMERULOSCLEROSIS, FOCAL SEGMENTAL, 6		HP:0012622	OMIM:614131	TAS				P		HPO:skoehler	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0000007	OMIM:614134	TAS				I		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0000407	OMIM:614134	TAS				P		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0000483	PMID:16909383	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0002656	OMIM:614134	TAS				P		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0002857	PMID:16909383	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0003370	PMID:16909383	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0004322	PMID:16909383	PCS				P		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0005041	PMID:16909383	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0007964	OMIM:614134	TAS				P		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0011003	OMIM:614134	TAS				P		HPO:probinson	
OMIM	614134	#614134 STICKLER SYNDROME, TYPE IV; STL4		HP:0012368	PMID:16909383	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0000006	OMIM:614135	TAS				I		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0002654	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0002656	OMIM:614135	IEA				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0002758	OMIM:614135	TAS	HP:0003621			P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0002815	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0002829	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0003301	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0003365	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0003370	PMID:11565064	TAS				P		HPO:probinson	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0006398	PMID:11565064	TAS				P		HPO:probinson	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0006407	PMID:11565064	TAS				P		HPO:probinson	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0010582	PMID:11565064	PCS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0010585	PMID:11565064	PCS				P		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0011463	OMIM:614135	TAS				C		HPO:skoehler	
OMIM	614135	#614135 EPIPHYSEAL DYSPLASIA, MULTIPLE, 6; EDM6		HP:0030041	OMIM:614135	TAS				P		HPO:skoehler	
OMIM	614149	%614149 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9; NDNC9;;ANONYCHIA-ONYCHOLYSIS, ISOLATED;;ONYCHODYSTROPHY;;NAIL DYSPLASIA		HP:0000007	OMIM:614149	TAS				I		HPO:skoehler	
OMIM	614149	%614149 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9; NDNC9;;ANONYCHIA-ONYCHOLYSIS, ISOLATED;;ONYCHODYSTROPHY;;NAIL DYSPLASIA		HP:0001802	OMIM:614149	TAS				P		HPO:skoehler	
OMIM	614149	%614149 NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9; NDNC9;;ANONYCHIA-ONYCHOLYSIS, ISOLATED;;ONYCHODYSTROPHY;;NAIL DYSPLASIA		HP:0008400	OMIM:614149	TAS				P		HPO:skoehler	
OMIM	614152	DEAFNESS, AUTOSOMAL DOMINANT 64; DFNA64		HP:0000006	OMIM:614152	TAS				I		HPO:skoehler	
OMIM	614152	DEAFNESS, AUTOSOMAL DOMINANT 64; DFNA64		HP:0000360	OMIM:614152	IEA				P		HPO:skoehler	
OMIM	614152	DEAFNESS, AUTOSOMAL DOMINANT 64; DFNA64		HP:0000407	OMIM:614152	TAS				P		HPO:skoehler	
OMIM	614152	DEAFNESS, AUTOSOMAL DOMINANT 64; DFNA64		HP:0003676	OMIM:614152	TAS				C		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000006	PMID:22744658	PCS				I		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000365	PMID:22492559	PCS		HP:0040284		P		HP:probinson	31/42
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000508	PMID:22492559	PCS		HP:0040284		P		HP:probinson	4/44
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000511	PMID:22492559	PCS		HP:0040284		P		HP:probinson	7/39
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000514	PMID:22492559	PCS		HP:0040284		P		HPO:skoehler	24/39
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0000639	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001252	PMID:22744658	PCS		HP:0040284		P		HP:probinson	4/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001260	PMID:22744658,PMID:22492559	PCS		HP:0040284		P		HPO:skoehler	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001272	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001276	PMID:22744658	PCS		HP:0040284		P		HP:probinson	4/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001308	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	10/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001324	PMID:22744658	PCS		HP:0040284		P		HP:probinson	5/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0001347	PMID:22744658	TAS		HP:0040284		P		HPO:skoehler	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0002015	PMID:22744658	PCS		HP:0040284		P		HP:probinson	6/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0002066	PMID:22492559	PCS				P		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0002070	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0002078	PMID:22744658	PCS		HP:0040284		P		HP:probinson	14/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0002311	OMIM:614153	TAS				P		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0003202	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	9/14
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0003445	PMID:22744658	IEA				P		HP:probinson	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0003487	PMID:22492559	PCS				P		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0003676	PMID:22492559	PCS				C		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0007772	OMIM:614153	TAS				P		HPO:skoehler	
OMIM	614153	#614153 SPINOCEREBELLAR ATAXIA 36; SCA36		HP:0012473	PMID:22744658	PCS		HP:0040284		P		HPO:skoehler	13/14
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0000006	OMIM:614156	TAS				I		HPO:skoehler	
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0000007	OMIM:614156	TAS				I		HPO:skoehler	
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0001081	OMIM:614156	TAS				P		HPO:skoehler	
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0001396	OMIM:614156	TAS				P		HPO:skoehler	
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0001410	OMIM:614156	TAS				P		HPO:skoehler	
OMIM	614156	HYPERBILIVERDINEMIA; HBLVD		HP:0032003	OMIM:614156	IEA				P		HPO:skoehler	
OMIM	614157	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10; NDNC10		HP:0000007	OMIM:614157	TAS				I		HPO:skoehler	
OMIM	614157	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10; NDNC10		HP:0001806	OMIM:614157	TAS				P		HPO:skoehler	
OMIM	614157	NAIL DISORDER, NONSYNDROMIC CONGENITAL, 10; NDNC10		HP:0012542	OMIM:614157	TAS				P		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0000006	OMIM:614158	TAS				I		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0000421	OMIM:614158	TAS				P		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0000978	OMIM:614158	TAS				P		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0003010	OMIM:614158	TAS				P		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0031364	OMIM:614158	IEA				P		HPO:skoehler	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0032244	OMIM:614158	TAS				P		HP:probinson	
OMIM	614158	BLEEDING DISORDER, PLATELET-TYPE, 14; BDPLT14		HP:0032244	OMIM:614158	IEA				P		HPO:skoehler	
OMIM	614160	#614160 MUSCLE HYPERTROPHY; MSLHP		HP:0000007	OMIM:614160	TAS				I		HPO:probinson	
OMIM	614160	#614160 MUSCLE HYPERTROPHY; MSLHP		HP:0003712	OMIM:614160	TAS				P		HPO:probinson	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000006	OMIM:614162	TAS				I		HPO:probinson	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000819	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000821	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000823	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000938	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0000964	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT	HP:0003676	HP:0001888	OMIM:614162	TAS				P		HPO:skoehler	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0001890	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002014	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002205	OMIM:614162	TAS				P		HPO:skoehler	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002721	OMIM:614162	TAS				P		HPO:skoehler	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002728	OMIM:614162	TAS				P		HPO:probinson	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0002958	OMIM:614162	TAS				P		HPO:skoehler	
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0004322	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614162	#614162 IMMUNODEFICIENCY 31C; IMD31C;;CANDIDIASIS, FAMILIAL, 7; CANDF7;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT		HP:0011473	OMIM:614162	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614163	DELAYED SLEEP PHASE DISORDER, SUSCEPTIBILITY TO; DSPD		HP:0100785	OMIM:614163	IEA				P		HPO:skoehler	
OMIM	614164	%614164 GLUTATHIONE PEROXIDASE DEFICIENCY; GPXD		HP:0000007	OMIM:614164	TAS				I		HPO:skoehler	
OMIM	614164	%614164 GLUTATHIONE PEROXIDASE DEFICIENCY; GPXD		HP:0003265	OMIM:614164	TAS				P		HPO:skoehler	
OMIM	614164	%614164 GLUTATHIONE PEROXIDASE DEFICIENCY; GPXD		HP:0004863	OMIM:614164	TAS				P		HPO:skoehler	
OMIM	614165	#614165 PARAGANGLIOMAS 5; PGL5		HP:0000006	OMIM:614165	TAS				I		HPO:skoehler	
OMIM	614165	#614165 PARAGANGLIOMAS 5; PGL5		HP:0002668	OMIM:614165	IEA				P		HPO:skoehler	
OMIM	614167	#614167 MYOPIA 21, AUTOSOMAL DOMINANT; MYP21		HP:0000006	OMIM:614167	TAS				I		HPO:skoehler	
OMIM	614167	#614167 MYOPIA 21, AUTOSOMAL DOMINANT; MYP21	HP:0012828	HP:0011003	OMIM:614167	TAS				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000007	OMIM:614170	TAS				I		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000023	OMIM:614170	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000365	OMIM:614170	TAS				P		HPO:probinson	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000485	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000545	OMIM:614170	TAS				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000563	OMIM:614170	TAS				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000592	OMIM:614170	TAS				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0000647	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0001119	OMIM:614170	TAS				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0001288	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0001382	OMIM:614170	IEA				P		HPO:skoehler	
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0001537	OMIM:614170	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0002757	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0003326	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614170	BRITTLE CORNEA SYNDROME 2; BCS2		HP:0007720	OMIM:614170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0000007	OMIM:614171	TAS				I		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0001010	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0001107	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0001873	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0001882	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0006934	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614171	HERMANSKY-PUDLAK SYNDROME 9		HP:0007894	OMIM:614171	TAS				P		HPO:skoehler	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0000006	OMIM:614172	TAS				I		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0001875	OMIM:614172	TAS				P		HPO:skoehler	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0001888	OMIM:614172	IEA				P		HPO:skoehler	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0001915	OMIM:614172	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0002721	OMIM:614172	IEA				P		HPO:skoehler	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0002841	OMIM:614172	TAS				P		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0002863	OMIM:614172	IEA				P		HPO:skoehler	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0004429	OMIM:614172	TAS				P		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0011275	OMIM:614172	TAS				P		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0012176	OMIM:614172	TAS				P		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0012312	OMIM:614172	TAS				P		HPO:probinson	
OMIM	614172	IMMUNODEFICIENCY 21; IMD21		HP:0012324	OMIM:614172	IEA				P		HPO:skoehler	
OMIM	614173	JOUBERT SYNDROME 13; JBTS13		HP:0000007	PMID:26477546	PCS				I		HPO:skoehler	
OMIM	614173	JOUBERT SYNDROME 13; JBTS13		HP:0001302	OMIM:614173	IEA				P		HPO:skoehler	
OMIM	614173	JOUBERT SYNDROME 13; JBTS13		HP:0001320	PMID:21725307	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	614173	JOUBERT SYNDROME 13; JBTS13		HP:0002419	PMID:21725307	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000007	OMIM:614175	TAS				I		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000047	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000054	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000107	OMIM:614175	TAS				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000175	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000286	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000508	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0000960	OMIM:614175	TAS				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0001250	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0002085	OMIM:614175	TAS				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0002323	OMIM:614175	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0002419	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0045025	OMIM:614175	IEA				P		HPO:skoehler	
OMIM	614175	MECKEL SYNDROME, TYPE 10; MKS10		HP:0100259	OMIM:614175	TAS				P		HPO:skoehler	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0000007	PMID:21310491	PCS				I		HPO:probinson	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0000505	PMID:21310491	PCS				P		HPO:probinson	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0000510	OMIM:614180	IEA				P		HPO:skoehler	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0000662	PMID:21310491	PCS				P		HPO:probinson	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0007688	PMID:21310491	PCS				P		HPO:probinson	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0007737	PMID:21310491	PCS				P		HPO:probinson	
OMIM	614180	#614180 RETINITIS PIGMENTOSA 61; RP61		HP:0007843	PMID:21310491	PCS				P		HPO:probinson	
OMIM	614181	RETINITIS PIGMENTOSA 62; RP62		HP:0000007	OMIM:614181	TAS				I		HPO:skoehler	
OMIM	614181	RETINITIS PIGMENTOSA 62; RP62		HP:0000510	OMIM:614181	IEA				P		HPO:skoehler	
OMIM	614181	RETINITIS PIGMENTOSA 62; RP62		HP:0000543	OMIM:614181	TAS				P		HPO:skoehler	
OMIM	614181	RETINITIS PIGMENTOSA 62; RP62		HP:0000662	OMIM:614181	TAS				P		HPO:skoehler	
OMIM	614181	RETINITIS PIGMENTOSA 62; RP62		HP:0001123	OMIM:614181	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000006	OMIM:614185	TAS				I		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000219	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000293	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000316	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000319	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0000343	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001387	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001634	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001650	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001653	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001718	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0001773	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0002092	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0002093	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0002240	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0002750	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0003196	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0003300	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0004279	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0004322	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0010579	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614185	#614185 GELEOPHYSIC DYSPLASIA 2; GPHYSD2		HP:0040083	OMIM:614185	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000007	OMIM:614186	TAS				I		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000486	OMIM:614186	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000518	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000543	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000613	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000639	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0000662	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614186	LEBER CONGENITAL AMAUROSIS 16		HP:0007663	OMIM:614186	TAS				P		HPO:skoehler	
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD		HP:0000006	OMIM:614187	TAS				I		HPO:skoehler	
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD		HP:0000049	OMIM:614187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD		HP:0000316	OMIM:614187	TAS				P		HPO:skoehler	
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD		HP:0000365	OMIM:614187	TAS				P		HPO:skoehler	
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD		HP:0000579	OMIM:614187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614187	%614187 HYPERTELORISM, PREAURICULAR SINUS, PUNCTAL PITS, AND DEAFNESS; HPPD	HP:0012832	HP:0004467	OMIM:614187	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000007	OMIM:614188	TAS				I		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000243	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000248	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000262	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000316	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000327	OMIM:614188	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0000684	OMIM:614188	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0001085	OMIM:614188	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0001363	OMIM:614188	IEA				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0001822	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0004425	OMIM:614188	IEA				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0004440	OMIM:614188	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0004442	OMIM:614188	TAS				P		HPO:skoehler	
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0004443	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0004691	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0009803	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0011069	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0030084	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0030799	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614188	CRANIOSYNOSTOSIS AND DENTAL ANOMALIES; CRSDA		HP:0100798	OMIM:614188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614190	#614190 PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3; PPNAD3;;CUSHING SYNDROME, ADRENAL, DUE TO PPNAD3		HP:0000006	OMIM:614190	TAS				I		HPO:probinson	
OMIM	614190	#614190 PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3; PPNAD3;;CUSHING SYNDROME, ADRENAL, DUE TO PPNAD3		HP:0003118	OMIM:614190	TAS				P		HPO:probinson	
OMIM	614190	#614190 PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3; PPNAD3;;CUSHING SYNDROME, ADRENAL, DUE TO PPNAD3		HP:0008221	OMIM:614190	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000006	OMIM:614192	TAS				I		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000219	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000256	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000337	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000343	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000455	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0000494	OMIM:614192	TAS				P		HPO:probinson	
OMIM	614192	#614192 MACROCEPHALY, MACROSOMIA, FACIAL DYSMORPHISM SYNDROME; MMFD		HP:0001999	OMIM:614192	IEA				P		HPO:skoehler	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0000006	OMIM:614195	TAS				I		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0000238	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0000316	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0000356	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0000512	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0007035	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0007291	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0007700	OMIM:614195	IEA				P		HPO:skoehler	
OMIM	614195	#614195 CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME; CAASDS		HP:0011488	OMIM:614195	TAS				P		HPO:probinson	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0000007	OMIM:614196	TAS				I		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0000093	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0000097	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0000100	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0000969	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0003073	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0003828	OMIM:614196	TAS				C		HPO:skoehler	
OMIM	614196	#614196 NEPHROTIC SYNDROME, TYPE 6; NPHS6		HP:0005576	OMIM:614196	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0000007	OMIM:614198	TAS				I		HPO:probinson	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0000218	OMIM:614198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0000508	OMIM:614198	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0000544	OMIM:614198	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0001270	OMIM:614198	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0001288	OMIM:614198	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0002104	OMIM:614198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0003307	OMIM:614198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0003388	OMIM:614198	TAS				P		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0003473	OMIM:614198	TAS				P		HPO:probinson	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0003593	OMIM:614198	TAS				C		HPO:skoehler	
OMIM	614198	MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16		HP:0003828	OMIM:614198	TAS				C		HPO:skoehler	
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000007	OMIM:614199	TAS				I		HPO:probinson	
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000093	OMIM:614199	TAS				P		HPO:probinson	
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000100	OMIM:614199	TAS	HP:0003577			P		HPO:probinson	
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000486	OMIM:614199	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000545	OMIM:614199	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0000639	OMIM:614199	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	614199	#614199 NEPHROTIC SYNDROME, TYPE 5, WITH OR WITHOUT OCULAR ABNORMALITIES;NPHS5		HP:0003774	OMIM:614199	TAS				P		HPO:probinson	
OMIM	614200	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN Ia DEFICIENCY;;GP Ia DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY		HP:0000006	OMIM:614200	TAS				I	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN IA DEFICIENCY;;GP IA DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY	HPO:skoehler	
OMIM	614200	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN Ia DEFICIENCY;;GP Ia DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY		HP:0000978	OMIM:614200	TAS				P	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN IA DEFICIENCY;;GP IA DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY	HPO:skoehler	
OMIM	614200	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN Ia DEFICIENCY;;GP Ia DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY	HP:0012825	HP:0001873	OMIM:614200	TAS				P	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN IA DEFICIENCY;;GP IA DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY	HPO:skoehler	
OMIM	614200	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN Ia DEFICIENCY;;GP Ia DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY		HP:0003577	OMIM:614200	TAS				C	%614200 BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9;;GLYCOPROTEIN IA DEFICIENCY;;GP IA DEFICIENCY;;COLLAGEN PLATELET RECEPTOR DEFICIENCY	HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0000007	OMIM:614201	TAS				I		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0000132	OMIM:614201	TAS				P		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0000421	OMIM:614201	TAS				P		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0000978	OMIM:614201	TAS				P		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0003010	OMIM:614201	TAS				P		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0003593	OMIM:614201	TAS				C		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0003828	OMIM:614201	TAS				C		HPO:skoehler	
OMIM	614201	BLEEDING DISORDER, PLATELET-TYPE, 11; BDPLT11		HP:0031364	OMIM:614201	IEA				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000007	OMIM:614202	TAS				I		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000219	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000268	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000272	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000276	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000307	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000316	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000319	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000322	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000431	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000448	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000494	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0000718	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0001250	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0001263	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0001513	OMIM:614202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0002342	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0004523	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614202	#614202 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15; MRT15		HP:0011229	OMIM:614202	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0000006	OMIM:614203	TAS				I		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0001300	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0002063	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0002067	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0002172	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0002304	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0002322	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614203	#614203 PARKINSON DISEASE 17; PARK17		HP:0100660	OMIM:614203	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0000007	OMIM:614204	TAS				I		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0000221	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0001036	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0001945	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0002164	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0003765	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0008404	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0010783	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0025092	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0025252	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0030151	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0040313	OMIM:614204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614204	PSORIASIS 14, PUSTULAR		HP:0200039	OMIM:614204	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000007	OMIM:614205	TAS				I		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000268	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000272	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000307	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000325	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000411	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000463	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0000470	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0001385	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0001518	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0002007	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0003100	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0003307	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0004322	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0004570	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0010306	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614205	#614205 THREE M SYNDROME 3; 3M3;;3@M SYNDROME 3		HP:0011800	OMIM:614205	TAS				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0000007	OMIM:614207	TAS				I		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0000175	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0000252	OMIM:614207	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0000431	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0000455	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0001250	OMIM:614207	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0001256	OMIM:614207	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0001263	OMIM:614207	TAS				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0001290	OMIM:614207	TAS				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0001344	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0002059	OMIM:614207	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0002905	OMIM:614207	TAS				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0003155	OMIM:614207	TAS				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0003196	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0003577	OMIM:614207	TAS				C		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0010804	OMIM:614207	IEA				P		HPO:skoehler	
OMIM	614207	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 3; HPMRS3		HP:0010864	OMIM:614207	TAS				P		HPO:skoehler	
OMIM	614208	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16		HP:0000007	OMIM:614208	TAS				I		HPO:skoehler	
OMIM	614208	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16		HP:0000664	OMIM:614208	TAS				P		HPO:skoehler	
OMIM	614208	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16		HP:0001249	OMIM:614208	TAS				P		HPO:skoehler	
OMIM	614208	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 16		HP:0001250	OMIM:614208	TAS				P		HPO:skoehler	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0000003	OMIM:614209	TAS				P		HPO:probinson	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0000007	OMIM:614209	TAS				I		HPO:probinson	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0000062	OMIM:614209	TAS				P		HPO:skoehler	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0000932	OMIM:614209	TAS				P		HPO:probinson	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0001762	OMIM:614209	TAS				P		HPO:probinson	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0002085	OMIM:614209	TAS				P		HPO:probinson	
OMIM	614209	#614209 MECKEL SYNDROME, TYPE 9; MKS9		HP:0009826	OMIM:614209	TAS				P		HPO:skoehler	
OMIM	614211	%614211 DEAFNESS, AUTOSOMAL DOMINANT 33; DFNA33		HP:0000006	OMIM:614211	TAS				I		HPO:skoehler	
OMIM	614211	%614211 DEAFNESS, AUTOSOMAL DOMINANT 33; DFNA33		HP:0000360	OMIM:614211	TAS				P		HPO:skoehler	
OMIM	614211	%614211 DEAFNESS, AUTOSOMAL DOMINANT 33; DFNA33		HP:0000407	OMIM:614211	TAS				P		HPO:skoehler	
OMIM	614211	%614211 DEAFNESS, AUTOSOMAL DOMINANT 33; DFNA33		HP:0003676	OMIM:614211	TAS				C		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0000006	OMIM:614212	TAS				I		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0000007	OMIM:614212	TAS				I		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0001250	OMIM:614212	TAS				P		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0001259	OMIM:614212	TAS				P		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0001298	OMIM:614212	IEA				P		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0001945	OMIM:614212	IEA				P		HPO:skoehler	
OMIM	614212	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 4; IIAE4		HP:0002181	OMIM:614212	TAS				P		HPO:skoehler	
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0000007	OMIM:614213	TAS				I		HPO:skoehler	
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0001263	OMIM:614213	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0001265	OMIM:614213	TAS				P		HPO:skoehler	
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0001284	OMIM:614213	TAS				P		HPO:skoehler	
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0003676	OMIM:614213	TAS				C		HPO:skoehler	
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0004322	OMIM:614213	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614213	#614213 NEUROPATHY, HEREDITARY SENSORY, TYPE IIC; HSN2C		HP:0009830	OMIM:614213	IEA				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000007	OMIM:614219	TAS				I		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000252	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000256	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000294	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000316	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000347	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000369	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000411	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000414	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000486	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000519	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000568	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000648	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000954	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0000965	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001057	OMIM:614219	IEA				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001250	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001263	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001290	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001321	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001562	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0001792	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0002059	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0002126	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0005280	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0006951	OMIM:614219	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0025356	OMIM:614219	IEA				P		HPO:skoehler	
OMIM	614219	ADAMS-OLIVER SYNDROME 2; AOS2		HP:0045025	OMIM:614219	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000007	OMIM:614222	TAS				I		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000046	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000054	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000189	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000248	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000294	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000347	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000400	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000482	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000519	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000568	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3	HP:0012825	HP:0000581	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000594	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000639	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000648	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0000998	OMIM:614222	IEA				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0001250	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0001371	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002079	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002119	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002120	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002126	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002187	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002510	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002714	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0002751	OMIM:614222	TAS				P		HPO:probinson	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0003196	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0004209	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0005484	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0008734	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0008897	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0008936	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614222	WARBURG MICRO SYNDROME 3; WARBM3		HP:0011448	OMIM:614222	TAS				P		HPO:skoehler	
OMIM	614224	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS		HP:0000007	OMIM:614224	TAS				I		HPO:skoehler	
OMIM	614224	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS		HP:0001642	OMIM:614224	TAS				P		HPO:skoehler	
OMIM	614224	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS		HP:0012231	OMIM:614224	TAS				P		HPO:skoehler	
OMIM	614224	RETINAL ARTERIAL MACROANEURYSM WITH SUPRAVALVULAR PULMONIC STENOSIS		HP:0025355	OMIM:614224	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000007	OMIM:614225	TAS				I		HPO:probinson	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000028	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000046	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000054	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000059	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000248	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000294	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000400	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000426	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000482	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2	HP:0012832	HP:0000519	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000568	OMIM:614225	TAS				P		HPO:probinson	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0000648	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0001264	OMIM:614225	IEA				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0001344	OMIM:614225	IEA				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0001371	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0001845	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0002079	OMIM:614225	TAS				P		HPO:probinson	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0002126	OMIM:614225	TAS				P		HPO:probinson	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0002283	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0003196	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0005484	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0007965	OMIM:614225	TAS				P		HPO:probinson	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0008897	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0008936	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0010722	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0010864	OMIM:614225	TAS				P		HPO:skoehler	
OMIM	614225	WARBURG MICRO SYNDROME 2; WARBM2		HP:0011344	OMIM:614225	TAS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000006	PMID:21802063	PCS				I		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000175	OMIM:614226	TAS				P		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000252	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000520	OMIM:614226	TAS				P		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000574	OMIM:614226	TAS				P		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000601	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0000664	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0001263	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0001274	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0001360	PMID:21802063	PCS				P		HPO:probinson	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0001748	OMIM:614226	TAS				P		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0003745	OMIM:614226	TAS				I		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0003828	OMIM:614226	TAS				C		HPO:skoehler	
OMIM	614226	HOLOPROSENCEPHALY 11		HP:0410030	OMIM:614226	TAS				P		HPO:skoehler	
OMIM	614227	%614227 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3; HNFJ3		HP:0000006	OMIM:614227	TAS				I		HPO:skoehler	
OMIM	614227	%614227 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3; HNFJ3		HP:0000083	OMIM:614227	TAS				P		HPO:skoehler	
OMIM	614227	%614227 HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3; HNFJ3		HP:0000112	OMIM:614227	IEA				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0000006	OMIM:614228	TAS				I		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0001265	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0001270	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0001761	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0002359	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0002460	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0002527	OMIM:614228	IEA				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0002936	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0003431	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0003677	OMIM:614228	TAS				C		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0003690	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614228	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2O; CMT2O		HP:0009046	OMIM:614228	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0000007	OMIM:614229	TAS				I		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0000639	OMIM:614229	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0001260	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0001263	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0001272	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0002015	OMIM:614229	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0002070	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0002078	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0003677	OMIM:614229	TAS				C		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0007772	OMIM:614229	TAS				P		HPO:skoehler	
OMIM	614229	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 11; SCAR11		HP:0025356	OMIM:614229	IEA				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000006	OMIM:614230	TAS				I		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000286	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000293	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000311	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000322	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000347	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000348	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000369	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000407	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000411	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000431	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000470	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000494	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000508	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0000581	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0001159	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0001249	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0001290	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0002714	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0003745	OMIM:614230	TAS				I		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0007759	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0012385	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614230	CHROMOSOME 8Q21.11 DELETION SYNDROME		HP:0012745	OMIM:614230	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000007	OMIM:614231	TAS				I		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000028	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000046	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000135	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000212	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000218	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000252	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000293	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000341	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000463	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000508	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000648	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000819	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000938	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0000952	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0001263	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0001319	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0001321	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0001348	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002079	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002123	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002187	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002205	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002521	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002756	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0002910	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0003577	OMIM:614231	TAS				C		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0008936	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0009879	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0010804	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0011968	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0012448	OMIM:614231	TAS				P		HPO:skoehler	
OMIM	614231	MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME		HP:0012594	OMIM:614231	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614233	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1		HP:0000006	PMID:16709486	PCS				I		HPO:probinson	
OMIM	614233	HYPERPIGMENTATION, FAMILIAL PROGRESSIVE, 1		HP:0000953	PMID:16709486	PCS				P		HPO:probinson	
OMIM	614237	HYPOTRICHOSIS 9; HYPT9		HP:0000007	PMID:20054564	PCS				I		HP:probinson	
OMIM	614237	HYPOTRICHOSIS 9; HYPT9		HP:0002209	PMID:20054564	PCS				P		HP:probinson	
OMIM	614237	HYPOTRICHOSIS 9; HYPT9		HP:0002231	PMID:20054564	PCS				P		HP:probinson	
OMIM	614238	HYPOTRICHOSIS 10; HYPT10		HP:0000653	OMIM:614238	IEA				P		HPO:skoehler	
OMIM	614238	HYPOTRICHOSIS 10; HYPT10		HP:0002231	OMIM:614238	IEA				P		HPO:skoehler	
OMIM	614238	HYPOTRICHOSIS 10; HYPT10		HP:0045075	OMIM:614238	IEA				P		HPO:skoehler	
OMIM	614249	#614249 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18; MRT18		HP:0000007	OMIM:614249	TAS				I		HPO:probinson	
OMIM	614249	#614249 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18; MRT18		HP:0001249	OMIM:614249	TAS				P		HPO:probinson	
OMIM	614250	#614250 NARCOLEPSY 7; NRCLP7		HP:0000006	OMIM:614250	TAS				I		HPO:skoehler	
OMIM	614250	#614250 NARCOLEPSY 7; NRCLP7		HP:0001513	OMIM:614250	TAS				P		HPO:skoehler	
OMIM	614250	#614250 NARCOLEPSY 7; NRCLP7		HP:0002189	OMIM:614250	TAS				P		HPO:skoehler	
OMIM	614250	#614250 NARCOLEPSY 7; NRCLP7		HP:0002524	OMIM:614250	TAS				P		HPO:skoehler	
OMIM	614250	#614250 NARCOLEPSY 7; NRCLP7		HP:0030050	OMIM:614250	TAS				P		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0000006	OMIM:614251	TAS				I		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0001300	OMIM:614251	TAS				P		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0002063	OMIM:614251	TAS				P		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0002067	OMIM:614251	TAS				P		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0002322	OMIM:614251	TAS				P		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0003587	OMIM:614251	TAS				C		HPO:skoehler	
OMIM	614251	#614251 PARKINSON DISEASE 18; PARK18		HP:0100315	OMIM:614251	TAS				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0000006	OMIM:614254	TAS				I		HPO:probinson	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001249	OMIM:614254	TAS				P		HPO:probinson	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001250	OMIM:614254	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001257	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001336	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001344	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0001347	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002019	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002059	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002072	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002079	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002126	OMIM:614254	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002353	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0002540	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0003593	OMIM:614254	IEA				C		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0010553	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0010864	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0011968	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0100660	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0100704	OMIM:614254	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614254	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD		HP:0100716	OMIM:614254	IEA				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0000006	OMIM:614255	IEA				I		HPO:probinson	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0000252	OMIM:614255	TAS				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0000639	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0000648	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001249	OMIM:614255	IEA		HP:0040284		P		HPO:probinson	1/1
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001250	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001257	OMIM:614255	IEA		HP:0040284		P		HPO:probinson	1/1
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001263	OMIM:614255	TAS				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001272	OMIM:614255	TAS				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001290	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001344	OMIM:614255	IEA				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001347	OMIM:614255	TAS				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001371	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0001762	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0002059	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0002540	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0003477	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0003487	OMIM:614255	TAS				P		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0003676	OMIM:614255	TAS				C		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0003828	OMIM:614255	TAS				C		HPO:skoehler	
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9	HP:0012825	HP:0006855	OMIM:614255	IEA		HP:0040284		P		HPO:probinson	1/1
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0008936	OMIM:614255	IEA		HP:0040284		P		HPO:probinson	1/1
OMIM	614255	MENTAL RETARDATION, AUTOSOMAL DOMINANT 9; MRD9		HP:0100704	OMIM:614255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614256	#614256 MENTAL RETARDATION, AUTOSOMAL DOMINANT 10; MRD10		HP:0000006	OMIM:614256	TAS				I		HPO:probinson	
OMIM	614256	#614256 MENTAL RETARDATION, AUTOSOMAL DOMINANT 10; MRD10		HP:0001249	OMIM:614256	TAS		HP:0040284		P		HPO:probinson	1/1
OMIM	614257	#614257 MENTAL RETARDATION, AUTOSOMAL DOMINANT 11; MRD11		HP:0000006	OMIM:614257	TAS				I		HPO:probinson	
OMIM	614257	#614257 MENTAL RETARDATION, AUTOSOMAL DOMINANT 11; MRD11		HP:0001249	OMIM:614257	TAS		HP:0040284		P		HPO:probinson	1/1
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000007	OMIM:614261	TAS				I		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000076	OMIM:614261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000175	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000253	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000316	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000327	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000340	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000365	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000369	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000445	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000508	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0000648	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001156	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001250	OMIM:614261	TAS	HP:0003593			P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001285	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001290	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001336	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001508	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001518	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001629	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001655	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001667	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0001792	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0002059	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0002079	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0003196	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0003577	OMIM:614261	TAS				C		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0004322	OMIM:614261	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0009882	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0010721	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0011344	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0012448	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614261	MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME		HP:0030084	OMIM:614261	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0000007	OMIM:614262	TAS				I		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0000293	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0001047	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0001629	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0001631	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0001642	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0001845	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0002021	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0002099	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0002804	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614262	614262 ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY; APUG		HP:0012385	OMIM:614262	TAS				P		HPO:skoehler	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0000007	OMIM:614265	TAS				I		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0001263	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0001508	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0001944	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0001993	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0002013	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0002014	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0011169	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614265	#614265 COMBINED MALONIC AND METHYLMALONIC ACIDURIA; CMAMMA		HP:0012120	OMIM:614265	TAS				P		HPO:probinson	
OMIM	614266	#614266 BARRETT ESOPHAGUS;;BARRETT METAPLASIAADENOCARCINOMA OF ESOPHAGUS, INCLUDED		HP:0001428	OMIM:614266	TAS				I		HPO:probinson	
OMIM	614266	#614266 BARRETT ESOPHAGUS;;BARRETT METAPLASIAADENOCARCINOMA OF ESOPHAGUS, INCLUDED		HP:0002020	PMID:14791960	PCS				P		HPO:lccarmody	
OMIM	614266	#614266 BARRETT ESOPHAGUS;;BARRETT METAPLASIAADENOCARCINOMA OF ESOPHAGUS, INCLUDED		HP:0004791	PMID:14791960	PCS		HP:0040281		P		HPO:lccarmody	HP:0040281
OMIM	614266	#614266 BARRETT ESOPHAGUS;;BARRETT METAPLASIAADENOCARCINOMA OF ESOPHAGUS, INCLUDED		HP:0011459	OMIM:614266	TAS				P		HPO:probinson	
OMIM	614266	#614266 BARRETT ESOPHAGUS;;BARRETT METAPLASIAADENOCARCINOMA OF ESOPHAGUS, INCLUDED		HP:0100580	OMIM:614266	TAS				P		HPO:probinson	
OMIM	614278	#614278 PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY; PAFAD		HP:0040175	OMIM:614278	IEA				P		HPO:skoehler	
OMIM	614278	#614278 PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE DEFICIENCY; PAFAD		HP:0040178	OMIM:614278	IEA				P		HPO:skoehler	
OMIM	614279	#614279 46,XY SEX REVERSAL 8; SRXY8;;MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;TDD		HP:0000007	OMIM:614279	TAS				I		HPO:skoehler	
OMIM	614279	#614279 46,XY SEX REVERSAL 8; SRXY8;;MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;TDD		HP:0000028	OMIM:614279	TAS				P		HPO:skoehler	
OMIM	614279	#614279 46,XY SEX REVERSAL 8; SRXY8;;MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;TDD		HP:0000037	OMIM:614279	TAS				P		HPO:skoehler	
OMIM	614279	#614279 46,XY SEX REVERSAL 8; SRXY8;;MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;TDD		HP:0000062	OMIM:614279	TAS				P		HPO:skoehler	
OMIM	614279	#614279 46,XY SEX REVERSAL 8; SRXY8;;MALE PSEUDOHERMAPHRODITISM DUE TO DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;TDD		HP:0012245	OMIM:614279	TAS				P		HPO:skoehler	
OMIM	614280	%614280 EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9; EJM9		HP:0000006	OMIM:614280	TAS				I		HPO:skoehler	
OMIM	614280	%614280 EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9; EJM9		HP:0002121	OMIM:614280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614280	%614280 EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 9; EJM9		HP:0002373	OMIM:614280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0000007	OMIM:614284	TAS				I		HPO:skoehler	
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0000407	OMIM:614284	TAS				P		HPO:skoehler	
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0000541	OMIM:614284	TAS				P		HPO:skoehler	
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0004322	OMIM:614284	IEA				P		HPO:skoehler	
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0007773	OMIM:614284	TAS				P		HPO:skoehler	
OMIM	614284	STICKLER SYNDROME, TYPE V; STL5		HP:0011003	OMIM:614284	TAS				P		HPO:skoehler	
OMIM	614286	#614286 MYELODYSPLASTIC SYNDROME; MDS;;MYELODYSPLASTIC SYNDROME, SUSCEPTIBILITY TO, INCLUDED		HP:0001428	OMIM:614286	TAS				I		HPO:probinson	
OMIM	614286	#614286 MYELODYSPLASTIC SYNDROME; MDS;;MYELODYSPLASTIC SYNDROME, SUSCEPTIBILITY TO, INCLUDED		HP:0002863	OMIM:614286	TAS				P		HPO:probinson	
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0000007	OMIM:614292	TAS				I		HPO:skoehler	
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0000518	OMIM:614292	TAS				P		HPO:skoehler	
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0000541	OMIM:614292	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0001132	OMIM:614292	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0011003	OMIM:614292	TAS				P		HPO:skoehler	
OMIM	614292	#614292 MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION; MCVD		HP:0200071	OMIM:614292	TAS				P		HPO:skoehler	
OMIM	614293	#614293 HYDATIDIFORM MOLE, RECURRENT, 2; HYDM2;;HYDATIDIFORM MOLE, BIPARENTAL COMPLETE		HP:0000007	OMIM:614293	TAS				I		HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000006	OMIM:614294	TAS				I	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000023	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000028	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000175	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000204	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000316	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000470	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000494	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000767	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0000776	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0001263	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0001651	OMIM:614294	TAS		HP:0040283		P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0001671	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0001972	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0002058	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0003577	OMIM:614294	TAS				C	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0004322	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0007018	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0010804	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614294	CHROMOSOME 15q25 DELETION SYNDROME		HP:0100807	OMIM:614294	TAS				P	CHROMOSOME 15Q25 DELETION SYNDROME	HPO:skoehler	
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000006	OMIM:614296	TAS				I		HPO:skoehler	
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000365	OMIM:614296	TAS				P		HPO:skoehler	
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000501	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000648	OMIM:614296	TAS				P		HPO:skoehler	
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000709	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000716	OMIM:614296	TAS				P		HPO:skoehler	
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000717	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000738	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000739	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0000819	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614296	WOLFRAM-LIKE SYNDROME, AUTOSOMAL DOMINANT; WFSL		HP:0100753	OMIM:614296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000007	OMIM:614298	TAS				I		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000529	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000648	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000712	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000716	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000726	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0000750	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001251	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001257	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001260	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001263	OMIM:614298	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001265	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001272	OMIM:614298	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001288	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001300	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001337	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001347	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0001761	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0002180	OMIM:614298	IEA				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0002366	OMIM:614298	TAS	HP:0003584			P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0002460	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4	HP:0012825	HP:0003236	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0003487	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0003676	OMIM:614298	TAS				C		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0003691	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0003693	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0012048	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0100315	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614298	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 4		HP:0100710	OMIM:614298	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0000007	OMIM:614299	TAS				I		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0000505	OMIM:614299	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0000648	OMIM:614299	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001250	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001251	OMIM:614299	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001254	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001257	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001263	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001290	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001336	OMIM:614299	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001522	OMIM:614299	TAS				M		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001639	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0001644	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002013	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002071	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002240	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002376	OMIM:614299	IEA				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002415	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002421	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0002878	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0003128	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0003593	OMIM:614299	TAS				C		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0008972	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614299	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 WITH HYPERGLYCINEMIA; MMDS2		HP:0200134	OMIM:614299	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0000007	OMIM:614300	TAS				I		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0000256	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0000316	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0000407	OMIM:614300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0000750	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001250	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001263	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001290	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001396	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001397	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001410	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001508	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001631	OMIM:614300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001642	OMIM:614300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001680	OMIM:614300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0001786	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0002007	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0002059	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0002465	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0002904	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0002910	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0003202	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0003235	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0003593	OMIM:614300	TAS				C		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0003676	OMIM:614300	TAS				C		HPO:skoehler	
OMIM	614300	HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY		HP:0006580	OMIM:614300	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0000006	OMIM:614302	TAS				I		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0000467	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0001662	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0003560	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0003581	OMIM:614302	TAS				C		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0003677	OMIM:614302	TAS				C		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0003701	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0005110	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614302	#614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7		HP:0007126	OMIM:614302	TAS				P		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0000006	OMIM:614303	TAS				I		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0000482	OMIM:614303	TAS				P		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0000483	OMIM:614303	TAS				P		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0000519	OMIM:614303	IEA				P		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0000563	OMIM:614303	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614303	EDICT SYNDROME		HP:0007663	OMIM:614303	TAS				P		HPO:skoehler	
OMIM	614303	EDICT SYNDROME		HP:0007676	OMIM:614303	IEA				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000006	OMIM:614305	TAS				I		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000007	OMIM:614305	TAS				I		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000256	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000303	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000316	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000324	OMIM:614305	IEA				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0000365	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0002007	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0002164	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0002273	OMIM:614305	IEA				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0009381	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0010554	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614305	SCLEROSTEOSIS 2; SOST2		HP:0010628	OMIM:614305	TAS				P		HPO:skoehler	
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0000006	OMIM:614306	TAS				I		HPO:skoehler	
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0000609	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0000640	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0000646	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0000712	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0001249	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0001260	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0001310	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0007018	OMIM:614306	TAS				P		HPO:skoehler	
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0025312	OMIM:614306	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614306	COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA		HP:0100543	OMIM:614306	IEA				P		HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0000007	OMIM:614307	TAS				I	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0000505	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0000580	OMIM:614307	TAS		HP:0040282		P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	HP:0040282
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0000716	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0000815	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0001251	OMIM:614307	TAS		HP:0040283		P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	HP:0040283
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0001257	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0001260	OMIM:614307	IEA				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0001337	OMIM:614307	TAS		HP:0040283		P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	HP:0040283
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0002076	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0002133	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614307	ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY; AMACRD		HP:0007141	OMIM:614307	TAS				P	ALPHA-METHYLACYL-COA RACEMASE DEFICIENCY; AMACRD	HPO:skoehler	
OMIM	614321	#614321 MYOPATHY, DISTAL, TATEYAMA TYPE; MPDT		HP:0000006	OMIM:614321	TAS				I		HPO:skoehler	
OMIM	614321	#614321 MYOPATHY, DISTAL, TATEYAMA TYPE; MPDT		HP:0000467	OMIM:614321	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614321	#614321 MYOPATHY, DISTAL, TATEYAMA TYPE; MPDT		HP:0001761	OMIM:614321	TAS				P		HPO:skoehler	
OMIM	614321	#614321 MYOPATHY, DISTAL, TATEYAMA TYPE; MPDT		HP:0003236	OMIM:614321	TAS				P		HPO:skoehler	
OMIM	614321	#614321 MYOPATHY, DISTAL, TATEYAMA TYPE; MPDT		HP:0008981	OMIM:614321	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0000007	OMIM:614322	TAS				I		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0000252	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0000546	OMIM:614322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0000640	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0000648	OMIM:614322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001249	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001250	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001257	OMIM:614322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001260	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001263	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001265	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY	HP:0012825	HP:0001272	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0001510	OMIM:614322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0002066	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0002070	OMIM:614322	TAS				P		HPO:skoehler	
OMIM	614322	#614322 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 12; SCAR12;;SPINOCEREBELLAR ATAXIA WITH MENTAL RETARDATION AND EPILEPSY		HP:0003487	OMIM:614322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614323	NEVOID HYPERMELANOSIS, LINEAR AND WHORLED; LWNH		HP:0000006	OMIM:614323	TAS				I		HPO:skoehler	
OMIM	614323	NEVOID HYPERMELANOSIS, LINEAR AND WHORLED; LWNH		HP:0001880	OMIM:614323	TAS				P		HPO:skoehler	
OMIM	614323	NEVOID HYPERMELANOSIS, LINEAR AND WHORLED; LWNH		HP:0003593	OMIM:614323	TAS				C		HPO:skoehler	
OMIM	614323	NEVOID HYPERMELANOSIS, LINEAR AND WHORLED; LWNH		HP:0003745	OMIM:614323	TAS				I		HPO:skoehler	
OMIM	614323	NEVOID HYPERMELANOSIS, LINEAR AND WHORLED; LWNH		HP:0007572	OMIM:614323	TAS				P		HPO:skoehler	
OMIM	614324	#614324 OVARIAN DYSGENESIS 3; ODG3		HP:0000007	OMIM:614324	TAS				I		HPO:skoehler	
OMIM	614324	#614324 OVARIAN DYSGENESIS 3; ODG3		HP:0000786	OMIM:614324	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0000007	OMIM:614325	TAS				I		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0000154	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0000486	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0001290	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0001642	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002019	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002020	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002136	OMIM:614325	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002307	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002376	OMIM:614325	IEA				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002650	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0002883	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0010808	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0010864	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0011968	OMIM:614325	TAS				P		HPO:skoehler	
OMIM	614325	PITT-HOPKINS-LIKE SYNDROME 2; PTHSL2		HP:0200134	OMIM:614325	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0000006	OMIM:614326	TAS				I		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0000252	OMIM:614326	TAS				P		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0001156	OMIM:614326	IEA				P		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0001249	OMIM:614326	TAS				P		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0004322	OMIM:614326	TAS				P		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0005819	OMIM:614326	TAS				P		HPO:skoehler	
OMIM	614326	#614326 FEINGOLD SYNDROME 2; FGLDS2;;BRACHYDACTYLY WITH SHORT STATURE AND MICROCEPHALY		HP:0009778	OMIM:614326	TAS				P		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0000006	OMIM:614327	TAS				I		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0002858	OMIM:614327	TAS				P		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0005584	OMIM:614327	IEA				P		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0007716	OMIM:614327	TAS				P		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0012056	OMIM:614327	TAS				P		HPO:skoehler	
OMIM	614327	TUMOR PREDISPOSITION SYNDROME; TPDS		HP:0030078	OMIM:614327	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0000007	OMIM:614328	TAS				I		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0000498	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0001019	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0001805	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0001818	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0001880	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0002573	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0010783	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0011473	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614328	#614328 INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL; NISBD		HP:0200039	OMIM:614328	TAS				P		HPO:skoehler	
OMIM	614329	%614329 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 31; MRT31		HP:0000007	OMIM:614329	TAS				I		HPO:skoehler	
OMIM	614329	%614329 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 31; MRT31		HP:0001249	OMIM:614329	TAS				P		HPO:skoehler	
OMIM	614331	#614331 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6;;COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6		HP:0000006	OMIM:614331	TAS				I		HPO:probinson	
OMIM	614331	#614331 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6; HNPCC6;;COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 6		HP:0006716	OMIM:614331	TAS				P		HPO:probinson	
OMIM	614333	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29		HP:0000007	PMID:21629298	PCS				I		HPO:skoehler	
OMIM	614333	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29		HP:0001252	PMID:21629298	PCS				P		HPO:probinson	
OMIM	614333	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29	HP:0012825	HP:0001270	PMID:21629298	PCS				P		HPO:probinson	
OMIM	614333	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29		HP:0001344	PMID:21629298	PCS				P		HPO:probinson	
OMIM	614333	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 29		HP:0010864	PMID:21629298	PCS				P		HPO:skoehler	
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0000006	OMIM:614335	TAS				I		HPO:skoehler	
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0001762	OMIM:614335	IEA		HP:0040284		P		HPO:skoehler	9/12
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0001838	OMIM:614335	IEA		HP:0040284		P		HPO:skoehler	3/12
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0002804	OMIM:614335	IEA				P		HPO:skoehler	
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0005684	OMIM:614335	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0008366	OMIM:614335	IEA		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0009473	OMIM:614335	IEA		HP:0040284		P		HPO:skoehler	5/12
OMIM	614335	ARTHROGRYPOSIS, DISTAL, TYPE 1B		HP:0012385	OMIM:614335	TAS				P		HPO:skoehler	
OMIM	614337	#614337 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4; HNPCC4		HP:0000006	OMIM:614337	TAS				I		HPO:probinson	
OMIM	614337	#614337 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4; HNPCC4		HP:0006716	OMIM:614337	TAS				P		HPO:probinson	
OMIM	614337	#614337 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4; HNPCC4		HP:0012114	OMIM:614337	TAS				P		HPO:probinson	
OMIM	614337	#614337 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 4; HNPCC4		HP:0100615	OMIM:614337	TAS				P		HPO:probinson	
OMIM	614338	PANCREATIC LIPASE DEFICIENCY		HP:0000007	OMIM:614338	TAS				I		HPO:probinson	
OMIM	614338	PANCREATIC LIPASE DEFICIENCY		HP:0002570	OMIM:614338	TAS				P		HPO:probinson	
OMIM	614338	PANCREATIC LIPASE DEFICIENCY		HP:0045014	OMIM:614338	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0000007	OMIM:614340	TAS				I		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0000252	OMIM:614340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0000718	OMIM:614340	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0001249	OMIM:614340	IEA				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0001263	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0001290	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0001347	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0001510	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0002465	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0005280	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614340	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27		HP:0011800	OMIM:614340	TAS				P		HPO:skoehler	
OMIM	614341	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33		HP:0000007	OMIM:614341	TAS				I		HPO:skoehler	
OMIM	614341	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33		HP:0001159	OMIM:614341	TAS				P		HPO:skoehler	
OMIM	614341	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33		HP:0001831	OMIM:614341	TAS				P		HPO:skoehler	
OMIM	614341	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33		HP:0001999	OMIM:614341	TAS				P		HPO:skoehler	
OMIM	614341	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 33		HP:0002342	OMIM:614341	TAS				P		HPO:skoehler	
OMIM	614342	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30		HP:0000007	OMIM:614342	TAS				I		HPO:skoehler	
OMIM	614342	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30		HP:0000158	OMIM:614342	TAS				P		HPO:skoehler	
OMIM	614342	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30		HP:0000252	OMIM:614342	TAS				P		HPO:skoehler	
OMIM	614342	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30		HP:0001510	OMIM:614342	TAS				P		HPO:skoehler	
OMIM	614342	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 30		HP:0010864	OMIM:614342	TAS				P		HPO:skoehler	
OMIM	614343	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19		HP:0000007	OMIM:614343	TAS				I		HPO:skoehler	
OMIM	614343	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19		HP:0001270	OMIM:614343	TAS				P		HPO:skoehler	
OMIM	614343	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19		HP:0001760	OMIM:614343	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614343	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 19		HP:0002342	OMIM:614343	TAS				P		HPO:skoehler	
OMIM	614344	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 23		HP:0000007	OMIM:614344	TAS				I		HPO:skoehler	
OMIM	614344	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 23	HP:0012826	HP:0001270	OMIM:614344	TAS				P		HPO:skoehler	
OMIM	614344	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 23		HP:0010864	OMIM:614344	TAS				P		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0000007	OMIM:614345	TAS				I		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0000252	OMIM:614345	TAS				P		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0000750	OMIM:614345	TAS				P		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0001270	OMIM:614345	TAS				P		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0001510	OMIM:614345	TAS				P		HPO:skoehler	
OMIM	614345	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 24		HP:0002342	OMIM:614345	TAS				P		HPO:skoehler	
OMIM	614346	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25		HP:0000007	OMIM:614346	TAS				I		HPO:skoehler	
OMIM	614346	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25		HP:0000739	OMIM:614346	TAS				P		HPO:skoehler	
OMIM	614346	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25		HP:0000750	OMIM:614346	TAS				P		HPO:skoehler	
OMIM	614346	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25		HP:0001270	OMIM:614346	TAS				P		HPO:skoehler	
OMIM	614346	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 25		HP:0002342	OMIM:614346	TAS				P		HPO:skoehler	
OMIM	614347	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28		HP:0000007	OMIM:614347	TAS				I		HPO:skoehler	
OMIM	614347	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28		HP:0000252	OMIM:614347	TAS				P		HPO:skoehler	
OMIM	614347	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28		HP:0000750	OMIM:614347	TAS				P		HPO:skoehler	
OMIM	614347	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28	HP:0012826	HP:0001270	OMIM:614347	TAS				P		HPO:skoehler	
OMIM	614347	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 28		HP:0002342	OMIM:614347	TAS				P		HPO:skoehler	
OMIM	614350	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5		HP:0000006	OMIM:614350	TAS				I		HPO:probinson	
OMIM	614350	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5		HP:0003829	OMIM:614350	TAS				C		HPO:skoehler	
OMIM	614350	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5		HP:0006716	OMIM:614350	TAS				P		HPO:probinson	
OMIM	614350	COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 5		HP:0012114	OMIM:614350	TAS				P		HPO:probinson	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0000006	OMIM:614369	TAS				I		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0001265	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0001284	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0001337	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0001609	OMIM:614369	TAS		HP:0040284		P		HPO:skoehler	53%
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0001760	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0002460	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0003676	OMIM:614369	TAS				C		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0003693	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0008180	OMIM:614369	TAS				P		HPO:skoehler	
OMIM	614369	PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS; PNMHH		HP:0009830	OMIM:614369	IEA				P		HPO:skoehler	
OMIM	614370	#614370 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5; SMDP5;;PULMONARY ALVEOLAR PROTEINOSIS 5;;PAP DUE TO CSF2RB DEFICIENCY;;CSF2RB DEFICIENCY		HP:0000007	OMIM:614370	TAS				I		HPO:skoehler	
OMIM	614370	#614370 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5; SMDP5;;PULMONARY ALVEOLAR PROTEINOSIS 5;;PAP DUE TO CSF2RB DEFICIENCY;;CSF2RB DEFICIENCY		HP:0002093	OMIM:614370	TAS				P		HPO:skoehler	
OMIM	614370	#614370 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5; SMDP5;;PULMONARY ALVEOLAR PROTEINOSIS 5;;PAP DUE TO CSF2RB DEFICIENCY;;CSF2RB DEFICIENCY		HP:0002094	OMIM:614370	TAS				P		HPO:skoehler	
OMIM	614370	#614370 SURFACTANT METABOLISM DYSFUNCTION, PULMONARY, 5; SMDP5;;PULMONARY ALVEOLAR PROTEINOSIS 5;;PAP DUE TO CSF2RB DEFICIENCY;;CSF2RB DEFICIENCY		HP:0006517	OMIM:614370	TAS				P		HPO:skoehler	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0000006	OMIM:614372	TAS				I		HPO:skoehler	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0001508	PMID:769701	PCS				P		HPO:lccarmody	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0001581	PMID:7707811	PCS				P		HPO:lccarmody	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0002742	PMID:7707811	PCS				P		HPO:lccarmody	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0005353	PMID:7707811	PCS				P		HPO:lccarmody	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0005381	PMID:7707811	PCS				P		HPO:lccarmody	
OMIM	614372	MANNOSE-BINDING LECTIN DEFICIENCY		HP:0031699	PMID:7707811	PCS				P		HPO:lccarmody	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0000007	OMIM:614373	TAS				I		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0001257	OMIM:614373	TAS				P		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0001324	OMIM:614373	IEA				P		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0001347	OMIM:614373	TAS				P		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0002127	OMIM:614373	TAS				P		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0002366	OMIM:614373	TAS				P		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0003677	OMIM:614373	TAS				C		HPO:skoehler	
OMIM	614373	AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE; ALS16		HP:0007354	OMIM:614373	IEA				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000007	OMIM:614376	TAS				I		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000023	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000089	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000093	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000099	OMIM:614376	IEA				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000219	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000293	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000518	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000545	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0000774	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0001156	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0001773	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0003016	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0003259	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0003774	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0004743	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0006644	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0008081	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0008905	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614376	SHORT-RIB THORACIC DYSPLASIA 5 WITH OR WITHOUT POLYDACTYLY; SRTD5		HP:0100866	OMIM:614376	TAS				P		HPO:skoehler	
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0000007	OMIM:614377	TAS				I		HPO:skoehler	
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0000089	OMIM:614377	TAS				P		HPO:skoehler	
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0000090	OMIM:614377	IEA				P		HPO:skoehler	
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0000556	OMIM:614377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0001407	OMIM:614377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0001737	OMIM:614377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0003774	OMIM:614377	TAS				P		HPO:skoehler	
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0010442	OMIM:614377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614377	NEPHRONOPHTHISIS 13		HP:0012595	OMIM:614377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000007	OMIM:614378	TAS				I		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000112	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000233	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000293	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000319	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000411	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000510	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000540	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000767	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000774	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000968	OMIM:614378	IEA				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0000973	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0001382	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0001385	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0002007	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0003774	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0004322	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0004442	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0005528	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0006532	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0008081	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0009836	OMIM:614378	TAS				P		HPO:skoehler	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0009882	OMIM:614378	TAS				P		HPO:probinson	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0010174	OMIM:614378	TAS				P		HPO:probinson	
OMIM	614378	CRANIOECTODERMAL DYSPLASIA 4		HP:0010554	OMIM:614378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614379	#614379 COMPLEMENT COMPONENT 4B DEFICIENCY; C4BD ;;C4B DEFICIENCY		HP:0001287	OMIM:614379	IEA				P		HPO:skoehler	
OMIM	614379	#614379 COMPLEMENT COMPONENT 4B DEFICIENCY; C4BD ;;C4B DEFICIENCY		HP:0045044	OMIM:614379	IEA				P		HPO:skoehler	
OMIM	614379	#614379 COMPLEMENT COMPONENT 4B DEFICIENCY; C4BD ;;C4B DEFICIENCY		HP:0200120	OMIM:614379	IEA				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0000007	OMIM:614380	TAS				I		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0000099	OMIM:614380	TAS				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0000979	OMIM:614380	TAS				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0000992	OMIM:614380	TAS				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0002633	OMIM:614380	TAS				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0002725	OMIM:614380	TAS				P		HPO:skoehler	
OMIM	614380	#614380 COMPLEMENT COMPONENT 4A DEFICIENCY; C4AD;;C4A DEFICIENCY		HP:0004431	OMIM:614380	TAS				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000007	OMIM:614381	IEA				I		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000044	OMIM:614381	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000545	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000666	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000668	OMIM:614381	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000677	OMIM:614381	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0000684	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001151	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001256	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001257	OMIM:614381	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001260	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001272	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001310	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0001347	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0002015	OMIM:614381	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0002075	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0002079	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0002080	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0002415	OMIM:614381	IEA				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0004322	OMIM:614381	TAS				P		HPO:skoehler	
OMIM	614381	LEUKODYSTROPHY, HYPOMYELINATING, 8, WITH OR WITHOUT OLIGODONTIA AND/OR HYPOGONADOTROPIC HYPOGONADISM		HP:0006808	OMIM:614381	IEA				P		HPO:probinson	
OMIM	614385	#614385 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7; HNPCC7		HP:0000006	OMIM:614385	TAS				I		HPO:probinson	
OMIM	614385	#614385 COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7; HNPCC7		HP:0006716	OMIM:614385	TAS				P		HPO:probinson	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000006	OMIM:614388	TAS				I		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000007	OMIM:614388	TAS				I		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000252	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000307	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000486	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000490	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000648	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000657	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0000666	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001263	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001284	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001290	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001298	OMIM:614388	IEA				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001508	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001522	OMIM:614388	TAS				M		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0001558	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0002059	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0002133	OMIM:614388	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0003128	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0003676	OMIM:614388	TAS				C		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0003828	OMIM:614388	TAS				C		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0007256	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0011968	OMIM:614388	TAS				P		HPO:skoehler	
OMIM	614388	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 1		HP:0200134	OMIM:614388	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614389	#614389 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1; RPRGL1;;RPRGL;;RPL;;ABORTION, SPONTANEOUS, RECURRENT;;FETAL LOSS, RECURRENT, SUSCEPTIBILITY TO;;MISCARRIAGE, RECURRENT;;EMBRYONIC LOSS, RECURRENT;;STILLBIRTH, RECURRENT		HP:0000006	OMIM:614389	TAS				I		HPO:skoehler	
OMIM	614389	#614389 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 1; RPRGL1;;RPRGL;;RPL;;ABORTION, SPONTANEOUS, RECURRENT;;FETAL LOSS, RECURRENT, SUSCEPTIBILITY TO;;MISCARRIAGE, RECURRENT;;EMBRYONIC LOSS, RECURRENT;;STILLBIRTH, RECURRENT		HP:0200067	OMIM:614389	TAS				P		HPO:skoehler	
OMIM	614390	#614390 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2; RPRGL2		HP:0000006	OMIM:614390	TAS				I		HPO:skoehler	
OMIM	614390	#614390 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 2; RPRGL2		HP:0200067	OMIM:614390	TAS				P		HPO:skoehler	
OMIM	614391	#614391 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3; RPRGL3		HP:0000006	OMIM:614391	TAS				I		HPO:skoehler	
OMIM	614391	#614391 PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3; RPRGL3		HP:0200067	OMIM:614391	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0000007	OMIM:614399	TAS				I		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0000175	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0000218	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0000767	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001250	OMIM:614399	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001265	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001270	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001284	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001319	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001508	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001558	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001611	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0001762	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002015	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002091	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002098	OMIM:614399	IEA				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002421	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002650	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0002878	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0003577	OMIM:614399	TAS				C		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0003828	OMIM:614399	TAS				C		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0006597	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0009046	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0010628	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614399	#614399 MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET;EMARDDMYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET,MILD VARIANT, INCLUDED		HP:0100490	OMIM:614399	TAS				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11		HP:0000007	OMIM:614402	TAS				I		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11	HP:0012832	HP:0000175	OMIM:614402	TAS				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11	HP:0012832	HP:0000204	OMIM:614402	TAS				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11		HP:0000568	OMIM:614402	IEA				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11		HP:0001263	OMIM:614402	TAS				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11		HP:0001274	OMIM:614402	TAS				P		HPO:skoehler	
OMIM	614402	#614402 MICROPHTHALMIA, SYNDROMIC 11; MCOPS11		HP:0012687	OMIM:614402	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000007	OMIM:614407	TAS				I		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000179	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000253	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000337	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000343	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000395	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000400	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0000448	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001063	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001182	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001290	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001321	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001332	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001344	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001347	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001508	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001510	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001662	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001678	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0001952	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0002078	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0002079	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0002080	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0002187	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0004209	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0004523	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0009183	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614407	MICROCEPHALY, CEREBELLAR HYPOPLASIA, AND CARDIAC CONDUCTION DEFECT SYNDROME		HP:0009879	OMIM:614407	TAS				P		HPO:skoehler	
OMIM	614408	#614408 MYOPATHY, CENTRONUCLEAR, 3; CNM3		HP:0000006	OMIM:614408	TAS				I		HPO:skoehler	
OMIM	614408	#614408 MYOPATHY, CENTRONUCLEAR, 3; CNM3		HP:0001324	OMIM:614408	TAS				P		HPO:skoehler	
OMIM	614408	#614408 MYOPATHY, CENTRONUCLEAR, 3; CNM3		HP:0003236	OMIM:614408	TAS				P		HPO:skoehler	
OMIM	614408	#614408 MYOPATHY, CENTRONUCLEAR, 3; CNM3		HP:0003394	OMIM:614408	TAS				P		HPO:skoehler	
OMIM	614408	#614408 MYOPATHY, CENTRONUCLEAR, 3; CNM3		HP:0100305	OMIM:614408	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000007	OMIM:614409	TAS				I		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000020	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000365	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000518	OMIM:614409	TAS	HP:0003577			P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000639	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000726	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0000789	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0001249	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0001258	OMIM:614409	IEA				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0001260	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0001272	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0001761	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002059	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002061	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002064	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002079	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002166	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002346	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002406	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002650	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0002808	OMIM:614409	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0003487	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0003676	OMIM:614409	TAS				C		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0003677	OMIM:614409	TAS				C		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0006986	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0007340	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0008003	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0011448	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0011449	OMIM:614409	TAS				P		HPO:skoehler	
OMIM	614409	SPASTIC PARAPLEGIA 46, AUTOSOMAL RECESSIVE; SPG46		HP:0020036	OMIM:614409	IEA				P		HPO:skoehler	
OMIM	614411	#614411 GLYCEROL QUANTITATIVE TRAIT LOCUS; GLYCQTL;;GLYCEROL RELEASE DURING EXERCISE, DEFECTIVEBODY MASS INDEX QUANTITATIVE TRAIT LOCUS 17, INCLUDED; BMIQ17, INCLUDED		HP:0000007	OMIM:614411	TAS				I		HPO:skoehler	
OMIM	614414	%614414 DEAFNESS, AUTOSOMAL RECESSIVE 96; DFNB96		HP:0000007	OMIM:614414	TAS				I		HPO:skoehler	
OMIM	614414	%614414 DEAFNESS, AUTOSOMAL RECESSIVE 96; DFNB96		HP:0000365	OMIM:614414	TAS				P		HPO:skoehler	
OMIM	614415	CHILBLAIN LUPUS 2; CHBL2		HP:0000006	OMIM:614415	TAS				I		HPO:skoehler	
OMIM	614415	CHILBLAIN LUPUS 2; CHBL2		HP:0000969	OMIM:614415	IEA				P		HPO:skoehler	
OMIM	614415	CHILBLAIN LUPUS 2; CHBL2		HP:0000992	OMIM:614415	TAS				P		HPO:skoehler	
OMIM	614415	CHILBLAIN LUPUS 2; CHBL2		HP:0002633	OMIM:614415	IEA				P		HPO:skoehler	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0000007	PMID:22019272	PCS				I		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0000248	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0001166	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0001363	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0002085	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0003041	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614416	#614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES;RHFCA		HP:0012165	PMID:22019272	PCS				P		HPO:probinson	
OMIM	614417	EPILEPSY, FAMILIAL TEMPORAL LOBE, 5		HP:0000006	OMIM:614417	TAS				I		HPO:skoehler	
OMIM	614417	EPILEPSY, FAMILIAL TEMPORAL LOBE, 5		HP:0000007	OMIM:614417	TAS				I		HPO:skoehler	
OMIM	614417	EPILEPSY, FAMILIAL TEMPORAL LOBE, 5		HP:0001250	OMIM:614417	IEA				P		HPO:skoehler	
OMIM	614418	FEBRILE SEIZURES, FAMILIAL, 11; FEB11		HP:0000007	OMIM:614418	TAS				I		HPO:skoehler	
OMIM	614418	FEBRILE SEIZURES, FAMILIAL, 11; FEB11		HP:0002069	OMIM:614418	TAS				P		HPO:skoehler	
OMIM	614418	FEBRILE SEIZURES, FAMILIAL, 11; FEB11		HP:0002373	OMIM:614418	TAS				P		HPO:skoehler	
OMIM	614418	FEBRILE SEIZURES, FAMILIAL, 11; FEB11		HP:0410170	OMIM:614418	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614420	#614420 SYSTEMIC LUPUS ERYTHEMATOSUS 16; SLEB16		HP:0000007	OMIM:614420	TAS				I		HPO:skoehler	
OMIM	614420	#614420 SYSTEMIC LUPUS ERYTHEMATOSUS 16; SLEB16		HP:0000123	OMIM:614420	TAS				P		HPO:skoehler	
OMIM	614420	#614420 SYSTEMIC LUPUS ERYTHEMATOSUS 16; SLEB16		HP:0002725	OMIM:614420	IEA				P		HPO:skoehler	
OMIM	614422	%614422 CATARACT, CONGENITAL, CERULEAN TYPE, 5; CCA5		HP:0000006	OMIM:614422	TAS				I		HPO:skoehler	
OMIM	614422	%614422 CATARACT, CONGENITAL, CERULEAN TYPE, 5; CCA5		HP:0000519	OMIM:614422	IEA				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000007	OMIM:614424	TAS				I		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000107	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000194	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000238	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000272	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000286	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000316	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000322	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000348	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000358	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000369	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000426	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000486	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000490	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000494	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000508	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000568	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000589	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000639	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000737	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0000822	OMIM:614424	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614424	JOUBERT SYNDROME 14		HP:0001251	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0001263	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0001290	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0001305	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0001510	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0002084	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0002553	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0010804	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0010864	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0025514	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614424	JOUBERT SYNDROME 14		HP:0100259	OMIM:614424	TAS				P		HPO:skoehler	
OMIM	614429	#614429 VENTRICULAR SEPTAL DEFECT 1; VSD1		HP:0000006	OMIM:614429	TAS				I		HPO:skoehler	
OMIM	614429	#614429 VENTRICULAR SEPTAL DEFECT 1; VSD1		HP:0001629	OMIM:614429	TAS				P		HPO:skoehler	
OMIM	614429	#614429 VENTRICULAR SEPTAL DEFECT 1; VSD1		HP:0001631	OMIM:614429	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614429	#614429 VENTRICULAR SEPTAL DEFECT 1; VSD1		HP:0001642	OMIM:614429	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614430	#614430 ATRIOVENTRICULAR SEPTAL DEFECT 4; AVSD4		HP:0000006	OMIM:614430	TAS				I		HPO:skoehler	
OMIM	614430	#614430 ATRIOVENTRICULAR SEPTAL DEFECT 4; AVSD4		HP:0010445	OMIM:614430	TAS				P		HPO:skoehler	
OMIM	614431	#614431 VENTRICULAR SEPTAL DEFECT 2; VSD2		HP:0000006	OMIM:614431	TAS				I		HPO:skoehler	
OMIM	614431	#614431 VENTRICULAR SEPTAL DEFECT 2; VSD2		HP:0011682	OMIM:614431	TAS				P		HPO:skoehler	
OMIM	614432	#614432 VENTRICULAR SEPTAL DEFECT 3; VSD3		HP:0000006	OMIM:614432	TAS				I		HPO:skoehler	
OMIM	614432	#614432 VENTRICULAR SEPTAL DEFECT 3; VSD3		HP:0001629	OMIM:614432	TAS				P		HPO:skoehler	
OMIM	614432	#614432 VENTRICULAR SEPTAL DEFECT 3; VSD3		HP:0001631	OMIM:614432	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614432	#614432 VENTRICULAR SEPTAL DEFECT 3; VSD3		HP:0001643	OMIM:614432	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614432	#614432 VENTRICULAR SEPTAL DEFECT 3; VSD3		HP:0004415	OMIM:614432	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614433	#614433 ATRIAL SEPTAL DEFECT 8; ASD8		HP:0000006	PMID:16287139	PCS				I		HPO:skoehler	
OMIM	614433	#614433 ATRIAL SEPTAL DEFECT 8; ASD8		HP:0001631	PMID:16287139	PCS		HP:0040284		P		HPO:skoehler	2/2
OMIM	614433	#614433 ATRIAL SEPTAL DEFECT 8; ASD8		HP:0010772	PMID:16287139	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	614434	#614434 CUTIS LAXA, AUTOSOMAL DOMINANT 2; ADCL2		HP:0000006	OMIM:614434	TAS				I		HPO:probinson	
OMIM	614434	#614434 CUTIS LAXA, AUTOSOMAL DOMINANT 2; ADCL2		HP:0000973	OMIM:614434	TAS				P		HPO:probinson	
OMIM	614434	#614434 CUTIS LAXA, AUTOSOMAL DOMINANT 2; ADCL2		HP:0001653	OMIM:614434	TAS				P		HPO:probinson	
OMIM	614434	#614434 CUTIS LAXA, AUTOSOMAL DOMINANT 2; ADCL2		HP:0002650	OMIM:614434	TAS				P		HPO:probinson	
OMIM	614434	#614434 CUTIS LAXA, AUTOSOMAL DOMINANT 2; ADCL2		HP:0100678	OMIM:614434	TAS				P		HPO:probinson	
OMIM	614435	#614435 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2		HP:0000006	OMIM:614435	TAS				I		HPO:skoehler	
OMIM	614435	#614435 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2		HP:0001629	OMIM:614435	TAS				P		HPO:skoehler	
OMIM	614435	#614435 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2		HP:0004383	OMIM:614435	TAS				P		HPO:skoehler	
OMIM	614435	#614435 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2		HP:0010883	OMIM:614435	TAS				P		HPO:skoehler	
OMIM	614435	#614435 HYPOPLASTIC LEFT HEART SYNDROME 2; HLHS2		HP:0011560	OMIM:614435	TAS				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0000006	OMIM:614436	TAS				I		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0000007	OMIM:614436	TAS				I		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0000007	PMID:20865121	PCS				I		HP:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0000764	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0001265	OMIM:614436	TAS				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0001284	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0001761	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0001765	OMIM:614436	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0002380	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0002460	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0002936	OMIM:614436	TAS				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003376	OMIM:614436	TAS				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003378	OMIM:614436	IEA				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003431	OMIM:614436	IEA				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003677	PMID:22012984	TAS				C		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003693	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0003829	OMIM:614436	TAS				C		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0006886	OMIM:614436	TAS				P		HPO:probinson	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0009027	OMIM:614436	TAS				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0040078	OMIM:614436	IEA				P		HPO:skoehler	
OMIM	614436	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P; CMT2P		HP:0040083	OMIM:614436	IEA				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000007	OMIM:614437	TAS				I		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000023	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000218	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000252	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000316	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000347	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000369	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000377	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000414	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000444	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000494	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000520	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000767	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000776	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000973	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0000977	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001166	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001290	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001382	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001548	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001562	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0001662	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0002097	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0004937	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0004942	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0004955	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0005280	OMIM:614437	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0010444	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0010759	OMIM:614437	TAS				P		HPO:probinson	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0011220	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614437	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB		HP:0045025	OMIM:614437	TAS				P		HPO:skoehler	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000007	OMIM:614438	TAS				I		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000023	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000028	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000233	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000239	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000316	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000358	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000418	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000581	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000592	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000750	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000963	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0000973	OMIM:614438	IEA				P		HPO:skoehler	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0001087	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0001249	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0002213	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0002987	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0007392	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0008070	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0010648	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614438	#614438 CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIIB; ARCL3B;;DE BARSY SYNDROME B		HP:0011220	OMIM:614438	TAS				P		HPO:probinson	
OMIM	614441	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2; PHOAR2		HP:0000007	OMIM:614441	TAS				I		HPO:skoehler	
OMIM	614441	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2; PHOAR2		HP:0001217	OMIM:614441	TAS				P		HPO:skoehler	
OMIM	614441	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2; PHOAR2		HP:0002829	OMIM:614441	TAS				P		HPO:skoehler	
OMIM	614441	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2; PHOAR2		HP:0030314	OMIM:614441	TAS				P		HPO:skoehler	
OMIM	614441	HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 2; PHOAR2		HP:0100774	OMIM:614441	IEA				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000006	OMIM:614450	TAS				I		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000158	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000316	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000684	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000851	OMIM:614450	TAS				P		HPO:probinson	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0000958	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0001374	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0001510	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0001539	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0001609	OMIM:614450	IEA				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0001903	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002019	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002136	OMIM:614450	IEA				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002329	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002645	OMIM:614450	IEA				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002750	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0002930	OMIM:614450	TAS				P		HPO:probinson	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0004324	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0004482	OMIM:614450	TAS				P		HPO:skoehler	
OMIM	614450	HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 6; CHNG6		HP:0012559	PMID:22168587	TAS				P		HPO:probinson	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0000006	OMIM:614455	TAS				I		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0000093	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0000097	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0001171	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0001265	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0001284	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0001761	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0001765	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0002460	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0002936	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0003376	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0003383	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0003447	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0003676	OMIM:614455	TAS				C		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0003774	OMIM:614455	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0007149	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0008944	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614455	#614455 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE E; CMTDIE;;CHARCOT-MARIE-TOOTH NEUROPATHY WITH FOCAL SEGMENTAL GLOMERULONEPHRITIS		HP:0009027	OMIM:614455	TAS				P		HPO:skoehler	
OMIM	614456	#614456 MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8; CMM8;;MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO		HP:0000006	PMID:22080950	PCS				I		HPO:probinson	
OMIM	614456	#614456 MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8; CMM8;;MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO		HP:0005584	OMIM:614456	IEA				P		HPO:skoehler	
OMIM	614456	#614456 MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8; CMM8;;MELANOMA AND RENAL CELL CARCINOMA, SUSCEPTIBILITY TO		HP:0012056	PMID:22080950	PCS				P		HPO:probinson	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000007	OMIM:614457	TAS				I		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000023	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000252	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000649	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000958	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0000962	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0001263	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0001371	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0001510	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0002099	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0002123	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0002187	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0002510	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0003577	OMIM:614457	TAS				C		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0008064	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0010783	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0011003	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0012444	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0012448	OMIM:614457	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614457	#614457 ICHTHYOSIS, SPASTIC QUADRIPLEGIA, AND MENTAL RETARDATION; ISQMR		HP:0040189	OMIM:614457	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0000007	OMIM:614458	TAS				I		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001250	OMIM:614458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001251	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001257	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001263	OMIM:614458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001290	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001332	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0001712	OMIM:614458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)	HP:0025303	HP:0002321	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)		HP:0002371	OMIM:614458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614458	THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE)	HP:0025303	HP:0003128	OMIM:614458	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0000007	OMIM:614462	TAS				I		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0000252	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001250	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001270	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001290	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001298	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001336	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001371	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001510	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0001639	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002059	OMIM:614462	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002093	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002104	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002151	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002360	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002415	OMIM:614462	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0002510	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0003128	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0011344	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0011968	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614462	HYPERGLYCINEMIA, LACTIC ACIDOSIS, AND SEIZURES		HP:0012736	OMIM:614462	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0000007	OMIM:614464	TAS				I		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0000054	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0000062	OMIM:614464	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614464	JOUBERT SYNDROME 15		HP:0000090	OMIM:614464	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614464	JOUBERT SYNDROME 15		HP:0000488	OMIM:614464	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614464	JOUBERT SYNDROME 15		HP:0000556	OMIM:614464	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614464	JOUBERT SYNDROME 15		HP:0000657	OMIM:614464	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614464	JOUBERT SYNDROME 15		HP:0001249	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0001251	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0001263	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0001290	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0002419	OMIM:614464	TAS				P		HPO:skoehler	
OMIM	614464	JOUBERT SYNDROME 15		HP:0010442	OMIM:614464	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000007	OMIM:614465	TAS				I		HPO:skoehler	
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000090	OMIM:614465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000107	OMIM:614465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000556	OMIM:614465	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000589	OMIM:614465	TAS				P		HPO:skoehler	
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0000657	OMIM:614465	TAS				P		HPO:skoehler	
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0001305	OMIM:614465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0002084	OMIM:614465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0002419	OMIM:614465	TAS				P		HPO:skoehler	
OMIM	614465	#614465 JOUBERT SYNDROME 16; JBTS16		HP:0010442	OMIM:614465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0000006	OMIM:614468	TAS				I		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0000872	OMIM:614468	TAS				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0001025	OMIM:614468	IEA				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0001045	OMIM:614468	TAS				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0002099	OMIM:614468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0002719	OMIM:614468	TAS				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0002958	OMIM:614468	IEA				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0003193	OMIM:614468	TAS				P		HPO:skoehler	
OMIM	614468	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3; FCAS3		HP:0010783	OMIM:614468	IEA				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0000006	OMIM:614470	TAS				I		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001744	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001875	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001876	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001878	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001909	OMIM:614470	TAS				P		HPO:probinson	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0001973	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0002205	OMIM:614470	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0002240	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0002665	OMIM:614470	TAS				P		HPO:probinson	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0002729	OMIM:614470	TAS				P		HPO:probinson	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0002731	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0005523	OMIM:614470	TAS				P		HPO:probinson	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0010702	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0012311	OMIM:614470	TAS				P		HPO:skoehler	
OMIM	614470	RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD		HP:0100827	OMIM:614470	IEA				P		HPO:skoehler	
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0000007	OMIM:614473	TAS				I		HPO:skoehler	
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0000121	OMIM:614473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0000822	OMIM:614473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0001635	OMIM:614473	TAS				P		HPO:skoehler	
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0001658	OMIM:614473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0001717	OMIM:614473	TAS				P		HPO:skoehler	
OMIM	614473	#614473 ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2; GACI2		HP:0004912	OMIM:614473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614474	#614474 ATRIOVENTRICULAR SEPTAL DEFECT 5; AVSD5		HP:0000006	OMIM:614474	TAS				I		HPO:skoehler	
OMIM	614474	#614474 ATRIOVENTRICULAR SEPTAL DEFECT 5; AVSD5		HP:0006695	OMIM:614474	IEA				P		HPO:skoehler	
OMIM	614474	#614474 ATRIOVENTRICULAR SEPTAL DEFECT 5; AVSD5		HP:0011623	OMIM:614474	TAS				P		HPO:skoehler	
OMIM	614475	#614475 ATRIAL SEPTAL DEFECT 9; ASD9		HP:0000006	OMIM:614475	TAS				I		HPO:skoehler	
OMIM	614475	#614475 ATRIAL SEPTAL DEFECT 9; ASD9		HP:0001684	OMIM:614475	TAS				P		HPO:skoehler	
OMIM	614475	#614475 ATRIAL SEPTAL DEFECT 9; ASD9		HP:0002092	OMIM:614475	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0000007	OMIM:614480	TAS				I		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0001395	OMIM:614480	TAS				P		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0001397	OMIM:614480	TAS				P		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0001744	OMIM:614480	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0002155	OMIM:614480	IEA				P		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0002240	OMIM:614480	TAS				P		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0002910	OMIM:614480	TAS				P		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0003593	OMIM:614480	TAS				C		HPO:skoehler	
OMIM	614480	#614480 HYPERTRIGLYCERIDEMIA, TRANSIENT INFANTILE; HTGTI		HP:0004322	OMIM:614480	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0000007	OMIM:614482	TAS				I		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0000365	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0000518	OMIM:614482	TAS	HP:0003577			P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0000519	OMIM:614482	IEA				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0000639	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0001250	OMIM:614482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0001263	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0001272	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0001290	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0001344	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0002059	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0003429	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0003593	OMIM:614482	TAS				C		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0003676	OMIM:614482	TAS				C		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0010837	OMIM:614482	TAS				P		HPO:skoehler	
OMIM	614482	CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION; CCHLND		HP:0025356	OMIM:614482	IEA				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0000006	OMIM:614483	TAS				I		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0001250	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0001257	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0001263	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0002119	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0002132	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0002170	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0002301	OMIM:614483	TAS				P		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0003828	OMIM:614483	TAS				C		HPO:skoehler	
OMIM	614483	#614483 PORENCEPHALY 2; POREN2		HP:0003829	OMIM:614483	TAS				C		HPO:skoehler	
OMIM	614485	#614485 TRIGONOCEPHALY 2; TRIGNO2;;CRANIOSYNOSTOSIS, METOPIC		HP:0000006	OMIM:614485	TAS				I		HPO:skoehler	
OMIM	614485	#614485 TRIGONOCEPHALY 2; TRIGNO2;;CRANIOSYNOSTOSIS, METOPIC		HP:0000243	OMIM:614485	TAS				P		HPO:skoehler	
OMIM	614485	#614485 TRIGONOCEPHALY 2; TRIGNO2;;CRANIOSYNOSTOSIS, METOPIC		HP:0000252	OMIM:614485	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614485	#614485 TRIGONOCEPHALY 2; TRIGNO2;;CRANIOSYNOSTOSIS, METOPIC		HP:0000316	OMIM:614485	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614485	#614485 TRIGONOCEPHALY 2; TRIGNO2;;CRANIOSYNOSTOSIS, METOPIC		HP:0011330	OMIM:614485	TAS				P		HPO:skoehler	
OMIM	614486	#614486 THROMBOPHILIA DUE TO THROMBOMODULIN DEFECT; THPH12		HP:0002625	OMIM:614486	TAS				P		HPO:probinson	
OMIM	614486	#614486 THROMBOPHILIA DUE TO THROMBOMODULIN DEFECT; THPH12		HP:0100724	OMIM:614486	TAS				P		HPO:probinson	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:614487	TAS				I		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0000508	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0000657	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001272	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001310	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001324	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001332	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0001336	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002015	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002069	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002075	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002123	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002313	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0002497	OMIM:614487	IEA				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0003202	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:614487	TAS				C		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:614487	TAS				C		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0003828	OMIM:614487	TAS				C		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0007141	OMIM:614487	TAS				P		HPO:skoehler	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0012240	OMIM:614487	TAS				P		HPO:probinson	
OMIM	614487	SPASTIC ATAXIA 5, AUTOSOMAL RECESSIVE		HP:0100543	OMIM:614487	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0000006	OMIM:614491	TAS				I		HPO:skoehler	
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0000822	OMIM:614491	TAS				P		HPO:skoehler	
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0002153	OMIM:614491	TAS				P		HPO:skoehler	
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0004918	OMIM:614491	TAS				P		HPO:probinson	
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0008242	OMIM:614491	IEA				P		HPO:skoehler	
OMIM	614491	#614491 PSEUDOHYPOALDOSTERONISM, TYPE IIB; PHA2B		HP:0011423	OMIM:614491	TAS				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0000006	OMIM:614492	TAS				I		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0000822	OMIM:614492	TAS				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0001942	OMIM:614492	TAS				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0002153	OMIM:614492	TAS				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0004918	OMIM:614492	TAS				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0008242	OMIM:614492	IEA				P		HPO:skoehler	
OMIM	614492	PSEUDOHYPOALDOSTERONISM, TYPE IIC		HP:0011423	OMIM:614492	TAS				P		HPO:skoehler	
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0000007	PMID:22231303	PCS				I		HPO:probinson	
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0000964	PMID:22231303	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0001873	PMID:22231303	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0002719	PMID:22231303	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0005415	PMID:22231303	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0012178	PMID:22231303	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	614493	#614493 WISKOTT-ALDRICH SYNDROME 2; WAS2;;WIPF1 DEFICIENCY		HP:0030253	PMID:22231303	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	614494	%614494 RETINITIS PIGMENTOSA 63; RP63		HP:0000006	OMIM:614494	TAS				I		HPO:skoehler	
OMIM	614494	%614494 RETINITIS PIGMENTOSA 63; RP63		HP:0000510	OMIM:614494	IEA				P		HPO:skoehler	
OMIM	614494	%614494 RETINITIS PIGMENTOSA 63; RP63		HP:0000543	OMIM:614494	TAS				P		HPO:skoehler	
OMIM	614494	%614494 RETINITIS PIGMENTOSA 63; RP63		HP:0000622	OMIM:614494	TAS				P		HPO:skoehler	
OMIM	614494	%614494 RETINITIS PIGMENTOSA 63; RP63		HP:0000662	OMIM:614494	TAS				P		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0000006	OMIM:614495	TAS				I		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0000007	OMIM:614495	TAS				I		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0000822	OMIM:614495	TAS				P		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0002153	OMIM:614495	TAS				P		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0004918	OMIM:614495	TAS				P		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0008242	OMIM:614495	IEA				P		HPO:skoehler	
OMIM	614495	#614495 PSEUDOHYPOALDOSTERONISM, TYPE IID; PHA2D;;FAMILIAL HYPERKALEMIC HYPERTENSION; FHHT		HP:0011423	OMIM:614495	TAS				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0000006	OMIM:614496	TAS				I		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0000822	OMIM:614496	TAS				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0001942	OMIM:614496	TAS				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0002153	OMIM:614496	TAS				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0004918	OMIM:614496	TAS				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0008242	OMIM:614496	IEA				P		HPO:skoehler	
OMIM	614496	PSEUDOHYPOALDOSTERONISM, TYPE IIE; PHA2E		HP:0011423	OMIM:614496	TAS				P		HPO:skoehler	
OMIM	614497	#614497 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7; MCOPCB7		HP:0000006	OMIM:614497	TAS				I		HPO:skoehler	
OMIM	614497	#614497 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7; MCOPCB7		HP:0000568	OMIM:614497	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614497	#614497 MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 7; MCOPCB7		HP:0000589	OMIM:614497	IEA				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0000007	OMIM:614498	TAS				I		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0000253	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0000347	OMIM:614498	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0000648	OMIM:614498	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0001263	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0001276	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0001371	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0001522	OMIM:614498	TAS				M		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0001662	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002063	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002104	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002123	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002169	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002171	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0002529	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0003487	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0003676	OMIM:614498	IEA				C		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0003739	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0012332	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0012448	OMIM:614498	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614498	RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL; RMFSL		HP:0031165	OMIM:614498	TAS				P		HPO:skoehler	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0000007	OMIM:614499	TAS				I		HPO:probinson	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0000750	OMIM:614499	TAS				P		HPO:skoehler	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0001249	OMIM:614499	TAS				P		HPO:probinson	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0001250	OMIM:614499	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0001302	OMIM:614499	IEA				P		HPO:skoehler	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0001339	OMIM:614499	TAS				P		HPO:skoehler	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0001355	OMIM:614499	TAS				P		HPO:skoehler	
OMIM	614499	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34		HP:0040194	OMIM:614499	TAS				P		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000007	PMID:22177090	PCS				I		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000510	PMID:22177090	PCS				P		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000518	OMIM:614500	TAS				P		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000529	PMID:22177090	PCS				P		HPO:probinson	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000543	PMID:22177090	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000548	PMID:22177090	PCS				P		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000613	PMID:22177090	PCS				P		HPO:probinson	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0000662	PMID:22177090	PCS				P		HPO:probinson	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0007401	PMID:22177090	PCS				P		HPO:skoehler	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0007663	PMID:22177090	PCS				P		HPO:probinson	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0007737	PMID:22177090	IEA		HP:0040284		P		HPO:probinson	2/6
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0007843	PMID:22177090	PCS		HP:0040284		P		HPO:probinson	4/6
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0025147	PMID:22177090	PCS				P		HPO:probinson	
OMIM	614500	CONE-ROD DYSTROPHY 16		HP:0100259	PMID:22177090	PCS		HP:0040284		P		HPO:skoehler	2/6
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000007	OMIM:614501	TAS				I		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000154	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000158	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000414	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000486	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0000666	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001182	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001250	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001263	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001265	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001290	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001537	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001607	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001647	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001650	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0001999	OMIM:614501	IEA				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0002079	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0002119	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0002353	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0003429	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0004279	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0011304	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0011968	OMIM:614501	TAS	HP:0003623			P		HPO:skoehler	
OMIM	614501	PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM		HP:0012802	OMIM:614501	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000007	OMIM:614504	TAS				I		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000365	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000505	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000543	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000613	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0000666	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B	HP:0012825	HP:0002078	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614504	#614504 USHER SYNDROME, TYPE IIIB; USH3B		HP:0002194	OMIM:614504	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0000007	OMIM:614507	TAS				I		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0000486	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0001263	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0001290	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0001410	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0001508	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0002019	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0002020	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0003593	OMIM:614507	TAS				C		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0003642	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614507	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IR		HP:0410018	OMIM:614507	TAS				P		HPO:skoehler	
OMIM	614508	#614508 MIRROR MOVEMENTS 2; MRMV2		HP:0000006	OMIM:614508	TAS				I		HPO:skoehler	
OMIM	614508	#614508 MIRROR MOVEMENTS 2; MRMV2		HP:0001335	OMIM:614508	IEA				P		HPO:skoehler	
OMIM	614508	#614508 MIRROR MOVEMENTS 2; MRMV2		HP:0003829	OMIM:614508	TAS		HP:0040284		C		HPO:skoehler	50%
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0000007	OMIM:614514	TAS				I		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0000618	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0000979	OMIM:614514	IEA				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0001342	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0002204	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0002638	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0004420	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0004855	OMIM:614514	IEA				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0005305	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0005521	OMIM:614514	TAS				P		HPO:skoehler	
OMIM	614514	THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL RECESSIVE; THPH6		HP:0100724	OMIM:614514	IEA				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0000218	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY	HP:0012825	HP:0000316	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001250	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001263	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001290	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001508	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001520	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001537	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001792	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001873	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001875	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0001903	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0002126	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0002919	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0003128	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0003355	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0003745	OMIM:614520	TAS				I		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0005280	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0005528	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0006610	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0011220	OMIM:614520	TAS				P		HPO:skoehler	
OMIM	614520	ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNEL DEFICIENCY		HP:0012448	OMIM:614520	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614521	#614521 THROMBOCYTHEMIA 3; THCYT3;;THROMBOCYTOSIS 3		HP:0000006	OMIM:614521	TAS				I		HPO:skoehler	
OMIM	614521	#614521 THROMBOCYTHEMIA 3; THCYT3;;THROMBOCYTOSIS 3		HP:0001428	OMIM:614521	TAS				I		HPO:skoehler	
OMIM	614521	#614521 THROMBOCYTHEMIA 3; THCYT3;;THROMBOCYTOSIS 3		HP:0001894	OMIM:614521	IEA				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000006	OMIM:614524	TAS				I		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000007	OMIM:614524	TAS				I		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000272	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000347	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000463	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000773	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000926	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0000946	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0001538	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0001591	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0003016	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0003021	OMIM:614524	IEA				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0003173	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0003175	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0003196	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0005257	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614524	FIBROCHONDROGENESIS 2; FBCG2		HP:0011800	OMIM:614524	TAS				P		HPO:skoehler	
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000006	OMIM:614526	TAS				I		HPO:skoehler	
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000185	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000297	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000319	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000325	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000347	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000490	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000494	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000501	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000568	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0000659	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0001156	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0001249	OMIM:614526	TAS				P		HPO:skoehler	
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0001250	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0001631	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0002032	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0008936	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614526	CHROMOSOME 17Q12 DUPLICATION SYNDROME		HP:0011304	OMIM:614526	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000003	OMIM:614527	TAS	HP:0003577			P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000006	OMIM:614527	TAS				I	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000010	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000028	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000089	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000122	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000126	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000138	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000151	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000177	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000218	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000272	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000278	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000286	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000303	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000324	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000347	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000348	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000411	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000494	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000535	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000540	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000666	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000717	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000750	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0000998	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0001249	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0001773	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0001792	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0001795	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0002007	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0002384	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0002553	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0002650	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0002910	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0003250	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0003774	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0004279	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0004322	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0004719	OMIM:614527	IEA				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0005280	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0005343	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0005999	OMIM:614527	TAS				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0008404	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0008619	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0008661	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0009824	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0010511	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0011856	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0031909	OMIM:614527	IEA				P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0100753	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614527	CHROMOSOME 17q12 DELETION SYNDROME		HP:0100807	OMIM:614527	TAS		HP:0040283		P	CHROMOSOME 17Q12 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000218	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000260	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000286	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000316	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000347	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000348	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000358	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000369	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000377	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000431	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000470	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000581	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000582	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0000774	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0001263	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0001290	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0001508	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0001518	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0002007	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0002033	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0002645	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0003745	OMIM:614541	TAS				I		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0005280	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0006610	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0008897	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614541	CHROMOSOME 16Q22 DELETION SYNDROME		HP:0012745	OMIM:614541	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000007	OMIM:614557	TAS				I		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000015	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000023	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000185	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000410	OMIM:614557	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000545	OMIM:614557	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000938	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000974	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000977	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0000978	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001252	OMIM:614557	TAS	HP:0003623			P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001270	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001537	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001643	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001757	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001762	OMIM:614557	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0001763	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0002421	OMIM:614557	TAS	HP:0011463			P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0002751	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0003198	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0003202	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0003467	OMIM:614557	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0007502	OMIM:614557	TAS				P		HPO:skoehler	
OMIM	614557	EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2; EDSKSCL2		HP:0031649	OMIM:614557	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0000006	OMIM:614558	TAS				I		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0000253	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0000717	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0001249	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0001263	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0001290	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0002059	OMIM:614558	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0002376	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0011097	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614558	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 13		HP:0200134	OMIM:614558	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000007	OMIM:614559	TAS				I		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000253	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000407	OMIM:614559	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000486	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000556	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000639	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0000648	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001250	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001251	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001265	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001272	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001284	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001290	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0001508	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0002079	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0002120	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0002305	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0003593	OMIM:614559	TAS				C		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0007108	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0010864	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614559	INFANTILE CEREBELLAR-RETINAL DEGENERATION		HP:0011344	OMIM:614559	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0000007	OMIM:614561	TAS				I		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001250	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001251	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001257	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001260	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001263	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001268	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001288	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001332	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0001337	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0002071	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0002301	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0002352	OMIM:614561	IEA				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0002415	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0002514	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0003676	OMIM:614561	TAS				C		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0003828	OMIM:614561	TAS				C		HPO:skoehler	
OMIM	614561	LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS		HP:0007256	OMIM:614561	TAS				P		HPO:skoehler	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0000006	OMIM:614563	TAS				I		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0000252	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0000494	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001249	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001252	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001265	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001288	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001302	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001321	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001357	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001760	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0001999	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0002079	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0002365	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0002510	OMIM:614563	TAS		HP:0040284		P		HPO:probinson	3/8
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0003477	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0007359	OMIM:614563	TAS				P		HPO:skoehler	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0011220	OMIM:614563	TAS				P		HPO:probinson	
OMIM	614563	MENTAL RETARDATION, AUTOSOMAL DOMINANT 13		HP:0200055	OMIM:614563	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0000006	OMIM:614564	TAS				I		HPO:skoehler	
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0000444	OMIM:614564	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0000670	OMIM:614564	TAS				P		HPO:skoehler	
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0001009	OMIM:614564	TAS				P		HPO:skoehler	
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0001596	OMIM:614564	TAS				P		HPO:skoehler	
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0001807	OMIM:614564	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0003002	OMIM:614564	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614564	#614564 CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL; FCTCS;;TELANGIECTASIA, CUTANEOUS, AND CANCER SYNDROME, FAMILIAL		HP:0006297	OMIM:614564	TAS				P		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0000007	OMIM:614565	TAS				I		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0000486	OMIM:614565	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0000545	OMIM:614565	TAS				P		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E	HP:0012826	HP:0000639	OMIM:614565	TAS				P		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0001419	OMIM:614565	TAS				I		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0007642	OMIM:614565	TAS				P		HPO:skoehler	
OMIM	614565	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E		HP:0007663	OMIM:614565	TAS				P		HPO:skoehler	
OMIM	614569	MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE		HP:0001028	PMID:8408836	PCS				P		HPO:probinson	
OMIM	614569	MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE		HP:0002756	PMID:8408836	PCS				P		HPO:probinson	
OMIM	614569	MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE		HP:0005701	PMID:8408836	PCS				P		HPO:probinson	
OMIM	614569	MULTIPLE ENCHONDROMATOSIS, MAFFUCCI TYPE		HP:0006765	PMID:8408836	PCS		HP:0040284		P		HPO:probinson	30%
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0000007	OMIM:614575	TAS				I		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0000640	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0001151	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0001260	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0001265	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0001272	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0002066	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0002070	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0002172	OMIM:614575	IEA				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0002403	OMIM:614575	TAS				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0003447	OMIM:614575	IEA				P		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0003581	OMIM:614575	TAS				C		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0003677	OMIM:614575	TAS				C		HPO:skoehler	
OMIM	614575	CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME; CANVAS		HP:0008568	OMIM:614575	IEA				P		HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000007	OMIM:614576	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000114	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000252	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000278	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000286	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000962	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0000966	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001249	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001250	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L	HP:0012825	HP:0001263	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001396	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001403	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001413	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001508	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001511	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001522	OMIM:614576	TAS				M	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001873	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001876	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001892	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0001903	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002028	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002037	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002059	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002119	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002240	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002719	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002721	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002904	OMIM:614576	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0002910	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0003577	OMIM:614576	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0004313	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0005435	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0007185	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0008936	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0012301	OMIM:614576	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	
OMIM	614576	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl; CDG2L		HP:0100259	OMIM:614576	TAS		HP:0040283		P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIL; CDG2L	HPO:skoehler	HP:0040283
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0000007	OMIM:614582	TAS				I		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0001263	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0001508	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0001639	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0002094	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0002151	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0002240	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0002910	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0003348	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614582	#614582 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 9; COXPD9		HP:0011968	OMIM:614582	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000006	OMIM:614583	TAS		HP:0040284		I		HPO:probinson	5/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000154	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000202	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000219	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000243	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	7/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000278	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000307	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000316	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	7/8
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000343	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000365	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	5/6
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000377	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000465	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000470	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000506	OMIM:614583	IEA				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000508	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	8/8
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000568	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000589	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	5/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0000637	OMIM:614583	TAS				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0001249	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	5/5
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0001250	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	7/8
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0001274	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0001302	OMIM:614583	IEA				P		HPO:skoehler	
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0001339	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	7/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0002119	OMIM:614583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0002553	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	7/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0004322	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	3/7
OMIM	614583	BARAITSER-WINTER SYNDROME 2; BRWS2		HP:0005484	OMIM:614583	TAS		HP:0040284		P		HPO:probinson	4/7
OMIM	614588	DYSTONIA 21; DYT21		HP:0000006	OMIM:614588	TAS				I		HPO:skoehler	
OMIM	614588	DYSTONIA 21; DYT21		HP:0000473	OMIM:614588	TAS				P		HPO:skoehler	
OMIM	614588	DYSTONIA 21; DYT21		HP:0000643	OMIM:614588	TAS				P		HPO:skoehler	
OMIM	614588	DYSTONIA 21; DYT21		HP:0011462	OMIM:614588	TAS				C		HPO:skoehler	
OMIM	614588	DYSTONIA 21; DYT21		HP:0012049	OMIM:614588	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000006	OMIM:614592	TAS				I		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000212	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000272	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000316	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000347	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000369	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0000894	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0001007	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0001090	OMIM:614592	IEA				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0001156	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0001433	OMIM:614592	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0001591	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0004440	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0008665	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614592	BENT BONE DYSPLASIA SYNDROME; BBDS		HP:0011800	OMIM:614592	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0000006	OMIM:614594	TAS				I		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0000975	OMIM:614594	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0000982	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0000989	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0001036	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0001371	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0002164	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0002289	OMIM:614594	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0007759	OMIM:614594	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0008070	OMIM:614594	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0008392	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614594	#614594 PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTICPLAQUES;;OLMSTED SYNDROME; OLMS		HP:0008404	OMIM:614594	TAS				P		HPO:skoehler	
OMIM	614595	#614595 PREECLAMPSIA/ECLAMPSIA 5; PEE5		HP:0000006	OMIM:614595	TAS				I		HPO:probinson	
OMIM	614595	#614595 PREECLAMPSIA/ECLAMPSIA 5; PEE5		HP:0100601	OMIM:614595	TAS				P		HPO:probinson	
OMIM	614595	#614595 PREECLAMPSIA/ECLAMPSIA 5; PEE5		HP:0100602	OMIM:614595	IEA				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0000007	OMIM:614602	TAS				I		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0000316	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0000445	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0001394	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0001508	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0001511	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0001518	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002014	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002224	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002235	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002240	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002299	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002583	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0002721	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0008070	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0009886	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0011220	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0011473	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0012115	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0030056	OMIM:614602	TAS				P		HPO:skoehler	
OMIM	614602	TRICHOHEPATOENTERIC SYNDROME 2		HP:0040303	OMIM:614602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000006	OMIM:614607	TAS				I		HPO:probinson	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000154	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000158	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000179	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000280	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000294	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000377	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000445	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000463	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000505	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000527	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000574	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000750	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0000998	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001156	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001249	OMIM:614607	TAS				P		HPO:probinson	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001250	OMIM:614607	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001263	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001273	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001290	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0001792	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0002209	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0002719	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0002750	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0004322	OMIM:614607	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0005280	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0009835	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0011968	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0030680	OMIM:614607	TAS				P		HPO:skoehler	
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0200104	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614607	COFFIN-SIRIS SYNDROME 2		HP:0200105	OMIM:614607	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000006	OMIM:614608	TAS				I		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000154	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000158	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000252	OMIM:614608	TAS		HP:0040284		P		HPO:probinson	2/3
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000280	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000365	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000445	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000463	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000505	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000527	OMIM:614608	TAS				P		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000574	OMIM:614608	TAS				P		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000696	OMIM:614608	TAS				P		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0000998	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001007	OMIM:614608	TAS		HP:0040284		P		HPO:probinson	3/4
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001249	OMIM:614608	TAS				P		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001250	OMIM:614608	TAS		HP:0040284		P		HPO:probinson	2/4
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001263	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001273	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001290	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001321	OMIM:614608	TAS		HP:0040284		P		HPO:probinson	2/3
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0001511	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0002209	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0002650	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0002750	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0004322	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0005280	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0009835	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0011968	OMIM:614608	TAS				P		HPO:probinson	
OMIM	614608	COFFIN-SIRIS SYNDROME 3		HP:0030680	OMIM:614608	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000006	OMIM:614609	TAS				I		HPO:probinson	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000154	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000158	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000252	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	4/5
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000280	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000365	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000445	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000463	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000505	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	5/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000527	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	6/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000574	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	6/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0000998	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001007	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	6/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001249	OMIM:614609	TAS				P		HPO:probinson	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001250	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	2/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001263	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001273	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001290	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001305	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	1/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0001511	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0002209	OMIM:614609	TAS		HP:0040284		P		HPO:probinson	3/6
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0002650	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0002750	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0004322	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0005280	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0009835	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0009928	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0011968	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614609	COFFIN-SIRIS SYNDROME 4		HP:0030680	OMIM:614609	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000006	OMIM:614613	TAS				I		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000028	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000047	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000272	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000303	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000311	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000463	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000635	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000717	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000750	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000752	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000819	OMIM:614613	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0000851	OMIM:614613	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE	HP:0012828	HP:0001156	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0001249	OMIM:614613	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0001263	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0001511	OMIM:614613	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0001513	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0002286	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0002297	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0002516	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0003196	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0003416	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0003502	OMIM:614613	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0003577	OMIM:614613	TAS				C		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0005280	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0005616	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0009803	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0010049	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0010579	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0010743	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614613	ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE		HP:0011800	OMIM:614613	TAS				P		HPO:skoehler	
OMIM	614614	#614614 DEAFNESS, AUTOSOMAL DOMINANT 4B; DFNA4B		HP:0000006	OMIM:614614	TAS				I		HPO:skoehler	
OMIM	614614	#614614 DEAFNESS, AUTOSOMAL DOMINANT 4B; DFNA4B		HP:0000365	OMIM:614614	IEA				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0000007	OMIM:614615	TAS				I		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0000657	OMIM:614615	TAS				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0001159	OMIM:614615	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0001251	OMIM:614615	TAS				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0001263	OMIM:614615	TAS				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0001320	OMIM:614615	TAS				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17	HP:0025303	HP:0002883	OMIM:614615	TAS				P		HPO:skoehler	
OMIM	614615	#614615 JOUBERT SYNDROME 17; JBTS17		HP:0010442	OMIM:614615	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614616	#614616 DIARRHEA 6; DIAR6		HP:0000006	OMIM:614616	TAS				I		HPO:skoehler	
OMIM	614616	#614616 DIARRHEA 6; DIAR6		HP:0002014	OMIM:614616	IEA				P		HPO:skoehler	
OMIM	614616	#614616 DIARRHEA 6; DIAR6		HP:0002027	OMIM:614616	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614616	#614616 DIARRHEA 6; DIAR6		HP:0100502	OMIM:614616	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614617	%614617 DEAFNESS, AUTOSOMAL RECESSIVE 86; DFNB86		HP:0000007	OMIM:614617	TAS				I		HPO:skoehler	
OMIM	614617	%614617 DEAFNESS, AUTOSOMAL RECESSIVE 86; DFNB86		HP:0000365	OMIM:614617	IEA				P		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0000006	OMIM:614618	TAS				I		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0000007	OMIM:614618	TAS				I		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0001276	OMIM:614618	TAS				P		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0002104	OMIM:614618	TAS	HP:0003623			P		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0002267	OMIM:614618	IEA				P		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0003552	OMIM:614618	TAS				P		HPO:skoehler	
OMIM	614618	#614618 HYPEREKPLEXIA 3; HKPX3		HP:0003593	OMIM:614618	TAS				C		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0000007	OMIM:614619	TAS				I		HPO:probinson	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0000483	OMIM:614619	IEA				P		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0000545	OMIM:614619	IEA				P		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0000565	OMIM:614619	TAS		HP:0040284		P		HPO:probinson	7/9
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0001276	OMIM:614619	TAS				P		HPO:probinson	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0001336	OMIM:614619	IEA				P		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0001347	OMIM:614619	IEA				P		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0002267	OMIM:614619	TAS				P		HPO:probinson	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0003593	OMIM:614619	IEA				C		HPO:skoehler	
OMIM	614619	HYPEREKPLEXIA 2; HKPX2		HP:0030904	OMIM:614619	IEA				P		HPO:skoehler	
OMIM	614621	#614621 UV-SENSITIVE SYNDROME 2; UVSS2		HP:0000007	OMIM:614621	TAS				I		HPO:skoehler	
OMIM	614621	#614621 UV-SENSITIVE SYNDROME 2; UVSS2		HP:0000992	OMIM:614621	TAS				P		HPO:skoehler	
OMIM	614621	#614621 UV-SENSITIVE SYNDROME 2; UVSS2		HP:0001480	OMIM:614621	TAS				P		HPO:skoehler	
OMIM	614621	#614621 UV-SENSITIVE SYNDROME 2; UVSS2		HP:0003224	OMIM:614621	TAS				P		HPO:skoehler	
OMIM	614621	#614621 UV-SENSITIVE SYNDROME 2; UVSS2		HP:0003593	OMIM:614621	TAS				C		HPO:skoehler	
OMIM	614622	%614622 KERATOCONUS 5; KTCN5		HP:0000006	OMIM:614622	TAS				I		HPO:skoehler	
OMIM	614622	%614622 KERATOCONUS 5; KTCN5		HP:0000563	OMIM:614622	TAS				P		HPO:skoehler	
OMIM	614623	%614623 KERATOCONUS 6; KTCN6		HP:0000006	OMIM:614623	TAS				I		HPO:skoehler	
OMIM	614623	%614623 KERATOCONUS 6; KTCN6		HP:0000563	OMIM:614623	TAS				P		HPO:skoehler	
OMIM	614628	%614628 KERATOCONUS 8; KTCN8		HP:0000006	OMIM:614628	TAS				I		HPO:skoehler	
OMIM	614628	%614628 KERATOCONUS 8; KTCN8		HP:0000563	OMIM:614628	TAS				P		HPO:skoehler	
OMIM	614629	%614629 KERATOCONUS 7; KTCN7		HP:0000006	OMIM:614629	TAS				I		HPO:skoehler	
OMIM	614629	%614629 KERATOCONUS 7; KTCN7		HP:0000563	OMIM:614629	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0000007	OMIM:614640	TAS				I		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0000958	OMIM:614640	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0000992	OMIM:614640	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0001009	OMIM:614640	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0001480	OMIM:614640	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0003224	OMIM:614640	TAS				P		HPO:skoehler	
OMIM	614640	#614640 UV-SENSITIVE SYNDROME 3; UVSS3		HP:0003593	OMIM:614640	TAS				C		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000007	OMIM:614643	TAS				I		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000238	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000256	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000278	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000369	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000490	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000501	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000518	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000541	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000568	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000609	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0000659	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001181	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001284	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001290	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001302	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001305	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001321	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001338	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0001558	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002007	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002079	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002084	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002126	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002187	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002282	OMIM:614643	IEA				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0002365	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0003236	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0003560	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0007260	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0007968	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0007973	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0008551	OMIM:614643	TAS				P		HPO:skoehler	
OMIM	614643	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 7; MDDGA7		HP:0031882	OMIM:614643	IEA				P		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0000007	OMIM:614650	TAS				I		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0000093	OMIM:614650	TAS				P		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0000097	OMIM:614650	TAS				P		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0000100	OMIM:614650	TAS				P		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0000407	OMIM:614650	TAS				P		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0001250	OMIM:614650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0001967	OMIM:614650	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0003593	OMIM:614650	TAS				C		HPO:skoehler	
OMIM	614650	#614650 COENZYME Q10 DEFICIENCY, PRIMARY, 6; COQ10D6		HP:0003678	OMIM:614650	TAS				C		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0000007	OMIM:614651	TAS				I		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0000256	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0000648	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0000965	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0001256	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0001284	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0001513	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0001653	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0001659	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0002092	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0002151	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614651	#614651 COENZYME Q10 DEFICIENCY, PRIMARY, 2; COQ10D2		HP:0009830	OMIM:614651	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0000007	OMIM:614652	TAS				I		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0000093	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0000100	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0000969	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0001319	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0002133	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0002151	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0011968	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614652	#614652 COENZYME Q10 DEFICIENCY, PRIMARY, 3; COQ10D3		HP:0100704	OMIM:614652	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000007	OMIM:614653	TAS				I		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000194	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000218	OMIM:614653	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000331	OMIM:614653	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000369	OMIM:614653	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000522	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000559	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000763	OMIM:614653	IEA				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0000975	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001188	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001284	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001319	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001371	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001510	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001649	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001662	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001762	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0001945	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0002093	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0002104	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0003093	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0007610	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614653	#614653 NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI; HSAN6;;HSAN VI		HP:0011968	OMIM:614653	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0000007	OMIM:614654	TAS				I		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5	HP:0031375	HP:0001250	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001263	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001272	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001276	OMIM:614654	IEA				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001290	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001298	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001332	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001347	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001511	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001612	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001662	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0001712	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0002059	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0002093	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0002151	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0003128	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0003348	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0005484	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614654	COENZYME Q10 DEFICIENCY, PRIMARY, 5; COQ10D5		HP:0011968	OMIM:614654	TAS				P		HPO:skoehler	
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0000006	OMIM:614662	TAS				I		HPO:skoehler	
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0000855	OMIM:614662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0000956	OMIM:614662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0001513	OMIM:614662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0005616	OMIM:614662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614662	#614662 CORTISONE REDUCTASE DEFICIENCY 2; CORTRD2		HP:0012411	OMIM:614662	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614665	#614665 MECONIUM ILEUS		HP:0000007	OMIM:614665	TAS				I		HPO:skoehler	
OMIM	614665	#614665 MECONIUM ILEUS		HP:0004388	OMIM:614665	TAS				P		HPO:skoehler	
OMIM	614665	#614665 MECONIUM ILEUS		HP:0004401	OMIM:614665	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000006	OMIM:614669	TAS				I		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000007	OMIM:614669	TAS				I		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000160	OMIM:614669	TAS		HP:0040284		P		HPO:skoehler	52%
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000162	OMIM:614669	TAS		HP:0040284		P		HPO:skoehler	46%
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000175	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000256	OMIM:614669	TAS		HP:0040284		P		HPO:skoehler	25%
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000311	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000358	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000369	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000678	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0000689	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0002104	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0004453	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0007627	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0007628	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0008537	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0008559	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0009088	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0025267	OMIM:614669	TAS				P		HPO:skoehler	
OMIM	614669	AURICULOCONDYLAR SYNDROME 2; ARCND2		HP:0031013	OMIM:614669	IEA				P		HPO:skoehler	
OMIM	614672	#614672 CARDIOMYOPATHY, DILATED, 2B; CMD2B		HP:0000007	OMIM:614672	TAS				I		HPO:skoehler	
OMIM	614672	#614672 CARDIOMYOPATHY, DILATED, 2B; CMD2B		HP:0001635	OMIM:614672	TAS				P		HPO:skoehler	
OMIM	614672	#614672 CARDIOMYOPATHY, DILATED, 2B; CMD2B		HP:0001644	OMIM:614672	TAS				P		HPO:skoehler	
OMIM	614672	#614672 CARDIOMYOPATHY, DILATED, 2B; CMD2B		HP:0005110	OMIM:614672	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8		HP:0000007	OMIM:614673	TAS				I		HPO:skoehler	
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8	HP:0012828	HP:0000252	OMIM:614673	TAS				P		HPO:skoehler	
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8		HP:0000278	OMIM:614673	TAS				P		HPO:skoehler	
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8		HP:0000340	OMIM:614673	TAS				P		HPO:skoehler	
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8		HP:0003577	OMIM:614673	TAS				C		HPO:skoehler	
OMIM	614673	#614673 MICROCEPHALY 8, PRIMARY, AUTOSOMAL RECESSIVE; MCPH8		HP:0010864	OMIM:614673	TAS				P		HPO:skoehler	
OMIM	614674	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT		HP:0000006	OMIM:614674	TAS				I		HPO:skoehler	
OMIM	614674	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT		HP:0001945	OMIM:614674	IEA				P		HPO:skoehler	
OMIM	614674	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT		HP:0002076	OMIM:614674	TAS				P		HPO:skoehler	
OMIM	614674	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT		HP:0003118	OMIM:614674	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614674	PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT		HP:0200067	OMIM:614674	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614675	BONE MARROW FAILURE SYNDROME 1; BMFS1		HP:0000006	OMIM:614675	TAS				I		HPO:skoehler	
OMIM	614675	BONE MARROW FAILURE SYNDROME 1; BMFS1		HP:0000365	OMIM:614675	TAS				P		HPO:skoehler	
OMIM	614675	BONE MARROW FAILURE SYNDROME 1; BMFS1		HP:0001915	OMIM:614675	TAS				P		HPO:skoehler	
OMIM	614675	BONE MARROW FAILURE SYNDROME 1; BMFS1		HP:0002863	OMIM:614675	TAS				P		HPO:skoehler	
OMIM	614675	BONE MARROW FAILURE SYNDROME 1; BMFS1		HP:0005528	OMIM:614675	IEA				P		HPO:skoehler	
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0000006	OMIM:614676	TAS				I		HPO:skoehler	
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0001634	OMIM:614676	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0001638	OMIM:614676	IEA				P		HPO:skoehler	
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0001699	OMIM:614676	TAS		HP:0040283		M		HPO:skoehler	HP:0040283
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0001712	OMIM:614676	TAS				P		HPO:skoehler	
OMIM	614676	%614676 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21; CMH21		HP:0011675	OMIM:614676	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000007	OMIM:614678	TAS				I		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000253	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000486	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000556	OMIM:614678	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000639	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0000657	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001250	OMIM:614678	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001257	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001263	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001272	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001290	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001308	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001344	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001347	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001371	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001510	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0001760	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0002059	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0002093	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0002350	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0002421	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0002827	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0003202	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0003577	OMIM:614678	TAS				C		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0003828	OMIM:614678	TAS				C		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0008936	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0011968	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614678	PONTOCEREBELLAR HYPOPLASIA, TYPE 1B		HP:0012473	OMIM:614678	TAS				P		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0000007	OMIM:614679	TAS				I		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0001696	OMIM:614679	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0002110	OMIM:614679	TAS				P		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0002205	OMIM:614679	TAS				P		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0002257	OMIM:614679	TAS				P		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0003577	OMIM:614679	TAS				C		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0005938	OMIM:614679	TAS				P		HPO:probinson	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0011109	OMIM:614679	TAS				P		HPO:skoehler	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0012265	OMIM:614679	TAS				P		HPO:probinson	
OMIM	614679	CILIARY DYSKINESIA, PRIMARY, 17; CILD17		HP:0012735	OMIM:614679	IEA				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000007	OMIM:614684	TAS				I		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000028	OMIM:614684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000054	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000154	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000219	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000316	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000343	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000349	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000396	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000431	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000574	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000582	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000767	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0000768	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0001156	OMIM:614684	IEA				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0001256	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0001500	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0001698	OMIM:614684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0001999	OMIM:614684	IEA				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0006610	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0009789	OMIM:614684	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0009803	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0010805	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0030084	OMIM:614684	IEA				P		HPO:skoehler	
OMIM	614684	HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITAL ABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES		HP:0200055	OMIM:614684	TAS				P		HPO:skoehler	
OMIM	614687	ALAR CLEFT, ISOLATED		HP:0003745	OMIM:614687	TAS				I		HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000407	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:iea	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000486	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000508	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000639	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000657	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0000902	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001249	OMIM:614688	TAS		HP:0040281		P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	HP:0040281
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001250	OMIM:614688	TAS		HP:0040283		P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	HP:0040283
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001263	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001290	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001310	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001344	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001347	PMID:21651769	PCS		HP:0040284		P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	3/3
OMIM	614688	Pontine tegmental cap dysplasia		HP:0001508	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002015	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002079	OMIM:614688	TAS		HP:0040283		P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	HP:0040283
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002599	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002650	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002835	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0002937	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0003745	OMIM:614688	TAS				I	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0005216	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0010628	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0011448	OMIM:614688	TAS		HP:0040283		P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	HP:0040283
OMIM	614688	Pontine tegmental cap dysplasia		HP:0011968	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0012155	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:skoehler	
OMIM	614688	Pontine tegmental cap dysplasia		HP:0030975	OMIM:614688	TAS				P	PONTINE TEGMENTAL CAP DYSPLASIA	HPO:probinson	
OMIM	614691	#614691 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 5; CATC5		HP:0000007	OMIM:614691	TAS				I		HPO:skoehler	
OMIM	614691	#614691 CATARACT, AUTOSOMAL RECESSIVE CONGENITAL 5; CATC5		HP:0000519	OMIM:614691	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0000006	OMIM:614696	TAS				I		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0001260	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0001265	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0001284	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0001348	OMIM:614696	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0002015	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0002145	OMIM:614696	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0002380	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0002483	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0002747	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0003202	OMIM:614696	TAS				P		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0003487	OMIM:614696	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0003581	OMIM:614696	TAS				C		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0003678	OMIM:614696	TAS				C		HPO:skoehler	
OMIM	614696	#614696 AMYOTROPHIC LATERAL SCLEROSIS 17; ALS17;;AMYOTROPHIC LATERAL SCLEROSIS, CHMP2B-RELATED		HP:0007354	OMIM:614696	IEA				P		HPO:skoehler	
OMIM	614699	#614699 IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7		HP:0000007	OMIM:614699	TAS				I		HPO:skoehler	
OMIM	614699	#614699 IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7		HP:0002028	OMIM:614699	TAS				P		HPO:skoehler	
OMIM	614699	#614699 IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7		HP:0002205	OMIM:614699	TAS				P		HPO:skoehler	
OMIM	614699	#614699 IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7		HP:0002720	OMIM:614699	TAS				P		HPO:skoehler	
OMIM	614699	#614699 IMMUNODEFICIENCY, COMMON VARIABLE, 7; CVID7		HP:0002721	OMIM:614699	IEA				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0000007	OMIM:614700	TAS				I		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0000403	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0000509	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0000821	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001369	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001508	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001510	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001873	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001875	OMIM:614700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001876	OMIM:614700	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0001890	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002028	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002090	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002099	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002110	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002583	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002716	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002720	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002721	OMIM:614700	IEA				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0002850	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0003676	OMIM:614700	TAS				C		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0005263	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0006528	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0011108	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614700	#614700 IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY; CVID8		HP:0100759	OMIM:614700	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000006	OMIM:614701	TAS				I		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000175	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000219	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000252	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000319	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000343	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000431	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000574	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000664	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0000965	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0001156	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0001159	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0001263	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0002020	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0002553	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0002937	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0004322	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0008428	OMIM:614701	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614701	#614701 CORNELIA DE LANGE SYNDROME 4; CDLS4		HP:0100777	OMIM:614701	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0000007	OMIM:614702	TAS				I		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0000648	OMIM:614702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001250	OMIM:614702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001257	OMIM:614702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001263	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001290	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001332	OMIM:614702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001508	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001518	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001639	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001942	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0001943	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0002151	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0002465	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0003128	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0003348	OMIM:614702	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0003577	OMIM:614702	TAS				C		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0011675	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0011968	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614702	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 10		HP:0100543	OMIM:614702	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0000007	OMIM:614706	TAS				I		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11	HP:0003676	HP:0000505	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0000556	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0000648	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0001251	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0001268	OMIM:614706	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0001272	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0002123	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0002353	OMIM:614706	TAS				P		HPO:skoehler	
OMIM	614706	#614706 CEROID LIPOFUSCINOSIS, NEURONAL, 11; CLN11		HP:0003678	OMIM:614706	TAS				C		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000007	OMIM:614707	TAS				I		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000407	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000467	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000572	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000639	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000648	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0000718	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001171	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001251	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001283	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001284	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001290	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001308	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0001992	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0002015	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0002093	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0002312	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0002375	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0002751	OMIM:614707	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0003676	OMIM:614707	TAS				C		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0003690	OMIM:614707	IEA				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2	HP:0012828	HP:0003700	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0003828	OMIM:614707	TAS				C		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0007141	OMIM:614707	IEA				P		HPO:skoehler	
OMIM	614707	BROWN-VIALETTO-VAN LAERE SYNDROME 2; BVVLS2		HP:0010628	OMIM:614707	TAS				P		HPO:skoehler	
OMIM	614714	POROKERATOSIS 7, MULTIPLE TYPES; POROK7		HP:0000006	OMIM:614714	TAS				I		HPO:skoehler	
OMIM	614714	POROKERATOSIS 7, MULTIPLE TYPES; POROK7		HP:0001036	OMIM:614714	IEA				P		HPO:skoehler	
OMIM	614714	POROKERATOSIS 7, MULTIPLE TYPES; POROK7		HP:0200044	OMIM:614714	TAS				P		HPO:skoehler	
OMIM	614723	#614723 ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY; APRTD;;APRT DEFICIENCY;;UROLITHIASIS, 2,8-@DIHYDROXYADENINE;;UROLITHIASIS, DHA;;NEPHROLITHIASIS, DHA		HP:0000007	OMIM:614723	TAS				I		HPO:skoehler	
OMIM	614723	#614723 ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY; APRTD;;APRT DEFICIENCY;;UROLITHIASIS, 2,8-@DIHYDROXYADENINE;;UROLITHIASIS, DHA;;NEPHROLITHIASIS, DHA		HP:0000083	OMIM:614723	TAS				P		HPO:skoehler	
OMIM	614723	#614723 ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY; APRTD;;APRT DEFICIENCY;;UROLITHIASIS, 2,8-@DIHYDROXYADENINE;;UROLITHIASIS, DHA;;NEPHROLITHIASIS, DHA		HP:0000787	OMIM:614723	TAS				P		HPO:probinson	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000007	OMIM:614727	TAS				I		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000272	OMIM:614727	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000358	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000369	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000705	OMIM:614727	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0000939	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001250	OMIM:614727	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001263	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001290	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001324	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001388	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001508	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001873	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0001955	OMIM:614727	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0002240	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0002500	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0002656	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0002751	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0002910	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0003236	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0004322	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0005484	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0011800	OMIM:614727	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0100252	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614727	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIK		HP:0100255	OMIM:614727	TAS				P		HPO:skoehler	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0000007	OMIM:614728	TAS				I		HPO:probinson	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0000252	OMIM:614728	TAS				P		HPO:probinson	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0000750	OMIM:614728	TAS				P		HPO:probinson	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0001249	OMIM:614728	TAS				P		HPO:skoehler	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0001263	OMIM:614728	TAS				P		HPO:probinson	
OMIM	614728	#614728 SECKEL SYNDROME 6; SCKL6		HP:0004322	OMIM:614728	TAS				P		HPO:probinson	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000006	OMIM:614732	TAS				I		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000028	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000047	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000054	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000256	OMIM:614732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000369	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000824	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0000835	OMIM:614732	TAS	HP:0003577			P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0001263	OMIM:614732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0001511	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0002150	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0002656	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0002750	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0003072	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0003196	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0005280	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0008897	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0011220	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614732	#614732 INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIACONGENITA, AND GENITAL ANOMALIES;;IMAGE SYNDROME		HP:0100255	OMIM:614732	TAS				P		HPO:skoehler	
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0000007	OMIM:614736	TAS				I		HPO:skoehler	
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0000028	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0000127	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0000826	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0000851	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0001250	OMIM:614736	IEA				P		HPO:skoehler	
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0001325	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0001508	OMIM:614736	TAS				P		HPO:skoehler	
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0001943	OMIM:614736	TAS				P		HPO:skoehler	
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0002153	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614736	GLUCOCORTICOID DEFICIENCY 4 WITH OR WITHOUT MINERALOCORTICOID DEFICIENCY; GCCD4		HP:0002902	OMIM:614736	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0000007	OMIM:614739	TAS				I		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0000252	OMIM:614739	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0000407	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001249	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001250	OMIM:614739	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001257	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001263	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001272	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001290	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001298	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001332	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001344	OMIM:614739	IEA				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001508	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001943	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0001987	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0002071	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0002151	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0002376	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0002540	OMIM:614739	IEA				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0002719	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0003128	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0003256	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0003535	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0003828	OMIM:614739	IEA				C		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0011968	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0012444	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0025356	OMIM:614739	IEA				P		HPO:skoehler	
OMIM	614739	3-METHYLGLUTACONIC ACIDURIA WITH DEAFNESS, ENCEPHALOPATHY, AND LEIGH-LIKE SYNDROME; MEGDEL		HP:0040187	OMIM:614739	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0000007	OMIM:614741	TAS				I		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0000219	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0000253	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0000286	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0000343	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001250	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001263	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001290	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001298	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001583	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001943	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0001992	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0002098	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0002151	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0002240	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0003128	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0003542	OMIM:614741	TAS				P		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0003577	OMIM:614741	TAS				C		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0003828	OMIM:614741	TAS				C		HPO:skoehler	
OMIM	614741	MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY		HP:0009830	OMIM:614741	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0000006	OMIM:614742	TAS				I		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0001394	OMIM:614742	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0001909	OMIM:614742	TAS				P		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0001915	OMIM:614742	TAS				P		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0002206	OMIM:614742	TAS				P		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0002216	OMIM:614742	TAS				P		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0003581	OMIM:614742	TAS				C		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0003829	OMIM:614742	TAS				C		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0005528	OMIM:614742	TAS				P		HPO:skoehler	
OMIM	614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		HP:0012324	OMIM:614742	IEA				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0000006	OMIM:614743	TAS				I		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0001394	OMIM:614743	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0001909	OMIM:614743	TAS				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0001915	OMIM:614743	TAS				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0002206	OMIM:614743	TAS				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0002216	OMIM:614743	TAS				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0003581	OMIM:614743	TAS				C		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0003829	OMIM:614743	TAS				C		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0005528	OMIM:614743	TAS				P		HPO:skoehler	
OMIM	614743	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 2; PFBMFT2		HP:0012324	OMIM:614743	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000007	OMIM:614744	TAS				I		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000286	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000319	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000347	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000358	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000369	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000407	OMIM:614744	TAS				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000463	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000508	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000565	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0000750	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0001260	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0002015	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0002058	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0002714	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0003196	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0003577	OMIM:614744	IEA				C		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0003680	OMIM:614744	TAS				C		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0005280	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0010628	OMIM:614744	TAS				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0011800	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0011968	OMIM:614744	IEA				P		HPO:skoehler	
OMIM	614744	FACIAL PARESIS, HEREDITARY CONGENITAL, 3; HCFP3		HP:0025312	OMIM:614744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000007	OMIM:614748	TAS				I		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000083	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000092	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000093	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000097	PMID:22512483	PCS	HP:0003577	HP:0040284		P		HPO:probinson	3/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000100	PMID:22512483	PCS	HP:0003577	HP:0040284		P		HPO:probinson	3/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000160	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000252	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000311	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000316	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000400	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000535	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000653	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000771	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0000774	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0001030	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0001252	OMIM:614748	IEA				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0001806	OMIM:614748	IEA				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0002098	PMID:22512483	PCS	HP:0003577	HP:0040284		P		HPO:probinson	3/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0002205	PMID:22512483	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0002209	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0002213	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0002643	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0003073	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0005972	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0006530	PMID:22512483	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0008066	PMID:22512483	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0008404	PMID:22512483	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0010783	OMIM:614748	IEA				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0011220	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614748	INTERSTITIAL LUNG DISEASE, NEPHROTIC SYNDROME, AND EPIDERMOLYSIS BULLOSA, CONGENITAL; ILNEB		HP:0012213	OMIM:614748	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000007	OMIM:614749	TAS				I		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000076	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000175	OMIM:614749	IEA				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000252	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000316	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000431	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000455	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000582	OMIM:614749	IEA				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000637	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0000750	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0001249	OMIM:614749	IEA				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0001250	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0001290	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0001510	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0001631	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0002023	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0002025	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0002119	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0002251	OMIM:614749	IEA				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0003155	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0003196	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0003577	OMIM:614749	TAS				C		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0006118	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0010055	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0010804	OMIM:614749	TAS				P		HPO:skoehler	
OMIM	614749	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2; HPMRS2		HP:0011326	OMIM:614749	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0000006	OMIM:614750	TAS				I		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0000007	OMIM:614750	TAS				I		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0000508	OMIM:614750	TAS				P		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0001270	OMIM:614750	TAS				P		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0001290	OMIM:614750	TAS				P		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0002650	OMIM:614750	TAS				P		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0003677	OMIM:614750	TAS				C		HPO:skoehler	
OMIM	614750	MYASTHENIC SYNDROME, CONGENITAL, 13		HP:0003701	OMIM:614750	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0000006	OMIM:614751	TAS				I		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0001265	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0001284	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0001761	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0002460	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0003431	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614751	NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB		HP:0003693	OMIM:614751	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000006	OMIM:614753	TAS				I		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0000160	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000232	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000256	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0000275	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0000276	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0000303	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000348	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000483	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000486	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000494	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000540	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000639	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000739	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0000750	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0000767	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2	HP:0012837	HP:0000965	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0001249	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0001270	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0001290	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0001548	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0002119	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0002650	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0002673	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0005616	OMIM:614753	TAS				P		HPO:probinson	
OMIM	614753	SOTOS SYNDROME 2		HP:0006288	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614753	SOTOS SYNDROME 2		HP:0100807	OMIM:614753	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000006	OMIM:614756	TAS				I		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000160	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000179	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000276	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000307	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000316	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000337	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000343	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000369	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000411	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000414	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000463	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000486	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000494	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000718	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000750	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0000752	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001250	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001256	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001260	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001263	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR	HP:0012825	HP:0001310	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001319	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0001321	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002003	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002019	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002020	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002120	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002275	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0002317	OMIM:614756	TAS				P		HPO:skoehler	
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0100540	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0400005	OMIM:614756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614756	CEREBELLAR ATAXIA, NONPROGRESSIVE, WITH MENTAL RETARDATION; CANPMR		HP:0410170	OMIM:614756	IEA				P		HPO:skoehler	
OMIM	614779	#614779 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6		HP:0000007	OMIM:614779	TAS				I		HPO:skoehler	
OMIM	614779	#614779 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6		HP:0001651	OMIM:614779	TAS				P		HPO:skoehler	
OMIM	614779	#614779 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6		HP:0001669	OMIM:614779	TAS				P		HPO:skoehler	
OMIM	614779	#614779 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6		HP:0003363	OMIM:614779	TAS				P		HPO:skoehler	
OMIM	614779	#614779 HETEROTAXY, VISCERAL, 6, AUTOSOMAL; HTX6		HP:0003828	OMIM:614779	TAS				C		HPO:skoehler	
OMIM	614782	#614782 TREMOR, HEREDITARY ESSENTIAL, 4; ETM4		HP:0000006	OMIM:614782	TAS				I		HPO:skoehler	
OMIM	614782	#614782 TREMOR, HEREDITARY ESSENTIAL, 4; ETM4		HP:0002174	OMIM:614782	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000007	OMIM:614800	TAS				I		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000233	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000248	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000276	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000286	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000316	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000324	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000341	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000343	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000470	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000486	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000520	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000540	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000545	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000574	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000648	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000954	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0000973	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0001156	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0001159	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0001252	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0001852	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0002057	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0002213	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0002750	OMIM:614800	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0002983	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0004322	OMIM:614800	IEA				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH	HP:0003676	HP:0007663	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0008897	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0011516	OMIM:614800	IEA				P		HPO:skoehler	
OMIM	614800	SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY; SOPH		HP:0200068	OMIM:614800	TAS				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0000006	OMIM:614807	TAS				I		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0001290	OMIM:614807	TAS				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0001324	OMIM:614807	IEA				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0003326	OMIM:614807	TAS				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0003687	OMIM:614807	IEA				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4		HP:0012378	OMIM:614807	IEA				P		HPO:skoehler	
OMIM	614807	MYOPATHY, CENTRONUCLEAR, 4; CNM4	HP:0012825	HP:0100543	OMIM:614807	TAS				P		HPO:skoehler	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0000006	PMID:22801503	PCS				I		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0001257	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0001260	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0001324	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0002015	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0002380	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0003202	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614808	#614808 AMYOTROPHIC LATERAL SCLEROSIS 18; ALS18		HP:0007354	PMID:22801503	PCS				P		HPO:probinson	
OMIM	614809	#614809 CFHR5 DEFICIENCY		HP:0000006	OMIM:614809	TAS				I		HPO:skoehler	
OMIM	614809	#614809 CFHR5 DEFICIENCY		HP:0000099	OMIM:614809	TAS				P		HPO:skoehler	
OMIM	614809	#614809 CFHR5 DEFICIENCY		HP:0000790	OMIM:614809	TAS				P		HPO:skoehler	
OMIM	614809	#614809 CFHR5 DEFICIENCY		HP:0003676	OMIM:614809	TAS				C		HPO:skoehler	
OMIM	614809	#614809 CFHR5 DEFICIENCY		HP:0003774	OMIM:614809	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000007	OMIM:614813	TAS				I		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000060	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000164	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000252	OMIM:614813	TAS	HP:0003581			P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000256	OMIM:614813	TAS	HP:0011463			P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000276	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000303	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000307	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000316	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000325	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000448	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000490	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000798	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0000819	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001156	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001263	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001290	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001518	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001620	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0001792	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0002164	OMIM:614813	IEA				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0002376	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0002515	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0003187	OMIM:614813	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0003498	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0004590	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0008070	OMIM:614813	TAS	HP:0003581			P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0008551	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0008839	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0009882	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0010049	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0010579	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0010743	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0011220	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0030084	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0100864	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614813	SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS		HP:0200055	OMIM:614813	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0000006	OMIM:614814	TAS				I		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0000252	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0000581	OMIM:614814	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0001057	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0001263	OMIM:614814	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0004691	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0009882	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0010743	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0010760	OMIM:614814	TAS				P		HPO:skoehler	
OMIM	614814	ADAMS-OLIVER SYNDROME 3		HP:0012745	OMIM:614814	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0000007	OMIM:614815	TAS				I		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0000085	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0000496	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0001249	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0001388	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0001511	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0001629	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0002419	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18	HP:0012828	HP:0002751	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0010442	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614815	#614815 JOUBERT SYNDROME 18; JBTS18		HP:0012385	OMIM:614815	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000006	OMIM:614816	TAS				I		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000023	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000098	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000218	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000278	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000316	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000494	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000766	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0000978	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0001166	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0001634	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0001647	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0001762	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0001763	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0002097	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0002107	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0002616	OMIM:614816	IEA				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0002647	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0002650	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0003302	OMIM:614816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0005116	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0005692	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0100775	OMIM:614816	TAS				P		HPO:skoehler	
OMIM	614816	#614816 LOEYS-DIETZ SYNDROME, TYPE 4; LDS4;;ANEURYSM, AORTIC AND CEREBRAL, WITH ARTERIAL TORTUOSITY AND SKELETALMANIFESTATIONS		HP:0410151	PMID:23608731	PCS				P		HPO:lccarmody	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0000007	OMIM:614817	TAS				I		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0000090	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0000093	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0000790	OMIM:614817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0001970	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0002910	OMIM:614817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0003076	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0003138	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0003259	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0003676	OMIM:614817	TAS				C		HPO:skoehler	
OMIM	614817	INTERSTITIAL NEPHRITIS, KARYOMEGALIC		HP:0003774	OMIM:614817	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0000007	OMIM:614819	TAS				I		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0000545	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0000594	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0001083	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0001156	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0001387	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0001642	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0001650	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0004322	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0007906	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614819	WEILL-MARCHESANI SYNDROME 3		HP:0030961	OMIM:614819	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0000006	OMIM:614820	TAS				I		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0000639	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001249	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001251	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001260	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001263	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001266	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001268	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0001332	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0002133	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2	HP:0025303	HP:0002301	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614820	ALTERNATING HEMIPLEGIA OF CHILDHOOD 2		HP:0200072	OMIM:614820	TAS				P		HPO:skoehler	
OMIM	614822	#614822 SPERMATOGENIC FAILURE 10; SPGF10;;SPERMATOGENIC FAILURE WITH DEFECTIVE SPERM ANNULUS		HP:0000006	OMIM:614822	TAS				I		HPO:skoehler	
OMIM	614822	#614822 SPERMATOGENIC FAILURE 10; SPGF10;;SPERMATOGENIC FAILURE WITH DEFECTIVE SPERM ANNULUS		HP:0000789	OMIM:614822	TAS				P		HPO:skoehler	
OMIM	614822	#614822 SPERMATOGENIC FAILURE 10; SPGF10;;SPERMATOGENIC FAILURE WITH DEFECTIVE SPERM ANNULUS		HP:0012864	OMIM:614822	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614823	#614823 AORTIC VALVE DISEASE 2; AOVD2;;BICUSPID AORTIC VALVE;;AORTIC VALVE STENOSIS		HP:0000006	OMIM:614823	TAS				I		HPO:skoehler	
OMIM	614823	#614823 AORTIC VALVE DISEASE 2; AOVD2;;BICUSPID AORTIC VALVE;;AORTIC VALVE STENOSIS		HP:0001647	OMIM:614823	TAS				P		HPO:skoehler	
OMIM	614823	#614823 AORTIC VALVE DISEASE 2; AOVD2;;BICUSPID AORTIC VALVE;;AORTIC VALVE STENOSIS		HP:0001680	OMIM:614823	TAS				P		HPO:skoehler	
OMIM	614823	#614823 AORTIC VALVE DISEASE 2; AOVD2;;BICUSPID AORTIC VALVE;;AORTIC VALVE STENOSIS		HP:0004963	OMIM:614823	TAS				P		HPO:skoehler	
OMIM	614826	%614826 NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT; NYS7		HP:0000006	OMIM:614826	TAS				I		HPO:skoehler	
OMIM	614826	%614826 NYSTAGMUS 7, CONGENITAL, AUTOSOMAL DOMINANT; NYS7		HP:0007811	OMIM:614826	TAS	HP:0003577			P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0000007	OMIM:614830	TAS				I		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0000238	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0000568	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0001263	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0001290	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0001321	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0002119	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0003560	OMIM:614830	IEA				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0007260	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614830	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 8		HP:0007973	OMIM:614830	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0000007	OMIM:614831	TAS				I		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0000508	OMIM:614831	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0000565	OMIM:614831	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0000571	OMIM:614831	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0000666	OMIM:614831	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001249	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001250	OMIM:614831	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001260	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001263	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001272	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001290	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001310	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001337	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001347	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0001763	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0002075	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0002119	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0003593	OMIM:614831	TAS				C		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0003677	OMIM:614831	TAS				C		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0004322	OMIM:614831	TAS	HP:0003581			P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0006951	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0007068	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614831	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 13		HP:0007256	OMIM:614831	TAS				P		HPO:skoehler	
OMIM	614832	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4		HP:0000007	OMIM:614832	TAS				I		HPO:probinson	
OMIM	614832	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4		HP:0000705	OMIM:614832	TAS				P		HPO:probinson	
OMIM	614832	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4		HP:0006285	OMIM:614832	TAS				P		HPO:probinson	
OMIM	614832	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA4		HP:0006297	OMIM:614832	TAS				P		HPO:skoehler	
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0000007	PMID:26608784	PCS				I	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0000252	PMID:26608784	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	6/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0000750	PMID:22939636	PCS				P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001250	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	4/4
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001257	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	1/4
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001260	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	2/4
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001272	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	1/3
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001274	PMID:26608784	PCS	HP:0003577	HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	1/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001339	PMID:26608784	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	1/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0001371	PMID:26608784	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	2/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0002126	PMID:26608784,PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	1/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0002342	PMID:22939636	PCS				P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0002353	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	2/2
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0004322	PMID:26608784	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	6/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0004325	PMID:26608784	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	6/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0006989	PMID:26608784	PCS	HP:0003577	HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HP:probinson	1/6
OMIM	614833	Microcephaly, short stature, and polymicrogyria with seizures		HP:0007256	PMID:22939636	PCS		HP:0040284		P	MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH SEIZURES	HPO:skoehler	2/2
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000007	OMIM:614837	IEA				I		HPO:probinson	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000013	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000027	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000028	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000044	OMIM:614837	IEA				P		HPO:probinson	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000054	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000458	OMIM:614837	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000771	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000786	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0000938	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0002750	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0008213	OMIM:614837	IEA				P		HPO:skoehler	
OMIM	614837	HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA; HH8		HP:0008734	OMIM:614837	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000006	OMIM:614838	TAS				I		HPO:probinson	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000044	OMIM:614838	TAS				P		HPO:probinson	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000054	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000175	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000458	OMIM:614838	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000771	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0000939	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0008734	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0030084	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614838	HYPOGONADOTROPIC HYPOGONADISM 9 WITH OR WITHOUT ANOSMIA		HP:0410030	OMIM:614838	TAS				P		HPO:skoehler	
OMIM	614839	#614839 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA; HH10		HP:0000007	OMIM:614839	IEA				I		HPO:probinson	
OMIM	614839	#614839 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA; HH10		HP:0000044	OMIM:614839	IEA				P		HPO:probinson	
OMIM	614839	#614839 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA; HH10		HP:0000458	OMIM:614839	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614839	#614839 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA; HH10		HP:0000786	OMIM:614839	TAS				P		HPO:skoehler	
OMIM	614839	#614839 HYPOGONADOTROPIC HYPOGONADISM 10 WITH OR WITHOUT ANOSMIA; HH10		HP:0001256	OMIM:614839	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0000007	PMID:19079066	IEA				I		HPO:probinson	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0000028	OMIM:614840	TAS				P		HPO:skoehler	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0000044	PMID:19079066	IEA				P		HPO:probinson	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0000054	OMIM:614840	TAS				P		HPO:skoehler	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0000786	OMIM:614840	TAS				P		HPO:skoehler	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0008197	PMID:19079066	IEA				P		HPO:probinson	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0008734	OMIM:614840	TAS				P		HPO:skoehler	
OMIM	614840	#614840 HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA; HH11		HP:0030260	OMIM:614840	TAS				P		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000007	PMID:19535795	PCS				I		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000013	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000028	OMIM:614841	TAS				P		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000044	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000054	PMID:19535795	PCS				P		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000458	OMIM:614841	TAS		HP:0040282		P		HPO:probinson	HP:0040282
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000786	OMIM:614841	TAS				P		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0000823	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0002555	PMID:19535795	PCS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0008214	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0008724	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0008734	OMIM:614841	TAS				P		HPO:skoehler	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0030339	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614841	HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA		HP:0040171	OMIM:614841	TAS				P		HPO:probinson	
OMIM	614842	#614842 HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13		HP:0000007	OMIM:614842	IEA				I		HPO:probinson	
OMIM	614842	#614842 HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13		HP:0000013	OMIM:614842	TAS				P		HPO:skoehler	
OMIM	614842	#614842 HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13		HP:0000044	OMIM:614842	IEA				P		HPO:probinson	
OMIM	614842	#614842 HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13		HP:0000458	OMIM:614842	IEA		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	614842	#614842 HYPOGONADOTROPIC HYPOGONADISM 13 WITH OR WITHOUT ANOSMIA; HH13		HP:0002750	OMIM:614842	TAS				P		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0000006	OMIM:614844	TAS				I		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0000007	OMIM:614844	TAS				I		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0000090	OMIM:614844	TAS				P		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0000113	OMIM:614844	TAS				P		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0000546	OMIM:614844	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0001320	OMIM:614844	TAS				P		HPO:skoehler	
OMIM	614844	#614844 NEPHRONOPHTHISIS 14; NPHP14JOUBERT SYNDROME 19, INCLUDED; JBTS19, INCLUDED		HP:0001696	OMIM:614844	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0000007	OMIM:614845	TAS				I		HPO:skoehler	
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0000090	OMIM:614845	TAS				P		HPO:skoehler	
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0000546	OMIM:614845	TAS				P		HPO:skoehler	
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0000618	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0000639	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0001250	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0001263	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0001320	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0001399	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0001513	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614845	#614845 NEPHRONOPHTHISIS 15; NPHP15		HP:0010442	OMIM:614845	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614847	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12		HP:0000006	OMIM:614847	TAS				I		HPO:skoehler	
OMIM	614847	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12		HP:0001249	OMIM:614847	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614847	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12		HP:0002069	OMIM:614847	TAS				P		HPO:skoehler	
OMIM	614847	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12		HP:0003828	OMIM:614847	TAS				C		HPO:skoehler	
OMIM	614847	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12		HP:0003829	OMIM:614847	TAS				C		HPO:skoehler	
OMIM	614850	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6; IIAE6		HP:0000006	OMIM:614850	TAS				I		HPO:probinson	
OMIM	614850	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6; IIAE6		HP:0000007	OMIM:614850	TAS				I		HPO:probinson	
OMIM	614850	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6; IIAE6		HP:0003829	OMIM:614850	IEA				C		HPO:skoehler	
OMIM	614850	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 6; IIAE6		HP:0012302	OMIM:614850	TAS				P		HPO:probinson	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000007	OMIM:614851	TAS				I		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000013	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000252	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000448	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000601	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0000786	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0001191	OMIM:614851	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0001250	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0001385	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0001511	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0002750	OMIM:614851	TAS	HP:0011463			P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0003067	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0003510	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0004626	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0008551	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0010864	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0011344	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0011787	OMIM:614851	TAS				P		HPO:skoehler	
OMIM	614851	SECKEL SYNDROME 7; SCKL7		HP:0030084	OMIM:614851	IEA				P		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0000007	OMIM:614852	TAS				I		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0000252	OMIM:614852	TAS				P		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0000718	OMIM:614852	TAS				P		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0001335	OMIM:614852	TAS				P		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0009879	OMIM:614852	TAS				P		HPO:skoehler	
OMIM	614852	#614852 MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE; MCPH9		HP:0100710	OMIM:614852	TAS				P		HPO:skoehler	
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000007	OMIM:614856	TAS				I		HPO:skoehler	
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000233	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000325	OMIM:614856	TAS				P		HPO:skoehler	
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000337	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000343	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000411	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000527	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000592	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000637	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000768	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000926	OMIM:614856	TAS				P		HPO:skoehler	
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0000939	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0001166	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0001290	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0001382	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0001537	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0002194	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0002645	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0002751	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0003083	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0003202	OMIM:614856	TAS				P		HPO:skoehler	
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0004322	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0004325	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614856	OSTEOGENESIS IMPERFECTA, TYPE XIII		HP:0011001	OMIM:614856	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0000007	OMIM:614857	TAS				I		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0000023	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0000028	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0000316	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0000347	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001254	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001263	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001290	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001510	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001631	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001680	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001873	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001875	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0001903	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002020	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002059	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002092	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002156	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002160	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002533	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002789	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0002912	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0003145	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0003223	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0003524	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0003577	OMIM:614857	TAS				C		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0006610	OMIM:614857	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0011968	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614857	METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, CBLJ TYPE		HP:0012120	OMIM:614857	TAS				P		HPO:skoehler	
OMIM	614858	#614858 HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA; HH14		HP:0000006	OMIM:614858	TAS				I		HPO:skoehler	
OMIM	614858	#614858 HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA; HH14		HP:0000028	OMIM:614858	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614858	#614858 HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA; HH14		HP:0000458	OMIM:614858	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614858	#614858 HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA; HH14		HP:0000786	OMIM:614858	TAS				P		HPO:skoehler	
OMIM	614858	#614858 HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA; HH14		HP:0008734	OMIM:614858	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0000007	OMIM:614859	TAS				I		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0000113	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0000348	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0000369	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0000431	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0001250	OMIM:614859	TAS				P		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A	HP:0003676	HP:0001284	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A	HP:0003676	HP:0001290	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0002240	OMIM:614859	TAS				P		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0002617	OMIM:614859	IEA				P		HPO:skoehler	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0008872	OMIM:614859	TAS				P		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0008935	OMIM:614859	TAS				P		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0010655	OMIM:614859	TAS				P		HPO:probinson	
OMIM	614859	PEROXISOME BIOGENESIS DISORDER 3A (ZELLWEGER); PBD3A		HP:0012368	OMIM:614859	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0000006	OMIM:614860	TAS				I		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0000473	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0001272	OMIM:614860	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614860	DYSTONIA 23; DYT23		HP:0001288	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0001336	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0001618	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0002120	OMIM:614860	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614860	DYSTONIA 23; DYT23		HP:0002346	OMIM:614860	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614860	DYSTONIA 23; DYT23		HP:0002356	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0002451	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0002530	OMIM:614860	TAS				P		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0003581	OMIM:614860	TAS				C		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0003676	OMIM:614860	TAS				C		HPO:skoehler	
OMIM	614860	DYSTONIA 23; DYT23		HP:0011675	OMIM:614860	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614861	#614861 DEAFNESS, AUTOSOMAL RECESSIVE 98; DFNB98		HP:0000007	OMIM:614861	TAS				I		HPO:skoehler	
OMIM	614861	#614861 DEAFNESS, AUTOSOMAL RECESSIVE 98; DFNB98	HP:0012829	HP:0000407	OMIM:614861	TAS				P		HPO:skoehler	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0000007	OMIM:614862	TAS				I		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0000107	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0000316	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0000537	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0000582	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0001250	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)	HP:0012829	HP:0001290	OMIM:614862	TAS				P		HPO:skoehler	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0001522	OMIM:614862	TAS				M		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0002240	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0002878	OMIM:614862	TAS				P		HPO:skoehler	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0005280	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0008872	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0008935	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614862	PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER)		HP:0010655	OMIM:614862	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000006	OMIM:614863	IEA				I		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000007	OMIM:614863	TAS				I		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000070	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000256	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000316	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000407	OMIM:614863	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000505	OMIM:614863	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000510	OMIM:614863	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000639	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000648	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000762	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0000954	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001249	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001250	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001251	PMID:21937992	PCS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001263	OMIM:614863	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001288	OMIM:614863	IEA				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001290	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001319	OMIM:614863	TAS				P		HPO:probinson	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0001410	OMIM:614863	IEA				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0002240	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614863	PEROXISOME BIOGENESIS DISORDER 4B; PBD4B		HP:0003196	OMIM:614863	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000007	OMIM:614866	TAS				I		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000028	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000175	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000239	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000286	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000311	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000316	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000347	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000348	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000369	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000518	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000580	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000952	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0000954	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001088	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001093	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001249	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001250	OMIM:614866	TAS				P		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001263	OMIM:614866	TAS				P		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001284	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001290	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001401	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001433	OMIM:614866	TAS				P		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001508	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001511	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001627	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001744	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001762	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0001840	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0002033	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0002126	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0002240	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0002764	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0002967	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0004734	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0007227	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0007759	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0008665	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0008935	OMIM:614866	TAS				P		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0010655	OMIM:614866	TAS				P		HPO:probinson	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0011039	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0012368	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0012385	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614866	PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER)		HP:0100540	OMIM:614866	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000007	OMIM:614867	TAS				I		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000407	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000505	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000510	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000514	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000639	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0000657	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001260	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001263	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001265	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001272	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001290	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001310	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001319	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001337	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001410	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0001761	OMIM:614867	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0002317	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0003677	OMIM:614867	TAS				C		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0003828	OMIM:614867	TAS				C		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0008167	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0009046	OMIM:614867	TAS				P		HPO:skoehler	
OMIM	614867	PEROXISOME BIOGENESIS DISORDER 5B		HP:0010571	OMIM:614867	TAS				P		HPO:probinson	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0000007	OMIM:614868	TAS				I		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0001631	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0001875	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0001888	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0002718	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0002721	OMIM:614868	IEA				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0002841	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0004429	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614868	#614868 T-CELL IMMUNODEFICIENCY, RECURRENT INFECTIONS, AND AUTOIMMUNITY WITHOR WITHOUT CARDIAC MALFORMATIONS; TIIAC;;STK4 DEFICIENCY;;MST1 DEFICIENCY		HP:0200043	OMIM:614868	TAS				P		HPO:skoehler	
OMIM	614869	#614869 USHER SYNDROME, TYPE IJ; USH1J		HP:0000007	OMIM:614869	TAS				I		HPO:skoehler	
OMIM	614869	#614869 USHER SYNDROME, TYPE IJ; USH1J		HP:0000510	OMIM:614869	TAS				P		HPO:skoehler	
OMIM	614869	#614869 USHER SYNDROME, TYPE IJ; USH1J		HP:0001270	OMIM:614869	TAS				P		HPO:skoehler	
OMIM	614869	#614869 USHER SYNDROME, TYPE IJ; USH1J		HP:0001751	OMIM:614869	TAS				P		HPO:skoehler	
OMIM	614869	#614869 USHER SYNDROME, TYPE IJ; USH1J		HP:0003577	OMIM:614869	TAS				C		HPO:skoehler	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0000007	OMIM:614870	TAS				I		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0000369	OMIM:614870	IEA				P		HPO:skoehler	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0001250	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0001290	OMIM:614870	IEA				P		HPO:skoehler	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0001302	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0001410	OMIM:614870	IEA				P		HPO:skoehler	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0002240	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0003678	OMIM:614870	IEA				C		HPO:skoehler	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0008872	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0008935	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0010655	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0011344	OMIM:614870	TAS				P		HPO:probinson	
OMIM	614870	PEROXISOME BIOGENESIS DISORDER 6A (ZELLWEGER); PBD6A		HP:0030048	OMIM:614870	IEA				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000007	OMIM:614871	TAS				I		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000407	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000505	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000556	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000639	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0000641	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001251	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001260	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001263	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001265	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001272	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001290	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001319	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001410	OMIM:614871	TAS				P		HPO:probinson	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0001761	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0002080	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0002500	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0002936	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0003677	OMIM:614871	TAS				C		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0003693	OMIM:614871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0003828	OMIM:614871	TAS				C		HPO:skoehler	
OMIM	614871	PEROXISOME BIOGENESIS DISORDER 6B		HP:0007772	OMIM:614871	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000007	OMIM:614872	TAS				I		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000218	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000343	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000348	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000358	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000369	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000518	OMIM:614872	IEA				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000639	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0000952	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0001250	OMIM:614872	TAS				P		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0001522	OMIM:614872	TAS				M		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0001762	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0002240	OMIM:614872	TAS				P		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0005469	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0006829	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0008935	OMIM:614872	TAS				P		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0010655	OMIM:614872	TAS				P		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0011968	OMIM:614872	TAS				P		HPO:probinson	
OMIM	614872	PEROXISOME BIOGENESIS DISORDER 7A (ZELLWEGER); PBD7A		HP:0012368	OMIM:614872	TAS				P		HPO:skoehler	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0000007	OMIM:614873	TAS				I		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0000407	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0000505	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0000556	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0001263	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0001319	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614873	#614873 PEROXISOME BIOGENESIS DISORDER 7B; PBD7B		HP:0001410	OMIM:614873	TAS				P		HPO:probinson	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:614874	TAS				I		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0000403	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:614874	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0003251	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0003593	OMIM:614874	TAS				C		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0004469	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0011108	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0012208	OMIM:614874	TAS				P		HPO:probinson	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0012256	OMIM:614874	TAS				P		HPO:probinson	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0012262	OMIM:614874	TAS				P		HPO:probinson	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0012265	OMIM:614874	IEA				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS	HP:0031796	HP:0012384	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614874	#614874 CILIARY DYSKINESIA, PRIMARY, 18; CILD18;;CILIARY DYSKINESIA, PRIMARY, 18, WITH OR WITHOUT SITUS INVERSUS		HP:0200073	OMIM:614874	TAS				P		HPO:skoehler	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0000007	OMIM:614876	TAS				I		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0000162	OMIM:614876	TAS				P		HPO:skoehler	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0000518	OMIM:614876	TAS				P		HPO:skoehler	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0000952	OMIM:614876	TAS				P		HPO:skoehler	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0001250	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0001290	OMIM:614876	TAS				P		HPO:skoehler	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0001522	OMIM:614876	TAS				M		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0001629	PMID:9837814	PCS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0002240	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0008872	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0008935	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0010655	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0011344	OMIM:614876	TAS				P		HPO:probinson	
OMIM	614876	PEROXISOME BIOGENESIS DISORDER 8A (ZELLWEGER); PBD8A		HP:0031956	OMIM:614876	IEA				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000007	OMIM:614877	TAS				I		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000407	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000505	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000518	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000556	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000639	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0000648	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001260	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001263	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001310	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001319	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001410	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0001508	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0002015	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0002019	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0002313	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0002415	OMIM:614877	IEA				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0003676	OMIM:614877	TAS				C		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0006855	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0007371	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0008167	OMIM:614877	TAS				P		HPO:probinson	
OMIM	614877	PEROXISOME BIOGENESIS DISORDER 8B; PBD8B		HP:0100543	OMIM:614877	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0000006	OMIM:614878	TAS				I		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0000518	OMIM:614878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0002720	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0002829	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0002850	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0002958	OMIM:614878	IEA				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0003593	OMIM:614878	TAS				C		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0006515	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0010783	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0011950	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0100279	OMIM:614878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0100658	OMIM:614878	TAS				P		HPO:skoehler	
OMIM	614878	#614878 AUTOINFLAMMATION, ANTIBODY DEFICIENCY, AND IMMUNE DYSREGULATION, PLCG2-ASSOCIATED;APLAID		HP:0200020	OMIM:614878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0000007	OMIM:614879	TAS				I		HPO:probinson	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0000407	OMIM:614879	TAS				P		HPO:probinson	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0000510	OMIM:614879	TAS				P		HPO:probinson	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0000518	OMIM:614879	TAS	HP:0003577			P		HPO:probinson	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0001249	OMIM:614879	TAS				P		HPO:probinson	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0001761	OMIM:614879	IEA				P		HPO:skoehler	
OMIM	614879	PEROXISOME BIOGENESIS DISORDER 9B; PBD9B		HP:0010571	OMIM:614879	TAS				P		HPO:probinson	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0000006	OMIM:614880	TAS				I		HPO:skoehler	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0000028	OMIM:614880	TAS				P		HPO:skoehler	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0000054	OMIM:614880	TAS				P		HPO:skoehler	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0000175	OMIM:614880	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0000786	OMIM:614880	TAS				P		HPO:skoehler	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0002857	OMIM:614880	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0008734	OMIM:614880	TAS				P		HPO:skoehler	
OMIM	614880	HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA		HP:0012506	OMIM:614880	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0000007	OMIM:614881	TAS				I		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0001284	OMIM:614881	TAS				P		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0001288	OMIM:614881	TAS				P		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0001618	OMIM:614881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0001761	OMIM:614881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0002936	OMIM:614881	TAS				P		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0003202	OMIM:614881	TAS				P		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0003677	OMIM:614881	TAS				C		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0007269	OMIM:614881	IEA				P		HPO:skoehler	
OMIM	614881	SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5		HP:0009027	OMIM:614881	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000007	OMIM:614882	TAS				I		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000218	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000286	PMID:10958759	PCS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000316	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000337	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000347	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000348	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000448	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000494	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0000518	OMIM:614882	IEA				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0001250	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0001284	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0001290	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0001522	OMIM:614882	TAS				M		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0001558	OMIM:614882	TAS				P		HPO:skoehler	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0002240	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0008935	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0010655	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0011344	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614882	PEROXISOME BIOGENESIS DISORDER 10A (ZELLWEGER); PBD10A		HP:0011968	OMIM:614882	TAS				P		HPO:probinson	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000007	OMIM:614883	TAS				I		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000107	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000239	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000260	OMIM:614883	TAS				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000325	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000348	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0000463	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0001250	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0001263	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0001339	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0001410	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0001508	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0002104	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0002126	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0002910	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0003429	PMID:9194444	PCS				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0005280	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0005562	OMIM:614883	TAS				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0006829	OMIM:614883	TAS				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0008947	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614883	PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER)		HP:0100729	OMIM:614883	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0000007	OMIM:614885	TAS				I		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0000364	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0000365	OMIM:614885	TAS				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0000518	OMIM:614885	TAS				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0000572	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B	HP:0003676	HP:0001290	OMIM:614885	TAS				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0001324	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0003323	OMIM:614885	TAS				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0011398	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0011947	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614885	PEROXISOME BIOGENESIS DISORDER 11B		HP:0011968	OMIM:614885	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000007	OMIM:614886	TAS				I		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000124	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000238	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000252	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000260	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000267	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000286	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000325	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000431	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000448	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0000629	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001081	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001250	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001263	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001290	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001399	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001476	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001510	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001558	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001631	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001643	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0001719	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0002059	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0002904	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0002910	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0003103	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0003455	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0004322	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0004325	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0007305	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0009553	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0010461	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0011398	OMIM:614886	IEA				P		HPO:skoehler	
OMIM	614886	PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER)		HP:0030799	OMIM:614886	TAS				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000007	OMIM:614887	IEA				I		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000239	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000268	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000325	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000347	OMIM:614887	TAS				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000348	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000422	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000478	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0000952	OMIM:614887	TAS				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0001250	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0001290	OMIM:614887	TAS				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0001476	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0002240	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0002269	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0005469	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0011398	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614887	PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER)		HP:0011968	OMIM:614887	IEA				P		HPO:skoehler	
OMIM	614889	IMMUNODEFICIENCY 28; IMD28		HP:0000007	OMIM:614889	TAS				I		HPO:probinson	
OMIM	614889	IMMUNODEFICIENCY 28; IMD28		HP:0002721	OMIM:614889	IEA				P		HPO:skoehler	
OMIM	614889	IMMUNODEFICIENCY 28; IMD28		HP:0011274	OMIM:614889	TAS				P		HPO:probinson	
OMIM	614890	IMMUNODEFICIENCY 29		HP:0000007	OMIM:614890	TAS				I		HPO:skoehler	
OMIM	614890	IMMUNODEFICIENCY 29		HP:0002721	OMIM:614890	IEA				P		HPO:skoehler	
OMIM	614891	IMMUNODEFICIENCY 30; IMD30		HP:0000007	OMIM:614891	TAS				I		HPO:probinson	
OMIM	614891	IMMUNODEFICIENCY 30; IMD30		HP:0002721	OMIM:614891	TAS				P		HPO:probinson	
OMIM	614891	IMMUNODEFICIENCY 30; IMD30		HP:0011274	OMIM:614891	TAS				P		HPO:probinson	
OMIM	614892	IMMUNODEFICIENCY 31A; IMD31A		HP:0000006	OMIM:614892	IEA				I		HPO:skoehler	
OMIM	614892	IMMUNODEFICIENCY 31A; IMD31A		HP:0002721	OMIM:614892	IEA				P		HPO:skoehler	
OMIM	614892	IMMUNODEFICIENCY 31A; IMD31A		HP:0003829	OMIM:614892	TAS				C		HPO:skoehler	
OMIM	614892	IMMUNODEFICIENCY 31A; IMD31A		HP:0012302	OMIM:614892	IEA				P		HPO:skoehler	
OMIM	614893	IMMUNODEFICIENCY 32A		HP:0000006	PMID:21524210	PCS				I		HPO:probinson	
OMIM	614893	IMMUNODEFICIENCY 32A		HP:0002716	PMID:21524210	PCS				P		HPO:probinson	
OMIM	614893	IMMUNODEFICIENCY 32A		HP:0002719	PMID:21524210	PCS				P		HPO:probinson	
OMIM	614893	IMMUNODEFICIENCY 32A		HP:0002721	PMID:21524210	PCS				P		HPO:probinson	
OMIM	614894	MONOCYTE AND DENDRITIC CELL DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:614894	TAS				I		HPO:skoehler	
OMIM	614894	MONOCYTE AND DENDRITIC CELL DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0001508	OMIM:614894	TAS				P		HPO:skoehler	
OMIM	614894	MONOCYTE AND DENDRITIC CELL DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0002719	OMIM:614894	TAS				P		HPO:skoehler	
OMIM	614894	MONOCYTE AND DENDRITIC CELL DEFICIENCY, AUTOSOMAL RECESSIVE		HP:0003593	OMIM:614894	TAS				C		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0000007	OMIM:614895	TAS				I		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0001270	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0001284	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0001604	OMIM:614895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0001761	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0002355	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0002650	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0002936	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003202	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003387	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003400	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003431	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003677	OMIM:614895	TAS				C		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0003690	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0010871	OMIM:614895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614895	#614895 CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 4F; CMT4F		HP:0011096	OMIM:614895	TAS				P		HPO:skoehler	
OMIM	614896	#614896 SINOATRIAL NODE DYSFUNCTION AND DEAFNESS; SANDD		HP:0000007	OMIM:614896	TAS				I		HPO:skoehler	
OMIM	614896	#614896 SINOATRIAL NODE DYSFUNCTION AND DEAFNESS; SANDD		HP:0000365	OMIM:614896	IEA				P		HPO:skoehler	
OMIM	614896	#614896 SINOATRIAL NODE DYSFUNCTION AND DEAFNESS; SANDD		HP:0001662	OMIM:614896	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000006	OMIM:614897	TAS				I		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000027	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000028	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000054	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000458	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0000786	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614897	#614897 HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA; HH16		HP:0008734	OMIM:614897	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:614898	TAS				I		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0000750	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0000768	OMIM:614898	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0000998	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:614898	IEA				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0001276	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0001288	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0001332	OMIM:614898	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0002169	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0002808	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614898	SPASTIC PARAPLEGIA 53, AUTOSOMAL RECESSIVE		HP:0100543	OMIM:614898	TAS				P		HPO:skoehler	
OMIM	614899	#614899 DEAFNESS, AUTOSOMAL RECESSIVE 93; DFNB93		HP:0000007	OMIM:614899	TAS				I		HPO:skoehler	
OMIM	614899	#614899 DEAFNESS, AUTOSOMAL RECESSIVE 93; DFNB93		HP:0000365	OMIM:614899	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000006	OMIM:614900	TAS				I		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000104	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000175	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000402	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000413	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0000492	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0001647	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0001875	OMIM:614900	TAS				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0001903	OMIM:614900	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0002974	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0002984	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0003022	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0004322	OMIM:614900	TAS				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0005528	OMIM:614900	TAS				P		HPO:probinson	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0006368	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0009777	OMIM:614900	IEA				P		HPO:skoehler	
OMIM	614900	DIAMOND-BLACKFAN ANEMIA 11; DBA11		HP:0010972	OMIM:614900	TAS				P		HPO:probinson	
OMIM	614915	LETHAL CONGENITAL CONTRACTURE SYNDROME 4		HP:0000007	OMIM:614915	TAS				I		HPO:skoehler	
OMIM	614915	LETHAL CONGENITAL CONTRACTURE SYNDROME 4		HP:0003202	OMIM:614915	TAS				P		HPO:skoehler	
OMIM	614915	LETHAL CONGENITAL CONTRACTURE SYNDROME 4		HP:0005684	OMIM:614915	IEA				P		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0000006	OMIM:614916	TAS				I		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0001279	OMIM:614916	TAS				P		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0001695	OMIM:614916	TAS				P		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0001699	OMIM:614916	TAS				M		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0002321	OMIM:614916	TAS				P		HPO:skoehler	
OMIM	614916	#614916 VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4		HP:0004756	OMIM:614916	IEA				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000007	PMID:22581968	PCS				I		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000020	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000034	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000519	PMID:22581968	PCS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000639	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0000958	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0001256	PMID:22581968	PCS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0001271	PMID:22581968	PCS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0001284	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0001324	OMIM:614920	TAS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0001730	PMID:22581968	PCS				P		HPO:skoehler	
OMIM	614920	PEROXISOME BIOGENESIS DISORDER 14B		HP:0002076	PMID:22581968	PCS				P		HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000007	OMIM:614921	TAS				I	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000175	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000193	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000201	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000347	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0000823	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0001324	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0001397	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0001644	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0001649	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HP:0025303	HP:0001943	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0001976	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0002094	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0002910	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0003201	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0003236	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0003546	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0003642	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0004322	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0005305	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HP:0011010	HP:0012115	OMIM:614921	TAS				P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	
OMIM	614921	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE It; CDG1T;;CDG It; CDGIt;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV		HP:0012378	OMIM:614921	TAS		HP:0040283		P	#614921 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IT; CDG1T;;CDG IT; CDGIT;;PHOSPHOGLUCOMUTASE 1 DEFICIENCY;;PGM1 DEFICIENCY;;GLYCOGEN STORAGE DISEASE XIV; GSD14;;GSD XIV	HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000007	OMIM:614922	TAS				I		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000083	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000089	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000107	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000110	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0000365	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001250	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001254	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001263	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001265	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001284	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001290	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001302	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001308	OMIM:614922	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001336	OMIM:614922	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001344	OMIM:614922	IEA				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001397	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001410	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001522	OMIM:614922	TAS				M		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001638	OMIM:614922	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0001947	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0002079	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0002120	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0002151	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0002240	OMIM:614922	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0002490	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0003128	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0003198	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0003429	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0003577	OMIM:614922	TAS				C		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0003828	OMIM:614922	TAS				C		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0006829	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0009830	OMIM:614922	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0011968	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614922	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11		HP:0012448	OMIM:614922	TAS				P		HPO:skoehler	
OMIM	614923	#614923 BRANCHED-CHAIN KETOACID DEHYDROGENASE KINASE DEFICIENCY; BCKDKD;;BCKDK DEFICIENCY		HP:0000717	OMIM:614923	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614923	#614923 BRANCHED-CHAIN KETOACID DEHYDROGENASE KINASE DEFICIENCY; BCKDKD;;BCKDK DEFICIENCY		HP:0001249	OMIM:614923	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614923	#614923 BRANCHED-CHAIN KETOACID DEHYDROGENASE KINASE DEFICIENCY; BCKDKD;;BCKDK DEFICIENCY		HP:0001250	OMIM:614923	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614923	#614923 BRANCHED-CHAIN KETOACID DEHYDROGENASE KINASE DEFICIENCY; BCKDKD;;BCKDK DEFICIENCY		HP:0010892	OMIM:614923	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0000007	OMIM:614924	TAS				I		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0000175	OMIM:614924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0000505	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0000508	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0000602	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001250	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001263	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001285	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001319	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001332	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001344	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001396	OMIM:614924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001403	OMIM:614924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0001508	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002067	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002079	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002151	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002240	OMIM:614924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002352	OMIM:614924	IEA				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0002376	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0003128	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0003200	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0003593	OMIM:614924	TAS				C		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0006989	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0008347	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0011923	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614924	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 12; COXPD12		HP:0011924	OMIM:614924	TAS				P		HPO:skoehler	
OMIM	614926	#614926 PERRAULT SYNDROME 2; PRLTS2		HP:0000007	OMIM:614926	TAS				I		HPO:skoehler	
OMIM	614926	#614926 PERRAULT SYNDROME 2; PRLTS2		HP:0000407	OMIM:614926	TAS				P		HPO:skoehler	
OMIM	614927	%614927 ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE; ECTD5		HP:0000007	OMIM:614927	TAS				I		HPO:skoehler	
OMIM	614927	%614927 ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE; ECTD5		HP:0001802	OMIM:614927	TAS				P		HPO:skoehler	
OMIM	614927	%614927 ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE; ECTD5		HP:0002209	OMIM:614927	TAS				P		HPO:skoehler	
OMIM	614927	%614927 ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE; ECTD5		HP:0007436	OMIM:614927	IEA				P		HPO:skoehler	
OMIM	614927	%614927 ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE; ECTD5		HP:0008391	OMIM:614927	TAS				P		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0000007	OMIM:614928	TAS				I		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0001596	OMIM:614928	IEA				P		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0001810	OMIM:614928	TAS				P		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0007436	OMIM:614928	IEA				P		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0008070	OMIM:614928	IEA				P		HPO:skoehler	
OMIM	614928	ECTODERMAL DYSPLASIA 6, HAIR/NAIL TYPE; ECTD6		HP:0012746	OMIM:614928	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0000007	OMIM:614929	TAS				I		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0000535	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0000653	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0001006	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0001596	OMIM:614929	IEA				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0001806	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0001810	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0002299	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0007436	OMIM:614929	IEA				P		HPO:skoehler	
OMIM	614929	ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE; ECTD7		HP:0008391	OMIM:614929	TAS				P		HPO:skoehler	
OMIM	614931	#614931 ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE; ECTD9		HP:0000007	OMIM:614931	TAS				I		HPO:skoehler	
OMIM	614931	#614931 ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE; ECTD9		HP:0000968	OMIM:614931	IEA				P		HPO:skoehler	
OMIM	614931	#614931 ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE; ECTD9		HP:0001006	OMIM:614931	TAS				P		HPO:skoehler	
OMIM	614931	#614931 ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE; ECTD9		HP:0001598	OMIM:614931	TAS				P		HPO:skoehler	
OMIM	614931	#614931 ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE; ECTD9		HP:0008404	OMIM:614931	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0000007	OMIM:614932	TAS				I		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0000518	OMIM:614932	IEA				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0000639	OMIM:614932	IEA				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0000762	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0001265	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0001266	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0001332	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0001344	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0001510	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0002415	OMIM:614932	IEA				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0003202	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0006829	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614932	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 13; COXPD13		HP:0100660	OMIM:614932	TAS				P		HPO:skoehler	
OMIM	614934	#614934 DEAFNESS, AUTOSOMAL RECESSIVE 70; DFNB70		HP:0000007	OMIM:614934	TAS				I		HPO:skoehler	
OMIM	614934	#614934 DEAFNESS, AUTOSOMAL RECESSIVE 70; DFNB70	HP:0012832	HP:0000365	OMIM:614934	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0000007	OMIM:614935	TAS				I		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0000403	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0000789	OMIM:614935	IEA				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0001696	OMIM:614935	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0002110	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0004469	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0011108	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0012207	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0012259	OMIM:614935	TAS				P		HPO:probinson	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0012263	OMIM:614935	TAS				P		HPO:probinson	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0012265	OMIM:614935	IEA				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19	HP:0031796	HP:0012384	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0100582	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614935	CILIARY DYSKINESIA, PRIMARY, 19; CILD19		HP:0200073	OMIM:614935	TAS				P		HPO:skoehler	
OMIM	614936	%614936 KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE IB; PPKP1B		HP:0000006	OMIM:614936	TAS				I		HPO:skoehler	
OMIM	614936	%614936 KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE IB; PPKP1B		HP:0000962	OMIM:614936	TAS				P		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0000006	OMIM:614937	TAS				I		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0001251	OMIM:614937	TAS				P		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0001336	OMIM:614937	TAS				P		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0002359	OMIM:614937	IEA				P		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0002527	OMIM:614937	TAS				P		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0003581	OMIM:614937	TAS				C		HPO:skoehler	
OMIM	614937	MYOCLONUS, FAMILIAL CORTICAL; FCM		HP:0003677	OMIM:614937	TAS				C		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000006	OMIM:614940	IEA				I		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000232	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000290	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000668	OMIM:614940	TAS				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000958	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0000970	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0002561	OMIM:614940	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0006483	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0007607	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614940	ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT		HP:0008070	OMIM:614940	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000007	OMIM:614941	TAS				I		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000217	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000232	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000290	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000607	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000653	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000668	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000698	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000958	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000968	OMIM:614941	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0000970	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0002205	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0002209	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0002557	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0002561	OMIM:614941	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0005280	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0005338	OMIM:614941	TAS				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0006483	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0008070	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614941	ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD11B		HP:0012384	OMIM:614941	IEA				P		HPO:skoehler	
OMIM	614944	#614944 DEAFNESS, AUTOSOMAL RECESSIVE 84B; DFNB84B		HP:0000007	OMIM:614944	TAS				I		HPO:skoehler	
OMIM	614944	#614944 DEAFNESS, AUTOSOMAL RECESSIVE 84B; DFNB84B		HP:0000365	OMIM:614944	IEA				P		HPO:skoehler	
OMIM	614944	#614944 DEAFNESS, AUTOSOMAL RECESSIVE 84B; DFNB84B		HP:0001756	OMIM:614944	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614945	DEAFNESS, AUTOSOMAL RECESSIVE 18B; DFNB18B		HP:0000007	OMIM:614945	TAS				I		HPO:skoehler	
OMIM	614945	DEAFNESS, AUTOSOMAL RECESSIVE 18B; DFNB18B		HP:0000365	OMIM:614945	TAS				P		HPO:skoehler	
OMIM	614945	DEAFNESS, AUTOSOMAL RECESSIVE 18B; DFNB18B		HP:0001265	OMIM:614945	IEA				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0000007	OMIM:614946	TAS				I		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0000252	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0000365	OMIM:614946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0000505	OMIM:614946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001250	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14	HP:0012829	HP:0001263	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001272	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001290	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001336	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001510	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001522	OMIM:614946	TAS				M		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001873	OMIM:614946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0001903	OMIM:614946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002059	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002119	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002151	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002171	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002353	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0002506	OMIM:614946	IEA				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0003128	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0003355	OMIM:614946	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0003828	OMIM:614946	TAS				C		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0007366	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614946	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 14; COXPD14		HP:0011968	OMIM:614946	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000007	OMIM:614947	TAS				I		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000252	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000486	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000639	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000648	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0000750	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001250	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001251	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15	HP:0012825	HP:0001263	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001290	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001337	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001513	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001629	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0001716	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0002151	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0002311	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0002317	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0002490	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0002500	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0004322	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0005144	OMIM:614947	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0007256	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15		HP:0007663	OMIM:614947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614947	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 15; COXPD15	HP:0012825	HP:0100543	OMIM:614947	TAS				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0000006	OMIM:614954	TAS				I		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0001631	OMIM:614954	IEA				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0001636	OMIM:614954	TAS				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0001649	OMIM:614954	IEA				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0001678	OMIM:614954	IEA				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0005110	OMIM:614954	TAS				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0005301	OMIM:614954	TAS				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0011709	OMIM:614954	IEA				P		HPO:skoehler	
OMIM	614954	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 3; CHTD3		HP:0011712	OMIM:614954	IEA				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0000006	OMIM:614959	TAS				I		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0000252	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0000817	OMIM:614959	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0001257	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0001290	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002079	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002120	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002133	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002169	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002171	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002376	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002445	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0002529	OMIM:614959	TAS				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0003676	OMIM:614959	TAS				C		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0012448	OMIM:614959	IEA				P		HPO:skoehler	
OMIM	614959	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 14; EIEE14		HP:0200134	OMIM:614959	IEA				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000007	OMIM:614961	TAS				I		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000483	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000540	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000545	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000565	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000639	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0000998	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001249	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001257	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001263	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001290	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001321	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001344	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001347	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001761	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0001762	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002015	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002020	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002072	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002079	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002365	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002465	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0002804	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0003577	OMIM:614961	TAS				C		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0004684	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0005484	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0008936	OMIM:614961	TAS				P		HPO:skoehler	
OMIM	614961	PONTOCEREBELLAR HYPOPLASIA, TYPE 8		HP:0100704	OMIM:614961	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0000007	OMIM:614962	TAS				I		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0000054	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0000135	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0000771	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0000786	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0001513	OMIM:614962	IEA	HP:0011463	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0002591	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0002788	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0003292	OMIM:614962	IEA				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0006532	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0008734	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0100738	OMIM:614962	IEA				P		HPO:skoehler	
OMIM	614962	LEPTIN DEFICIENCY OR DYSFUNCTION		HP:0410018	OMIM:614962	TAS				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0000718	OMIM:614963	IEA	HP:0003593	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0000815	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0000823	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0000824	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0001513	OMIM:614963	IEA	HP:0003593	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0002591	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0002958	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0008245	OMIM:614963	IEA				P		HPO:skoehler	
OMIM	614963	#614963 LEPTIN RECEPTOR DEFICIENCY;;OBESITY, MORBID, NONSYNDROMIC 2		HP:0012286	OMIM:614963	IEA	HP:0003593	HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000007	OMIM:614969	TAS				I		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000054	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000062	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000215	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000253	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000286	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000347	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000400	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000431	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000639	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000648	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0000657	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001250	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001258	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7	HP:0012828	HP:0001263	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001290	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001321	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001336	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001344	OMIM:614969	IEA				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0001347	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0002059	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0002079	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0002104	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0003577	OMIM:614969	TAS				C		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0003745	OMIM:614969	TAS				I		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0005280	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614969	PONTOCEREBELLAR HYPOPLASIA, TYPE 7; PCH7		HP:0012110	OMIM:614969	TAS				P		HPO:skoehler	
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000007	OMIM:614970	IEA		HP:0040282		I		HPO:skoehler	HP:0040282
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000107	OMIM:614970	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000479	OMIM:614970	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000488	OMIM:614970	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000657	OMIM:614970	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000718	OMIM:614970	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0000742	OMIM:614970	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0001159	OMIM:614970	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0001263	OMIM:614970	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0001344	OMIM:614970	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0002093	OMIM:614970	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0002419	OMIM:614970	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0003577	OMIM:614970	TAS				C		HPO:skoehler	
OMIM	614970	#614970 JOUBERT SYNDROME 20; JBTS20		HP:0100259	OMIM:614970	IEA		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0000006	OMIM:614972	TAS				I		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0000007	OMIM:614972	TAS		HP:0040283		I		HPO:skoehler	HP:0040283
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0000952	OMIM:614972	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0000989	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0001406	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0001622	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0025116	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0200148	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614972	CHOLESTASIS, INTRAHEPATIC, OF PREGNANCY 3		HP:0200150	OMIM:614972	TAS				P		HPO:skoehler	
OMIM	614974	#614974 FOCAL FACIAL DERMAL DYSPLASIA 4; FFDD4		HP:0000007	OMIM:614974	TAS				I		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000007	OMIM:614976	TAS				I		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000028	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000049	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000054	PMID:23063620	PCS		HP:0040284		P		HPO:skoehler	1/4
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000189	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000218	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000243	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000248	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000263	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000278	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000286	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000316	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000369	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000407	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000411	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000431	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000463	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000465	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000470	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000535	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000582	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000767	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000768	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0000973	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001156	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001263	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001363	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001513	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001537	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001631	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001643	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001651	PMID:23063620	PCS	HP:0003577	HP:0040284		P		HPO:skoehler	2/5
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001669	PMID:23063620	PCS	HP:0003577	HP:0040284		P		HPO:skoehler	1/5
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001696	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0001762	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0002007	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0002553	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0002557	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0002558	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0002812	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0005280	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0006610	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0009933	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0010239	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0010554	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0011304	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0011800	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0012385	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0100258	OMIM:614976	TAS				P		HPO:skoehler	
OMIM	614976	#614976 CARPENTER SYNDROME 2; CRPT2		HP:0100259	OMIM:614976	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS		HP:0000006	OMIM:614979	TAS				I		HPO:skoehler	
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS		HP:0000572	OMIM:614979	IEA				P		HPO:skoehler	
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS		HP:0000970	OMIM:614979	TAS				P		HPO:skoehler	
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS		HP:0001025	OMIM:614979	TAS				P		HPO:skoehler	
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS		HP:0001744	OMIM:614979	IEA				P		HPO:skoehler	
OMIM	614979	SPLENOMEGALY, CYTOPENIA, AND VISION LOSS	HP:0012825	HP:0001876	OMIM:614979	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0000006	OMIM:614980	TAS				I		HPO:probinson	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001629	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001636	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001647	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001650	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001659	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0001682	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0004764	OMIM:614980	TAS				P		HPO:probinson	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0004942	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0005110	OMIM:614980	TAS				P		HPO:skoehler	
OMIM	614980	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2		HP:0032092	OMIM:614980	IEA				P		HPO:skoehler	
OMIM	614990	%614990 USHER SYNDROME, TYPE IK; USH1K		HP:0000007	OMIM:614990	TAS				I		HPO:skoehler	
OMIM	614990	%614990 USHER SYNDROME, TYPE IK; USH1K		HP:0000510	OMIM:614990	TAS				P		HPO:skoehler	
OMIM	614990	%614990 USHER SYNDROME, TYPE IK; USH1K		HP:0001270	OMIM:614990	TAS				P		HPO:skoehler	
OMIM	614990	%614990 USHER SYNDROME, TYPE IK; USH1K		HP:0001751	OMIM:614990	TAS				P		HPO:skoehler	
OMIM	614990	%614990 USHER SYNDROME, TYPE IK; USH1K		HP:0003577	OMIM:614990	TAS				C		HPO:skoehler	
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0000006	OMIM:615005	IEA				I		HPO:skoehler	
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0000708	OMIM:615005	IEA				P		HPO:skoehler	
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0000709	OMIM:615005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0000716	OMIM:615005	TAS				P		HPO:skoehler	
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0000718	OMIM:615005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0001249	OMIM:615005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0002133	OMIM:615005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0007359	OMIM:615005	IEA				P		HPO:skoehler	
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0012075	OMIM:615005	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615005	EPILEPSY, NOCTURNAL FRONTAL LOBE, 5; ENFL5		HP:0100543	OMIM:615005	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0000007	OMIM:615006	IEA				I		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0000737	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0000817	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0001263	OMIM:615006	TAS				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0001290	OMIM:615006	TAS				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0002187	OMIM:615006	TAS				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0002476	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0002521	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0002540	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0011097	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0011398	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615006	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 15; EIEE15		HP:0200134	OMIM:615006	IEA				P		HPO:skoehler	
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0000006	OMIM:615007	IEA				I		HPO:skoehler	
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0000639	OMIM:615007	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0000716	OMIM:615007	TAS				P		HPO:skoehler	
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0000726	OMIM:615007	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0001300	OMIM:615007	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0002076	OMIM:615007	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615007	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4; IBGC4		HP:0002135	OMIM:615007	IEA				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0000007	OMIM:615008	TAS				I		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0000093	OMIM:615008	TAS				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0000099	OMIM:615008	IEA				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0000100	OMIM:615008	TAS				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0001873	OMIM:615008	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0001878	OMIM:615008	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0001919	OMIM:615008	TAS				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0003676	OMIM:615008	TAS				C		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0003774	OMIM:615008	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0004722	OMIM:615008	TAS				P		HPO:skoehler	
OMIM	615008	NEPHROTIC SYNDROME, TYPE 7; NPHS7		HP:0005575	OMIM:615008	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000006	PMID:23159249	PCS				I		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000028	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000154	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000219	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000294	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000316	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000319	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000369	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000400	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000414	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000486	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000494	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000508	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000527	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000545	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000639	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS	HP:0012825	HP:0000664	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000699	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000718	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0000750	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001195	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001249	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001250	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001263	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001290	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001321	OMIM:615009	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001344	OMIM:615009	IEA				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001643	OMIM:615009	IEA				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001647	OMIM:615009	IEA				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001655	OMIM:615009	IEA				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001671	OMIM:615009	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001763	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0001833	OMIM:615009	IEA				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0002019	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0002389	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0002553	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0002580	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0002714	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0006610	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0011098	PMID:23159249	PCS				P		HPO:probinson	
OMIM	615009	SCHUURS-HOEIJMAKERS SYNDROME; SHMS		HP:0011968	OMIM:615009	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0000007	OMIM:615010	TAS				I		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0000252	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0000639	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6	HP:0012828	HP:0001263	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0001332	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0001337	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0001878	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0002063	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0002371	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0002376	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0002415	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0002514	OMIM:615010	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615010	AICARDI-GOUTIERES SYNDROME 6		HP:0006957	OMIM:615010	TAS				P		HPO:skoehler	
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0000007	OMIM:615022	TAS				I		HPO:probinson	
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0000982	OMIM:615022	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0001019	OMIM:615022	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0008064	OMIM:615022	TAS		HP:0040284		P		HPO:probinson	3/3
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0025092	OMIM:615022	TAS				P		HPO:skoehler	
OMIM	615022	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 7		HP:0025114	OMIM:615022	TAS				P		HPO:skoehler	
OMIM	615023	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9		HP:0000007	OMIM:615023	TAS				I		HPO:skoehler	
OMIM	615023	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9		HP:0007431	OMIM:615023	IEA				P		HPO:skoehler	
OMIM	615023	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9	HP:0012826	HP:0025092	OMIM:615023	TAS				P		HPO:skoehler	
OMIM	615023	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9		HP:0025114	OMIM:615023	TAS				P		HPO:skoehler	
OMIM	615024	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10		HP:0000007	OMIM:615024	TAS				I		HPO:skoehler	
OMIM	615024	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10		HP:0000982	OMIM:615024	TAS				P		HPO:skoehler	
OMIM	615024	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10		HP:0001019	OMIM:615024	IEA				P		HPO:skoehler	
OMIM	615024	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10		HP:0007431	OMIM:615024	IEA				P		HPO:skoehler	
OMIM	615024	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10; ARCI10		HP:0025114	OMIM:615024	TAS				P		HPO:skoehler	
OMIM	615025	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q; CMT2Q		HP:0000006	OMIM:615025	TAS				I		HPO:skoehler	
OMIM	615025	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q; CMT2Q		HP:0002355	OMIM:615025	TAS				P		HPO:skoehler	
OMIM	615025	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q; CMT2Q		HP:0003202	OMIM:615025	TAS				P		HPO:skoehler	
OMIM	615025	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q; CMT2Q		HP:0003474	OMIM:615025	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0000006	OMIM:615026	TAS				I		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0001942	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0001943	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0002033	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0003215	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0045045	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615026	RIBOFLAVIN DEFICIENCY		HP:0100504	OMIM:615026	IEA				P		HPO:skoehler	
OMIM	615028	EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:615028	TAS				I		HPO:skoehler	
OMIM	615028	EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE	HP:0012825	HP:0000962	OMIM:615028	TAS				P		HPO:skoehler	
OMIM	615028	EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE		HP:0001030	OMIM:615028	TAS				P		HPO:skoehler	
OMIM	615028	EPIDERMOLYSIS BULLOSA, NONSPECIFIC, AUTOSOMAL RECESSIVE		HP:0025092	OMIM:615028	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0000007	OMIM:615030	TAS				I		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0001258	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0001270	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0002079	OMIM:615030	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0002135	OMIM:615030	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0002317	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0002395	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0003487	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0003828	OMIM:615030	TAS				C		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0040083	OMIM:615030	TAS				P		HPO:skoehler	
OMIM	615030	#615030 SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56		HP:0100543	OMIM:615030	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:615031	TAS				I		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000248	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000294	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000311	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000338	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000470	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000475	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0000678	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:615031	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001284	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001290	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0001310	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0002020	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0002059	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0002064	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0002066	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0002079	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE	HP:0025303	HP:0002871	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615031	SPASTIC PARAPLEGIA 49, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:615031	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000098	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000256	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000307	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000316	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000336	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000445	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000494	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0000717	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0001249	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0001250	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0001763	PMID:24998929	PCS				P		HPO:probinson	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0002019	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0002360	OMIM:615032	TAS				P		HPO:skoehler	
OMIM	615032	AUTISM, SUSCEPTIBILITY TO, 18		HP:0025352	PMID:24998929	PCS				I		HPO:probinson	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000007	OMIM:615033	TAS				I		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000020	OMIM:615033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000218	OMIM:615033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000486	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000506	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0000609	OMIM:615033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0001249	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0001258	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0001260	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0001263	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0001347	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0002015	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0002019	OMIM:615033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0002079	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0002518	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0002607	OMIM:615033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0003487	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0003676	OMIM:615033	TAS				C		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0004322	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615033	#615033 SPASTIC PARAPLEGIA 54, AUTOSOMAL RECESSIVE; SPG54		HP:0007340	OMIM:615033	TAS				P		HPO:skoehler	
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0000006	OMIM:615034	TAS				I		HPO:skoehler	
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0000473	OMIM:615034	TAS				P		HPO:skoehler	
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0000643	OMIM:615034	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0002346	OMIM:615034	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0002346	OMIM:615034	TAS				P		HPO:skoehler	
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0003829	OMIM:615034	TAS				C		HPO:skoehler	
OMIM	615034	#615034 DYSTONIA 24; DYT24		HP:0012048	OMIM:615034	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0000007	OMIM:615035	TAS				I		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0000486	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0000603	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0000639	OMIM:615035	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0000648	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0001249	OMIM:615035	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0001258	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0001263	OMIM:615035	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0001324	OMIM:615035	IEA				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0001762	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0002079	OMIM:615035	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0002169	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0002355	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0002936	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0003376	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0003383	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0003477	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0003487	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0003828	OMIM:615035	TAS				C		HPO:skoehler	
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0007663	OMIM:615035	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615035	SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE; SPG55		HP:0100543	OMIM:615035	TAS				P		HPO:skoehler	
OMIM	615040	#615040 EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1		HP:0000006	OMIM:615040	TAS				I		HPO:skoehler	
OMIM	615040	#615040 EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1		HP:0003593	OMIM:615040	TAS				C		HPO:skoehler	
OMIM	615040	#615040 EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1	HP:0025303	HP:0012531	OMIM:615040	TAS				P		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0000007	OMIM:615041	TAS				I		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0000133	OMIM:615041	TAS				P		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0003560	OMIM:615041	TAS				P		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0007033	OMIM:615041	TAS				P		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0007260	OMIM:615041	TAS				P		HPO:skoehler	
OMIM	615041	#615041 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10; MDDGA10		HP:0007973	OMIM:615041	TAS				P		HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000007	OMIM:615042	TAS				I	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000218	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000219	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000347	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000486	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000601	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0000648	OMIM:615042	TAS		HP:0040282		P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	HP:0040282
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu	HP:0031375	HP:0001250	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0001263	PMID:19901254	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu	HP:0012828	HP:0001290	PMID:19901254	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0001321	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0001522	OMIM:615042	TAS				M	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002058	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002375	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002476	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002643	PMID:19901254	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002650	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002803	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0002910	PMID:19901254	IEA				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0003160	PMID:23109149	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0003196	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0003236	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0003577	OMIM:615042	TAS				C	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0005484	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0006829	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0011968	OMIM:615042	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:skoehler	
OMIM	615042	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu; CDG1U;;CDG Iu; CDGIu		HP:0012762	PMID:19901254	TAS				P	#615042 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IU; CDG1U;;CDG IU; CDGIU	HPO:nvasilevsky	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0000007	OMIM:615043	TAS				I		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001257	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001258	OMIM:615043	IEA				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43	HP:0012825	HP:0001260	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001265	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001288	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001324	OMIM:615043	IEA				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001347	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0001761	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0002936	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0003487	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0003677	OMIM:615043	TAS				C		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0003693	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0003828	OMIM:615043	TAS				C		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0006380	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615043	SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43		HP:0006466	OMIM:615043	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0000006	OMIM:615048	TAS				I		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001265	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001284	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001324	OMIM:615048	IEA				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001337	OMIM:615048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001761	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001763	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0001765	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0002355	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0002380	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0002936	OMIM:615048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ	HP:0012825	HP:0003202	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0003236	OMIM:615048	TAS				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0003394	OMIM:615048	IEA				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0003677	OMIM:615048	TAS				C		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0007269	OMIM:615048	IEA				P		HPO:skoehler	
OMIM	615048	SPINAL MUSCULAR ATROPHY, JOKELA TYPE; SMAJ		HP:0008981	OMIM:615048	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615058	#615058 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F		HP:0000007	OMIM:615058	TAS				I		HPO:skoehler	
OMIM	615058	#615058 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F		HP:0000486	OMIM:615058	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615058	#615058 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F		HP:0000545	OMIM:615058	TAS				P		HPO:skoehler	
OMIM	615058	#615058 NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F		HP:0007642	OMIM:615058	TAS				P		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0000006	OMIM:615059	TAS				I		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0001006	OMIM:615059	IEA				P		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0001596	OMIM:615059	IEA				P		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0002221	OMIM:615059	TAS				P		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0100840	OMIM:615059	TAS				P		HPO:skoehler	
OMIM	615059	HYPOTRICHOSIS 11; HYPT11		HP:0200102	OMIM:615059	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000007	OMIM:615065	TAS				I		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000059	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000175	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000221	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000311	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000347	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000414	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000463	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000470	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0000508	OMIM:615065	IEA				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0001181	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0001762	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0001848	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0002553	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0002650	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0002804	OMIM:615065	IEA				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0002827	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0002987	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0003199	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0003307	OMIM:615065	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D		HP:0004322	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615065	ARTHROGRYPOSIS, DISTAL, TYPE 5D; DA5D	HP:0012825	HP:0012385	OMIM:615065	TAS				P		HPO:skoehler	
OMIM	615066	#615066 OSTEOGENESIS IMPERFECTA, TYPE XIV; OI14 ;;OI, TYPE XIV		HP:0000007	OMIM:615066	IEA				I		HPO:skoehler	
OMIM	615066	#615066 OSTEOGENESIS IMPERFECTA, TYPE XIV; OI14 ;;OI, TYPE XIV		HP:0000938	OMIM:615066	IEA				P		HPO:skoehler	
OMIM	615066	#615066 OSTEOGENESIS IMPERFECTA, TYPE XIV; OI14 ;;OI, TYPE XIV		HP:0002757	OMIM:615066	IEA				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0000007	OMIM:615067	TAS				I		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0000403	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0001696	OMIM:615067	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0002110	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0006532	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0011108	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0012256	OMIM:615067	TAS				P		HPO:probinson	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0012265	OMIM:615067	TAS				P		HPO:probinson	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0012735	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0031417	OMIM:615067	IEA				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0100750	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615067	CILIARY DYSKINESIA, PRIMARY, 20; CILD20		HP:0200073	OMIM:615067	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000007	OMIM:615071	TAS				I		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000154	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000252	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000272	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000322	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000369	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000431	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000445	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0000490	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0001263	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0002650	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0003510	OMIM:615071	IEA				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0004325	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0005280	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0010864	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615071	ALAZAMI SYNDROME		HP:0012471	OMIM:615071	TAS				P		HPO:skoehler	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0000006	OMIM:615072	TAS				I		HPO:skoehler	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0000007	OMIM:615072	TAS				I		HPO:skoehler	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0001156	OMIM:615072	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0001776	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0004220	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0004322	OMIM:615072	TAS				P		HPO:skoehler	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0009295	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0009439	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0009577	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615072	#615072 BRACHYDACTYLY, TYPE A1, C; BDA1C		HP:0009882	PMID:20683927	PCS				P		HPO:lccarmody	
OMIM	615073	DYSTONIA 25		HP:0000006	OMIM:615073	TAS				I		HPO:skoehler	
OMIM	615073	DYSTONIA 25		HP:0000473	OMIM:615073	TAS				P		HPO:skoehler	
OMIM	615073	DYSTONIA 25		HP:0002451	OMIM:615073	TAS				P		HPO:skoehler	
OMIM	615073	DYSTONIA 25		HP:0012049	OMIM:615073	TAS				P		HPO:skoehler	
OMIM	615073	DYSTONIA 25		HP:0031008	OMIM:615073	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000006	PMID:23644463	PCS				I		HPO:probinson	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000154	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000219	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000316	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000322	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000337	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000431	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000455	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000486	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000490	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000540	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000581	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000748	PMID:23644463	PCS				P		HPO:probinson	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0000752	OMIM:615074	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0001263	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0001319	PMID:23644463	PCS				P		HPO:probinson	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0002463	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0002465	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0003593	OMIM:615074	TAS				C		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0008070	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0010511	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0010864	PMID:23644463	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0045025	OMIM:615074	IEA				P		HPO:skoehler	
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0100033	OMIM:615074	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615074	MENTAL RETARDATION, AUTOSOMAL DOMINANT 18; MRD18		HP:0100807	OMIM:615074	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000006	OMIM:615075	TAS				I		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000219	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000252	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000343	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000486	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0000540	OMIM:615075	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0001249	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0001263	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19	HP:0003676	HP:0001264	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0001290	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0002079	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0002167	OMIM:615075	TAS				P		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0003593	OMIM:615075	TAS				C		HPO:skoehler	
OMIM	615075	MENTAL RETARDATION, AUTOSOMAL DOMINANT 19; MRD19		HP:0030490	OMIM:615075	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615081	#615081 SPERMATOGENIC FAILURE 11; SPGF11		HP:0000006	OMIM:615081	TAS				I		HPO:skoehler	
OMIM	615081	#615081 SPERMATOGENIC FAILURE 11; SPGF11		HP:0000789	OMIM:615081	TAS				P		HPO:skoehler	
OMIM	615081	#615081 SPERMATOGENIC FAILURE 11; SPGF11		HP:0012864	OMIM:615081	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615082	#615082 C3HEX, ABILITY TO SMELL		HP:0000006	OMIM:615082	TAS				I		HPO:skoehler	
OMIM	615083	COLORECTAL CANCER, SUSCEPTIBILITY TO, 12; CRCS12		HP:0000006	OMIM:615083	TAS				I		HPO:skoehler	
OMIM	615083	COLORECTAL CANCER, SUSCEPTIBILITY TO, 12; CRCS12		HP:0003581	OMIM:615083	TAS				C		HPO:skoehler	
OMIM	615083	COLORECTAL CANCER, SUSCEPTIBILITY TO, 12; CRCS12		HP:0030731	OMIM:615083	IEA				P		HPO:skoehler	
OMIM	615083	COLORECTAL CANCER, SUSCEPTIBILITY TO, 12; CRCS12		HP:0200063	OMIM:615083	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0000007	OMIM:615084	TAS				I		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0000252	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0000508	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0000590	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0000815	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001249	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001265	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001321	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001611	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001618	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0001644	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002014	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002018	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002093	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002094	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002719	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0002808	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11	HP:0012825	HP:0003236	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0003306	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0003388	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0003546	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0003676	OMIM:615084	TAS				C		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0003700	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0007126	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0008443	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0010628	OMIM:615084	TAS				P		HPO:skoehler	
OMIM	615084	MITOCHONDRIAL DNA DEPLETION SYNDROME 11		HP:0011675	OMIM:615084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0000007	OMIM:615085	TAS				I		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0000256	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0000648	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0001508	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0001744	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0001873	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0001903	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0002007	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0002240	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0010628	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0011002	OMIM:615085	IEA				P		HPO:skoehler	
OMIM	615085	#615085 OSTEOPETROSIS, AUTOSOMAL RECESSIVE 8; OPTB8		HP:0011968	OMIM:615085	TAS				P		HPO:skoehler	
OMIM	615092	#615092 LEFT VENTRICULAR NONCOMPACTION 7; LVNC7		HP:0000006	OMIM:615092	TAS				I		HPO:skoehler	
OMIM	615092	#615092 LEFT VENTRICULAR NONCOMPACTION 7; LVNC7		HP:0011664	OMIM:615092	TAS				P		HPO:probinson	
OMIM	615092	#615092 LEFT VENTRICULAR NONCOMPACTION 7; LVNC7		HP:0030682	OMIM:615092	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000007	OMIM:615095	TAS				I		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10	HP:0012828	HP:0000252	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000340	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000347	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000426	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000453	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0000518	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0001257	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0001272	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0001511	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0001518	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10	HP:0012828	HP:0002059	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0002171	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0002804	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0003577	OMIM:615095	TAS				C		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0011344	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0012448	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615095	MICROCEPHALY 10, PRIMARY, AUTOSOMAL RECESSIVE; MCPH10		HP:0012736	OMIM:615095	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000006	OMIM:615102	TAS				I		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000028	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000175	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000294	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000331	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000358	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000369	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000508	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000520	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME	HP:0012825	HP:0000767	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0000774	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001256	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME	HP:0012825	HP:0001263	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001511	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001561	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001622	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001629	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001631	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0001642	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0002079	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0002558	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0002705	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0004322	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0010535	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0011968	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615102	TYSHCHENKO SYNDROME		HP:0100874	OMIM:615102	TAS				P		HPO:skoehler	
OMIM	615106	#615106 COWDEN SYNDROME 3; CWS3		HP:0000131	OMIM:615106	IEA				P		HPO:skoehler	
OMIM	615106	#615106 COWDEN SYNDROME 3; CWS3		HP:0003287	OMIM:615106	IEA				P		HPO:skoehler	
OMIM	615106	#615106 COWDEN SYNDROME 3; CWS3		HP:0005584	OMIM:615106	IEA				P		HPO:skoehler	
OMIM	615106	#615106 COWDEN SYNDROME 3; CWS3		HP:0100031	OMIM:615106	IEA				P		HPO:skoehler	
OMIM	615107	#615107 COWDEN SYNDROME 4; CWS4		HP:0000168	OMIM:615107	IEA				P		HPO:skoehler	
OMIM	615107	#615107 COWDEN SYNDROME 4; CWS4		HP:0009726	OMIM:615107	IEA				P		HPO:skoehler	
OMIM	615107	#615107 COWDEN SYNDROME 4; CWS4		HP:0010566	OMIM:615107	IEA				P		HPO:skoehler	
OMIM	615107	#615107 COWDEN SYNDROME 4; CWS4		HP:0012844	OMIM:615107	IEA				P		HPO:skoehler	
OMIM	615107	#615107 COWDEN SYNDROME 4; CWS4		HP:3000019	OMIM:615107	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000006	OMIM:615108	IEA				I		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000034	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000138	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000160	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000218	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000221	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000327	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000347	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000365	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000518	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000545	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000767	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000771	OMIM:615108	TAS				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000821	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000836	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000853	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000854	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0000972	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001031	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001102	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001249	OMIM:615108	TAS		HP:0040284		P		HPO:skoehler	12%
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001250	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001256	OMIM:615108	IEA		HP:0040284		P		HPO:skoehler	12%
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0001626	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0002080	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0002253	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0002650	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0002808	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0002858	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0003002	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0003581	OMIM:615108	TAS				C		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0004390	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0004481	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0006740	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0010609	OMIM:615108	IEA				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0010619	OMIM:615108	TAS				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0012871	OMIM:615108	TAS				P		HPO:skoehler	
OMIM	615108	COWDEN SYNDROME 5; CWS5		HP:0100646	OMIM:615108	TAS				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000006	OMIM:615109	IEA				I		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000034	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000138	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000160	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000218	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000221	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000327	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000347	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000365	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000518	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000545	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000767	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000771	OMIM:615109	TAS				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000821	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000836	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000853	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000854	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0000972	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001031	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001102	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001249	OMIM:615109	TAS		HP:0040284		P		HPO:skoehler	12%
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001250	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001256	OMIM:615109	IEA		HP:0040284		P		HPO:skoehler	12%
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0001626	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0002080	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0002253	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0002650	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0002808	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0002858	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0003002	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0003581	OMIM:615109	TAS				C		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0004390	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0004481	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0006740	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0010609	OMIM:615109	IEA				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0010619	OMIM:615109	TAS				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0012871	OMIM:615109	TAS				P		HPO:skoehler	
OMIM	615109	COWDEN SYNDROME 6; CWS6		HP:0100646	OMIM:615109	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000007	OMIM:615112	TAS				I		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000010	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000012	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000076	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000083	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000126	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0000805	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615112	UROFACIAL SYNDROME 2		HP:0002019	OMIM:615112	TAS				P		HPO:skoehler	
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000007	OMIM:615113	TAS				I		HPO:skoehler	
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000541	OMIM:615113	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000568	OMIM:615113	IEA				P		HPO:skoehler	
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000589	OMIM:615113	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000609	OMIM:615113	TAS				P		HPO:skoehler	
OMIM	615113	MICROPHTHALMIA, ISOLATED 8		HP:0000621	OMIM:615113	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0000007	OMIM:615119	TAS				I	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0000252	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0001290	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0001298	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0001397	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0001558	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0001638	OMIM:615119	IEA				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615119	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 2; CEMCOX2		HP:0002171	OMIM:615119	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 2; CEMCOX2	HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0000007	OMIM:615120	TAS				I		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0000218	OMIM:615120	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0000508	OMIM:615120	TAS				P		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0000774	OMIM:615120	TAS				P		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0002093	OMIM:615120	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0003388	OMIM:615120	TAS				P		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0003701	OMIM:615120	TAS				P		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0003828	OMIM:615120	TAS				C		HPO:skoehler	
OMIM	615120	MYASTHENIC SYNDROME, CONGENITAL, 8; CMS8		HP:0010628	OMIM:615120	TAS				P		HPO:skoehler	
OMIM	615121	STOMATIN-LIKE PROTEIN-2, HYPERPHOSPHORYLATION OF		HP:0000006	OMIM:615121	TAS				I		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0000007	OMIM:615122	TAS				I		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0001541	OMIM:615122	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0001744	OMIM:615122	TAS				P		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0001915	OMIM:615122	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0001945	OMIM:615122	TAS				P		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0002240	OMIM:615122	TAS				P		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0002665	OMIM:615122	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0002716	OMIM:615122	TAS				P		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0003828	OMIM:615122	TAS				C		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0004313	OMIM:615122	TAS				P		HPO:skoehler	
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0005523	OMIM:615122	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0012156	OMIM:615122	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615122	LYMPHOPROLIFERATIVE SYNDROME 2; LPFS2		HP:0020072	OMIM:615122	IEA				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0000006	OMIM:615127	TAS				I		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0001250	OMIM:615127	IEA				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0001336	OMIM:615127	IEA				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0001337	OMIM:615127	IEA				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0001340	OMIM:615127	TAS				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0001351	OMIM:615127	TAS				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0002069	OMIM:615127	TAS				P		HPO:skoehler	
OMIM	615127	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 4; FAME4		HP:0003680	OMIM:615127	TAS				C		HPO:skoehler	
OMIM	615134	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9; CMM9		HP:0000006	PMID:23348503	PCS				I		HPO:probinson	
OMIM	615134	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 9; CMM9		HP:0002861	PMID:23348503	PCS				P		HPO:probinson	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0000007	OMIM:615139	TAS				I		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0000272	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0000337	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0001999	OMIM:615139	IEA				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0002205	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0002653	OMIM:615139	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0002721	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0003577	OMIM:615139	TAS				C		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0004322	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0004482	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615139	#615139 FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS		HP:0007421	OMIM:615139	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000007	OMIM:615145	TAS				I		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000482	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000541	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000565	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000568	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0000612	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0007663	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615145	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 9		HP:0012043	OMIM:615145	TAS				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0000007	OMIM:615147	TAS				I		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0000482	OMIM:615147	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0000556	OMIM:615147	TAS				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0000612	OMIM:615147	IEA				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0001643	OMIM:615147	TAS				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0007663	OMIM:615147	TAS				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0030825	OMIM:615147	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0040137	OMIM:615147	IEA				P		HPO:skoehler	
OMIM	615147	RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME		HP:0200070	OMIM:615147	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0000007	OMIM:615155	TAS				I		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0000316	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0000431	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0002650	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0003083	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0004322	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615155	%615155 STEEL SYNDROME; STLS;;DISLOCATED HIPS AND RADIAL HEADS, CARPAL COALITION, SCOLIOSIS, ANDSHORT STATURE		HP:0011220	OMIM:615155	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0000006	OMIM:615156	TAS				I		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6	HP:0012825	HP:0000508	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0000544	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0000590	OMIM:615156	IEA				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0001288	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0001533	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0002870	OMIM:615156	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0002875	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003236	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6	HP:0012825	HP:0003325	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003326	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003391	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003394	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003546	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003677	OMIM:615156	TAS				C		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0003700	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615156	#615156 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 6; PEOA6;;PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, AUTOSOMAL DOMINANT, 6		HP:0010628	OMIM:615156	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000007	OMIM:615157	TAS				I		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000365	OMIM:615157	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000639	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000709	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000716	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000718	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000722	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000738	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0000739	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001260	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001263	OMIM:615157	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001272	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001310	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001324	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001332	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001337	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001347	OMIM:615157	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0001618	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002059	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002067	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002075	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2	HP:0003676	HP:0002180	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002186	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002311	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002313	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0002542	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0003202	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0003487	OMIM:615157	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0040078	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615157	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2; MC3DN2		HP:0100543	OMIM:615157	TAS				P		HPO:skoehler	
OMIM	615158	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3; MC3DN3		HP:0000007	OMIM:615158	TAS				I		HPO:skoehler	
OMIM	615158	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3; MC3DN3		HP:0001942	OMIM:615158	TAS				P		HPO:skoehler	
OMIM	615158	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3; MC3DN3		HP:0001943	OMIM:615158	TAS				P		HPO:skoehler	
OMIM	615158	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 3; MC3DN3		HP:0002151	OMIM:615158	IEA				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0000007	OMIM:615159	TAS				I		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001251	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001263	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001290	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001332	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001344	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0001347	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0002071	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0002151	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0002305	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0002540	OMIM:615159	IEA				P		HPO:skoehler	
OMIM	615159	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4; MC3DN4		HP:0010864	OMIM:615159	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0000007	OMIM:615160	TAS				I		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0001410	OMIM:615160	IEA				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0001942	OMIM:615160	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0001943	OMIM:615160	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0001987	OMIM:615160	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0002151	OMIM:615160	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0002910	OMIM:615160	IEA				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0003542	OMIM:615160	TAS				P		HPO:skoehler	
OMIM	615160	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 5; MC3DN5		HP:0100543	OMIM:615160	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000007	PMID:20950399	PCS				I		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000219	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000232	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000272	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000280	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000316	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000337	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000343	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000347	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000348	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000369	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000445	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000494	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0000664	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0001007	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0001249	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0001263	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0001290	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0002714	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0003022	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0004325	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0005469	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0008551	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0009928	PMID:20950399	PCS				P		HPO:probinson	
OMIM	615162	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35		HP:0030084	OMIM:615162	TAS				P		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000006	OMIM:615163	TAS				I		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000505	OMIM:615163	IEA				P		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000543	OMIM:615163	TAS				P		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000548	OMIM:615163	IEA				P		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000603	OMIM:615163	TAS				P		HPO:skoehler	
OMIM	615163	CONE-ROD DYSTROPHY 17; CORD17		HP:0000613	OMIM:615163	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0000006	OMIM:615170	TAS				I		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME	HP:0012828	HP:0001159	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0001181	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0001773	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0004279	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0009778	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0010049	OMIM:615170	TAS				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0012385	OMIM:615170	IEA				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0030084	OMIM:615170	IEA				P		HPO:skoehler	
OMIM	615170	WAHAB SYNDROME		HP:0031013	OMIM:615170	IEA				P		HPO:skoehler	
OMIM	615179	#615179 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0000007	OMIM:615179	TAS				I		HPO:skoehler	
OMIM	615179	#615179 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5	HP:0012825	HP:0000613	OMIM:615179	TAS				P		HPO:skoehler	
OMIM	615179	#615179 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0000639	OMIM:615179	TAS				P		HPO:skoehler	
OMIM	615179	#615179 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0001022	OMIM:615179	IEA				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000007	OMIM:615181	TAS				I		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000238	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000518	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000541	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000545	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000568	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000609	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0000618	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11	HP:0012828	HP:0001263	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0001321	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0002126	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0002350	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0002352	OMIM:615181	IEA				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0003236	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0003560	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0006829	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0007033	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0007260	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0012110	OMIM:615181	TAS				P		HPO:skoehler	
OMIM	615181	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11; MDDGA11		HP:0100543	OMIM:615181	IEA				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0000007	OMIM:615182	TAS				I		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0000252	OMIM:615182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0000256	OMIM:615182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0000737	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0000817	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0001250	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0001263	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0001298	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0001321	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0002093	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0002094	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0002119	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0002240	OMIM:615182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0006829	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0010307	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0011968	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0012448	OMIM:615182	TAS				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0040144	OMIM:615182	IEA				P		HPO:skoehler	
OMIM	615182	#615182 COMBINED D-2- AND L-2-HYDROXYGLUTARIC ACIDURIA; D2L2AD		HP:0100704	OMIM:615182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615184	#615184 CARDIOMYOPATHY, DILATED, 1II; CMD1II		HP:0000006	OMIM:615184	TAS				I		HPO:skoehler	
OMIM	615184	#615184 CARDIOMYOPATHY, DILATED, 1II; CMD1II	HP:0012825	HP:0001644	OMIM:615184	TAS				P		HPO:skoehler	
OMIM	615184	#615184 CARDIOMYOPATHY, DILATED, 1II; CMD1II		HP:0001653	OMIM:615184	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0000006	OMIM:615185	TAS				I		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0001265	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0001761	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0001765	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0002936	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0003376	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0003383	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0003450	OMIM:615185	TAS				P		HPO:skoehler	
OMIM	615185	#615185 CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE F; CMTDIF		HP:0003677	OMIM:615185	TAS				C		HPO:skoehler	
OMIM	615188	#615188 CATARACT, MULTIPLE TYPES		HP:0000006	OMIM:615188	TAS				I		HPO:skoehler	
OMIM	615188	#615188 CATARACT, MULTIPLE TYPES		HP:0000519	OMIM:615188	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0000006	OMIM:615190	TAS				I		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0000007	OMIM:615190	TAS				I		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0000252	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0001263	OMIM:615190	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0001321	OMIM:615190	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0001511	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0001882	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0002583	OMIM:615190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0002721	OMIM:615190	IEA				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0003828	OMIM:615190	TAS				C		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0004313	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0005528	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0008404	OMIM:615190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0008897	OMIM:615190	TAS				P		HPO:skoehler	
OMIM	615190	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 5; DKCB5		HP:0010450	OMIM:615190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000007	OMIM:615191	TAS				I		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000238	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000256	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000365	OMIM:615191	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000518	OMIM:615191	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0000648	OMIM:615191	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615191	LISSENCEPHALY 5; LIS5	HP:0003676	HP:0001249	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0001250	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0001258	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0001290	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0001321	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002085	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002132	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002282	PMID:23472759	TAS				P		HPO:probinson	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002352	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002365	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0002500	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0003676	OMIM:615191	TAS				C		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0003828	OMIM:615191	TAS				C		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0007260	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0011344	OMIM:615191	TAS				P		HPO:skoehler	
OMIM	615191	LISSENCEPHALY 5; LIS5		HP:0025356	OMIM:615191	IEA				P		HPO:skoehler	
OMIM	615193	#615193 BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15;;MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED		HP:0000006	OMIM:615193	TAS				I		HPO:skoehler	
OMIM	615193	#615193 BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15;;MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED		HP:0000421	OMIM:615193	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615193	#615193 BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15;;MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED		HP:0001873	OMIM:615193	TAS				P		HPO:skoehler	
OMIM	615193	#615193 BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15;;MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED		HP:0011273	OMIM:615193	TAS				P		HPO:skoehler	
OMIM	615193	#615193 BLEEDING DISORDER, PLATELET-TYPE, 15; BDPLT15;;MACROTHROMBOCYTOPENIA, AUTOSOMAL DOMINANT, ACTN1-RELATED		HP:0011877	OMIM:615193	TAS				P		HPO:skoehler	
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0000007	OMIM:615198	TAS				I		HPO:skoehler	
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0001249	OMIM:615198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0001250	OMIM:615198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0001263	OMIM:615198	TAS				P		HPO:skoehler	
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0001290	OMIM:615198	TAS				P		HPO:skoehler	
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0003155	OMIM:615198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0100255	OMIM:615198	IEA				P		HPO:skoehler	
OMIM	615198	OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA		HP:0100923	OMIM:615198	TAS				P		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0000007	OMIM:615206	TAS				I		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0002090	OMIM:615206	TAS				P		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0002205	OMIM:615206	TAS				P		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0002721	OMIM:615206	TAS				P		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0003593	OMIM:615206	TAS				C		HPO:skoehler	
OMIM	615206	#615206 CARD11 IMMUNODEFICIENCY		HP:0004313	OMIM:615206	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0000007	OMIM:615207	TAS				I		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0001394	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0001399	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0001508	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0002028	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0002090	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0002110	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0002721	OMIM:615207	IEA				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0011108	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0030151	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615207	#615207 IL21R IMMUNODEFICIENCY		HP:0200124	OMIM:615207	TAS				P		HPO:skoehler	
OMIM	615214	#615214 AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT		HP:0000007	OMIM:615214	TAS				I		HPO:skoehler	
OMIM	615214	#615214 AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT		HP:0001875	OMIM:615214	TAS				P		HPO:skoehler	
OMIM	615214	#615214 AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT		HP:0002205	OMIM:615214	TAS				P		HPO:skoehler	
OMIM	615214	#615214 AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT		HP:0003593	OMIM:615214	TAS				C		HPO:skoehler	
OMIM	615214	#615214 AGAMMAGLOBULINEMIA 7, AUTOSOMAL RECESSIVE; AGM7;;AGAMMAGLOBULINEMIA, AUTOSOMAL RECESSIVE, DUE TO PIK3R1 DEFECT		HP:0004432	OMIM:615214	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0000007	OMIM:615217	TAS				I		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0000514	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0000639	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0000657	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001260	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001265	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001271	OMIM:615217	IEA				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001272	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001284	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001310	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0001324	OMIM:615217	IEA				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0002359	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0002936	OMIM:615217	TAS				P		HPO:skoehler	
OMIM	615217	ATAXIA-OCULOMOTOR APRAXIA 3; AOA3		HP:0003676	OMIM:615217	TAS				C		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000007	OMIM:615219	TAS				I		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000256	OMIM:615219	TAS				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000358	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000407	OMIM:615219	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000486	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000494	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000612	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0000648	OMIM:615219	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001104	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001249	OMIM:615219	TAS				P		HPO:probinson	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001250	OMIM:615219	TAS				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001270	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001334	OMIM:615219	TAS				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001339	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0001999	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0002007	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0002119	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0002282	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0003577	OMIM:615219	TAS				C		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0003828	OMIM:615219	IEA				C		HPO:skoehler	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0009879	OMIM:615219	TAS				P		HPO:probinson	
OMIM	615219	HYDROCEPHALUS, CONGENITAL, 2, WITH OR WITHOUT BRAIN OR EYE ANOMALIES; HYC2		HP:0030048	OMIM:615219	IEA				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0000007	OMIM:615220	TAS				I		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0000592	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0000883	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0000926	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0001263	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0001321	OMIM:615220	IEA				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0002650	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0004322	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0010636	OMIM:615220	IEA				P		HPO:skoehler	
OMIM	615220	OSTEOGENESIS IMPERFECTA, TYPE XV; OI15		HP:0012110	OMIM:615220	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0000007	OMIM:615222	TAS				I		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0000470	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0000768	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0000926	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0001552	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0001763	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0001783	OMIM:615222	IEA				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0002857	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0003025	OMIM:615222	IEA				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0003071	OMIM:615222	IEA				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2	HP:0012825	HP:0003311	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0003521	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0004325	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0006009	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2	HP:0012825	HP:0006429	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0008812	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0009803	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0010049	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615222	SMITH-MCCORT DYSPLASIA 2; SMC2		HP:0010743	OMIM:615222	TAS				P		HPO:skoehler	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0000006	OMIM:615224	TAS				I		HPO:skoehler	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0002076	OMIM:615224	IEA				P		HPO:skoehler	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0002077	PMID:23636092	PCS				P		HPO:lccarmody	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0002083	PMID:23636092	PCS				P		HPO:lccarmody	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0006979	PMID:15800623	PCS				P		HPO:lccarmody	
OMIM	615224	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 2; FASPS2		HP:0031873	OMIM:615224	IEA				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0000006	OMIM:615225	TAS				I		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0000343	OMIM:615225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0000470	OMIM:615225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0000968	OMIM:615225	IEA				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0000982	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0001036	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0002860	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0006094	OMIM:615225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0007502	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0008404	OMIM:615225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0011034	OMIM:615225	IEA				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0011496	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0025092	OMIM:615225	TAS				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0030731	OMIM:615225	IEA				P		HPO:skoehler	
OMIM	615225	PALMOPLANTAR CARCINOMA, MULTIPLE SELF-HEALING; MSPC		HP:0040180	OMIM:615225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615226	#615226 POLYDACTYLY, POSTAXIAL, TYPE A6; PAPA6		HP:0000007	OMIM:615226	TAS				I		HPO:skoehler	
OMIM	615226	#615226 POLYDACTYLY, POSTAXIAL, TYPE A6; PAPA6		HP:0001162	OMIM:615226	IEA				P		HPO:skoehler	
OMIM	615226	#615226 POLYDACTYLY, POSTAXIAL, TYPE A6; PAPA6		HP:0009374	OMIM:615226	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0000007	OMIM:615228	TAS				I		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0000639	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0000737	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0001250	OMIM:615228	IEA				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4	HP:0003676	HP:0001298	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0001321	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0002089	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0002104	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0003577	OMIM:615228	TAS				C		HPO:skoehler	
OMIM	615228	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4		HP:0025430	OMIM:615228	TAS				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0000007	OMIM:615233	TAS				I		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0000510	OMIM:615233	IEA				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0000543	OMIM:615233	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0000603	OMIM:615233	TAS				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0000662	OMIM:615233	TAS				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0001133	OMIM:615233	TAS				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0007663	OMIM:615233	TAS				P		HPO:skoehler	
OMIM	615233	#615233 RETINITIS PIGMENTOSA 66; RP66		HP:0007787	OMIM:615233	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0000006	OMIM:615234	TAS				I		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0000027	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0000135	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0000957	OMIM:615234	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0000980	OMIM:615234	IEA				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0001510	OMIM:615234	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0001744	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2	HP:0012828	HP:0001903	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0002240	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0003281	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0004447	OMIM:615234	IEA				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0025066	OMIM:615234	TAS				P		HPO:skoehler	
OMIM	615234	ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 2; AHMIO2		HP:0032231	OMIM:615234	IEA				P		HPO:skoehler	
OMIM	615235	#615235 CARDIOMYOPATHY, DILATED, 1JJ; CMD1JJ		HP:0000006	OMIM:615235	TAS				I		HPO:skoehler	
OMIM	615235	#615235 CARDIOMYOPATHY, DILATED, 1JJ; CMD1JJ	HP:0012828	HP:0001644	OMIM:615235	TAS				P		HPO:skoehler	
OMIM	615236	MICROCEPHALY - INTELLECTUAL DISABILITY - PHALANGEAL AND NEUROLOGICAL ANOMALIES		HP:0001249	OMIM:615236	IEA				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0000007	OMIM:615237	TAS				I		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0001508	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0002013	OMIM:615237	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0002028	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0002566	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0002570	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0030889	OMIM:615237	TAS				P		HPO:probinson	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0030897	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615237	CONGENITAL SHORT BOWEL SYNDROME		HP:0030914	OMIM:615237	TAS				P		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0000007	OMIM:615238	TAS				I		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0000956	OMIM:615238	TAS				P		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0001397	OMIM:615238	TAS				P		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0002155	OMIM:615238	TAS				P		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0002240	OMIM:615238	TAS				P		HPO:skoehler	
OMIM	615238	#615238 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5; FPLD5;;LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH CIDEC MUTATIONS		HP:0009125	OMIM:615238	IEA				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0000007	OMIM:615244	TAS				I		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0000093	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0000100	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0000407	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0000969	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0001249	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0001250	OMIM:615244	IEA				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0001967	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0003073	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0003623	OMIM:615244	TAS				C		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0003678	OMIM:615244	TAS				C		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0012577	OMIM:615244	TAS				P		HPO:probinson	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0012622	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615244	NEPHROTIC SYNDROME, TYPE 8; NPHS8		HP:0100704	OMIM:615244	TAS				P		HPO:skoehler	
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0000006	OMIM:615248	TAS				I		HPO:skoehler	
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0001635	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0001639	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0001644	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0001653	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0001712	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0005110	OMIM:615248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615248	CARDIOMYOPATHY, DILATED, 1KK; CMD1KK		HP:0005144	OMIM:615248	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000007	OMIM:615249	TAS				I		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000238	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000253	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000407	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000518	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000546	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000568	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0000589	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001090	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001250	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12	HP:0012828	HP:0001263	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001274	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001319	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001321	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0001371	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0002365	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0002421	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0002465	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0002650	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0002747	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0003236	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0003560	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0003577	OMIM:615249	TAS				C		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0007260	OMIM:615249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0007663	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0011968	OMIM:615249	TAS				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0025356	OMIM:615249	IEA				P		HPO:skoehler	
OMIM	615249	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 12; MDDGA12		HP:0031882	OMIM:615249	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615264	#615264 BLOOD GROUP, VEL SYSTEM; VELVEL-NULL PHENOTYPE, INCLUDED		HP:0000007	OMIM:615264	TAS				I		HPO:skoehler	
OMIM	615266	HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA; HH17		HP:0000006	OMIM:615266	TAS				I		HPO:skoehler	
OMIM	615266	HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA; HH17		HP:0000164	OMIM:615266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615266	HYPOGONADOTROPIC HYPOGONADISM 17 WITH OR WITHOUT ANOSMIA; HH17		HP:0000365	OMIM:615266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000006	OMIM:615267	TAS				I		HPO:skoehler	
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000007	OMIM:615267	IEA				I		HPO:skoehler	
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000135	OMIM:615267	TAS				P		HPO:skoehler	
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000164	OMIM:615267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000365	OMIM:615267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000458	OMIM:615267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000938	OMIM:615267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615267	HYPOGONADOTROPIC HYPOGONADISM 18 WITH OR WITHOUT ANOSMIA; HH18		HP:0000939	OMIM:615267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0000007	OMIM:615268	TAS				I		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0001249	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0001260	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0001272	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0002059	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0002078	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0002540	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0003577	OMIM:615268	TAS				C		HPO:skoehler	
OMIM	615268	#615268 CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME4; CAMRQ4;;CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH OR WITHOUT QUADRUPEDALLOCOMOTION 4		HP:0007371	OMIM:615268	TAS				P		HPO:skoehler	
OMIM	615269	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA; HH19		HP:0000006	OMIM:615269	TAS				I		HPO:skoehler	
OMIM	615269	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA; HH19		HP:0000164	OMIM:615269	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615269	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA; HH19		HP:0000365	OMIM:615269	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615269	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA; HH19		HP:0000938	OMIM:615269	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615269	HYPOGONADOTROPIC HYPOGONADISM 19 WITH OR WITHOUT ANOSMIA; HH19		HP:0000939	OMIM:615269	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615270	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA; HH20		HP:0000006	OMIM:615270	TAS				I		HPO:skoehler	
OMIM	615270	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA; HH20		HP:0000135	OMIM:615270	IEA				P		HPO:skoehler	
OMIM	615270	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA; HH20		HP:0000823	OMIM:615270	TAS				P		HPO:skoehler	
OMIM	615270	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA; HH20		HP:0000938	OMIM:615270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615270	HYPOGONADOTROPIC HYPOGONADISM 20 WITH OR WITHOUT ANOSMIA; HH20		HP:0000939	OMIM:615270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615271	HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA; HH21		HP:0000006	OMIM:615271	TAS				I		HPO:skoehler	
OMIM	615271	HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA; HH21		HP:0000365	OMIM:615271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615271	HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA; HH21		HP:0000938	OMIM:615271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615271	HYPOGONADOTROPIC HYPOGONADISM 21 WITH OR WITHOUT ANOSMIA; HH21		HP:0000939	OMIM:615271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0000007	OMIM:615272	TAS				I		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0000252	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0000369	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0002032	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0003593	OMIM:615272	TAS				C		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0004322	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0005528	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0005912	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615272	#615272 FANCONI ANEMIA, COMPLEMENTATION GROUP Q; FANCQ		HP:0009777	OMIM:615272	TAS				P		HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000007	PMID:24651605	PCS				I	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000248	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000252	PMID:24651605	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	6/8
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000275	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000297	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000316	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000463	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000486	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000508	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000522	PMID:24651605	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000711	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	2/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000939	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000954	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000970	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0000975	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001250	PMID:24651605,PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	4/8
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001263	PMID:24651605,PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	8/8
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001265	PMID:24651605	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	6/8
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001271	PMID:25220016	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001290	OMIM:615273	TAS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001310	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001336	OMIM:615273	IEA				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001773	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0001945	PMID:25220016	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002072	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002098	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002151	OMIM:615273	IEA		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	HP:0040284
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002205	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002240	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002305	PMID:27388694	IEA				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002345	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002487	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002650	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0002910	PMID:24651605	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	6/7
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0003448	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	2/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0004325	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0006254	OMIM:615273	IEA		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	HP:0040284
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0007021	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	2/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0007957	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	2/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0008954	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0009938	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0010536	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	1/11
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv	HP:0012825	HP:0012448	PMID:24651605	TAS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	1/2
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0012520	OMIM:615273	IEA				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0012531	PMID:25220016	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0012706	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0012708	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0012804	OMIM:615273	IEA				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0025455	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0025458	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0025460	PMID:27388694	PCS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0025460	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0030906	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	10/11
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0030978	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:probinson	7/9
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0030980	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	12/12
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0031146	PMID:27388694	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	10/11
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0031162	PMID:27388694	IEA		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HP:probinson	11/11
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0200055	OMIM:61527	TAS				P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:skoehler	
OMIM	615273	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iv; CDG1V;;CDG Iv; CDGIv		HP:0200136	PMID:25220016	PCS		HP:0040284		P	#615273 CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IV; CDG1V;;CDG IV; CDGIV	HPO:lccarmody	2/2
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0000006	OMIM:615274	TAS				I		HPO:probinson	
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0000518	OMIM:615274	TAS				P		HPO:probinson	
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0000519	OMIM:615274	IEA				P		HPO:skoehler	
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0007971	OMIM:615274	IEA				P		HPO:skoehler	
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0100018	OMIM:615274	IEA				P		HPO:skoehler	
OMIM	615274	CATARACT 15, MULTIPLE TYPES; CTRCT15		HP:0100019	OMIM:615274	IEA				P		HPO:skoehler	
OMIM	615277	CATARACT 19, MULTIPLE TYPES; CTRCT19		HP:0000007	PMID:11917274	PCS				I		HPO:probinson	
OMIM	615277	CATARACT 19, MULTIPLE TYPES; CTRCT19		HP:0000639	OMIM:615277	TAS				P		HPO:skoehler	
OMIM	615277	CATARACT 19, MULTIPLE TYPES; CTRCT19		HP:0000646	OMIM:615277	IEA				P		HPO:skoehler	
OMIM	615277	CATARACT 19, MULTIPLE TYPES; CTRCT19		HP:0007780	PMID:11917274	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000006	PMID:21797849	PCS				I		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000218	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000280	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000337	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000358	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000369	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000463	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000508	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0000545	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0001263	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0001634	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0002212	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0002213	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0002223	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0003477	PMID:21797849	PCS				P		HPO:probinson	
OMIM	615278	#615278 CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2		HP:0008070	OMIM:615278	TAS				P		HPO:probinson	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0000154	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0000639	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0000767	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0000975	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001250	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001252	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001263	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001508	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001639	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0001642	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0002046	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0002212	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0002650	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0004349	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0008050	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615279	#615279 CARDIOFACIOCUTANEOUS SYNDROME 3; CFC3		HP:0040180	OMIM:615279	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000341	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000348	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000486	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000506	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000519	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000545	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000609	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000639	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000766	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000974	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0000975	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001003	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001252	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001263	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001321	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001642	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0001646	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0002046	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0002079	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0002223	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0002650	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0004322	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0010438	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615280	#615280 CARDIOFACIOCUTANEOUS SYNDROME 4; CFC4		HP:0030047	OMIM:615280	IEA				P		HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0000007	OMIM:615281	TAS				I	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0000639	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0001256	OMIM:615281	TAS		HP:0040283		P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	HP:0040283
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0001257	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0001270	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0001347	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0002079	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0002352	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0003429	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0003487	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0003593	OMIM:615281	TAS				C	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0003676	OMIM:615281	TAS				C	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615281	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-tRNA SYNTHETASE DEFICIENCY		HP:0008936	OMIM:615281	TAS				P	#615281 HYPOMYELINATION WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LEGSPASTICITY; HBSL;;ASPARTYL-TRNA SYNTHETASE DEFICIENCY	HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0000006	OMIM:615282	TAS				I		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0000252	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0001250	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0001263	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0001344	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0001511	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0001989	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0002079	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0002126	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0002510	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0002539	OMIM:615282	IEA				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0002804	OMIM:615282	TAS				P		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0003577	OMIM:615282	TAS				C		HPO:skoehler	
OMIM	615282	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2		HP:0003828	OMIM:615282	TAS				C		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000007	OMIM:615284	TAS				I		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000020	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000252	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000486	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000602	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0000762	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0001159	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0001249	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0001284	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0001288	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0001763	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0002650	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0002936	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0003383	OMIM:615284	TAS				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0003676	OMIM:615284	TAS				C		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0003690	OMIM:615284	IEA				P		HPO:skoehler	
OMIM	615284	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3		HP:0012444	OMIM:615284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0000007	OMIM:615285	TAS				I		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001263	OMIM:615285	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001508	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001744	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001873	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001875	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001882	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001903	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0001978	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0002240	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0002719	OMIM:615285	IEA				P		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0003593	OMIM:615285	TAS				C		HPO:skoehler	
OMIM	615285	NEUTROPENIA, SEVERE CONGENITAL, 5, AUTOSOMAL RECESSIVE; SCN5		HP:0010702	OMIM:615285	TAS				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000007	OMIM:615286	TAS				I		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000252	OMIM:615286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000286	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000348	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000506	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000565	OMIM:615286	TAS				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000582	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000718	OMIM:615286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000752	OMIM:615286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0000824	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001249	OMIM:615286	TAS				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001250	OMIM:615286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001257	OMIM:615286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001274	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001290	OMIM:615286	TAS				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001508	OMIM:615286	TAS				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0001999	OMIM:615286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0003593	OMIM:615286	TAS				C		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0011220	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0012444	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615286	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 36; MRT36		HP:0012448	OMIM:615286	IEA				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000007	OMIM:615287	TAS				I		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000054	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000107	OMIM:615287	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000110	OMIM:615287	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000126	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000238	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0000618	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001093	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001250	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001257	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001263	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001274	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001305	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0001321	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0002085	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0002282	OMIM:615287	IEA				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0002323	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0002365	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0002539	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0003236	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0003560	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0003577	OMIM:615287	TAS				C		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0006829	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0007260	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0007759	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0007973	OMIM:615287	TAS				P		HPO:skoehler	
OMIM	615287	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13; MDDGA13		HP:0008734	OMIM:615287	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0000006	OMIM:615290	TAS				I		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001257	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2	HP:0012839	HP:0001265	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001270	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2	HP:0012839	HP:0001284	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001347	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001385	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001762	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0001771	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0002380	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0002515	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003273	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003307	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003327	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003391	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003691	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0003828	OMIM:615290	TAS				C		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0006380	OMIM:615290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0007269	OMIM:615290	IEA				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0009046	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615290	#615290 SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2, AUTOSOMALDOMINANT; SMALED2		HP:0040083	OMIM:615290	TAS				P		HPO:skoehler	
OMIM	615293	#615293 MYOFIBROMATOSIS, INFANTILE, 2; IMF2		HP:0000006	OMIM:615293	TAS				I		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0000007	OMIM:615294	TAS				I		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0000403	OMIM:615294	TAS				P		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0002110	OMIM:615294	TAS				P		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0011109	OMIM:615294	TAS				P		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0012265	OMIM:615294	IEA				P		HPO:skoehler	
OMIM	615294	CILIARY DYSKINESIA, PRIMARY, 21; CILD21		HP:0100750	OMIM:615294	TAS				P		HPO:skoehler	
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0000007	OMIM:615297	TAS				I		HPO:skoehler	
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0000965	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001537	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001629	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001631	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001643	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001800	OMIM:615297	TAS				P		HPO:skoehler	
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0001831	OMIM:615297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615297	#615297 ADAMS-OLIVER SYNDROME 4; AOS4		HP:0100797	OMIM:615297	TAS				P		HPO:skoehler	
OMIM	615298	#615298 SYMPHALANGISM, PROXIMAL, 1B; SYM1B		HP:0001763	OMIM:615298	IEA				P		HPO:skoehler	
OMIM	615298	#615298 SYMPHALANGISM, PROXIMAL, 1B; SYM1B		HP:0006143	OMIM:615298	IEA				P		HPO:skoehler	
OMIM	615298	#615298 SYMPHALANGISM, PROXIMAL, 1B; SYM1B		HP:0009177	OMIM:615298	IEA				P		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0000007	OMIM:615300	TAS				I		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0000013	OMIM:615300	TAS				P		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0000130	OMIM:615300	IEA				P		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0000786	OMIM:615300	IEA				P		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0001730	OMIM:615300	IEA				P		HPO:skoehler	
OMIM	615300	PERRAULT SYNDROME 4		HP:0008209	OMIM:615300	IEA				P		HPO:skoehler	
OMIM	615312	%615312 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0000007	OMIM:615312	TAS				I		HPO:skoehler	
OMIM	615312	%615312 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0000613	OMIM:615312	TAS				P		HPO:skoehler	
OMIM	615312	%615312 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0000639	OMIM:615312	TAS				P		HPO:skoehler	
OMIM	615312	%615312 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0001022	OMIM:615312	IEA				P		HPO:skoehler	
OMIM	615312	%615312 ALBINISM, OCULOCUTANEOUS, TYPE V; OCA5		HP:0007750	OMIM:615312	TAS				P		HPO:skoehler	
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000006	OMIM:615314	TAS				I		HPO:skoehler	
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000294	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000486	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000508	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000717	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0000954	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0001156	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0001263	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0001363	OMIM:615314	IEA				P		HPO:skoehler	
OMIM	615314	#615314 CRANIOSYNOSTOSIS 3; CRS3		HP:0001822	OMIM:615314	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R		HP:0000007	OMIM:615325	TAS				I		HPO:skoehler	
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R		HP:0002987	OMIM:615325	TAS				P		HPO:skoehler	
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R		HP:0003560	OMIM:615325	TAS				P		HPO:skoehler	
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R		HP:0003676	OMIM:615325	TAS				C		HPO:skoehler	
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R	HP:0012825	HP:0003691	OMIM:615325	TAS				P		HPO:skoehler	
OMIM	615325	#615325 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2R; LGMD2R	HP:0012825	HP:0010628	OMIM:615325	TAS				P		HPO:skoehler	
OMIM	615327	#615327 DOWLING-DEGOS DISEASE 2; DDD2		HP:0000006	PMID:25229252	PCS				I		HPO:skoehler	
OMIM	615327	#615327 DOWLING-DEGOS DISEASE 2; DDD2		HP:0007502	OMIM:615327	TAS				P		HPO:probinson	
OMIM	615327	#615327 DOWLING-DEGOS DISEASE 2; DDD2		HP:0007588	PMID:25229252	PCS				P		HPO:probinson	
OMIM	615327	#615327 DOWLING-DEGOS DISEASE 2; DDD2		HP:0009719	OMIM:615327	TAS				P		HPO:probinson	
OMIM	615327	#615327 DOWLING-DEGOS DISEASE 2; DDD2		HP:0045059	PMID:25229252	PCS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000007	OMIM:615328	TAS				I		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000252	OMIM:615328	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000670	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000750	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000966	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0000972	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0001249	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0003577	OMIM:615328	TAS				C		HPO:skoehler	
OMIM	615328	#615328 SHAHEEN SYNDROME; SHNS		HP:0006297	OMIM:615328	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000007	OMIM:615330	TAS				I		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000218	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000252	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000278	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000505	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000639	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000648	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000737	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0000969	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001250	OMIM:615330	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001298	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001511	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001561	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001942	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0001954	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002059	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002079	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002126	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002376	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002415	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002510	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002804	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0002878	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0003128	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0003287	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0003577	OMIM:615330	TAS				C		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0003676	OMIM:615330	IEA				C		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0003828	OMIM:615330	IEA				C		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0006610	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0006829	OMIM:615330	TAS				P		HPO:skoehler	
OMIM	615330	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 3; MMDS3		HP:0100543	OMIM:615330	IEA				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0000007	OMIM:615338	TAS				I		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0000572	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0000648	OMIM:615338	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16	HP:0012828	HP:0001263	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0001269	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0001290	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0001332	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0001336	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0002059	OMIM:615338	IEA				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0002071	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0002133	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0002376	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0003676	OMIM:615338	TAS				C		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0005484	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0006829	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0012448	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0025356	OMIM:615338	IEA				P		HPO:skoehler	
OMIM	615338	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16; EIEE16		HP:0200134	OMIM:615338	TAS				P		HPO:skoehler	
OMIM	615342	#615342 PULMONARY HYPERTENSION, PRIMARY, 2; PPH2		HP:0000006	OMIM:615342	TAS				I		HPO:skoehler	
OMIM	615342	#615342 PULMONARY HYPERTENSION, PRIMARY, 2; PPH2		HP:0002092	OMIM:615342	TAS				P		HPO:skoehler	
OMIM	615342	#615342 PULMONARY HYPERTENSION, PRIMARY, 2; PPH2		HP:0003676	OMIM:615342	TAS				C		HPO:skoehler	
OMIM	615342	#615342 PULMONARY HYPERTENSION, PRIMARY, 2; PPH2		HP:0003829	OMIM:615342	TAS				C		HPO:skoehler	
OMIM	615342	#615342 PULMONARY HYPERTENSION, PRIMARY, 2; PPH2		HP:0005317	OMIM:615342	TAS				P		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0000006	OMIM:615343	TAS				I		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0002092	OMIM:615343	IEA				P		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0002094	OMIM:615343	TAS				P		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0003829	OMIM:615343	TAS				C		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0004890	OMIM:615343	TAS				P		HPO:skoehler	
OMIM	615343	#615343 PULMONARY HYPERTENSION, PRIMARY, 3; PPH3		HP:0005317	OMIM:615343	TAS				P		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0000006	OMIM:615344	IEA				I		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0002092	OMIM:615344	IEA				P		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0003676	OMIM:615344	TAS				C		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0003829	OMIM:615344	TAS				C		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0005317	OMIM:615344	TAS				P		HPO:skoehler	
OMIM	615344	PULMONARY HYPERTENSION, PRIMARY, 4		HP:0011675	OMIM:615344	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615346	#615346 PRECOCIOUS PUBERTY, CENTRAL, 2; CPPB2		HP:0000006	OMIM:615346	TAS				I		HPO:skoehler	
OMIM	615346	#615346 PRECOCIOUS PUBERTY, CENTRAL, 2; CPPB2		HP:0005616	OMIM:615346	TAS				P		HPO:skoehler	
OMIM	615346	#615346 PRECOCIOUS PUBERTY, CENTRAL, 2; CPPB2		HP:0010314	OMIM:615346	TAS				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0000007	OMIM:615348	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0000765	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0001371	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0001989	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0002015	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0002375	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0002878	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0003715	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0003798	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615348	#615348 NEMALINE MYOPATHY 8; NEM8		HP:0010628	OMIM:615348	IEA				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000007	OMIM:615349	TAS				I		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000175	OMIM:615349	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000520	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000592	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000767	OMIM:615349	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000926	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000973	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0000974	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0001263	OMIM:615349	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0001290	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0001762	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0002656	OMIM:615349	IEA				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0002751	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0002827	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0003015	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0004233	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0004325	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0008070	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0009702	OMIM:615349	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0011220	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0011341	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615349	EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 2; EDSSPD2		HP:0012368	OMIM:615349	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0000007	OMIM:615350	TAS				I		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0000175	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0000252	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0000407	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001251	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001263	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001321	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001324	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001344	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0001562	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0002540	OMIM:615350	IEA				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0003236	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0003560	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0003577	OMIM:615350	TAS				C		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0010864	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0011968	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0012110	OMIM:615350	TAS				P		HPO:skoehler	
OMIM	615350	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 14; MDDGA14		HP:0030046	OMIM:615350	IEA				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000007	OMIM:615351	TAS				I		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000252	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000486	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000508	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000518	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0000639	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001249	OMIM:615351	IEA				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001250	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001263	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001276	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001290	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001321	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001344	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001371	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001558	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0001657	OMIM:615351	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0002058	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0002421	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0003236	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0003560	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0003741	OMIM:615351	IEA				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0003828	OMIM:615351	TAS				C		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0009055	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0011968	OMIM:615351	TAS				P		HPO:skoehler	
OMIM	615351	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14; MDDGB14		HP:0030046	OMIM:615351	IEA				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0000007	OMIM:615352	TAS				I		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0000252	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0000518	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0000639	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0001250	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0001256	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0001270	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0001290	OMIM:615352	TAS				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0001638	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0002093	OMIM:615352	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0003236	OMIM:615352	TAS				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0003546	OMIM:615352	TAS				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0003560	OMIM:615352	TAS				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0003701	OMIM:615352	TAS				P		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0003828	OMIM:615352	TAS				C		HPO:skoehler	
OMIM	615352	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 14; MDDGC14		HP:0030046	OMIM:615352	IEA				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000006	OMIM:615355	TAS				I		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000028	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	9/13
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000286	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000316	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000369	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000465	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	15/21
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000470	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000494	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000508	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000766	PMID:25124994	PCS				P		HPO:probinson	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000766	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	5/19
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000953	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	6/17
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000962	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0000974	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	6/17
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001249	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	4/18
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001508	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001561	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001629	PMID:25124994	PCS				P		HPO:probinson	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001631	PMID:25124994	PCS				P		HPO:probinson	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001639	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001642	OMIM:615355	TAS				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001643	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	3/22
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0001712	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	14/23
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0002202	OMIM:615355	IEA				P		HPO:skoehler	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0002212	PMID:25124994	PCS				P		HPO:probinson	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0002212	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	9/20
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0004322	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	7/20
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0004482	PMID:25124994	PCS				P		HPO:probinson	
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0004482	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	11/19
OMIM	615355	NOONAN SYNDROME 8; NS8		HP:0007517	PMID:25124994	PCS		HP:0040284		P		HPO:probinson	8/16
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000007	OMIM:615356	TAS				I		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000252	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000486	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000518	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000522	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0000545	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001249	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001250	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001251	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001260	OMIM:615356	IEA				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001263	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001272	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001290	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001332	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001337	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001385	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001397	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0001511	OMIM:615356	IEA				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002059	OMIM:615356	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002072	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002240	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002305	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002353	OMIM:615356	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002355	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002465	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002515	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002540	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002571	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002650	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0002910	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003236	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003307	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003326	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003391	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003394	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0003429	OMIM:615356	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0004322	OMIM:615356	TAS				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0006785	OMIM:615356	IEA				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0011098	OMIM:615356	IEA				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0011968	OMIM:615356	IEA				P		HPO:skoehler	
OMIM	615356	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S; LGMD2S		HP:0100633	OMIM:615356	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615360	Leber congenital amaurosis 17		HP:0000007	PMID:23307924	PCS				I	LEBER CONGENITAL AMAUROSIS 17	HPO:skoehler	
OMIM	615360	Leber congenital amaurosis 17		HP:0032284	PMID:23307924	TAS		HP:0040284		P	LEBER CONGENITAL AMAUROSIS 17	HP:probinson	1/1
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0000006	OMIM:615361	TAS				I		HPO:skoehler	
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0002135	OMIM:615361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0002901	OMIM:615361	TAS				P		HPO:skoehler	
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0003394	OMIM:615361	TAS				P		HPO:skoehler	
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0003401	OMIM:615361	TAS				P		HPO:skoehler	
OMIM	615361	#615361 HYPOCALCEMIA, AUTOSOMAL DOMINANT 2; HYPOC2		HP:0008897	OMIM:615361	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0000007	OMIM:615362	TAS				I		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0000712	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0000716	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0000726	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001250	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001251	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001260	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001272	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001336	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001337	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0001347	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0002071	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0002476	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0002506	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0003487	OMIM:615362	TAS				P		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0003581	OMIM:615362	TAS				C		HPO:skoehler	
OMIM	615362	CEROID LIPOFUSCINOSIS, NEURONAL, 13; CLN13		HP:0003676	OMIM:615362	TAS				C		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000007	OMIM:615363	TAS				I		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000013	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000786	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000842	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000938	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0000956	OMIM:615363	IEA				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0001061	OMIM:615363	IEA				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0001952	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615363	ESTROGEN RESISTANCE; ESTRR		HP:0002750	OMIM:615363	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0000007	OMIM:615368	TAS				I		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0000573	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0000762	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0000883	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001284	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001290	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001371	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001518	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001522	OMIM:615368	TAS				M		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001558	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0001561	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0002093	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0002803	OMIM:615368	IEA				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0003236	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0003577	OMIM:615368	TAS				C		HPO:skoehler	
OMIM	615368	LETHAL CONGENITAL CONTRACTURE SYNDROME 5		HP:0003687	OMIM:615368	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0000006	OMIM:615369	TAS				I		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0000729	OMIM:615369	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0000992	OMIM:615369	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0001249	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0001263	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002121	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002123	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002133	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002353	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002373	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0002376	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0010819	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615369	#615369 EPILEPTIC ENCEPHALOPATHY, CHILDHOOD-ONSET; EEOC		HP:0200134	OMIM:615369	TAS				P		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0000006	OMIM:615373	TAS				I		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0001635	OMIM:615373	TAS				P		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0001644	OMIM:615373	IEA				P		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0001653	OMIM:615373	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0001711	OMIM:615373	TAS				P		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0005162	OMIM:615373	IEA				P		HPO:skoehler	
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0011675	OMIM:615373	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615373	LEFT VENTRICULAR NONCOMPACTION 8; LVNC8		HP:0030682	OMIM:615373	IEA				P		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0000007	OMIM:615374	TAS				I		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0000548	OMIM:615374	IEA				P		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0000603	OMIM:615374	TAS				P		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0008001	OMIM:615374	TAS				P		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0011003	OMIM:615374	TAS				P		HPO:skoehler	
OMIM	615374	CONE-ROD DYSTROPHY 18		HP:0025010	OMIM:615374	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0000007	OMIM:615376	TAS				I		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0001284	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0001761	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0001765	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0002460	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0002936	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0003387	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0003431	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615376	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE C		HP:0008180	OMIM:615376	TAS				P		HPO:skoehler	
OMIM	615377	ATRIAL FIBRILLATION, FAMILIAL, 13; ATFB13		HP:0000006	OMIM:615377	TAS				I		HPO:skoehler	
OMIM	615377	ATRIAL FIBRILLATION, FAMILIAL, 13; ATFB13		HP:0001650	OMIM:615377	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615377	ATRIAL FIBRILLATION, FAMILIAL, 13; ATFB13		HP:0004757	OMIM:615377	TAS				P		HPO:skoehler	
OMIM	615377	ATRIAL FIBRILLATION, FAMILIAL, 13; ATFB13		HP:0031295	OMIM:615377	IEA				P		HPO:skoehler	
OMIM	615378	#615378 ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14		HP:0000006	PMID:19808477	PCS				I		HPO:probinson	
OMIM	615378	#615378 ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14		HP:0000822	OMIM:615378	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615378	#615378 ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14		HP:0004757	PMID:19808477	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	615378	#615378 ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14		HP:0012248	PMID:19808477	PCS		HP:0040284		P		HPO:probinson	1/2
OMIM	615378	#615378 ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14		HP:0012251	PMID:19808477	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000006	OMIM:615381	TAS				I		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000028	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000135	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000160	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000347	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000407	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000444	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000520	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000678	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000819	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000855	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0000939	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0001009	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0001371	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0001397	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0001620	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0002155	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0002240	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0002650	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0002808	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0002910	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0004334	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0009125	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0100324	OMIM:615381	IEA				P		HPO:skoehler	
OMIM	615381	MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL		HP:0100679	OMIM:615381	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0000007	OMIM:615382	TAS				I		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0000083	OMIM:615382	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0000090	OMIM:615382	IEA				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0000105	OMIM:615382	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0000113	OMIM:615382	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001395	OMIM:615382	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001396	OMIM:615382	TAS				P		HPO:skoehler	
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001639	OMIM:615382	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001642	OMIM:615382	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001643	OMIM:615382	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001650	OMIM:615382	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615382	#615382 NEPHRONOPHTHISIS 16; NPHP16		HP:0001696	OMIM:615382	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0000007	OMIM:615386	TAS				I		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0000571	OMIM:615386	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0000639	OMIM:615386	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0000750	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0001257	OMIM:615386	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0001263	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0001272	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0001310	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0001347	OMIM:615386	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0002066	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0002075	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0002080	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0003593	OMIM:615386	TAS				C		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0003677	OMIM:615386	TAS				C		HPO:skoehler	
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0008003	OMIM:615386	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615386	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14		HP:0100543	OMIM:615386	TAS				P		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0000007	OMIM:615387	TAS				I		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0001508	OMIM:615387	TAS				P		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0002716	OMIM:615387	TAS				P		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0002719	OMIM:615387	TAS				P		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0002960	OMIM:615387	TAS				P		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0003593	OMIM:615387	TAS				C		HPO:skoehler	
OMIM	615387	T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY		HP:0032061	OMIM:615387	IEA				P		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0000007	OMIM:615395	TAS				I		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0001414	OMIM:615395	TAS				P		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0001639	OMIM:615395	TAS				P		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16	HP:0012825	HP:0002151	OMIM:615395	TAS				P		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0002910	OMIM:615395	TAS				P		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0003593	OMIM:615395	TAS				C		HPO:skoehler	
OMIM	615395	#615395 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 16; COXPD16		HP:0003828	OMIM:615395	TAS				C		HPO:skoehler	
OMIM	615396	#615396 LEFT VENTRICULAR NONCOMPACTION 10; LVNC10CARDIOMYOPATHY, DILATED, 1MM, INCLUDED; CMD1MM, INCLUDED		HP:0000006	OMIM:615396	TAS				I		HPO:skoehler	
OMIM	615396	#615396 LEFT VENTRICULAR NONCOMPACTION 10; LVNC10CARDIOMYOPATHY, DILATED, 1MM, INCLUDED; CMD1MM, INCLUDED		HP:0001644	OMIM:615396	TAS				P		HPO:skoehler	
OMIM	615396	#615396 LEFT VENTRICULAR NONCOMPACTION 10; LVNC10CARDIOMYOPATHY, DILATED, 1MM, INCLUDED; CMD1MM, INCLUDED		HP:0030682	OMIM:615396	IEA				P		HPO:skoehler	
OMIM	615397	#615397 MECKEL SYNDROME, TYPE 11; MKS11		HP:0000007	OMIM:615397	TAS				I		HPO:skoehler	
OMIM	615397	#615397 MECKEL SYNDROME, TYPE 11; MKS11		HP:0000113	OMIM:615397	TAS				P		HPO:skoehler	
OMIM	615397	#615397 MECKEL SYNDROME, TYPE 11; MKS11		HP:0001562	OMIM:615397	TAS				P		HPO:skoehler	
OMIM	615397	#615397 MECKEL SYNDROME, TYPE 11; MKS11		HP:0002085	OMIM:615397	TAS				P		HPO:skoehler	
OMIM	615397	#615397 MECKEL SYNDROME, TYPE 11; MKS11		HP:0010442	OMIM:615397	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000007	OMIM:615398	TAS				I		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000071	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000107	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000121	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000164	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000194	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000218	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000248	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3	HP:0012825	HP:0000256	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000341	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000343	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000348	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000463	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000486	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000505	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000540	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000565	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000639	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000767	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000938	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0000939	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001250	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001251	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001263	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001272	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001290	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001321	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3	HP:0012825	HP:0001520	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001643	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0001723	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002002	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002059	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002150	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002353	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002376	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002650	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002714	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0002750	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0003022	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0003186	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0003196	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0003487	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0003593	OMIM:615398	TAS				C		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0005280	OMIM:615398	TAS				P		HPO:skoehler	
OMIM	615398	MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 3; MCAHS3		HP:0011448	OMIM:615398	IEA				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0000006	OMIM:615399	TAS				I		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0001025	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0001428	OMIM:615399	TAS				I		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0001878	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0002014	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0002027	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0002094	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0002315	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0002829	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0004818	OMIM:615399	IEA				P		HPO:skoehler	
OMIM	615399	#615399 PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2		HP:0012378	OMIM:615399	TAS				P		HPO:skoehler	
OMIM	615400	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5; FAME5		HP:0000007	OMIM:615400	TAS				I		HPO:skoehler	
OMIM	615400	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5; FAME5		HP:0001337	OMIM:615400	IEA				P		HPO:skoehler	
OMIM	615400	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5; FAME5		HP:0002069	OMIM:615400	TAS				P		HPO:skoehler	
OMIM	615400	EPILEPSY, FAMILIAL ADULT MYOCLONIC, 5; FAME5		HP:0011157	OMIM:615400	IEA				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0000007	OMIM:615401	TAS				I		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0000752	OMIM:615401	TAS				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0001263	OMIM:615401	TAS				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0001888	OMIM:615401	TAS				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0002205	OMIM:615401	TAS				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0002721	OMIM:615401	IEA				P		HPO:skoehler	
OMIM	615401	#615401 IMMUNODEFICIENCY 8; IMD8		HP:0003593	OMIM:615401	TAS				C		HPO:skoehler	
OMIM	615402	Dyschromatosis universalis hereditaria 3		HP:0000006	PMID:23519333	PCS				I	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3	HPO:skoehler	
OMIM	615402	Dyschromatosis universalis hereditaria 3		HP:0001034	PMID:23519333	PCS	HP:0011463			P	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3	HP:probinson	
OMIM	615402	Dyschromatosis universalis hereditaria 3		HP:0020073	PMID:23519333	PCS	HP:0011463			P	DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3	HP:probinson	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0000006	OMIM:615411	TAS				I		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0000252	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0000639	OMIM:615411	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0001250	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0001263	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0001302	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0001511	OMIM:615411	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0002079	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0002282	OMIM:615411	IEA				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0002510	OMIM:615411	TAS				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0002539	OMIM:615411	IEA				P		HPO:skoehler	
OMIM	615411	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 3; CDCBM3		HP:0031882	OMIM:615411	IEA				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0000006	OMIM:615412	TAS				I		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0000252	OMIM:615412	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0000518	OMIM:615412	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0001250	OMIM:615412	TAS				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0001263	OMIM:615412	TAS				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0001302	OMIM:615412	IEA				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0002282	OMIM:615412	IEA				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0002510	OMIM:615412	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0002539	OMIM:615412	IEA				P		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0003828	OMIM:615412	TAS				C		HPO:skoehler	
OMIM	615412	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 4; CDCBM4		HP:0031882	OMIM:615412	IEA				P		HPO:skoehler	
OMIM	615413	Spermatogenic failure 12		HP:0000006	PMID:23315541	PCS				I	SPERMATOGENIC FAILURE 12	HPO:skoehler	
OMIM	615413	Spermatogenic failure 12		HP:0000027	PMID:23315541	PCS				P	SPERMATOGENIC FAILURE 12	HPO:skoehler	
OMIM	615413	Spermatogenic failure 12		HP:0000789	PMID:23315541	PCS				P	SPERMATOGENIC FAILURE 12	HPO:skoehler	
OMIM	615413	Spermatogenic failure 12		HP:0012863	PMID:23315541	PCS				P	SPERMATOGENIC FAILURE 12	HPO:lccarmody	
OMIM	615414	#615414 MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE; MCPH11		HP:0000007	OMIM:615414	TAS				I		HPO:skoehler	
OMIM	615414	#615414 MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE; MCPH11		HP:0000252	OMIM:615414	TAS				P		HPO:skoehler	
OMIM	615414	#615414 MICROCEPHALY 11, PRIMARY, AUTOSOMAL RECESSIVE; MCPH11		HP:0004322	OMIM:615414	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0000007	OMIM:615415	TAS				I		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0000105	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0000800	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001395	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001396	OMIM:615415	IEA				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001562	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001639	OMIM:615415	IEA				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001642	OMIM:615415	IEA				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001650	OMIM:615415	IEA				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001660	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001696	OMIM:615415	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001746	OMIM:615415	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0001762	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0002089	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0002240	OMIM:615415	IEA				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0002980	OMIM:615415	TAS				P		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0003577	OMIM:615415	TAS				C		HPO:skoehler	
OMIM	615415	RENAL-HEPATIC-PANCREATIC DYSPLASIA 2; RHPD2		HP:0003826	OMIM:615415	TAS				M		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0000007	OMIM:615418	TAS				I		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0000518	OMIM:615418	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0001324	OMIM:615418	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0001513	OMIM:615418	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0001639	OMIM:615418	TAS				P		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0003128	OMIM:615418	TAS				P		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0003202	OMIM:615418	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0003326	OMIM:615418	TAS				P		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0003546	OMIM:615418	TAS				P		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0003677	OMIM:615418	TAS				C		HPO:skoehler	
OMIM	615418	#615418 MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE); MTDPS12		HP:0100543	OMIM:615418	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000007	OMIM:615419	TAS				I		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000028	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000154	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000219	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000248	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000252	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000319	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000325	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000347	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000369	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000400	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000417	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000486	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000639	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000648	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000768	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0000817	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0001250	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1	HP:0012829	HP:0001263	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0001347	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0002019	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0002020	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0002465	OMIM:615419	IEA				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0002510	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0002650	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0003196	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0003202	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0003431	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0003676	OMIM:615419	TAS				C		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0007256	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1	HP:0012828	HP:0008897	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0008936	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0011220	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0011968	OMIM:615419	TAS				P		HPO:skoehler	
OMIM	615419	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 1; IHPRF1		HP:0025356	OMIM:615419	IEA				P		HPO:skoehler	
OMIM	615420	#615420 MYOPIA 22, AUTOSOMAL DOMINANT; MYP22		HP:0000006	OMIM:615420	TAS				I		HPO:skoehler	
OMIM	615420	#615420 MYOPIA 22, AUTOSOMAL DOMINANT; MYP22		HP:0000545	OMIM:615420	IEA				P		HPO:skoehler	
OMIM	615420	#615420 MYOPIA 22, AUTOSOMAL DOMINANT; MYP22		HP:0007663	OMIM:615420	TAS				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0000708	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0000924	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0002145	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0003198	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0003202	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0003236	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0003560	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0003687	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0100295	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615422	#615422 INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 2; IBMPFD2 ;;MULTISYSTEM PROTEINOPATHY 2; MSP2		HP:0100614	OMIM:615422	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0000006	OMIM:615424	IEA				I		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0003155	OMIM:615424	TAS				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0003198	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0003701	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0003805	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0006785	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0008180	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0010991	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615424	INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3; IBMPFD3		HP:0100299	OMIM:615424	IEA				P		HPO:skoehler	
OMIM	615425	#615425 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2; EBSB2		HP:0000007	OMIM:615425	TAS				I		HPO:skoehler	
OMIM	615425	#615425 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2; EBSB2		HP:0001075	OMIM:615425	TAS				P		HPO:skoehler	
OMIM	615425	#615425 EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 2; EBSB2		HP:0008404	OMIM:615425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0000006	PMID:23455423	PCS				I		HPO:probinson	
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0003155	PMID:23455423	PCS				P		HPO:probinson	
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0003560	PMID:23455423	PCS	HP:0003584			P		HPO:probinson	
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0003805	PMID:23455423	PCS				P		HPO:probinson	
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0007354	OMIM:615426	IEA				P		HPO:skoehler	
OMIM	615426	AMYOTROPHIC LATERAL SCLEROSIS 20; ALS20		HP:0100299	PMID:23455423	PCS				P		HPO:probinson	
OMIM	615429	#615429 DEAFNESS, AUTOSOMAL RECESSIVE 88; DFNB88		HP:0000007	OMIM:615429	TAS				I		HPO:skoehler	
OMIM	615429	#615429 DEAFNESS, AUTOSOMAL RECESSIVE 88; DFNB88		HP:0000365	OMIM:615429	IEA				P		HPO:skoehler	
OMIM	615431	#615431 MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23		HP:0000007	PMID:23830514	PCS				I		HPO:probinson	
OMIM	615431	#615431 MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23		HP:0000505	PMID:23830514	PCS				P		HPO:probinson	
OMIM	615431	#615431 MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23		HP:0007663	OMIM:615431	TAS				P		HPO:skoehler	
OMIM	615431	#615431 MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23		HP:0007800	PMID:23830514	PCS				P		HPO:probinson	
OMIM	615431	#615431 MYOPIA 23, AUTOSOMAL RECESSIVE; MYP23		HP:0011003	PMID:23830514	PCS				P		HPO:probinson	
OMIM	615432	#615432 SPECIFIC LANGUAGE IMPAIRMENT 5; SLI5		HP:0000006	OMIM:615432	TAS				I		HPO:skoehler	
OMIM	615432	#615432 SPECIFIC LANGUAGE IMPAIRMENT 5; SLI5		HP:0000729	OMIM:615432	TAS				P		HPO:skoehler	
OMIM	615432	#615432 SPECIFIC LANGUAGE IMPAIRMENT 5; SLI5		HP:0001263	OMIM:615432	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615432	#615432 SPECIFIC LANGUAGE IMPAIRMENT 5; SLI5		HP:0002463	OMIM:615432	TAS				P		HPO:skoehler	
OMIM	615432	#615432 SPECIFIC LANGUAGE IMPAIRMENT 5; SLI5		HP:0003829	OMIM:615432	TAS				C		HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000006	OMIM:615433	TAS				I	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000028	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000049	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000054	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000248	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000268	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000286	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000316	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000322	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000369	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000400	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000486	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000508	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000545	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000717	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0000750	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0001274	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0001357	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0002119	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0002705	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0006988	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0007018	OMIM:615433	TAS		HP:0040283		P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	615433	#615433 CHROMOSOME 3q13.31 DELETION SYNDROME		HP:0008734	OMIM:615433	TAS				P	#615433 CHROMOSOME 3Q13.31 DELETION SYNDROME	HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0000007	OMIM:615434	TAS				I		HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0000510	OMIM:615434	IEA				P		HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0000543	OMIM:615434	TAS				P		HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0001696	OMIM:615434	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0007401	OMIM:615434	IEA				P		HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0007663	OMIM:615434	TAS				P		HPO:skoehler	
OMIM	615434	RETINITIS PIGMENTOSA WITH OR WITHOUT SITUS INVERSUS		HP:0007787	OMIM:615434	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0000006	OMIM:615436	TAS				I		HPO:skoehler	
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0002647	OMIM:615436	IEA				P		HPO:skoehler	
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0005112	OMIM:615436	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0006702	OMIM:615436	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0012727	OMIM:615436	TAS				P		HPO:skoehler	
OMIM	615436	AORTIC ANEURYSM, FAMILIAL THORACIC 8; AAT8		HP:0030882	OMIM:615436	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0000007	PMID:22607940	PCS				I		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0000252	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0000293	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0000407	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001250	PMID:22607940	PCS				P		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001263	PMID:22607940	PCS				P		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001290	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001397	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001508	PMID:22607940	PCS				P		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001903	PMID:22607940	PCS				P		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0001972	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0002007	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0002194	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0002240	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0002910	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0003128	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0003256	OMIM:615438	TAS				P		HPO:skoehler	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0006554	PMID:22607940	PCS				P		HPO:probinson	
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0010511	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615438	INFANTILE LIVER FAILURE SYNDROME 1		HP:0100807	OMIM:615438	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0000006	OMIM:615439	TAS				I		HPO:skoehler	
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0000529	OMIM:615439	TAS				P		HPO:skoehler	
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0011506	OMIM:615439	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0011506	OMIM:615439	IEA				P		HPO:skoehler	
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0011510	OMIM:615439	IEA				P		HPO:skoehler	
OMIM	615439	MACULAR DEGENERATION, AGE-RELATED, 13; ARMD13		HP:0200056	OMIM:615439	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0000007	OMIM:615440	TAS				I		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0000252	OMIM:615440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0000365	OMIM:615440	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001263	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001290	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001508	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001510	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001635	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0001639	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615440	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17		HP:0003128	OMIM:615440	TAS				P		HPO:skoehler	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0000007	PMID:22422768	TAS				I		HPO:skoehler	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0001259	PMID:22422768	PCS				P		HPO:lccarmody	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0001279	PMID:22422768	PCS				P		HPO:lccarmody	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0001695	PMID:22422768	PCS				P		HPO:lccarmody	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0003701	PMID:22422768	PCS				P		HPO:skoehler	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0004756	PMID:22422768	IEA				P		HPO:skoehler	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0006682	OMIM:615441	IEA				P		HPO:skoehler	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0031273	PMID:22422768	PCS				P		HPO:lccarmody	
OMIM	615441	VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5		HP:0031677	PMID:22422768	PCS				P		HPO:lccarmody	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0000007	OMIM:615444	TAS				I		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0000403	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0000789	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0001696	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0002110	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0004469	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0011108	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0012207	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0012259	OMIM:615444	IEA				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0012265	OMIM:615444	IEA				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0012384	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0100582	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615444	CILIARY DYSKINESIA, PRIMARY, 22; CILD22		HP:0200073	OMIM:615444	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0000007	OMIM:615451	TAS				I		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0000403	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0001696	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0002110	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0004469	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0011108	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0012265	OMIM:615451	IEA				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0012384	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615451	CILIARY DYSKINESIA, PRIMARY, 23; CILD23		HP:0200073	OMIM:615451	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6		HP:0000007	OMIM:615453	TAS				I		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6		HP:0001298	OMIM:615453	IEA				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6	HP:0025303	HP:0001987	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6		HP:0002151	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6	HP:0025303	HP:0002910	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6	HP:0025303	HP:0003128	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6		HP:0005974	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615453	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6; MC3DN6	HP:0025303	HP:0006554	OMIM:615453	TAS				P		HPO:skoehler	
OMIM	615457	#615457 BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18; BMIQ18;;OBESITY, SUSCEPTIBILITY TO		HP:0000006	OMIM:615457	TAS				I		HPO:skoehler	
OMIM	615457	#615457 BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18; BMIQ18;;OBESITY, SUSCEPTIBILITY TO	HP:0012828	HP:0001513	OMIM:615457	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000007	OMIM:615458	TAS				I		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000358	OMIM:615458	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000445	OMIM:615458	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000455	OMIM:615458	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000482	OMIM:615458	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0000506	OMIM:615458	TAS				P		HPO:skoehler	
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0007787	OMIM:615458	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615458	MICROCORNEA, MYOPIC CHORIORETINAL ATROPHY, AND TELECANTHUS; MMCAT		HP:0200065	OMIM:615458	IEA				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000006	OMIM:615465	TAS				I		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000028	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000047	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000054	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000175	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000204	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000252	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000286	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000316	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000358	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000369	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000445	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000601	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0000873	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0001159	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS	HP:0012828	HP:0001263	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0001274	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0001319	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0001363	OMIM:615465	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0003228	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0005466	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0006870	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0008213	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0025356	OMIM:615465	IEA				P		HPO:skoehler	
OMIM	615465	HARTSFIELD SYNDROME; HRTFDS		HP:0100257	OMIM:615465	TAS				P		HPO:skoehler	
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0000007	OMIM:615468	TAS				I		HPO:skoehler	
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0000939	OMIM:615468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0001510	OMIM:615468	TAS				P		HPO:skoehler	
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0002718	OMIM:615468	TAS				P		HPO:skoehler	
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0002721	OMIM:615468	TAS				P		HPO:skoehler	
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0002750	OMIM:615468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615468	#615468 IMMUNODEFICIENCY 12; IMD12		HP:0004429	OMIM:615468	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000007	OMIM:615471	TAS				I		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000047	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000232	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000252	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000275	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000286	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000411	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000494	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000518	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000574	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0000639	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001250	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001251	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)	HP:0012828	HP:0001263	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001266	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001272	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001290	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001298	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001332	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001357	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001508	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001510	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001518	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001639	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001773	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001875	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0001947	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002015	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002020	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002059	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002079	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002151	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002415	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002650	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002719	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0002910	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0003128	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0003202	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0003348	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0011120	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0011675	OMIM:615471	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0012448	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615471	MITOCHONDRIAL DNA DEPLETION SYNDROME 13 (ENCEPHALOMYOPATHIC TYPE)		HP:0200125	OMIM:615471	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0000006	OMIM:615473	TAS				I		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0001263	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0001332	OMIM:615473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0001344	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0002059	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0002072	OMIM:615473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0002079	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0002305	OMIM:615473	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0002521	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0010818	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0012448	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615473	#615473 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 17; EIEE17		HP:0200134	OMIM:615473	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0000006	OMIM:615474	TAS				I		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0000787	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0000822	OMIM:615474	TAS	HP:0003623			P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0001263	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0001629	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0001655	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0001712	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0002069	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0002092	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0002305	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0002510	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0002900	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0003351	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0100021	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0100704	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0200114	OMIM:615474	TAS				P		HPO:skoehler	
OMIM	615474	PRIMARY ALDOSTERONISM, SEIZURES, AND NEUROLOGIC ABNORMALITIES		HP:0200128	OMIM:615474	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0000007	OMIM:615476	TAS				I		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0000348	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0000494	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0000508	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0001263	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0001265	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0001290	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0002121	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0002353	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0002553	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0007074	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0007359	OMIM:615476	TAS				P		HPO:skoehler	
OMIM	615476	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 18		HP:0200134	OMIM:615476	IEA				P		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24		HP:0000007	OMIM:615481	TAS				I		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24		HP:0000789	OMIM:615481	TAS				P		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24		HP:0002110	OMIM:615481	TAS				P		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24		HP:0011108	OMIM:615481	TAS				P		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24		HP:0012265	OMIM:615481	IEA				P		HPO:skoehler	
OMIM	615481	CILIARY DYSKINESIA, PRIMARY, 24; CILD24	HP:0031796	HP:0012384	OMIM:615481	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0000007	OMIM:615482	TAS				I		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0000789	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0001696	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0002110	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0003593	OMIM:615482	TAS				C		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0006510	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0011108	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0012263	OMIM:615482	TAS				P		HPO:skoehler	
OMIM	615482	CILIARY DYSKINESIA, PRIMARY, 25; CILD25		HP:0012265	OMIM:615482	IEA				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000006	OMIM:615483	TAS				I		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000709	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000716	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000726	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000739	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0000741	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0001260	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0001300	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0002072	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0002076	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0002135	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0002305	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0002321	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0003676	OMIM:615483	TAS				C		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0100034	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615483	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5; IBGC5		HP:0100660	OMIM:615483	TAS				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000154	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000218	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000232	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000252	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000316	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000426	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000455	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000486	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000494	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0000582	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0001249	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0001250	OMIM:615485	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0001344	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0001508	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0001519	OMIM:615485	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0002079	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0002540	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0002553	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0003196	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0008850	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0011344	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0011968	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615485	BAINBRIDGE-ROPERS SYNDROME; BRPS		HP:0031936	OMIM:615485	IEA				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0000007	OMIM:615486	TAS				I		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0000821	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001217	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001394	OMIM:615486	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001397	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001410	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001508	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001903	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0001941	OMIM:615486	IEA				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0002093	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0002094	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0002240	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0002910	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0003355	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0003676	OMIM:615486	TAS				C		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0003828	OMIM:615486	TAS				C		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0006517	OMIM:615486	IEA				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0006530	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615486	INTERSTITIAL LUNG AND LIVER DISEASE; ILLD		HP:0012735	OMIM:615486	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0000007	OMIM:615490	TAS				I		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001284	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001290	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001324	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001605	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001761	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0001762	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0002093	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0002136	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0002540	OMIM:615490	IEA				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0002779	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0003199	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0003380	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0003477	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0006380	OMIM:615490	TAS				P		HPO:skoehler	
OMIM	615490	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R; CMT2R		HP:0040078	OMIM:615490	IEA				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0000007	OMIM:615491	TAS				I		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0000529	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0000545	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0000639	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0000648	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001258	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001272	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001310	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001371	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001761	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0001763	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002059	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002080	OMIM:615491	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002180	OMIM:615491	IEA				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002273	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002380	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002411	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002486	OMIM:615491	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0002599	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0003487	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0003676	OMIM:615491	TAS				C		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0007141	OMIM:615491	IEA				P		HPO:skoehler	
OMIM	615491	SPASTIC PARAPLEGIA 79, AUTOSOMAL RECESSIVE; SPG79		HP:0011448	OMIM:615491	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0000007	OMIM:615493	TAS				I		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0000718	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0000752	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0001250	OMIM:615493	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0001257	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0001290	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0002342	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615493	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37		HP:0003763	OMIM:615493	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0000007	OMIM:615500	TAS				I		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0000403	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0000789	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0001696	OMIM:615500	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0002110	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0004469	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0011108	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0012207	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0012256	OMIM:615500	IEA				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0012265	OMIM:615500	IEA				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26	HP:0031796	HP:0012384	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615500	CILIARY DYSKINESIA, PRIMARY, 26; CILD26		HP:0200073	OMIM:615500	TAS				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0000817	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0001263	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0001321	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0001347	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0002059	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0002069	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0002126	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0002179	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0002421	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0003166	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0003537	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0003570	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0003643	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0005268	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0008936	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0011968	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615501	MOLYBDENUM COFACTOR DEFICIENCY, COMPLEMENTATION GROUP C; MOCODC		HP:0012110	OMIM:615501	IEA				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000006	OMIM:615502	TAS				I		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000028	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000164	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000175	OMIM:615502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000233	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000252	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000486	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000540	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0000729	OMIM:615502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001249	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001263	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001290	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001631	OMIM:615502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001643	OMIM:615502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0001680	OMIM:615502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0004322	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615502	MENTAL RETARDATION, AUTOSOMAL DOMINANT 21		HP:0011968	OMIM:615502	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000007	OMIM:615503	TAS				I		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000062	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000256	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000773	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000774	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0001156	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0001159	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0001508	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0001561	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0001629	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0002089	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0002980	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0003026	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0004322	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0005280	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0006644	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0010454	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0100258	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0100259	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615503	#615503 SHORT RIB-POLYDACTYLY SYNDROME, TYPE VI; SRPS6		HP:0100732	OMIM:615503	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0000007	OMIM:615504	TAS				I		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0000403	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0002110	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0004469	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0011108	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0012265	OMIM:615504	IEA				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27	HP:0031796	HP:0012384	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615504	CILIARY DYSKINESIA, PRIMARY, 27; CILD27		HP:0200073	OMIM:615504	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0000007	OMIM:615505	TAS				I		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0000403	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0001696	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0002110	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0004469	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0011108	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0012265	OMIM:615505	IEA				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28	HP:0031796	HP:0012384	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615505	CILIARY DYSKINESIA, PRIMARY, 28; CILD28		HP:0200073	OMIM:615505	TAS				P		HPO:skoehler	
OMIM	615506	#615506 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5		HP:0000006	OMIM:615506	TAS				I		HPO:skoehler	
OMIM	615506	#615506 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5		HP:0001009	OMIM:615506	TAS				P		HPO:skoehler	
OMIM	615506	#615506 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5		HP:0001409	OMIM:615506	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615506	#615506 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5		HP:0002910	OMIM:615506	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615506	#615506 TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 5; HHT5		HP:0004406	OMIM:615506	TAS				P		HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0000007	OMIM:615508	TAS				I	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0000982	OMIM:615508	IEA				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001006	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001019	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001510	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001581	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001629	OMIM:615508	TAS		HP:0040283		P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	HP:0040283
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0001642	OMIM:615508	TAS		HP:0040283		P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	HP:0040283
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0002205	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0003228	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0003765	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0025114	OMIM:615508	IEA				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0040162	OMIM:615508	IEA				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615508	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IgE; EPKHE		HP:0100792	OMIM:615508	TAS				P	ERYTHRODERMA, CONGENITAL, WITH PALMOPLANTAR KERATODERMA, HYPOTRICHOSIS, AND HYPER-IGE; EPKHE	HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000007	OMIM:615510	TAS				I		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000365	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000486	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000522	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000639	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000962	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0000966	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001249	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001263	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001278	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001288	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001290	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0001611	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0002015	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0002571	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0003474	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0009916	OMIM:615510	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615510	ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME		HP:0011968	OMIM:615510	TAS				P		HPO:skoehler	
OMIM	615511	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY		HP:0000007	OMIM:615511	TAS				I		HPO:skoehler	
OMIM	615511	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY		HP:0001290	OMIM:615511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615511	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY		HP:0001324	OMIM:615511	TAS				P		HPO:skoehler	
OMIM	615511	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY		HP:0003201	OMIM:615511	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615511	MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY		HP:0003750	OMIM:615511	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0000007	OMIM:615512	TAS				I		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0000543	OMIM:615512	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0000952	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001081	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001082	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001257	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001263	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001265	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001290	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001332	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001337	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001635	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001744	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001895	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0001897	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0002317	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0002747	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0002808	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0003198	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0003202	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0003323	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0004870	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615512	TRIOSEPHOSPHATE ISOMERASE DEFICIENCY		HP:0009830	OMIM:615512	TAS				P		HPO:skoehler	
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0000006	PMID:24136356	PCS				I		HPO:skoehler	
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0001744	PMID:24136356	PCS		HP:0040284		P		HPO:skoehler	10/17
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0002110	PMID:24136356	PCS		HP:0040284		P		HPO:skoehler	12/16
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0002716	PMID:24165795	PCS		HP:0040284		P		HPO:skoehler	5/7
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0002721	PMID:24165795	PCS				P		HPO:skoehler	
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0003496	PMID:24136356	PCS		HP:0040284		P		HP:probinson	14/17
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0005403	PMID:24136356	PCS		HP:0040284		P		HP:probinson	12/17
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0005425	PMID:24165795	PCS	HP:0011463			P		HPO:skoehler	
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0008348	PMID:24136356	PCS		HP:0040284		P		HP:probinson	10/11
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0012476	PMID:24136356	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0030381	PMID:24136356	PCS		HP:0040284		P		HP:probinson	14/16
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0030388	PMID:24136356	PCS		HP:0040284		P		HP:probinson	8/16
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0100658	PMID:24136356	PCS				P		HPO:skoehler	
OMIM	615513	#615513 IMMUNODEFICIENCY 14; IMD14;;ACTIVATED PI3K-DELTA SYNDROME; APDS;;P110-DELTA-ACTIVATING MUTATION CAUSING SENESCENT T CELLS, LYMPHADENOPATHY,AND IMMUNODEFICIENCY; PASLI		HP:0410018	PMID:24136356	PCS		HP:0040284		P		HPO:skoehler	17/17
OMIM	615515	AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19		HP:0000006	OMIM:615515	TAS				I		HPO:skoehler	
OMIM	615515	AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19		HP:0002747	OMIM:615515	TAS				P		HPO:skoehler	
OMIM	615515	AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19		HP:0003581	OMIM:615515	TAS				C		HPO:skoehler	
OMIM	615515	AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19		HP:0006957	OMIM:615515	TAS				P		HPO:skoehler	
OMIM	615515	AMYOTROPHIC LATERAL SCLEROSIS 19; ALS19		HP:0007354	OMIM:615515	IEA				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000007	OMIM:615516	TAS				I		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000189	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000303	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000486	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000635	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000718	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000742	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0000752	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001249	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001250	OMIM:615516	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001263	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001290	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001357	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0001852	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0002317	OMIM:615516	TAS				P		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0003593	OMIM:615516	TAS				C		HPO:skoehler	
OMIM	615516	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 38; MRT38		HP:0031987	OMIM:615516	IEA				P		HPO:skoehler	
OMIM	615517	#615517 HEMOCHROMATOSIS, TYPE 5; HFE5;;IRON OVERLOAD, AUTOSOMAL DOMINANT		HP:0000006	OMIM:615517	TAS				I		HPO:skoehler	
OMIM	615517	#615517 HEMOCHROMATOSIS, TYPE 5; HFE5;;IRON OVERLOAD, AUTOSOMAL DOMINANT		HP:0003281	OMIM:615517	TAS				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0000006	OMIM:615518	TAS				I		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0000403	OMIM:615518	TAS				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0001888	OMIM:615518	TAS				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0002090	OMIM:615518	IEA				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0002721	OMIM:615518	IEA				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0011108	OMIM:615518	TAS				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0011945	OMIM:615518	TAS				P		HPO:skoehler	
OMIM	615518	IMMUNODEFICIENCY 13; IMD13		HP:0032275	OMIM:615518	IEA				P		HPO:skoehler	
OMIM	615522	COLE DISEASE; COLED		HP:0000006	OMIM:615522	TAS				I		HPO:skoehler	
OMIM	615522	COLE DISEASE; COLED		HP:0000962	OMIM:615522	TAS				P		HPO:skoehler	
OMIM	615522	COLE DISEASE; COLED		HP:0000982	OMIM:615522	IEA				P		HPO:skoehler	
OMIM	615522	COLE DISEASE; COLED		HP:0025092	OMIM:615522	TAS				P		HPO:skoehler	
OMIM	615522	COLE DISEASE; COLED		HP:0025114	OMIM:615522	TAS				P		HPO:skoehler	
OMIM	615523	#615523 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8; FECD8		HP:0000006	OMIM:615523	TAS				I		HPO:skoehler	
OMIM	615523	#615523 CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8; FECD8		HP:0001131	OMIM:615523	IEA				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000006	OMIM:615524	TAS				I		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000007	OMIM:615524	TAS				I		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000028	OMIM:615524	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000278	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000347	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000431	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000455	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000528	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000568	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000776	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0000813	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0001249	OMIM:615524	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0001629	OMIM:615524	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0002089	OMIM:615524	TAS				P		HPO:skoehler	
OMIM	615524	MICROPHTHALMIA, SYNDROMIC 12		HP:0005156	OMIM:615524	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615527	#615527 CANDIDIASIS, FAMILIAL, 8; CANDF8;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:615527	TAS				I		HPO:skoehler	
OMIM	615527	#615527 CANDIDIASIS, FAMILIAL, 8; CANDF8;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0000158	OMIM:615527	TAS				P		HPO:skoehler	
OMIM	615527	#615527 CANDIDIASIS, FAMILIAL, 8; CANDF8;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0000498	OMIM:615527	TAS				P		HPO:skoehler	
OMIM	615527	#615527 CANDIDIASIS, FAMILIAL, 8; CANDF8;;CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL RECESSIVE		HP:0012203	OMIM:615527	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0000007	OMIM:615528	TAS				I		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0000571	OMIM:615528	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0000738	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001249	OMIM:615528	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001250	OMIM:615528	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001257	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001260	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001300	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001332	OMIM:615528	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0001337	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0002063	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0002067	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0002172	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0002362	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0003677	OMIM:615528	TAS				C		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0003678	OMIM:615528	TAS				C		HPO:skoehler	
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0007256	OMIM:615528	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615528	PARKINSON DISEASE 19A, JUVENILE-ONSET		HP:0100543	OMIM:615528	TAS				P		HPO:skoehler	
OMIM	615529	#615529 CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO; CRS5		HP:0000006	OMIM:615529	TAS				I		HPO:skoehler	
OMIM	615529	#615529 CRANIOSYNOSTOSIS 5, SUSCEPTIBILITY TO; CRS5		HP:0001363	OMIM:615529	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0000007	OMIM:615530	TAS				I		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0000605	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0000658	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001260	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001268	OMIM:615530	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001300	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001332	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001337	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0001621	OMIM:615530	IEA				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0002063	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0002067	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0002172	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0002362	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0003676	OMIM:615530	TAS				C		HPO:skoehler	
OMIM	615530	PARKINSON DISEASE 20, EARLY-ONSET; PARK20		HP:0025401	OMIM:615530	TAS				P		HPO:skoehler	
OMIM	615537	RETICULATE ACROPIGMENTATION OF KITAMURA; RAK		HP:0000006	OMIM:615537	TAS				I		HPO:skoehler	
OMIM	615537	RETICULATE ACROPIGMENTATION OF KITAMURA; RAK		HP:0000962	OMIM:615537	IEA				P		HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0000418	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0000463	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0000537	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0000582	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0001250	OMIM:615538	IEA				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0001263	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0002591	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0003745	OMIM:615538	TAS				I	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0007018	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615538	CHROMOSOME 22q13 DUPLICATION SYNDROME		HP:0007302	OMIM:615538	TAS				P	CHROMOSOME 22Q13 DUPLICATION SYNDROME	HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000007	OMIM:615539	TAS				I		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000023	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000160	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000218	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000248	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000297	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000316	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000343	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000411	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000494	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000506	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000592	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0000678	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0001166	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0001181	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0001634	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0001653	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0001655	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2	HP:0012832	HP:0001762	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0002007	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0002059	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0002194	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0002829	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0003324	OMIM:615539	TAS				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0003326	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0011800	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615539	EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2; EDSMC2		HP:0012385	OMIM:615539	IEA				P		HPO:skoehler	
OMIM	615540	#615540 DEAFNESS, AUTOSOMAL RECESSIVE 76; DFNB76		HP:0000007	OMIM:615540	TAS				I		HPO:skoehler	
OMIM	615540	#615540 DEAFNESS, AUTOSOMAL RECESSIVE 76; DFNB76		HP:0000408	OMIM:615540	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000007	OMIM:615541	TAS				I		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000252	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000340	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000400	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000448	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000486	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000490	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000664	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000718	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000733	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39	HP:0012828	HP:0000750	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0000752	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0001249	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0001263	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0002751	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0003593	OMIM:615541	TAS				C		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0004322	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615541	#615541 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39		HP:0040080	OMIM:615541	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0000006	OMIM:615542	TAS				I		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0000028	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0000051	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0000054	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0000062	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0001636	OMIM:615542	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0008715	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615542	#615542 TESTICULAR ANOMALIES WITH OR WITHOUT CONGENITAL HEART DISEASE; TACHD		HP:0030260	OMIM:615542	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0000006	OMIM:615544	TAS				I		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0000486	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0000750	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0001250	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0001263	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0002282	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615544	#615544 PERIVENTRICULAR NODULAR HETEROTOPIA 6; PVNH6		HP:0002521	OMIM:615544	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000007	OMIM:615546	TAS				I		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000028	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000047	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000048	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000054	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000089	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000218	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000260	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000272	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000286	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000316	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000327	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000341	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000347	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000405	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000407	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000413	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000431	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000508	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000581	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000689	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000774	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000894	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000938	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0000960	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0001249	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0001290	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0001388	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0001510	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0001762	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002079	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002282	OMIM:615546	IEA				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002650	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002652	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002714	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0002779	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0003577	OMIM:615546	TAS				C		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0004689	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0008551	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0010044	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0010537	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0010554	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0010804	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0011800	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0011968	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0012745	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0030084	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615546	VAN MALDERGEM SYNDROME 2; VMLDS2		HP:0040079	OMIM:615546	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000006	OMIM:615547	TAS				I		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000028	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000054	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000135	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000194	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000278	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000280	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000288	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000303	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000341	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000545	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000565	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0000574	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001156	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001182	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001249	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001250	OMIM:615547	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001263	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001319	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001344	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001371	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001513	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001531	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001773	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001838	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0001989	OMIM:615547	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002007	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002019	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002020	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002540	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002591	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002650	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002804	OMIM:615547	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0002808	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0003593	OMIM:615547	TAS				C		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0004283	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0004322	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0010535	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0011968	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0012385	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0012745	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0030084	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0031936	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0100710	OMIM:615547	IEA				P		HPO:skoehler	
OMIM	615547	SCHAAF-YANG SYNDROME; SHFYNG		HP:0200055	OMIM:615547	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0000006	OMIM:615548	TAS				I		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0000975	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0000989	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7	HP:0012825	HP:0001270	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7	HP:0012825	HP:0001324	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0002014	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0002019	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0007021	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0012332	OMIM:615548	TAS				P		HPO:skoehler	
OMIM	615548	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII; HSAN7		HP:0100716	OMIM:615548	IEA				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0000006	OMIM:615550	TAS				I		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0001199	OMIM:615550	TAS				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0001629	OMIM:615550	TAS				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0001895	OMIM:615550	TAS				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0001896	OMIM:615550	TAS				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0001972	OMIM:615550	TAS				P		HPO:skoehler	
OMIM	615550	#615550 DIAMOND-BLACKFAN ANEMIA 12; DBA12		HP:0030270	OMIM:615550	TAS				P		HPO:probinson	
OMIM	615551	EPISODIC PAIN SYNDROME, FAMILIAL, 2		HP:0000006	OMIM:615551	TAS				I		HPO:skoehler	
OMIM	615551	EPISODIC PAIN SYNDROME, FAMILIAL, 2		HP:0003581	OMIM:615551	TAS				C		HPO:skoehler	
OMIM	615551	EPISODIC PAIN SYNDROME, FAMILIAL, 2		HP:0031005	OMIM:615551	TAS				P		HPO:skoehler	
OMIM	615552	EPISODIC PAIN SYNDROME, FAMILIAL, 3		HP:0000006	OMIM:615552	TAS				I		HPO:skoehler	
OMIM	615552	EPISODIC PAIN SYNDROME, FAMILIAL, 3		HP:0012332	OMIM:615552	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	615552	EPISODIC PAIN SYNDROME, FAMILIAL, 3		HP:0012531	OMIM:615552	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0000007	OMIM:615553	TAS				I		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0000252	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0000308	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0000729	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0001249	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0001250	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0001263	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0001290	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0002804	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0002827	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0004976	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615553	ARTHROGRYPOSIS, MENTAL RETARDATION, AND SEIZURES		HP:0100490	OMIM:615553	TAS				P		HPO:skoehler	
OMIM	615554	#615554 MULTIPLE FIBROADENOMAS OF THE BREAST; MFAB		HP:0000006	PMID:18779591	PCS				I		HPO:skoehler	
OMIM	615554	#615554 MULTIPLE FIBROADENOMAS OF THE BREAST; MFAB	HP:0030651	HP:0010619	PMID:18779591	PCS				P		HP:probinson	
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000006	OMIM:615555	TAS				I		HPO:skoehler	
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000007	OMIM:615555	IEA				I		HPO:skoehler	
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000132	OMIM:615555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000789	OMIM:615555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000870	OMIM:615555	TAS				P		HPO:skoehler	
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0000876	OMIM:615555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0031109	OMIM:615555	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615555	HYPERPROLACTINEMIA; HPRL		HP:0100829	OMIM:615555	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0000007	OMIM:615558	TAS				I		HPO:skoehler	
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0000510	OMIM:615558	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0000546	OMIM:615558	TAS				P		HPO:skoehler	
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0001251	OMIM:615558	TAS				P		HPO:skoehler	
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0001315	OMIM:615558	TAS				P		HPO:skoehler	
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0001927	OMIM:615558	TAS				P		HPO:skoehler	
OMIM	615558	#615558 HYPOBETALIPOPROTEINEMIA, FAMILIAL, 1; FHBL1;;HYPOBETALIPOPROTEINEMIA, FAMILIAL; FHBL;;ACANTHOCYTOSIS WITH HYPOBETALIPOPROTEINEMIA;;HYPOBETALIPOPROTEINEMIA, NORMOTRIGLYCERIDEMIC		HP:0003563	OMIM:615558	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0000007	OMIM:615559	TAS				I		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0000100	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0001744	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0001878	OMIM:615559	IEA				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0001973	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0002240	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0002716	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0002719	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0002829	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0003593	OMIM:615559	TAS				C		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0012578	OMIM:615559	TAS				P		HPO:skoehler	
OMIM	615559	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3		HP:0100827	OMIM:615559	IEA				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000007	OMIM:615560	TAS				I		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000265	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000308	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000369	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000410	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000522	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000592	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000670	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0000689	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0001182	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0002342	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0003691	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2	HP:0012832	HP:0004467	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0007678	OMIM:615560	TAS				P		HPO:skoehler	
OMIM	615560	OTOFACIOCERVICAL SYNDROME 2		HP:0030084	OMIM:615560	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615561	#615561 COMPLEMENT FACTOR B DEFICIENCY; CFBD		HP:0002090	OMIM:615561	IEA				P		HPO:skoehler	
OMIM	615561	#615561 COMPLEMENT FACTOR B DEFICIENCY; CFBD		HP:0002586	OMIM:615561	IEA				P		HPO:skoehler	
OMIM	615561	#615561 COMPLEMENT FACTOR B DEFICIENCY; CFBD		HP:0005381	OMIM:615561	IEA				P		HPO:skoehler	
OMIM	615561	#615561 COMPLEMENT FACTOR B DEFICIENCY; CFBD		HP:0005416	OMIM:615561	IEA				P		HPO:skoehler	
OMIM	615565	#615565 RETINITIS PIGMENTOSA 67; RP67		HP:0000007	OMIM:615565	TAS				I		HPO:skoehler	
OMIM	615565	#615565 RETINITIS PIGMENTOSA 67; RP67		HP:0000510	OMIM:615565	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0000007	OMIM:615573	TAS				I		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0000093	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0000097	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0000100	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0000969	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0003073	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0003676	OMIM:615573	TAS				C		HPO:skoehler	
OMIM	615573	NEPHROTIC SYNDROME, TYPE 9; NPHS9		HP:0003774	OMIM:615573	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0000007	OMIM:615574	TAS				I		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0000253	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0000340	OMIM:615574	IEA				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0000347	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0000400	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001176	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001250	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY	HP:0003676	HP:0001298	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001321	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001347	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001508	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0001833	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002079	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002093	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002119	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002267	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002510	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002521	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0002539	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0003676	OMIM:615574	TAS				C		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0008936	OMIM:615574	IEA				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0009879	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0011968	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0012110	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0012448	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0012736	OMIM:615574	TAS				P		HPO:probinson	
OMIM	615574	ASPARAGINE SYNTHETASE DEFICIENCY		HP:0100704	OMIM:615574	TAS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0000006	OMIM:615575	TAS				I		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0001761	OMIM:615575	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0002355	PMID:24207122	PCS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0002380	PMID:24207122	PCS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003394	OMIM:615575	TAS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003431	PMID:24207122	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003444	PMID:24207122	PCS				P		HPO:probinson	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003677	OMIM:615575	TAS				C		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003701	PMID:24207122	PCS		HP:0040284		P		HPO:probinson	11/11
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0003828	OMIM:615575	TAS				C		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0007210	OMIM:615575	TAS				P		HPO:probinson	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0007269	PMID:24207122	PCS				P		HPO:probinson	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0007340	OMIM:615575	TAS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0009005	OMIM:615575	TAS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0009046	PMID:24207122	PCS				P		HPO:skoehler	
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0009072	PMID:24207122	PCS		HP:0040284		P		HPO:probinson	10/11
OMIM	615575	#615575 NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; HMN2D;;HMN IID;;NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IID; DHMN2D;;SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL DOMINANT, CALF-PREDOMINANT		HP:0031108	OMIM:615575	TAS				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0000006	OMIM:615577	TAS				I		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0000824	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0001263	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0001596	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0001943	OMIM:615577	IEA				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0002099	OMIM:615577	TAS				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0002205	OMIM:615577	TAS				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0002721	OMIM:615577	IEA				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0003765	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0003828	OMIM:615577	TAS				C		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0004313	OMIM:615577	TAS				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0008404	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0011734	OMIM:615577	TAS				P		HPO:skoehler	
OMIM	615577	IMMUNODEFICIENCY, COMMON VARIABLE, 10; CVID10		HP:0030804	OMIM:615577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0000007	OMIM:615578	TAS				I		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0000505	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0000750	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001256	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001290	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001310	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001337	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001511	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0001972	OMIM:615578	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0002151	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0003128	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0003202	OMIM:615578	TAS				P		HPO:skoehler	
OMIM	615578	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 18		HP:0003828	OMIM:615578	TAS				C		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000006	PMID:25835445	PCS				I		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000023	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000098	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	12/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000175	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	5/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000193	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	11/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000218	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000248	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000268	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000276	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5	HP:0012825	HP:0000278	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000283	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000316	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	14/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000319	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000494	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000508	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000520	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000577	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000592	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5	HP:0012825	HP:0000767	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	11/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000768	PMID:25835445	PCS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0000978	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001166	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	16/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001265	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001270	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001319	OMIM:615582	TAS				P		HP:probinson	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001342	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001382	PMID:25835445	PCS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001518	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001629	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001653	PMID:25835445	PCS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001655	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001659	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001762	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0001763	OMIM:615582	TAS		HP:0040284		P		HPO:skoehler	14/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0002036	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0002751	PMID:25835445	PCS		HP:0040284		P		HPO:skoehler	11/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0002758	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0003199	PMID:25835445	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0003302	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0004322	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0004933	PMID:25835445	PCS		HP:0040284		P		HP:probinson	3/43
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0010646	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0010665	PMID:25835445	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0011800	OMIM:615582	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0012771	OMIM:615582	TAS				P		HPO:skoehler	
OMIM	615582	LOEYS-DIETZ SYNDROME 5		HP:0410151	PMID:23608731	PCS				P		HPO:lccarmody	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000006	OMIM:615583	TAS				I	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000089	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000104	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000107	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000219	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000252	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000341	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000343	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000431	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000470	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0000589	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0001263	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0001671	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0002059	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0002650	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0002827	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0002937	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0002948	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0003196	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0003577	OMIM:615583	TAS				C	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0004322	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0009237	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0011968	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615583	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8q24.3 DELETION SYNDROME		HP:0030084	OMIM:615583	TAS				P	#615583 VERHEIJ SYNDROME; VRJS;;CHROMOSOME 8Q24.3 DELETION SYNDROME	HPO:skoehler	
OMIM	615589	%615589 OTOSCLEROSIS 10; OTSC10		HP:0000006	OMIM:615589	TAS				I		HPO:skoehler	
OMIM	615589	%615589 OTOSCLEROSIS 10; OTSC10		HP:0000362	OMIM:615589	IEA				P		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0000007	OMIM:615592	TAS				I		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0001508	OMIM:615592	TAS				P		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0002028	OMIM:615592	TAS				P		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0002721	OMIM:615592	TAS				P		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0003593	OMIM:615592	TAS				C		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0004432	OMIM:615592	TAS				P		HPO:skoehler	
OMIM	615592	#615592 IMMUNODEFICIENCY 15; IMD15		HP:0011947	OMIM:615592	TAS				P		HPO:skoehler	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0000007	PMID:23897980	PCS				I		HPO:probinson	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0001744	PMID:20156905	PCS				P		HPO:probinson	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0001876	PMID:20156905	PCS				P		HPO:probinson	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0002721	OMIM:615593	IEA				P		HPO:skoehler	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0003621	OMIM:615593	TAS				C		HPO:skoehler	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0004844	PMID:20156905	PCS				P		HPO:probinson	
OMIM	615593	IMMUNODEFICIENCY 16		HP:0100726	PMID:20156905	PCS	HP:0011463	HP:0040284		P		HPO:probinson	3/3
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0000007	OMIM:615595	TAS				I		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0001319	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0001397	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0001508	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0002098	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0003128	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615595	#615595 COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19; COXPD19		HP:0011968	OMIM:615595	TAS				P		HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0000007	OMIM:615596	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0000252	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001249	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001250	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001263	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001272	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001290	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0001508	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0003577	OMIM:615596	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0011968	OMIM:615596	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615596	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw; CDG1W		HP:0012345	OMIM:615596	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IW; CDG1W	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000007	OMIM:615597	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000028	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000046	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000054	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000252	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0000648	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001249	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001250	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X	HP:0012828	HP:0001263	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001272	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001290	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001410	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001508	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001511	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0001873	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0002098	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0003577	OMIM:615597	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0003819	OMIM:615597	TAS				M	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0011968	OMIM:615597	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615597	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ix; CDG1X		HP:0012345	OMIM:615597	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IX; CDG1X	HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0000007	OMIM:615598	TAS				I		HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0007410	OMIM:615598	TAS				P		HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0025080	OMIM:615598	TAS				P		HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0025092	OMIM:615598	TAS				P		HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0025114	OMIM:615598	TAS				P		HPO:skoehler	
OMIM	615598	PALMOPLANTAR KERATODERMA, NAGASHIMA TYPE; PPKN		HP:0032007	OMIM:615598	IEA				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0000007	OMIM:615599	TAS				I		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0000639	OMIM:615599	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001249	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001257	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001263	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001347	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001647	OMIM:615599	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0001760	OMIM:615599	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0002079	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0002465	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0003487	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0005484	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615599	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40		HP:0012448	OMIM:615599	TAS				P		HPO:skoehler	
OMIM	615604	#615604 L-FERRITIN DEFICIENCY; LFTD		HP:0000006	OMIM:615604	TAS				I		HPO:skoehler	
OMIM	615604	#615604 L-FERRITIN DEFICIENCY; LFTD		HP:0000007	OMIM:615604	TAS				I		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0000006	OMIM:615605	TAS				I		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0000093	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0001942	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0002748	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0002979	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0003076	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0003109	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0003355	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0003828	OMIM:615605	TAS				C		HPO:skoehler	
OMIM	615605	#615605 FANCONI RENOTUBULAR SYNDROME 3; FRTS3		HP:0004322	OMIM:615605	TAS				P		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000007	OMIM:615607	TAS				I		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000403	OMIM:615607	TAS				P		HPO:probinson	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000964	OMIM:615607	TAS				P		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0001508	OMIM:615607	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0001890	OMIM:615607	IEA		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002205	OMIM:615607	TAS				P		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002242	OMIM:615607	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002721	OMIM:615607	TAS				P		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0003828	OMIM:615607	IEA				C		HPO:skoehler	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0005415	OMIM:615607	TAS				P		HPO:probinson	
OMIM	615607	#615607 IMMUNODEFICIENCY 17; IMD17;;CD3-GAMMA DEFICIENCY;;SCID-LIKE IMMUNODEFICIENCY, T CELL-PARTIAL, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0031123	OMIM:615607	TAS				P		HPO:probinson	
OMIM	615612	DEVELOPMENTAL DYSPLASIA OF THE HIP 2; DDH2		HP:0000006	OMIM:615612	TAS				I		HPO:skoehler	
OMIM	615612	DEVELOPMENTAL DYSPLASIA OF THE HIP 2; DDH2		HP:0001385	PMID:23716478	PCS				P		HPO:nvasilevsky	
OMIM	615612	DEVELOPMENTAL DYSPLASIA OF THE HIP 2; DDH2		HP:0002673	OMIM:615612	IEA				P		HPO:skoehler	
OMIM	615612	DEVELOPMENTAL DYSPLASIA OF THE HIP 2; DDH2		HP:0008843	PMID:23716478	PCS		HP:0040284		P		HPO:nvasilevsky	40%
OMIM	615612	DEVELOPMENTAL DYSPLASIA OF THE HIP 2; DDH2		HP:0030838	OMIM:615612	TAS				P		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0000007	OMIM:615615	TAS				I		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0000403	OMIM:615615	TAS				P		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0001888	OMIM:615615	TAS		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0002205	OMIM:615615	TAS				P		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0002721	OMIM:615615	TAS				P		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0003593	OMIM:615615	TAS				C		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0003828	OMIM:615615	TAS				C		HPO:skoehler	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0030253	OMIM:615615	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0031123	OMIM:615615	TAS				P		HPO:probinson	
OMIM	615615	#615615 IMMUNODEFICIENCY 18; IMD18;;CD3-EPSILON DEFICIENCYIMMUNODEFICIENCY 18, SEVERE COMBINED IMMUNODEFICIENCY VARIANT, INCLUDED;;IMMUNODEFICIENCY 18, SCID VARIANT, INCLUDED		HP:0045080	PMID:15546002	PCS				P		HPO:probinson	
OMIM	615616	#615616 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 13; ARVC13		HP:0000006	OMIM:615616	TAS				I		HPO:skoehler	
OMIM	615616	#615616 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 13; ARVC13		HP:0004756	OMIM:615616	TAS				P		HPO:skoehler	
OMIM	615616	#615616 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13; ARVD13;;ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 13; ARVC13		HP:0011710	OMIM:615616	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000007	OMIM:615617	TAS				I		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0000403	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0001508	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0001888	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002014	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002205	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0002721	OMIM:615617	TAS				P		HPO:skoehler	
OMIM	615617	#615617 IMMUNODEFICIENCY 19; IMD19;;CD3-DELTA DEFICIENCY;;SEVERE COMBINED IMMUNODEFICIENCY, T CELL-NEGATIVE, B CELL-POSITIVE,NK CELL-POSITIVE;;SCID, T CELL-NEGATIVE, B CELL-POSITIVE, NK CELL-POSITIVE		HP:0003593	OMIM:615617	TAS				C		HPO:skoehler	
OMIM	615619	CHOLANGIOCARCINOMA		HP:0030153	OMIM:615619	IEA				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0000006	OMIM:615625	TAS				I		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0000007	OMIM:615625	TAS				I		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0001258	OMIM:615625	IEA				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0001347	OMIM:615625	TAS				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0001761	OMIM:615625	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0002064	OMIM:615625	TAS				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0002839	OMIM:615625	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0003487	OMIM:615625	TAS				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0003552	OMIM:615625	TAS				P		HPO:skoehler	
OMIM	615625	#615625 SPASTIC PARAPLEGIA 72, AUTOSOMAL RECESSIVE; SPG72SPASTIC PARAPLEGIA 72, AUTOSOMAL DOMINANT		HP:0003677	OMIM:615625	TAS				C		HPO:skoehler	
OMIM	615629	#615629 DEAFNESS, AUTOSOMAL DOMINANT 56; DFNA56		HP:0000006	OMIM:615629	TAS				I		HPO:skoehler	
OMIM	615629	#615629 DEAFNESS, AUTOSOMAL DOMINANT 56; DFNA56		HP:0000365	OMIM:615629	IEA				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000007	OMIM:615630	TAS				I		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000090	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000202	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000238	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000546	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000657	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000662	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000773	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001156	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001162	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001249	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001320	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001395	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001396	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001399	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001513	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001591	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001629	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001744	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0001952	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0002119	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0002240	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0002857	OMIM:615630	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0003026	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0004322	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0005257	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0006644	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0010230	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615630	#615630 SHORT-RIB THORACIC DYSPLASIA 10 WITH OR WITHOUT POLYDACTYLY; SRTD10		HP:0012622	OMIM:615630	TAS				P		HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0000007	OMIM:615631	TAS				I	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0000952	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0000980	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0001159	OMIM:615631	TAS		HP:0040283		P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	HP:0040283
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0001744	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0001792	OMIM:615631	TAS		HP:0040283		P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	HP:0040283
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0001923	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0002240	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0004322	OMIM:615631	TAS		HP:0040283		P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	HP:0040283
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0004447	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0010972	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0011273	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615631	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib; CDAN1B;;CDA, TYPE Ib		HP:0012132	OMIM:615631	TAS				P	#615631 ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE IB; CDAN1B;;CDA, TYPE IB	HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0000006	OMIM:615632	TAS				I		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0000962	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0001822	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0002600	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0002754	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0003040	OMIM:615632	IEA				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0003390	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0003474	OMIM:615632	IEA				P		HPO:skoehler	
OMIM	615632	NEUROPATHY, HEREDITARY SENSORY, TYPE IF; HSN1F		HP:0009771	OMIM:615632	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000007	OMIM:615633	TAS				I		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000028	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000121	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000510	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000750	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000774	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000888	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0001156	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0001513	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0001561	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0001591	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0002093	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0002205	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0003026	OMIM:615633	TAS				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0006644	OMIM:615633	IEA				P		HPO:skoehler	
OMIM	615633	#615633 SHORT-RIB THORACIC DYSPLASIA 11 WITH OR WITHOUT POLYDACTYLY; SRTD11		HP:0100259	OMIM:615633	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0000007	OMIM:615636	TAS				I		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0000107	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0000407	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0000486	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0000488	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0000508	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0000528	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0000657	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0001249	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0001251	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0001263	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0001290	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0001591	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0002079	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0002085	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0002089	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0002094	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0002104	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0002365	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0003577	OMIM:615636	TAS				C		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0003828	OMIM:615636	TAS				C		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0004719	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0007291	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615636	JOUBERT SYNDROME 21		HP:0009932	OMIM:615636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615636	JOUBERT SYNDROME 21		HP:0011933	OMIM:615636	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000007	OMIM:615637	TAS				I		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000256	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000278	OMIM:615637	IEA				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000303	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000455	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000494	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000733	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0000739	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0001249	OMIM:615637	IEA				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0001250	OMIM:615637	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0001263	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0001290	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0002007	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0003577	OMIM:615637	TAS				C		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0004209	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615637	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41		HP:0030799	OMIM:615637	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0000007	OMIM:615643	TAS				I		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0000716	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0000722	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0001260	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0001263	OMIM:615643	IEA				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0001265	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0001268	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0001761	OMIM:615643	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002063	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002067	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002079	OMIM:615643	IEA				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002180	OMIM:615643	IEA				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002313	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002376	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0002510	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0003676	OMIM:615643	TAS				C		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0003693	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0007002	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0012048	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615643	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6; NBIA6		HP:0040083	OMIM:615643	TAS				P		HPO:skoehler	
OMIM	615649	%615649 DEAFNESS, AUTOSOMAL DOMINANT 54; DFNA54		HP:0000006	OMIM:615649	TAS				I		HPO:skoehler	
OMIM	615649	%615649 DEAFNESS, AUTOSOMAL DOMINANT 54; DFNA54		HP:0000365	OMIM:615649	IEA				P		HPO:skoehler	
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0000007	OMIM:615651	TAS				I		HPO:skoehler	
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0000532	OMIM:615651	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0001123	OMIM:615651	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0001138	OMIM:615651	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0002066	OMIM:615651	TAS				P		HPO:skoehler	
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0002070	OMIM:615651	TAS				P		HPO:skoehler	
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0002315	OMIM:615651	TAS				P		HPO:skoehler	
OMIM	615651	#615651 LEUKOENCEPHALOPATHY WITH ATAXIA; LKPAT		HP:0002352	OMIM:615651	TAS				P		HPO:skoehler	
OMIM	615654	%615654 DEAFNESS, AUTOSOMAL DOMINANT 58; DFNA58		HP:0000006	OMIM:615654	TAS				I		HPO:skoehler	
OMIM	615654	%615654 DEAFNESS, AUTOSOMAL DOMINANT 58; DFNA58		HP:0000360	OMIM:615654	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615654	%615654 DEAFNESS, AUTOSOMAL DOMINANT 58; DFNA58		HP:0000365	OMIM:615654	IEA				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000006	OMIM:615656	TAS				I		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000175	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000316	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000337	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000722	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000729	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0000750	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001238	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001249	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001250	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001251	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001263	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001290	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001357	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0001627	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0002312	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0003829	OMIM:615656	TAS				C		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0007018	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0011968	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615656	CHROMOSOME 15Q11.2 DELETION SYNDROME		HP:0040082	OMIM:615656	TAS				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0000007	OMIM:615658	TAS				I		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0000572	OMIM:615658	TAS				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0000648	OMIM:615658	TAS				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0001258	OMIM:615658	IEA				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0001347	OMIM:615658	TAS				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0002540	OMIM:615658	IEA				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0003474	OMIM:615658	IEA				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0003487	OMIM:615658	TAS				P		HPO:skoehler	
OMIM	615658	SPASTIC PARAPLEGIA 57, AUTOSOMAL RECESSIVE; SPG57		HP:0007141	OMIM:615658	IEA				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000007	OMIM:615663	TAS				I		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000028	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000046	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000054	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000160	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000248	OMIM:615663	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000294	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000431	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000482	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000490	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000501	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000508	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4	HP:0012832	HP:0000519	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0000568	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4	HP:0003676	HP:0000648	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0001007	OMIM:615663	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0001250	OMIM:615663	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0001272	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0001371	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0002079	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0002120	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0002510	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0003199	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0005484	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0007095	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0008734	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0008850	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615663	#615663 WARBURG MICRO SYNDROME 4; WARBM4		HP:0010864	OMIM:615663	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0000007	OMIM:615665	TAS				I		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0000089	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0000550	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0000568	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0000589	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0001159	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0001162	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0001263	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0001511	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0001999	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0002419	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615665	#615665 JOUBERT SYNDROME 22; JBTS22		HP:0007973	OMIM:615665	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000006	OMIM:615668	TAS				I		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000331	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000343	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000347	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000358	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000448	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000508	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000565	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000637	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0000750	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001249	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001250	OMIM:615668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001263	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001290	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001510	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0001519	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0002003	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0002615	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0009765	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0010511	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0045082	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615668	CHROMOSOME 5Q12 DELETION SYNDROME		HP:0100807	OMIM:615668	TAS				P		HPO:skoehler	
OMIM	615670	#615670 SCHWANNOMATOSIS 2; SWNTS2		HP:0000006	OMIM:615670	TAS				I		HPO:skoehler	
OMIM	615670	#615670 SCHWANNOMATOSIS 2; SWNTS2		HP:0003828	OMIM:615670	TAS				C		HPO:skoehler	
OMIM	615670	#615670 SCHWANNOMATOSIS 2; SWNTS2		HP:0003829	OMIM:615670	TAS				C		HPO:skoehler	
OMIM	615670	#615670 SCHWANNOMATOSIS 2; SWNTS2		HP:0010302	OMIM:615670	TAS				P		HPO:skoehler	
OMIM	615670	#615670 SCHWANNOMATOSIS 2; SWNTS2		HP:0100008	OMIM:615670	TAS				P		HPO:skoehler	
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0000007	PMID:24336167	PCS				I		HPO:probinson	
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0000252	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0000508	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0000602	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0000648	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0001251	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0001270	OMIM:615673	TAS				P		HPO:skoehler	
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0001328	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	15/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0001332	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	10/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0001337	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	10/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0002071	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	10/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0002072	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	10/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0002310	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	10/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0002355	OMIM:615673	TAS				P		HPO:skoehler	
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0003236	OMIM:615673	TAS				P		HPO:skoehler	
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0003477	OMIM:615673	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0003701	PMID:24336167	PCS		HP:0040284		P		HPO:probinson	15/15
OMIM	615673	MYOPATHY WITH EXTRAPYRAMIDAL SIGNS		HP:0009046	OMIM:615673	TAS				P		HPO:skoehler	
OMIM	615674	%615674 DOWLING-DEGOS DISEASE 3; DDD3		HP:0000006	OMIM:615674	TAS				I		HPO:skoehler	
OMIM	615674	%615674 DOWLING-DEGOS DISEASE 3; DDD3		HP:0007441	PMID:16575392	TAS				P		HPO:lccarmody	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0000007	PMID:24482476	PCS				I		HPO:probinson	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0001257	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0001260	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0001317	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0001347	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0002061	OMIM:615681	TAS				P		HPO:skoehler	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0002064	OMIM:615681	TAS				P		HPO:skoehler	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0002169	OMIM:615681	TAS				P		HPO:skoehler	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0002355	PMID:24482476	PCS				P		HPO:probinson	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0002943	OMIM:615681	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0003202	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0003487	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:615681	TAS				C		HPO:skoehler	
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0006844	OMIM:615681	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615681	SPASTIC PARAPLEGIA 62, AUTOSOMAL RECESSIVE		HP:0030051	OMIM:615681	TAS				P		HPO:skoehler	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0000007	PMID:24482476	PCS				I		HPO:probinson	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0000252	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0000519	OMIM:615683	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0000718	OMIM:615683	TAS				P		HPO:skoehler	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0000823	OMIM:615683	TAS				P		HPO:skoehler	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0001249	PMID:24482476	PCS				P		HPO:probinson	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0001258	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0001260	PMID:24482476	PCS				P		HPO:probinson	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0001288	PMID:24482476	PCS				P		HPO:probinson	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0001762	OMIM:615683	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0002342	OMIM:615683	TAS				P		HPO:skoehler	
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0002500	PMID:24482476	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	615683	SPASTIC PARAPLEGIA 64, AUTOSOMAL RECESSIVE; SPG64		HP:0003202	OMIM:615683	TAS				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0000007	OMIM:615685	TAS				I		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0000763	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0001258	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0001271	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0002355	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0002540	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0003438	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0007083	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615685	SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE; SPG61		HP:0012407	OMIM:615685	IEA				P		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0000007	OMIM:615686	IEA				I		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0001258	OMIM:615686	IEA				P		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0001347	OMIM:615686	IEA				P		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0002079	OMIM:615686	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0002518	OMIM:615686	IEA				P		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0003202	OMIM:615686	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0004322	OMIM:615686	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0012407	OMIM:615686	IEA				P		HPO:skoehler	
OMIM	615686	SPASTIC PARAPLEGIA 63, AUTOSOMAL RECESSIVE; SPG63		HP:0031936	OMIM:615686	IEA				P		HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000007	PMID:24552284	PCS				I	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000602	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000648	OMIM:615688	TAS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000713	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000822	OMIM:615688	TAS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000965	PMID:24552284	PCS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0000979	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001251	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001297	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HP:probinson	5/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001369	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001409	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HP:probinson	1/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001744	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	5/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001876	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HP:probinson	2/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001882	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	2/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001894	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	3/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001903	PMID:24552284	PCS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset	HP:0031796	HP:0001945	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0001974	OMIM:615688	TAS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002027	PMID:24552285	PCS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002040	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HP:probinson	1/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002240	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	4/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002301	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002315	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002381	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002617	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002633	OMIM:615688	IEA				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002721	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0002910	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	5/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0003326	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0003828	OMIM:615688	TAS				C	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0004313	OMIM:615688	TAS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0009830	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0012219	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0012490	OMIM:615688	TAS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0025343	OMIM:615688	TAS		HP:0040283		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	HP:0040283
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0030351	PMID:24552284	PCS		HP:0040284		P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HP:probinson	3/5
OMIM	615688	Polyarteritis nodosa, childhood-onset		HP:0030880	PMID:24552285	PCS				P	POLYARTERITIS NODOSA, CHILDHOOD-ONSET	HPO:skoehler	
OMIM	615696	DOWLING-DEGOS DISEASE 4; DDD4		HP:0000006	OMIM:615696	TAS				I		HPO:skoehler	
OMIM	615696	DOWLING-DEGOS DISEASE 4; DDD4		HP:0025092	OMIM:615696	TAS				P		HPO:skoehler	
OMIM	615696	DOWLING-DEGOS DISEASE 4; DDD4		HP:0025114	OMIM:615696	IEA				P		HPO:skoehler	
OMIM	615697	EPILEPSY, FAMILIAL TEMPORAL LOBE, 6; ETL6		HP:0002373	OMIM:615697	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615697	EPILEPSY, FAMILIAL TEMPORAL LOBE, 6; ETL6		HP:0003829	OMIM:615697	IEA				C		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0000007	PMID:24268657	IEA				I		HPO:probinson	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0000027	OMIM:615703	TAS				P		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0000789	OMIM:615703	TAS				P		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0000798	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	6/6
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0000822	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	11/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0000855	OMIM:615703	TAS				P		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0001249	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	3/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0001397	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	11/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0001513	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	10/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0001635	OMIM:615703	TAS				P		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF		HP:0001658	OMIM:615703	TAS				P		HPO:skoehler	
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0002155	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	4/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0003124	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	4/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0003141	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	2/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0003233	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	6/11
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0005181	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	5/15
OMIM	615703	#615703 MORBID OBESITY AND SPERMATOGENIC FAILURE; MOSPGF	HP:0012828	HP:0005978	PMID:24268657	IEA		HP:0040284		P		HPO:probinson	3/11
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0000006	OMIM:615704	TAS				I		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0000518	OMIM:615704	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0000823	OMIM:615704	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0000966	OMIM:615704	TAS				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0001029	OMIM:615704	TAS	HP:0003577			P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0001055	OMIM:615704	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0001324	OMIM:615704	IEA				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0001596	OMIM:615704	TAS				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0002164	OMIM:615704	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0002206	OMIM:615704	IEA				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0002240	OMIM:615704	TAS				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0002650	OMIM:615704	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0003202	OMIM:615704	TAS				P		HPO:skoehler	
OMIM	615704	POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP		HP:0003236	OMIM:615704	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0000007	OMIM:615705	TAS				I		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0000639	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001249	OMIM:615705	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001250	OMIM:615705	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001251	OMIM:615705	IEA				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001260	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001265	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001270	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001272	OMIM:615705	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0001347	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0002317	OMIM:615705	TAS				P		HPO:skoehler	
OMIM	615705	#615705 SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 15; SCAR15;;SALIH ATAXIA		HP:0003676	OMIM:615705	TAS				C		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000007	OMIM:615706	TAS				I		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000162	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000193	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000278	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000293	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000347	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0000402	OMIM:615706	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0008513	OMIM:615706	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0008751	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615706	#615706 AURICULOCONDYLAR SYNDROME 3; ARCND3		HP:0030022	OMIM:615706	TAS				P		HPO:skoehler	
OMIM	615707	IMMUNODEFICIENCY 20; IMD20		HP:0000007	OMIM:615707	TAS				I		HPO:skoehler	
OMIM	615707	IMMUNODEFICIENCY 20; IMD20		HP:0000403	OMIM:615707	TAS				P		HPO:skoehler	
OMIM	615707	IMMUNODEFICIENCY 20; IMD20		HP:0002721	OMIM:615707	IEA				P		HPO:skoehler	
OMIM	615707	IMMUNODEFICIENCY 20; IMD20		HP:0011108	OMIM:615707	TAS				P		HPO:skoehler	
OMIM	615709	SACRAL AGENESIS WITH VERTEBRAL ANOMALIES; SAVA		HP:0000007	OMIM:615709	TAS				I		HPO:skoehler	
OMIM	615709	SACRAL AGENESIS WITH VERTEBRAL ANOMALIES; SAVA		HP:0003468	OMIM:615709	IEA				P		HPO:skoehler	
OMIM	615709	SACRAL AGENESIS WITH VERTEBRAL ANOMALIES; SAVA		HP:0003577	OMIM:615709	TAS				C		HPO:skoehler	
OMIM	615709	SACRAL AGENESIS WITH VERTEBRAL ANOMALIES; SAVA		HP:0010305	OMIM:615709	IEA				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0000007	OMIM:615710	TAS				I		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0001511	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0001545	OMIM:615710	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0001734	OMIM:615710	IEA				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002014	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002024	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002247	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002566	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002594	OMIM:615710	IEA				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0002904	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0003074	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0005235	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0005912	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0011467	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615710	MITCHELL-RILEY SYNDROME; MTCHRS		HP:0011985	OMIM:615710	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0000007	OMIM:615715	TAS				I		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0000252	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0001319	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0001873	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0001882	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0001903	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615715	#615715 BONE MARROW FAILURE SYNDROME 2; BMFS2		HP:0005528	OMIM:615715	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000007	OMIM:615716	TAS				I		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000175	OMIM:615716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000219	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000252	OMIM:615716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000316	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000431	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000455	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0000582	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0001249	OMIM:615716	IEA				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4	HP:0012837	HP:0001250	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4	HP:0012828	HP:0001263	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0001290	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0001510	OMIM:615716	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0002540	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0003155	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0003593	OMIM:615716	TAS				C		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0003763	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0004305	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615716	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4		HP:0010804	OMIM:615716	TAS				P		HPO:skoehler	
OMIM	615721	#615721 RENAL HYPODYSPLASIA/APLASIA 2; RHDA2		HP:0000007	OMIM:615721	TAS				I		HPO:skoehler	
OMIM	615721	#615721 RENAL HYPODYSPLASIA/APLASIA 2; RHDA2		HP:0001582	OMIM:615721	TAS				P		HPO:skoehler	
OMIM	615721	#615721 RENAL HYPODYSPLASIA/APLASIA 2; RHDA2		HP:0002009	OMIM:615721	TAS				P		HPO:skoehler	
OMIM	615721	#615721 RENAL HYPODYSPLASIA/APLASIA 2; RHDA2		HP:0002089	OMIM:615721	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0000006	OMIM:615722	TAS				I		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0000486	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0000543	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0000639	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0000648	OMIM:615722	IEA				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0001123	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0001182	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0001249	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0001263	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0007663	OMIM:615722	TAS				P		HPO:skoehler	
OMIM	615722	BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS		HP:0100704	OMIM:615722	IEA				P		HPO:skoehler	
OMIM	615723	PREMATURE OVARIAN FAILURE 8; POF8		HP:0000007	OMIM:615723	TAS				I		HPO:skoehler	
OMIM	615723	PREMATURE OVARIAN FAILURE 8; POF8		HP:0000786	OMIM:615723	TAS				P		HPO:skoehler	
OMIM	615723	PREMATURE OVARIAN FAILURE 8; POF8		HP:0000837	OMIM:615723	TAS				P		HPO:skoehler	
OMIM	615723	PREMATURE OVARIAN FAILURE 8; POF8		HP:0008209	OMIM:615723	TAS				P		HPO:skoehler	
OMIM	615723	PREMATURE OVARIAN FAILURE 8; POF8		HP:0100615	OMIM:615723	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615724	#615724 PREMATURE OVARIAN FAILURE 9; POF9		HP:0000007	OMIM:615724	TAS				I		HPO:skoehler	
OMIM	615724	#615724 PREMATURE OVARIAN FAILURE 9; POF9		HP:0000141	OMIM:615724	TAS				P		HPO:skoehler	
OMIM	615724	#615724 PREMATURE OVARIAN FAILURE 9; POF9		HP:0000837	OMIM:615724	TAS				P		HPO:skoehler	
OMIM	615724	#615724 PREMATURE OVARIAN FAILURE 9; POF9		HP:0008209	OMIM:615724	IEA				P		HPO:skoehler	
OMIM	615725	#615725 RETINITIS PIGMENTOSA 68; RP68		HP:0000007	OMIM:615725	TAS				I		HPO:skoehler	
OMIM	615725	#615725 RETINITIS PIGMENTOSA 68; RP68		HP:0000510	OMIM:615725	IEA				P		HPO:skoehler	
OMIM	615725	#615725 RETINITIS PIGMENTOSA 68; RP68		HP:0000662	OMIM:615725	TAS				P		HPO:skoehler	
OMIM	615725	#615725 RETINITIS PIGMENTOSA 68; RP68		HP:0001105	OMIM:615725	TAS				P		HPO:skoehler	
OMIM	615725	#615725 RETINITIS PIGMENTOSA 68; RP68		HP:0001123	OMIM:615725	TAS				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0000221	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0000230	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0000975	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0000982	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0002745	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0007556	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0008401	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0008404	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0010765	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0040181	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615726	#615726 PACHYONYCHIA CONGENITA 3; PC3		HP:0200040	OMIM:615726	IEA				P		HPO:skoehler	
OMIM	615728	#615728 PACHYONYCHIA CONGENITA 4; PC4		HP:0000006	OMIM:615728	IEA				I		HPO:skoehler	
OMIM	615728	#615728 PACHYONYCHIA CONGENITA 4; PC4		HP:0000982	OMIM:615728	IEA				P		HPO:skoehler	
OMIM	615728	#615728 PACHYONYCHIA CONGENITA 4; PC4		HP:0008404	OMIM:615728	IEA				P		HPO:skoehler	
OMIM	615728	#615728 PACHYONYCHIA CONGENITA 4; PC4		HP:0012035	OMIM:615728	IEA				P		HPO:skoehler	
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0000007	OMIM:615731	TAS				I		HPO:skoehler	
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0000175	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0000218	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0000347	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0000774	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0001270	OMIM:615731	TAS				P		HPO:skoehler	
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0001324	OMIM:615731	TAS				P		HPO:skoehler	
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0001623	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0001989	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0002093	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0002650	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0002804	OMIM:615731	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615731	#615731 NEMALINE MYOPATHY 9; NEM9		HP:0003828	OMIM:615731	TAS				C		HPO:skoehler	
OMIM	615735	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE		HP:0000006	OMIM:615735	TAS				I		HPO:skoehler	
OMIM	615735	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE		HP:0000982	OMIM:615735	TAS				P		HPO:skoehler	
OMIM	615735	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL OR DIFFUSE		HP:0025092	OMIM:615735	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0000006	OMIM:615744	TAS				I		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0001249	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0001263	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0002121	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0002133	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0002373	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0006813	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0010819	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615744	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 19; EIEE19		HP:0200134	OMIM:615744	TAS				P		HPO:skoehler	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0000007	PMID:23275345	PCS				I		HPO:skoehler	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0001297	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0001638	OMIM:615745	IEA				P		HPO:skoehler	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0001662	OMIM:615745	TAS				P		HPO:skoehler	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0001692	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0001962	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0002094	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0003238	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0006698	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0025478	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0100699	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615745	#615745 ATRIAL STANDSTILL 2; ATRST2;;ATRIAL DILATION AND STANDSTILL;;CARDIOMYOPATHY, ATRIAL DILATED, WITH ATRIAL STANDSTILL		HP:0200127	PMID:23275345	PCS				P		HPO:lccarmody	
OMIM	615749	ECULIZUMAB, POOR RESPONSE TO		HP:0000006	OMIM:615749	TAS				I		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0000007	OMIM:615750	TAS				I		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0000802	OMIM:615750	TAS				P		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0000822	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0000965	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0001250	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0001269	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0002015	OMIM:615750	TAS				P		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0002140	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0002571	OMIM:615750	TAS				P		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0003828	OMIM:615750	TAS				C		HPO:skoehler	
OMIM	615750	MOYAMOYA DISEASE 6 WITH ACHALASIA		HP:0030880	OMIM:615750	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0000007	OMIM:615751	TAS				I		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001254	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001263	OMIM:615751	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001942	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001943	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001950	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001987	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0001993	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0002151	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO	HP:0025303	HP:0002789	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0002919	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0003128	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0003348	OMIM:615751	TAS				P		HPO:skoehler	
OMIM	615751	CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO		HP:0003828	OMIM:615751	TAS				C		HPO:skoehler	
OMIM	615752	#615752 POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR ;;PMGR		HP:0000007	OMIM:615752	IEA				I		HPO:skoehler	
OMIM	615752	#615752 POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR ;;PMGR		HP:0001249	OMIM:615752	IEA				P		HPO:skoehler	
OMIM	615752	#615752 POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR ;;PMGR		HP:0001250	OMIM:615752	IEA				P		HPO:skoehler	
OMIM	615752	#615752 POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR ;;PMGR		HP:0002463	OMIM:615752	IEA				P		HPO:skoehler	
OMIM	615752	#615752 POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE; BPPR ;;PMGR		HP:0012650	OMIM:615752	IEA				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0000007	OMIM:615758	TAS				I		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0001508	OMIM:615758	TAS				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0002014	OMIM:615758	TAS				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0002205	OMIM:615758	TAS				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0002721	OMIM:615758	IEA				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0002960	OMIM:615758	TAS				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0003593	OMIM:615758	TAS				C		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0005407	OMIM:615758	IEA				P		HPO:skoehler	
OMIM	615758	IMMUNODEFICIENCY 22; IMD22		HP:0012490	OMIM:615758	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000007	OMIM:615760	TAS				I		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000252	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000253	OMIM:615760	IEA				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000286	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000340	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000341	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000358	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000369	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0000601	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY	HP:0012829	HP:0001263	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0001290	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0001347	OMIM:615760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0002059	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0002079	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0002119	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0002133	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0003429	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0003676	OMIM:615760	TAS				C		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0006855	OMIM:615760	TAS				P		HPO:skoehler	
OMIM	615760	MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY		HP:0009879	OMIM:615760	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000006	OMIM:615761	TAS				I		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000028	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000047	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000219	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000248	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000319	OMIM:615761	IEA				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000347	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000463	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000483	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000486	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000545	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000582	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000664	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000678	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000722	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0000750	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0001249	OMIM:615761	IEA				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0001263	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0002307	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0002650	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0002714	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0002808	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0003307	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615761	MENTAL RETARDATION, AUTOSOMAL DOMINANT 23; MRD23		HP:0005280	OMIM:615761	TAS				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0000006	OMIM:615763	TAS				I		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0001250	OMIM:615763	TAS				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5	HP:0012828	HP:0001263	OMIM:615763	TAS				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0001290	OMIM:615763	TAS				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0002079	OMIM:615763	TAS				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0002119	OMIM:615763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0002365	OMIM:615763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0002521	OMIM:615763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0002539	OMIM:615763	IEA				P		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0003828	OMIM:615763	TAS				C		HPO:skoehler	
OMIM	615763	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 5		HP:0009879	OMIM:615763	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0000007	OMIM:615767	TAS				I		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0001508	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0001510	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0002028	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0002037	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0002205	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0002721	OMIM:615767	IEA				P		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0003593	OMIM:615767	TAS				C		HPO:skoehler	
OMIM	615767	IMMUNODEFICIENCY, COMMON VARIABLE, 11; CVID11		HP:0004313	OMIM:615767	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0000007	OMIM:615768	TAS				I		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0000135	OMIM:615768	IEA				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0000544	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0000639	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0001257	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0001260	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0001272	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0001321	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0001337	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0002070	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0002078	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0002317	OMIM:615768	TAS				P		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0003676	OMIM:615768	TAS				C		HPO:skoehler	
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0011448	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615768	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16; SCAR16		HP:0100543	OMIM:615768	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615770	ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15		HP:0000007	OMIM:615770	TAS				I		HPO:skoehler	
OMIM	615770	ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15		HP:0004749	OMIM:615770	TAS				P		HPO:skoehler	
OMIM	615770	ATRIAL FIBRILLATION, FAMILIAL, 15; ATFB15		HP:0005110	OMIM:615770	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0000006	OMIM:615771	TAS				I		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0000252	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0000568	OMIM:615771	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0000750	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0001251	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6	HP:0012828	HP:0001263	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0001321	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0002126	OMIM:615771	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0002365	OMIM:615771	TAS				P		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0002539	OMIM:615771	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0003577	OMIM:615771	TAS				C		HPO:skoehler	
OMIM	615771	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 6; CDCBM6		HP:0007973	OMIM:615771	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615774	#615774 OOCYTE MATURATION DEFECT; OOMD		HP:0000007	OMIM:615774	TAS				I		HPO:skoehler	
OMIM	615774	#615774 OOCYTE MATURATION DEFECT; OOMD		HP:0000789	OMIM:615774	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000007	OMIM:615777	TAS				I		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000175	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000311	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000343	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000520	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000592	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000767	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000768	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000774	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000894	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0000954	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001249	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001290	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001388	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001763	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001769	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001863	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0001956	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0002656	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0002673	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0003016	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0003026	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0004233	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0004322	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0004482	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0005280	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0009803	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0010049	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0011304	OMIM:615777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615777	DESBUQUOIS DYSPLASIA 2		HP:0012368	OMIM:615777	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0000006	OMIM:615779	TAS				I		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0001629	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0001636	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0001650	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0001680	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0004383	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615779	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4; CHTD4		HP:0006695	OMIM:615779	TAS				P		HPO:skoehler	
OMIM	615780	RETINITIS PIGMENTOSA 69		HP:0000007	OMIM:615780	TAS				I		HPO:probinson	
OMIM	615780	RETINITIS PIGMENTOSA 69		HP:0000510	OMIM:615780	IEA				P		HPO:skoehler	
OMIM	615780	RETINITIS PIGMENTOSA 69		HP:0000550	OMIM:615780	TAS	HP:0003596			P		HPO:probinson	
OMIM	615780	RETINITIS PIGMENTOSA 69		HP:0000580	OMIM:615780	TAS				P		HPO:skoehler	
OMIM	615780	RETINITIS PIGMENTOSA 69		HP:0001133	OMIM:615780	TAS				P		HPO:probinson	
OMIM	615785	WHITE SPONGE NEVUS 2; WSN2		HP:0000006	OMIM:615785	TAS				I		HPO:skoehler	
OMIM	615785	WHITE SPONGE NEVUS 2; WSN2		HP:0000969	OMIM:615785	IEA				P		HPO:skoehler	
OMIM	615785	WHITE SPONGE NEVUS 2; WSN2		HP:0025092	OMIM:615785	TAS				P		HPO:skoehler	
OMIM	615785	WHITE SPONGE NEVUS 2; WSN2		HP:0040009	OMIM:615785	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000007	PMID:24389050	TAS				I		HPO:probinson	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000252	PMID:24389050	TAS		HP:0040284		P		HPO:probinson	2/2
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000308	OMIM:615789	IEA				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000348	PMID:24389050	TAS				P		HPO:probinson	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000463	PMID:24389050	TAS				P		HPO:probinson	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000506	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000520	PMID:24389050	TAS				P		HPO:probinson	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000535	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0000938	PMID:24389050	TAS		HP:0040284		P		HPO:probinson	2/2
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0001156	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0001518	PMID:24389050	TAS		HP:0040284		P		HPO:probinson	2/2
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0001762	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0001903	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0002007	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0002384	OMIM:615789	IEA				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0002719	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0003510	PMID:24389050	TAS		HP:0040284		P		HPO:probinson	2/2
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0004823	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0005280	PMID:24389050	TAS				P		HPO:probinson	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0005585	OMIM:615789	IEA				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0005590	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0009623	OMIM:615789	IEA				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0009882	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0011003	OMIM:615789	IEA				P		HPO:skoehler	
OMIM	615789	SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF		HP:0012736	OMIM:615789	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000007	OMIM:615802	TAS				I		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000154	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000164	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000252	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000400	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000470	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000512	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0000556	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001249	OMIM:615802	IEA				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001250	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001257	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001263	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001319	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001321	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0001344	OMIM:615802	IEA				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0002059	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0002079	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0004322	OMIM:615802	TAS				P		HPO:skoehler	
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0012448	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615802	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42		HP:0100704	OMIM:615802	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000007	OMIM:615803	TAS				I		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000028	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000218	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000219	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000253	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000430	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000431	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000520	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000527	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000565	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000637	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000639	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0000817	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001250	OMIM:615803	IEA				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001257	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10	HP:0012829	HP:0001263	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001298	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001344	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001347	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0001510	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0002079	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0002119	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0002120	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0002553	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0003196	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0003577	OMIM:615803	TAS				C		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0009879	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615803	PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10		HP:0012448	OMIM:615803	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0000007	OMIM:615807	TAS				I		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0000086	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0000252	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0000347	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0000444	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0001249	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0001263	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0002176	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8	HP:0012828	HP:0002751	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615807	SECKEL SYNDROME 8; SCKL8		HP:0004322	OMIM:615807	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000007	OMIM:615809	TAS				I		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000158	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000188	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000253	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000297	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000341	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000377	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000494	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0000648	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0001250	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0001257	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9	HP:0012829	HP:0001263	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0002079	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0002119	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0002120	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0002169	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0003477	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0008936	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0011800	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615809	PONTOCEREBELLAR HYPOPLASIA, TYPE 9		HP:0100704	OMIM:615809	TAS				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0000006	OMIM:615812	TAS				I		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3	HP:0012828	HP:0000822	OMIM:615812	TAS				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0001297	OMIM:615812	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0001658	OMIM:615812	IEA				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0001956	OMIM:615812	TAS				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0003124	OMIM:615812	TAS				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0005145	OMIM:615812	IEA				P		HPO:skoehler	
OMIM	615812	ABDOMINAL OBESITY-METABOLIC SYNDROME 3; AOMS3		HP:0012743	OMIM:615812	IEA				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000007	OMIM:615816	TAS				I		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000218	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000405	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000407	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000793	OMIM:615816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0000964	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001249	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001251	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001260	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001263	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001265	OMIM:615816	IEA				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001290	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001875	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001878	OMIM:615816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0001888	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0002099	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0002110	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0002205	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0002650	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0002721	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0003193	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0003474	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0010783	OMIM:615816	IEA				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0040148	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0100543	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615816	IMMUNODEFICIENCY 23; IMD23		HP:0200029	OMIM:615816	TAS				P		HPO:skoehler	
OMIM	615817	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43		HP:0000007	OMIM:615817	TAS				I		HPO:skoehler	
OMIM	615817	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43		HP:0001249	OMIM:615817	IEA				P		HPO:skoehler	
OMIM	615817	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43		HP:0001257	OMIM:615817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615817	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43		HP:0001263	OMIM:615817	TAS				P		HPO:skoehler	
OMIM	615817	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43		HP:0004322	OMIM:615817	TAS				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0000006	OMIM:615821	TAS				I		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0000982	OMIM:615821	TAS				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0000989	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001036	OMIM:615821	TAS				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001279	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001644	OMIM:615821	TAS				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001649	OMIM:615821	IEA				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001808	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0001820	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0002224	OMIM:615821	TAS				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0008064	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0008404	OMIM:615821	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0009804	OMIM:615821	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0010783	OMIM:615821	IEA				P		HPO:skoehler	
OMIM	615821	CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR, KERATODERMA, AND TOOTH AGENESIS; DCWHKTA		HP:0030816	OMIM:615821	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000007	OMIM:615824	TAS				I		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000028	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000286	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000582	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000664	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000718	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0000752	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0001250	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0001263	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0001319	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0001511	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0001942	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0002049	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0002465	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0003593	OMIM:615824	TAS				C		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0005280	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615824	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 7; MC3DN7		HP:0100259	OMIM:615824	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000006	OMIM:615828	TAS				I		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000179	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000303	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000718	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000720	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000817	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0000960	OMIM:615828	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0001249	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0001263	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0001288	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0002719	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0010804	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615828	MENTAL RETARDATION, AUTOSOMAL DOMINANT 24; MRD24		HP:0011228	OMIM:615828	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000006	OMIM:615829	TAS				I		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000316	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000347	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000369	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000494	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000565	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0000582	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0001249	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0001263	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0001290	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0001508	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0001601	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0002079	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0002870	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0005280	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0006951	OMIM:615829	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615829	XIA-GIBBS SYNDROME		HP:0009879	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0009909	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0012448	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615829	XIA-GIBBS SYNDROME		HP:0025267	OMIM:615829	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000006	OMIM:615830	TAS				I		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000712	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000716	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000819	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000822	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000938	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000939	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0000978	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0001007	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0001030	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0001061	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0001579	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0001596	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0003701	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0004324	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4	HP:0012832	HP:0008221	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0025383	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615830	PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4		HP:0500011	OMIM:615830	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0000007	OMIM:615833	TAS				I		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0001250	OMIM:615833	IEA				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21	HP:0012829	HP:0001263	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0001276	OMIM:615833	IEA				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0001290	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0001558	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0008936	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0011968	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0012444	OMIM:615833	IEA				P		HPO:skoehler	
OMIM	615833	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 21; EIEE21		HP:0200134	OMIM:615833	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000006	OMIM:615834	IEA				I		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000154	OMIM:615834	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000160	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000248	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000252	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000316	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000322	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000369	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000486	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000494	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000508	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000574	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000717	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0000750	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0001249	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0001263	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0001276	OMIM:615834	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0001518	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0001999	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0002553	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0002650	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0002804	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0002808	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0004322	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0005274	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0006184	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0011968	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0012471	OMIM:615834	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0012745	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0012810	OMIM:615834	TAS				P		HPO:skoehler	
OMIM	615834	MENTAL RETARDATION, AUTOSOMAL DOMINANT 26		HP:0100021	OMIM:615834	IEA				P		HPO:skoehler	
OMIM	615837	DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101		HP:0000007	OMIM:615837	TAS				I		HPO:skoehler	
OMIM	615837	DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101		HP:0008619	OMIM:615837	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0000007	OMIM:615838	TAS				I		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0000543	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0000544	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0000577	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0000639	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001249	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001251	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001254	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001260	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001263	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001285	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001288	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001290	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001298	OMIM:615838	IEA				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8	HP:0012828	HP:0001324	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001348	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001508	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0001903	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002059	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002079	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002151	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002376	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002518	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0002878	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0003128	OMIM:615838	TAS				P		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0003676	OMIM:615838	TAS				C		HPO:skoehler	
OMIM	615838	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 8; MC3DN8		HP:0003678	OMIM:615838	TAS				C		HPO:skoehler	
OMIM	615841	SPERMATOGENIC FAILURE 13; SPGF13		HP:0000007	OMIM:615841	TAS				I		HPO:skoehler	
OMIM	615841	SPERMATOGENIC FAILURE 13; SPGF13		HP:0000027	OMIM:615841	TAS				P		HPO:skoehler	
OMIM	615842	SPERMATOGENIC FAILURE 14; SPGF14		HP:0000007	OMIM:615842	TAS				I		HPO:skoehler	
OMIM	615842	SPERMATOGENIC FAILURE 14; SPGF14		HP:0000027	OMIM:615842	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0000006	OMIM:615846	TAS				I		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0000100	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0000252	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0000496	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0000737	OMIM:615846	TAS	HP:0003623			P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001047	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001249	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001250	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001263	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001285	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001290	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001332	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001344	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001511	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001744	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0001873	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0002059	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0002135	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0002240	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0002376	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0002633	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0003828	OMIM:615846	TAS				C		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0003829	OMIM:615846	TAS				C		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7	HP:0012828	HP:0008936	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0010702	OMIM:615846	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615846	AICARDI-GOUTIERES SYNDROME 7		HP:0011968	OMIM:615846	TAS				P		HPO:skoehler	
OMIM	615848	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10; CMM10		HP:0000006	OMIM:615848	TAS				I		HPO:skoehler	
OMIM	615848	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10; CMM10		HP:0002861	OMIM:615848	IEA				P		HPO:skoehler	
OMIM	615848	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10; CMM10		HP:0003581	OMIM:615848	TAS				C		HPO:skoehler	
OMIM	615848	MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10; CMM10		HP:0003829	OMIM:615848	TAS				C		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000006	OMIM:615849	TAS				I		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000028	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000054	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000135	OMIM:615849	IEA				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000175	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000204	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000601	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0000873	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0001263	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0003828	OMIM:615849	TAS				C		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0003829	OMIM:615849	TAS				C		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0004322	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0010627	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0011755	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0011800	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0040075	OMIM:615849	TAS				P		HPO:skoehler	
OMIM	615849	CULLER-JONES SYNDROME; CJS		HP:0100259	OMIM:615849	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0000007	OMIM:615851	TAS				I		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0000253	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0000737	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0000939	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0001250	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E	HP:0012828	HP:0001263	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E	HP:0003676	HP:0001272	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0001319	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0001371	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E	HP:0003676	HP:0002059	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0002079	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0002179	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0002187	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E	HP:0003676	HP:0002510	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0002650	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0003593	OMIM:615851	TAS				C		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0003676	OMIM:615851	TAS				C		HPO:skoehler	
OMIM	615851	PONTOCEREBELLAR HYPOPLASIA, TYPE 2E; PCH2E		HP:0004322	OMIM:615851	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000007	OMIM:615859	TAS				I		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000294	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000322	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000341	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000377	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000455	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000506	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000574	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0000629	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0001250	OMIM:615859	IEA				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0001263	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0002079	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0002521	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0003593	OMIM:615859	TAS				C		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23	HP:0012825	HP:0012110	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0012471	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0100704	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615859	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23; EIEE23		HP:0200134	OMIM:615859	TAS				P		HPO:skoehler	
OMIM	615860	CONE-ROD DYSTROPHY 19; CORD19		HP:0000007	OMIM:615860	TAS				I		HPO:skoehler	
OMIM	615860	CONE-ROD DYSTROPHY 19; CORD19		HP:0000548	OMIM:615860	IEA				P		HPO:skoehler	
OMIM	615860	CONE-ROD DYSTROPHY 19; CORD19		HP:0000556	OMIM:615860	TAS				P		HPO:skoehler	
OMIM	615861	FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME		HP:0000007	PMID:24814193	PCS				I		HPO:skoehler	
OMIM	615861	FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME		HP:0012579	PMID:24814193	PCS	HP:0011463	HP:0040284		P		HPO:skoehler	1/1
OMIM	615861	FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME		HP:0012588	PMID:24814193	PCS	HP:0011463	HP:0040284		P		HPO:skoehler	1/4
OMIM	615861	FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME		HP:0031266	PMID:24814193	PCS	HP:0011463			P		HPO:probinson	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0000007	OMIM:615862	TAS				I		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0000090	OMIM:615862	TAS				P		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0000092	OMIM:615862	TAS				P		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0000238	OMIM:615862	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0000486	OMIM:615862	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0001249	OMIM:615862	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0001396	OMIM:615862	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0001970	OMIM:615862	TAS				P		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0003774	OMIM:615862	TAS				P		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0004722	OMIM:615862	TAS				P		HPO:skoehler	
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0006580	OMIM:615862	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615862	NEPHRONOPHTHISIS 18; NPHP18		HP:0032118	OMIM:615862	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	615863	DIARRHEA 7; DIAR7		HP:0000007	OMIM:615863	TAS				I		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0002013	OMIM:615863	TAS				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0002014	OMIM:615863	IEA				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0002243	OMIM:615863	TAS				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0003073	OMIM:615863	TAS				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0003077	OMIM:615863	TAS				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0003124	OMIM:615863	TAS				P		HPO:skoehler	
OMIM	615863	DIARRHEA 7; DIAR7		HP:0011473	OMIM:615863	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000006	OMIM:615866	IEA				I		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000194	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000232	OMIM:615866	TAS				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000252	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000293	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000322	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000331	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000358	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000369	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000430	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000527	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0000998	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0001249	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0001256	OMIM:615866	TAS				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0001510	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0001511	OMIM:615866	TAS				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0001999	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0002553	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0003189	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0003196	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0004322	OMIM:615866	TAS				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0005280	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0005288	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0009882	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0009891	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0009929	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0011800	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0011937	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0012471	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0012745	OMIM:615866	IEA				P		HPO:skoehler	
OMIM	615866	MENTAL RETARDATION, AUTOSOMAL DOMINANT 27		HP:0030084	OMIM:615866	TAS				P		HPO:skoehler	
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0000006	OMIM:615871	TAS				I		HPO:skoehler	
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0000708	OMIM:615871	TAS				P		HPO:skoehler	
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0001249	OMIM:615871	TAS				P		HPO:skoehler	
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0001251	OMIM:615871	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0002373	OMIM:615871	TAS				P		HPO:skoehler	
OMIM	615871	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 24; EIEE24		HP:0200134	OMIM:615871	TAS				P		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0000007	OMIM:615872	TAS				I		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0000789	OMIM:615872	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0002110	OMIM:615872	TAS				P		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0002205	OMIM:615872	TAS				P		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0003676	OMIM:615872	TAS				C		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0012265	OMIM:615872	IEA				P		HPO:skoehler	
OMIM	615872	CILIARY DYSKINESIA, PRIMARY, 29; CILD29		HP:0100750	OMIM:615872	TAS				P		HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000006	OMIM:615873	TAS				I	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000154	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	13/56
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000179	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	20/55
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000219	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	45/64
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000232	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	25/55
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000280	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	11/65
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000319	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000343	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	22/56
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000368	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	10/68
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000431	PMID:29724491	TAS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	33/66
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000455	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	15/57
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000486	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000494	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	20/60
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000505	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000508	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000540	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000625	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000625	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	12/63
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000687	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	18/52
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000722	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000729	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000733	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000752	PMID:28221363	PCS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0000824	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:probinson	5/46
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001249	OMIM:615873	IEA				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001250	OMIM:615873	TAS		HP:0040283		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	HP:0040283
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001263	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001290	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001388	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001513	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0001627	OMIM:615873	TAS		HP:0040283		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	HP:0040283
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0002463	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0002719	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0003196	PMID:29724491	TAS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	31/63
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0003593	OMIM:615873	TAS				C	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0004322	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0006288	PMID:28221363	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	44/54
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0009890	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	33/66
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0011220	PMID:29724491	TAS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	42/64
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0011968	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0045025	PMID:29724491	PCS		HP:0040284		P	HELSMOORTEL-VAN DER AA SYNDROME	HP:probinson	14/58
OMIM	615873	Helsmoortel-van der Aa syndrome		HP:0200055	OMIM:615873	TAS				P	HELSMOORTEL-VAN DER AA SYNDROME	HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000006	OMIM:615877	TAS				I		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000007	OMIM:615877	TAS				I		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000047	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000256	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000286	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000482	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000486	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000518	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000527	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000528	OMIM:615877	IEA				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000568	OMIM:615877	IEA				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000589	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000629	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000639	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000647	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0000826	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0001763	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0002342	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0008905	OMIM:615877	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0009918	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615877	MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS		HP:0011220	OMIM:615877	TAS				P		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0000007	OMIM:615878	TAS				I		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0001399	OMIM:615878	TAS				P		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0001402	OMIM:615878	TAS				P		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0001406	OMIM:615878	TAS				P		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0001409	OMIM:615878	TAS				P		HPO:skoehler	
OMIM	615878	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 4		HP:0003676	OMIM:615878	TAS				C		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000006	OMIM:615879	TAS				I		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000098	OMIM:615879	TAS				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000256	OMIM:615879	TAS				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000311	OMIM:615879	TAS				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000581	OMIM:615879	TAS				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0000609	OMIM:615879	IEA				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0001249	OMIM:615879	TAS				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0001250	OMIM:615879	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0001290	OMIM:615879	IEA				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0001537	OMIM:615879	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0001631	OMIM:615879	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0002650	OMIM:615879	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0007099	OMIM:615879	IEA				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0040197	OMIM:615879	IEA				P		HPO:skoehler	
OMIM	615879	TATTON-BROWN-RAHMAN SYNDROME; TBRS		HP:0045025	OMIM:615879	IEA				P		HPO:skoehler	
OMIM	615881	PLASMA TRIGLYCERIDE LEVEL QUANTITATIVE TRAIT LOCUS		HP:0000006	OMIM:615881	TAS				I		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0000006	OMIM:615883	TAS				I		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0000616	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0001371	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0002522	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0002527	OMIM:615883	IEA				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0002901	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003236	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003306	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003324	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003677	OMIM:615883	TAS				C		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003701	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0003828	OMIM:615883	IEA				C		HPO:skoehler	
OMIM	615883	MYOPATHY, TUBULAR AGGREGATE, 2; TAM2		HP:0009027	OMIM:615883	TAS				P		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0000006	OMIM:615885	TAS				I		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0001006	OMIM:615885	IEA				P		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0002217	OMIM:615885	IEA				P		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0011359	OMIM:615885	IEA				P		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0100840	OMIM:615885	TAS				P		HPO:skoehler	
OMIM	615885	HYPOTRICHOSIS 12; HYPT12		HP:0200102	OMIM:615885	TAS				P		HPO:skoehler	
OMIM	615887	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5		HP:0000007	OMIM:615887	TAS				I		HPO:skoehler	
OMIM	615887	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5		HP:0000670	OMIM:615887	TAS				P		HPO:skoehler	
OMIM	615887	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA5; AI2A5		HP:0000705	OMIM:615887	TAS				P		HPO:skoehler	
OMIM	615888	BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18		HP:0000007	OMIM:615888	TAS				I		HPO:skoehler	
OMIM	615888	BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18		HP:0000421	OMIM:615888	TAS				P		HPO:skoehler	
OMIM	615888	BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18		HP:0003010	OMIM:615888	TAS				P		HPO:skoehler	
OMIM	615888	BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18		HP:0003540	OMIM:615888	IEA				P		HPO:skoehler	
OMIM	615888	BLEEDING DISORDER, PLATELET-TYPE, 18; BDPLT18		HP:0003593	OMIM:615888	TAS				C		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0000007	OMIM:615889	TAS				I		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0000639	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0000716	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0000726	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001251	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001257	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001260	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001272	OMIM:615889	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001332	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0001337	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0002180	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0002186	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0002371	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0003676	OMIM:615889	TAS				C		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0006970	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0006980	OMIM:615889	IEA				P		HPO:skoehler	
OMIM	615889	LEUKOENCEPHALOPATHY, PROGRESSIVE, WITH OVARIAN FAILURE; LKENP		HP:0008209	OMIM:615889	TAS				P		HPO:skoehler	
OMIM	615892	OROFACIAL CLEFT 14		HP:0000007	PMID:23860042	PCS				I		HPO:skoehler	
OMIM	615892	OROFACIAL CLEFT 14		HP:0000161	PMID:23519333	PCS				P		HP:probinson	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0000007	OMIM:615895	TAS				I		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0000508	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0000964	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0001508	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0001510	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0001644	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002240	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002650	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002716	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002719	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002721	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0002910	OMIM:615895	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0003236	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0003326	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0003676	OMIM:615895	TAS				C		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0003701	OMIM:615895	TAS				P		HPO:skoehler	
OMIM	615895	POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1		HP:0003828	OMIM:615895	TAS				C		HPO:skoehler	
OMIM	615896	#615896 HYPOTRICHOSIS 13; HYPT13;;HYPOTRICHOSIS WITH WOOLLY HAIR		HP:0000006	OMIM:615896	TAS				I		HPO:skoehler	
OMIM	615896	#615896 HYPOTRICHOSIS 13; HYPT13;;HYPOTRICHOSIS WITH WOOLLY HAIR		HP:0000535	PMID:22592156	PCS				P		HPO:lccarmody	
OMIM	615896	#615896 HYPOTRICHOSIS 13; HYPT13;;HYPOTRICHOSIS WITH WOOLLY HAIR		HP:0001006	OMIM:615896	TAS				P		HPO:skoehler	
OMIM	615896	#615896 HYPOTRICHOSIS 13; HYPT13;;HYPOTRICHOSIS WITH WOOLLY HAIR		HP:0002224	OMIM:615896	IEA				P		HPO:skoehler	
OMIM	615896	#615896 HYPOTRICHOSIS 13; HYPT13;;HYPOTRICHOSIS WITH WOOLLY HAIR		HP:0008070	PMID:22592156	PCS				P		HPO:lccarmody	
OMIM	615897	Immunodeficiency 24		HP:0000007	PMID:24870241	PCS				I	IMMUNODEFICIENCY 24	HPO:probinson	
OMIM	615897	Immunodeficiency 24		HP:0001888	PMID:24870241	PCS				P	IMMUNODEFICIENCY 24	HPO:probinson	
OMIM	615897	Immunodeficiency 24		HP:0002721	OMIM:615897	IEA				P	IMMUNODEFICIENCY 24	HPO:skoehler	
OMIM	615897	Immunodeficiency 24		HP:0004429	PMID:24870241	PCS		HP:0040284		P	IMMUNODEFICIENCY 24	HP:probinson	8/8
OMIM	615897	Immunodeficiency 24		HP:0008348	PMID:24870241	PCS		HP:0040284		P	IMMUNODEFICIENCY 24	HPO:probinson	3/3
OMIM	615897	Immunodeficiency 24		HP:0030253	PMID:24870241	PCS		HP:0040284		P	IMMUNODEFICIENCY 24	HPO:probinson	1/4
OMIM	615897	Immunodeficiency 24		HP:0031691	PMID:24870241	PCS				P	IMMUNODEFICIENCY 24	HP:probinson	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0000007	OMIM:615905	TAS				I		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0000252	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0000668	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0000684	OMIM:615905	IEA				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0001251	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0001257	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0001263	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0001290	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0002133	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0002500	OMIM:615905	IEA				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0004305	OMIM:615905	IEA				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0008936	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0012448	OMIM:615905	IEA				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0031165	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615905	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA; EIEE25		HP:0200134	OMIM:615905	TAS				P		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0000006	OMIM:615907	TAS				I		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0000034	OMIM:615907	TAS				P		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0000962	OMIM:615907	IEA				P		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0001004	OMIM:615907	IEA				P		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0003828	OMIM:615907	TAS				C		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0100658	OMIM:615907	IEA				P		HPO:skoehler	
OMIM	615907	LYMPHEDEMA, HEREDITARY, ID; LMPH1D		HP:0100797	OMIM:615907	TAS				P		HPO:skoehler	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0000006	OMIM:615909	TAS				I		HPO:probinson	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0001897	OMIM:615909	TAS				P		HPO:skoehler	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0003828	OMIM:615909	TAS				C		HPO:skoehler	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0003829	OMIM:615909	TAS				C		HPO:skoehler	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0011463	OMIM:615909	TAS				C		HPO:probinson	
OMIM	615909	DIAMOND-BLACKFAN ANEMIA 13; DBA13		HP:0030270	OMIM:615909	TAS				P		HPO:probinson	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0000006	OMIM:615911	TAS				I		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0000407	OMIM:615911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0000508	OMIM:615911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0000727	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001251	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001260	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001265	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001283	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001284	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0001300	OMIM:615911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0002015	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0002120	OMIM:615911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0002145	OMIM:615911	IEA				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0003487	OMIM:615911	TAS				P		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0003676	OMIM:615911	TAS				C		HPO:skoehler	
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0003701	OMIM:615911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615911	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2; FTDALS2		HP:0007354	OMIM:615911	IEA				P		HPO:skoehler	
OMIM	615916	CARDIOMYOPATHY, DILATED, 1NN		HP:0000006	OMIM:615916	TAS				I		HPO:skoehler	
OMIM	615916	CARDIOMYOPATHY, DILATED, 1NN		HP:0001644	OMIM:615916	TAS				P		HPO:skoehler	
OMIM	615916	CARDIOMYOPATHY, DILATED, 1NN		HP:0001653	OMIM:615916	TAS				P		HPO:skoehler	
OMIM	615916	CARDIOMYOPATHY, DILATED, 1NN		HP:0004308	OMIM:615916	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0000007	OMIM:615917	TAS				I		HPO:skoehler	
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0000252	OMIM:615917	TAS				P		HPO:skoehler	
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0000508	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0000590	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0001250	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0001251	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0001263	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0001290	OMIM:615917	TAS				P		HPO:skoehler	
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0001999	OMIM:615917	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615917	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 20		HP:0003593	OMIM:615917	TAS				C		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0000007	OMIM:615918	TAS				I		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0001263	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0001290	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0001397	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0002079	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0002151	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0002509	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0003577	OMIM:615918	TAS				C		HPO:skoehler	
OMIM	615918	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21		HP:0008936	OMIM:615918	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0000007	OMIM:615919	TAS				I		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0000252	OMIM:615919	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0000524	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0000613	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0000992	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001251	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001260	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001263	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001272	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001371	OMIM:615919	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0001761	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0002015	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0002180	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0002317	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0003323	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0003676	OMIM:615919	TAS				C		HPO:skoehler	
OMIM	615919	ATAXIA-TELANGIECTASIA-LIKE DISORDER 2; ATLD2		HP:0004322	OMIM:615919	TAS				P		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000006	OMIM:615922	TAS				I		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000510	OMIM:615922	IEA				P		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000543	OMIM:615922	TAS				P		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000546	OMIM:615922	TAS				P		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000662	OMIM:615922	TAS				P		HPO:skoehler	
OMIM	615922	RETINITIS PIGMENTOSA 70; RP70		HP:0000980	OMIM:615922	IEA				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0000006	OMIM:615923	TAS				I		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0000098	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0000938	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0001166	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0001847	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0002650	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0010055	OMIM:615923	TAS				P		HPO:skoehler	
OMIM	615923	EPIPHYSEAL CHONDRODYSPLASIA, MIURA TYPE; ECDM		HP:0040019	OMIM:615923	IEA				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0000007	OMIM:615924	TAS				I		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0000750	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0000752	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001250	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001251	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001257	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001268	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD	HP:0003676	HP:0001298	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001332	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001336	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001337	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0001347	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002059	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002155	OMIM:615924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002240	OMIM:615924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002273	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002371	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002376	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0002529	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0003676	OMIM:615924	TAS				C		HPO:skoehler	
OMIM	615924	ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY; PELD		HP:0007256	OMIM:615924	TAS				P		HPO:skoehler	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0000006	OMIM:615925	TAS				I		HPO:probinson	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0000007	OMIM:615925	TAS				I		HPO:probinson	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0000824	OMIM:615925	IEA				P		HPO:skoehler	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0002750	OMIM:615925	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0004322	OMIM:615925	TAS				P		HPO:probinson	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0008897	OMIM:615925	TAS				P		HPO:probinson	
OMIM	615925	GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL; GHDP		HP:0012506	OMIM:615925	TAS		HP:0040283		P		HPO:probinson	HP:0040283
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000007	OMIM:615926	TAS				I		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000011	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000028	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000076	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000126	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000278	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000490	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000618	OMIM:615926	IEA				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000824	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0000873	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0001250	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0001257	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS	HP:0012828	HP:0001263	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0002020	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0002079	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0002827	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0003228	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0005484	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0008245	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0011220	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615926	WEBB-DATTANI SYNDROME; WEDAS		HP:0012448	OMIM:615926	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0000006	OMIM:615934	TAS				I		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0000965	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001009	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001387	OMIM:615934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001508	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001510	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001882	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001894	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001903	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0001945	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0002205	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0002729	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0002829	OMIM:615934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0003326	OMIM:615934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0003565	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0003623	OMIM:615934	TAS				C		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0003828	OMIM:615934	TAS				C		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0006530	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0008404	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0010702	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0010783	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0025300	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0030880	OMIM:615934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0100614	OMIM:615934	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615934	STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET; SAVI		HP:0200039	OMIM:615934	TAS				P		HPO:skoehler	
OMIM	615935	PANCREATIC AGENESIS 2; PAGEN2		HP:0000007	OMIM:615935	TAS				I		HPO:skoehler	
OMIM	615935	PANCREATIC AGENESIS 2; PAGEN2		HP:0001518	OMIM:615935	TAS				P		HPO:skoehler	
OMIM	615935	PANCREATIC AGENESIS 2; PAGEN2		HP:0002570	OMIM:615935	TAS				P		HPO:skoehler	
OMIM	615935	PANCREATIC AGENESIS 2; PAGEN2		HP:0002594	OMIM:615935	IEA				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0000006	OMIM:615937	TAS				I		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0000238	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0000256	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0000965	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0000974	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0001162	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0001249	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0001250	OMIM:615937	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0002079	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0002119	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0002126	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0007206	OMIM:615937	TAS				P		HPO:skoehler	
OMIM	615937	#615937 MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2;MPPH2		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0000006	OMIM:615938	TAS				I		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0000238	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0000256	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0001162	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3	HP:0012828	HP:0001263	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0001344	OMIM:615938	IEA				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0001355	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0002119	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0002126	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0003577	OMIM:615938	TAS				C		HPO:skoehler	
OMIM	615938	MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3; MPPH3		HP:0011220	OMIM:615938	TAS				P		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0000007	OMIM:615942	TAS				I		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0000233	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0000343	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0001249	OMIM:615942	IEA				P		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0001250	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0001263	OMIM:615942	TAS				P		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0001763	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0003593	OMIM:615942	TAS				C		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0003828	OMIM:615942	TAS				C		HPO:skoehler	
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0005280	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0005469	OMIM:615942	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615942	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44		HP:0100543	OMIM:615942	TAS				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0000006	OMIM:615945	TAS				I		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0000639	OMIM:615945	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0001251	OMIM:615945	TAS				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0001260	OMIM:615945	TAS				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0001272	OMIM:615945	IEA				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0001337	OMIM:615945	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0002015	OMIM:615945	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0002317	OMIM:615945	TAS				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0002359	OMIM:615945	TAS				P		HPO:skoehler	
OMIM	615945	SPINOCEREBELLAR ATAXIA 37; SCA37		HP:0003677	OMIM:615945	TAS				C		HPO:skoehler	
OMIM	615946	MYOPIA 24, AUTOSOMAL DOMINANT; MYP24		HP:0000006	OMIM:615946	TAS				I		HPO:skoehler	
OMIM	615946	MYOPIA 24, AUTOSOMAL DOMINANT; MYP24	HP:0012828	HP:0000545	OMIM:615946	TAS				P		HPO:skoehler	
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0000007	OMIM:615947	TAS				I		HPO:skoehler	
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0000660	OMIM:615947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0001508	OMIM:615947	TAS				P		HPO:skoehler	
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0001744	OMIM:615947	TAS				P		HPO:skoehler	
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0002240	OMIM:615947	TAS				P		HPO:skoehler	
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0002583	OMIM:615947	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615947	HYPERLIPOPROTEINEMIA, TYPE ID		HP:0010980	OMIM:615947	IEA				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000007	OMIM:615948	TAS				I		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000054	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000175	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000180	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000243	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000252	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000506	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0000582	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0001344	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0001999	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0002079	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0002419	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0003577	OMIM:615948	TAS				C		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0008753	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0010297	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0010864	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0011069	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0011802	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0032118	OMIM:615948	IEA				P		HPO:skoehler	
OMIM	615948	OROFACIODIGITAL SYNDROME XIV; OFD14		HP:0100259	OMIM:615948	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000006	OMIM:615952	TAS				I		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000164	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000819	OMIM:615952	IEA				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000821	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000823	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0000964	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0001369	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0001890	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0001973	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0002608	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0002719	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0004313	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0004322	OMIM:615952	TAS				P		HPO:skoehler	
OMIM	615952	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1; ADMIO1		HP:0006515	OMIM:615952	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0000006	OMIM:615954	TAS				I		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0000311	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0000716	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0000822	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0000939	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0001428	OMIM:615954	TAS				I		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0003074	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0008231	OMIM:615954	TAS				P		HPO:skoehler	
OMIM	615954	ACTH-INDEPENDENT MACRONODULAR ADRENAL HYPERPLASIA 2; AIMAH2		HP:0012743	OMIM:615954	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0000006	OMIM:615957	TAS				I		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0000514	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0000639	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0001260	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0001272	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0002066	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0002070	OMIM:615957	TAS				P		HPO:skoehler	
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0003477	OMIM:615957	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615957	SPINOCEREBELLAR ATAXIA 38; SCA38		HP:0003677	OMIM:615957	TAS				C		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000007	OMIM:615959	TAS				I		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000160	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000218	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000278	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000347	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0000602	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0001270	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0001284	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0001290	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0001644	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5	HP:0012828	HP:0002093	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0003273	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0003327	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0003593	OMIM:615959	TAS				C		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0006829	OMIM:615959	TAS	HP:0003623			P		HPO:skoehler	
OMIM	615959	MYOPATHY, CENTRONUCLEAR, 5		HP:0010628	OMIM:615959	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000007	OMIM:615960	TAS				I		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000486	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000545	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000556	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000639	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000646	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000657	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0000750	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0001105	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0001270	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0001290	OMIM:615960	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0001320	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0002198	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0002282	OMIM:615960	IEA				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0002350	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0002518	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0003828	OMIM:615960	TAS				C		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0007033	OMIM:615960	TAS				P		HPO:skoehler	
OMIM	615960	PORETTI-BOLTSHAUSER SYNDROME; PTBHS		HP:0030329	PMID:25105227	PCS				P		HPO:probinson	
OMIM	615961	#615961 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD		HP:0000823	PMID:21396577	PCS				P		HPO:skoehler	
OMIM	615961	#615961 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD		HP:0001530	PMID:21396577	PCS				P		HPO:skoehler	
OMIM	615961	#615961 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD		HP:0008189	PMID:21396577	PCS				P		HPO:skoehler	
OMIM	615961	#615961 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD		HP:0030353	PMID:21396577	PCS				P		HPO:skoehler	
OMIM	615961	#615961 ACID-LABILE SUBUNIT DEFICIENCY; ACLSD		HP:0045046	OMIM:615961	TAS				P		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0000006	OMIM:615962	TAS				I		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0000739	OMIM:615962	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0000789	OMIM:615962	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0000822	OMIM:615962	TAS				P		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0000858	OMIM:615962	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0001007	OMIM:615962	TAS				P		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0001943	OMIM:615962	TAS				P		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0012378	OMIM:615962	TAS				P		HPO:skoehler	
OMIM	615962	GLUCOCORTICOID RESISTANCE, GENERALIZED; GCCR		HP:0200114	OMIM:615962	TAS				P		HPO:skoehler	
OMIM	615963	VESICOURETERAL REFLUX 8; VUR8		HP:0000006	OMIM:615963	TAS				I		HPO:skoehler	
OMIM	615963	VESICOURETERAL REFLUX 8; VUR8		HP:0000010	OMIM:615963	TAS				P		HPO:skoehler	
OMIM	615963	VESICOURETERAL REFLUX 8; VUR8		HP:0000076	OMIM:615963	TAS				P		HPO:skoehler	
OMIM	615963	VESICOURETERAL REFLUX 8; VUR8		HP:0000081	OMIM:615963	TAS				P		HPO:skoehler	
OMIM	615963	VESICOURETERAL REFLUX 8; VUR8		HP:0001382	OMIM:615963	TAS				P		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000007	OMIM:615966	TAS				I		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000054	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000219	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000252	OMIM:615966	TAS				P		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000331	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000343	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000369	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000407	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000431	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000490	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0000505	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0001250	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0001302	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0001320	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0001511	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0002079	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26	HP:0031796	HP:0002783	OMIM:615966	TAS				P		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0003429	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0003593	OMIM:615966	TAS				C		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0004430	OMIM:615966	TAS				P		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0009879	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0010557	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0011107	OMIM:615966	TAS				P		HPO:skoehler	
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0011220	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615966	IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES; IMD26		HP:0012444	OMIM:615966	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615969	ALPHA-FETOPROTEIN DEFICIENCY; AFPD		HP:0000007	PMID:15280901	PCS				I		HPO:skoehler	
OMIM	615969	ALPHA-FETOPROTEIN DEFICIENCY; AFPD		HP:0045057	PMID:15280901	PCS				P		HPO:skoehler	
OMIM	615970	ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF; HPAFP		HP:0000006	PMID:14699509	PCS				I		HPO:probinson	
OMIM	615970	ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF; HPAFP		HP:0006254	PMID:14699509	PCS				P		HPO:probinson	
OMIM	615972	NANOPHTHALMOS 4; NNO4		HP:0000006	OMIM:615972	TAS				I		HPO:skoehler	
OMIM	615972	NANOPHTHALMOS 4; NNO4		HP:0000568	OMIM:615972	IEA				P		HPO:skoehler	
OMIM	615972	NANOPHTHALMOS 4; NNO4		HP:0007663	OMIM:615972	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615972	NANOPHTHALMOS 4; NNO4		HP:0012426	OMIM:615972	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0000007	OMIM:615973	TAS				I		HPO:skoehler	
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0000548	OMIM:615973	IEA				P		HPO:skoehler	
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0000551	OMIM:615973	TAS				P		HPO:skoehler	
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0000603	OMIM:615973	IEA				P		HPO:skoehler	
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0000639	OMIM:615973	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0001133	OMIM:615973	TAS				P		HPO:skoehler	
OMIM	615973	CONE-ROD DYSTROPHY 20; CORD20		HP:0007663	OMIM:615973	TAS				P		HPO:skoehler	
OMIM	615974	DEAFNESS, AUTOSOMAL RECESSIVE 102; DFNB102		HP:0000007	PMID:24741995	PCS				I		HPO:probinson	
OMIM	615974	DEAFNESS, AUTOSOMAL RECESSIVE 102; DFNB102		HP:0003577	OMIM:615974	TAS				C		HPO:skoehler	
OMIM	615974	DEAFNESS, AUTOSOMAL RECESSIVE 102; DFNB102		HP:0012715	PMID:24741995	PCS				P		HPO:probinson	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0000006	OMIM:615978	IEA				I		HPO:skoehler	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0002721	OMIM:615978	IEA				P		HPO:skoehler	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0002754	PMID:28902581	IEA				P		HPO:probinson	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0005661	OMIM:615978	TAS				P		HPO:skoehler	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0008940	PMID:28902581	PCS				P		HPO:probinson	
OMIM	615978	#615978 IMMUNODEFICIENCY 27B; IMD27B ;;IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT;; IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT		HP:0011274	OMIM:615978	IEA				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000007	OMIM:615979	TAS				I		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000280	OMIM:615979	TAS				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000336	OMIM:615979	TAS				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000431	OMIM:615979	TAS				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000490	OMIM:615979	TAS				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0000574	OMIM:615979	TAS				P		HPO:skoehler	
OMIM	615979	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45; MRT45		HP:0001249	OMIM:615979	IEA				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0000007	OMIM:615980	TAS				I		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0000819	OMIM:615980	IEA				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0000855	OMIM:615980	TAS				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0001397	OMIM:615980	TAS				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0003119	OMIM:615980	TAS				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0003236	OMIM:615980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0003560	OMIM:615980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0003701	OMIM:615980	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0009125	OMIM:615980	IEA				P		HPO:skoehler	
OMIM	615980	LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6; FPLD6		HP:0012743	OMIM:615980	IEA				P		HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0000007	PMID:11285252	PCS				I	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0000135	OMIM:615981	TAS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0000510	PMID:23829372	PCS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0000546	OMIM:615981	TAS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0000819	PMID:23829372	PCS				P	BARDET-BIEDL SYNDROME 2	HP:probinson	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001162	PMID:11285252	PCS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001249	PMID:11285252	PCS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001263	PMID:16823392	PCS		HP:0040284		P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	2/2
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001513	PMID:11285252	PCS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001631	OMIM:615981	TAS		HP:0040283		P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	HP:0040283
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001644	PMID:7802002	PCS		HP:0040283		P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	HP:0040283
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001647	OMIM:615981	TAS		HP:0040283		P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	HP:0040283
OMIM	615981	Bardet-Biedl syndrome 2		HP:0001830	PMID:11285252	PCS				P	BARDET-BIEDL SYNDROME 2	HP:probinson	
OMIM	615981	Bardet-Biedl syndrome 2		HP:0003241	OMIM:615981	TAS				P	BARDET-BIEDL SYNDROME 2	HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000007	OMIM:615982	TAS				I		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000028	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000107	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000135	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000164	OMIM:615982	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000510	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000546	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0000662	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0001156	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0001159	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0001249	OMIM:615982	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0001513	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0003241	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615982	BARDET-BIEDL SYNDROME 4; BBS4		HP:0010442	OMIM:615982	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0000007	OMIM:615983	TAS				I		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0000135	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0000510	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0001156	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0001159	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0001513	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0003241	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0007754	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0010442	OMIM:615983	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615983	BARDET-BIEDL SYNDROME 5; BBS5		HP:0100543	OMIM:615983	TAS				P		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0000007	OMIM:615984	TAS				I		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0000510	OMIM:615984	TAS				P		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0001249	OMIM:615984	TAS				P		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0001513	OMIM:615984	TAS				P		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0003241	OMIM:615984	TAS				P		HPO:skoehler	
OMIM	615984	BARDET-BIEDL SYNDROME 7; BBS7		HP:0010442	OMIM:615984	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000007	OMIM:615985	TAS				I		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000047	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000110	OMIM:615985	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000135	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000248	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0000510	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0001249	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0001263	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0001513	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0001696	OMIM:615985	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0010442	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615985	BARDET-BIEDL SYNDROME 8; BBS8		HP:0100543	OMIM:615985	TAS				P		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0000007	OMIM:615986	TAS				I		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0000510	OMIM:615986	TAS				P		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0001249	OMIM:615986	TAS				P		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0001513	OMIM:615986	TAS				P		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0003828	OMIM:615986	TAS				C		HPO:skoehler	
OMIM	615986	BARDET-BIEDL SYNDROME 9; BBS9		HP:0010442	OMIM:615986	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0000007	OMIM:615987	TAS				I		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0000083	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0000107	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0000135	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0000510	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0001513	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0010442	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615987	BARDET-BIEDL SYNDROME 10; BBS10		HP:0100543	OMIM:615987	TAS				P		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0000007	OMIM:615988	TAS				I		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0000077	OMIM:615988	TAS				P		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0000135	OMIM:615988	TAS				P		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0000488	OMIM:615988	TAS				P		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0001513	OMIM:615988	TAS				P		HPO:skoehler	
OMIM	615988	BARDET-BIEDL SYNDROME 11; BBS11		HP:0010442	OMIM:615988	TAS				P		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0000007	OMIM:615989	TAS				I		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0000077	OMIM:615989	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0000135	OMIM:615989	TAS				P		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0000510	OMIM:615989	TAS				P		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0001513	OMIM:615989	TAS				P		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0010442	OMIM:615989	TAS				P		HPO:skoehler	
OMIM	615989	BARDET-BIEDL SYNDROME 12; BBS12		HP:0100543	OMIM:615989	TAS				P		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0000007	OMIM:615990	TAS				I		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0000510	OMIM:615990	TAS				P		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0001249	OMIM:615990	TAS				P		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0001263	OMIM:615990	TAS				P		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0001513	OMIM:615990	TAS				P		HPO:skoehler	
OMIM	615990	BARDET-BIEDL SYNDROME 13; BBS13		HP:0010442	OMIM:615990	TAS				P		HPO:skoehler	
OMIM	615991	BARDET-BIEDL SYNDROME 14; BBS14		HP:0000007	OMIM:615991	TAS				I		HPO:skoehler	
OMIM	615991	BARDET-BIEDL SYNDROME 14; BBS14		HP:0000510	OMIM:615991	TAS				P		HPO:skoehler	
OMIM	615991	BARDET-BIEDL SYNDROME 14; BBS14		HP:0001249	OMIM:615991	TAS				P		HPO:skoehler	
OMIM	615991	BARDET-BIEDL SYNDROME 14; BBS14		HP:0001263	OMIM:615991	TAS				P		HPO:skoehler	
OMIM	615991	BARDET-BIEDL SYNDROME 14; BBS14		HP:0001513	OMIM:615991	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000007	OMIM:615993	TAS				I		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000083	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000104	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000107	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000110	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000135	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000365	OMIM:615993	IEA				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000403	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000510	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0000546	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0001249	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0001263	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0001513	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0002098	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0003241	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0011950	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615993	BARDET-BIEDL SYNDROME 16; BBS16		HP:0100543	OMIM:615993	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0000007	OMIM:615994	TAS				I		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0000107	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0000135	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0000546	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0000548	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0001156	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0001263	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0001513	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0001696	OMIM:615994	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0003241	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0003774	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0100260	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615994	BARDET-BIEDL SYNDROME 17; BBS17		HP:0100543	OMIM:615994	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0000007	OMIM:615995	TAS				I		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0000083	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0000510	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0000518	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0001156	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0001513	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615995	BARDET-BIEDL SYNDROME 18; BBS18		HP:0100543	OMIM:615995	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0000007	OMIM:615996	TAS				I		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0000083	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0000135	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0000510	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0001249	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0001513	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0003241	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0004409	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	615996	BARDET-BIEDL SYNDROME 19; BBS19		HP:0010442	OMIM:615996	TAS				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0000007	OMIM:616000	IEA				I		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0000939	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0002615	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0003073	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0003077	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0009125	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616000	#616000 ANALBUMINEMIA; ANALBA		HP:0012378	OMIM:616000	IEA				P		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0000007	OMIM:616001	TAS				I		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0000319	OMIM:616001	TAS				P		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0000385	OMIM:616001	TAS				P		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0000455	OMIM:616001	TAS				P		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0002557	OMIM:616001	IEA				P		HPO:skoehler	
OMIM	616001	BREASTS AND/OR NIPPLES, APLASIA OR HYPOPLASIA OF, 2; BNAH2		HP:0002561	OMIM:616001	TAS				P		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0000006	OMIM:616002	TAS				I		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0000089	OMIM:616002	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0000093	OMIM:616002	TAS				P		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0000097	OMIM:616002	TAS				P		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0000100	OMIM:616002	TAS				P		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0003774	OMIM:616002	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0003828	OMIM:616002	TAS				C		HPO:skoehler	
OMIM	616002	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7; FSGS7		HP:0003829	OMIM:616002	TAS				C		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0000006	OMIM:616005	TAS				I		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0001888	OMIM:616005	IEA				P		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0002205	OMIM:616005	TAS				P		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0002718	OMIM:616005	TAS				P		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0002721	OMIM:616005	IEA				P		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0002960	OMIM:616005	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0004313	OMIM:616005	TAS				P		HPO:skoehler	
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0005550	OMIM:616005	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616005	IMMUNODEFICIENCY 36; IMD36		HP:0012191	OMIM:616005	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000007	PMID:24913602	PCS				I		HPO:skoehler	
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000160	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	6/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000286	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000316	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000365	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	2/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000581	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	6/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0000939	PMID:24913602	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0001004	PMID:24913602	PCS				P		HPO:skoehler	
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0001159	PMID:24913602	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0001256	PMID:24913602	PCS		HP:0040284		P		HPO:probinson	7/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0001510	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	5/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0002593	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	7/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0005183	PMID:24913602	PCS				P		HPO:skoehler	
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0005280	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	8/9
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0006521	PMID:24913602	PCS				P		HPO:skoehler	
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0008551	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	8/8
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0012368	PMID:24913602	PCS				P		HPO:skoehler	
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0012385	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	5/8
OMIM	616006	#616006 HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 2; HKLLS2		HP:0040079	PMID:24913602	PCS		HP:0040284		P		HPO:skoehler	8/8
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000007	OMIM:616007	TAS				I		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000343	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000407	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000518	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000639	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000763	OMIM:616007	IEA				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000824	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0000938	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0001265	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0001270	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0001371	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0001374	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0002650	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0002936	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0003416	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0004322	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0005280	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616007	CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA; CAGSSS		HP:0007141	OMIM:616007	TAS				P		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0000007	OMIM:616022	TAS				I		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0000403	OMIM:616022	TAS				P		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0001508	OMIM:616022	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0001875	OMIM:616022	TAS				P		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0002205	OMIM:616022	TAS				P		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0002718	OMIM:616022	TAS				P		HPO:skoehler	
OMIM	616022	NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE; SCN6		HP:0004322	OMIM:616022	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0000007	OMIM:616025	TAS				I		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0000158	OMIM:616025	IEA				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0000431	OMIM:616025	TAS				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0001249	OMIM:616025	IEA				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0001250	OMIM:616025	IEA				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11	HP:0012829	HP:0001263	OMIM:616025	TAS				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0001344	OMIM:616025	IEA				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0002521	OMIM:616025	TAS				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0003155	OMIM:616025	TAS				P		HPO:skoehler	
OMIM	616025	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 11; GPIBD11		HP:0010804	OMIM:616025	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0000006	OMIM:616026	TAS				I		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0000093	OMIM:616026	IEA				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0000121	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0000819	OMIM:616026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0001520	OMIM:616026	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0001943	OMIM:616026	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0002240	OMIM:616026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0002748	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0003076	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0003109	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0003355	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0003537	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616026	FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG; FRTS4		HP:0004322	OMIM:616026	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0000006	OMIM:616028	TAS				I		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0000023	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001048	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001057	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001156	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001159	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001250	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001537	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001642	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001655	OMIM:616028	IEA				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001667	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001744	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001810	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0001971	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0002040	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0002092	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0025107	OMIM:616028	TAS				P		HPO:skoehler	
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0030242	OMIM:616028	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616028	ADAMS-OLIVER SYNDROME 5; AOS5		HP:0030718	OMIM:616028	IEA				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0000007	OMIM:616029	TAS				I		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0000668	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME	HP:0012825	HP:0000962	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0001798	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0002015	OMIM:616029	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0002099	OMIM:616029	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0004322	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0006297	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0008404	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616029	ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME		HP:0025092	OMIM:616029	TAS				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000007	OMIM:616030	TAS				I		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000028	OMIM:616030	TAS				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000054	OMIM:616030	TAS				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000135	OMIM:616030	IEA				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000458	OMIM:616030	TAS				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0000786	OMIM:616030	TAS				P		HPO:skoehler	
OMIM	616030	HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA; HH22		HP:0008734	OMIM:616030	TAS				P		HPO:skoehler	
OMIM	616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8		HP:0000006	OMIM:616032	TAS				I		HPO:skoehler	
OMIM	616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8		HP:0000093	OMIM:616032	TAS				P		HPO:skoehler	
OMIM	616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8		HP:0000097	OMIM:616032	TAS				P		HPO:skoehler	
OMIM	616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8		HP:0000100	OMIM:616032	TAS				P		HPO:skoehler	
OMIM	616032	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8; FSGS8		HP:0003774	OMIM:616032	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000007	OMIM:616033	TAS				I		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000252	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000445	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000470	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000786	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000825	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0000939	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0001249	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0001250	OMIM:616033	IEA				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0001270	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0001388	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0002650	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0004322	OMIM:616033	TAS				P		HPO:skoehler	
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0025383	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616033	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1		HP:0025515	OMIM:616033	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0000007	OMIM:616034	TAS				I	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0000252	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0000639	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001250	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001257	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD	HP:0012829	HP:0001263	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001266	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001298	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001319	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001332	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001508	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0001522	OMIM:616034	TAS				M	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0002059	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0002119	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0002161	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0002415	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0002445	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0008315	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616034	2,4-DIENOYL-CoA REDUCTASE DEFICIENCY; DECRD		HP:0100704	OMIM:616034	TAS				P	2,4-DIENOYL-COA REDUCTASE DEFICIENCY; DECRD	HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0000007	OMIM:616037	TAS				I		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0000403	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0001696	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0001742	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0002099	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0002110	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0002205	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0004469	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0012256	OMIM:616037	IEA				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0012265	OMIM:616037	IEA				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0012735	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0100582	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616037	CILIARY DYSKINESIA, PRIMARY, 30; CILD30		HP:0200073	OMIM:616037	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000007	OMIM:616038	TAS				I		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000175	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000218	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000252	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000316	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000340	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000347	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000369	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000377	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000457	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0000470	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0001511	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0001558	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0001838	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0002650	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0003577	OMIM:616038	TAS				C		HPO:skoehler	
OMIM	616038	NEU-LAXOVA SYNDROME 2; NLS2		HP:0008064	OMIM:616038	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0000007	OMIM:616039	TAS				I		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0001265	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0001284	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0001761	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0002936	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0003376	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0003383	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0003677	OMIM:616039	TAS				C		HPO:skoehler	
OMIM	616039	CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D; CMTRID		HP:0009027	OMIM:616039	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0000006	OMIM:616040	TAS				I		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0000365	OMIM:616040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0001265	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0001284	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0001288	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0001761	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0001765	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0002460	OMIM:616040	TAS				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0003202	OMIM:616040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0003388	OMIM:616040	IEA				P		HPO:skoehler	
OMIM	616040	MYASTHENIC SYNDROME, CONGENITAL, 7, PRESYNAPTIC; CMS7		HP:0003701	OMIM:616040	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616042	DEAFNESS, AUTOSOMAL RECESSIVE 103; DFNB103		HP:0000007	OMIM:616042	TAS				I		HPO:skoehler	
OMIM	616042	DEAFNESS, AUTOSOMAL RECESSIVE 103; DFNB103		HP:0000407	OMIM:616042	TAS				P		HPO:skoehler	
OMIM	616042	DEAFNESS, AUTOSOMAL RECESSIVE 103; DFNB103		HP:0003593	OMIM:616042	TAS				C		HPO:skoehler	
OMIM	616042	DEAFNESS, AUTOSOMAL RECESSIVE 103; DFNB103		HP:0008568	OMIM:616042	TAS				P		HPO:skoehler	
OMIM	616044	DEAFNESS, AUTOSOMAL DOMINANT 65; DFNA65		HP:0000006	OMIM:616044	IEA				I		HPO:skoehler	
OMIM	616044	DEAFNESS, AUTOSOMAL DOMINANT 65; DFNA65		HP:0001730	OMIM:616044	IEA				P		HPO:skoehler	
OMIM	616044	DEAFNESS, AUTOSOMAL DOMINANT 65; DFNA65		HP:0003677	OMIM:616044	TAS				C		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0000007	OMIM:616045	TAS				I		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0000252	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001250	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001290	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001298	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001508	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001511	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0001635	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0002092	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0003348	OMIM:616045	TAS				P		HPO:skoehler	
OMIM	616045	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22		HP:0003577	OMIM:616045	TAS				C		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0000006	OMIM:616050	TAS				I		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0000988	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0001508	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0001744	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC	HP:0025303	HP:0001876	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC	HP:0025303	HP:0001945	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0002829	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0003281	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0003326	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0004322	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0004387	OMIM:616050	IEA				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC		HP:0005208	OMIM:616050	IEA				P		HPO:skoehler	
OMIM	616050	AUTOINFLAMMATION WITH INFANTILE ENTEROCOLITIS; AIFEC	HP:0025303	HP:0005521	OMIM:616050	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:616051	TAS				I		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000311	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000340	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000347	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000448	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001321	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001338	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001511	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001773	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004979	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0009879	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616051	MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE		HP:0200055	OMIM:616051	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0000007	OMIM:616052	TAS				I		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0000158	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0001324	OMIM:616052	IEA				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0003236	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0003677	OMIM:616052	TAS				C		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0003691	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0006785	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0008981	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616052	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7; MDDGC7		HP:0030046	OMIM:616052	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0000006	OMIM:616053	TAS				I		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0001260	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0001310	OMIM:616053	IEA				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0001347	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0002075	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0002080	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0002136	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0002313	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0002317	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0003581	OMIM:616053	TAS				C		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0003677	OMIM:616053	TAS				C		HPO:skoehler	
OMIM	616053	SPINOCEREBELLAR ATAXIA 40; SCA40		HP:0006879	OMIM:616053	TAS				P		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0000006	OMIM:616055	TAS				I		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0000639	OMIM:616055	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616055	EPISODIC ATAXIA, TYPE 8	HP:0025303	HP:0001251	OMIM:616055	TAS				P		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0001260	OMIM:616055	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616055	EPISODIC ATAXIA, TYPE 8	HP:0025303	HP:0001324	OMIM:616055	TAS				P		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8	HP:0025303	HP:0001350	OMIM:616055	TAS				P		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0002080	OMIM:616055	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0002131	OMIM:616055	IEA				P		HPO:skoehler	
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0002411	OMIM:616055	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616055	EPISODIC ATAXIA, TYPE 8		HP:0003680	OMIM:616055	TAS				C		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0000006	OMIM:616056	TAS				I		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0001250	OMIM:616056	TAS				P		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0001263	OMIM:616056	TAS				P		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0001290	OMIM:616056	TAS				P		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0001344	OMIM:616056	IEA				P		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0002521	OMIM:616056	TAS				P		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0003593	OMIM:616056	TAS				C		HPO:skoehler	
OMIM	616056	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 26; EIEE26		HP:0200134	OMIM:616056	TAS				P		HPO:skoehler	
OMIM	616059	MIRROR MOVEMENTS 3; MRMV3		HP:0000007	OMIM:616059	TAS				I		HPO:skoehler	
OMIM	616059	MIRROR MOVEMENTS 3; MRMV3		HP:0001335	OMIM:616059	IEA				P		HPO:skoehler	
OMIM	616063	POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK8		HP:0000006	OMIM:616063	TAS				I		HPO:skoehler	
OMIM	616063	POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK8		HP:0200034	OMIM:616063	IEA				P		HPO:skoehler	
OMIM	616063	POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK8		HP:0200044	OMIM:616063	IEA				P		HPO:skoehler	
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0000006	OMIM:616067	TAS				I		HPO:skoehler	
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0000062	OMIM:616067	TAS				P		HPO:skoehler	
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0000063	OMIM:616067	TAS				P		HPO:skoehler	
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0000133	OMIM:616067	IEA				P		HPO:skoehler	
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0000729	OMIM:616067	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616067	46,XY SEX REVERSAL 9; SRXY9		HP:0012245	OMIM:616067	IEA				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0000007	OMIM:616069	TAS				I		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0000527	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0000822	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0000969	OMIM:616069	IEA				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0001508	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0001944	OMIM:616069	IEA				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0002013	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0002014	OMIM:616069	IEA				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0006532	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0025092	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0100501	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0200034	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616069	INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2; NISBD2		HP:0200039	OMIM:616069	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000006	OMIM:616078	TAS				I		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000189	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000218	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000219	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000248	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000276	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000307	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000316	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000369	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000494	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000508	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000664	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0000678	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0001249	OMIM:616078	IEA				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0001250	OMIM:616078	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0001270	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0001344	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616078	MENTAL RETARDATION, AUTOSOMAL DOMINANT 29; MRD29		HP:0007018	OMIM:616078	TAS				P		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA		HP:0000006	OMIM:616079	TAS				I		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA		HP:0000543	OMIM:616079	TAS				P		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA		HP:0000556	OMIM:616079	TAS				P		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA		HP:0000603	OMIM:616079	IEA				P		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA	HP:0012825	HP:0000613	OMIM:616079	TAS				P		HPO:skoehler	
OMIM	616079	RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA		HP:0000662	OMIM:616079	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12		HP:0000007	OMIM:616080	TAS				I		HPO:skoehler	
OMIM	616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12		HP:0000252	OMIM:616080	TAS				P		HPO:skoehler	
OMIM	616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12		HP:0000340	OMIM:616080	TAS				P		HPO:skoehler	
OMIM	616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12		HP:0001256	OMIM:616080	TAS				P		HPO:skoehler	
OMIM	616080	MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE; MCPH12		HP:0009879	OMIM:616080	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0000007	OMIM:616081	TAS				I		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0000365	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0000505	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0001263	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0001285	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0001320	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C	HP:0012828	HP:0001324	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0001371	OMIM:616081	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0001508	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0002079	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0002120	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0002878	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0007269	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616081	PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C		HP:0011968	OMIM:616081	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000006	OMIM:616083	TAS				I		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000154	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000316	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000508	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000718	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0000750	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0001256	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0001263	OMIM:616083	TAS				P		HPO:skoehler	
OMIM	616083	MENTAL RETARDATION, AUTOSOMAL DOMINANT 30; MRD30		HP:0001999	OMIM:616083	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0000007	OMIM:616084	TAS				I		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0000121	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0000407	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0000510	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001250	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001251	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001263	OMIM:616084	TAS				P		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001290	OMIM:616084	TAS				P		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001317	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001510	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001638	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001888	OMIM:616084	IEA				P		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0001924	OMIM:616084	TAS				P		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0002059	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0002299	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0003128	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0003355	OMIM:616084	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0003828	OMIM:616084	TAS				C		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0004313	OMIM:616084	TAS				P		HPO:skoehler	
OMIM	616084	SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS, AND DEVELOPMENTAL DELAY; SIFD		HP:0004840	OMIM:616084	TAS				P		HPO:skoehler	
OMIM	616089	#616089 BLOOD GROUP, GERBICH SYSTEM; GE ;;GERBICH BLOOD GROUP SYSTEM		HP:0004445	OMIM:616089	IEA				P		HPO:skoehler	
OMIM	616089	#616089 BLOOD GROUP, GERBICH SYSTEM; GE ;;GERBICH BLOOD GROUP SYSTEM		HP:0010970	OMIM:616089	IEA				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0000007	OMIM:616094	TAS				I		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0001265	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0001270	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0001319	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0003236	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0003391	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0003551	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0003560	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12		HP:0003593	OMIM:616094	TAS				C		HPO:skoehler	
OMIM	616094	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12; MDDGC12	HP:0012825	HP:0100543	OMIM:616094	TAS				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0000006	OMIM:616095	TAS				I		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0000007	OMIM:616095	TAS				I		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0001249	OMIM:616095	TAS				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0001263	OMIM:616095	TAS				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D	HP:0012828	HP:0001993	OMIM:616095	TAS				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0002919	OMIM:616095	IEA				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0011968	OMIM:616095	TAS				P		HPO:skoehler	
OMIM	616095	MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D		HP:0012734	OMIM:616095	TAS				P		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0000007	OMIM:616098	TAS				I		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0001250	OMIM:616098	TAS				P		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0002383	OMIM:616098	TAS				P		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0002719	OMIM:616098	TAS				P		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0002721	OMIM:616098	TAS				P		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0003593	OMIM:616098	TAS				C		HPO:skoehler	
OMIM	616098	IMMUNODEFICIENCY 37; IMD37		HP:0004313	OMIM:616098	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0000007	OMIM:616099	TAS				I		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0000535	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0000653	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0000982	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0002209	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0002231	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0040149	OMIM:616099	TAS				P		HPO:skoehler	
OMIM	616099	PALMOPLANTAR KERATODERMA AND WOOLLY HAIR; PPKWH		HP:0040149	OMIM:616099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0000006	OMIM:616100	TAS				I		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0000964	OMIM:616100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0001744	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0001888	OMIM:616100	IEA				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0001890	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0001973	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0002014	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0002240	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0002716	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0002788	OMIM:616100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0003765	OMIM:616100	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0003829	OMIM:616100	TAS				C		HPO:skoehler	
OMIM	616100	AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V; ALPS5		HP:0004313	OMIM:616100	TAS				P		HPO:skoehler	
OMIM	616106	PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO; PSORS15		HP:0000006	OMIM:616106	TAS				I		HPO:skoehler	
OMIM	616106	PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO; PSORS15		HP:0003765	OMIM:616106	IEA				P		HPO:skoehler	
OMIM	616106	PSORIASIS 15, PUSTULAR, SUSCEPTIBILITY TO; PSORS15		HP:0008404	OMIM:616106	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0000007	OMIM:616108	TAS				I		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0000272	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0000556	OMIM:616108	IEA				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS	HP:0012825	HP:0000582	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0000687	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0000689	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0001070	OMIM:616108	IEA				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0001263	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0004322	OMIM:616108	TAS				P		HPO:skoehler	
OMIM	616108	RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME; RDJCSS		HP:0025356	OMIM:616108	IEA				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0000007	OMIM:616111	TAS				I		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0001263	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0001290	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0001510	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0001943	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0002151	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0003128	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0003577	OMIM:616111	TAS				C		HPO:skoehler	
OMIM	616111	MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9		HP:0011968	OMIM:616111	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0000007	OMIM:616113	TAS				I		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0000135	OMIM:616113	IEA				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001251	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001260	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001270	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001271	OMIM:616113	IEA				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001321	OMIM:616113	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001332	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001730	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0001943	OMIM:616113	IEA				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0002342	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0004322	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0008897	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616113	POLYENDOCRINE-POLYNEUROPATHY SYNDROME; PEPNS		HP:0011787	OMIM:616113	TAS				P		HPO:skoehler	
OMIM	616115	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4		HP:0000006	OMIM:616115	TAS				I		HPO:skoehler	
OMIM	616115	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4	HP:0025303	HP:0002829	OMIM:616115	TAS				P		HPO:skoehler	
OMIM	616115	FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 4		HP:0025303	OMIM:616115	TAS				C		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0000007	OMIM:616116	TAS				I		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0000713	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0000718	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0001249	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0001250	OMIM:616116	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0001263	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0001290	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0001510	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0002360	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616116	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46		HP:0002465	OMIM:616116	TAS				P		HPO:skoehler	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0000006	PMID:24925317	IEA				I		HPO:probinson	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0001635	OMIM:616117	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0001644	PMID:24925317	IEA				P		HPO:probinson	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0001649	OMIM:616117	IEA				P		HPO:skoehler	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0001692	PMID:24925317	IEA				P		HPO:probinson	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0004749	OMIM:616117	TAS				P		HPO:skoehler	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0005110	OMIM:616117	TAS				P		HPO:skoehler	
OMIM	616117	CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY; CCDD		HP:0011711	PMID:24925317	IEA				P		HPO:probinson	
OMIM	616118	#616118 MACULAR DEGENERATION, EARLY-ONSET; EOMD		HP:0000006	PMID:24899048	PCS				I		HPO:skoehler	
OMIM	616118	#616118 MACULAR DEGENERATION, EARLY-ONSET; EOMD		HP:0000608	PMID:24899048	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	616118	#616118 MACULAR DEGENERATION, EARLY-ONSET; EOMD		HP:0007663	PMID:24899048	PCS				P		HPO:skoehler	
OMIM	616118	#616118 MACULAR DEGENERATION, EARLY-ONSET; EOMD		HP:0011506	PMID:24899048	PCS	HP:0011462	HP:0040284		P		HPO:skoehler	1/4
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0000007	PMID:22859821	PCS				I		HPO:probinson	
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0001250	PMID:25307056	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0002135	PMID:25307056	IEA				P		HPO:skoehler	
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0002716	PMID:22859821	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0002721	OMIM:616126	IEA				P		HPO:skoehler	
OMIM	616126	IMMUNODEFICIENCY 38 WITH BASAL GANGLIA CALCIFICATION; IMD38		HP:0011274	PMID:22859821	PCS				P		HPO:probinson	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0000007	OMIM:616127	TAS				I		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001249	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001260	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001263	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001290	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001310	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001321	OMIM:616127	IEA				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0001337	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0002078	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0002317	OMIM:616127	TAS				P		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0003593	OMIM:616127	TAS				C		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0003677	OMIM:616127	TAS				C		HPO:skoehler	
OMIM	616127	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 17; SCAR17		HP:0003680	OMIM:616127	TAS				C		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000007	OMIM:616138	TAS				I		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000133	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000218	OMIM:616138	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5	HP:0012825	HP:0000602	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000639	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000786	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0000815	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0001250	OMIM:616138	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0001251	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0001265	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0001761	OMIM:616138	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5	HP:0012825	HP:0002151	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0002403	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5		HP:0003390	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616138	PERRAULT SYNDROME 5; PRLTS5	HP:0012825	HP:0003542	OMIM:616138	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0000006	OMIM:616139	TAS				I		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001249	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001250	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001257	OMIM:616139	IEA				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001263	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001290	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001332	OMIM:616139	IEA				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0001344	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0002072	OMIM:616139	IEA				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0002521	OMIM:616139	IEA				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0003828	OMIM:616139	TAS				C		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0100660	OMIM:616139	IEA				P		HPO:skoehler	
OMIM	616139	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 27; EIEE27		HP:0200134	OMIM:616139	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0000007	OMIM:616140	TAS				I		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0000252	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0000639	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001249	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001257	OMIM:616140	IEA				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001260	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001263	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001310	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0001347	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0002071	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0002079	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0002080	OMIM:616140	TAS				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0002415	OMIM:616140	IEA				P		HPO:skoehler	
OMIM	616140	LEUKODYSTROPHY, HYPOMYELINATING, 9; HLD9		HP:0003828	OMIM:616140	TAS				C		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000007	OMIM:616145	TAS				I		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000023	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000028	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000162	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000175	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000204	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000218	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000347	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000369	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000377	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000470	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000476	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000767	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000768	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0000954	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001250	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001263	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001373	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001388	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001511	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001537	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001629	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001651	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001680	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0001762	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0002623	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0004209	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0008897	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0009464	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0012385	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616145	CATEL-MANZKE SYNDROME; CATMANS		HP:0030368	OMIM:616145	TAS				P		HPO:skoehler	
OMIM	616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4		HP:0000006	OMIM:616151	IEA				I		HPO:skoehler	
OMIM	616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4		HP:0007677	OMIM:616151	IEA				P		HPO:skoehler	
OMIM	616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4		HP:0007754	OMIM:616151	IEA				P		HPO:skoehler	
OMIM	616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4		HP:0011510	OMIM:616151	IEA				P		HPO:skoehler	
OMIM	616151	MACULAR DYSTROPHY, VITELLIFORM, 4; VMD4		HP:0030515	OMIM:616151	IEA				P		HPO:skoehler	
OMIM	616152	#616152 MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5		HP:0000006	OMIM:616152	IEA				I		HPO:skoehler	
OMIM	616152	#616152 MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5		HP:0000603	OMIM:616152	IEA				P		HPO:skoehler	
OMIM	616152	#616152 MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5		HP:0007677	OMIM:616152	IEA				P		HPO:skoehler	
OMIM	616152	#616152 MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5		HP:0007754	OMIM:616152	IEA				P		HPO:skoehler	
OMIM	616152	#616152 MACULAR DYSTROPHY, VITELLIFORM, 5; VMD5		HP:0030515	OMIM:616152	IEA				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000007	OMIM:616154	TAS				I		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000219	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000252	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000280	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000343	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000400	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0000518	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001249	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001250	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001257	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER	HP:0012828	HP:0001263	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001272	OMIM:616154	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001290	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0001510	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616154	PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER		HP:0002553	OMIM:616154	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0000007	OMIM:616155	TAS				I		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0001265	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0001284	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0001762	OMIM:616155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0002650	OMIM:616155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0002936	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0003376	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0003677	OMIM:616155	TAS				C		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0003701	OMIM:616155	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0007141	OMIM:616155	IEA				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0009027	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616155	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S; CMT2S		HP:0040078	OMIM:616155	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000006	OMIM:616158	TAS				I		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000194	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000218	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000486	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000506	OMIM:616158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0000639	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0001249	OMIM:616158	IEA				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0001250	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31	HP:0012828	HP:0001263	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0001319	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0001336	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0001344	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0002058	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0002093	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0002136	OMIM:616158	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0003429	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0003828	OMIM:616158	TAS				C		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0011220	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0011968	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616158	MENTAL RETARDATION, AUTOSOMAL DOMINANT 31; MRD31		HP:0012448	OMIM:616158	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0000007	OMIM:616165	TAS				I		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0000602	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0001283	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0001290	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0001558	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0001561	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0001622	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0002747	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0002804	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0003202	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0003324	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0006829	OMIM:616165	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616165	NEMALINE MYOPATHY 10		HP:0010628	OMIM:616165	TAS				P		HPO:skoehler	
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0000006	OMIM:616166	TAS				I		HPO:skoehler	
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0000218	OMIM:616166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0000767	OMIM:616166	TAS				P		HPO:skoehler	
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0000768	OMIM:616166	TAS				P		HPO:skoehler	
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0001166	OMIM:616166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0001634	OMIM:616166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0005110	OMIM:616166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616166	AORTIC ANEURYSM, FAMILIAL THORACIC 9; AAT9		HP:0012727	OMIM:616166	TAS				P		HPO:skoehler	
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0000007	OMIM:616170	TAS				I		HPO:skoehler	
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0000543	OMIM:616170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0000603	OMIM:616170	IEA				P		HPO:skoehler	
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0007663	OMIM:616170	TAS				P		HPO:skoehler	
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0007754	OMIM:616170	IEA				P		HPO:skoehler	
OMIM	616170	MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT; CCMD		HP:0011504	OMIM:616170	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000007	OMIM:616171	TAS				I		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000252	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000340	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000347	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000448	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000482	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000488	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000505	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000518	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000520	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000543	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000568	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0000648	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0001249	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0001250	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2	HP:0012829	HP:0001263	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0001272	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0001511	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0002059	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0003577	OMIM:616171	TAS				C		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0004322	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0007401	OMIM:616171	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616171	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2		HP:0009879	OMIM:616171	TAS				P		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0000006	OMIM:616172	TAS				I		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0001263	OMIM:616172	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0002069	OMIM:616172	TAS				P		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0002121	OMIM:616172	TAS				P		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0002373	OMIM:616172	IEA				P		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0002384	OMIM:616172	TAS				P		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0003828	OMIM:616172	TAS				C		HPO:skoehler	
OMIM	616172	GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 9; GEFSP9		HP:0010819	OMIM:616172	TAS				P		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0000007	OMIM:616176	TAS				I		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0000132	OMIM:616176	TAS				P		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0000421	OMIM:616176	TAS				P		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0001903	OMIM:616176	TAS				P		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0007420	OMIM:616176	TAS				P		HPO:skoehler	
OMIM	616176	BLEEDING DISORDER, PLATELET-TYPE, 19; BDPLT19		HP:0040185	OMIM:616176	TAS				P		HPO:skoehler	
OMIM	616185	OVARIAN DYSGENESIS 4; ODG4		HP:0000007	OMIM:616185	TAS				I		HPO:skoehler	
OMIM	616185	OVARIAN DYSGENESIS 4; ODG4		HP:0000786	OMIM:616185	TAS				P		HPO:skoehler	
OMIM	616185	OVARIAN DYSGENESIS 4; ODG4		HP:0002750	OMIM:616185	TAS				P		HPO:skoehler	
OMIM	616185	OVARIAN DYSGENESIS 4; ODG4		HP:0004322	OMIM:616185	TAS				P		HPO:skoehler	
OMIM	616185	OVARIAN DYSGENESIS 4; ODG4		HP:0004325	OMIM:616185	TAS				P		HPO:skoehler	
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0000006	OMIM:616187	TAS				I		HPO:skoehler	
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001250	OMIM:616187	IEA				P		HPO:skoehler	
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001251	OMIM:616187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001268	OMIM:616187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001272	OMIM:616187	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001336	OMIM:616187	TAS				P		HPO:skoehler	
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0001337	OMIM:616187	TAS				P		HPO:skoehler	
OMIM	616187	EPILEPSY, PROGRESSIVE MYOCLONIC 7; EPM7		HP:0003676	OMIM:616187	TAS				C		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0000007	OMIM:616188	TAS				I		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0000483	OMIM:616188	TAS				P		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0000541	OMIM:616188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0000545	OMIM:616188	TAS				P		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0000556	OMIM:616188	IEA				P		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0001513	OMIM:616188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0007663	OMIM:616188	TAS				P		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0007722	OMIM:616188	IEA				P		HPO:skoehler	
OMIM	616188	RETINAL DYSTROPHY AND OBESITY; RDOB		HP:0500087	OMIM:616188	IEA				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0000007	OMIM:616192	TAS				I		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0000407	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0001272	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0001284	OMIM:616192	IEA				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0002059	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0002066	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0003487	OMIM:616192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0004322	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0007366	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0009830	OMIM:616192	IEA				P		HPO:skoehler	
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0100543	OMIM:616192	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616192	ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS; ACPHD		HP:0100651	OMIM:616192	TAS				P		HPO:skoehler	
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0000007	OMIM:616193	TAS				I		HPO:skoehler	
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0001249	OMIM:616193	IEA				P		HPO:skoehler	
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0001263	OMIM:616193	TAS				P		HPO:skoehler	
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0001290	OMIM:616193	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0002384	OMIM:616193	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0002465	OMIM:616193	TAS				P		HPO:skoehler	
OMIM	616193	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 47		HP:0003593	OMIM:616193	TAS				C		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0000007	OMIM:616198	TAS				I		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0000505	OMIM:616198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001250	OMIM:616198	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001263	OMIM:616198	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001290	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001511	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001635	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0001638	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0002151	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0003128	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0003828	OMIM:616198	TAS				C		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0011675	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616198	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23		HP:0011968	OMIM:616198	TAS				P		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0000007	OMIM:616199	TAS				I		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0002355	OMIM:616199	IEA				P		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0002460	OMIM:616199	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0003202	OMIM:616199	TAS				P		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0003325	OMIM:616199	TAS				P		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0003677	OMIM:616199	TAS				C		HPO:skoehler	
OMIM	616199	POLYGLUCOSAN BODY MYOPATHY 2; PGBM2		HP:0003828	OMIM:616199	TAS				C		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0000007	OMIM:616200	TAS				I		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0000325	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0000347	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0000414	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0000426	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS	HP:0012825	HP:0000767	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0001402	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0001763	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0002007	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0002750	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0002987	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0003202	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0004322	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0004325	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0005659	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS	HP:0012832	HP:0007787	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0009125	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0030084	OMIM:616200	IEA				P		HPO:skoehler	
OMIM	616200	RUIJS-AALFS SYNDROME; RJALS		HP:0200021	OMIM:616200	TAS				P		HPO:skoehler	
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0000007	OMIM:616201	TAS				I		HPO:skoehler	
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0001508	OMIM:616201	TAS				P		HPO:skoehler	
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0001642	OMIM:616201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0001647	OMIM:616201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0001653	OMIM:616201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0001662	OMIM:616201	TAS				P		HPO:skoehler	
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0004749	OMIM:616201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0005110	OMIM:616201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616201	CHRONIC ATRIAL AND INTESTINAL DYSRHYTHMIA; CAID		HP:0011704	OMIM:616201	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000007	OMIM:616202	TAS				I		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000252	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000369	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000470	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000535	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000675	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000679	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0000689	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0001182	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0001249	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0001263	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0001321	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0001601	OMIM:616202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0002213	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0002650	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0003100	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0003593	OMIM:616202	TAS				C		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0004322	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0006511	OMIM:616202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0008070	OMIM:616202	TAS				P		HPO:skoehler	
OMIM	616202	CEREBELLOFACIODENTAL SYNDROME		HP:0012110	OMIM:616202	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0000007	OMIM:616204	TAS				I		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0000543	OMIM:616204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0000565	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0000639	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0000657	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001260	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001263	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18	HP:0012828	HP:0001272	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001290	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001310	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001347	OMIM:616204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0001371	OMIM:616204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0002066	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0002075	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0002078	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0002311	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0002465	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0003487	OMIM:616204	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0003593	OMIM:616204	TAS				C		HPO:skoehler	
OMIM	616204	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18		HP:0100543	OMIM:616204	TAS				P		HPO:skoehler	
OMIM	616208	AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS22		HP:0000006	OMIM:616208	TAS				I		HPO:skoehler	
OMIM	616208	AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS22		HP:0002145	OMIM:616208	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616208	AMYOTROPHIC LATERAL SCLEROSIS 22 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA; ALS22		HP:0007354	OMIM:616208	IEA				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0000006	OMIM:616209	TAS				I		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0002151	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0003236	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0003546	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0003677	OMIM:616209	TAS				C		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0003722	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0004322	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0008994	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616209	MYOPATHY, ISOLATED MITOCHONDRIAL, AUTOSOMAL DOMINANT; IMMD		HP:0010628	OMIM:616209	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0000007	OMIM:616211	TAS				I		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0000253	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0000512	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0000546	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0000648	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28	HP:0031375	HP:0001250	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0001257	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28	HP:0012829	HP:0001263	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0001347	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0002059	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0002063	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0002079	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0002375	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0003828	OMIM:616211	TAS				C		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0008936	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0012448	OMIM:616211	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616211	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28; EIEE28		HP:0200134	OMIM:616211	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0000007	OMIM:616212	TAS				I		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0000252	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0000340	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001250	OMIM:616212	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001257	OMIM:616212	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001263	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001270	OMIM:616212	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001302	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001338	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0001347	OMIM:616212	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0002079	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0002119	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0002126	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0002282	OMIM:616212	IEA				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0002509	OMIM:616212	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0003593	OMIM:616212	TAS				C		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0009879	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616212	LISSENCEPHALY 6 WITH MICROCEPHALY; LIS6		HP:0100543	OMIM:616212	TAS				P		HPO:skoehler	
OMIM	616214	HYPERPROINSULINEMIA		HP:0000006	OMIM:616214	TAS				I		HPO:skoehler	
OMIM	616214	HYPERPROINSULINEMIA		HP:0000842	OMIM:616214	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616214	HYPERPROINSULINEMIA		HP:0003074	OMIM:616214	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0000006	OMIM:616216	TAS				I		HPO:skoehler	
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0000421	OMIM:616216	TAS				P		HPO:skoehler	
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0000967	OMIM:616216	TAS				P		HPO:skoehler	
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0000978	OMIM:616216	TAS				P		HPO:skoehler	
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0001873	OMIM:616216	TAS				P		HPO:skoehler	
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0001875	OMIM:616216	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616216	THROMBOCYTOPENIA 5; THC5		HP:0001903	OMIM:616216	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0000007	OMIM:616217	TAS				I		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0000090	OMIM:616217	IEA				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0000090	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0001395	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0001396	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0001408	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0001744	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0002240	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616217	NEPHRONOPHTHISIS 19; NPHP19		HP:0003774	OMIM:616217	TAS				P		HPO:skoehler	
OMIM	616219	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5; CFEOM5		HP:0000007	OMIM:616219	TAS				I		HPO:skoehler	
OMIM	616219	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5; CFEOM5		HP:0000508	OMIM:616219	TAS				P		HPO:skoehler	
OMIM	616219	FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5; CFEOM5		HP:0003577	OMIM:616219	TAS				C		HPO:skoehler	
OMIM	616220	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9; FSGS9		HP:0000007	OMIM:616220	TAS				I		HPO:skoehler	
OMIM	616220	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9; FSGS9		HP:0000097	OMIM:616220	TAS				P		HPO:skoehler	
OMIM	616220	FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9; FSGS9		HP:0000100	OMIM:616220	TAS				P		HPO:skoehler	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0000007	PMID:24305999	PCS				I		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0000705	PMID:24305999	PCS				P		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0006286	PMID:24305999	PCS				P		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0006297	PMID:24305999	PCS				P		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0009102	PMID:24305999	PCS				P		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0009722	PMID:24319098	PCS				P		HPO:probinson	
OMIM	616221	#616221 AMELOGENESIS IMPERFECTA, TYPE IH; AI1H		HP:0200095	OMIM:616221	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000028	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000175	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000193	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000218	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000238	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000322	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000347	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000358	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000403	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000445	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0000463	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0000750	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001270	OMIM:616222	IEA				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001290	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001371	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001382	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001511	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001518	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001622	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001773	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0001956	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0002007	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0002155	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0002650	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0003124	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0003745	OMIM:616222	TAS				I		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0004322	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0004482	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0004904	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0005280	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0008734	OMIM:616222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616222	TEMPLE SYNDROME		HP:0011220	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0011968	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0025502	OMIM:616222	IEA				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0030084	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616222	TEMPLE SYNDROME		HP:0200055	OMIM:616222	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0000007	OMIM:616224	TAS				I		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0000508	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0000824	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0001270	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0001290	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0001324	OMIM:616224	IEA				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0002515	OMIM:616224	IEA				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0003577	OMIM:616224	TAS				C		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0004322	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0010804	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616224	MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22		HP:0011968	OMIM:616224	TAS				P		HPO:skoehler	
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0000007	PMID:23404334	IEA				I		HPO:probinson	
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15	HP:0012825	HP:0000508	PMID:23404334	IEA		HP:0040284		P		HPO:probinson	1/7
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0002355	OMIM:616227	IEA				P		HPO:skoehler	
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0002359	PMID:23404334	IEA				P		HPO:probinson	
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0002828	PMID:23404334	IEA		HP:0040284		P		HPO:probinson	6/7
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0003403	PMID:23404334	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0003473	PMID:23404334	IEA		HP:0040284		P		HPO:probinson	2/2
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0003677	OMIM:616227	IEA				C		HPO:skoehler	
OMIM	616227	MYASTHENIC SYNDROME, CONGENITAL, 15; CMS15		HP:0030205	PMID:23404334	IEA		HP:0040284		P		HPO:probinson	4/4
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0000007	OMIM:616228	TAS				I		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0000218	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0001270	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0001290	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0001371	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0001763	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0002515	OMIM:616228	TAS				P		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0002650	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003200	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003307	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003325	OMIM:616228	TAS				P		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003391	OMIM:616228	TAS				P		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003473	OMIM:616228	TAS				P		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003677	OMIM:616228	TAS				C		HPO:skoehler	
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0003691	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616228	MYASTHENIC SYNDROME, CONGENITAL, 14		HP:0008180	OMIM:616228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0000007	OMIM:616229	TAS				I		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0000365	OMIM:616229	TAS				P		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0000923	OMIM:616229	TAS				P		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0001518	OMIM:616229	TAS				P		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0003027	OMIM:616229	IEA				P		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0003577	OMIM:616229	TAS				C		HPO:skoehler	
OMIM	616229	OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16		HP:0008905	OMIM:616229	IEA				P		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0000007	OMIM:616230	TAS				I		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0000726	OMIM:616230	TAS				P		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0001249	OMIM:616230	TAS				P		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0001336	OMIM:616230	IEA				P		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0002069	OMIM:616230	TAS				P		HPO:skoehler	
OMIM	616230	EPILEPSY, PROGRESSIVE MYOCLONIC, 8; EPM8		HP:0003676	OMIM:616230	TAS				C		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0000006	OMIM:616231	TAS				I		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0003236	OMIM:616231	TAS				P		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0003326	OMIM:616231	TAS				P		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0003388	OMIM:616231	TAS				P		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0003394	OMIM:616231	TAS				P		HPO:skoehler	
OMIM	616231	MYOPATHY, VACUOLAR, WITH CASQ1 AGGREGATES; VMCQA		HP:0003701	OMIM:616231	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000007	OMIM:616239	TAS				I		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000097	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000252	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000508	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000639	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0000648	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001250	OMIM:616239	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001256	OMIM:616239	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001257	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001260	OMIM:616239	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001272	OMIM:616239	IEA				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001274	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0001290	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0002151	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0002171	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0002180	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0002529	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0003198	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0003202	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0003236	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0003701	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0010628	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0011968	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0100704	OMIM:616239	TAS				P		HPO:skoehler	
OMIM	616239	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 24; COXPD24		HP:0200114	OMIM:616239	IEA				P		HPO:skoehler	
OMIM	616247	LONG QT SYNDROME 14; LQT14		HP:0000006	OMIM:616247	TAS				I		HPO:skoehler	
OMIM	616247	LONG QT SYNDROME 14; LQT14		HP:0001663	OMIM:616247	IEA				P		HPO:skoehler	
OMIM	616247	LONG QT SYNDROME 14; LQT14		HP:0001695	OMIM:616247	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616247	LONG QT SYNDROME 14; LQT14		HP:0001699	OMIM:616247	TAS				M		HPO:skoehler	
OMIM	616247	LONG QT SYNDROME 14; LQT14		HP:0005184	OMIM:616247	IEA				P		HPO:skoehler	
OMIM	616248	LETHAL CONGENITAL CONTRACTURE SYNDROME 6; LCCS6		HP:0000007	OMIM:616248	TAS				I		HPO:skoehler	
OMIM	616248	LETHAL CONGENITAL CONTRACTURE SYNDROME 6; LCCS6		HP:0000256	OMIM:616248	TAS				P		HPO:skoehler	
OMIM	616248	LETHAL CONGENITAL CONTRACTURE SYNDROME 6; LCCS6		HP:0001558	OMIM:616248	TAS				P		HPO:skoehler	
OMIM	616248	LETHAL CONGENITAL CONTRACTURE SYNDROME 6; LCCS6		HP:0002803	OMIM:616248	IEA				P		HPO:skoehler	
OMIM	616249	LONG QT SYNDROME 15; LQT15		HP:0000006	OMIM:616249	TAS				I		HPO:skoehler	
OMIM	616249	LONG QT SYNDROME 15; LQT15		HP:0001662	OMIM:616249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616249	LONG QT SYNDROME 15; LQT15		HP:0001663	OMIM:616249	IEA				P		HPO:skoehler	
OMIM	616249	LONG QT SYNDROME 15; LQT15		HP:0001695	OMIM:616249	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616249	LONG QT SYNDROME 15; LQT15		HP:0005184	OMIM:616249	IEA				P		HPO:skoehler	
OMIM	616255	SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES		HP:0000006	OMIM:616255	TAS				I		HPO:skoehler	
OMIM	616255	SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES		HP:0002750	OMIM:616255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616255	SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES		HP:0003508	OMIM:616255	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000007	OMIM:616258	TAS				I		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000089	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000104	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000148	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000193	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000252	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000340	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000347	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000369	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000431	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0000463	OMIM:616258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0001274	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0001321	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0001511	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0001562	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0001838	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0002804	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616258	MECKEL SYNDROME 12; MKS12		HP:0006872	OMIM:616258	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000006	OMIM:616260	TAS				I		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000158	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS	HP:0012825	HP:0000238	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000256	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000270	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000303	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000445	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000463	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000506	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000574	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000739	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000750	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000938	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0000998	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001097	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001249	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001250	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001279	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001288	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001290	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001528	OMIM:616260	IEA				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0001943	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002003	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002020	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002090	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002104	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002119	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002120	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002312	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002389	OMIM:616260	IEA				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0002650	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0010280	OMIM:616260	IEA				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0025356	OMIM:616260	IEA				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0030880	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0040216	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616260	TENORIO SYNDROME; TNORS		HP:0100021	OMIM:616260	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000007	OMIM:616263	TAS				I		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000049	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000219	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000248	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000253	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000316	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000407	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000577	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0000821	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001249	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001251	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001263	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET	HP:0003676	HP:0001272	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001290	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001395	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001508	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0001762	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0002240	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0002460	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0002570	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0002827	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0003577	OMIM:616263	TAS				C		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0003676	OMIM:616263	TAS				C		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0004322	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0009623	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0011800	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616263	NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET		HP:0100732	OMIM:616263	TAS				P		HPO:skoehler	
OMIM	616265	#616265 PEELING SKIN SYNDROME 3; PSS3		HP:0000007	OMIM:616265	TAS				I		HPO:skoehler	
OMIM	616265	#616265 PEELING SKIN SYNDROME 3; PSS3		HP:0040190	OMIM:616265	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000006	OMIM:616266	TAS				I		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000023	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000205	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000293	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000343	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000347	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000431	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000470	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0000750	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0001181	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0001263	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0001272	OMIM:616266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0001290	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0001537	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002000	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002020	OMIM:616266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002059	OMIM:616266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002093	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002650	OMIM:616266	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002803	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0002987	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0003273	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0003577	OMIM:616266	TAS				C		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0006380	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0009931	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616266	CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY		HP:0012385	OMIM:616266	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0000007	OMIM:616267	TAS				I		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0000657	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0001251	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0001272	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0001284	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0001332	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0002445	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0003678	OMIM:616267	TAS				C		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0009830	OMIM:616267	TAS				P		HPO:skoehler	
OMIM	616267	ATAXIA-OCULOMOTOR APRAXIA 4; AOA4		HP:0100543	OMIM:616267	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000006	OMIM:616268	TAS				I		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000164	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000219	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000252	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000286	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000308	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000341	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000358	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000369	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000426	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000455	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000486	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0000508	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001249	OMIM:616268	IEA				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001250	OMIM:616268	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001263	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001319	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001344	OMIM:616268	IEA				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001357	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001363	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001629	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001631	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0001643	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0002098	OMIM:616268	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0002643	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0002714	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0011968	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616268	MENTAL RETARDATION, AUTOSOMAL DOMINANT 32; MRD32		HP:0100704	OMIM:616268	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000007	OMIM:616269	TAS				I		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000303	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000343	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000400	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000581	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000718	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0000742	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0001263	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0001344	OMIM:616269	IEA				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0002515	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0002540	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0010864	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48	HP:0003676	HP:0030186	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616269	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48; MRT48		HP:0200055	OMIM:616269	TAS				P		HPO:skoehler	
OMIM	616270	#616270 AMELOGENESIS IMPERFECTA, TYPE IF; AI1F ;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF; AI1F		HP:0000007	OMIM:616270	IEA				I		HPO:skoehler	
OMIM	616270	#616270 AMELOGENESIS IMPERFECTA, TYPE IF; AI1F ;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF; AI1F		HP:0000705	OMIM:616270	IEA				P		HPO:skoehler	
OMIM	616270	#616270 AMELOGENESIS IMPERFECTA, TYPE IF; AI1F ;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF; AI1F		HP:0006297	OMIM:616270	IEA				P		HPO:skoehler	
OMIM	616270	#616270 AMELOGENESIS IMPERFECTA, TYPE IF; AI1F ;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF; AI1F		HP:0009722	OMIM:616270	IEA				P		HPO:skoehler	
OMIM	616270	#616270 AMELOGENESIS IMPERFECTA, TYPE IF; AI1F ;;AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE IF; AI1F		HP:0011073	OMIM:616270	IEA				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0000007	OMIM:616271	TAS				I		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0000252	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0000518	OMIM:616271	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001249	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001250	OMIM:616271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001257	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001263	OMIM:616271	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001272	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001319	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001510	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001875	OMIM:616271	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0001999	OMIM:616271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0002059	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0002071	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0002376	OMIM:616271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0002719	OMIM:616271	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0003577	OMIM:616271	TAS				C		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0003676	OMIM:616271	TAS				C		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0007256	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616271	3-METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT, AND NEUTROPENIA; MEGCANN		HP:0011968	OMIM:616271	TAS				P		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0000007	OMIM:616276	TAS				I		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001250	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001319	OMIM:616276	TAS				P		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001321	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001511	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001639	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001643	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0001662	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0002015	OMIM:616276	TAS				P		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0002093	OMIM:616276	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0002151	OMIM:616276	TAS				P		HPO:skoehler	
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0002650	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0004383	OMIM:616276	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616276	COENZYME Q10 DEFICIENCY, PRIMARY, 7; COQ10D7		HP:0200134	OMIM:616276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0000007	OMIM:616277	TAS				I	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0000365	OMIM:616277	TAS		HP:0040283		P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	HP:0040283
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0000639	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0001257	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D	HP:0012828	HP:0001263	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0001290	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0001332	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0001629	OMIM:616277	TAS		HP:0040283		P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	HP:0040283
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D	HP:0025303	HP:0002104	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0002151	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0002490	OMIM:616277	TAS				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616277	MITOCHONDRIAL SHORT-CHAIN ENOYL-CoA HYDRATASE 1 DEFICIENCY; ECHS1D		HP:0002928	OMIM:616277	IEA				P	MITOCHONDRIAL SHORT-CHAIN ENOYL-COA HYDRATASE 1 DEFICIENCY; ECHS1D	HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0000007	OMIM:616278	TAS				I		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0000952	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0001395	OMIM:616278	TAS				P		HPO:probinson	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0001399	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0001744	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0001891	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0002240	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0002910	OMIM:616278	TAS				P		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0003593	OMIM:616278	TAS				C		HPO:skoehler	
OMIM	616278	#616278 BILE ACID SYNTHESIS DEFECT, CONGENITAL, 5; CBAS5		HP:0003676	OMIM:616278	TAS				C		HPO:skoehler	
OMIM	616279	#616279 CATARACT 43; CTRCT43		HP:0000006	OMIM:616279	TAS				I		HPO:skoehler	
OMIM	616279	#616279 CATARACT 43; CTRCT43		HP:0000523	OMIM:616279	IEA				P		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0000006	OMIM:616280	TAS				I		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0001284	OMIM:616280	TAS				P		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0002936	OMIM:616280	TAS				P		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0003376	OMIM:616280	TAS				P		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0003477	OMIM:616280	TAS				P		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0003677	OMIM:616280	TAS				C		HPO:skoehler	
OMIM	616280	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U; CMT2U		HP:0009027	OMIM:616280	TAS				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0000007	OMIM:616281	IEA				I		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0000252	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001249	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001257	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001260	OMIM:616281	TAS				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001263	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001290	OMIM:616281	TAS				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001298	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001344	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001347	OMIM:616281	TAS				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0001508	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0002069	OMIM:616281	IEA				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0002079	OMIM:616281	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0002307	OMIM:616281	TAS				P		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0003676	OMIM:616281	TAS				C		HPO:skoehler	
OMIM	616281	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 49; MRT49		HP:0005484	OMIM:616281	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0000006	OMIM:616282	TAS				I		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0001258	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0001347	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0001760	OMIM:616282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0002355	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73	HP:0012825	HP:0003202	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0003487	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0003581	OMIM:616282	TAS				C		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73		HP:0003677	OMIM:616282	TAS				C		HPO:skoehler	
OMIM	616282	SPASTIC PARAPLEGIA 73, AUTOSOMAL DOMINANT; SPG73	HP:0012825	HP:0003701	OMIM:616282	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0000007	OMIM:616286	TAS				I		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0000347	OMIM:616286	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001272	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001284	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001290	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001349	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001561	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0001989	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0002059	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0002079	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7	HP:0012839	HP:0002804	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0003202	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0003470	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0006380	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0012697	OMIM:616286	IEA				P		HPO:skoehler	
OMIM	616286	LETHAL CONGENITAL CONTRACTURE SYNDROME 7; LCCS7		HP:0200136	OMIM:616286	TAS				P		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8		HP:0000007	OMIM:616287	TAS				I		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8		HP:0001284	OMIM:616287	TAS				P		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8		HP:0001290	OMIM:616287	TAS				P		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8		HP:0001349	OMIM:616287	TAS				P		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8	HP:0012839	HP:0002804	OMIM:616287	TAS				P		HPO:skoehler	
OMIM	616287	LETHAL CONGENITAL CONTRACTURE SYNDROME 8		HP:0200136	OMIM:616287	TAS				P		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0000007	OMIM:616289	TAS				I		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0000642	OMIM:616289	TAS				P		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0000648	OMIM:616289	TAS				P		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0000980	OMIM:616289	IEA				P		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0007663	OMIM:616289	TAS				P		HPO:skoehler	
OMIM	616289	OPTIC ATROPHY 9; OPA9		HP:0030528	OMIM:616289	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0000007	OMIM:616291	TAS				I		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0000639	OMIM:616291	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0001260	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0001270	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0001272	OMIM:616291	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0001310	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0002066	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0002070	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0002075	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0002345	OMIM:616291	TAS				P		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0003676	OMIM:616291	TAS				C		HPO:skoehler	
OMIM	616291	LICHTENSTEIN-KNORR SYNDROME; LIKNS		HP:0004322	OMIM:616291	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000007	OMIM:616294	TAS				I		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000218	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000238	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000256	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000262	OMIM:616294	IEA				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000308	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000316	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000325	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000494	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000520	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000592	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000767	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000883	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000926	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0000938	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0001562	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0001620	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0002007	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0002645	OMIM:616294	IEA				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0002808	OMIM:616294	IEA				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0002868	OMIM:616294	IEA				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0004322	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0004440	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0004443	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0008897	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616294	COLE-CARPENTER SYNDROME 2; CLCRP2		HP:0011800	OMIM:616294	TAS				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0000007	OMIM:616295	TAS				I		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0000982	OMIM:616295	TAS				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0001806	OMIM:616295	IEA				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0001820	OMIM:616295	IEA				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0025092	OMIM:616295	TAS				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0030318	OMIM:616295	TAS				P		HPO:skoehler	
OMIM	616295	PEELING SKIN WITH LEUKONYCHIA, ACRAL PUNCTATE KERATOSES, CHEILITIS, AND KNUCKLE PADS; PLACK		HP:0040189	OMIM:616295	IEA				P		HPO:skoehler	
OMIM	616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2		HP:0000006	OMIM:616298	TAS				I		HPO:skoehler	
OMIM	616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2		HP:0000501	OMIM:616298	TAS				P		HPO:skoehler	
OMIM	616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2		HP:0000962	OMIM:616298	TAS				P		HPO:skoehler	
OMIM	616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2		HP:0001650	OMIM:616298	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616298	SINGLETON-MERTEN SYNDROME 2; SGMRT2		HP:0004322	OMIM:616298	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0000007	OMIM:616299	TAS				I		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001263	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001272	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001285	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001332	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001410	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001522	OMIM:616299	TAS				M		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0001662	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0002071	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0002092	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0002151	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0002500	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0002910	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0003128	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0003573	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0003593	OMIM:616299	TAS				C		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0008936	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616299	LIPOYLTRANSFERASE 1 DEFICIENCY; LIPT1D		HP:0012448	OMIM:616299	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000007	OMIM:616300	TAS				I		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000028	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000062	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000089	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000107	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000175	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000180	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000280	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000308	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000316	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000400	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000448	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000568	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000695	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000773	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000774	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0000888	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0001305	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0001321	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0001539	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0001591	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0001643	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0002084	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0002089	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0002093	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0002419	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0002692	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0003177	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0003180	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0004482	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0008839	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0008905	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0010297	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0011315	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0011800	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0100258	OMIM:616300	TAS				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0100259	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616300	SHORT-RIB THORACIC DYSPLASIA 13 WITH OR WITHOUT POLYDACTYLY; SRTD13		HP:0410030	OMIM:616300	IEA				P		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0000007	OMIM:616304	TAS				I		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17	HP:0012825	HP:0000508	OMIM:616304	TAS				P		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0001265	OMIM:616304	TAS				P		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0001324	OMIM:616304	IEA				P		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0002355	OMIM:616304	TAS				P		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0003577	OMIM:616304	TAS				C		HPO:skoehler	
OMIM	616304	MYASTHENIC SYNDROME, CONGENITAL, 17; CMS17		HP:0011968	OMIM:616304	TAS				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0000007	OMIM:616307	TAS				I		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0000090	OMIM:616307	TAS				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0000980	OMIM:616307	IEA				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0001407	OMIM:616307	TAS				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0001737	OMIM:616307	TAS				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0002617	OMIM:616307	IEA				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0007401	OMIM:616307	IEA				P		HPO:skoehler	
OMIM	616307	SENIOR-LOKEN SYNDROME 8; SLSN8		HP:0007663	OMIM:616307	TAS				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0000006	OMIM:616311	IEA				I		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0000252	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0000646	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0001249	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0002650	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0002750	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0004322	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0004325	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0007018	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616311	#616311 MENTAL RETARDATION, AUTOSOMAL DOMINANT 33; MRD33		HP:0200065	OMIM:616311	IEA				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000006	OMIM:616313	TAS				I		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000218	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000275	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000276	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000508	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0000602	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0001319	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0001371	OMIM:616313	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0003198	OMIM:616313	IEA				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0003202	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0003388	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0003577	OMIM:616313	TAS				C		HPO:skoehler	
OMIM	616313	MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A		HP:0010628	OMIM:616313	TAS				P		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0000007	OMIM:616314	TAS				I		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0001319	OMIM:616314	TAS				P		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0001324	OMIM:616314	TAS				P		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C	HP:0025303	HP:0002093	OMIM:616314	TAS				P		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0003198	OMIM:616314	IEA				P		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0003577	OMIM:616314	TAS				C		HPO:skoehler	
OMIM	616314	MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C		HP:0011968	OMIM:616314	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0000006	OMIM:616321	TAS				I		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0000508	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0001319	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0002015	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A	HP:0025303	HP:0002093	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0002540	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0003198	OMIM:616321	IEA				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A	HP:0012828	HP:0003324	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0003388	OMIM:616321	TAS				P		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0003593	OMIM:616321	TAS				C		HPO:skoehler	
OMIM	616321	MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A		HP:0003676	OMIM:616321	TAS				C		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0000007	OMIM:616322	TAS				I		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0000218	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0000467	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0000508	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0000602	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0001319	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0001558	OMIM:616322	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0002093	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0003388	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0003593	OMIM:616322	TAS				C		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0010628	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616322	MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B		HP:0011968	OMIM:616322	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0000007	OMIM:616323	TAS				I		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0000218	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0000508	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0001290	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0002015	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C	HP:0025303	HP:0002093	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0003577	OMIM:616323	TAS				C		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0010628	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0011968	OMIM:616323	TAS				P		HPO:skoehler	
OMIM	616323	MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C		HP:0012378	OMIM:616323	IEA				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0000007	OMIM:616324	TAS				I		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0000467	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0000508	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0000602	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0001319	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0002093	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0003388	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0003593	OMIM:616324	TAS				C		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0010628	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616324	MYASTHENIC SYNDROME, CONGENITAL, 4B, FAST-CHANNEL; CMS4B		HP:0011968	OMIM:616324	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0000007	OMIM:616325	TAS				I		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0000467	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0000508	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0000602	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0001319	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9	HP:0025303	HP:0002093	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0003388	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0003391	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0003593	OMIM:616325	TAS				C		HPO:skoehler	
OMIM	616325	MYASTHENIC SYNDROME, CONGENITAL, 9, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS9		HP:0010628	OMIM:616325	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0000007	OMIM:616326	TAS				I		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0000218	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0000276	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0000508	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0001319	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0001558	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11	HP:0025303	HP:0002093	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0002804	OMIM:616326	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0003388	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0003391	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0003577	OMIM:616326	TAS				C		HPO:skoehler	
OMIM	616326	MYASTHENIC SYNDROME, CONGENITAL, 11, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS11		HP:0011968	OMIM:616326	TAS				P		HPO:skoehler	
OMIM	616329	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13		HP:0000006	OMIM:616329	TAS				I		HPO:skoehler	
OMIM	616329	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13		HP:0004904	OMIM:616329	IEA				P		HPO:skoehler	
OMIM	616329	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13		HP:0009800	OMIM:616329	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0000006	OMIM:616330	TAS				I		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0000508	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001251	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001260	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001263	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001284	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001324	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001371	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0001558	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0002093	OMIM:616330	TAS	HP:0003623			P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0002355	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0002465	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0003388	OMIM:616330	TAS				P		HPO:skoehler	
OMIM	616330	MYASTHENIC SYNDROME, CONGENITAL, 18; CMS18		HP:0003577	OMIM:616330	TAS				C		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000006	OMIM:616331	TAS				I		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000028	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000054	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000207	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000212	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000219	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000256	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000316	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000343	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000347	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000348	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000405	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000407	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000463	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000520	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000678	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0000689	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0001156	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0001537	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0002007	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0002684	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0003027	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0003196	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0003577	OMIM:616331	TAS				C		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0004322	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0009882	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0011001	OMIM:616331	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0011304	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0011800	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616331	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 2; DRS2		HP:0030084	OMIM:616331	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0000007	OMIM:616335	TAS				I		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0000252	OMIM:616335	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0000568	OMIM:616335	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0000639	OMIM:616335	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3	HP:0012825	HP:0001263	OMIM:616335	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0001999	OMIM:616335	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0003577	OMIM:616335	TAS				C		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0007663	OMIM:616335	TAS				P		HPO:skoehler	
OMIM	616335	MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 3; MCCRP3		HP:0007731	PMID:25817018	PCS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0000007	OMIM:616339	TAS				I		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0000252	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0000639	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0000643	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001250	OMIM:616339	IEA				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001257	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29	HP:0012829	HP:0001263	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001284	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001290	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001298	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001508	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0001511	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29	HP:0003676	HP:0002059	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0002072	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0002827	OMIM:616339	TAS	HP:0003577			P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0003429	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0003577	OMIM:616339	TAS				C		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0004322	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0009830	OMIM:616339	TAS				P		HPO:skoehler	
OMIM	616339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 29; EIEE29		HP:0200134	OMIM:616339	IEA				P		HPO:skoehler	
OMIM	616340	#616340 DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA67		HP:0000006	OMIM:616341	TAS				I		HPO:skoehler	
OMIM	616340	#616340 DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA67		HP:0000360	OMIM:616341	TAS				P		HPO:skoehler	
OMIM	616340	#616340 DEAFNESS, AUTOSOMAL DOMINANT 67; DFNA67		HP:0000407	OMIM:616341	TAS				P		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0000006	PMID:25839329	PCS				I		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0000733	PMID:25839329	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30	HP:0012829	HP:0001263	PMID:25839329	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0001298	OMIM:616341	TAS				P		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0001344	PMID:25839329	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0001522	PMID:25839329	PCS		HP:0040284		M		HPO:probinson	2/6
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0002069	OMIM:616341	TAS				P		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0002098	PMID:25839329	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0002123	PMID:25839329	PCS		HP:0040284		P		HPO:skoehler	2/6
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0002521	OMIM:616341	TAS				P		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0011968	PMID:25839329	PCS				P		HPO:skoehler	
OMIM	616341	#616341 EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30; EIEE30		HP:0200134	OMIM:616341	IEA				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0000007	OMIM:616342	TAS				I		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0000252	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0000293	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0000347	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0000470	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001004	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001007	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001188	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001250	OMIM:616342	IEA				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001263	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001274	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001284	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001321	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0001339	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0002804	OMIM:616342	TAS				P		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0003577	OMIM:616342	TAS				C		HPO:skoehler	
OMIM	616342	LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA; LIS7		HP:0031882	OMIM:616342	IEA				P		HPO:skoehler	
OMIM	616345	#616345 IMMUNODEFICIENCY 39; IMD39		HP:0000007	OMIM:616345	IEA				I		HPO:skoehler	
OMIM	616345	#616345 IMMUNODEFICIENCY 39; IMD39		HP:0002721	OMIM:616345	IEA				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0000006	OMIM:616346	TAS				I		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0001249	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31	HP:0031375	HP:0001250	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0001263	OMIM:616346	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0001290	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0001344	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0002059	OMIM:616346	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0002355	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0002376	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0002521	OMIM:616346	IEA				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0002540	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0100716	OMIM:616346	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616346	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 31; EIEE31		HP:0200134	OMIM:616346	TAS				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000006	OMIM:616351	IEA				I		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000286	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000319	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000365	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000463	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000582	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000664	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000687	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0000733	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0001249	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0001263	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0001488	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0001562	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0001773	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002058	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002069	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002136	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002208	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002212	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0002307	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0003763	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0004691	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0005484	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0006610	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0008936	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616351	#616351 MENTAL RETARDATION, AUTOSOMAL DOMINANT 34; MRD34		HP:0100704	OMIM:616351	IEA				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0000007	OMIM:616353	TAS				I		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0000252	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0000670	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001000	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001251	OMIM:616353	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001263	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001321	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001508	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001511	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0001596	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0003593	OMIM:616353	TAS				C		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0003828	OMIM:616353	TAS				C		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0008070	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616353	DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 6		HP:0008404	OMIM:616353	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000007	OMIM:616354	TAS				I		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000158	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000218	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000280	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000283	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000286	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000289	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000343	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000407	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000463	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000639	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000678	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000684	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000729	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0000998	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001156	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001250	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001251	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001257	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20	HP:0012828	HP:0001263	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001265	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20	HP:0003676	HP:0001272	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001290	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001321	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001344	OMIM:616354	IEA				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0001762	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0002120	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0002186	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0002540	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0002650	OMIM:616354	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0003487	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0003593	OMIM:616354	TAS				C		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0004482	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0011220	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0012385	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0012471	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0012745	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0012810	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616354	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 20; SCAR20		HP:0030084	OMIM:616354	TAS				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000006	OMIM:616355	TAS				I		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000194	OMIM:616355	TAS				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000238	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000256	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000297	OMIM:616355	TAS				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35	HP:0012825	HP:0000316	OMIM:616355	TAS				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000341	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000486	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000490	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000494	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0000545	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001249	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001250	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001263	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001290	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001344	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001374	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0001943	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0002021	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0002028	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0002119	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616355	MENTAL RETARDATION, AUTOSOMAL DOMINANT 35; MRD35		HP:0005988	OMIM:616355	IEA				P		HPO:skoehler	
OMIM	616357	#616357 DEAFNESS, AUTOSOMAL DOMINANT 40; DFNA40		HP:0000006	PMID:12471561	PCS				I		HPO:skoehler	
OMIM	616357	#616357 DEAFNESS, AUTOSOMAL DOMINANT 40; DFNA40		HP:0000407	PMID:12471561	PCS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0000006	OMIM:616361	TAS				I		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0001300	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0001337	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0002063	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0002067	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0002172	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0003677	OMIM:616361	TAS				C		HPO:skoehler	
OMIM	616361	PARKINSON DISEASE 21; PARK21		HP:0100315	OMIM:616361	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000006	OMIM:616362	IEA				I		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000194	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000238	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000252	OMIM:616362	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000297	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000315	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36	HP:0012825	HP:0000316	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000324	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000463	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000494	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000505	PMID:25533962	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/3
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0000767	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001249	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001250	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001252	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36	HP:0012828	HP:0001263	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001290	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001344	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001357	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0001382	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0002079	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0002119	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0002194	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0002540	OMIM:616362	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0005487	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0009179	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0010055	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0010721	OMIM:616362	IEA				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0010804	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616362	MENTAL RETARDATION, AUTOSOMAL DOMINANT 36; MRD36		HP:0012448	OMIM:616362	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000006	OMIM:616364	TAS				I		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000194	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000218	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000248	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000252	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000297	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000303	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000307	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000322	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000356	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000358	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000369	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000455	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000470	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000483	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000486	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000510	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000512	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000540	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000545	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000612	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000648	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000649	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0000708	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0001156	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0001249	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0001263	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0001290	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0001388	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002019	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002020	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002059	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002079	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002173	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0002714	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0004322	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0005280	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0008619	OMIM:616364	IEA				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0011800	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0011968	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0030680	OMIM:616364	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0100704	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616364	WHITE-SUTTON SYNDROME		HP:0100716	OMIM:616364	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0000006	OMIM:616366	TAS				I		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0001249	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32	HP:0031375	HP:0001250	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0001251	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0001336	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0001337	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0001344	OMIM:616366	IEA				P		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0003593	OMIM:616366	TAS				C		HPO:skoehler	
OMIM	616366	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32; EIEE32		HP:0200134	OMIM:616366	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000006	OMIM:616367	TAS				I		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000072	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000162	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000175	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000211	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000232	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA	HP:0012825	HP:0000324	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000327	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000347	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000369	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000378	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000384	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000402	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000405	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000411	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000431	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000535	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000652	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000653	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000678	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0000680	OMIM:616367	TAS				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0001596	OMIM:616367	IEA				P		HPO:skoehler	
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0001647	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0004467	OMIM:616367	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616367	MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA		HP:0005321	OMIM:616367	IEA				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000006	OMIM:616368	TAS				I		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000028	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000076	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000085	OMIM:616368	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000280	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000311	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000316	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000365	OMIM:616368	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000518	OMIM:616368	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000520	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000527	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000574	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0000648	OMIM:616368	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001156	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001249	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001263	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001513	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001601	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001643	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0001671	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0002020	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0002714	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0002777	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0003196	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0003577	OMIM:616368	TAS				C		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0004322	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0006528	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0011951	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616368	CHOPS SYNDROME; CHOPS		HP:0100874	OMIM:616368	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0000007	OMIM:616370	TAS				I		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0000505	OMIM:616370	IEA				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0000639	OMIM:616370	IEA				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0000648	OMIM:616370	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0001257	OMIM:616370	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0001290	OMIM:616370	IEA				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0001344	OMIM:616370	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0001347	OMIM:616370	IEA				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0002415	OMIM:616370	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0002518	OMIM:616370	TAS				P		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0003676	OMIM:616370	IEA				C		HPO:skoehler	
OMIM	616370	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 4; MMDS4		HP:0031358	OMIM:616370	IEA				P		HPO:skoehler	
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0000006	OMIM:616371	TAS				I		HPO:skoehler	
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0002206	OMIM:616371	TAS				P		HPO:skoehler	
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0002216	OMIM:616371	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0003581	OMIM:616371	TAS				C		HPO:skoehler	
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0003829	OMIM:616371	TAS				C		HPO:skoehler	
OMIM	616371	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 4; PFBMFT4		HP:0005528	OMIM:616371	IEA				P		HPO:skoehler	
OMIM	616373	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3; PFBMFT3		HP:0000006	OMIM:616373	TAS				I		HPO:skoehler	
OMIM	616373	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3; PFBMFT3		HP:0002206	OMIM:616373	TAS				P		HPO:skoehler	
OMIM	616373	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3; PFBMFT3		HP:0003581	OMIM:616373	TAS				C		HPO:skoehler	
OMIM	616373	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 3; PFBMFT3		HP:0003829	OMIM:616373	TAS				C		HPO:skoehler	
OMIM	616389	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G		HP:0000007	OMIM:616389	IEA				I		HPO:skoehler	
OMIM	616389	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G		HP:0000543	OMIM:616389	IEA				P		HPO:skoehler	
OMIM	616389	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G		HP:0000618	OMIM:616389	IEA				P		HPO:skoehler	
OMIM	616389	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1G; CSNB1G		HP:0007642	OMIM:616389	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0000007	OMIM:616390	IEA				I		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0000144	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0000992	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0001249	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0002208	OMIM:616390	TAS				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0002299	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0002664	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0004322	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0007479	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0045055	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616390	TRICHOTHIODYSTROPHY 2, PHOTOSENSITIVE		HP:0100543	OMIM:616390	IEA				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000006	OMIM:616393	TAS				I		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000232	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000286	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000369	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000490	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000494	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0000718	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0001250	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0001263	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0001319	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0001344	OMIM:616393	IEA				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0002714	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0003593	OMIM:616393	TAS				C		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0005280	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0010804	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616393	MENTAL RETARDATION, AUTOSOMAL DOMINANT 38; MRD38		HP:0010864	OMIM:616393	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000007	OMIM:616394	TAS				I		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000510	OMIM:616394	IEA				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000543	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000618	OMIM:616394	IEA				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000750	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0000969	OMIM:616394	IEA				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0001513	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0001733	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0002910	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0007843	OMIM:616394	TAS				P		HPO:skoehler	
OMIM	616394	RETINITIS PIGMENTOSA 71; RP71		HP:0011510	OMIM:616394	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0000007	OMIM:616395	IEA				I		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0000144	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0000518	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0001019	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0001249	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0002099	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0002299	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0004322	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0007479	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0009473	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616395	#616395 TRICHOTHIODYSTROPHY 3, PHOTOSENSITIVE; TTD3 ;;TRICHOTHIODYSTROPHY, COMPLEMENTATION GROUP A; TTDA		HP:0045055	OMIM:616395	IEA				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0000006	OMIM:616398	TAS				I		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0000473	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0000643	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0000716	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0000739	OMIM:616398	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0001260	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0001336	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0003676	OMIM:616398	TAS				C		HPO:skoehler	
OMIM	616398	DYSTONIA 26, MYOCLONIC; DYT26		HP:0012049	OMIM:616398	TAS				P		HPO:skoehler	
OMIM	616399	BRUGADA SYNDROME 9; BRGDA9		HP:0000006	OMIM:616399	TAS				I		HPO:skoehler	
OMIM	616399	BRUGADA SYNDROME 9; BRGDA9		HP:0001962	OMIM:616399	TAS				P		HPO:skoehler	
OMIM	616399	BRUGADA SYNDROME 9; BRGDA9		HP:0012251	OMIM:616399	IEA				P		HPO:skoehler	
OMIM	616399	BRUGADA SYNDROME 9; BRGDA9		HP:0031972	OMIM:616399	IEA				P		HPO:skoehler	
OMIM	616400	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2; FNEPPK2		HP:0000006	OMIM:616400	TAS				I		HPO:skoehler	
OMIM	616400	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2; FNEPPK2		HP:0000962	OMIM:616400	TAS				P		HPO:skoehler	
OMIM	616400	PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC, FOCAL 2; FNEPPK2		HP:0000982	OMIM:616400	IEA				P		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0000007	OMIM:616402	TAS				I		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0000252	OMIM:616402	TAS				P		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0000718	OMIM:616402	TAS				P		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0001249	OMIM:616402	TAS				P		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0001250	OMIM:616402	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14	HP:0012828	HP:0001263	OMIM:616402	TAS				P		HPO:skoehler	
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0001321	OMIM:616402	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616402	MICROCEPHALY 14, PRIMARY, AUTOSOMAL RECESSIVE; MCPH14		HP:0002465	OMIM:616402	TAS				P		HPO:skoehler	
OMIM	616407	BROWN SYNDROME		HP:0000006	OMIM:616407	TAS				I		HPO:skoehler	
OMIM	616407	BROWN SYNDROME		HP:0000651	PMID:1757853	TAS				P		HPO:lccarmody	
OMIM	616407	BROWN SYNDROME		HP:0031622	PMID:1757853	TAS				P		HPO:lccarmody	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0000006	OMIM:616409	TAS				I		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0000718	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0001250	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33	HP:0012828	HP:0001263	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0001319	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0001344	OMIM:616409	IEA				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0002317	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0002521	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0003593	OMIM:616409	TAS				C		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0005484	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616409	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 33; EIEE33		HP:0200134	OMIM:616409	TAS				P		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0000006	OMIM:616410	TAS				I		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0001251	OMIM:616410	IEA				P		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0001272	OMIM:616410	TAS				P		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0002172	OMIM:616410	IEA				P		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0002317	OMIM:616410	TAS				P		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0003581	OMIM:616410	TAS				C		HPO:skoehler	
OMIM	616410	SPINOCEREBELLAR ATAXIA 41; SCA41		HP:0003676	OMIM:616410	TAS				C		HPO:skoehler	
OMIM	616411	DYSTONIA 27; DYT27		HP:0000007	OMIM:616411	TAS				I		HPO:skoehler	
OMIM	616411	DYSTONIA 27; DYT27		HP:0002174	OMIM:616411	TAS				P		HPO:skoehler	
OMIM	616411	DYSTONIA 27; DYT27		HP:0002356	OMIM:616411	TAS				P		HPO:skoehler	
OMIM	616411	DYSTONIA 27; DYT27		HP:0012048	OMIM:616411	TAS				P		HPO:skoehler	
OMIM	616411	DYSTONIA 27; DYT27		HP:0012049	OMIM:616411	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0000006	OMIM:616413	TAS				I		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0000716	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0000726	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0001250	OMIM:616413	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0001260	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0001266	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0001300	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0002135	OMIM:616413	IEA				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0002354	OMIM:616413	TAS				P		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0003581	OMIM:616413	TAS				C		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0003676	OMIM:616413	TAS				C		HPO:skoehler	
OMIM	616413	BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 6; IBGC6		HP:0031814	OMIM:616413	IEA				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0000006	OMIM:616414	TAS				I		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0001369	OMIM:616414	IEA				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0002098	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0002789	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0002829	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0003565	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0003829	OMIM:616414	TAS				C		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0006530	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0008653	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0012735	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616414	AUTOIMMUNE INTERSTITIAL LUNG, JOINT, AND KIDNEY DISEASE; AILJK		HP:0040223	OMIM:616414	TAS				P		HPO:skoehler	
OMIM	616415	FAMILIAL ADENOMATOUS POLYPOSIS 3		HP:0000007	OMIM:616415	TAS				I		HPO:skoehler	
OMIM	616415	FAMILIAL ADENOMATOUS POLYPOSIS 3		HP:0002858	OMIM:616415	TAS				P		HPO:skoehler	
OMIM	616415	FAMILIAL ADENOMATOUS POLYPOSIS 3		HP:0003002	OMIM:616415	TAS				P		HPO:skoehler	
OMIM	616415	FAMILIAL ADENOMATOUS POLYPOSIS 3		HP:0008069	OMIM:616415	TAS				P		HPO:skoehler	
OMIM	616415	FAMILIAL ADENOMATOUS POLYPOSIS 3		HP:0009725	OMIM:616415	TAS				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0000006	OMIM:616418	TAS				I		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0000007	OMIM:616418	TAS				I		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0000252	OMIM:616418	TAS				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0001249	OMIM:616418	TAS				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0001250	OMIM:616418	TAS				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0001263	OMIM:616418	TAS				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0001344	OMIM:616418	IEA				P		HPO:skoehler	
OMIM	616418	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION; HOMGSMR		HP:0002917	OMIM:616418	IEA				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000007	OMIM:616420	TAS				I		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000253	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000272	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000319	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000325	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000341	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000343	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000365	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000369	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000414	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000463	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000494	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000582	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0000639	OMIM:616420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001166	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001250	OMIM:616420	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001257	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10	HP:0012828	HP:0001263	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001344	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001347	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0001508	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0002079	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0002120	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0002415	OMIM:616420	IEA				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0002540	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0003196	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0003202	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0003429	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0003487	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0003676	OMIM:616420	TAS				C		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0008936	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616420	LEUKODYSTROPHY, HYPOMYELINATING, 10		HP:0012471	OMIM:616420	TAS				P		HPO:skoehler	
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0000006	OMIM:616421	TAS				I		HPO:skoehler	
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0001249	OMIM:616421	TAS				P		HPO:skoehler	
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0001251	OMIM:616421	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0001337	OMIM:616421	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0002121	OMIM:616421	TAS				P		HPO:skoehler	
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0002650	OMIM:616421	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616421	MYOCLONIC-ATONIC EPILEPSY		HP:0025097	OMIM:616421	TAS				P		HPO:skoehler	
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0000006	OMIM:616425	TAS				I		HPO:skoehler	
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0000054	OMIM:616425	TAS				P		HPO:skoehler	
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0000062	OMIM:616425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0000150	OMIM:616425	TAS				P		HPO:skoehler	
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0008734	OMIM:616425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0012245	OMIM:616425	IEA				P		HPO:skoehler	
OMIM	616425	46,XY SEX REVERSAL 10; SRXY10		HP:0100621	OMIM:616425	TAS				P		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0000006	OMIM:616428	TAS				I		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0000528	OMIM:616428	IEA				P		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0000567	OMIM:616428	TAS				P		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0000568	OMIM:616428	TAS				P		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0000612	OMIM:616428	TAS				P		HPO:skoehler	
OMIM	616428	MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10; MCOPCB10		HP:0025492	OMIM:616428	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000007	OMIM:616430	TAS				I		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000316	OMIM:616430	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000343	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000369	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000431	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000463	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000768	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0000824	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0001263	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0001272	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0001290	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0002059	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0002617	OMIM:616430	IEA				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0003196	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0003577	OMIM:616430	TAS				C		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0004322	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0005280	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616430	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 25; COXPD25		HP:0011968	OMIM:616430	TAS				P		HPO:skoehler	
OMIM	616433	IMMUNODEFICIENCY 40; IMD40		HP:0000007	OMIM:616433	TAS				I		HPO:skoehler	
OMIM	616433	IMMUNODEFICIENCY 40; IMD40		HP:0001888	OMIM:616433	IEA				P		HPO:skoehler	
OMIM	616433	IMMUNODEFICIENCY 40; IMD40		HP:0002721	OMIM:616433	TAS				P		HPO:skoehler	
OMIM	616433	IMMUNODEFICIENCY 40; IMD40		HP:0003577	OMIM:616433	TAS				C		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0000007	OMIM:616435	TAS				I		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0001873	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0001876	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0001903	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0004322	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0005528	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0009778	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616435	FANCONI ANEMIA, COMPLEMENTATION GROUP T; FANCT		HP:0009942	OMIM:616435	TAS				P		HPO:skoehler	
OMIM	616436	EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7		HP:0000006	OMIM:616436	TAS				I		HPO:skoehler	
OMIM	616436	EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7		HP:0003829	OMIM:616436	TAS				C		HPO:skoehler	
OMIM	616436	EPILEPSY, FAMILIAL TEMPORAL LOBE, 7; ETL7		HP:0011158	OMIM:616436	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0000006	OMIM:616437	TAS				I		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0000734	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0000741	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0000751	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0001260	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0001265	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0001283	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0001347	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002015	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002120	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002145	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002300	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002366	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002380	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0002463	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0003202	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0003676	OMIM:616437	TAS				C		HPO:skoehler	
OMIM	616437	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3		HP:0007354	OMIM:616437	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0000006	OMIM:616439	TAS				I		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0000734	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0000741	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0000751	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0001260	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0001265	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0001283	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0001347	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002015	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002120	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002145	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002300	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002366	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002380	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0002463	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0003202	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0003581	OMIM:616439	TAS				C		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0003676	OMIM:616439	TAS				C		HPO:skoehler	
OMIM	616439	FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4		HP:0007354	OMIM:616439	TAS				P		HPO:skoehler	
OMIM	616445	CANDIDIASIS, FAMILIAL, 9; CANDF9		HP:0000007	OMIM:616445	TAS				I		HPO:skoehler	
OMIM	616445	CANDIDIASIS, FAMILIAL, 9; CANDF9		HP:0011107	OMIM:616445	TAS				P		HPO:skoehler	
OMIM	616445	CANDIDIASIS, FAMILIAL, 9; CANDF9		HP:0012203	OMIM:616445	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000007	OMIM:616449	TAS				I		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000047	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000126	OMIM:616449	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000175	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000232	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000252	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000286	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000316	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000322	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000482	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000486	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000494	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000508	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0000518	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0001250	OMIM:616449	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0001257	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0001263	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0001290	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0001671	OMIM:616449	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0002079	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0002119	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0002650	OMIM:616449	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0002808	OMIM:616449	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0003577	OMIM:616449	TAS				C		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0003764	OMIM:616449	IEA				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0008070	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616449	BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS		HP:0010804	OMIM:616449	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0000007	OMIM:616451	TAS				I		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0000648	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0001123	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0001258	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0001284	OMIM:616451	IEA				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0001347	OMIM:616451	IEA				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0002936	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0003477	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0003487	OMIM:616451	TAS				P		HPO:skoehler	
OMIM	616451	SPASTIC PARAPLEGIA 74, AUTOSOMAL RECESSIVE; SPG74		HP:0003677	OMIM:616451	TAS				C		HPO:skoehler	
OMIM	616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA		HP:0000006	OMIM:616452	TAS				I		HPO:skoehler	
OMIM	616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA		HP:0001744	OMIM:616452	TAS				P		HPO:skoehler	
OMIM	616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA		HP:0002719	OMIM:616452	TAS				P		HPO:skoehler	
OMIM	616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA		HP:0002850	OMIM:616452	TAS				P		HPO:skoehler	
OMIM	616452	B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA		HP:0100827	OMIM:616452	IEA				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000006	OMIM:616455	TAS				I		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000158	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000212	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000349	OMIM:616455	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000407	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000430	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000431	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000456	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000470	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000527	OMIM:616455	IEA				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000574	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0000664	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0001249	OMIM:616455	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0001290	OMIM:616455	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0002002	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0002808	OMIM:616455	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0004322	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0005322	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616455	ZIMMERMANN-LABAND SYNDROME 2; ZLS2		HP:0012471	OMIM:616455	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0000007	OMIM:616457	TAS				I		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001263	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001290	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001903	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001927	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001947	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0001981	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50	HP:0012825	HP:0001987	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0002133	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0002136	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0002376	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0002465	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0003593	OMIM:616457	TAS				C		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0003676	OMIM:616457	TAS				C		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0004823	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0012345	OMIM:616457	IEA				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0012444	OMIM:616457	IEA				P		HPO:skoehler	
OMIM	616457	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 50; EIEE50		HP:0200134	OMIM:616457	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000007	OMIM:616459	TAS				I		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000160	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000219	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000252	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000369	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0000490	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001010	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001156	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001263	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001290	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001344	OMIM:616459	IEA				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001388	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0001852	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0002317	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0002540	OMIM:616459	IEA				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0003196	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0003577	OMIM:616459	TAS				C		HPO:skoehler	
OMIM	616459	AL-RAQAD SYNDROME; ARS		HP:0012368	OMIM:616459	TAS				P		HPO:skoehler	
OMIM	616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50		HP:0000007	OMIM:616460	TAS				I		HPO:skoehler	
OMIM	616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50		HP:0000252	OMIM:616460	TAS				P		HPO:skoehler	
OMIM	616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50		HP:0000407	OMIM:616460	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50		HP:0001256	OMIM:616460	TAS				P		HPO:skoehler	
OMIM	616460	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 50; MRT50		HP:0003593	OMIM:616460	TAS				C		HPO:skoehler	
OMIM	616461	EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8		HP:0000006	OMIM:616461	TAS				I		HPO:skoehler	
OMIM	616461	EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8		HP:0002384	OMIM:616461	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000006	OMIM:616462	TAS				I		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000175	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000252	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000278	OMIM:616462	IEA				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000327	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000347	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000400	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000453	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0000494	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0001643	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0002980	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0004322	OMIM:616462	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0004325	OMIM:616462	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0008551	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0008807	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0009892	OMIM:616462	IEA				P		HPO:skoehler	
OMIM	616462	ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN		HP:0011800	OMIM:616462	TAS				P		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000006	OMIM:616468	TAS				I		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000518	OMIM:616468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000529	OMIM:616468	TAS				P		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000533	OMIM:616468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000541	OMIM:616468	IEA				P		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0000545	OMIM:616468	TAS				P		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6	HP:0003676	HP:0001489	OMIM:616468	TAS				P		HPO:skoehler	
OMIM	616468	EXUDATIVE VITREORETINOPATHY 6; EVR6		HP:0030490	OMIM:616468	IEA				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0000007	OMIM:616469	TAS				I		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0000510	OMIM:616469	IEA				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0000543	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0000613	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0000662	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0001133	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0007663	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0007787	OMIM:616469	TAS				P		HPO:skoehler	
OMIM	616469	RETINITIS PIGMENTOSA 72; RP72		HP:0500087	OMIM:616469	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0000218	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0001270	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0001284	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0001371	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0001382	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0002093	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0002751	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0003741	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616470	#616470 ULLRICH CONGENITAL MUSCULAR DYSTROPHY 2; UCMD2		HP:0010628	OMIM:616470	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0001290	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0001324	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0001371	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0001388	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0002808	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0003198	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0003236	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0009046	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0025403	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616471	BETHLEM MYOPATHY 2; BTHLM2		HP:0031936	OMIM:616471	IEA				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0000007	OMIM:616479	TAS				I		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0000508	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2	HP:0003676	HP:0000544	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0000590	OMIM:616479	IEA				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0001251	OMIM:616479	IEA				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0001260	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0001272	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0001324	OMIM:616479	IEA				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0001347	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0002015	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0002093	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0002151	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0002172	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0002317	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003202	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003236	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003326	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003487	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003546	OMIM:616479	TAS				P		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0003676	OMIM:616479	TAS				C		HPO:skoehler	
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0011712	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616479	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 2; PEOB2		HP:0100543	OMIM:616479	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0000007	OMIM:616481	TAS				I		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0002110	OMIM:616481	TAS				P		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0002205	OMIM:616481	TAS				P		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0002643	OMIM:616481	TAS				P		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0003577	OMIM:616481	TAS				C		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0012263	OMIM:616481	TAS				P		HPO:skoehler	
OMIM	616481	CILIARY DYSKINESIA, PRIMARY, 32; CILD32		HP:0012265	OMIM:616481	IEA				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000006	OMIM:616482	TAS				I		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000238	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000260	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000365	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000388	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000577	OMIM:616482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000926	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0000956	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001249	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001250	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001263	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001355	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001582	OMIM:616482	IEA				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0001635	OMIM:616482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002007	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002020	OMIM:616482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002079	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002092	OMIM:616482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002808	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002871	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0002938	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0003027	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0003510	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0005280	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0008905	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0010535	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0011003	OMIM:616482	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616482	ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN		HP:0011800	OMIM:616482	TAS				P		HPO:skoehler	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0000007	PMID:26073778	PCS				I		HPO:skoehler	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0000952	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0001250	PMID:26073778	PCS		HP:0040284		P		HPO:nvasilevsky	1/10
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0001254	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0001638	PMID:26073778	PCS		HP:0040284		P		HPO:nvasilevsky	1/10
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0001943	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0001987	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0002013	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0002480	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0002910	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0003256	PMID:26073778	PCS				P		HPO:nvasilevsky	
OMIM	616483	INFANTILE LIVER FAILURE SYNDROME 2		HP:0006554	PMID:26073778	PCS	HP:0003593			P		HPO:nvasilevsky	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:616486	TAS				I		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000253	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000582	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE	HP:0012828	HP:0001263	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001285	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001290	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001321	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001344	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001762	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002064	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002079	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002119	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002365	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002540	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:616486	TAS				C		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003676	OMIM:616486	TAS				C		HPO:skoehler	
OMIM	616486	MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE		HP:0010864	OMIM:616486	TAS				P		HPO:skoehler	
OMIM	616487	EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY; EBSND		HP:0000007	OMIM:616487	TAS				I		HPO:skoehler	
OMIM	616487	EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY; EBSND		HP:0007556	OMIM:616487	TAS				P		HPO:skoehler	
OMIM	616487	EPIDERMOLYSIS BULLOSA SIMPLEX WITH NAIL DYSTROPHY; EBSND		HP:0008404	OMIM:616487	TAS				P		HPO:skoehler	
OMIM	616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8		HP:0000007	OMIM:616488	TAS				I		HPO:skoehler	
OMIM	616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8		HP:0000559	OMIM:616488	TAS				P		HPO:skoehler	
OMIM	616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8		HP:0000966	OMIM:616488	TAS				P		HPO:skoehler	
OMIM	616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8		HP:0002719	OMIM:616488	IEA				P		HPO:skoehler	
OMIM	616488	NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII; HSAN8		HP:0012804	OMIM:616488	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000006	OMIM:616489	TAS				I		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000028	OMIM:616489	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000047	OMIM:616489	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000062	OMIM:616489	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000278	OMIM:616489	IEA				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000325	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000369	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0000995	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0001270	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0001290	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0001419	OMIM:616489	TAS				I		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0001643	OMIM:616489	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0002750	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0004322	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0004325	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0004482	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0008872	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0011220	OMIM:616489	TAS				P		HPO:skoehler	
OMIM	616489	GROWTH RESTRICTION, SEVERE, WITH DISTINCTIVE FACIES; GRDF		HP:0040019	OMIM:616489	IEA				P		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0000007	OMIM:616490	TAS				I		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0000496	OMIM:616490	TAS				P		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0000589	OMIM:616490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0001263	OMIM:616490	TAS				P		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0002104	OMIM:616490	TAS				P		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0002789	OMIM:616490	TAS				P		HPO:skoehler	
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0006989	OMIM:616490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0007033	OMIM:616490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616490	JOUBERT SYNDROME 23; JBTS23		HP:0010442	OMIM:616490	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0000006	OMIM:616491	TAS				I		HPO:skoehler	
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0001265	OMIM:616491	TAS				P		HPO:skoehler	
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0002936	OMIM:616491	TAS				P		HPO:skoehler	
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0003401	OMIM:616491	IEA				P		HPO:skoehler	
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0003676	OMIM:616491	TAS				C		HPO:skoehler	
OMIM	616491	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V; CMT2V		HP:0010871	OMIM:616491	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0000007	OMIM:616494	TAS				I		HPO:skoehler	
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0000164	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0000545	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001249	OMIM:616494	TAS				P		HPO:skoehler	
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001251	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001257	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001263	OMIM:616494	TAS				P		HPO:skoehler	
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001272	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001337	OMIM:616494	TAS				P		HPO:skoehler	
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0001337	OMIM:616494	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0002079	OMIM:616494	TAS				P		HPO:skoehler	
OMIM	616494	LEUKODYSTROPHY, HYPOMYELINATING, 11; HLD11		HP:0002415	OMIM:616494	TAS				P		HPO:skoehler	
OMIM	616500	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3; CEMCOX3		HP:0000007	OMIM:616500	TAS				I	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 3; CEMCOX3	HPO:skoehler	
OMIM	616500	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3; CEMCOX3		HP:0001639	OMIM:616500	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 3; CEMCOX3	HPO:skoehler	
OMIM	616500	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 3; CEMCOX3		HP:0003577	OMIM:616500	TAS				C	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 3; CEMCOX3	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0000007	OMIM:616501	TAS				I	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0000331	OMIM:616501	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0001252	OMIM:616501	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0001639	OMIM:616501	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0003128	OMIM:616501	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616501	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASE DEFICIENCY 4; CEMCOX4		HP:0030682	OMIM:616501	TAS				P	CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME C OXIDASE DEFICIENCY 4; CEMCOX4	HPO:skoehler	
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0000007	OMIM:616502	TAS				I		HPO:skoehler	
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0000556	OMIM:616502	IEA				P		HPO:skoehler	
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0000613	OMIM:616502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0000662	OMIM:616502	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0007401	OMIM:616502	TAS				P		HPO:skoehler	
OMIM	616502	CONE-ROD DYSTROPHY 21; CORD21		HP:0007663	OMIM:616502	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000007	OMIM:616503	TAS				I		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000219	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000316	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000325	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000347	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000369	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000463	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0000775	OMIM:616503	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001181	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001196	OMIM:616503	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001511	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001558	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001561	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0001762	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0002089	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0002650	OMIM:616503	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0002803	OMIM:616503	IEA				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0003198	OMIM:616503	IEA				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0005280	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0009487	OMIM:616503	TAS				P		HPO:skoehler	
OMIM	616503	LETHAL CONGENITAL CONTRACTURE SYNDROME 9; LCCS9		HP:0031013	OMIM:616503	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000007	OMIM:616505	TAS				I		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000189	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000341	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000414	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000463	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000529	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000577	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000639	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0000648	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001182	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001251	OMIM:616505	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001263	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001265	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001272	OMIM:616505	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001290	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001310	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001324	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001336	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001337	OMIM:616505	IEA				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001347	OMIM:616505	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001371	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0001761	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0002936	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0003186	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0003376	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0003487	OMIM:616505	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0003828	OMIM:616505	TAS				C		HPO:skoehler	
OMIM	616505	NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB; HMSN6B		HP:0010804	OMIM:616505	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0000007	OMIM:616507	TAS				I		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0000750	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0000926	OMIM:616507	IEA				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0000939	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0000977	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0001252	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0001270	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0001324	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0002650	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0002953	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0003199	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0004322	OMIM:616507	TAS		HP:0040282		P		HPO:skoehler	HP:0040282
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0006086	OMIM:616507	TAS				P		HPO:skoehler	
OMIM	616507	OSTEOGENESIS IMPERFECTA, TYPE XVII; OI17		HP:0030746	OMIM:616507	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616509	CATARACT 44; CTRCT44		HP:0000007	OMIM:616509	TAS				I		HPO:skoehler	
OMIM	616509	CATARACT 44; CTRCT44	HP:0012828	HP:0000519	OMIM:616509	TAS				P		HPO:skoehler	
OMIM	616509	CATARACT 44; CTRCT44		HP:0000572	OMIM:616509	TAS				P		HPO:skoehler	
OMIM	616511	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14; MODY14		HP:0000006	OMIM:616511	TAS				I		HPO:skoehler	
OMIM	616511	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14; MODY14		HP:0000819	OMIM:616511	TAS				P		HPO:skoehler	
OMIM	616511	MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 14; MODY14		HP:0004904	OMIM:616511	IEA				P		HPO:skoehler	
OMIM	616515	DEAFNESS, AUTOSOMAL RECESSIVE 104; DFNB104		HP:0000007	OMIM:616515	TAS				I		HPO:skoehler	
OMIM	616515	DEAFNESS, AUTOSOMAL RECESSIVE 104; DFNB104		HP:0000399	OMIM:616515	TAS				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0000007	OMIM:616516	TAS				I		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0001288	OMIM:616516	TAS				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0001324	OMIM:616516	IEA				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0002155	OMIM:616516	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0002650	OMIM:616516	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0002987	OMIM:616516	TAS				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0003141	OMIM:616516	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0003236	OMIM:616516	TAS				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0003560	OMIM:616516	TAS				P		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0003676	OMIM:616516	TAS				C		HPO:skoehler	
OMIM	616516	EMERY-DREIFUSS MUSCULAR DYSTROPHY 3, AUTOSOMAL RECESSIVE; EDMD3		HP:0011675	OMIM:616516	TAS				P		HPO:skoehler	
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0000007	PMID:26029869	PCS				I		HPO:probinson	
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0000603	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0000613	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0000639	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	4/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0007401	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0007663	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0007750	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0011516	PMID:26029869	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616517	ACHROMATOPSIA 7; ACHM7		HP:0030825	OMIM:616517	IEA				P		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0000006	OMIM:616521	TAS				I		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0000718	OMIM:616521	TAS				P		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0000750	OMIM:616521	TAS				P		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0001249	OMIM:616521	TAS				P		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0001263	OMIM:616521	TAS				P		HPO:skoehler	
OMIM	616521	MENTAL RETARDATION, AUTOSOMAL DOMINANT 39		HP:0001513	OMIM:616521	TAS		HP:0040281		P		HPO:skoehler	HP:0040281
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0000007	OMIM:616531	TAS				I		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0000268	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0000347	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0001321	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0001762	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0002126	OMIM:616531	IEA				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0002804	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0003577	OMIM:616531	TAS				C		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0007033	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0008796	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616531	POLYMICROGYRIA, PERISYLVIAN, WITH CEREBELLAR HYPOPLASIA AND ARTHROGRYPOSIS; PMGYCHA		HP:0010557	OMIM:616531	TAS				P		HPO:skoehler	
OMIM	616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7		HP:0000006	OMIM:616532	TAS				I		HPO:skoehler	
OMIM	616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7		HP:0001250	OMIM:616532	TAS				P		HPO:skoehler	
OMIM	616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7		HP:0002315	OMIM:616532	TAS				P		HPO:skoehler	
OMIM	616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7		HP:0002383	OMIM:616532	IEA				P		HPO:skoehler	
OMIM	616532	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 7; IIAE7		HP:0031179	OMIM:616532	TAS				P		HPO:skoehler	
OMIM	616534	THYROID CANCER, NONMEDULLARY, 4; NMTC4		HP:0000006	OMIM:616534	TAS				I		HPO:skoehler	
OMIM	616534	THYROID CANCER, NONMEDULLARY, 4; NMTC4		HP:0000853	OMIM:616534	IEA				P		HPO:skoehler	
OMIM	616534	THYROID CANCER, NONMEDULLARY, 4; NMTC4		HP:0040198	OMIM:616534	TAS				P		HPO:skoehler	
OMIM	616535	THYROID CANCER, NONMEDULLARY, 5; NMTC5		HP:0000006	OMIM:616535	TAS				I		HPO:skoehler	
OMIM	616535	THYROID CANCER, NONMEDULLARY, 5; NMTC5		HP:0040198	OMIM:616535	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000007	OMIM:616538	TAS				I		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000238	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000256	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000518	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000545	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000556	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000557	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0000568	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9	HP:0012828	HP:0001263	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0001290	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0001320	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0001344	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002079	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002119	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002126	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002350	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002415	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002421	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002514	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0002878	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0003236	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0003560	OMIM:616538	TAS				P		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0003593	OMIM:616538	TAS				C		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0003828	OMIM:616538	TAS				C		HPO:skoehler	
OMIM	616538	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 9; MDDGA9		HP:0031882	OMIM:616538	IEA				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0000007	OMIM:616539	TAS				I		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0000160	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0000325	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0000592	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001257	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001263	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001265	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001290	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001324	OMIM:616539	IEA				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001347	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001394	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0001508	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0002024	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0002151	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0002465	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0002875	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0003487	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0003546	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0011922	OMIM:616539	IEA		HP:0040280		P		HPO:skoehler	HP:0040280
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0012444	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616539	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 26; COXPD26		HP:0012448	OMIM:616539	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0000007	OMIM:616540	TAS				I		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0000171	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0001263	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0001336	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0002066	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0002119	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0002133	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0002650	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0003676	OMIM:616540	TAS				C		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0003700	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616540	EPILEPSY, PROGRESSIVE MYOCLONIC, 9; EPM9		HP:0009778	OMIM:616540	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000007	OMIM:616541	TAS				I		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000023	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000028	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000054	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000086	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000089	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000122	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000252	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000276	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000325	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000331	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000340	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000348	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000407	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000426	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000444	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000455	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000490	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000518	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000601	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000639	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000692	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000750	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000763	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000819	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000821	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000855	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0000956	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001260	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001263	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001310	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001511	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001620	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001644	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001761	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED	HP:0012825	HP:0001888	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001903	OMIM:616541	IEA				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0001956	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0002075	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0002119	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0002136	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0002186	OMIM:616541	IEA				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0003119	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0003189	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0004322	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED	HP:0012825	HP:0006855	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0009826	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0009879	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0030084	OMIM:616541	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616541	SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED		HP:0100543	OMIM:616541	TAS				P		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0000007	OMIM:616544	TAS				I		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0000510	OMIM:616544	IEA				P		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0000662	OMIM:616544	TAS				P		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0000980	OMIM:616544	IEA				P		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0001105	OMIM:616544	TAS				P		HPO:skoehler	
OMIM	616544	RETINITIS PIGMENTOSA 73; RP73		HP:0001133	OMIM:616544	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000007	OMIM:616546	TAS				I		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000054	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000175	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000238	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000369	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000377	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000470	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000480	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000773	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000774	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0000776	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001265	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001290	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001320	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001561	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001631	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0001789	OMIM:616546	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0002089	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0002126	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0002323	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0002419	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0002983	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0005280	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0006660	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0100258	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616546	SHORT-RIB THORACIC DYSPLASIA 14 WITH POLYDACTYLY		HP:0100259	OMIM:616546	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000007	OMIM:616549	TAS				I		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000218	OMIM:616549	IEA				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000219	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000232	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000252	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000343	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000347	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000369	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000414	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000430	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000465	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000470	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0000508	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0001290	OMIM:616549	IEA				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0001638	OMIM:616549	IEA				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0002162	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0002944	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0002949	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0003198	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0003502	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4		HP:0003798	OMIM:616549	IEA				P		HPO:skoehler	
OMIM	616549	KLIPPEL-FEIL SYNDROME 4, AUTOSOMAL RECESSIVE, WITH NEMALINE MYOPATHY AND FACIAL DYSMORPHISM; KFS4	HP:0012832	HP:0008807	OMIM:616549	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0000006	OMIM:616553	TAS				I		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0000007	OMIM:616553	TAS				I		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0000164	OMIM:616553	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0000252	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0001263	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0001321	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0001511	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0001915	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0002745	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6	HP:0003676	HP:0005528	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0008404	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616553	DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6		HP:0010450	OMIM:616553	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000006	OMIM:616559	TAS				I		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000028	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000316	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000465	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000470	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000494	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000508	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0000535	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0001263	OMIM:616559	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0001642	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0001671	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0001680	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0002212	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0004322	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616559	NOONAN SYNDROME 9; NS9		HP:0040180	OMIM:616559	TAS				P		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74		HP:0000007	OMIM:616562	TAS				I		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74		HP:0000510	OMIM:616562	IEA				P		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74	HP:0012826	HP:0000543	OMIM:616562	TAS				P		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74		HP:0000580	OMIM:616562	TAS				P		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74		HP:0001115	OMIM:616562	TAS				P		HPO:skoehler	
OMIM	616562	RETINITIS PIGMENTOSA 74; RP74		HP:0001133	OMIM:616562	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000006	OMIM:616564	TAS				I		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000028	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000316	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000470	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000494	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000508	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000535	OMIM:616564	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0000766	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0001642	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0001671	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0001680	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0001718	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0002212	OMIM:616564	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616564	NOONAN SYNDROME 10; NS10		HP:0004322	OMIM:616564	TAS				P		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0000007	OMIM:616566	TAS				I		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0002650	OMIM:616566	IEA				P		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0002937	OMIM:616566	IEA				P		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0002947	OMIM:616566	TAS				P		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0003316	OMIM:616566	IEA				P		HPO:skoehler	
OMIM	616566	SPONDYLOCOSTAL DYSOSTOSIS 6, AUTOSOMAL RECESSIVE; SCDO6		HP:0003416	OMIM:616566	TAS				P		HPO:skoehler	
OMIM	616568	GLIOMA SUSCEPTIBILITY 9; GLM9		HP:0000006	OMIM:616568	TAS				I		HPO:skoehler	
OMIM	616568	GLIOMA SUSCEPTIBILITY 9; GLM9		HP:0001909	OMIM:616568	IEA				P		HPO:skoehler	
OMIM	616568	GLIOMA SUSCEPTIBILITY 9; GLM9		HP:0003581	OMIM:616568	TAS				C		HPO:skoehler	
OMIM	616568	GLIOMA SUSCEPTIBILITY 9; GLM9		HP:0003829	OMIM:616568	TAS				C		HPO:skoehler	
OMIM	616568	GLIOMA SUSCEPTIBILITY 9; GLM9		HP:0009592	OMIM:616568	IEA				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000007	OMIM:616570	TAS				I		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000175	OMIM:616570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000252	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000347	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000369	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000568	OMIM:616570	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000969	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0000992	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0001263	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0001511	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0001558	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0001762	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0001838	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616570	CEREBROOCULOFACIOSKELETAL SYNDROME 3; COFS3		HP:0002804	OMIM:616570	TAS				P		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0000006	OMIM:616576	TAS				I		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0001581	OMIM:616576	TAS				P		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0001596	OMIM:616576	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0001873	OMIM:616576	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0001878	OMIM:616576	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0002721	OMIM:616576	TAS				P		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0003828	OMIM:616576	TAS				C		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0004313	OMIM:616576	TAS				P		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0005425	OMIM:616576	TAS				P		HPO:skoehler	
OMIM	616576	IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12		HP:0006510	OMIM:616576	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0000007	OMIM:616577	TAS				I		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0000252	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0000407	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0000486	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0000639	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001250	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001257	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001263	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001344	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001508	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0001873	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0002079	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0002353	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0002509	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0002650	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0002721	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0003429	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0008936	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0010864	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0011968	OMIM:616577	TAS				P		HPO:skoehler	
OMIM	616577	EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME; EHLMRS		HP:0100704	OMIM:616577	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000006	OMIM:616579	TAS				I		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000194	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000218	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000232	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000252	OMIM:616579	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000276	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000286	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000297	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000307	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000322	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000369	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000486	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000540	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000582	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0000733	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0001249	OMIM:616579	IEA				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0001263	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0001290	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0001344	OMIM:616579	IEA				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0001382	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0002020	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0002066	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0002205	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0003577	OMIM:616579	TAS				C		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0007328	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0010804	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616579	MENTAL RETARDATION, AUTOSOMAL DOMINANT 40; MRD40		HP:0011968	OMIM:616579	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000006	OMIM:616580	TAS				I		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000028	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000194	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000218	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000268	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000276	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000430	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000474	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000494	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000508	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000637	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000677	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000767	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0000960	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001249	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001263	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001290	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001363	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001385	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0001845	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0002019	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0002465	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0002650	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0002714	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0003186	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0005338	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0006610	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0008551	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0011968	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0012811	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616580	AU-KLINE SYNDROME		HP:0100259	OMIM:616580	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0000006	OMIM:616583	TAS				I		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0000211	OMIM:616583	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0000926	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0000946	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0002655	OMIM:616583	IEA				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0002673	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0002751	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0002829	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0004568	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616583	SPONDYLOEPIPHYSEAL DYSPLASIA, STANESCU TYPE		HP:0025258	OMIM:616583	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0000007	OMIM:616586	TAS				I		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0000016	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0000252	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0000518	OMIM:616586	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001249	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001257	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001258	OMIM:616586	IEA				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001263	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001288	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001337	OMIM:616586	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001344	OMIM:616586	IEA				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001347	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0001999	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0002445	OMIM:616586	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0003202	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0003487	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0003676	OMIM:616586	TAS				C		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0004322	OMIM:616586	TAS				P		HPO:skoehler	
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0007024	OMIM:616586	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616586	SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B		HP:0009027	OMIM:616586	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0000006	OMIM:616589	TAS				I		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0000089	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0000965	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001156	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001159	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001362	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001395	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001409	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001629	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001660	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001800	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0001849	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0002040	OMIM:616589	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0005180	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616589	ADAMS-OLIVER SYNDROME 6; AOS6		HP:0007385	OMIM:616589	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000006	OMIM:616592	TAS				I		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000219	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000307	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000336	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000431	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000494	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000508	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000520	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000716	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000739	OMIM:616592	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000963	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0000974	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0001030	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0001548	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0001833	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0002344	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0002944	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616592	KOSAKI OVERGROWTH SYNDROME; KOGS		HP:0011220	OMIM:616592	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000006	OMIM:616602	TAS				I		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000248	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000252	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000262	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000270	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000294	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000316	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000348	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000407	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000486	OMIM:616602	IEA				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0000508	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001252	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001252	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001263	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6	HP:0012825	HP:0001272	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001274	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001290	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001290	OMIM:616602	TAS				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001305	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001357	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0001363	OMIM:616602	IEA				P		HPO:skoehler	
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0002650	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616602	CRANIOSYNOSTOSIS 6; CRS6		HP:0003298	OMIM:616602	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000006	OMIM:616603	TAS				I		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000122	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000252	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000270	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000325	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000337	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000369	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000411	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000486	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000519	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000729	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000938	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0000973	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001181	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001263	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001290	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001348	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001511	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001659	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0001762	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0002645	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0002677	OMIM:616603	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0002827	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0007957	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0011220	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0011968	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0025356	OMIM:616603	IEA				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0100678	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616603	CUTIS LAXA, AUTOSOMAL DOMINANT 3; ADCL3		HP:0100790	OMIM:616603	TAS				P		HPO:skoehler	
OMIM	616604	CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB		HP:0000006	OMIM:616604	TAS				I	CHROMOSOME 14Q32 DUPLICATION SYNDROME, 700-KB	HPO:skoehler	
OMIM	616604	CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB		HP:0003829	OMIM:616604	TAS				C	CHROMOSOME 14Q32 DUPLICATION SYNDROME, 700-KB	HPO:skoehler	
OMIM	616604	CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB		HP:0011974	OMIM:616604	TAS				P	CHROMOSOME 14Q32 DUPLICATION SYNDROME, 700-KB	HPO:skoehler	
OMIM	616604	CHROMOSOME 14q32 DUPLICATION SYNDROME, 700-KB		HP:0012324	OMIM:616604	TAS				P	CHROMOSOME 14Q32 DUPLICATION SYNDROME, 700-KB	HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000218	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000252	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000268	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000286	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000316	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000369	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000463	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000470	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000494	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0000580	OMIM:616606	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0001249	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0001263	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0001290	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0001510	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0002133	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0002465	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0003593	OMIM:616606	TAS				C		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0003745	OMIM:616606	TAS				I		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0005280	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616606	RING CHROMOSOME 14 SYNDROME		HP:0005469	OMIM:616606	TAS				P		HPO:skoehler	
OMIM	616617	HEIMLER SYNDROME 2		HP:0000007	OMIM:616617	TAS				I		HPO:skoehler	
OMIM	616617	HEIMLER SYNDROME 2		HP:0000678	OMIM:616617	TAS				P		HPO:skoehler	
OMIM	616617	HEIMLER SYNDROME 2		HP:0001763	OMIM:616617	TAS				P		HPO:skoehler	
OMIM	616617	HEIMLER SYNDROME 2		HP:0001820	OMIM:616617	TAS				P		HPO:skoehler	
OMIM	616622	IMMUNODEFICIENCY 42		HP:0000007	OMIM:616622	TAS				I		HPO:skoehler	
OMIM	616622	IMMUNODEFICIENCY 42		HP:0000778	OMIM:616622	TAS				P		HPO:skoehler	
OMIM	616622	IMMUNODEFICIENCY 42		HP:0003593	OMIM:616622	TAS				C		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0000006	OMIM:616625	TAS				I		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0001761	OMIM:616625	TAS				P		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0001765	OMIM:616625	TAS				P		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0002936	OMIM:616625	TAS				P		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0003376	OMIM:616625	TAS				P		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0003438	OMIM:616625	TAS				P		HPO:skoehler	
OMIM	616625	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2W		HP:0003828	OMIM:616625	TAS				C		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000007	OMIM:616629	TAS				I		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000090	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000135	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000486	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000510	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000608	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0000639	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0001263	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0001395	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0001396	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0001513	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0001970	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0003774	OMIM:616629	TAS				P		HPO:skoehler	
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0008802	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616629	SENIOR-LOKEN SYNDROME 9		HP:0010442	OMIM:616629	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616631	POROKERATOSIS 9, MULTIPLE TYPES; POROK9		HP:0200044	OMIM:616631	IEA				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0000007	OMIM:616632	TAS				I		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0000252	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0000648	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0001250	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0001290	OMIM:616632	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0002079	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0002465	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0004322	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616632	SEIZURES, CORTICAL BLINDNESS, AND MICROCEPHALY SYNDROME		HP:0100704	OMIM:616632	TAS				P		HPO:skoehler	
OMIM	616636	IMMUNODEFICIENCY 44		HP:0000007	OMIM:616636	TAS				I		HPO:skoehler	
OMIM	616636	IMMUNODEFICIENCY 44		HP:0001298	OMIM:616636	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616636	IMMUNODEFICIENCY 44		HP:0003828	OMIM:616636	TAS				C		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000006	OMIM:616638	TAS				I		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000154	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000194	OMIM:616638	IEA				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000219	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000256	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000260	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000316	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000319	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000331	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000343	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000348	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000486	OMIM:616638	IEA				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000494	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0000957	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001249	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001250	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001290	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001537	OMIM:616638	IEA				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001540	OMIM:616638	IEA				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001869	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001873	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0001943	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0002007	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0002212	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0002720	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0003196	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0005280	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0006191	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0007206	PMID:22497611	PCS				P		HPO:lccarmody	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0008905	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0009882	OMIM:616638	IEA				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0010241	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0011800	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616638	SMITH-KINGSMORE SYNDROME		HP:0012650	OMIM:616638	TAS				P		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0000007	PMID:22961547	PCS				I		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0000020	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0000709	OMIM:616640	TAS				P		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0000726	OMIM:616640	TAS				P		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0000738	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0001260	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0001336	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0001347	OMIM:616640	TAS				P		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0002073	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0002123	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0002300	OMIM:616640	TAS				P		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0002497	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0002510	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0003676	OMIM:616640	TAS				C		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0003828	OMIM:616640	TAS				C		HPO:skoehler	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0011999	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616640	EPILEPSY, PROGRESSIVE MYOCLONIC, 10		HP:0100318	PMID:22961547	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0000007	OMIM:616645	TAS				I		HPO:skoehler	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0001249	OMIM:616645	TAS				P		HPO:skoehler	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0001263	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0002059	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0002133	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0002188	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0002376	OMIM:616645	IEA				P		HPO:skoehler	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0002540	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0003593	PMID:26333769	PCS				C		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0003781	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0005484	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0006813	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0007256	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616645	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 34; EIEE34		HP:0007334	PMID:26333769	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0000007	PMID:26224535	PCS				I		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0000252	PMID:26224535	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0000518	PMID:26224535	PCS		HP:0040284		P		HPO:probinson	3/7
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0000737	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001263	PMID:26224535	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001298	OMIM:616647	TAS				P		HPO:skoehler	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001511	OMIM:616647	TAS				P		HPO:skoehler	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001522	PMID:26224535	PCS				M		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001620	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0001638	OMIM:616647	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0002059	OMIM:616647	TAS				P		HPO:skoehler	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0002133	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0002188	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0003593	PMID:26224535	PCS				C		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0006829	OMIM:616647	TAS				P		HPO:skoehler	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0011968	PMID:26224535	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0012444	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616647	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 35		HP:0200085	PMID:26224535	PCS				P		HPO:probinson	
OMIM	616648	OPTIC ATROPHY 8		HP:0000006	PMID:21349918	PCS				I		HPO:probinson	
OMIM	616648	OPTIC ATROPHY 8		HP:0000407	PMID:21349918	PCS				P		HPO:probinson	
OMIM	616648	OPTIC ATROPHY 8		HP:0000572	OMIM:616648	TAS				P		HPO:skoehler	
OMIM	616648	OPTIC ATROPHY 8		HP:0000603	PMID:21349918	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616648	OPTIC ATROPHY 8		HP:0000648	PMID:21349918	PCS				P		HPO:probinson	
OMIM	616648	OPTIC ATROPHY 8		HP:0001634	PMID:21349918	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	616648	OPTIC ATROPHY 8		HP:0001653	OMIM:616648	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616648	OPTIC ATROPHY 8		HP:0006958	PMID:21349918	IEA		HP:0040284		P		HPO:probinson	3/5
OMIM	616648	OPTIC ATROPHY 8		HP:0007104	PMID:21349918	PCS				P		HPO:probinson	
OMIM	616648	OPTIC ATROPHY 8		HP:0030455	PMID:21349918	PCS				P		HPO:probinson	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0000006	OMIM:616649	TAS				I		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0000952	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0001744	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0001878	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0001923	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0002904	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616649	SPHEROCYTOSIS, TYPE 2		HP:0004444	OMIM:616649	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000007	PMID:26522830	PCS				I		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000219	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000252	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	5/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000343	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000403	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000430	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000460	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000463	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000494	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000556	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000637	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000954	PMID:26522830	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0000964	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001156	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001252	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	5/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001256	PMID:16901296	PCS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001263	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	5/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001290	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001511	PMID:16901296	PCS		HP:0040284		P		HPO:skoehler	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001622	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001629	PMID:26522830	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001744	PMID:26522830	PCS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001831	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0001880	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0002240	PMID:26522830	PCS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0002655	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0002714	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0002716	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0003273	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0003301	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0004209	PMID:26522830	PCS		HP:0040284		P		HPO:skoehler	4/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0004322	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0004625	PMID:26522830	PCS				P		HPO:probinson	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0006361	PMID:26522830	PCS				P		HPO:probinson	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0006532	OMIM:616651	TAS				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0008897	PMID:16901296	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0010049	PMID:26522830	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0011231	OMIM:616651	IEA				P		HPO:skoehler	
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0011927	PMID:26522830	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616651	ROIFMAN SYNDROME; RFMN		HP:0012817	PMID:26522830	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000006	OMIM:616652	TAS				I		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000218	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000219	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000319	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000325	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000445	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000486	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000582	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0000762	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001249	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001263	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001284	OMIM:616652	IEA				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001290	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001388	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001508	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001671	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0001760	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0002066	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0002136	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0002317	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0002465	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0002936	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0003396	OMIM:616652	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0003577	OMIM:616652	TAS				C		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0007108	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0011968	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0012450	OMIM:616652	TAS				P		HPO:skoehler	
OMIM	616652	YUAN-HAREL-LUPSKI SYNDROME; YUHAL		HP:0031936	OMIM:616652	IEA				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0000007	OMIM:616654	TAS				I		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0000540	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0000639	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001162	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001257	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24	HP:0012828	HP:0001263	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001288	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001290	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001302	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001310	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001321	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001344	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001347	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0001762	OMIM:616654	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616654	JOUBERT SYNDROME 24		HP:0002126	OMIM:616654	TAS				P		HPO:skoehler	
OMIM	616654	JOUBERT SYNDROME 24		HP:0003593	OMIM:616654	TAS				C		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0000007	OMIM:616657	TAS				I		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0000253	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0000737	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0000752	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0001249	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0001250	OMIM:616657	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM	HP:0012828	HP:0001263	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0001290	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0001344	OMIM:616657	IEA				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0001347	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0002059	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0002079	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0002510	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0002540	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0003487	OMIM:616657	TAS				P		HPO:skoehler	
OMIM	616657	SPASTIC TETRAPLEGIA, THIN CORPUS CALLOSUM, AND PROGRESSIVE MICROCEPHALY; SPATCCM		HP:0003577	OMIM:616657	TAS				C		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0000007	OMIM:616668	TAS				I		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0001155	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0001284	OMIM:616668	IEA				P		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0001337	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0001761	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0002079	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0002751	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0002936	OMIM:616668	TAS				P		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0003477	OMIM:616668	TAS				P		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0003677	OMIM:616668	TAS				C		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0006466	OMIM:616668	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0009027	OMIM:616668	TAS				P		HPO:skoehler	
OMIM	616668	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X; CMT2X		HP:0100543	OMIM:616668	TAS				P		HPO:skoehler	
OMIM	616669	IMMUNODEFICIENCY 45		HP:0000007	OMIM:616669	TAS				I		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0000007	OMIM:616672	TAS				I		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0000505	OMIM:616672	IEA				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001263	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001284	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001321	OMIM:616672	IEA				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001332	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001336	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001414	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0001508	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002059	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002072	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002079	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002133	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002151	OMIM:616672	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002179	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0002273	OMIM:616672	IEA				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0005484	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0006829	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0010841	OMIM:616672	IEA				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0011968	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616672	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 27; COXPD27		HP:0200134	OMIM:616672	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:616680	TAS				I		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000483	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000501	OMIM:616680	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000540	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0000648	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0001272	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0001310	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0001319	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0002119	OMIM:616680	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0002313	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0002464	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0002522	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0002600	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0003677	OMIM:616680	TAS				C		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0007371	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0007663	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0009830	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616680	SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE		HP:0100543	OMIM:616680	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:616681	TAS				I		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000028	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000194	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000340	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000347	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000501	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000506	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000508	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001181	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001274	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002510	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004325	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0006380	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616681	MICROCEPHALY 16, PRIMARY, AUTOSOMAL RECESSIVE		HP:0009879	OMIM:616681	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000007	OMIM:616682	TAS				I		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000028	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000256	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000280	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000316	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0000486	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0001250	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0001263	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0001290	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0001629	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0001845	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0002019	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0002020	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0002465	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0002650	OMIM:616682	TAS				P		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0003593	OMIM:616682	TAS				C		HPO:skoehler	
OMIM	616682	SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME; SSMS		HP:0005326	OMIM:616682	IEA				P		HPO:skoehler	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0000007	OMIM:616683	PCS				I		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0000011	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0000365	OMIM:616683	TAS				P		HPO:skoehler	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0000648	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0001249	OMIM:616683	TAS				P		HPO:skoehler	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0001257	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0001272	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0001344	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0001371	PMID:26307567,PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0002019	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0002079	PMID:26307567,PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0002119	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0002384	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0002465	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0005484	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0005968	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0006808	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0007281	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0007663	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0008936	PMID:26307567	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0011344	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0011398	PMID:27120463	PCS				P		HPO:probinson	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0012332	OMIM:616683	TAS				P		HPO:skoehler	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0012448	OMIM:616683	TAS				P		HPO:skoehler	
OMIM	616683	LEUKODYSTROPHY, HYPOMYELINATING, 12		HP:0100704	OMIM:616683	TAS				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0000007	PMID:24027061	PCS				I		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K	HP:0012825	HP:0000407	PMID:24027061	PCS				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0000666	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0001251	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0001284	OMIM:616684	IEA				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0001332	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0002151	PMID:24027061	PCS				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0002355	PMID:24027061	PCS				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0002751	PMID:24027061	PCS				P		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0003202	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0003388	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0003447	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0003677	OMIM:616684	TAS				C		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0003828	OMIM:616684	TAS				C		HPO:skoehler	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0009830	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616684	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4K; CMT4K		HP:0011096	PMID:24027061	PCS				P		HPO:probinson	
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0000006	OMIM:616685	TAS				I		HPO:skoehler	
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0002069	OMIM:616685	TAS				P		HPO:skoehler	
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0002121	OMIM:616685	TAS				P		HPO:skoehler	
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0002123	OMIM:616685	TAS				P		HPO:skoehler	
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0002373	OMIM:616685	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616685	EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14		HP:0003829	OMIM:616685	TAS				C		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0000006	OMIM:616687	TAS				I		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0001284	OMIM:616687	IEA				P		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0001761	OMIM:616687	TAS				P		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0001765	OMIM:616687	TAS				P		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0002936	OMIM:616687	TAS				P		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0003236	OMIM:616687	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0003676	OMIM:616687	TAS				C		HPO:skoehler	
OMIM	616687	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Y; CMT2Y		HP:0003828	OMIM:616687	TAS				C		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0000006	OMIM:616688	TAS				I		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0000020	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0000365	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001171	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001263	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001270	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001276	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001284	OMIM:616688	IEA				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001290	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001620	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0001761	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0002355	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0002380	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0002411	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0002650	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0002936	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0003394	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0003677	OMIM:616688	TAS				C		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0003701	OMIM:616688	IEA				P		HPO:skoehler	
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0007256	OMIM:616688	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616688	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Z; CMT2Z		HP:0009027	OMIM:616688	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0000006	OMIM:616689	TAS				I		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0000952	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0001744	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0001878	OMIM:616689	TAS	HP:0003577			P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0001923	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0001927	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0002240	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0002904	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0004823	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0005518	OMIM:616689	TAS				P		HPO:skoehler	
OMIM	616689	DEHYDRATED HEREDITARY STOMATOCYTOSIS 2; DHS2		HP:0025548	OMIM:616689	IEA				P		HPO:skoehler	
OMIM	616697	DEAFNESS, AUTOSOMAL DOMINANT 69		HP:0000006	PMID:26522471	PCS				I		HPO:probinson	
OMIM	616697	DEAFNESS, AUTOSOMAL DOMINANT 69		HP:0000407	PMID:26522471	PCS				P		HPO:probinson	
OMIM	616705	DEAFNESS, AUTOSOMAL RECESSIVE 97		HP:0000007	PMID:25941349	PCS				I		HPO:skoehler	
OMIM	616705	DEAFNESS, AUTOSOMAL RECESSIVE 97		HP:0000407	PMID:25941349	PCS	HP:0003593	HP:0040284		P		HP:probinson	9/9
OMIM	616707	DEAFNESS, AUTOSOMAL DOMINANT 68		HP:0000006	PMID:25816005	PCS				I		HPO:skoehler	
OMIM	616707	DEAFNESS, AUTOSOMAL DOMINANT 68		HP:0000407	PMID:25816005	PCS	HP:0003621	HP:0040284		P		HP:probinson	10/10
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000006	PMID:26264232	PCS				I		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000219	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000248	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000280	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000293	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000316	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000337	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000358	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000365	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000377	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000407	OMIM:616708	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000414	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000470	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000483	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000486	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000490	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000545	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000574	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000664	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000713	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000718	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000739	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0000750	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0001007	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0001250	PMID:26264232	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0001263	PMID:26264232	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0001290	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0002019	PMID:26264232	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0002079	OMIM:616708	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0002360	PMID:26264232	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0002714	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0003186	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0003593	OMIM:616708	TAS				C		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0005280	PMID:26264232	PCS				P		HPO:probinson	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0007018	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0011220	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0011800	OMIM:616708	TAS				P		HPO:skoehler	
OMIM	616708	DESANTO-SHINAWI SYNDROME		HP:0011968	PMID:26264232	PCS		HP:0040284		P		HPO:probinson	4/6
OMIM	616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22		HP:0000006	OMIM:616710	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22		HP:0001288	OMIM:616710	IEA				P		HPO:skoehler	
OMIM	616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22		HP:0001347	OMIM:616710	IEA				P		HPO:skoehler	
OMIM	616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22		HP:0002067	OMIM:616710	IEA				P		HPO:skoehler	
OMIM	616710	PARKINSON DISEASE 22, AUTOSOMAL DOMINANT; PARK22		HP:0002322	OMIM:616710	IEA				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0000007	OMIM:616716	TAS				I		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0000252	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0000519	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0000763	OMIM:616716	IEA				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001250	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001263	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001265	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001324	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001761	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0001762	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0002099	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0002136	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0002812	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0002943	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0003021	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0003025	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0003700	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0004322	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0004325	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0009830	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0010544	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0010864	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0011703	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616716	RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, TYPE 5; RCDP5		HP:0100864	OMIM:616716	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0000007	OMIM:616719	TAS				I		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001256	OMIM:616719	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001257	OMIM:616719	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001265	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001270	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001272	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001337	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001347	OMIM:616719	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001395	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001399	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001744	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0001762	OMIM:616719	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0002066	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0002240	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0002359	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0002936	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616719	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 21		HP:0007141	OMIM:616719	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000007	OMIM:616720	TAS				I		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000218	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000278	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000347	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000369	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000508	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0000768	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0001270	OMIM:616720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0001283	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0001290	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0001761	OMIM:616720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0002020	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0002093	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0002421	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0002783	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0003306	OMIM:616720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0003546	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0003577	OMIM:616720	TAS				C		HPO:skoehler	
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0010628	OMIM:616720	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616720	MYASTHENIC SYNDROME, CONGENITAL, 19		HP:0011968	OMIM:616720	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000007	OMIM:616721	TAS				I		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000365	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000483	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000486	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000639	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0000938	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0001250	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN	HP:0012829	HP:0001263	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0001272	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN	HP:0012829	HP:0001290	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0001363	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0001382	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0002059	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0002187	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0002540	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0002719	OMIM:616721	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0003577	OMIM:616721	TAS				C		HPO:skoehler	
OMIM	616721	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIN		HP:0004322	OMIM:616721	TAS				P		HPO:skoehler	
OMIM	616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT		HP:0000006	OMIM:616722	TAS				I		HPO:skoehler	
OMIM	616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT		HP:0000519	OMIM:616722	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT		HP:0001105	OMIM:616722	TAS				P		HPO:skoehler	
OMIM	616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT		HP:0007663	OMIM:616722	TAS				P		HPO:skoehler	
OMIM	616722	RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT		HP:0011484	OMIM:616722	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000007	OMIM:616723	TAS				I		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000252	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000272	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000286	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000316	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000369	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000470	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000486	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA	HP:0012825	HP:0000508	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000729	OMIM:616723	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000926	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0000938	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001249	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001270	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001290	OMIM:616723	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001363	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001845	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0001999	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0002678	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0002750	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA	HP:0012825	HP:0002944	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0002980	OMIM:616723	IEA				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0003196	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0003275	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0004322	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0005280	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0006461	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0008551	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0010049	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0010585	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0010804	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0012471	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616723	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, FADEN-ALKURAYA TYPE; SEMDFA		HP:0100864	OMIM:616723	TAS				P		HPO:skoehler	
OMIM	616724	TOOTH AGENESIS, SELECTIVE, 7		HP:0000006	OMIM:616724	TAS				I		HPO:skoehler	
OMIM	616724	TOOTH AGENESIS, SELECTIVE, 7		HP:0000679	OMIM:616724	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616724	TOOTH AGENESIS, SELECTIVE, 7		HP:0006349	OMIM:616724	TAS				P		HPO:skoehler	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0000007	OMIM:616726	TAS				I		HPO:skoehler	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0000403	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0000405	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0002110	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0002257	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0002837	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0006532	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0012265	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0012735	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616726	CILIARY DYSKINESIA, PRIMARY, 33		HP:0100750	PMID:26387594	PCS				P		HPO:probinson	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000006	PMID:26656649	PCS				I		HPO:probinson	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000028	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000041	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000219	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000248	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000256	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000431	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000463	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000494	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000508	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000577	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000592	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000657	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000664	OMIM:616728	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000687	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0000750	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001182	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001263	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001270	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001290	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001382	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0001800	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002007	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002019	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002079	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002144	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002188	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002553	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002558	OMIM:616728	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0002714	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0003396	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0003468	PMID:26656649	PCS				P		HPO:probinson	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0004209	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0004322	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0006895	PMID:26656649	PCS				P		HPO:probinson	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0009778	OMIM:616728	TAS				P		HPO:skoehler	
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0011220	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0011968	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	1/2
OMIM	616728	CLEFT PALATE, PSYCHOMOTOR RETARDATION, AND DISTINCTIVE FACIAL FEATURES		HP:0012430	PMID:26656649	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000007	PMID:26411495	PCS				I		HPO:probinson	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000092	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000093	PMID:26411495	PCS				P		HPO:probinson	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000097	PMID:26411495	PCS		HP:0040284		P		HPO:probinson	8/10
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000100	PMID:26411495	PCS				P		HPO:probinson	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000175	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000218	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000319	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000340	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000341	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000347	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000750	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0000794	OMIM:616730	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001166	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001263	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001629	OMIM:616730	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001644	OMIM:616730	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001967	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0001999	OMIM:616730	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0003073	PMID:26411495	PCS				P		HPO:probinson	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0003124	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0003676	OMIM:616730	TAS				C		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0003774	PMID:26411495	PCS				P		HPO:probinson	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0003828	OMIM:616730	TAS				C		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0009944	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0012579	OMIM:616730	TAS				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0030084	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616730	NEPHROTIC SYNDROME, TYPE 11; NPHS11		HP:0410030	OMIM:616730	IEA				P		HPO:skoehler	
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0000007	OMIM:616732	TAS				I		HPO:skoehler	
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0000543	OMIM:616732	TAS				P		HPO:skoehler	
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0000603	OMIM:616732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0000613	OMIM:616732	TAS				P		HPO:skoehler	
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0000639	OMIM:616732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0001251	OMIM:616732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0001256	OMIM:616732	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616732	OPTIC ATROPHY 10 WITH OR WITHOUT ATAXIA, MENTAL RETARDATION, AND SEIZURES		HP:0007663	OMIM:616732	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0000007	PMID:26084283	PCS				I		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0000110	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0000365	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0000505	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0000822	OMIM:616733	IEA				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001252	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001263	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001270	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001271	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001290	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001324	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001371	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001511	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001518	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0001562	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0002089	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0002098	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0003259	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0003577	OMIM:616733	TAS				C		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0005932	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0008897	OMIM:616733	TAS				P		HPO:skoehler	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0011096	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0011968	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616733	COENZYME Q10 DEFICIENCY, PRIMARY, 8; COQ10D8		HP:0012531	PMID:26084283	PCS				P		HPO:probinson	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000006	OMIM:616734	TAS				I		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000028	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000046	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000047	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000160	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000175	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000252	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000286	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000316	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000347	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000358	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000369	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000470	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000475	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000482	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000494	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000568	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000581	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000582	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000670	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000691	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000750	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0000767	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001182	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001249	OMIM:616734	IEA				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001250	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001270	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001290	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0001763	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0002079	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0004279	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0004322	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0006610	OMIM:616734	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0008551	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0012368	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616734	SKIN CREASES, CONGENITAL SYMMETRIC CIRCUMFERENTIAL, 2; CSCSC2		HP:0012745	OMIM:616734	TAS				P		HPO:skoehler	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0000006	PMID:26188006	PCS				I		HPO:probinson	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0002080	PMID:26188006	PCS				P		HPO:probinson	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0002174	PMID:26188006	PCS				P		HPO:probinson	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0003677	OMIM:616736	TAS				C		HPO:skoehler	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0003828	OMIM:616736	TAS				C		HPO:skoehler	
OMIM	616736	TREMOR, HEREDITARY ESSENTIAL, 5		HP:0003831	OMIM:616736	TAS				C		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000023	PMID:26708094	PCS	HP:0011463	HP:0040283		P		HPO:probinson	HP:0040283
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000028	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000047	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000122	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000126	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000154	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000219	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000253	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000316	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000319	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000322	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000341	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000343	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000358	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000369	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000407	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000414	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000431	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000454	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000494	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS	HP:0012825	HP:0000508	PMID:26708094	IEA		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000577	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000582	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000648	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000664	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000687	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000689	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0000708	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001004	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001182	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001249	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001250	OMIM:616737	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001251	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	1/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001263	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001272	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	1/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001290	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001321	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001344	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001643	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	1/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001671	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001873	OMIM:616737	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0001999	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002079	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002119	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002120	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002518	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002553	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002714	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002719	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0002721	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0003764	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0007655	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0009623	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0011220	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0011800	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0011877	PMID:26708094	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0012385	PMID:26708094	PCS	HP:0011463	HP:0040284		P		HPO:probinson	2/2
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0030084	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616737	TAKENOUCHI-KOSAKI SYNDROME; TKS		HP:0045075	OMIM:616737	IEA				P		HPO:skoehler	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0000006	OMIM:616738	TAS				I		HPO:skoehler	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0000034	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0000407	OMIM:616738	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0001873	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0001875	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0001903	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0001905	OMIM:616738	TAS				P		HPO:skoehler	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0002974	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0006394	OMIM:616738	TAS				P		HPO:probinson	
OMIM	616738	RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2		HP:0010557	PMID:20091385	PCS				P		HPO:probinson	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0000007	PMID:26206890	PCS				I		HPO:probinson	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0000252	OMIM:616739	TAS				P		HPO:skoehler	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0000750	PMID:26206890	PCS				P		HPO:probinson	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0001249	PMID:26206890	PCS				P		HPO:probinson	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0001263	PMID:26206890	PCS				P		HPO:probinson	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0001270	OMIM:616739	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0003593	OMIM:616739	TAS				C		HPO:skoehler	
OMIM	616739	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 51		HP:0010864	OMIM:616739	TAS				P		HPO:skoehler	
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0000007	PMID:26642240	PCS				I		HPO:probinson	
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0000509	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	3/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0001287	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	2/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0001508	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	4/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0001875	PMID:26642240	PCS				P		HPO:probinson	
OMIM	616740	IMMUNODEFICIENCY 46; IMD46	HP:0012825	HP:0001903	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0002028	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	10/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0002721	OMIM:616740	IEA				P		HPO:skoehler	
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0004313	PMID:26642240	PCS				P		HPO:probinson	
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0004854	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0005425	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	11/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0009098	PMID:26642240	IEA		HP:0040284		P		HPO:probinson	1/14
OMIM	616740	IMMUNODEFICIENCY 46; IMD46		HP:0100806	PMID:26642240	PCS		HP:0040284		P		HPO:probinson	5/14
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0000006	PMID:26642243	PCS				I		HPO:probinson	
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0000155	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	11/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0000988	OMIM:616744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0001873	OMIM:616744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0001878	OMIM:616744	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0001888	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	2/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0001954	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	2/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0002583	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	2/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0003249	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	10/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0003493	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	3/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0005764	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	5/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0012122	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	3/11
OMIM	616744	AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE		HP:0025343	PMID:26642243	PCS		HP:0040284		P		HPO:probinson	3/11
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0000007	PMID:26437028	PCS				I		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001631	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001646	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	1/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001669	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	4/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001696	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001702	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	1/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0001748	OMIM:616749	TAS				P		HPO:skoehler	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0002566	OMIM:616749	TAS				P		HPO:skoehler	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0004762	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0004935	OMIM:616749	TAS				P		HPO:skoehler	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0004971	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	2/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0005160	OMIM:616749	TAS				P		HPO:skoehler	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0006695	OMIM:616749	TAS				P		HPO:skoehler	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0011560	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	1/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0011565	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0011611	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0011671	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0012020	PMID:26437028	PCS		HP:0040284		P		HPO:probinson	1/14
OMIM	616749	HETEROTAXY, VISCERAL, 7, AUTOSOMAL		HP:0030853	PMID:26437028	PCS				P		HPO:probinson	
OMIM	616754	BOMBAY PHENOTYPE		HP:0000007	OMIM:616754	TAS				I		HPO:skoehler	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000007	PMID:26424145	IEA				I		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000252	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000407	PMID:26424145	PCS		HP:0040284		P		HPO:probinson	3/8
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000486	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000545	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0000556	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001249	OMIM:616756	TAS				P		HPO:skoehler	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001250	PMID:26424145	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001251	OMIM:616756	TAS				P		HPO:skoehler	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001252	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001263	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001290	OMIM:616756	TAS				P		HPO:skoehler	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001332	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001513	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0001762	PMID:26424145	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002059	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002061	PMID:26424145	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002079	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002123	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002136	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002376	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002515	PMID:26424145	PCS		HP:0040284		P		HPO:probinson	3/8
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002540	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002650	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002808	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002827	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0002938	PMID:26424145	PCS				P		HPO:probinson	
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0004322	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616756	SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES		HP:0012448	OMIM:616756	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0000007	PMID:26160856	PCS				I		HPO:probinson	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0000653	PMID:26160856	PCS				P		HPO:probinson	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0001006	PMID:26902920	PCS				P		HPO:probinson	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0002209	PMID:26160856	PCS				P		HPO:probinson	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0002212	PMID:26160856	PCS				P		HPO:probinson	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0002213	OMIM:616760	TAS				P		HPO:skoehler	
OMIM	616760	WOOLLY HAIR, AUTOSOMAL RECESSIVE 3		HP:0009886	PMID:26902920	PCS				P		HPO:probinson	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0000007	PMID:26573021	PCS				I		HPO:probinson	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0000252	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0000639	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	2/5
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0001250	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	1/4
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0001263	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0001290	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0001332	PMID:26573021	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0002415	OMIM:616763	TAS				P		HPO:skoehler	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0003593	OMIM:616763	TAS				C		HPO:skoehler	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0005484	OMIM:616763	TAS				P		HPO:skoehler	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0007204	PMID:26573021	PCS				P		HPO:probinson	
OMIM	616763	LEUKODYSTROPHY AND ACQUIRED MICROCEPHALY WITH OR WITHOUT DYSTONIA		HP:0010864	OMIM:616763	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0000007	PMID:26595769	PCS				I		HPO:probinson	
OMIM	616777	SECKEL SYNDROME 9		HP:0000010	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0000062	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0000252	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0000275	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0000276	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0000347	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0000411	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0000444	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0000776	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0000998	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001263	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0001511	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0001518	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001558	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001561	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001629	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001631	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0001762	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0002099	OMIM:616777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616777	SECKEL SYNDROME 9		HP:0002119	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616777	SECKEL SYNDROME 9		HP:0002205	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616777	SECKEL SYNDROME 9		HP:0004322	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616777	SECKEL SYNDROME 9		HP:0004971	OMIM:616777	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616777	SECKEL SYNDROME 9		HP:0008665	OMIM:616777	TAS				P		HPO:skoehler	
OMIM	616777	SECKEL SYNDROME 9		HP:0009879	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616777	SECKEL SYNDROME 9		HP:0030799	PMID:26595769	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0000006	PMID:26063658	PCS				I		HPO:probinson	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0000726	OMIM:616779	IEA				P		HPO:skoehler	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0001250	OMIM:616779	IEA				P		HPO:skoehler	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0001268	PMID:26063658	PCS				P		HPO:probinson	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0001288	OMIM:616779	IEA				P		HPO:skoehler	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0002315	OMIM:616779	IEA				P		HPO:skoehler	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0002326	OMIM:616779	IEA				P		HPO:skoehler	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0007236	PMID:26063658	PCS				P		HPO:probinson	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0012520	PMID:26063658	PCS				P		HPO:probinson	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0025012	PMID:26063658	PCS				P		HPO:probinson	
OMIM	616779	CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 2; CADASIL2		HP:0030890	PMID:26063658	PCS				P		HPO:probinson	
OMIM	616780	OOCYTE MATURATION DEFECT 2; OOMD2		HP:0000006	OMIM:616780	TAS				I		HPO:skoehler	
OMIM	616780	OOCYTE MATURATION DEFECT 2; OOMD2		HP:0000007	OMIM:616780	TAS				I		HPO:skoehler	
OMIM	616780	OOCYTE MATURATION DEFECT 2; OOMD2		HP:0008222	PMID:27273344	PCS				P		HPO:probinson	
OMIM	616780	OOCYTE MATURATION DEFECT 2; OOMD2		HP:0031516	PMID:26789871	PCS				P		HPO:lccarmody	
OMIM	616780	OOCYTE MATURATION DEFECT 2; OOMD2		HP:0031516	OMIM:616780	IEA				P		HPO:skoehler	
OMIM	616781	JOUBERT SYNDROME 25		HP:0000007	PMID:26477546	PCS				I		HPO:probinson	
OMIM	616781	JOUBERT SYNDROME 25		HP:0000512	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0000657	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0001251	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0001263	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0001290	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0001321	OMIM:616781	TAS				P		HPO:skoehler	
OMIM	616781	JOUBERT SYNDROME 25		HP:0002419	PMID:26477546	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616781	JOUBERT SYNDROME 25		HP:0003593	OMIM:616781	TAS				C		HPO:skoehler	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000007	PMID:26714646	PCS				I		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000054	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000175	OMIM:616784	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616784	JOUBERT SYNDROME 26		HP:0000316	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000463	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000508	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000639	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000824	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0000871	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0001263	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0001290	OMIM:616784	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616784	JOUBERT SYNDROME 26		HP:0001321	OMIM:616784	TAS				P		HPO:skoehler	
OMIM	616784	JOUBERT SYNDROME 26		HP:0002007	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0002788	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0003577	OMIM:616784	TAS				C		HPO:skoehler	
OMIM	616784	JOUBERT SYNDROME 26		HP:0004322	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0007068	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0011787	PMID:26714646	PCS				P		HPO:probinson	
OMIM	616784	JOUBERT SYNDROME 26		HP:0410030	OMIM:616784	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616788	OROFACIAL CLEFT 15		HP:0000006	PMID:25954033	PCS				I		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000028	OMIM:616788	TAS				P		HPO:skoehler	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000286	OMIM:616788	TAS				P		HPO:skoehler	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000316	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000369	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000411	OMIM:616788	TAS				P		HPO:skoehler	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000414	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000582	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000653	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0000954	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0007651	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0009890	OMIM:616788	TAS				P		HPO:skoehler	
OMIM	616788	OROFACIAL CLEFT 15		HP:0010294	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0011800	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0012905	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0045075	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0100271	OMIM:616788	TAS				P		HPO:skoehler	
OMIM	616788	OROFACIAL CLEFT 15		HP:0100336	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0100337	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616788	OROFACIAL CLEFT 15		HP:0200153	PMID:25954033	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000006	PMID:25758992	PCS				I		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000028	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000154	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000158	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000194	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000232	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000248	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000311	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000316	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000325	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000341	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000369	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000400	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000414	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000470	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000486	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000582	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000589	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0000717	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001251	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001260	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001263	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001270	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001290	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001357	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001655	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001669	OMIM:616789	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0001762	OMIM:616789	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0002007	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0002342	PMID:25167861	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0002465	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0002719	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0003593	OMIM:616789	TAS				C		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0005280	OMIM:616789	TAS				P		HPO:skoehler	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0011220	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616789	MENTAL RETARDATION AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS		HP:0030084	PMID:25758992	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0000007	PMID:26522469	PCS				I		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001263	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001290	OMIM:616794	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001324	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001558	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001561	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0001635	OMIM:616794	TAS				P		HPO:skoehler	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0002027	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0002151	OMIM:616794	TAS				P		HPO:skoehler	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0002878	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0003200	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0003542	OMIM:616794	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0003593	PMID:26522469	PCS				C		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0003828	OMIM:616794	TAS				C		HPO:skoehler	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0004396	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0004900	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0008347	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0011923	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616794	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 28		HP:0012378	PMID:26522469	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000006	PMID:26456284	PCS				I		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000012	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	4/14
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000020	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	2/14
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000651	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000666	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000716	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0000716	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	3/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0001152	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	6/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0001260	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	12/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0001272	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0001337	OMIM:616795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0001347	OMIM:616795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0002015	PMID:26456284	IEA		HP:0040284		P		HPO:probinson	4/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0002064	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	4/13
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0002317	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0002317	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	9/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0002497	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0003487	OMIM:616795	PCS		HP:0040284		P		HPO:probinson	4/15
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0003677	OMIM:616795	TAS				C		HPO:skoehler	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0006938	PMID:26456284	PCS		HP:0040284		P		HPO:probinson	6/13
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0007001	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0031166	OMIM:616795	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616795	SPINOCEREBELLAR ATAXIA 42		HP:0100543	PMID:26456284	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000007	PMID:26708753	PCS				I		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000194	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000219	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000248	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000252	PMID:26708753	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000286	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000297	PMID:26708751	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000319	PMID:26545877	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000322	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000325	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000337	PMID:26545877	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000348	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000358	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000369	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000414	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000426	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000448	PMID:26545877	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000463	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000470	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000494	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000508	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000565	PMID:26708751	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000639	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0000938	PMID:26708753	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001182	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001250	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001257	PMID:26708753	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001290	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001344	PMID:26708751	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001357	PMID:26545877	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001511	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0001531	PMID:26708753	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002007	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002019	PMID:26708751	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002059	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002079	PMID:26708751	PCS		HP:0040284		P		HPO:probinson	1/4
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002187	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002283	PMID:26708753	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002465	OMIM:616801	IEA				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002540	OMIM:616801	IEA				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0002650	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0003273	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0004326	PMID:26708753	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0007069	PMID:26708753	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0011220	PMID:26545877	PCS				P		HPO:probinson	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0011968	OMIM:616801	TAS				P		HPO:skoehler	
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0012389	PMID:26708753	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0012736	PMID:26708753	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616801	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2; IHPRF2		HP:0100660	OMIM:616801	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000006	PMID:26111154	PCS				I		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000194	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000286	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000324	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000358	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000369	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000414	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000431	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000486	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000494	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000545	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000648	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000678	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000739	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000750	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0000768	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001249	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001263	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001290	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001763	OMIM:616803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001845	OMIM:616803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0001847	OMIM:616803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0002007	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0002650	PMID:26111154	PCS				P		HPO:probinson	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0005280	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0008428	OMIM:616803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0030084	OMIM:616803	TAS				P		HPO:skoehler	
OMIM	616803	LAMB-SHAFFER SYNDROME		HP:0100807	OMIM:616803	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616806	WILMS TUMOR 6		HP:0002667	PMID:26551668	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000007	PMID:26293662	PCS				I		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000023	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000154	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000218	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000252	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000341	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000391	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000414	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000463	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000470	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000486	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000490	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000519	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000637	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000718	OMIM:616809	TAS				P		HPO:nvasilevsky	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000736	OMIM:616809	TAS				P		HPO:nvasilevsky	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000750	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000752	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0000938	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001250	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001263	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001371	PMID:26293662	TAS				P		HPO:nvasilevsky	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001385	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001510	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0001561	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0002013	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0002027	PMID:26293662	TAS				P		HPO:nvasilevsky	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0002376	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0002617	OMIM:616809	IEA				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0002987	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0003155	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0003236	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0003273	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0003577	PMID:26293662	PCS				C		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0004691	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0004742	PMID:26293662	TAS				P		HPO:nvasilevsky	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0005274	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0005280	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0006118	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0006380	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0008936	OMIM:616809,PMID:26293662	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0009748	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0009826	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0010844	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0010943	PMID:26293662	PCS				P		HPO:probinson	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0011968	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0030084	OMIM:616809	TAS				P		HPO:skoehler	
OMIM	616809	HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 6		HP:0100704	OMIM:616809	IEA				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0000007	PMID:26626369	PCS				I		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0000252	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0000488	OMIM:616811	TAS				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0000648	OMIM:616811	TAS				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001138	PMID:26626369	PCS	HP:0003621			P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001250	PMID:26626369	PCS	HP:0011463			P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001257	OMIM:616811	TAS				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001263	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001272	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001290	OMIM:616811	TAS				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0001332	OMIM:616811	TAS				P		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002151	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002188	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002283	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002416	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002490	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0002922	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0003577	OMIM:616811	TAS				C		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0003593	PMID:26626369	PCS				C		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0003676	OMIM:616811	TAS				C		HPO:skoehler	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0009830	PMID:26626369	PCS	HP:0003621			P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0011923	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0011924	PMID:26626369	PCS				P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0011968	PMID:26626369	PCS	HP:0011463			P		HPO:probinson	
OMIM	616811	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29		HP:0040078	PMID:26626369	PCS	HP:0003621			P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0000007	PMID:26642364	PCS				I		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0001279	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0001678	OMIM:616812	IEA				P		HPO:skoehler	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0001688	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003236	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003325	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003560	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003687	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003690	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0003701	OMIM:616812	IEA				P		HPO:skoehler	
OMIM	616812	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2X; LGMD2X		HP:0006957	PMID:26642364	PCS				P		HPO:probinson	
OMIM	616814	PREIMPLANTATION EMBRYONIC LETHALITY 1		HP:0000007	OMIM:616814	TAS				I		HPO:skoehler	
OMIM	616814	PREIMPLANTATION EMBRYONIC LETHALITY 1		HP:0008222	PMID:26537248	TAS				P		HPO:lccarmody	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000007	PMID:26358778	PCS				I		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000028	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000194	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000276	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000486	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0000750	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0001263	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0001319	OMIM:616816	TAS				P		HPO:skoehler	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0001558	OMIM:616816	TAS				P		HPO:skoehler	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0001629	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0002058	OMIM:616816	TAS				P		HPO:skoehler	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0002079	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0002747	OMIM:616816	TAS				P		HPO:skoehler	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0003198	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0003557	OMIM:616816	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0006829	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0006897	OMIM:616816	IEA				P		HPO:skoehler	
OMIM	616816	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR		HP:0006956	PMID:26358778	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000007	PMID:26159176	PCS				I		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000028	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000089	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000160	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000252	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000286	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000293	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000347	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000365	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000400	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000407	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000494	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000592	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000601	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000677	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000767	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000821	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0000823	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001015	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001250	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001257	PMID:26307080	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001260	PMID:26307080	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001348	PMID:26307080	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001511	OMIM:616817	TAS				P		HPO:skoehler	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001518	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001620	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0001988	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002066	PMID:26307080	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002078	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002079	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002213	OMIM:616817	TAS				P		HPO:skoehler	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002365	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002714	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002750	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0002751	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0003307	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0003468	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0004322	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0004570	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0008070	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0010864	PMID:26159176	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0012448	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0030186	PMID:26307080	PCS				P		HPO:probinson	
OMIM	616817	MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2		HP:0200021	OMIM:616817	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0000006	PMID:25782674	PCS				I		HPO:probinson	
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0000093	PMID:25782674	PCS		HP:0040284		P		HPO:probinson	1/8
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0000790	PMID:25782674	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0000794	PMID:25782674	PCS				P		HPO:probinson	
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0000822	PMID:25782674	PCS		HP:0040284		P		HPO:probinson	3/10
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0003676	OMIM:616818	TAS				C		HPO:skoehler	
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0003774	PMID:25782674	PCS		HP:0040284		P		HPO:probinson	2/11
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0011462	PMID:25782674	PCS				C		HPO:probinson	
OMIM	616818	IGA NEPHROPATHY, SUSCEPTIBILITY TO, 3		HP:0012574	PMID:25782674	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000007	PMID:25388005	PCS				I		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000232	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000294	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000341	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000358	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000369	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000411	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000463	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000486	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000527	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0000574	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001007	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001249	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001251	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001263	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001320	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001321	OMIM:616819	TAS				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001338	OMIM:616819	IEA				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0001344	OMIM:616819	IEA				P		HPO:skoehler	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0007370	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0008070	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0011451	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616819	CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND CEREBELLAR ATAXIA; CCAFCA		HP:0012724	PMID:25388005	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0000007	PMID:25589244	PCS				I		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0001324	OMIM:616827	IEA				P		HPO:skoehler	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0001644	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0001762	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0002273	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0003202	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0003236	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0003560	OMIM:616827	TAS				P		HPO:skoehler	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0003676	OMIM:616827	TAS				C		HPO:skoehler	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0006673	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0008981	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0009025	OMIM:616827	TAS				P		HPO:skoehler	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0011463	PMID:25589244	PCS				C		HPO:probinson	
OMIM	616827	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2W; LGMD2W		HP:0030284	PMID:25589244	PCS				P		HPO:probinson	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0000007	PMID:26833332	PCS				I		HPO:probinson	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0000276	OMIM:616828	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0000494	OMIM:616828	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0000508	OMIM:616828	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001250	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	1/4
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001263	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001290	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001394	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001399	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	2/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001433	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0001744	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0002240	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO	HP:0003676	HP:0002611	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0002910	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0003124	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0003141	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0003202	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0003236	OMIM:616828	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0003593	OMIM:616828	TAS				C		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0006579	OMIM:616828	TAS				P		HPO:skoehler	
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0010639	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0010837	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0012345	PMID:26833332	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616828	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIO		HP:0025321	PMID:26833332	PCS				P		HPO:probinson	
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0000007	PMID:26833330	PCS				I		HPO:probinson	
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0001263	OMIM:616829	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0001290	OMIM:616829	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0001397	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0001410	OMIM:616829	TAS				P		HPO:skoehler	
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0002910	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0003124	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0003141	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0003155	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0010837	PMID:26833330	PCS				P		HPO:probinson	
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0012347	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616829	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIP		HP:0012358	PMID:26833330	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000006	PMID:24852293	PCS				I		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000147	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000272	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000276	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000303	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000307	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000348	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000403	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000494	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000718	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000729	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000739	OMIM:616831	IEA				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000750	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0000858	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001007	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001249	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001250	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001263	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001290	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001350	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001513	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001548	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0001833	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0002119	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0002308	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0002591	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0003189	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0003396	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0004233	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0004322	OMIM:616831	TAS				P		HPO:skoehler	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0009890	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0011220	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616831	LUSCAN-LUMISH SYNDROME; LLS		HP:0100962	PMID:24852293	PCS				P		HPO:probinson	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0000006	PMID:26849110	PCS				I		HPO:probinson	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0000121	OMIM:616833	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0001677	OMIM:616833	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0001712	OMIM:616833	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0002653	OMIM:616833	TAS				P		HPO:skoehler	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0002757	PMID:26849110	PCS				P		HPO:probinson	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0002758	PMID:26849110	PCS				P		HPO:probinson	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0003155	OMIM:616833	TAS				P		HPO:skoehler	
OMIM	616833	PAGET DISEASE OF BONE 6		HP:0003581	OMIM:616833	TAS				C		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0000007	PMID:21285510	PCS				I		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0000252	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0000498	OMIM:616834	TAS				P		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0000519	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0000823	OMIM:616834	TAS				P		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0001256	OMIM:616834	TAS				P		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0001263	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0001508	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0002750	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0002829	OMIM:616834	TAS				P		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0003146	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0003563	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0003765	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0004322	OMIM:616834	TAS				P		HPO:skoehler	
OMIM	616834	MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS		HP:0008064	PMID:21285510	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000006	OMIM:616835	IEA				I		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000028	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000059	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000175	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000308	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000348	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000358	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000402	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000405	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000430	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000457	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000463	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000486	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000494	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000621	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000750	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000823	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0000824	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001249	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001270	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001385	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001508	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001518	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001537	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001601	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0001852	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002007	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002020	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002097	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002205	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002750	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0002786	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0003196	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0003510	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0005280	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0005819	PMID:26637980	PCS				P		HPO:probinson	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0006443	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0008551	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0009879	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0011800	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0011968	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0012448	OMIM:616835	IEA				P		HPO:skoehler	
OMIM	616835	MEIER-GORLIN SYNDROME 6; MGORS6		HP:0012471	PMID:26637980	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616839	EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE		HP:0000007	PMID:26933868	PCS				I		HPO:probinson	
OMIM	616839	EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE		HP:0003200	PMID:26933868	PCS				P		HPO:probinson	
OMIM	616839	EXERCISE INTOLERANCE, RIBOFLAVIN-RESPONSIVE		HP:0003546	PMID:26933868	PCS				P		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000007	PMID:26942284	PCS				I		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0000726	OMIM:616840	TAS				P		HPO:skoehler	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001257	OMIM:616840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001268	PMID:26942284	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001300	PMID:26942284	PCS				P		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0001347	OMIM:616840	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002063	PMID:26942284	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002120	OMIM:616840	TAS				P		HPO:skoehler	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002185	PMID:26942284	PCS				P		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002304	OMIM:616840	TAS				P		HPO:skoehler	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002322	PMID:26942284	PCS				P		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0002451	PMID:26942284	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0003676	OMIM:616840	TAS				C		HPO:skoehler	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0007256	PMID:26942284	PCS				P		HPO:probinson	
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0012332	PMID:26942284	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616840	PARKINSON DISEASE 23, AUTOSOMAL RECESSIVE EARLY-ONSET		HP:0100315	PMID:26942284	PCS				P		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000007	PMID:26333996	PCS				I		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000034	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000282	PMID:26333996	PCS				P		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000286	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	3/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000347	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000365	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000378	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000465	PMID:26333996	PCS				P		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000767	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0000821	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001004	PMID:26333996	PCS				P		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001263	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001541	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001561	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001631	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001744	PMID:26333996	PCS				P		HPO:probinson	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001744	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0001790	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0002020	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0002593	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0002619	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0002625	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0002650	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0004322	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0004392	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	1/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0007430	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0010310	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	2/10
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0031188	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0100539	OMIM:616843	TAS				P		HPO:skoehler	
OMIM	616843	LYMPHEDEMA, HEREDITARY, III		HP:0100658	PMID:26333996	PCS		HP:0040284		P		HPO:probinson	4/10
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0000006	PMID:25758993	PCS				I		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0000750	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0002275	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0004209	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0004220	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0009566	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0009568	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0009638	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0009650	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616849	BRACHYDACTYLY, TYPE A1, D		HP:0010241	PMID:25758993	PCS				P		HPO:probinson	
OMIM	616851	CATARACT 45		HP:0000007	PMID:25804400	PCS				I		HPO:probinson	
OMIM	616851	CATARACT 45		HP:0000519	PMID:25804400	PCS	HP:0003577			P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0000006	PMID:25938801	PCS				I		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0001265	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0001284	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0001315	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0001771	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0002650	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003307	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003323	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003557	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003677	OMIM:616852	TAS				C		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003687	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003691	PMID:25938801	PCS		HP:0040284		P		HPO:probinson	9/11
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003722	PMID:25938801	PCS		HP:0040284		P		HPO:probinson	12/12
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0003828	OMIM:616852	TAS				C		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0009025	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0009027	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0009130	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0010628	PMID:25938801	PCS				P		HPO:probinson	
OMIM	616852	MYOPATHY, SCAPULOHUMEROPERONEAL		HP:0031189	OMIM:616852	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000007	PMID:26598328	PCS				I		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000010	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000076	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000089	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000218	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000248	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000456	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000457	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000470	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000664	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0000668	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001047	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001057	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001263	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001274	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001562	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001631	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0001655	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0002023	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0002553	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0002656	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0003196	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0003417	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0003510	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0006989	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0008070	OMIM:616854	TAS				P		HPO:skoehler	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0008551	PMID:26598328	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616854	EVEN-PLUS SYNDROME		HP:0010575	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616854	EVEN-PLUS SYNDROME		HP:0011800	PMID:26598328	PCS				P		HPO:probinson	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0000006	PMID:26522472	PCS				I		HPO:probinson	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0000256	PMID:26522472	PCS				P		HPO:probinson	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0000853	OMIM:616858	IEA				P		HPO:skoehler	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0000872	OMIM:616858	TAS				P		HPO:skoehler	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0001028	PMID:26522472	PCS				P		HPO:probinson	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0002895	PMID:26522472	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0003002	OMIM:616858	TAS				P		HPO:skoehler	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0012740	OMIM:616858	IEA				P		HPO:skoehler	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0012844	PMID:26522472	PCS				P		HPO:probinson	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0030075	OMIM:616858	TAS				P		HPO:skoehler	
OMIM	616858	COWDEN SYNDROME 7; CWS7		HP:0200008	OMIM:616858	TAS				P		HPO:skoehler	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0000007	PMID:24334290	PCS				I		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0000486	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0000505	OMIM:616859	TAS				P		HPO:skoehler	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0000639	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0000648	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0001250	PMID:24334290	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0001260	PMID:24334290	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0001264	PMID:24334290	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0001288	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0001347	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0002079	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0002154	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0002415	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0002497	PMID:24334290	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0002928	PMID:24334290	PCS				P		HPO:probinson	
OMIM	616859	SPASTICITY, CHILDHOOD-ONSET, WITH HYPERGLYCINEMIA		HP:0003487	PMID:21471552	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0000007	PMID:25342667	PCS				I		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0000952	OMIM:616860	TAS				P		HPO:skoehler	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0001394	OMIM:616860	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0001433	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0001744	OMIM:616860	TAS				P		HPO:skoehler	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0001903	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0002240	OMIM:616860	TAS				P		HPO:skoehler	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0002908	PMID:17485548	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0002910	PMID:17485548	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0003281	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0005978	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0011273	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0012132	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0012465	PMID:25342667	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0025066	PMID:17485548	PCS				P		HPO:probinson	
OMIM	616860	ANEMIA, SIDEROBLASTIC, 3, PYRIDOXINE-REFRACTORY; SIDBA3		HP:0032231	OMIM:616860	IEA				P		HPO:skoehler	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000006	PMID:26365382	PCS				I	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000028	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	3/4
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000054	OMIM:616863	TAS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:skoehler	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000239	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000243	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000270	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000369	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000486	PMID:26365382	PCS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000718	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	5/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000729	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	5/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0000750	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	6/6
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001249	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	7/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001250	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	5/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001252	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	4/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001263	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	7/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001290	OMIM:616863	TAS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:skoehler	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001344	OMIM:616863	IEA				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:skoehler	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001822	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0001999	OMIM:616863	TAS		HP:0040283		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:skoehler	HP:0040283
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0002186	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	3/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0004209	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/7
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0010536	PMID:26365382	PCS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0011098	OMIM:616863	TAS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:skoehler	
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0012412	PMID:26365382	PCS		HP:0040284		P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	1/2
OMIM	616863	CHROMOSOME 16p13.2 DELETION SYNDROME		HP:0030223	PMID:26365382	PCS				P	CHROMOSOME 16P13.2 DELETION SYNDROME	HPO:probinson	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000007	PMID:26924529	PCS				I		HPO:probinson	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000160	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000218	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000308	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000316	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0000966	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001263	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001284	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001290	OMIM:616866	TAS				P		HPO:skoehler	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001324	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001558	PMID:26924529	PCS	HP:0011461	HP:0040284		P		HPO:probinson	4/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001562	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001622	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001635	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	1/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001638	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001643	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001655	PMID:26924529	PCS	HP:0003577	HP:0040284		P		HPO:probinson	1/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0001684	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0002015	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0002089	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0002643	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0002804	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0003447	OMIM:616866	IEA				P		HPO:skoehler	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0003477	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0003557	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0003577	OMIM:616866	TAS				C		HPO:skoehler	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0003700	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0005855	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0006829	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0007269	OMIM:616866	TAS				P		HPO:skoehler	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0009110	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616866	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 1; SMABF1		HP:0100295	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0000007	PMID:26924529	PCS				I		HPO:probinson	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001263	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001284	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001290	OMIM:616867	TAS				P		HPO:skoehler	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001324	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001558	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001561	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001622	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001643	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0001655	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002015	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002089	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002536	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002643	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002804	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0002878	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0003447	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0003477	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0003557	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0003577	OMIM:616867	TAS				C		HPO:skoehler	
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0005855	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0006829	PMID:26924529	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	616867	SPINAL MUSCULAR ATROPHY WITH CONGENITAL BONE FRACTURES 2		HP:0007269	PMID:26924529	PCS				P		HPO:probinson	
OMIM	616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL		HP:0000007	PMID:26358773	PCS				I		HPO:probinson	
OMIM	616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL		HP:0001561	PMID:26358773	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL		HP:0002037	OMIM:616868	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL		HP:0003270	PMID:26358773	PCS				P		HPO:probinson	
OMIM	616868	DIARRHEA 8, SECRETORY SODIUM, CONGENITAL		HP:0005208	PMID:26358773	PCS	HP:0003577			P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0000006	PMID:26712909	PCS				I		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0000964	OMIM:616871	TAS				P		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0001882	PMID:26712909	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0002099	OMIM:616871	TAS				P		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0002665	OMIM:616871	TAS				P		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0002725	OMIM:616871	TAS				P		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0002863	PMID:25920683	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0003581	OMIM:616871	TAS				C		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0003829	OMIM:616871	TAS				C		HPO:skoehler	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0004808	PMID:25920683	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0005505	PMID:25920683	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0005528	PMID:26712909	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0012311	PMID:25920683	PCS				P		HPO:probinson	
OMIM	616871	MYELOPROLIFERATIVE/LYMPHOPROLIFERATIVE NEOPLASMS, FAMILIAL (MULTIPLE TYPES), SUSCEPTIBILITY TO; MPLPF		HP:0031688	OMIM:616871	IEA				P		HPO:skoehler	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0000006	PMID:26981933	PCS				I		HPO:probinson	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0001876	OMIM:616873	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0002718	PMID:26981933	PCS				P		HPO:probinson	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0002721	OMIM:616873	IEA				P		HPO:skoehler	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0003829	OMIM:616873	TAS				C		HPO:skoehler	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0004313	PMID:26981933	PCS				P		HPO:probinson	
OMIM	616873	IMMUNODEFICIENCY, COMMON VARIABLE, 13; CVID13		HP:0010976	PMID:26981933	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000007	PMID:26942288	PCS				I		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000188	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000212	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000278	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000294	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000316	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000322	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	3/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000347	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000483	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000490	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000512	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000540	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000545	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000565	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000648	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000649	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0000750	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001212	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	3/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001249	OMIM:616875	TAS				P		HPO:skoehler	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001250	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	1/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001263	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001265	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	5/6
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001272	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001290	OMIM:616875	TAS				P		HPO:skoehler	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0001332	OMIM:616875	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0002023	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0002059	OMIM:616875	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0002079	OMIM:616875	TAS				P		HPO:skoehler	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0002509	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0002650	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0003676	OMIM:616875	TAS				C		HPO:skoehler	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0005484	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	3/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0007371	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	6/6
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0008755	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0008936	PMID:26942288	PCS		HP:0040284		P		HPO:probinson	6/7
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0025356	OMIM:616875	IEA				P		HPO:skoehler	
OMIM	616875	CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR		HP:0100704	PMID:26942288	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0000007	PMID:26805781	PCS				I		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0000252	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0000407	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0000648	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0000821	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001249	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001250	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	9/12
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001251	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001260	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001263	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	12/12
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001264	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001288	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001290	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001324	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001332	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001344	OMIM:616878	IEA				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001639	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001663	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001664	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	2/12
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001695	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001942	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001943	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	9/12
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0001987	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	9/11
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002058	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002059	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002066	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002151	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	9/11
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002169	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN	HP:0003676	HP:0002180	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002307	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002370	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002510	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002910	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002913	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0002919	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0003128	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0003236	PMID:26805782	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0004756	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	2/12
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0005184	PMID:26805781	PCS		HP:0040284		P		HPO:probinson	6/11
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0006801	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0008942	PMID:26805781	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0010314	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0012411	OMIM:616878	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0045045	PMID:26805782	PCS				P		HPO:probinson	
OMIM	616878	METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN		HP:0200136	OMIM:616878	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0000007	OMIM:616881	TAS				I		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0000505	OMIM:616881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0000639	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0000648	OMIM:616881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001251	OMIM:616881	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001257	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001263	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001290	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001344	OMIM:616881	IEA				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001371	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0001508	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0002169	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0002415	OMIM:616881	IEA				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0002518	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0003593	OMIM:616881	TAS				C		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0011968	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616881	LEUKODYSTROPHY, HYPOMYELINATING, 13; HLD13		HP:0012448	OMIM:616881	TAS				P		HPO:skoehler	
OMIM	616882	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3; FASPS3		HP:0000006	OMIM:616882	TAS				I		HPO:skoehler	
OMIM	616882	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3; FASPS3		HP:0000716	OMIM:616882	TAS				P		HPO:skoehler	
OMIM	616882	ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 3; FASPS3		HP:0031873	OMIM:616882	IEA				P		HPO:skoehler	
OMIM	616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52		HP:0000007	PMID:26566883	PCS				I		HPO:probinson	
OMIM	616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52		HP:0001250	PMID:26566883	PCS				P		HPO:probinson	
OMIM	616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52		HP:0001263	OMIM:616887	TAS				P		HPO:skoehler	
OMIM	616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52		HP:0003593	OMIM:616887	TAS				C		HPO:skoehler	
OMIM	616887	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 52		HP:0010864	PMID:26566883	PCS				P		HPO:probinson	
OMIM	616890	SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY; SFMMP		HP:0000007	OMIM:616890	TAS				I		HPO:skoehler	
OMIM	616890	SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY; SFMMP		HP:0000407	OMIM:616890	TAS				P		HPO:skoehler	
OMIM	616890	SPLIT-FOOT MALFORMATION WITH MESOAXIAL POLYDACTYLY; SFMMP		HP:0012725	OMIM:616890	IEA				P		HPO:skoehler	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0000007	PMID:26878725	PCS				I		HPO:probinson	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0000097	OMIM:616892	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0000790	OMIM:616892	TAS				P		HPO:skoehler	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0001967	OMIM:616892	TAS				P		HPO:skoehler	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0003676	OMIM:616892	TAS				C		HPO:skoehler	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0003774	OMIM:616892	TAS				P		HPO:skoehler	
OMIM	616892	NEPHROTIC SYNDROME, TYPE 12		HP:0012588	OMIM:616892	PCS	HP:0011463	HP:0040284		P		HPO:probinson	7/7
OMIM	616893	NEPHROTIC SYNDROME, TYPE 13		HP:0000007	PMID:26878725	PCS				I		HPO:probinson	
OMIM	616893	NEPHROTIC SYNDROME, TYPE 13		HP:0000097	PMID:26878725	PCS				P		HPO:probinson	
OMIM	616893	NEPHROTIC SYNDROME, TYPE 13		HP:0003774	PMID:26878725	PCS				P		HPO:probinson	
OMIM	616893	NEPHROTIC SYNDROME, TYPE 13		HP:0012588	PMID:26878725	PCS				P		HPO:probinson	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000006	OMIM:616894	TAS				I		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000028	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000175	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000212	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000256	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000286	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000316	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000343	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000347	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000365	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000369	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000431	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000463	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000465	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000470	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000506	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000520	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000527	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000582	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000592	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0000689	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0001156	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0001545	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0001629	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0001643	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0001655	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0002007	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0002650	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0002714	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0002808	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0003027	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0003196	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0004322	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0004935	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0005180	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0005280	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0006349	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0009803	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0010954	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0011304	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0011800	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0030084	OMIM:616894	TAS				P		HPO:skoehler	
OMIM	616894	ROBINOW SYNDROME, AUTOSOMAL DOMINANT 3		HP:0410030	OMIM:616894	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0000007	PMID:26561570	PCS				I		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0000407	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0000546	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0001612	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0001623	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0001639	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0002104	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0002179	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0003202	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0008872	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0008936	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0011410	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616896	MITOCHONDRIAL DNA DEPLETION SYNDROME 14		HP:0012736	PMID:26561570	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000007	PMID:26365339	PCS				I		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000047	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000054	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000126	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000175	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000248	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000252	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000316	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000347	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000358	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000369	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000431	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000463	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000465	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000470	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000506	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000773	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000923	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000926	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0000938	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001181	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001195	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001321	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001371	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001511	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001518	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001541	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001561	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001629	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001639	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001640	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0001789	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0002089	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0002119	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0002202	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0002265	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0002645	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0003015	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0003097	OMIM:616897	TAS				P		HPO:skoehler	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0003196	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0003978	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0004331	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0005257	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0005855	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0006640	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0009826	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0011220	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0012368	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0031107	OMIM:616897	TAS				P		HPO:probinson	
OMIM	616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE		HP:0100333	PMID:26365339	PCS				P		HPO:probinson	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000006	OMIM:616898	TAS				I		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000175	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000232	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000322	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000348	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000358	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0000369	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0001249	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0001263	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0001629	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0001631	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0002553	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0003577	OMIM:616898	TAS				C		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0010804	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616898	CHROMOSOME 15Q14 DELETION SYNDROME		HP:0410030	OMIM:616898	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000007	PMID:27040692	PCS				I		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000158	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	2/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000212	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000256	OMIM:616900	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000280	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000340	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000341	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000414	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000426	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000463	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0000490	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0001250	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0001265	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0001298	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0001320	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0001321	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002059	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002079	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002119	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002263	PMID:27040692	IEA		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002376	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002465	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002518	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0002553	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0003577	OMIM:616900	TAS				C		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0003828	OMIM:616900	TAS				C		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0006829	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0006989	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0010804	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0011471	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012444	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012471	OMIM:616900	TAS				P		HPO:skoehler	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012510	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012697	PMID:27040692	PCS				P		HPO:probinson	
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012708	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0012736	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	5/5
OMIM	616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3		HP:0100704	PMID:27040692	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000007	OMIM:616901	TAS				I		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000077	OMIM:616901	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000164	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000243	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000286	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000316	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000347	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000369	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000494	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0000653	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001249	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001263	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001305	OMIM:616901	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001363	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001629	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0001800	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0003577	OMIM:616901	TAS				C		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0004322	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0005280	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0011220	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0030799	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR		HP:0045075	OMIM:616901	TAS				P		HPO:skoehler	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0000006	PMID:26010655	PCS				I		HPO:probinson	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0000526	OMIM:616902	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0000717	PMID:26010655	PCS				P		HPO:probinson	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0000750	OMIM:616902	TAS				P		HPO:skoehler	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0001249	OMIM:616902	TAS				P		HPO:skoehler	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0001250	PMID:26010655	PCS				P		HPO:probinson	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0001263	PMID:26010655	PCS				P		HPO:probinson	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0002463	PMID:26010655	PCS				P		HPO:probinson	
OMIM	616902	CHROMOSOME 11P13 DELETION SYNDROME, DISTAL		HP:0003829	OMIM:616902	TAS				C		HPO:skoehler	
OMIM	616903	THIOPURINES, POOR METABOLISM OF, 2		HP:0000006	OMIM:616903	TAS				I		HPO:skoehler	
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0000007	PMID:27153400	PCS				I		HPO:probinson	
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:616907	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:616907	TAS				P		HPO:skoehler	
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0001260	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0001310	OMIM:616907	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0001761	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	5/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0002061	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	8/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0002066	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0002395	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0002650	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	1/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0002936	OMIM:616907	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0003202	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0003390	OMIM:616907	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0003487	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	6/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0007340	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	5/7
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0007350	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	7/8
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0008081	OMIM:616907	TAS				P		HPO:skoehler	
OMIM	616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE		HP:0009830	PMID:27153400	PCS		HP:0040284		P		HPO:probinson	2/8
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000007	PMID:26216346	PCS				I		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000028	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000047	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000252	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000286	OMIM:616910	IEA				P		HPO:skoehler	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000316	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000369	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000405	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0000486	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0001249	OMIM:616910	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0001263	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0001511	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0002719	OMIM:616910	IEA				P		HPO:skoehler	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0003175	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0003196	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0004313	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0004432	OMIM:616910	IEA				P		HPO:skoehler	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0010442	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3		HP:0012368	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0000007	PMID:26216346	IEA				I		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0000286	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0000316	OMIM:616911	PCS				P		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0001249	PMID:26216346	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0001263	OMIM:616911	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0001270	PMID:26216346	PCS		HP:0040284		P		HPO:probinson	2/3
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0002719	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0003577	OMIM:616911	TAS				C		HPO:skoehler	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0004313	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0004432	OMIM:616911	IEA				P		HPO:skoehler	
OMIM	616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4		HP:0005280	PMID:26216346	PCS				P		HPO:probinson	
OMIM	616913	BLEEDING DISORDER, PLATELET-TYPE, 20		HP:0000006	OMIM:616913	TAS				I		HPO:skoehler	
OMIM	616913	BLEEDING DISORDER, PLATELET-TYPE, 20		HP:0000132	OMIM:616913	TAS				P		HPO:skoehler	
OMIM	616913	BLEEDING DISORDER, PLATELET-TYPE, 20		HP:0000421	OMIM:616913	TAS				P		HPO:skoehler	
OMIM	616913	BLEEDING DISORDER, PLATELET-TYPE, 20		HP:0000978	OMIM:616913	TAS				P		HPO:skoehler	
OMIM	616913	BLEEDING DISORDER, PLATELET-TYPE, 20		HP:0001873	OMIM:616913	TAS				P		HPO:skoehler	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000006	PMID:20979188	PCS				I		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000098	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000238	OMIM:616914	IEA				P		HPO:skoehler	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000256	OMIM:616914	TAS				P		HPO:skoehler	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000278	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000426	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000460	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000494	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000520	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000767	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000822	OMIM:616914	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0000978	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001083	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001166	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001187	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001363	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001511	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001562	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001622	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001634	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0001763	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0002616	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0002705	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0003758	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0008081	OMIM:616914	TAS				P		HPO:skoehler	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0011003	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0011220	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0030799	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS		HP:0100775	PMID:26860060	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0000007	PMID:26996948	PCS				I		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0000750	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001250	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001251	OMIM:616917	TAS				P		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001263	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001265	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001290	PMID:26996948	PCS	HP:0003577			P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001321	OMIM:616917	TAS				P		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001344	OMIM:616917	IEA				P		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0001511	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0002059	OMIM:616917	TAS				P		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0002079	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0002187	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0003577	OMIM:616917	TAS				C		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0006829	OMIM:616917	TAS				P		HPO:skoehler	
OMIM	616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53		HP:0011193	PMID:26996948	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000007	PMID:27018474	PCS				I		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000179	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000232	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000252	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000260	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000269	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000316	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000341	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000358	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000369	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000377	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000431	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000463	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000505	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000568	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0000817	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001188	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001250	OMIM:616920	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001263	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001290	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001305	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001510	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001561	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0001629	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002020	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002059	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002079	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002188	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002283	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0002705	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0005280	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0005487	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0006801	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0007370	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0008936	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0011220	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0011611	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0100490	PMID:27018474	PCS				P		HPO:probinson	
OMIM	616920	HEART AND BRAIN MALFORMATION SYNDROME		HP:0410030	OMIM:616920	TAS				P		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0000007	PMID:27058446	PCS				I		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0001250	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0001260	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0001270	OMIM:616921	TAS				P		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0001337	OMIM:616921	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002072	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002307	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002310	OMIM:616921	TAS				P		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002317	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002359	OMIM:616921	TAS				P		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0002487	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0003593	OMIM:616921	TAS				C		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0008936	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0011968	OMIM:616921	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0100248	OMIM:616921	IEA				P		HPO:skoehler	
OMIM	616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD		HP:0100660	PMID:27058446	PCS				P		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0000006	PMID:27058447	PCS				I		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0001249	PMID:27058447	PCS				P		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0001268	PMID:27058447	PCS				P		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0001300	PMID:27058447	PCS				P		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0002072	PMID:27058447	PCS				P		HPO:probinson	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0003680	OMIM:616922	TAS				C		HPO:skoehler	
OMIM	616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2		HP:0010994	PMID:27058447	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0000006	PMID:27040688	PCS				I		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0001265	OMIM:616924	TAS				P		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0001761	OMIM:616924	TAS				P		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0002021	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0002359	OMIM:616924	TAS				P		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0002495	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0002515	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0002936	OMIM:616924	TAS				P		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003198	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003200	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003236	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003390	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003445	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003484	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003487	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003555	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003557	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003676	OMIM:616924	TAS				C		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003701	OMIM:616924	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003805	PMID:27040688	PCS				P		HPO:probinson	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0003828	OMIM:616924	TAS				C		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0007141	OMIM:616924	IEA				P		HPO:skoehler	
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0007210	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0007340	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	4/4
OMIM	616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC		HP:0009129	PMID:27040688	PCS		HP:0040284		P		HPO:probinson	3/4
OMIM	616937	THROMBOCYTOPENIA 6		HP:0000006	PMID:26936507	PCS				I		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0000490	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0000601	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0000939	OMIM:616937	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616937	THROMBOCYTOPENIA 6		HP:0001873	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0002003	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0004406	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0011974	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616937	THROMBOCYTOPENIA 6		HP:0031020	PMID:26936507	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000006	PMID:23906836	PCS				I		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000154	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000179	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000219	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000252	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000280	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000294	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000322	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000445	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000508	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000527	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0000574	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001166	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001249	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001250	OMIM:616938	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001263	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001305	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001321	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001344	PMID:23906836	IEA				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001511	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001631	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001800	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001810	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0001852	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0002079	OMIM:616938	TAS				P		HPO:skoehler	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0002209	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0002719	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0004322	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0005280	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0009882	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0009928	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616938	COFFIN-SIRIS SYNDROME 5		HP:0011968	PMID:23906836	PCS				P		HPO:probinson	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0000007	PMID:27123486	PCS				I		HPO:probinson	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0001249	OMIM:616939	TAS				P		HPO:skoehler	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0001263	PMID:27123486	PCS				P		HPO:probinson	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0002072	PMID:27123486	PCS				P		HPO:probinson	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0002457	PMID:27123486	PCS				P		HPO:probinson	
OMIM	616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION		HP:0002465	PMID:27123486	PCS				P		HPO:probinson	
OMIM	616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT		HP:0000006	PMID:24216514	PCS				I		HPO:probinson	
OMIM	616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT		HP:0000403	PMID:24216514	PCS		HP:0040284		P		HPO:probinson	2/4
OMIM	616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT		HP:0003593	OMIM:616941	TAS				C		HPO:skoehler	
OMIM	616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT		HP:0004432	PMID:24216514	PCS				P		HPO:probinson	
OMIM	616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT		HP:0010976	PMID:24216514	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000007	PMID:26996949	PCS				I		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000252	OMIM:616943	TAS				P		HPO:skoehler	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000482	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000565	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000639	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0000958	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0001270	OMIM:616943	TAS				P		HPO:skoehler	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0001518	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0001761	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002136	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002217	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002299	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002342	OMIM:616943	TAS				P		HPO:skoehler	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002423	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002673	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0002750	OMIM:616943	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0004322	OMIM:616943	TAS				P		HPO:skoehler	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0004440	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0008064	OMIM:616943	IEA				P		HPO:skoehler	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0008619	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0008883	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6		HP:0045055	PMID:26996949	PCS				P		HPO:probinson	
OMIM	616944	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41		HP:0000006	PMID:25102098	PCS				I		HPO:probinson	
OMIM	616944	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41		HP:0001249	PMID:25102098	PCS				P		HPO:probinson	
OMIM	616944	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41		HP:0001250	OMIM:616944	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616944	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41		HP:0001263	PMID:25102098	PCS				P		HPO:probinson	
OMIM	616946	PREMATURE OVARIAN FAILURE 11		HP:0000006	PMID:26218421	PCS				I		HPO:probinson	
OMIM	616946	PREMATURE OVARIAN FAILURE 11		HP:0000869	PMID:26218421	PCS				P		HPO:probinson	
OMIM	616946	PREMATURE OVARIAN FAILURE 11		HP:0000876	PMID:26218421	PCS				P		HPO:probinson	
OMIM	616946	PREMATURE OVARIAN FAILURE 11		HP:0008232	PMID:26218421	PCS				P		HPO:probinson	
OMIM	616947	PREMATURE OVARIAN FAILURE 12		HP:0000007	PMID:25062452	PCS				I		HPO:probinson	
OMIM	616947	PREMATURE OVARIAN FAILURE 12		HP:0000568	PMID:25062452	PCS				P		HPO:probinson	
OMIM	616947	PREMATURE OVARIAN FAILURE 12		HP:0000786	PMID:25062452	PCS				P		HPO:probinson	
OMIM	616947	PREMATURE OVARIAN FAILURE 12		HP:0007754	PMID:25062452	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0000007	PMID:26157035	PCS				I		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0000639	OMIM:616948	TAS				P		HPO:skoehler	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0001249	OMIM:616948	TAS				P		HPO:skoehler	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0001260	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0001272	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0001310	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0001347	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0002061	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0002078	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0002079	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0002080	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0002317	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0003677	OMIM:616948	TAS				C		HPO:skoehler	
OMIM	616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22		HP:0007256	PMID:26157035	PCS				P		HPO:probinson	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0000007	PMID:24658003	PCS				I		HPO:probinson	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0001249	PMID:24658003	PCS				P		HPO:probinson	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0001250	PMID:24658003	PCS	HP:0011463			P		HPO:probinson	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0001251	PMID:24658003	PCS				P		HPO:probinson	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0001290	OMIM:616949	IEA				P		HPO:skoehler	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0002902	OMIM:616949	IEA				P		HPO:skoehler	
OMIM	616949	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 23; SCAR23		HP:0003388	OMIM:616949	IEA				P		HPO:skoehler	
OMIM	616950	SPERMATOGENIC FAILURE 15; SPGF15		HP:0000007	PMID:25899990	PCS				I		HPO:probinson	
OMIM	616950	SPERMATOGENIC FAILURE 15; SPGF15		HP:0002835	OMIM:616950	IEA				P		HPO:skoehler	
OMIM	616950	SPERMATOGENIC FAILURE 15; SPGF15		HP:0011961	PMID:25899990	PCS				P		HPO:probinson	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0000007	OMIM:616954	TAS				I		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0000252	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0000365	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0000767	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0001251	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0001257	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS	HP:0012829	HP:0001263	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0001290	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0001344	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0002751	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0003577	OMIM:616954	TAS				C		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0100022	OMIM:616954	TAS				P		HPO:skoehler	
OMIM	616954	YOU-HOOVER-FONG SYNDROME; YHFS		HP:0100704	OMIM:616954	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0000007	PMID:26494905	PCS				I		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0000543	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0000545	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0000662	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0000980	OMIM:616959	IEA				P		HPO:skoehler	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0001903	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0004445	OMIM:616959	TAS				P		HPO:skoehler	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0007722	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0011273	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0025066	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0030529	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0030609	PMID:26494905	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0040303	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616959	RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM		HP:0100014	PMID:26494905	PCS				P		HPO:probinson	
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0000007	PMID:26047794	PCS				I		HPO:probinson	
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0000103	PMID:26047794	PCS		HP:0040284		P		HPO:probinson	11/14
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0000117	PMID:26047794	PCS				P		HPO:probinson	
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0001252	PMID:26047794	PCS		HP:0040284		P		HPO:probinson	4/15
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0001508	PMID:26047794	PCS		HP:0040284		P		HPO:probinson	11/15
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0002148	PMID:26047794	PCS				P		HPO:probinson	
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0002150	PMID:26047794	PCS		HP:0040284		P		HPO:probinson	12/15
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0003072	PMID:26047794	PCS				P		HPO:probinson	
OMIM	616963	HYPERCALCEMIA, INFANTILE 2		HP:0012408	PMID:26047794	PCS				P		HPO:probinson	
OMIM	616968	DEAFNESS, AUTOSOMAL DOMINANT 70		HP:0000006	PMID:26196677	PCS				I		HPO:probinson	
OMIM	616968	DEAFNESS, AUTOSOMAL DOMINANT 70		HP:0000408	PMID:26196677	PCS				P		HPO:probinson	
OMIM	616968	DEAFNESS, AUTOSOMAL DOMINANT 70		HP:0003677	OMIM:616968	TAS				C		HPO:skoehler	
OMIM	616968	DEAFNESS, AUTOSOMAL DOMINANT 70		HP:0003828	OMIM:616968	TAS				C		HPO:skoehler	
OMIM	616969	DEAFNESS, AUTOSOMAL DOMINANT 66		HP:0000006	PMID:26197441	PCS				I		HPO:probinson	
OMIM	616969	DEAFNESS, AUTOSOMAL DOMINANT 66		HP:0000407	PMID:26197441	PCS				P		HPO:probinson	
OMIM	616969	DEAFNESS, AUTOSOMAL DOMINANT 66		HP:0003828	OMIM:616969	TAS				C		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0000006	OMIM:616973	TAS				I		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0000126	OMIM:616973	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0000175	OMIM:616973	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0000486	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0000639	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0001249	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0001250	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0001263	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0001290	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0001508	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0002353	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0002509	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0003593	OMIM:616973	TAS				C		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0007772	OMIM:616973	TAS				P		HPO:skoehler	
OMIM	616973	MENTAL RETARDATION, AUTOSOMAL DOMINANT 42		HP:0100704	OMIM:616973	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0000007	OMIM:616974	TAS				I		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0001290	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0001410	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0001508	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0001712	OMIM:616974	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0002020	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0002151	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0002490	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0002910	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0003128	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0003348	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0003577	OMIM:616974	TAS				C		HPO:skoehler	
OMIM	616974	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 30		HP:0011968	OMIM:616974	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000006	OMIM:616975	TAS				I		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000028	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000047	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000076	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000286	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000347	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000358	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000369	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000463	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000486	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000494	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000568	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000581	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000589	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000648	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0000729	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001260	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001263	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001290	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001320	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001511	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0001629	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0002007	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0002020	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0002079	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0002119	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0003593	OMIM:616975	TAS				C		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0004322	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0011229	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616975	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART		HP:0011968	OMIM:616975	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000006	OMIM:616977	TAS				I		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000160	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000252	OMIM:616977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000426	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000431	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000729	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000739	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0000752	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001182	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001249	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001250	OMIM:616977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001263	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001290	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001344	OMIM:616977	IEA				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0001999	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0002019	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0002020	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0002059	OMIM:616977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0002079	OMIM:616977	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0003593	OMIM:616977	TAS				C		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0011968	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616977	MENTAL RETARDATION, AUTOSOMAL DOMINANT 43; MRD43		HP:0100710	OMIM:616977	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0000007	OMIM:616981	TAS				I		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0000639	OMIM:616981	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001249	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001250	OMIM:616981	IEA				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001257	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001263	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001266	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001272	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001288	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001290	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001336	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0001344	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0002059	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0002063	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0002376	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	616981	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 37; EIEE37		HP:0200134	OMIM:616981	TAS				P		HPO:skoehler	
OMIM	617004	POLYCYSTIC LIVER DISEASE 2		HP:0000006	OMIM:617004	TAS				I		HPO:skoehler	
OMIM	617004	POLYCYSTIC LIVER DISEASE 2		HP:0001407	OMIM:617004	TAS				P		HPO:skoehler	
OMIM	617004	POLYCYSTIC LIVER DISEASE 2		HP:0002240	OMIM:617004	TAS				P		HPO:skoehler	
OMIM	617004	POLYCYSTIC LIVER DISEASE 2		HP:0003581	OMIM:617004	TAS				C		HPO:skoehler	
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0000007	OMIM:617006	TAS				I		HPO:skoehler	
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0000093	OMIM:617006	TAS				P		HPO:skoehler	
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0000100	OMIM:617006	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0002960	OMIM:617006	IEA				P		HPO:skoehler	
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0003593	OMIM:617006	TAS				C		HPO:skoehler	
OMIM	617006	AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2; ADMIO2		HP:0012579	OMIM:617006	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0000007	OMIM:617008	TAS				I		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0000252	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0000577	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0000605	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0000639	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0001250	OMIM:617008	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0001263	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0001264	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0002015	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0002465	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0002510	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0003593	OMIM:617008	TAS				C		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0003828	OMIM:617008	TAS				C		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0007256	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617008	CEREBRAL PALSY, SPASTIC QUADRIPLEGIC, 3		HP:0100543	OMIM:617008	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000007	OMIM:617011	TAS				I		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000098	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000218	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000238	OMIM:617011	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000256	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000272	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000276	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000303	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000316	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000325	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000358	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000369	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000400	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000426	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000472	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000494	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000520	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0000582	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001166	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001176	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001249	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001250	OMIM:617011	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001263	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001272	OMIM:617011	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001290	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001344	OMIM:617011	IEA				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001355	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001388	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001763	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0001833	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002007	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002066	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002119	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002120	OMIM:617011	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002650	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0002808	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0003307	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0003577	OMIM:617011	TAS				C		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0007074	OMIM:617011	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0011220	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617011	MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR		HP:0045075	OMIM:617011	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0000007	OMIM:617013	TAS				I		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001249	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001257	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001263	OMIM:617013	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001272	OMIM:617013	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001288	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001300	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001337	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0001371	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0002059	OMIM:617013	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0002067	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0002376	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0002650	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0003487	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0003676	OMIM:617013	TAS				C		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0005484	OMIM:617013	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0008936	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0011448	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617013	HYPERMANGANESEMIA WITH DYSTONIA 2		HP:0012048	OMIM:617013	TAS				P		HPO:skoehler	
OMIM	617014	NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:617014	TAS				I		HPO:skoehler	
OMIM	617014	NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE		HP:0001875	OMIM:617014	TAS				P		HPO:skoehler	
OMIM	617014	NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE		HP:0002719	OMIM:617014	TAS				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0000006	OMIM:617017	TAS				I		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0000007	OMIM:617017	TAS				I		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0001265	OMIM:617017	TAS				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0001284	OMIM:617017	TAS				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0002317	OMIM:617017	TAS				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0002936	OMIM:617017	TAS				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0003581	OMIM:617017	TAS				C		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0003677	OMIM:617017	TAS				C		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0007141	OMIM:617017	IEA				P		HPO:skoehler	
OMIM	617017	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T; CMT2T		HP:0009027	OMIM:617017	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0000006	OMIM:617018	TAS				I		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0000571	OMIM:617018	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0000639	OMIM:617018	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0001260	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0001265	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0001272	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0001337	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0001761	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0002063	OMIM:617018	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0002066	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0002070	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0002936	OMIM:617018	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0003581	OMIM:617018	TAS				C		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0003677	OMIM:617018	TAS				C		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0003693	OMIM:617018	TAS				P		HPO:skoehler	
OMIM	617018	SPINOCEREBELLAR ATAXIA 43; SCA43		HP:0009763	OMIM:617018	IEA				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0000007	OMIM:617020	TAS				I		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0000556	OMIM:617020	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0001251	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0001263	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0001276	OMIM:617020	IEA				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0001290	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0001332	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0002133	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0002187	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0003593	OMIM:617020	TAS				C		HPO:skoehler	
OMIM	617020	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 38; EIEE38		HP:0200134	OMIM:617020	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0000007	OMIM:617021	TAS				I		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0000822	OMIM:617021	IEA				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001250	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001410	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001511	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001562	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001629	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001643	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001873	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0001924	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0002093	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0002353	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0003128	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0003577	OMIM:617021	TAS				C		HPO:skoehler	
OMIM	617021	HYDROPS, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA; HLASA		HP:0011675	OMIM:617021	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000007	OMIM:617022	TAS				I		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000189	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000218	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000343	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000347	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000470	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000473	OMIM:617022	IEA				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000778	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0000885	OMIM:617022	IEA				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001181	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001511	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001539	OMIM:617022	IEA				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001562	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001629	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001640	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001762	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001789	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0001989	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0002089	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0002623	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0002943	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0010557	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617022	LETHAL CONGENITAL CONTRACTURE SYNDROME 10; LCCS10		HP:0025258	OMIM:617022	TAS				P		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0000007	OMIM:617023	TAS				I		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0000545	OMIM:617023	TAS				P		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0000662	OMIM:617023	TAS				P		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0000980	OMIM:617023	IEA				P		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0007994	OMIM:617023	TAS				P		HPO:skoehler	
OMIM	617023	RETINITIS PIGMENTOSA 75; RP75		HP:0031790	OMIM:617023	IEA				P		HPO:skoehler	
OMIM	617024	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H		HP:0000007	OMIM:617024	TAS				I		HPO:skoehler	
OMIM	617024	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H		HP:0000540	OMIM:617024	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617024	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H		HP:0000613	OMIM:617024	TAS				P		HPO:skoehler	
OMIM	617024	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H		HP:0000662	OMIM:617024	TAS				P		HPO:skoehler	
OMIM	617024	NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1H; CSNB1H		HP:0025573	OMIM:617024	IEA				P		HPO:skoehler	
OMIM	617025	NEVUS COMEDONICUS		HP:0001428	OMIM:617025	TAS				I		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0000007	OMIM:617026	TAS				I		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0000253	OMIM:617026	TAS				P		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0000486	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001249	OMIM:617026	TAS				P		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001250	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001257	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001270	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001290	OMIM:617026	TAS				P		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0001347	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0002120	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0002540	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0003487	OMIM:617026	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0003577	OMIM:617026	TAS				C		HPO:skoehler	
OMIM	617026	PONTOCEREBELLAR HYPOPLASIA, TYPE 2F		HP:0003828	OMIM:617026	TAS				C		HPO:skoehler	
OMIM	617027	HYPERALDOSTERONISM, FAMILIAL, TYPE IV		HP:0000006	OMIM:617027	TAS				I		HPO:skoehler	
OMIM	617027	HYPERALDOSTERONISM, FAMILIAL, TYPE IV		HP:0000822	OMIM:617027	TAS				P		HPO:skoehler	
OMIM	617028	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54		HP:0000007	OMIM:617028	TAS				I		HPO:skoehler	
OMIM	617028	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54		HP:0000750	OMIM:617028	TAS				P		HPO:skoehler	
OMIM	617028	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54		HP:0000752	OMIM:617028	TAS				P		HPO:skoehler	
OMIM	617028	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 54		HP:0001249	OMIM:617028	TAS				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0000007	OMIM:617030	TAS				I		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0002600	OMIM:617030	TAS				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0003198	OMIM:617030	IEA				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0003555	OMIM:617030	TAS				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0003677	OMIM:617030	TAS				C		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0003693	OMIM:617030	TAS				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0003805	OMIM:617030	IEA				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0008180	OMIM:617030	TAS				P		HPO:skoehler	
OMIM	617030	MYOPATHY, DISTAL, 5; MPD5		HP:0010628	OMIM:617030	TAS				P		HPO:skoehler	
OMIM	617035	PATENT DUCTUS ARTERIOSUS 2		HP:0000006	OMIM:617035	TAS				I		HPO:skoehler	
OMIM	617035	PATENT DUCTUS ARTERIOSUS 2		HP:0001643	OMIM:617035	TAS				P		HPO:skoehler	
OMIM	617039	PATENT DUCTUS ARTERIOSUS 3		HP:0000006	OMIM:617039	TAS				I		HPO:skoehler	
OMIM	617039	PATENT DUCTUS ARTERIOSUS 3		HP:0001643	OMIM:617039	TAS				P		HPO:skoehler	
OMIM	617041	DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS; DURS3		HP:0000006	OMIM:617041	TAS				I		HPO:skoehler	
OMIM	617041	DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS; DURS3		HP:0000542	OMIM:617041	TAS				P		HPO:skoehler	
OMIM	617041	DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS; DURS3		HP:0000634	OMIM:617041	TAS				P		HPO:skoehler	
OMIM	617041	DUANE RETRACTION SYNDROME 3 WITH OR WITHOUT DEAFNESS; DURS3		HP:0000661	OMIM:617041	IEA				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0000007	OMIM:617044	TAS				I		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0000554	OMIM:617044	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0000722	OMIM:617044	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0000733	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0001249	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0001290	OMIM:617044	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0001629	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0001643	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0001655	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0003508	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0007018	OMIM:617044	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617044	SHORT STATURE, DEVELOPMENTAL DELAY, AND CONGENITAL HEART DEFECTS		HP:0100716	OMIM:617044	TAS				P		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:617046	TAS				I		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:617046	TAS				P		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:617046	TAS				P		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:617046	TAS				P		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0003677	OMIM:617046	TAS				C		HPO:skoehler	
OMIM	617046	SPASTIC PARAPLEGIA 77, AUTOSOMAL RECESSIVE		HP:0007210	OMIM:617046	TAS				P		HPO:skoehler	
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0000006	OMIM:617047	TAS				I		HPO:skoehler	
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0001635	OMIM:617047	TAS				P		HPO:skoehler	
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0001653	OMIM:617047	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0002094	OMIM:617047	TAS				P		HPO:skoehler	
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0005110	OMIM:617047	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617047	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26		HP:0031295	OMIM:617047	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0000007	OMIM:617049	TAS				I		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0000952	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0000969	OMIM:617049	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0001394	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0001399	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0001508	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0001943	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0001987	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0002910	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0003678	OMIM:617049	TAS				C		HPO:skoehler	
OMIM	617049	CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC, 5		HP:0008151	OMIM:617049	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000007	OMIM:617050	TAS				I		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000252	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000278	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000319	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000369	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000400	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000601	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0000639	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0001107	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0001290	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0001332	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0001744	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0001875	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002059	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002069	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002123	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002205	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002240	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002353	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0002721	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0003593	OMIM:617050	TAS				C		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0006530	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0008936	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0011968	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617050	HERMANSKY-PUDLAK SYNDROME 10		HP:0012448	OMIM:617050	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0000007	OMIM:617051	TAS				I		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0000252	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0000280	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0000486	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0001263	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0001290	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0002059	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0002119	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0002187	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0003593	OMIM:617051	TAS				C		HPO:skoehler	
OMIM	617051	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 55		HP:0100702	OMIM:617051	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000007	OMIM:617052	TAS				I		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000252	OMIM:617052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000286	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000316	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000347	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000365	OMIM:617052	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000378	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000483	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000494	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000540	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000545	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000556	OMIM:617052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000668	OMIM:617052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000691	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000705	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000962	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0000964	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001000	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001374	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001382	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001508	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001511	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001738	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001792	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001876	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001915	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0001999	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0003812	OMIM:617052	IEA				C		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0004322	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0004349	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0004808	OMIM:617052	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0005528	OMIM:617052	TAS				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0006297	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0008404	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0100255	OMIM:617052	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617052	BONE MARROW FAILURE SYNDROME 3; BMFS3		HP:0100840	OMIM:617052	IEA				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000006	OMIM:617053	TAS				I		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000010	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000028	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000047	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000049	OMIM:617053	IEA				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000238	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000815	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000846	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0000967	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001250	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001263	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001270	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001511	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001643	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001762	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001838	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001873	OMIM:617053	IEA				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001882	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001888	OMIM:617053	IEA				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001903	OMIM:617053	IEA				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0001943	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002020	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002028	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002043	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002153	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002170	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002571	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002650	OMIM:617053	TAS	HP:0003577			P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002718	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002863	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0002902	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0004059	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0004322	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0004325	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0006270	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0008734	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0010550	OMIM:617053	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0010557	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE	HP:0031796	HP:0011951	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0030260	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617053	MIRAGE SYNDROME; MIRAGE		HP:0100806	OMIM:617053	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0000007	OMIM:617054	TAS				I		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0000750	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0001276	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0001347	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0002015	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0002307	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0002317	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0002376	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0003676	OMIM:617054	TAS				C		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0006957	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617054	STRIATONIGRAL DEGENERATION, CHILDHOOD-ONSET		HP:0012179	OMIM:617054	TAS				P		HPO:skoehler	
OMIM	617055	CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3		HP:0000218	OMIM:617055	IEA				P		HPO:skoehler	
OMIM	617055	CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3		HP:0000293	OMIM:617055	IEA				P		HPO:skoehler	
OMIM	617055	CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3		HP:0002015	OMIM:617055	IEA				P		HPO:skoehler	
OMIM	617055	CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3		HP:0003593	OMIM:617055	IEA				C		HPO:skoehler	
OMIM	617055	CRISPONI/COLD-INDUCED SWEATING SYNDROME 3; CISS3		HP:0011968	OMIM:617055	IEA				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0000006	OMIM:617056	TAS				I		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0000097	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0000107	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0000112	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0001511	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0001875	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0001903	OMIM:617056	TAS	HP:0003577			P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0001997	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0002149	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0002617	OMIM:617056	IEA				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0002719	OMIM:617056	IEA				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0003676	OMIM:617056	TAS				C		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0004322	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0012622	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617056	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 4; HNFJ4		HP:0100543	OMIM:617056	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000006	OMIM:617061	TAS				I		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000218	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000252	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000347	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000348	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000400	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000494	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000574	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000582	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000664	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000668	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000678	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000718	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000722	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0000750	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0001156	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0001182	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0001249	OMIM:617061	IEA				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0001250	OMIM:617061	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0001270	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0002465	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0002719	OMIM:617061	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0002808	OMIM:617061	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0003196	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0004691	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0007018	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0011968	OMIM:617061	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0012471	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617061	MENTAL RETARDATION, AUTOSOMAL DOMINANT 44; MRD44		HP:0030084	OMIM:617061	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000006	OMIM:617062	TAS				I		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000218	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000219	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000252	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000286	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000316	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000347	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000369	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000431	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000463	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000508	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000664	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0000750	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001156	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001249	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001263	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001290	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001302	OMIM:617062	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001344	OMIM:617062	IEA				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001382	OMIM:617062	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0001508	OMIM:617062	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0002019	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0002553	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0002650	OMIM:617062	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0002720	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0004315	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0007018	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0009879	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0010819	OMIM:617062	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0011968	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617062	OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS		HP:0030084	OMIM:617062	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000007	OMIM:617063	TAS				I		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000028	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000047	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000054	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000076	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000160	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000175	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000218	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000253	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000260	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000365	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000453	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000486	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000520	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0000545	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001217	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001263	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001388	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001629	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001631	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0001674	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0002023	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0002025	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0002089	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0002650	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0002979	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0004322	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0004325	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0004442	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0004691	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0006498	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0007099	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0008551	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0008665	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0012227	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0045074	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0100258	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617063	MEIER-GORLIN SYNDROME 7		HP:0100867	OMIM:617063	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0000007	OMIM:617065	TAS				I		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40	HP:0031375	HP:0001250	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0001257	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0001266	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0001336	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0002120	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0002187	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0002521	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617065	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 40		HP:0200134	OMIM:617065	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0000007	OMIM:617066	TAS				I		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0000218	OMIM:617066	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0000467	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0000767	OMIM:617066	IEA				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0000958	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0001270	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0002650	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0002747	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0003306	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0003560	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0003577	OMIM:617066	TAS				C		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0003687	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0006829	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617066	MUSCULAR DYSTROPHY, CONGENITAL, DAVIGNON-CHAUVEAU TYPE; MDCDC		HP:0007502	OMIM:617066	TAS				P		HPO:skoehler	
OMIM	617068	PORTAL HYPERTENSION, NONCIRRHOTIC		HP:0000007	OMIM:617068	TAS				I		HPO:skoehler	
OMIM	617068	PORTAL HYPERTENSION, NONCIRRHOTIC		HP:0001409	OMIM:617068	TAS				P		HPO:skoehler	
OMIM	617068	PORTAL HYPERTENSION, NONCIRRHOTIC		HP:0001744	OMIM:617068	TAS				P		HPO:skoehler	
OMIM	617068	PORTAL HYPERTENSION, NONCIRRHOTIC		HP:0002240	OMIM:617068	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0000007	OMIM:617069	TAS				I		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0000508	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0000590	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0001260	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0002015	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0002151	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0003202	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0003236	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0003691	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0003701	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0003737	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0008972	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617069	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 3		HP:0010628	OMIM:617069	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0000007	OMIM:617070	TAS				I		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0000407	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0000508	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0000590	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0001265	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0001618	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0002015	OMIM:617070	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0002120	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0002151	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0002460	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003200	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003202	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003236	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003477	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003581	OMIM:617070	TAS				C		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003701	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0003737	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617070	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4		HP:0100543	OMIM:617070	TAS				P		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0000007	OMIM:617072	TAS				I		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0001324	OMIM:617072	IEA				P		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0003236	OMIM:617072	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0003306	OMIM:617072	TAS				P		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0003560	OMIM:617072	IEA				P		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0003677	OMIM:617072	TAS				C		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0006466	OMIM:617072	TAS				P		HPO:skoehler	
OMIM	617072	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Y; LGMD2Y		HP:0100297	OMIM:617072	TAS				P		HPO:skoehler	
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0000006	OMIM:617073	TAS				I		HPO:skoehler	
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0000691	OMIM:617073	TAS				P		HPO:skoehler	
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0000958	OMIM:617073	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0001592	OMIM:617073	IEA				P		HPO:skoehler	
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0008070	OMIM:617073	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617073	TOOTH AGENESIS, SELECTIVE, 8; STHAG8		HP:0045075	OMIM:617073	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617075	NASOPHARYNGEAL CARCINOMA, SUSCEPTIBILITY TO, 3		HP:0000006	OMIM:617075	TAS				I		HPO:skoehler	
OMIM	617080	SEIZURES, BENIGN FAMILIAL INFANTILE, 5		HP:0000006	OMIM:617080	TAS				I		HPO:skoehler	
OMIM	617080	SEIZURES, BENIGN FAMILIAL INFANTILE, 5		HP:0002069	OMIM:617080	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0000007	OMIM:617082	TAS				I		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0000252	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0000365	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0000505	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0000998	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0001257	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA	HP:0012829	HP:0001263	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0001290	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0001508	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0001511	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0002120	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0002133	OMIM:617082	TAS				P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0002650	OMIM:617082	TAS	HP:0003577			P		HPO:skoehler	
OMIM	617082	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IAA		HP:0003577	OMIM:617082	TAS				C		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0000007	OMIM:617086	TAS				I		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0000252	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0000505	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0000544	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0000648	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001250	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001257	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001263	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001272	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001344	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0001347	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0002015	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0002521	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0002540	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0003593	OMIM:617086	TAS				C		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0003676	OMIM:617086	TAS				C		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0006829	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617086	ENCEPHALOPATHY DUE TO DEFECTIVE MITOCHONDRIAL AND PEROXISOMAL FISSION 2		HP:0009830	OMIM:617086	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0000007	OMIM:617087	TAS				I		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0000365	OMIM:617087	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0000543	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0000648	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0001265	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0001761	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002194	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002355	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002650	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002747	OMIM:617087	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002808	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0002936	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0003477	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0003701	OMIM:617087	IEA				P		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0003828	OMIM:617087	TAS				C		HPO:skoehler	
OMIM	617087	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B		HP:0009027	OMIM:617087	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000007	OMIM:617088	TAS				I		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000148	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000191	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000286	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000369	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000494	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000668	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000773	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000888	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0000894	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001156	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001162	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001561	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001643	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001680	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0001744	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0002240	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0004322	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0005280	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0006695	OMIM:617088	TAS				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0010566	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0011069	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617088	SHORT-RIB THORACIC DYSPLASIA 15 WITH POLYDACTYLY; SRTD15		HP:0030010	OMIM:617088	IEA				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:617090	TAS				I		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000104	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000252	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000316	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000340	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000400	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0000414	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001249	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001250	OMIM:617090	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001257	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001263	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001274	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001321	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0001508	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002119	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0002365	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003577	OMIM:617090	TAS				C		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0003828	OMIM:617090	TAS				C		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0004322	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0009879	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617090	MICROCEPHALY 17, PRIMARY, AUTOSOMAL RECESSIVE		HP:0012471	OMIM:617090	TAS				P		HPO:skoehler	
OMIM	617091	CILIARY DYSKINESIA, PRIMARY, 34; CILD34		HP:0000007	OMIM:617091	TAS				I		HPO:skoehler	
OMIM	617091	CILIARY DYSKINESIA, PRIMARY, 34; CILD34		HP:0000789	OMIM:617091	IEA				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0000007	OMIM:617092	TAS				I		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0001696	OMIM:617092	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0002110	OMIM:617092	TAS				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0002205	OMIM:617092	IEA				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0002257	OMIM:617092	TAS				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0003577	OMIM:617092	TAS				C		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0011109	OMIM:617092	TAS				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0012735	OMIM:617092	IEA				P		HPO:skoehler	
OMIM	617092	CILIARY DYSKINESIA, PRIMARY, 35; CILD35		HP:0100582	OMIM:617092	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0000007	OMIM:617093	TAS				I		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0000081	OMIM:617093	IEA				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0000126	OMIM:617093	IEA				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0000252	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0000407	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001249	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001250	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001257	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001263	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001290	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001397	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001410	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001508	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0001511	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0002910	OMIM:617093	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0003577	OMIM:617093	TAS				C		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0003828	OMIM:617093	TAS				C		HPO:skoehler	
OMIM	617093	GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY; GRIDHH		HP:0008897	OMIM:617093	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0000007	OMIM:617099	TAS				I		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0001386	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0001508	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0001974	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0002014	OMIM:617099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0002633	OMIM:617099	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0002716	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0002829	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0003326	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0009125	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0011897	OMIM:617099	TAS				P		HPO:skoehler	
OMIM	617099	AUTOINFLAMMATION, PANNICULITIS, AND DERMATOSIS SYNDROME; AIPDS		HP:0012490	OMIM:617099	IEA				P		HPO:skoehler	
OMIM	617100	FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4		HP:0000007	OMIM:617100	TAS				I		HPO:skoehler	
OMIM	617100	FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4		HP:0000854	OMIM:617100	TAS				P		HPO:skoehler	
OMIM	617100	FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4		HP:0009592	OMIM:617100	TAS				P		HPO:skoehler	
OMIM	617100	FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4		HP:0012126	OMIM:617100	TAS				P		HPO:skoehler	
OMIM	617100	FAMILIAL ADENOMATOUS POLYPOSIS 4; FAP4		HP:0012740	OMIM:617100	IEA				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000006	OMIM:617101	TAS				I		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000219	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000232	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000252	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000278	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000286	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000369	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000378	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000396	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000486	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000494	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0000592	OMIM:617101	IEA				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0001249	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0001263	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0001272	OMIM:617101	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0001382	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0003577	OMIM:617101	TAS				C		HPO:skoehler	
OMIM	617101	INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN		HP:0011800	OMIM:617101	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000007	OMIM:617102	TAS				I		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000268	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000293	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000348	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000369	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000431	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000506	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000540	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000670	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000687	OMIM:617102	IEA				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0000774	OMIM:617102	IEA				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0001156	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0001270	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0001852	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0002079	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0002098	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0003180	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0004322	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0005280	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0009826	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0009882	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0010049	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0010230	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0010306	OMIM:617102	IEA				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0010743	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0011800	OMIM:617102	TAS				P		HPO:skoehler	
OMIM	617102	SHORT-RIB THORACIC DYSPLASIA 16 WITH OR WITHOUT POLYDACTYLY; SRTD16		HP:0100259	OMIM:617102	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0000006	OMIM:617105	TAS				I		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0000252	OMIM:617105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0000737	OMIM:617105	IEA				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001250	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001254	OMIM:617105	IEA				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001257	OMIM:617105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001263	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001290	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001344	OMIM:617105	IEA				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0001371	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002059	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002079	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002187	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002376	OMIM:617105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002521	OMIM:617105	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002540	OMIM:617105	IEA				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0002751	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0003623	OMIM:617105	TAS				C		HPO:skoehler	
OMIM	617105	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 41; EIEE41		HP:0200134	OMIM:617105	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0000006	OMIM:617106	TAS				I		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0000565	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0000639	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001249	OMIM:617106	IEA				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001250	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001251	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001263	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001276	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001290	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001337	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001347	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0001371	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0002305	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0002353	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617106	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42; EIEE42		HP:0200134	OMIM:617106	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000007	OMIM:617107	TAS				I		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000107	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000110	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000158	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000256	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000286	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000311	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000316	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000400	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000407	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000486	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000490	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000494	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0000589	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001176	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001256	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001263	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001520	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001548	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001629	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001634	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001763	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001833	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0001847	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0002619	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0002667	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0002979	OMIM:617107	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0004712	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0011800	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0012471	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617107	THAUVIN-ROBINET-FAIVRE SYNDROME		HP:0030037	OMIM:617107	TAS				P		HPO:skoehler	
OMIM	617108	SESSILE SERRATED POLYPOSIS CANCER SYNDROME		HP:0000006	OMIM:617108	TAS				I		HPO:skoehler	
OMIM	617108	SESSILE SERRATED POLYPOSIS CANCER SYNDROME		HP:0032222	PMID:27081527	PCS				P		HP:probinson	
OMIM	617111	MACULAR DYSTROPHY, PATTERNED, 3; MDPT3		HP:0000006	OMIM:617111	TAS				I		HPO:skoehler	
OMIM	617111	MACULAR DYSTROPHY, PATTERNED, 3; MDPT3		HP:0000510	OMIM:617111	TAS				P		HPO:skoehler	
OMIM	617111	MACULAR DYSTROPHY, PATTERNED, 3; MDPT3		HP:0007401	OMIM:617111	IEA				P		HPO:skoehler	
OMIM	617111	MACULAR DYSTROPHY, PATTERNED, 3; MDPT3		HP:0007663	OMIM:617111	TAS				P		HPO:skoehler	
OMIM	617111	MACULAR DYSTROPHY, PATTERNED, 3; MDPT3		HP:0011506	OMIM:617111	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0000006	OMIM:617113	TAS				I		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0000752	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0001249	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0001250	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0001251	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0001263	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0001290	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0003593	OMIM:617113	TAS				C		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0100660	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617113	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 43		HP:0200134	OMIM:617113	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0000007	OMIM:617114	TAS				I		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0001265	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0001762	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0001771	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0002355	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0002540	OMIM:617114	IEA				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0002808	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0002987	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0003202	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0003236	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0003306	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0003307	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0003677	OMIM:617114	TAS				C		HPO:skoehler	
OMIM	617114	MYOPATHY, MYOFIBRILLAR, 7; MFM7		HP:0010628	OMIM:617114	TAS				P		HPO:skoehler	
OMIM	617115	PEELING SKIN SYNDROME 5		HP:0000007	OMIM:617115	TAS				I		HPO:skoehler	
OMIM	617115	PEELING SKIN SYNDROME 5		HP:0000962	OMIM:617115	TAS				P		HPO:skoehler	
OMIM	617115	PEELING SKIN SYNDROME 5		HP:0025092	OMIM:617115	TAS				P		HPO:skoehler	
OMIM	617116	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2		HP:0000006	OMIM:617116	TAS				I		HPO:skoehler	
OMIM	617116	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2		HP:0001250	OMIM:617116	IEA				P		HPO:skoehler	
OMIM	617116	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2		HP:0003829	OMIM:617116	TAS				C		HPO:skoehler	
OMIM	617116	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 2; FFEVF2		HP:0032046	PMID:27173016	PCS	HP:0011463	HP:0040284		P		HPO:nvasilevsky	1/2
OMIM	617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3		HP:0000006	OMIM:617118	TAS				I		HPO:skoehler	
OMIM	617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3		HP:0001250	OMIM:617118	IEA				P		HPO:skoehler	
OMIM	617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3		HP:0003829	OMIM:617118	TAS				C		HPO:skoehler	
OMIM	617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3		HP:0032046	PMID:27173016	PCS		HP:0040284		P		HPO:nvasilevsky	1/10
OMIM	617118	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 3; FFEVF3		HP:0032052	PMID:26285051	IEA		HP:0040284		P		HPO:nvasilevsky	3/6
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0000007	OMIM:617119	TAS				I		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0000135	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0000252	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0000510	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0001249	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0001513	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617119	BARDET-BIEDL SYNDROME 20		HP:0010442	OMIM:617119	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0000007	OMIM:617120	TAS				I		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0000639	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0000657	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0001249	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0001251	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0001263	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0001290	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617120	JOUBERT SYNDROME 27		HP:0002419	OMIM:617120	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0000007	OMIM:617121	TAS				I		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0000488	OMIM:617121	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617121	JOUBERT SYNDROME 28		HP:0000639	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0000657	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0001249	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0001251	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0001263	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617121	JOUBERT SYNDROME 28		HP:0001290	OMIM:617121	TAS				P		HPO:skoehler	
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0000007	OMIM:617123	TAS				I		HPO:skoehler	
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0000662	OMIM:617123	TAS				P		HPO:skoehler	
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0007663	OMIM:617123	TAS				P		HPO:skoehler	
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0011505	OMIM:617123	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0030329	OMIM:617123	IEA				P		HPO:skoehler	
OMIM	617123	RETINITIS PIGMENTOSA 76; RP76		HP:0500087	OMIM:617123	IEA				P		HPO:skoehler	
OMIM	617125	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56		HP:0000007	OMIM:617125	TAS				I		HPO:skoehler	
OMIM	617125	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 56		HP:0001249	OMIM:617125	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000007	OMIM:617126	TAS				I		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000028	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000160	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000218	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000219	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000252	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000294	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000343	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000426	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000430	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000448	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000527	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000574	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000664	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000678	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0000752	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0001007	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0001249	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0001263	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0001319	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0002465	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0002553	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0004322	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617126	ALAZAMI-YUAN SYNDROME		HP:0010055	OMIM:617126	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0000007	OMIM:617127	TAS				I		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0000180	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0000316	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0000431	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0000463	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0001274	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0002119	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0002419	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0010055	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617127	OROFACIODIGITAL SYNDROME XV		HP:0012368	OMIM:617127	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0000007	OMIM:617132	TAS				I		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0000298	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0000737	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0000817	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001250	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001257	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001272	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001290	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001298	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001332	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001344	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0001508	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0002020	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0002059	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0002079	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0002305	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0004322	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0005484	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0010864	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0011968	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617132	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 44		HP:0012448	OMIM:617132	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0000007	OMIM:617133	TAS				I		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0000518	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0000639	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0001260	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0001272	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0002064	OMIM:617133	IEA				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0002066	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0002070	OMIM:617133	TAS				P		HPO:skoehler	
OMIM	617133	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24		HP:0003676	OMIM:617133	TAS				C		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000006	OMIM:617137	TAS				I		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000011	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000028	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000175	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000193	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000201	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000218	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000293	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000294	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000307	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000316	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000322	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000336	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000369	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000377	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000405	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000407	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000431	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000455	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000465	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000494	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000574	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000592	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000767	OMIM:617137	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0000823	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001007	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001256	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001374	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001607	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001642	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001643	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001647	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001655	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0001762	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002002	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002020	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002021	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002650	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002777	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0002949	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0003083	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0003199	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0003273	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0005280	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0008872	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0009487	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0010049	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0010307	OMIM:617137	IEA				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0010743	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0012385	OMIM:617137	TAS				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0040019	OMIM:617137	IEA				P		HPO:skoehler	
OMIM	617137	FRONTOMETAPHYSEAL DYSPLASIA 2; FMD2		HP:0100279	OMIM:617137	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000006	OMIM:617140	TAS				I		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000085	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000122	OMIM:617140	IEA				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000160	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000164	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000175	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000218	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000219	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000322	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000324	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000369	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000431	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000486	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000490	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000494	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000540	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000648	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0000772	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001249	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001250	OMIM:617140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001263	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001290	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001321	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001363	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001371	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001382	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001508	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0001773	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002007	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002079	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002119	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002376	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002650	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002808	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0002937	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0004322	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0005280	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0011968	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0030680	OMIM:617140	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0100702	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0100704	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617140	ZTTK SYNDROME; ZTTKS		HP:0200055	OMIM:617140	TAS				P		HPO:skoehler	
OMIM	617141	ANIRIDIA 2		HP:0000006	OMIM:617141	TAS				I		HPO:skoehler	
OMIM	617142	ANIRIDIA 3		HP:0000006	OMIM:617142	TAS				I		HPO:skoehler	
OMIM	617142	ANIRIDIA 3		HP:0000501	OMIM:617142	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617142	ANIRIDIA 3		HP:0000518	OMIM:617142	TAS				P		HPO:skoehler	
OMIM	617142	ANIRIDIA 3		HP:0000529	OMIM:617142	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0000007	OMIM:617143	TAS				I		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0000467	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0000508	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0000597	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0001283	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0001290	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0001561	OMIM:617143	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0001618	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002015	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002033	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002104	OMIM:617143	IEA				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002650	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002791	OMIM:617143	IEA				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002804	OMIM:617143	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0002808	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0003701	OMIM:617143	IEA				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0003828	OMIM:617143	TAS				C		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0010307	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0010628	OMIM:617143	TAS				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0031936	OMIM:617143	IEA				P		HPO:skoehler	
OMIM	617143	MYASTHENIC SYNDROME, CONGENITAL, 20, PRESYNAPTIC; CMS20		HP:0100543	OMIM:617143	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000007	OMIM:617145	TAS				I		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000020	OMIM:617145	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000365	OMIM:617145	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000511	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000639	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0000657	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001260	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001268	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001272	OMIM:617145	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001310	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001332	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001337	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0001347	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0002066	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0002070	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0002075	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0003676	OMIM:617145	TAS				C		HPO:skoehler	
OMIM	617145	NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET		HP:0007256	OMIM:617145	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0000007	PMID:27843126	PCS				I		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0000218	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0000219	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0000431	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001166	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	4/10
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001260	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	7/7
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001263	PMID:27843126	PCS		HP:0040284		P		HP:probinson	3/9
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001270	PMID:27843126	PCS	HP:0003593	HP:0040284		P		HPO:skoehler	10/10
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001284	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	9/9
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001319	PMID:27843126	PCS	HP:0003577	HP:0040284		P		HP:probinson	8/8
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001371	OMIM:617146	TAS	HP:0003577			P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001385	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001762	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001763	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	6/7
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0001852	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	7/9
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002020	PMID:27843126	PCS		HP:0040284		P		HP:probinson	2/11
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002058	PMID:27843126	PCS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002093	PMID:27843126	PCS	HP:0003623	HP:0040284		P		HPO:skoehler	6/6
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002136	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002421	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002540	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0002650	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	10/10
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0003189	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0003236	PMID:27843126	PCS		HP:0040284		P		HP:probinson	1/5
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0003390	OMIM:617146	TAS				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0003484	PMID:27843126	PCS		HP:0040284		P		HP:probinson	5/8
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0003676	OMIM:617146	TAS				C		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0004322	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	8/9
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0007010	OMIM:617146	IEA				P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0007340	PMID:27843126	PCS		HP:0040284		P		HP:probinson	8/9
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0008872	PMID:27843126	PCS		HP:0040284		P		HP:probinson	2/11
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0010871	OMIM:617146	TAS	HP:0003577			P		HPO:skoehler	
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0012385	PMID:27843126	PCS		HP:0040284		P		HPO:skoehler	6/10
OMIM	617146	ARTHROGRYPOSIS, DISTAL, WITH IMPAIRED PROPRIOCEPTION AND TOUCH		HP:0031936	OMIM:617146	IEA				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0000006	OMIM:617153	TAS				I		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0001250	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0001251	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0001263	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0001290	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0002079	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0002376	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0002521	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0003593	OMIM:617153	TAS				C		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0100704	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617153	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 45		HP:0200134	OMIM:617153	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0000007	OMIM:617156	TAS				I		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0000952	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001394	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15	HP:0003676	HP:0001399	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001414	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001508	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001511	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001522	OMIM:617156	TAS				M		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001541	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0001943	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0002910	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0003073	OMIM:617156	IEA				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0003256	OMIM:617156	TAS				P		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0003577	OMIM:617156	TAS				C		HPO:skoehler	
OMIM	617156	MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE); MTDPS15		HP:0003676	OMIM:617156	TAS				C		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000007	OMIM:617157	TAS				I		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000218	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000233	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000252	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000272	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000278	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000286	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000343	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000431	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000455	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000470	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000483	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000486	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000490	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000750	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0000852	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001156	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001249	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001250	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001263	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001290	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0001513	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0002007	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0003593	OMIM:617157	TAS				C		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0004322	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0005280	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0009891	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0010049	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0010743	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0012448	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0012745	OMIM:617157	TAS				P		HPO:skoehler	
OMIM	617157	SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES; SBIDDS		HP:0031936	OMIM:617157	IEA				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0000006	OMIM:617158	TAS				I		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003202	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003236	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003376	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003438	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003691	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0003805	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0009027	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617158	MYOPATHY, DISTAL, WITH RIMMED VACUOLES		HP:0010628	OMIM:617158	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000006	OMIM:617159	TAS				I		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000028	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000054	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000062	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000076	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000083	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000243	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000256	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000280	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000286	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000316	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000365	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000369	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000378	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000483	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000508	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000582	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0000894	PMID:27479907	PCS	HP:0003593	HP:0040284		P		HP:probinson	1/6
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001182	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001249	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001290	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001545	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001629	PMID:27479907	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001631	PMID:27479907	PCS		HP:0040284		P		HP:probinson	2/6
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001636	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0001680	PMID:27479907	PCS		HP:0040284		P		HP:probinson	1/6
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0002119	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0002141	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0002308	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0002645	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0003180	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0004322	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0012745	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617159	SIFRIM-HITZ-WEISS SYNDROME		HP:0100864	OMIM:617159	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0000006	OMIM:617162	TAS				I		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0000252	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46	HP:0031375	HP:0001250	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0001263	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0001276	OMIM:617162	IEA				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0001344	OMIM:617162	IEA				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0001508	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0001763	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0002015	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0002059	OMIM:617162	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0002521	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0003593	OMIM:617162	TAS				C		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0003812	OMIM:617162	IEA				C		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0008936	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0011968	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0100704	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617162	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 46; EIEE46		HP:0200134	OMIM:617162	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000006	OMIM:617164	TAS				I		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000046	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000047	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000054	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000175	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000218	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000252	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000278	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000347	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000483	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000545	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0000601	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001249	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001250	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001270	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001508	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001511	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0001629	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0002066	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0002673	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0002870	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0003016	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0004691	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0005616	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0006429	OMIM:617164	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0008905	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0011968	OMIM:617164	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617164	SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY		HP:0030799	OMIM:617164	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0000006	OMIM:617166	TAS				I		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0000543	OMIM:617166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0001272	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0001344	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002070	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002133	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002376	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002465	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002521	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0002540	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0003828	OMIM:617166	TAS				C		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0005484	OMIM:617166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0008936	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0010841	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0011968	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0012450	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0100704	OMIM:617166	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617166	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47		HP:0200134	OMIM:617166	TAS				P		HPO:skoehler	
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0000006	OMIM:617168	TAS				I		HPO:skoehler	
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0000218	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0000545	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0000678	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0001382	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0001519	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0001647	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0001653	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0001677	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0002616	OMIM:617168	IEA				P		HPO:skoehler	
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0002650	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0005112	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0005113	OMIM:617168	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617168	AORTIC ANEURYSM, FAMILIAL THORACIC 10; AAT10		HP:0100775	OMIM:617168	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617169	SOTOS SYNDROME 3		HP:0000007	OMIM:617169	TAS				I		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0000276	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0000303	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0000448	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0000752	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0001249	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0002465	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617169	SOTOS SYNDROME 3		HP:0004482	OMIM:617169	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0000007	OMIM:617171	TAS				I		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0000713	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0000718	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0000720	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0001249	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0001263	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0001290	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0001344	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0002133	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0002353	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0002360	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0003593	OMIM:617171	TAS				C		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0004305	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617171	DYSKINESIA, SEIZURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER		HP:0100660	OMIM:617171	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0000007	OMIM:617173	TAS				I		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0000512	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0000546	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0000639	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0000750	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0001249	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0001250	OMIM:617173	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0001263	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0001290	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0001662	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617173	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA		HP:0011704	OMIM:617173	TAS				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0000006	OMIM:617174	TAS				I		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0000023	OMIM:617174	IEA				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0000225	OMIM:617174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0000704	OMIM:617174	IEA				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0000978	OMIM:617174	TAS				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0001030	OMIM:617174	TAS				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0001382	OMIM:617174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0001382	OMIM:617174	TAS				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0001537	OMIM:617174	IEA				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0002650	OMIM:617174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0002664	OMIM:617174	TAS				P		HPO:skoehler	
OMIM	617174	EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2		HP:0002829	OMIM:617174	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0000007	OMIM:617175	TAS				I		HPO:skoehler	
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES	HP:0003676	HP:0000556	OMIM:617175	TAS				P		HPO:skoehler	
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0000853	OMIM:617175	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0000869	OMIM:617175	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0002206	OMIM:617175	TAS				P		HPO:skoehler	
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0007663	OMIM:617175	TAS				P		HPO:skoehler	
OMIM	617175	RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES		HP:0008209	OMIM:617175	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0000006	OMIM:617180	TAS				I		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0000316	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0000463	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0000520	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0001156	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0001290	OMIM:617180	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0001561	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0002000	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0002098	OMIM:617180	IEA				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0002205	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0002779	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0002780	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0005280	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0006530	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617180	CHITAYAT SYNDROME; CHYTS		HP:0012471	OMIM:617180	TAS				P		HPO:skoehler	
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0000007	OMIM:617182	TAS				I		HPO:skoehler	
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0000750	OMIM:617182	TAS				P		HPO:skoehler	
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0001249	OMIM:617182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0001263	OMIM:617182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0001290	OMIM:617182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0001662	OMIM:617182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0007010	OMIM:617182	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0007018	OMIM:617182	TAS				P		HPO:skoehler	
OMIM	617182	LANGUAGE DELAY AND ATTENTION DEFICIT-HYPERACTIVITY DISORDER/COGNITIVE IMPAIRMENT WITH OR WITHOUT CARDIAC ARRHYTHMIA; LADCI		HP:0011704	OMIM:617182	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000006	OMIM:617183	TAS				I		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000007	OMIM:617183	TAS				I		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000276	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000303	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000347	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000348	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000490	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000545	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000565	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000582	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000639	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000648	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0000750	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001249	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001251	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001257	OMIM:617183	IEA				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001263	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001272	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001290	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001385	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001639	OMIM:617183	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0001760	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0002007	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0002121	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0002540	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0002650	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0003196	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0003477	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0003593	OMIM:617183	TAS				C		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0003693	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0008936	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617183	HAREL-YOON SYNDROME; HAYOS		HP:0011968	OMIM:617183	TAS				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0000006	OMIM:617184	TAS				I		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0001265	OMIM:617184	TAS				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A	HP:0012829	HP:0001290	OMIM:617184	TAS				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0001639	OMIM:617184	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0001992	OMIM:617184	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0002540	OMIM:617184	IEA				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0002747	OMIM:617184	TAS				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0003128	OMIM:617184	TAS				P		HPO:skoehler	
OMIM	617184	MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A		HP:0003577	OMIM:617184	TAS				C		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0000007	OMIM:617186	TAS				I		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0000486	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0000639	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001250	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001251	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001259	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001290	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001298	OMIM:617186	IEA				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001337	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0001522	OMIM:617186	TAS				M		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002151	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002181	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002196	OMIM:617186	IEA				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002273	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002352	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002376	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0002490	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0003128	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0003678	OMIM:617186	TAS				C		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0012444	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0030915	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617186	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY; PEBEL		HP:0200041	OMIM:617186	TAS				P		HPO:skoehler	
OMIM	617187	SPERMATOGENIC FAILURE 16		HP:0000007	OMIM:617187	TAS				I		HPO:skoehler	
OMIM	617187	SPERMATOGENIC FAILURE 16		HP:0000789	OMIM:617187	TAS				P		HPO:skoehler	
OMIM	617187	SPERMATOGENIC FAILURE 16		HP:0012207	OMIM:617187	TAS				P		HPO:skoehler	
OMIM	617187	SPERMATOGENIC FAILURE 16		HP:0012869	OMIM:617187	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0000007	OMIM:617188	TAS				I		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0000252	OMIM:617188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0000729	OMIM:617188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001249	OMIM:617188	IEA				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001263	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001276	OMIM:617188	IEA				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001290	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001344	OMIM:617188	IEA				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0001347	OMIM:617188	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0002123	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0002126	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0002373	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0002540	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0003577	OMIM:617188	TAS				C		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0007359	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0008936	OMIM:617188	TAS				P		HPO:skoehler	
OMIM	617188	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 57; MRT57		HP:0031936	OMIM:617188	IEA				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000006	OMIM:617190	TAS				I		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000256	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000276	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000278	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000316	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000358	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000369	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000455	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000508	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000520	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000750	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0000939	OMIM:617190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001249	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001250	OMIM:617190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001263	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001290	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001631	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0001943	OMIM:617190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0002119	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0002553	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0002650	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0002808	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0003593	OMIM:617190	TAS				C		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0003764	OMIM:617190	IEA				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0005616	OMIM:617190	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0006191	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617190	SHASHI-PENA SYNDROME; SHAPNS		HP:0008872	OMIM:617190	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000007	OMIM:617193	TAS				I		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000297	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000316	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000347	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000582	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000648	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0000687	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001249	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001250	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001263	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001272	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001298	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001308	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001324	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0001344	OMIM:617193	IEA				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002019	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002079	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002119	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002171	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002376	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002506	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002510	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002529	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002650	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0002804	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0003202	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0003429	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0003828	OMIM:617193	TAS				C		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0005484	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0006829	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0007366	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0011968	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617193	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT		HP:0045075	OMIM:617193	TAS				P		HPO:skoehler	
OMIM	617194	LETHAL CONGENITAL CONTRACTURE SYNDROME 11		HP:0000007	OMIM:617194	TAS				I		HPO:skoehler	
OMIM	617194	LETHAL CONGENITAL CONTRACTURE SYNDROME 11		HP:0000278	OMIM:617194	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617194	LETHAL CONGENITAL CONTRACTURE SYNDROME 11		HP:0001558	OMIM:617194	TAS				P		HPO:skoehler	
OMIM	617194	LETHAL CONGENITAL CONTRACTURE SYNDROME 11		HP:0002089	OMIM:617194	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000006	OMIM:617201	TAS				I		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000028	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000175	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000347	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000365	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000486	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0000648	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001249	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001250	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001263	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001344	OMIM:617201	IEA				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001371	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0001999	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0002079	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0002282	OMIM:617201	IEA				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0002539	OMIM:617201	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0003577	OMIM:617201	TAS				C		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0004691	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617201	PERIVENTRICULAR NODULAR HETEROTOPIA 7; PVNH7		HP:0008936	OMIM:617201	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0000007	OMIM:617205	TAS				I		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0001629	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0001719	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0003363	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0004383	OMIM:617205	IEA				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0004935	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0011539	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617205	HETEROTAXY, VISCERAL, 8, AUTOSOMAL; HTX8		HP:0011579	OMIM:617205	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0000007	OMIM:617207	TAS				I		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0000648	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001249	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001250	OMIM:617207	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001251	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001260	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001263	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001272	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0001298	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0002079	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0002510	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0002650	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0003477	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0003593	OMIM:617207	TAS				C		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0003676	OMIM:617207	TAS				C		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0003693	OMIM:617207	IEA				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0006829	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0007269	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617207	ENCEPHALOPATHY, PROGRESSIVE, WITH AMYOTROPHY AND OPTIC ATROPHY; PEAMO		HP:0009027	OMIM:617207	TAS				P		HPO:skoehler	
OMIM	617213	SEDOHEPTULOKINASE DEFICIENCY; SHPKD		HP:0000007	PMID:25647543	PCS		HP:0040284		I		HPO:probinson	2/2
OMIM	617213	SEDOHEPTULOKINASE DEFICIENCY; SHPKD		HP:0025157	PMID:25647543	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617214	SPERMATOGENIC FAILURE 17		HP:0000007	OMIM:617214	TAS				I		HPO:skoehler	
OMIM	617214	SPERMATOGENIC FAILURE 17		HP:0000789	OMIM:617214	TAS				P		HPO:skoehler	
OMIM	617217	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6		HP:0000007	OMIM:617217	TAS				I		HPO:skoehler	
OMIM	617217	AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA6		HP:0200095	OMIM:617217	TAS				P		HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0000006	OMIM:617219	TAS				I	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0000072	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0000076	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0000787	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001182	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001249	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001250	OMIM:617219	TAS		HP:0040283		P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	HP:0040283
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001263	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001290	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001344	OMIM:617219	IEA				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001385	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0001762	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0002021	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0002617	OMIM:617219	IEA				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0003829	OMIM:617219	TAS				C	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0004209	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0008897	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617219	CHROMOSOME 19q13.11 DELETION SYNDROME, PROXIMAL		HP:0011968	OMIM:617219	TAS				P	CHROMOSOME 19Q13.11 DELETION SYNDROME, PROXIMAL	HPO:skoehler	
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0000007	OMIM:617222	TAS				I		HPO:skoehler	
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001250	OMIM:617222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001290	OMIM:617222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001635	OMIM:617222	TAS				P		HPO:skoehler	
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001639	OMIM:617222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001662	OMIM:617222	TAS				P		HPO:skoehler	
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001685	OMIM:617222	TAS				P		HPO:skoehler	
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0001942	OMIM:617222	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617222	SUDDEN CARDIAC FAILURE, INFANTILE		HP:0012819	OMIM:617222	TAS				P		HPO:skoehler	
OMIM	617223	SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED		HP:0000007	OMIM:617223	TAS				I		HPO:skoehler	
OMIM	617223	SUDDEN CARDIAC FAILURE, ALCOHOL-INDUCED		HP:0001685	OMIM:617223	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000007	OMIM:617225	TAS				I		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000605	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000639	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000718	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000726	OMIM:617225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0000738	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001251	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001258	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001260	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001272	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001288	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001300	OMIM:617225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001347	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0001761	OMIM:617225	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0002120	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0002510	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0002936	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617225	SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE		HP:0003487	OMIM:617225	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0000007	OMIM:617228	TAS				I		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0000252	OMIM:617228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0000518	OMIM:617228	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001250	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001263	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001276	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001290	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001508	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0001639	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0002151	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0003128	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0003348	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0003593	OMIM:617228	TAS				C		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0011968	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617228	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31		HP:0030682	OMIM:617228	TAS				P		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0000007	OMIM:617232	TAS				I		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0002093	OMIM:617232	TAS				P		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0003236	OMIM:617232	TAS				P		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0003677	OMIM:617232	TAS				C		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0003691	OMIM:617232	TAS				P		HPO:skoehler	
OMIM	617232	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2Z		HP:0008994	OMIM:617232	TAS				P		HPO:skoehler	
OMIM	617234	PREIMPLANTATION EMBRYONIC LETHALITY 2		HP:0000007	OMIM:617234	TAS				I		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0000006	OMIM:617235	TAS				I		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0000252	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0000508	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0000639	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0000980	OMIM:617235	IEA				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0001250	OMIM:617235	IEA				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0001290	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0001336	OMIM:617235	IEA				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0002015	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0002072	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0002305	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0003577	OMIM:617235	TAS				C		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0006980	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0007281	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0011968	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0012448	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617235	MYOCLONUS, INTRACTABLE, NEONATAL; NEIMY		HP:0100704	OMIM:617235	TAS				P		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0000007	OMIM:617236	TAS				I		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0000407	OMIM:617236	TAS				P		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0000608	OMIM:617236	TAS				P		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0000613	OMIM:617236	TAS				P		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0000639	OMIM:617236	TAS				P		HPO:skoehler	
OMIM	617236	CONE-ROD DYSTROPHY AND HEARING LOSS; CRDHL		HP:0001105	OMIM:617236	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000006	OMIM:617237	TAS				I		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000316	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000322	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000347	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000582	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000695	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0000973	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001007	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001249	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001250	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001263	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001290	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001344	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001537	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001880	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0001888	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0002058	OMIM:617237	IEA				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0002510	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0002645	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0003577	OMIM:617237	TAS				C		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0004415	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0004430	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0011123	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617237	IMMUNODEFICIENCY 49; IMD49		HP:0012745	OMIM:617237	TAS				P		HPO:skoehler	
OMIM	617238	MYOPIA 25, AUTOSOMAL DOMINANT		HP:0000006	OMIM:617238	TAS				I		HPO:skoehler	
OMIM	617238	MYOPIA 25, AUTOSOMAL DOMINANT		HP:0011003	OMIM:617238	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0000007	OMIM:617239	TAS				I		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0000508	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0000602	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0000639	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0001290	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0002093	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0002104	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0002355	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0003546	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0006380	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0010628	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0011968	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617239	MYASTHENIC SYNDROME, CONGENITAL, 21, PRESYNAPTIC		HP:0012378	OMIM:617239	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0000007	OMIM:617241	TAS				I		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0000260	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0000777	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0000964	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0001508	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0001999	OMIM:617241	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0002090	OMIM:617241	IEA				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0002097	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0008936	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0011133	OMIM:617241	IEA				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0011342	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0011946	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617241	LUNG DISEASE, IMMUNODEFICIENCY, AND CHROMOSOME BREAKAGE SYNDROME; LICS		HP:0011968	OMIM:617241	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0000007	OMIM:617243	TAS				I		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0000252	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0001873	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0001875	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0001903	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0004322	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0005528	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617243	FANCONI ANEMIA, COMPLEMENTATION GROUP V		HP:0006254	OMIM:617243	TAS				P		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0000006	OMIM:617244	TAS				I		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0000238	OMIM:617244	TAS				P		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0000252	OMIM:617244	TAS				P		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0001249	OMIM:617244	TAS				P		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0001510	OMIM:617244	TAS				P		HPO:skoehler	
OMIM	617244	FANCONI ANEMIA, COMPLEMENTATION GROUP R		HP:0002023	OMIM:617244	TAS				P		HPO:skoehler	
OMIM	617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0000007	OMIM:617247	TAS				I		HPO:skoehler	
OMIM	617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0000252	OMIM:617247	TAS				P		HPO:skoehler	
OMIM	617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0001510	OMIM:617247	TAS				P		HPO:skoehler	
OMIM	617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0001643	OMIM:617247	TAS				P		HPO:skoehler	
OMIM	617247	FANCONI ANEMIA, COMPLEMENTATION GROUP U		HP:0011835	OMIM:617247	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0000007	OMIM:617248	TAS				I		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0000407	OMIM:617248	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0000518	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001250	OMIM:617248	IEA				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001276	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001290	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001332	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001337	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001510	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001522	OMIM:617248	TAS				M		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001662	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0001875	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002033	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002059	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002079	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002104	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002119	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002151	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002490	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0002878	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0003535	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617248	3-METHYLGLUTACONIC ACIDURIA, TYPE VIII; MGCA8		HP:0005484	OMIM:617248	TAS				P		HPO:skoehler	
OMIM	617251	UNCOMBABLE HAIR SYNDROME 2		HP:0000007	OMIM:617251	TAS				I		HPO:skoehler	
OMIM	617251	UNCOMBABLE HAIR SYNDROME 2		HP:0001118	OMIM:617251	TAS				P		HPO:skoehler	
OMIM	617251	UNCOMBABLE HAIR SYNDROME 2		HP:0002235	OMIM:617251	TAS				P		HPO:skoehler	
OMIM	617251	UNCOMBABLE HAIR SYNDROME 2		HP:0003593	OMIM:617251	TAS				C		HPO:skoehler	
OMIM	617251	UNCOMBABLE HAIR SYNDROME 2		HP:0030056	OMIM:617251	TAS				P		HPO:skoehler	
OMIM	617252	UNCOMBABLE HAIR SYNDROME 3; UHS3		HP:0000007	OMIM:617252	TAS				I		HPO:skoehler	
OMIM	617252	UNCOMBABLE HAIR SYNDROME 3; UHS3		HP:0002212	OMIM:617252	IEA				P		HPO:skoehler	
OMIM	617252	UNCOMBABLE HAIR SYNDROME 3; UHS3		HP:0002235	OMIM:617252	TAS				P		HPO:skoehler	
OMIM	617252	UNCOMBABLE HAIR SYNDROME 3; UHS3		HP:0030056	OMIM:617252	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000007	OMIM:617253	TAS				I		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000252	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000308	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000541	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000819	OMIM:617253	IEA				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000822	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0000956	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0001397	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0001635	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0001714	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0001735	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0001952	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0003016	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0003076	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0003100	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0005112	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0008232	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0010579	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0010609	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0011969	OMIM:617253	TAS				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0031956	OMIM:617253	IEA				P		HPO:skoehler	
OMIM	617253	SECKEL SYNDROME 10; SCKL10		HP:0031964	OMIM:617253	IEA				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0000007	OMIM:617255	TAS				I		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0000252	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0000518	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0000648	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001249	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001250	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001257	OMIM:617255	IEA				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001263	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001339	OMIM:617255	IEA				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001344	OMIM:617255	IEA				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0001762	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0002079	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0002085	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0002119	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0002126	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0002365	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0003236	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0003593	OMIM:617255	TAS				C		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0008936	OMIM:617255	TAS				P		HPO:skoehler	
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0012447	OMIM:617255	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617255	LISSENCEPHALY 8; LIS8		HP:0031936	OMIM:617255	IEA				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000007	OMIM:617258	TAS				I		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000098	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000218	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000347	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000467	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000508	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0000678	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001265	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001284	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001319	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001611	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001761	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0001763	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0002015	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0002359	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0002650	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0002792	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003236	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003306	OMIM:617258	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003388	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003391	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003551	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003677	OMIM:617258	TAS				C		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003691	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003700	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0003798	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0009046	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0010628	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617258	MYOPATHY, MYOFIBRILLAR, 8		HP:0011947	OMIM:617258	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000006	OMIM:617260	TAS				I		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000107	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000110	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000154	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000252	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000280	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000286	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000307	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000319	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000325	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000377	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000494	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000506	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000540	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000582	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0000824	OMIM:617260	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001249	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001263	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001274	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001290	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001643	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001680	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001718	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001762	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0001763	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0002007	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0002079	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0002093	OMIM:617260	TAS	HP:0003623			P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0002119	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0002465	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0004322	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0004383	OMIM:617260	IEA				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0009765	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0011968	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0012745	OMIM:617260	TAS				P		HPO:skoehler	
OMIM	617260	GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF		HP:0031936	OMIM:617260	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000006	PMID:27389779	PCS				I		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000154	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000179	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000286	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000400	PMID:12	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000414	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000463	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000486	PMID:27389779	PCS		HP:0040284		P		HP:probinson	3/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000490	PMID:27389779	PCS		HP:0040284		P		HP:probinson	3/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000506	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000508	PMID:27389779	PCS		HP:0040284		P		HP:probinson	2/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000574	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000639	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000729	PMID:27389779	PCS		HP:0040284		P		HP:probinson	2/3
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0000938	PMID:27389779	PCS		HP:0040284		P		HP:probinson	3/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0001249	PMID:27389779	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0001250	PMID:27389779	PCS	HP:0003593	HP:0040284		P		HP:probinson	6/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0001263	PMID:27389779	PCS		HP:0040284		P		HP:probinson	7/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0001290	PMID:27389779	PCS		HP:0040284		P		HP:probinson	7/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0001999	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0002059	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0002119	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0002353	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0002705	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0005280	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0011220	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0011800	PMID:27389779	PCS				P		HP:probinson	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0031936	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0040288	PMID:27389779	PCS		HP:0040284		P		HP:probinson	4/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0045075	OMIM:617268	IEA				P		HPO:skoehler	
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0100023	PMID:27389779	PCS		HP:0040284		P		HP:probinson	4/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0100704	PMID:27389779	PCS		HP:0040284		P		HP:probinson	3/7
OMIM	617268	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL		HP:0100716	PMID:27389779	PCS		HP:0040284		P		HP:probinson	2/7
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0000007	PMID:25847581	PCS				I		HPO:probinson	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0000718	OMIM:617270	TAS				P		HPO:skoehler	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0000733	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0000750	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001249	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001263	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001264	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001266	OMIM:617270	TAS				P		HPO:skoehler	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001344	OMIM:617270	IEA				P		HPO:skoehler	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0001347	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0002421	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0003577	PMID:25847581	PCS				C		HPO:probinson	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0003676	OMIM:617270	TAS				C		HPO:skoehler	
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0004322	OMIM:617270	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0008936	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0011856	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617270	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 58; MRT58		HP:0100716	PMID:25847581	PCS		HP:0040284		P		HPO:probinson	2/2
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0000007	OMIM:617271	TAS				I		HPO:skoehler	
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0000090	OMIM:617271	TAS				P		HPO:skoehler	
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0000107	OMIM:617271	TAS				P		HPO:skoehler	
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0003676	OMIM:617271	TAS				C		HPO:skoehler	
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0003774	OMIM:617271	TAS				P		HPO:skoehler	
OMIM	617271	NEPHRONOPHTHISIS 20		HP:0003828	OMIM:617271	TAS				C		HPO:skoehler	
OMIM	617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E		HP:0000006	OMIM:617272	TAS				I		HPO:skoehler	
OMIM	617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E		HP:0000485	OMIM:617272	TAS				P		HPO:skoehler	
OMIM	617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E		HP:0000501	OMIM:617272	IEA				P		HPO:skoehler	
OMIM	617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E		HP:0000969	OMIM:617272	IEA				P		HPO:skoehler	
OMIM	617272	GLAUCOMA 3, PRIMARY CONGENITAL, E; GLC3E		HP:0007906	OMIM:617272	IEA				P		HPO:skoehler	
OMIM	617275	TOOTH AGENESIS, SELECTIVE, 9; STHAG9		HP:0000006	OMIM:617275	TAS				I		HPO:skoehler	
OMIM	617275	TOOTH AGENESIS, SELECTIVE, 9; STHAG9		HP:0001592	OMIM:617275	IEA				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0000007	OMIM:617276	TAS				I		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0000252	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0000510	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0000817	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0001263	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0001272	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0001290	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0001344	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0002059	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0002079	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0002133	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0002521	OMIM:617276	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0100660	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617276	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 48		HP:0200134	OMIM:617276	TAS				P		HPO:skoehler	
OMIM	617280	ATRIAL FIBRILLATION, FAMILIAL, 18		HP:0000006	OMIM:617280	TAS				I		HPO:skoehler	
OMIM	617280	ATRIAL FIBRILLATION, FAMILIAL, 18		HP:0001662	OMIM:617280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617280	ATRIAL FIBRILLATION, FAMILIAL, 18		HP:0001962	OMIM:617280	TAS				P		HPO:skoehler	
OMIM	617280	ATRIAL FIBRILLATION, FAMILIAL, 18		HP:0004754	OMIM:617280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617280	ATRIAL FIBRILLATION, FAMILIAL, 18		HP:0004757	OMIM:617280	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000194	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000215	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000238	OMIM:617281	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000280	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000322	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000448	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000527	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0000648	OMIM:617281	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001250	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001257	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001305	OMIM:617281	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001336	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001344	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0001347	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0002007	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0002353	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0002514	OMIM:617281	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0012736	OMIM:617281	TAS				P		HP:probinson	
OMIM	617281	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 49; EIEE49		HP:0200134	OMIM:617281	IEA				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0000007	OMIM:617282	TAS				I		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0000505	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0000639	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0000648	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001251	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001257	OMIM:617282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001260	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001270	OMIM:617282	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001288	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001336	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0001347	OMIM:617282	IEA				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0002015	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0002072	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0003676	OMIM:617282	TAS				C		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0003828	OMIM:617282	TAS				C		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0012179	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617282	DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG		HP:0100660	OMIM:617282	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0000006	OMIM:617284	TAS				I		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0000252	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0000414	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0000483	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0000496	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0001257	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0001260	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0001263	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0001270	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0001336	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0002544	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0003676	OMIM:617284	TAS				C		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0003829	OMIM:617284	TAS				C		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0004322	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0012048	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0012049	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0040083	OMIM:617284	TAS				P		HPO:skoehler	
OMIM	617284	DYSTONIA 28, CHILDHOOD-ONSET		HP:0100543	OMIM:617284	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0000007	OMIM:617290	TAS				I		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001249	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001250	OMIM:617290	IEA				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001263	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001276	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001336	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001942	OMIM:617290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0001999	OMIM:617290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0002093	OMIM:617290	TAS	HP:0003623			P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0002104	OMIM:617290	TAS	HP:0003623			P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0002119	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0002169	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0002465	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0005484	OMIM:617290	TAS				P		HPO:skoehler	
OMIM	617290	EPILEPSY, EARLY-ONSET, VITAMIN B6-DEPENDENT; EPVB6D		HP:0012444	OMIM:617290	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH		HP:0000006	OMIM:617294	TAS				I		HPO:skoehler	
OMIM	617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH		HP:0001810	OMIM:617294	TAS				P		HPO:skoehler	
OMIM	617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH		HP:0002231	OMIM:617294	TAS				P		HPO:skoehler	
OMIM	617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH		HP:0002293	OMIM:617294	IEA				P		HPO:skoehler	
OMIM	617294	EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED, WITH SCARRING AND HAIR LOSS; EBSSH		HP:0007435	OMIM:617294	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000006	OMIM:617296	TAS				I		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000293	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000483	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000490	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000540	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000565	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000639	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0000750	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0001249	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0001258	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0001263	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0001338	OMIM:617296	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0001347	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0002059	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0002509	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0003593	OMIM:617296	TAS				C		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0006956	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0007663	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0008936	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0011220	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617296	SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY		HP:0012448	OMIM:617296	TAS				P		HPO:skoehler	
OMIM	617297	AMELOGENESIS IMPERFECTA, TYPE IJ		HP:0000007	OMIM:617297	TAS				I		HPO:skoehler	
OMIM	617297	AMELOGENESIS IMPERFECTA, TYPE IJ		HP:0000670	OMIM:617297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617297	AMELOGENESIS IMPERFECTA, TYPE IJ		HP:0011094	OMIM:617297	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0000006	OMIM:617300	TAS				I		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0000282	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0001004	OMIM:617300	IEA				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0001631	OMIM:617300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0001698	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0001790	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0001903	OMIM:617300	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0002098	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0002619	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0003828	OMIM:617300	TAS				C		HPO:skoehler	
OMIM	617300	LYMPHATIC MALFORMATION 7; LMPHM7		HP:0100598	OMIM:617300	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000007	OMIM:617301	TAS				I		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000243	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000252	OMIM:617301	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000268	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000278	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000369	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000463	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000508	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000527	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000648	OMIM:617301	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0000648	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001188	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001263	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001276	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001298	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001388	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001762	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0001845	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002015	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002058	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002079	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE	HP:0031796	HP:0002104	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002119	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002169	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002267	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002804	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002816	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002827	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002878	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0002987	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0003273	OMIM:617301	TAS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0003577	OMIM:617301	TAS				C		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0005280	PMID:27773429	PCS				P		HPO:skoehler	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0008936	PMID:27773429	PCS				P		HP:probinson	
OMIM	617301	GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE		HP:0025116	PMID:27773429	PCS				P		HP:probinson	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000007	OMIM:617302	TAS				I		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000252	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000256	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000365	OMIM:617302	IEA				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000400	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000486	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000540	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000545	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000646	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000648	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0000752	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001249	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001263	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001290	OMIM:617302	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001310	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001321	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001344	OMIM:617302	IEA				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0001349	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0002352	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0002487	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0003593	OMIM:617302	TAS				C		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0004322	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0011800	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617302	OPTIC ATROPHY 11; OPA11		HP:0012444	OMIM:617302	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000007	OMIM:617303	TAS				I		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000092	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000093	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000097	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000158	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000280	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000286	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000431	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000445	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000470	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000506	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000527	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000648	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000664	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000767	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000768	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0000943	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001007	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001263	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001371	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001403	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001639	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001643	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001744	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001760	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001873	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0001903	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002098	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002205	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002208	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002240	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002514	OMIM:617303	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002680	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0002869	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0003593	OMIM:617303	TAS				C		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0005528	OMIM:617303	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0008807	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0011220	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0012444	OMIM:617303	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0012448	OMIM:617303	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617303	MUCOPOLYSACCHARIDOSIS-PLUS SYNDROME		HP:0012471	OMIM:617303	TAS				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0000007	OMIM:617304	TAS				I		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0000510	OMIM:617304	IEA				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0000662	OMIM:617304	TAS				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0001105	OMIM:617304	IEA				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77	HP:0003676	HP:0007663	OMIM:617304	TAS				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0007787	OMIM:617304	TAS				P		HPO:skoehler	
OMIM	617304	RETINITIS PIGMENTOSA 77; RP77		HP:0011505	OMIM:617304	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000007	OMIM:617306	TAS				I		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000256	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000347	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000358	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000568	OMIM:617306	IEA				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000586	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0000589	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0001290	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0002007	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0004467	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617306	COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD		HP:0011002	OMIM:617306	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0000007	OMIM:617308	TAS				I		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0000511	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0000750	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0001256	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0001263	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0001310	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0001350	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0002570	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0003593	OMIM:617308	TAS				C		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0045014	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617308	BILE ACID SYNTHESIS DEFECT, CONGENITAL, 6		HP:0100512	OMIM:617308	TAS				P		HPO:skoehler	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0000007	PMID:27839872	PCS				I	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0001087	PMID:11403040	PCS				P	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0007957	PMID:11403040	PCS				P	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011484	PMID:11403040	PCS				P	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011490	PMID:11403040	PCS				P	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617315	Anterior segment dysgenesis 6, multiple subtypes		HP:0011496	PMID:11403040	PCS				P	ANTERIOR SEGMENT DYSGENESIS 6, MULTIPLE SUBTYPES	HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0000007	PMID:27839872	PCS				I		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0000518	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0001083	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0001093	OMIM:617319	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0007676	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0009917	OMIM:617319	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0009918	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0012376	OMIM:617319	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0012805	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0025358	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617319	ANTERIOR SEGMENT DYSGENESIS 8		HP:0100693	PMID:27839872	PCS				P		HPO:probinson	
OMIM	617320	Ichthyosis, congenital, autosomal recessive 12		HP:0000007	PMID:27494380	PCS				I	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12	HPO:probinson	
OMIM	617320	Ichthyosis, congenital, autosomal recessive 12		HP:0040190	PMID:27494380	PCS				P	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 12	HPO:probinson	
OMIM	617321	Yao syndrome		HP:0000155	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	14/52
OMIM	617321	Yao syndrome		HP:0000217	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0000787	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0000988	PMID:26070941	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	49/54
OMIM	617321	Yao syndrome		HP:0001097	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0001369	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	41/52
OMIM	617321	Yao syndrome		HP:0001426	PMID:27984003	PCS				I	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0001701	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0001714	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0001824	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	22/54
OMIM	617321	Yao syndrome		HP:0001954	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	35/52
OMIM	617321	Yao syndrome		HP:0002014	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	34/52
OMIM	617321	Yao syndrome		HP:0002027	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	34/52
OMIM	617321	Yao syndrome		HP:0002099	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0002102	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0002829	PMID:27984003	PCS				P	YAO SYNDROME	HP:probinson	
OMIM	617321	Yao syndrome		HP:0003326	PMID:26070941	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	19/54
OMIM	617321	Yao syndrome		HP:0003565	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	14/48
OMIM	617321	Yao syndrome		HP:0100749	PMID:27984003	PCS		HP:0040284		P	YAO SYNDROME	HP:probinson	7/52
OMIM	617323	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59		HP:0000007	OMIM:617323	TAS				I		HPO:skoehler	
OMIM	617323	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59		HP:0000718	OMIM:617323	TAS				P		HPO:skoehler	
OMIM	617323	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59		HP:0001249	OMIM:617323	TAS				P		HPO:skoehler	
OMIM	617323	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59		HP:0011999	OMIM:617323	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000006	OMIM:617330	TAS				I		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000028	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000054	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000076	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000219	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000252	OMIM:617330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000276	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000286	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000300	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000316	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000325	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000331	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000348	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000358	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000369	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000396	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000426	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000455	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000483	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000486	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000490	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000494	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000664	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000733	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0000750	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001249	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001260	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001263	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001272	OMIM:617330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001290	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001310	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0001558	OMIM:617330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002002	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002015	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002020	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002058	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002186	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002421	OMIM:617330	IEA				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0002714	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0003186	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0003593	OMIM:617330	TAS				C		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0004322	OMIM:617330	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0011220	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0011228	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0011822	OMIM:617330	TAS				P		HPO:skoehler	
OMIM	617330	HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS		HP:0031936	OMIM:617330	IEA				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000006	OMIM:617333	TAS				I		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000154	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000160	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000252	OMIM:617333	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000311	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000316	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000322	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000337	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000343	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000377	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000431	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000486	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000494	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000508	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000581	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0000750	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0001249	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0001263	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0001290	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0001511	OMIM:617333	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0001762	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0002714	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0003577	OMIM:617333	TAS				C		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0003828	OMIM:617333	TAS				C		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0004322	OMIM:617333	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0011968	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0012368	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0012385	OMIM:617333	TAS				P		HPO:skoehler	
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0012447	OMIM:617333	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617333	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP		HP:0031936	OMIM:617333	IEA				P		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0000007	OMIM:617336	TAS				I		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0000218	OMIM:617336	TAS				P		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0000767	OMIM:617336	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0001638	OMIM:617336	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0001761	OMIM:617336	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0001762	OMIM:617336	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0002515	OMIM:617336	IEA				P		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0002792	OMIM:617336	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0003391	OMIM:617336	TAS				P		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0003677	OMIM:617336	TAS				C		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0003691	OMIM:617336	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0003798	OMIM:617336	IEA				P		HPO:skoehler	
OMIM	617336	NEMALINE MYOPATHY 11, AUTOSOMAL RECESSIVE; NEM11		HP:0010628	OMIM:617336	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0000006	OMIM:617337	TAS				I		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0000322	OMIM:617337	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0000695	OMIM:617337	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0000962	OMIM:617337	IEA				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0000966	OMIM:617337	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0007387	OMIM:617337	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0008404	OMIM:617337	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0011120	OMIM:617337	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0032152	OMIM:617337	IEA				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0040154	OMIM:617337	TAS				P		HPO:skoehler	
OMIM	617337	ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE; ECTD12		HP:0040162	OMIM:617337	IEA				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0000007	OMIM:617339	TAS				I		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0000486	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0000510	OMIM:617339	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51	HP:0012837	HP:0001250	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001263	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001265	OMIM:617339	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001272	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001332	OMIM:617339	IEA				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001344	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0001508	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002019	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002079	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002151	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002421	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002490	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002540	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0002558	OMIM:617339	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0003202	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0003487	OMIM:617339	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0011968	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0012448	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617339	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 51; EIEE51		HP:0200134	OMIM:617339	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0000007	OMIM:617341	TAS				I		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0000938	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001251	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001257	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001332	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001409	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001511	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0001876	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0002040	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0002216	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0002239	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617341	CEREBRORETINAL MICROANGIOPATHY WITH CALCIFICATIONS AND CYSTS 2		HP:0007763	OMIM:617341	TAS				P		HPO:skoehler	
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0000006	OMIM:617343	TAS				I		HPO:skoehler	
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0000787	OMIM:617343	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0000938	OMIM:617343	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0003072	OMIM:617343	TAS				P		HPO:skoehler	
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0006780	OMIM:617343	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617343	HYPERPARATHYROIDISM 4		HP:0008200	OMIM:617343	TAS				P		HPO:skoehler	
OMIM	617349	AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO		HP:0000006	OMIM:617349	TAS				I		HPO:skoehler	
OMIM	617349	AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO		HP:0002647	OMIM:617349	TAS				P		HPO:skoehler	
OMIM	617349	AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO		HP:0003828	OMIM:617349	TAS				C		HPO:skoehler	
OMIM	617349	AORTIC ANEURYSM, FAMILIAL THORACIC 11, SUSCEPTIBILITY TO		HP:0003829	OMIM:617349	TAS				C		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0000007	OMIM:617350	TAS				I		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0001257	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0001263	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0001290	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0002070	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0002123	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0002373	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0006813	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0007256	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0007270	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0007281	OMIM:617350	IEA				P		HPO:skoehler	
OMIM	617350	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 52; EIEE52		HP:0200134	OMIM:617350	TAS				P		HPO:skoehler	
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000085	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000268	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000278	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000286	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000325	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000358	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0000957	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001034	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001270	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	2/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001290	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	4/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001508	PMID:26248010	PCS	HP:0003577	HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	8/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0001511	PMID:26248010	PCS	HP:0030674			P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0002650	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0003307	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0003510	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	8/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0004691	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	1/8
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0011968	PMID:26248010	PCS	HP:0003577			P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	
OMIM	617352	Mulchandani-Bhoj-Conlin syndrome		HP:0030084	PMID:26248010	PCS		HP:0040284		P	MULCHANDANI-BHOJ-CONLIN SYNDROME	HP:probinson	2/8
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000006	OMIM:617360	TAS				I		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000160	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000219	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000252	OMIM:617360	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000286	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000316	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000322	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000358	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000369	OMIM:617360	IEA				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000431	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000486	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000508	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000582	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0000750	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001249	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001250	OMIM:617360	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001263	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001274	OMIM:617360	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001290	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001382	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001629	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0001631	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0002079	OMIM:617360	IEA				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0002472	OMIM:617360	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0011968	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0012385	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0012745	OMIM:617360	IEA				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0030084	OMIM:617360	TAS				P		HPO:skoehler	
OMIM	617360	CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD		HP:0031936	OMIM:617360	IEA				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000006	OMIM:617364	TAS				I		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000252	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000426	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000639	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000687	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000691	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000750	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000958	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0000963	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0001159	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0001263	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0001290	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0001808	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0002209	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0002650	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0005280	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0006323	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0011220	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0011304	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617364	CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA		HP:0011968	OMIM:617364	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000007	OMIM:617370	TAS				I		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000011	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000121	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000348	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000358	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000369	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000518	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0000639	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0001258	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0001263	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0001290	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0001347	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0003186	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617370	PEROXISOME BIOGENESIS DISORDER 10B		HP:0006579	OMIM:617370	TAS				P		HPO:skoehler	
OMIM	617383	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2		HP:0000006	PMID:27330106	PCS				I		HPO:skoehler	
OMIM	617383	AVASCULAR NECROSIS OF FEMORAL HEAD, PRIMARY, 2		HP:0005743	PMID:27330106	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0000007	PMID:28132689	PCS				I		HPO:skoehler	
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0000639	PMID:28132689	PCS		HP:0040284		P		HPO:skoehler	1/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0000750	PMID:28132689	PCS		HP:0040284		P		HPO:skoehler	2/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0001256	PMID:28132689	PCS		HP:0040284		P		HPO:skoehler	3/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0001263	PMID:28132689	PCS		HP:0040284		P		HPO:skoehler	4/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0001276	OMIM:617384	IEA				P		HPO:skoehler	
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0001300	PMID:28132689	PCS		HP:0040284		P		HPO:lccarmody	1/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0002067	OMIM:617384	IEA				P		HPO:lccarmody	
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0002136	OMIM:617384	IEA				P		HPO:skoehler	
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0002509	PMID:28132689	PCS		HP:0040284		P		HPO:lccarmody	1/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0007018	PMID:28132689	PCS		HP:0040284		P		HPO:lccarmody	1/5
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0008936	PMID:28132689	PCS		HP:0040284		P		HPO:lccarmody	1/6
OMIM	617384	HYPERPHENYLALANINEMIA, MILD, NON-BH4-DEFICIENT; HPANBH4		HP:0010553	PMID:28132689	PCS		HP:0040284		P		HPO:lccarmody	1/6
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000006	OMIM:617388	TAS				I		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000007	OMIM:617388	TAS				I		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000554	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000613	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000958	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0000962	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0001097	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0001508	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK	HP:0012826	HP:0001510	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0001744	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0001890	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0003261	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0003493	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0005764	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0011496	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0011859	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0025092	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0032061	OMIM:617388	IEA				P		HPO:skoehler	
OMIM	617388	AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK		HP:0100646	OMIM:617388	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0000007	OMIM:617389	TAS				I		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0000505	OMIM:617389	IEA				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0001290	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002079	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002133	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002151	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002187	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002344	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002510	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0002521	OMIM:617389	IEA				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0003236	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0011968	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617389	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 53; EIEE53		HP:0200134	OMIM:617389	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0000006	OMIM:617391	TAS				I		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0000252	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0001249	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0001250	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0001263	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0001290	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0001344	OMIM:617391	IEA				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0002119	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0002353	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0003593	OMIM:617391	TAS				C		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0012448	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617391	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 54; EIEE54		HP:0200134	OMIM:617391	TAS				P		HPO:skoehler	
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000007	OMIM:617392	TAS				I		HPO:skoehler	
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000294	OMIM:617392	TAS				P		HPO:skoehler	
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000316	OMIM:617392	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000431	OMIM:617392	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000653	OMIM:617392	TAS				P		HPO:skoehler	
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0000677	OMIM:617392	IEA				P		HPO:skoehler	
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0005280	OMIM:617392	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0012471	OMIM:617392	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617392	ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE; ECTD13		HP:0045074	OMIM:617392	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000006	OMIM:617393	TAS				I		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000252	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000455	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000518	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000733	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0000737	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001249	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001250	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001257	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001263	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001290	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001344	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001371	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0001508	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0002059	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0002355	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0002421	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0002650	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0011968	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617393	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION		HP:0012448	OMIM:617393	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0000007	OMIM:617394	TAS				I		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0000952	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0000989	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0001394	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0001409	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0001744	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0002240	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0002613	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0002910	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0003593	OMIM:617394	TAS				C		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0003676	OMIM:617394	TAS				C		HPO:skoehler	
OMIM	617394	SCLEROSING CHOLANGITIS, NEONATAL		HP:0030991	OMIM:617394	TAS				P		HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0000007	OMIM:617395	TAS				I	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0001250	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0001263	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0002079	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0002506	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0002510	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0002910	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0003593	OMIM:617395	TAS				C	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0005484	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0012345	OMIM:617395	IEA				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617395	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq; CDG2Q		HP:0012506	OMIM:617395	TAS				P	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIQ; CDG2Q	HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0000007	OMIM:617396	TAS				I		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0000158	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0000470	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0000668	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0000914	OMIM:617396	IEA				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0001156	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0001371	OMIM:617396	IEA				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0001792	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0002164	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0002673	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0002750	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0002812	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0002967	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0003300	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0003307	OMIM:617396	IEA				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0003423	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0004482	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0008070	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0008802	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0008824	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0010646	OMIM:617396	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0011800	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0100255	OMIM:617396	IEA				P		HPO:skoehler	
OMIM	617396	ANAUXETIC DYSPLASIA 2; ANXD2		HP:0100864	OMIM:617396	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0000007	OMIM:617397	TAS				I		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0000252	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0000967	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001250	OMIM:617397	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001254	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001290	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001321	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001342	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001410	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001541	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001643	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001662	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0001873	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002093	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002119	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002126	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002240	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002282	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002514	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0002910	OMIM:617397	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0003128	OMIM:617397	TAS				P		HPO:skoehler	
OMIM	617397	PSEUDO-TORCH SYNDROME 2		HP:0003577	OMIM:617397	TAS				C		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000007	OMIM:617402	TAS				I		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000218	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000307	OMIM:617402	IEA				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000316	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000325	OMIM:617402	IEA				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000343	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000369	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000455	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000621	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000639	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0000678	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001188	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001290	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001385	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001388	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001519	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001601	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001631	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001634	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001659	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001762	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0001763	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0002751	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0003758	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0004322	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0004325	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0005180	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0006380	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0008689	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0009933	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0010761	OMIM:617402	TAS				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0011712	OMIM:617402	IEA				P		HPO:skoehler	
OMIM	617402	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IIC; ARCL2C		HP:0200128	OMIM:617402	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000007	OMIM:617403	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000023	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000054	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000278	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000298	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000316	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000325	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000369	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000400	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000411	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000414	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000431	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000494	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000518	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000581	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000621	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0000750	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001250	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001270	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001290	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001508	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001519	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001631	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001635	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0001639	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0002079	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0002171	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617403	CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IID; ARCL2D		HP:0011712	OMIM:617403	IEA				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0000007	OMIM:617404	TAS				I		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0000252	OMIM:617404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0000486	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0000518	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0001249	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0001250	OMIM:617404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0001263	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0001270	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0001290	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0002061	OMIM:617404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0002093	OMIM:617404	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0002650	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0003236	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0003306	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0003307	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0003391	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0003676	OMIM:617404	TAS				C		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0004322	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0009126	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617404	MUSCULAR DYSTROPHY, CONGENITAL, WITH CATARACTS AND INTELLECTUAL DISABILITY		HP:0040083	OMIM:617404	TAS				P		HPO:skoehler	
OMIM	617405	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY		HP:0000007	OMIM:617405	TAS				I		HPO:skoehler	
OMIM	617405	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	617405	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY		HP:0001156	OMIM:617405	TAS				P		HPO:skoehler	
OMIM	617405	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY		HP:0004322	OMIM:617405	TAS				P		HPO:skoehler	
OMIM	617405	SHORT-RIB THORACIC DYSPLASIA 17 WITH OR WITHOUT POLYDACTYLY		HP:0010442	OMIM:617405	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000007	PMID:27008867	PCS				I		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000085	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000510	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000545	OMIM:617406	IEA				P		HPO:skoehler	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000548	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000618	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000668	OMIM:617406	IEA				P		HPO:skoehler	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0000750	PMID:26854863	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0001105	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0001133	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0001162	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0001513	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0002910	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0007750	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0030329	PMID:26854863	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0030483	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617406	BARDET-BIEDL SYNDROME 21; BBS21		HP:0030631	PMID:27008867	PCS				P		HPO:probinson	
OMIM	617408	DIAMOND-BLACKFAN ANEMIA 16		HP:0000006	OMIM:617408	TAS				I		HPO:skoehler	
OMIM	617408	DIAMOND-BLACKFAN ANEMIA 16		HP:0001631	OMIM:617408	TAS				P		HPO:skoehler	
OMIM	617408	DIAMOND-BLACKFAN ANEMIA 16		HP:0001642	OMIM:617408	TAS				P		HPO:skoehler	
OMIM	617408	DIAMOND-BLACKFAN ANEMIA 16		HP:0001903	OMIM:617408	TAS				P		HPO:skoehler	
OMIM	617409	DIAMOND-BLACKFAN ANEMIA 17		HP:0000006	PMID:25424902	PCS				I		HPO:skoehler	
OMIM	617409	DIAMOND-BLACKFAN ANEMIA 17		HP:0000953	PMID:25424902	PCS				P		HP:probinson	
OMIM	617409	DIAMOND-BLACKFAN ANEMIA 17		HP:0001903	PMID:25424902	PCS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000006	OMIM:617412	TAS				I		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000175	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000218	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000252	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000286	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000369	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000377	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000405	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000527	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000574	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000729	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0000954	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0001256	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0001270	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0001290	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0002299	OMIM:617412	IEA				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0002553	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0004322	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0005280	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0005469	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617412	BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD		HP:0011069	OMIM:617412	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000007	OMIM:617425	TAS				I		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000253	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000280	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000293	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000316	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000448	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000455	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000767	OMIM:617425	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000926	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0000954	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001019	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001156	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001216	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001249	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001250	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001270	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001407	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001880	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0001888	OMIM:617425	IEA				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0002023	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0002656	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0002673	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0002719	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA	HP:0003676	HP:0002751	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0003083	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0003090	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0003375	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0003498	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0004313	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0005280	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0008462	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0008936	OMIM:617425	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617425	IMMUNOSKELETAL DYSPLASIA WITH NEURODEVELOPMENTAL ABNORMALITIES; ISDNA		HP:0100255	OMIM:617425	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0000007	OMIM:617432	TAS				I		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0000252	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0000823	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0001256	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0001263	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0001518	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0002750	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0003828	OMIM:617432	TAS				C		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0004322	OMIM:617432	TAS				P		HPO:skoehler	
OMIM	617432	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60		HP:0012448	OMIM:617432	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0000007	OMIM:617433	TAS				I		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0000543	OMIM:617433	TAS				P		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0000662	OMIM:617433	IEA				P		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0001123	OMIM:617433	TAS				P		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0007663	OMIM:617433	TAS				P		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0011505	OMIM:617433	TAS				P		HPO:skoehler	
OMIM	617433	RETINITIS PIGMENTOSA 78; RP78		HP:0030786	OMIM:617433	TAS				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001250	OMIM:617435	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001257	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001263	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001272	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001332	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001337	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001344	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0001773	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002015	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002059	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002067	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002317	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002340	OMIM:617435	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002376	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002650	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0002808	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0007256	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0008936	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0010864	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0011448	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0011968	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617435	LOPES-MACIEL-RODAN SYNDROME; LOMARS		HP:0200055	OMIM:617435	IEA				P		HPO:skoehler	
OMIM	617439	CRANIOSYNOSTOSIS 7		HP:0000006	OMIM:617439	TAS				I		HPO:skoehler	
OMIM	617439	CRANIOSYNOSTOSIS 7		HP:0000750	OMIM:617439	TAS				P		HPO:skoehler	
OMIM	617439	CRANIOSYNOSTOSIS 7		HP:0001363	OMIM:617439	TAS				P		HPO:skoehler	
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0000007	OMIM:617441	TAS				I		HPO:skoehler	
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0001744	OMIM:617441	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0001873	OMIM:617441	TAS				P		HPO:skoehler	
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0001903	OMIM:617441	TAS				P		HPO:skoehler	
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0004823	OMIM:617441	TAS				P		HPO:skoehler	
OMIM	617441	THROMBOCYTOPENIA, ANEMIA, AND MYELOFIBROSIS; THAMY		HP:0011974	OMIM:617441	IEA				P		HPO:skoehler	
OMIM	617442	PREMATURE OVARIAN FAILURE 13		HP:0000007	OMIM:617442	TAS				I		HPO:skoehler	
OMIM	617442	PREMATURE OVARIAN FAILURE 13		HP:0000876	OMIM:617442	TAS				P		HPO:skoehler	
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0000006	OMIM:617443	IEA				I		HPO:skoehler	
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0000007	OMIM:617443	IEA				I		HPO:skoehler	
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0000132	OMIM:617443	IEA				P		HPO:skoehler	
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0000964	OMIM:617443	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0001873	OMIM:617443	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0003540	OMIM:617443	IEA				P		HPO:skoehler	
OMIM	617443	BLEEDING DISORDER, PLATELET-TYPE, 21; BDPLT21		HP:0003765	OMIM:617443	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000006	OMIM:617450	TAS				I		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000154	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000219	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000337	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000358	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000369	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000463	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000486	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000540	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000722	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000729	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000739	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0000750	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001156	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001249	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001263	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001290	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001773	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0001792	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD	HP:0031796	HP:0002013	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0002019	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0002020	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0002136	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0003307	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0004322	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0007018	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0011968	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617450	INTELLECTUAL DEVELOPMENTAL DISORDER WITH GASTROINTESTINAL DIFFICULTIES AND HIGH PAIN THRESHOLD		HP:0200055	OMIM:617450	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000007	OMIM:617452	TAS				I		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000028	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000218	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000219	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000248	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000252	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000276	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000278	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000343	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000365	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000369	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000400	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000411	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000426	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000431	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000470	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000494	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000527	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000637	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000729	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0000960	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001182	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001250	OMIM:617452	IEA				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001263	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001290	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001371	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001508	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001511	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001762	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0001845	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002079	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002119	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002510	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002540	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002553	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0002650	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0004322	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0005469	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0010864	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0011304	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617452	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA		HP:0011968	OMIM:617452	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0000006	OMIM:617460	TAS				I		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0000543	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0000613	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0000662	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0001133	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0007401	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617460	RETINITIS PIGMENTOSA 79		HP:0007663	OMIM:617460	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000006	OMIM:617466	TAS				I		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000047	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000136	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000143	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000378	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0000396	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0002023	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0002650	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0003298	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0004736	OMIM:617466	TAS				P		HPO:skoehler	
OMIM	617466	TOWNES-BROCKS SYNDROME 2; TBS2		HP:0008551	OMIM:617466	IEA				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000007	OMIM:617468	TAS				I		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000218	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000278	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000341	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000347	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000411	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000508	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000565	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0000678	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0001250	OMIM:617468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0001284	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0001290	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0001762	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0001989	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0002089	OMIM:617468	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0002421	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0002804	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0002987	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0003273	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0003577	OMIM:617468	TAS				C		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0003691	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0005684	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0006380	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0006466	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0006659	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617468	ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC, WITH MYELIN DEFECT		HP:0012385	OMIM:617468	TAS				P		HPO:skoehler	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0000369	PMID:28369036	PCS				P		HP:probinson	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0000377	OMIM:617475	IEA				P		HPO:skoehler	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0000403	OMIM:617475	IEA				P		HPO:skoehler	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0001508	PMID:28369036	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0001808	PMID:28369036	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0001873	OMIM:617475	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0001875	PMID:28369036	PCS		HP:0040284		P		HPO:skoehler	4/4
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0001903	OMIM:617475	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0002164	PMID:28369036	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0002718	PMID:28369036	PCS				P		HP:probinson	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0002863	OMIM:617475	IEA				P		HPO:skoehler	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0003577	PMID:28369036	PCS				C		HPO:skoehler	
OMIM	617475	SPECIFIC GRANULE DEFICIENCY 2; SGD2		HP:0012551	PMID:28369036	PCS				P		HP:probinson	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0000007	OMIM:617478	TAS				I		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0000083	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0000107	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0000252	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0001338	OMIM:617478	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0001629	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0001631	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0001636	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0001660	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0005301	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0007430	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0010773	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0011611	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0011662	OMIM:617478	IEA				P		HPO:skoehler	
OMIM	617478	STRUCTURAL HEART DEFECTS AND RENAL ANOMALIES SYNDROME; SHDRA		HP:0012020	OMIM:617478	TAS				P		HPO:skoehler	
OMIM	617480	46,XX SEX REVERSAL 4; SRXX4		HP:0000054	OMIM:617480	IEA				P		HPO:skoehler	
OMIM	617480	46,XX SEX REVERSAL 4; SRXX4		HP:0000062	OMIM:617480	IEA				P		HPO:skoehler	
OMIM	617480	46,XX SEX REVERSAL 4; SRXX4		HP:0000808	OMIM:617480	IEA				P		HPO:skoehler	
OMIM	617480	46,XX SEX REVERSAL 4; SRXX4		HP:0003829	OMIM:617480	IEA				C		HPO:skoehler	
OMIM	617480	46,XX SEX REVERSAL 4; SRXX4		HP:0008665	OMIM:617480	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000252	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000400	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000411	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000518	OMIM:617481	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000520	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0000648	OMIM:617481	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0001250	OMIM:617481	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0001272	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0001285	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0001290	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0001357	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0002079	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0002120	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0002169	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0003202	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0003577	OMIM:617481	IEA				C		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0003676	OMIM:617481	IEA				C		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0012448	OMIM:617481	IEA				P		HPO:skoehler	
OMIM	617481	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND VARIABLE BRAIN ANOMALIES; NMIHBA		HP:0012736	OMIM:617481	TAS				P		HP:probinson	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0000252	OMIM:617493	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001249	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001250	OMIM:617493	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001257	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001263	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001332	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0001344	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002059	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002072	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002079	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002119	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002305	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002421	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0002487	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617493	NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM		HP:0100660	OMIM:617493	IEA				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000006	OMIM:617506	TAS				I		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000028	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000218	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000256	OMIM:617506	IEA				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000316	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000358	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000369	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000391	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000396	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000465	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000470	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000475	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000494	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000508	OMIM:617506	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000609	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000750	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000767	OMIM:617506	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000768	OMIM:617506	IEA				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000957	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0000963	OMIM:617506	IEA				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001263	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001290	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001305	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001363	OMIM:617506	TAS		HP:0040283		P		HPO:skoehler	HP:0040283
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001363	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001382	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001480	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001508	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001629	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001642	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001643	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001653	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001655	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0001680	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0002217	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0002750	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0004322	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0004969	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0007099	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0008070	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0010648	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0011220	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617506	NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2		HP:0011712	OMIM:617506	TAS				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000278	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000286	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000293	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000340	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000341	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000648	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0000969	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001263	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL	HP:0003676	HP:0001272	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001302	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001319	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001336	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001344	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0001347	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002079	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002119	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002126	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002133	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002187	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0002521	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL		HP:0006829	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617507	PEHO-LIKE SYNDROME; PEHOL	HP:0003676	HP:0007105	OMIM:617507	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0001873	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0001878	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0002716	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0002719	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0002721	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0002958	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617514	IMMUNODEFICIENCY 52; IMD52		HP:0004313	OMIM:617514	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000047	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000049	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000054	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000278	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000316	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000324	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000347	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000365	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000369	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000486	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000639	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0000750	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001249	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001250	OMIM:617516	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001263	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001643	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001660	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0001671	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0009777	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0009778	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0012683	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617516	STANKIEWICZ-ISIDOR SYNDROME; STISS		HP:0100704	OMIM:617516	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0001250	OMIM:617519	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0001263	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0001284	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0001344	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0002058	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0003577	OMIM:617519	IEA				C		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0003693	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0003700	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0006829	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0007108	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617519	NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND		HP:0010628	OMIM:617519	IEA				P		HPO:skoehler	
OMIM	617520	MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT; MCPH18		HP:0000006	OMIM:617520	TAS				I		HPO:nvasilevsky	
OMIM	617520	MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT; MCPH18		HP:0000252	OMIM:617520	TAS				P		HPO:nvasilevsky	
OMIM	617520	MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT; MCPH18		HP:0001256	OMIM:617520	TAS				P		HPO:nvasilevsky	
OMIM	617520	MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT; MCPH18		HP:0002342	OMIM:617520	TAS				P		HPO:nvasilevsky	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000218	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000219	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000483	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000486	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000494	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000508	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000527	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000543	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000639	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000646	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0000649	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0001249	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0001270	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0002359	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617523	NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM		HP:0012110	OMIM:617523	IEA				P		HPO:skoehler	
OMIM	617524	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2; EKVP2		HP:0000982	OMIM:617524	IEA				P		HPO:skoehler	
OMIM	617524	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 2; EKVP2		HP:0010783	OMIM:617524	IEA				P		HPO:skoehler	
OMIM	617525	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3; EKVP3		HP:0000982	OMIM:617525	IEA				P		HPO:skoehler	
OMIM	617525	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3; EKVP3		HP:0010783	OMIM:617525	IEA				P		HPO:skoehler	
OMIM	617525	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3; EKVP3		HP:0025092	OMIM:617525	IEA				P		HPO:skoehler	
OMIM	617525	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 3; EKVP3		HP:0025114	OMIM:617525	IEA				P		HPO:skoehler	
OMIM	617526	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4; EKVP4		HP:0000007	OMIM:617526	TAS				I		HPO:skoehler	
OMIM	617526	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4; EKVP4		HP:0000972	OMIM:617526	IEA				P		HPO:skoehler	
OMIM	617526	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4; EKVP4		HP:0010783	OMIM:617526	IEA				P		HPO:skoehler	
OMIM	617526	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 4; EKVP4		HP:0025092	OMIM:617526	TAS				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000218	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000319	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000338	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000343	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000347	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000358	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000369	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000639	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000648	OMIM:617527	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000954	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000969	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0000975	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001249	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001250	OMIM:617527	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001263	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001276	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001283	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0001838	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002015	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002033	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002063	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002079	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002093	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002104	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002119	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002120	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0002267	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0003577	OMIM:617527	IEA				C		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0003828	OMIM:617527	IEA				C		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0005781	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0006980	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0010804	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0011398	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0012448	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0100259	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617527	NEURODEVELOPMENTAL DISORDER WITH PROGRESSIVE MICROCEPHALY, SPASTICITY, AND BRAIN ANOMALIES; NDMSBA		HP:0100807	OMIM:617527	IEA				P		HPO:skoehler	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000007	OMIM:617532	TAS				I		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000233	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000316	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000319	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000325	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000494	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0000739	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0001250	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0001263	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0001290	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0002342	OMIM:617532	TAS				P		HPO:skoehler	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0002553	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0005280	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617532	INTELLECTUAL DEVELOPMENTAL DISORDER WITH NEUROPSYCHIATRIC FEATURES; IDDNPF		HP:0008770	OMIM:617532	TAS				P		HPO:nvasilevsky	
OMIM	617537	RAHMAN SYNDROME		HP:0000006	OMIM:617537	TAS				I		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000256	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000293	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000483	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000486	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000506	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0000646	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0001249	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0001263	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0001276	OMIM:617537	TAS	HP:0003623			P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0001319	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0001762	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0002751	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0003764	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0005616	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617537	RAHMAN SYNDROME		HP:0012385	OMIM:617537	TAS				P		HPO:skoehler	
OMIM	617540	PITUITARY ADENOMA 5, MULTIPLE TYPES; PITA5		HP:0003581	OMIM:617540	IEA				C		HPO:skoehler	
OMIM	617540	PITUITARY ADENOMA 5, MULTIPLE TYPES; PITA5		HP:0003829	OMIM:617540	IEA				C		HPO:skoehler	
OMIM	617542	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2; HGPPS2		HP:0001249	OMIM:617542	IEA				P		HPO:skoehler	
OMIM	617542	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2; HGPPS2		HP:0001263	OMIM:617542	IEA				P		HPO:skoehler	
OMIM	617542	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2; HGPPS2		HP:0001274	OMIM:617542	IEA				P		HPO:skoehler	
OMIM	617542	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2; HGPPS2		HP:0001335	OMIM:617542	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617542	GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2; HGPPS2		HP:0001347	OMIM:617542	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617547	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA; RDMS		HP:0000556	OMIM:617547	IEA				P		HPO:skoehler	
OMIM	617547	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA; RDMS		HP:0000603	OMIM:617547	IEA				P		HPO:skoehler	
OMIM	617547	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA; RDMS		HP:0000613	OMIM:617547	IEA				P		HPO:skoehler	
OMIM	617547	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA; RDMS		HP:0000662	OMIM:617547	IEA				P		HPO:skoehler	
OMIM	617547	RETINAL DYSTROPHY WITH OR WITHOUT MACULAR STAPHYLOMA; RDMS		HP:0100018	OMIM:617547	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000179	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000272	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000307	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000324	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000337	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000358	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000377	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000486	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000494	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000629	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0000750	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0001249	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0001263	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0001332	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0001337	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0001388	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0002119	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0002500	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0002515	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0012448	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617557	GABRIELE-DE VRIES SYNDROME; GADEVS		HP:0100807	OMIM:617557	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0000007	OMIM:617560	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0000571	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0000639	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0001257	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0001260	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0001270	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0001272	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0001332	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0002070	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0002078	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0002415	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0003593	OMIM:617560	IEA				C		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0003676	OMIM:617560	IEA				C		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0007256	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617560	SPASTIC ATAXIA 8, AUTOSOMAL RECESSIVE, WITH HYPOMYELINATING LEUKODYSTROPHY; SPAX8		HP:0100543	OMIM:617560	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000098	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000278	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000286	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000311	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000316	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000337	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000369	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000400	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000431	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000494	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000508	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000518	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000545	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000750	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0000938	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001176	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001249	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001263	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001288	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001388	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001643	OMIM:617561	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001792	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001816	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0001833	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0002370	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0002650	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0002673	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0002866	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0003577	OMIM:617561	IEA				C		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0005280	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0005616	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0011304	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0012385	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0100807	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617561	COHEN-GIBSON SYNDROME; COGIS		HP:0400004	OMIM:617561	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0000488	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0000657	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0001249	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0001251	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0001263	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0001321	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0002085	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617562	MECKEL SYNDROME 13; MKS13		HP:0002419	OMIM:617562	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0000278	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0000488	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0000508	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0000657	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0001251	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0001263	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0002104	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0002119	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0002282	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0002419	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0002540	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0010864	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0011802	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617563	OROFACIODIGITAL SYNDROME XVI; OFD16		HP:0012745	OMIM:617563	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0000089	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0000160	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0000369	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0000508	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0008551	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617564	MEIER-GORLIN SYNDROME 8; MGORS8		HP:0012471	OMIM:617564	IEA				P		HPO:skoehler	
OMIM	617565	PERRAULT SYNDROME 6; PRLTS6		HP:0000013	OMIM:617565	IEA				P		HPO:skoehler	
OMIM	617565	PERRAULT SYNDROME 6; PRLTS6		HP:0000869	OMIM:617565	IEA				P		HPO:skoehler	
OMIM	617565	PERRAULT SYNDROME 6; PRLTS6		HP:0008209	OMIM:617565	IEA				P		HPO:skoehler	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0000007	OMIM:617571	TAS				I		HPO:nvasilevsky	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0000962	OMIM:617571	IEA				P		HPO:skoehler	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0000989	OMIM:617571	IEA				P		HPO:skoehler	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0010783	OMIM:617571	IEA				P		HPO:skoehler	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0025080	OMIM:617571	TAS				P		HPO:nvasilevsky	
OMIM	617571	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 14; ARCI14		HP:0040189	OMIM:617571	TAS				P		HPO:nvasilevsky	
OMIM	617572	EXUDATIVE VITREORETINOPATHY 7; EVR7		HP:0000546	OMIM:617572	IEA				P		HPO:skoehler	
OMIM	617572	EXUDATIVE VITREORETINOPATHY 7; EVR7		HP:0000639	OMIM:617572	IEA				P		HPO:skoehler	
OMIM	617572	EXUDATIVE VITREORETINOPATHY 7; EVR7		HP:0007773	OMIM:617572	IEA				P		HPO:skoehler	
OMIM	617572	EXUDATIVE VITREORETINOPATHY 7; EVR7		HP:0011530	OMIM:617572	IEA				P		HPO:skoehler	
OMIM	617574	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13; ARCI13		HP:0000007	OMIM:617574	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617574	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13; ARCI13		HP:0000972	OMIM:617574	IEA				P		HPO:skoehler	
OMIM	617574	ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 13; ARCI13		HP:0025114	OMIM:617574	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000028	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000054	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000093	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000097	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000100	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000135	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000486	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000508	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000821	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000846	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0000969	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001250	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001251	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001263	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001268	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001290	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001943	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0001967	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0002155	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0002376	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0003073	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0003676	OMIM:617575	IEA				C		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0003774	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0003828	OMIM:617575	IEA				C		HPO:skoehler	
OMIM	617575	NEPHROTIC SYNDROME, TYPE 14; NPHS14		HP:0008064	OMIM:617575	IEA				P		HPO:skoehler	
OMIM	617576	SPERMATOGENIC FAILURE 18; SPGF18		HP:0000789	OMIM:617576	IEA				P		HPO:skoehler	
OMIM	617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37		HP:0000821	OMIM:617577	IEA				P		HPO:skoehler	
OMIM	617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37		HP:0000853	OMIM:617577	IEA				P		HPO:skoehler	
OMIM	617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37		HP:0002257	OMIM:617577	IEA				P		HPO:skoehler	
OMIM	617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37		HP:0030828	OMIM:617577	IEA				P		HPO:skoehler	
OMIM	617577	CILIARY DYSKINESIA, PRIMARY, 37; CILD37		HP:0031417	OMIM:617577	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0000007	OMIM:617584	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0001263	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0001310	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0001321	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0002078	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0003680	OMIM:617584	IEA				C		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0031936	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617584	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25		HP:0100543	OMIM:617584	IEA				P		HPO:skoehler	
OMIM	617585	IMMUNODEFICIENCY 53; IMD53		HP:0002719	OMIM:617585	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0000509	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0000956	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0000988	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001369	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001371	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001508	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001873	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001888	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001903	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0001954	PMID:26524591	PCS				P		HP:probinson	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0002155	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0002716	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0002719	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0002829	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0002910	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0003565	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0009125	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0010702	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0012490	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0100539	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617591	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 3; PRAAS3		HP:0100614	OMIM:617591	IEA				P		HPO:skoehler	
OMIM	617592	SPERMATOGENIC FAILURE 19; SPGF19		HP:0000789	OMIM:617592	IEA				P		HPO:skoehler	
OMIM	617593	SPERMATOGENIC FAILURE 20; SPGF20		HP:0000789	OMIM:617593	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0000083	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0000508	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0000657	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0001251	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0001266	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0001332	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0001970	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0002355	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0002371	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0002376	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0002509	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0004719	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0008936	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0100543	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617595	BIRK-LANDAU-PEREZ SYNDROME; BILAPES		HP:0100660	OMIM:617595	IEA				P		HPO:skoehler	
OMIM	617598	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3; MVA3		HP:0001250	OMIM:617598	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617598	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3; MVA3		HP:0001263	OMIM:617598	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617598	MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3; MVA3		HP:0200024	OMIM:617598	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0000817	PMID:28334793	TAS				P		HPO:nvasilevsky	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55	HP:0031375	HP:0001250	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001263	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001344	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001347	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001371	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001382	PMID:28334793	TAS				P		HPO:nvasilevsky	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0001510	PMID:28334793	TAS				P		HPO:nvasilevsky	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0002079	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0002187	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0002421	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0002509	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0002521	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0003623	OMIM:617599	IEA				C		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0010841	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0011968	PMID:28334793	TAS				P		HPO:nvasilevsky	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0040195	PMID:28334793	TAS				P		HPO:nvasilevsky	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0100704	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617599	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 55; EIEE55		HP:0200134	OMIM:617599	IEA				P		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0000006	OMIM:617600	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0001249	OMIM:617600	IEA				P		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0001250	OMIM:617600	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0001263	OMIM:617600	IEA				P		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0002376	OMIM:617600	IEA				P		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0002465	OMIM:617600	IEA				P		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0003828	OMIM:617600	IEA				C		HPO:skoehler	
OMIM	617600	MENTAL RETARDATION, AUTOSOMAL DOMINANT 45; MRD45		HP:0007018	OMIM:617600	IEA				P		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0000006	OMIM:617601	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0001249	OMIM:617601	IEA				P		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0001250	OMIM:617601	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0001263	OMIM:617601	IEA				P		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0001344	OMIM:617601	IEA				P		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0002317	OMIM:617601	IEA				P		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0003828	OMIM:617601	IEA				C		HPO:skoehler	
OMIM	617601	MENTAL RETARDATION, AUTOSOMAL DOMINANT 46; MRD46		HP:0200134	OMIM:617601	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000307	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000331	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000337	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000460	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000670	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000678	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000963	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000965	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0000977	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001166	OMIM:617602	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001508	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001511	OMIM:617602	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001629	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001631	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0001680	OMIM:617602	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0002010	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0002019	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0002023	OMIM:617602	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0002566	OMIM:617602	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0003189	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0003196	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0012385	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617602	CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME; CHDSKM		HP:0040019	OMIM:617602	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0001156	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0001256	OMIM:617604	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0001263	OMIM:617604	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0002974	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0002984	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0003027	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0003083	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0003577	OMIM:617604	IEA				C		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0004209	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0006443	OMIM:617604	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0009879	OMIM:617604	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617604	MICROCEPHALY, SHORT STATURE, AND LIMB ABNORMALITIES; MISSLA		HP:0010049	OMIM:617604	IEA				P		HPO:skoehler	
OMIM	617605	DEAFNESS, AUTOSOMAL DOMINANT 71; DFNA71		HP:0000006	OMIM:617605	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617605	DEAFNESS, AUTOSOMAL DOMINANT 71; DFNA71		HP:0003676	OMIM:617605	IEA				C		HPO:skoehler	
OMIM	617606	DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72		HP:0000006	OMIM:617606	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617606	DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72		HP:0000360	OMIM:617606	IEA				P		HPO:skoehler	
OMIM	617606	DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72		HP:0000407	OMIM:617606	IEA				P		HPO:skoehler	
OMIM	617606	DEAFNESS, AUTOSOMAL DOMINANT 72; DFNA72		HP:0003676	OMIM:617606	IEA				C		HPO:skoehler	
OMIM	617607	AMELOGENESIS IMPERFECTA, TYPE IIIB; AI3B		HP:0000705	OMIM:617607	IEA				P		HPO:skoehler	
OMIM	617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15		HP:0000093	OMIM:617609	IEA				P		HPO:skoehler	
OMIM	617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15		HP:0000100	OMIM:617609	IEA				P		HPO:skoehler	
OMIM	617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15		HP:0003073	OMIM:617609	IEA				P		HPO:skoehler	
OMIM	617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15		HP:0003774	OMIM:617609	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617609	NEPHROTIC SYNDROME, TYPE 15; NPHS15		HP:0012579	OMIM:617609	IEA				P		HPO:skoehler	
OMIM	617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5		HP:0000113	OMIM:617610	IEA				P		HPO:skoehler	
OMIM	617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5		HP:0003677	OMIM:617610	IEA				C		HPO:skoehler	
OMIM	617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5		HP:0003774	OMIM:617610	IEA				P		HPO:skoehler	
OMIM	617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5		HP:0003828	OMIM:617610	IEA				C		HPO:skoehler	
OMIM	617610	POLYCYSTIC KIDNEY DISEASE 5; PKD5		HP:0004719	OMIM:617610	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0001250	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0001257	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0001263	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0001302	OMIM:617613	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0001347	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0002119	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0002151	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0002376	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0002415	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0003236	OMIM:617613	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0003593	OMIM:617613	IEA				C		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0003676	OMIM:617613	IEA				C		HPO:skoehler	
OMIM	617613	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 5; MMDS5		HP:0012448	OMIM:617613	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000215	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000280	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000293	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000347	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000463	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000486	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0000646	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0001249	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0001250	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0001263	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0001344	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0002019	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0002064	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0002079	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0002119	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0002136	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0003593	OMIM:617616	IEA				C		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0003828	OMIM:617616	IEA				C		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0005280	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0005338	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0011968	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0031936	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0040082	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617616	SKRABAN-DEARDORFF SYNDROME; SKDEAS		HP:0430028	OMIM:617616	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0000496	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0000508	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0000556	OMIM:617622	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0000750	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0001249	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0001250	OMIM:617622	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0001263	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0002104	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0002282	OMIM:617622	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0002789	OMIM:617622	IEA				P		HPO:skoehler	
OMIM	617622	JOUBERT SYNDROME 30; JBTS30		HP:0003577	OMIM:617622	IEA				C		HPO:skoehler	
OMIM	617629	SCHIZOPHRENIA 19; SCZD19		HP:0003829	OMIM:617629	IEA				C		HPO:skoehler	
OMIM	617629	SCHIZOPHRENIA 19; SCZD19		HP:0100753	OMIM:617629	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0000007	OMIM:617633	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0000639	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0000657	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0001260	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0001272	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0001284	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0001310	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0002070	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0002075	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0002317	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0002403	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0002936	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0003676	OMIM:617633	IEA				C		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0007141	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617633	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 26; SCAR26		HP:0007338	OMIM:617633	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0000006	OMIM:617635	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0000490	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0000750	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0001249	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0001250	OMIM:617635	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0001263	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0002020	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0002059	OMIM:617635	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0011968	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617635	MENTAL RETARDATION, AUTOSOMAL DOMINANT 47; MRD47		HP:0045074	OMIM:617635	IEA				P		HPO:skoehler	
OMIM	617638	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B		HP:0001047	OMIM:617638	IEA				P		HPO:skoehler	
OMIM	617638	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B		HP:0001880	OMIM:617638	IEA				P		HPO:skoehler	
OMIM	617638	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B		HP:0002090	OMIM:617638	IEA				P		HPO:skoehler	
OMIM	617638	IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS; IMD11B		HP:0002099	OMIM:617638	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000028	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000054	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000062	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000083	OMIM:617641	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000083	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000085	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000086	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000089	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000104	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000110	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000275	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000276	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000286	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000365	OMIM:617641	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000369	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000391	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000431	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000463	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000486	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0000750	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0001263	OMIM:617641	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0001270	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0002002	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0002617	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0003828	OMIM:617641	IEA				C		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0004719	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0005563	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0008551	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0008589	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0030037	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617641	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED		HP:0040080	OMIM:617641	IEA				P		HPO:skoehler	
OMIM	617642	POLYDACTYLY, POSTAXIAL, TYPE A7; PAPA7		HP:0100259	OMIM:617642	IEA				P		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0001263	OMIM:617643	IEA				P		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0001272	OMIM:617643	IEA				P		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0002353	OMIM:617643	IEA				P		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0002465	OMIM:617643	IEA				P		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0003593	OMIM:617643	IEA				C		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0003828	OMIM:617643	IEA				C		HPO:skoehler	
OMIM	617643	CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES; CADEDS		HP:0007334	OMIM:617643	IEA				P		HPO:skoehler	
OMIM	617644	SPERMATOGENIC FAILURE 21; SPGF21		HP:0000789	OMIM:617644	IEA				P		HPO:skoehler	
OMIM	617644	SPERMATOGENIC FAILURE 21; SPGF21		HP:0012207	OMIM:617644	IEA				P		HPO:skoehler	
OMIM	617644	SPERMATOGENIC FAILURE 21; SPGF21		HP:0012869	OMIM:617644	IEA				P		HPO:skoehler	
OMIM	617654	DEAFNESS, AUTOSOMAL RECESSIVE 108; DFNB108		HP:0000007	OMIM:617654	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617654	DEAFNESS, AUTOSOMAL RECESSIVE 108; DFNB108		HP:0003593	OMIM:617654	IEA				C		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0000175	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0000193	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0001249	OMIM:617660	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0001263	OMIM:617660	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0001631	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0001650	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0001718	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0002144	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0003316	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0004383	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0004590	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0005950	OMIM:617660	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0008755	OMIM:617660	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0010301	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617660	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1		HP:0010305	OMIM:617660	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0000089	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0000252	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0001643	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0002007	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0002937	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0004383	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617661	VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2; VCRL2		HP:0012622	OMIM:617661	IEA				P		HPO:skoehler	
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0000501	OMIM:617662	IEA				P		HPO:skoehler	
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0000520	OMIM:617662	IEA				P		HPO:skoehler	
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0000541	OMIM:617662	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0000567	OMIM:617662	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0000612	OMIM:617662	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617662	JOINT LAXITY, SHORT STATURE, AND MYOPIA; JLSM		HP:0011003	OMIM:617662	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0000508	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0000577	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0000639	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0000648	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001257	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001263	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001266	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001290	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001332	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0001344	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002019	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002020	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002151	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002376	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002490	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0002540	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0003676	OMIM:617664	IEA				C		HPO:skoehler	
OMIM	617664	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 32; COXPD32		HP:0011968	OMIM:617664	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0000739	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0001249	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0001251	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0001263	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0002133	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0002136	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0002353	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0002370	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0003593	OMIM:617665	IEA				C		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0007018	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617665	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56; EIEE56		HP:0008770	OMIM:617665	IEA				P		HPO:skoehler	
OMIM	617666	FRASER SYNDROME 2; FRASRS2		HP:0000089	OMIM:617666	IEA				P		HPO:skoehler	
OMIM	617666	FRASER SYNDROME 2; FRASRS2		HP:0000104	OMIM:617666	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0000046	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0000444	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0000445	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0001126	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0001831	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0002101	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617667	FRASER SYNDROME 3; FRASRS3		HP:0012725	OMIM:617667	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0000803	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0001250	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0001285	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0001298	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0001332	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0001344	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0002120	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0002151	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0002353	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0003348	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0003542	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0003577	OMIM:617668	IEA				C		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0007109	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0012448	OMIM:617668	IEA				P		HPO:skoehler	
OMIM	617668	ENCEPHALOPATHY, NEONATAL SEVERE, WITH LACTIC ACIDOSIS AND BRAIN ABNORMALITIES; NELABA		HP:0012736	OMIM:617668	TAS				P		HP:probinson	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0000648	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001250	OMIM:617669	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001257	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001263	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001274	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001298	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001332	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0001336	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0002015	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0002119	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0002120	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0002376	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0002521	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0003577	OMIM:617669	IEA				C		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0003676	OMIM:617669	IEA				C		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0011968	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0012110	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617669	ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND SPASTICITY; PEBAS		HP:0100704	OMIM:617669	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0000083	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0000103	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0000787	OMIM:617671	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617671	HELIX SYNDROME; HELIX		HP:0000958	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0000966	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0002046	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0002900	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0002918	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617671	HELIX SYNDROME; HELIX		HP:0003127	OMIM:617671	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001250	OMIM:617672	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001251	OMIM:617672	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001257	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001263	OMIM:617672	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001268	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001272	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001300	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0001332	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002015	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002063	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002072	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002079	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002120	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002180	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002187	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0002376	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0003447	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0007256	OMIM:617672	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0011096	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617672	NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA		HP:0011968	OMIM:617672	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000006	OMIM:617675	IEA				I		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000007	OMIM:617675	IEA				I		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000276	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000303	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000347	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000580	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000716	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000739	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000750	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000786	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000836	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000870	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0000980	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001012	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001256	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001265	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001270	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001290	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001310	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001324	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001337	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0001761	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002058	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002070	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002075	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002078	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002355	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002540	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002750	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0002936	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0003236	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0003326	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0003557	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0003693	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617675	MYOPATHY, MITOCHONDRIAL, AND ATAXIA; MMYAT		HP:0100753	OMIM:617675	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0000316	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0000324	OMIM:617681	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0000348	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0000698	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0007651	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0009743	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0009804	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0012368	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617681	BLEPHAROCHEILODONTIC SYNDROME 2; BCDS2		HP:0012905	OMIM:617681	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0000256	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0000307	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0000494	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0000629	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0001249	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0001250	OMIM:617682	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0001263	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0002007	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0002721	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0003593	OMIM:617682	IEA				C		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0011098	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617682	PILAROWSKI-BJORNSSON SYNDROME; PILBOS		HP:0011229	OMIM:617682	IEA				P		HPO:skoehler	
OMIM	617690	OVARIAN DYSGENESIS 5; ODG5		HP:0000013	OMIM:617690	IEA				P		HPO:skoehler	
OMIM	617690	OVARIAN DYSGENESIS 5; ODG5		HP:0000786	OMIM:617690	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0000750	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0001257	OMIM:617691	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0001260	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0001270	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0001272	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0001310	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0002066	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0002075	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0002359	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0003677	OMIM:617691	IEA				C		HPO:skoehler	
OMIM	617691	SPINOCEREBELLAR ATAXIA 44; SCA44		HP:0007338	OMIM:617691	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000007	PMID:28886341	PCS				I		HPO:probinson	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000219	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000248	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	1/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS	HP:0012832	HP:0000286	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/7
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000307	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000316	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000319	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000325	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000331	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	5/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000343	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000358	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000369	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000377	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000431	PMID:28886341	IEA		HP:0040284		P		HPO:probinson	3/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000455	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000494	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000506	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	7/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000664	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0000750	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0001249	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	9/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0001250	OMIM:617694	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0001263	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0001511	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0001572	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	2/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0002079	OMIM:617694	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0002136	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0002705	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0002937	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0004322	PMID:28886341	PCS				P		HPO:probinson	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0004325	PMID:28886341	PCS				P		HPO:probinson	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0005280	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	6/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0006191	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	4/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0007413	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0008897	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0025300	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	3/9
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0030084	OMIM:617694	IEA				P		HPO:skoehler	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0040195	PMID:28886341	PCS				P		HPO:probinson	
OMIM	617694	AL KAISSI SYNDROME; ALKAS		HP:0200055	PMID:28886341	PCS		HP:0040284		P		HPO:probinson	8/9
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000540	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000565	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000589	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000733	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000750	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0000817	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0001250	OMIM:617695	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0001257	OMIM:617695	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0001260	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0001263	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0001290	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002070	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002079	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002136	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002355	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002370	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0002540	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0003202	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0010864	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617695	PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11		HP:0040082	OMIM:617695	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001257	OMIM:617698	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001263	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001290	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001324	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001344	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0001508	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0002059	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0002151	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0002169	OMIM:617698	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0002500	OMIM:617698	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0002521	OMIM:617698	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0003535	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0010864	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617698	3-METHYLGLUTACONIC ACIDURIA, TYPE IX; MGCA9		HP:0031936	OMIM:617698	IEA				P		HPO:skoehler	
OMIM	617706	SPERMATOGENIC FAILURE 22; SPGF22		HP:0000027	OMIM:617706	IEA				P		HPO:skoehler	
OMIM	617706	SPERMATOGENIC FAILURE 22; SPGF22		HP:0000789	OMIM:617706	IEA				P		HPO:skoehler	
OMIM	617707	SPERMATOGENIC FAILURE 23; SPGF23		HP:0000027	OMIM:617707	IEA				P		HPO:skoehler	
OMIM	617707	SPERMATOGENIC FAILURE 23; SPGF23		HP:0000789	OMIM:617707	IEA				P		HPO:skoehler	
OMIM	617709	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES; NEDMAS		HP:0001250	OMIM:617709	IEA				P		HPO:skoehler	
OMIM	617709	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES; NEDMAS		HP:0001251	OMIM:617709	IEA				P		HPO:skoehler	
OMIM	617709	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES; NEDMAS		HP:0001263	OMIM:617709	IEA				P		HPO:skoehler	
OMIM	617709	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ATAXIA, AND SEIZURES; NEDMAS		HP:0002342	OMIM:617709	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0000510	OMIM:617710	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0000577	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0000639	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0000646	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0000648	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001249	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001250	OMIM:617710	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001263	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001272	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001310	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001324	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001332	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001344	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001347	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0001943	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002059	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002119	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002151	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002305	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002509	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0002510	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0003202	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0008936	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0011968	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617710	NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES; NEMMLAS		HP:0012448	OMIM:617710	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0000316	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0001249	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1	HP:0031375	HP:0001250	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0001257	OMIM:617711	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0001263	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0001344	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0002059	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0002317	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0002376	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0002521	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0010841	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0012448	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0100704	OMIM:617711	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617711	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 1; IECEE1		HP:0200134	OMIM:617711	IEA				P		HPO:skoehler	
OMIM	617712	OOCYTE MATURATION DEFECT 3; OOMD3		HP:0000006	OMIM:617712	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617712	OOCYTE MATURATION DEFECT 3; OOMD3		HP:0000789	OMIM:617712	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0000100	OMIM:617713	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0000483	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0000508	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0000590	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0000646	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0001638	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0001640	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0001712	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0002151	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0002910	OMIM:617713	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0003198	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0003236	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0003546	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0003581	OMIM:617713	IEA		HP:0040284		C		HPO:skoehler	HP:0040284
OMIM	617713	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 33; COXPD33		HP:0012378	OMIM:617713	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000365	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000505	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000510	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000602	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000639	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000648	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617717	AUDITORY NEUROPATHY AND OPTIC ATROPHY; ANOA		HP:0000980	OMIM:617717	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0001873	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0002633	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0002716	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0002719	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0003565	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0005537	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617718	PLATELET ABNORMALITIES WITH EOSINOPHILIA AND IMMUNE-MEDIATED INFLAMMATORY DISEASE; PLTEID		HP:0100827	OMIM:617718	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0000926	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0002650	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0002656	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0002970	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0004233	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0010585	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617719	EPIPHYSEAL DYSPLASIA, MULTIPLE, 7; EDM7		HP:0100864	OMIM:617719	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000093	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000096	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000100	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000160	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000218	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000286	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000316	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000340	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000341	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000347	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000369	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000486	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000490	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000494	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000505	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000568	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000750	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0000969	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001166	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001249	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001250	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001257	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001263	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001272	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001290	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001302	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001508	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001511	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0001967	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0002059	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0002079	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0002119	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0003073	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0003774	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0009879	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0011800	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617729	GALLOWAY-MOWAT SYNDROME 3; GAMOS3		HP:0012385	OMIM:617729	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0000096	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0000100	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0000316	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0000505	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0000750	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0001250	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0001257	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0001263	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0001321	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0001967	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0002059	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0002126	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617730	GALLOWAY-MOWAT SYNDROME 4; GAMOS4		HP:0003774	OMIM:617730	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000096	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000100	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000286	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000303	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000316	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000365	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0000490	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0001251	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0001257	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0001263	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0001302	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0001999	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0002119	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0003774	OMIM:617731	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0011096	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617731	GALLOWAY-MOWAT SYNDROME 5; GAMOS5		HP:0012444	OMIM:617731	IEA				P		HPO:skoehler	
OMIM	617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD		HP:0000220	OMIM:617732	IEA				P		HPO:skoehler	
OMIM	617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD		HP:0003593	OMIM:617732	IEA				C		HPO:skoehler	
OMIM	617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD		HP:0003680	OMIM:617732	IEA				C		HPO:skoehler	
OMIM	617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD		HP:0003828	OMIM:617732	IEA				C		HPO:skoehler	
OMIM	617732	FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD		HP:0011469	OMIM:617732	IEA				P		HPO:skoehler	
OMIM	617743	OOCYTE MATURATION DEFECT 4; OOMD4		HP:0000789	OMIM:617743	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0000750	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0001256	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0001263	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0001508	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0001510	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0001631	OMIM:617744	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0002352	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0002719	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0002721	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0003593	OMIM:617744	IEA				C		HPO:skoehler	
OMIM	617744	IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH		HP:0004313	OMIM:617744	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000160	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000175	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000218	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000248	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000260	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000316	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000322	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000347	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000349	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000365	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000369	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000378	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000396	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000430	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000431	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000453	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000636	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0000894	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0001263	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0001321	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0002000	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0002020	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0002023	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0002230	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0005487	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0008551	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0011800	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0012725	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617746	SWEENEY-COX SYNDROME; SWCOS		HP:0100807	OMIM:617746	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000006	PMID:28886345	PCS				I		HPO:probinson	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000252	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	4/7
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000256	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	2/7
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000369	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000377	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000407	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000426	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000463	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000637	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000708	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0000733	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	2/5
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001249	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	7/7
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001250	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	3/5
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001252	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	4/5
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001290	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001320	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001321	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001344	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0001999	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002079	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	4/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002126	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002195	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002198	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	1/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002280	PMID:28886345	IEA		HP:0040284		P		HPO:probinson	3/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0002553	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0006956	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	2/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0007033	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0008872	PMID:28886345	PCS		HP:0040284		P		HPO:probinson	3/6
OMIM	617751	MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48		HP:0009765	OMIM:617751	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000006	OMIM:617752	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000154	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000218	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000286	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000316	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000343	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000486	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000582	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000718	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000750	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0000752	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0001249	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0001250	OMIM:617752	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0001263	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0001999	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0002714	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0003196	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0005280	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617752	MENTAL RETARDATION, AUTOSOMAL DOMINANT 49; MRD49		HP:0045025	OMIM:617752	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000160	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000219	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000286	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000316	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000448	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000455	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000486	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000582	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0000750	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001238	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001249	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001263	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001763	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001845	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0001852	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0002500	OMIM:617755	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0010055	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0012745	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0030084	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617755	NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL		HP:0200055	OMIM:617755	IEA				P		HPO:skoehler	
OMIM	617756	ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 5; EKVP5		HP:0000972	OMIM:617756	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0000316	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0000639	OMIM:617757	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0000657	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0001251	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0001256	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0001260	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0001263	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0001317	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0002126	OMIM:617757	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617757	JOUBERT SYNDROME 32; JBTS32		HP:0002419	OMIM:617757	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0001270	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0001290	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0002460	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0002515	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0002650	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003202	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003307	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003388	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003394	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003677	OMIM:617760	IEA				C		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003701	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0003805	OMIM:617760	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0008981	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617760	MYOPATHY, CENTRONUCLEAR, 6, WITH FIBER-TYPE DISPROPORTION; CNM6		HP:0009025	OMIM:617760	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0000486	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0000639	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0000657	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0001263	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0001290	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0002078	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0002079	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0002119	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0002419	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617761	JOUBERT SYNDROME 31; JBTS31		HP:0100543	OMIM:617761	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0000280	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0000319	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0000340	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0000543	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0000574	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0001249	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0001257	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0001284	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0001332	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0002059	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0002079	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0002376	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0002415	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0003676	OMIM:617762	IEA				C		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0007281	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617762	LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO		HP:0009830	OMIM:617762	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000343	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000348	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000358	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000369	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000407	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000455	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000486	OMIM:617763	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000490	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000501	OMIM:617763	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000510	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000545	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000582	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000639	OMIM:617763	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000750	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0000821	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001131	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001156	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001256	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001270	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001272	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0001596	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0003828	OMIM:617763	IEA				C		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0008070	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0010761	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0011304	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0012448	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0012745	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617763	SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF		HP:0012810	OMIM:617763	IEA				P		HPO:skoehler	
OMIM	617765	IMMUNODEFICIENCY, COMMON VARIABLE, 14; CVID14		HP:0002721	OMIM:617765	IEA				P		HPO:skoehler	
OMIM	617765	IMMUNODEFICIENCY, COMMON VARIABLE, 14; CVID14		HP:0004313	OMIM:617765	IEA				P		HPO:skoehler	
OMIM	617767	JOUBERT SYNDROME 33; JBTS33		HP:0001251	OMIM:617767	IEA				P		HPO:skoehler	
OMIM	617767	JOUBERT SYNDROME 33; JBTS33		HP:0001263	OMIM:617767	IEA				P		HPO:skoehler	
OMIM	617767	JOUBERT SYNDROME 33; JBTS33		HP:0002104	OMIM:617767	IEA				P		HPO:skoehler	
OMIM	617767	JOUBERT SYNDROME 33; JBTS33		HP:0002419	OMIM:617767	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0000750	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0001249	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0001250	OMIM:617768	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0001263	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0001999	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0002650	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617768	KLEEFSTRA SYNDROME 2; KLEFS2		HP:0002808	OMIM:617768	IEA				P		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0000006	OMIM:617769	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0001260	OMIM:617769	IEA				P		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0001272	OMIM:617769	IEA				P		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0002066	OMIM:617769	IEA				P		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0002070	OMIM:617769	IEA				P		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0003581	OMIM:617769	IEA				C		HPO:skoehler	
OMIM	617769	SPINOCEREBELLAR ATAXIA 45; SCA45		HP:0003677	OMIM:617769	IEA				C		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0000006	OMIM:617770	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0000514	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0000639	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0001260	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0001272	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0001310	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0002066	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0002070	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0002403	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0003390	OMIM:617770	IEA				P		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0003581	OMIM:617770	IEA				C		HPO:skoehler	
OMIM	617770	SPINOCEREBELLAR ATAXIA 46; SCA46		HP:0003677	OMIM:617770	IEA				C		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0001263	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0002079	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0002123	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0002376	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0002521	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0003593	OMIM:617771	IEA				C		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0007270	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617771	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 57; EIEE57		HP:0200134	OMIM:617771	IEA				P		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0000006	OMIM:617772	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0001369	OMIM:617772	IEA				P		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0001945	OMIM:617772	IEA				P		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0002716	OMIM:617772	IEA				P		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0002829	OMIM:617772	IEA				P		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0003677	OMIM:617772	IEA				C		HPO:skoehler	
OMIM	617772	DEAFNESS, AUTOSOMAL DOMINANT 34, WITH OR WITHOUT INFLAMMATION; DFNA34		HP:0003828	OMIM:617772	IEA				C		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000007	OMIM:617773	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000276	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000303	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000316	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000358	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000369	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000414	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000448	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000527	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000574	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000664	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000718	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000750	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0000752	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001182	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001249	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001257	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001263	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001347	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001761	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0001762	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0002079	OMIM:617773	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0002353	OMIM:617773	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0002553	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0003199	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0003487	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0003593	OMIM:617773	IEA				C		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0005484	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0008936	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617773	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 61; MRT61		HP:0031936	OMIM:617773	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001250	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001256	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001876	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001888	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001889	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0001894	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0002719	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0002960	OMIM:617780	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0003223	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0004313	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617780	COMBINED IMMUNODEFICIENCY AND MEGALOBLASTIC ANEMIA WITH OR WITHOUT HYPERHOMOCYSTEINEMIA; CIMAH		HP:0004430	OMIM:617780	IEA				P		HPO:skoehler	
OMIM	617781	RETINITIS PIGMENTOSA 80; RP80		HP:0000529	OMIM:617781	IEA				P		HPO:skoehler	
OMIM	617781	RETINITIS PIGMENTOSA 80; RP80		HP:0000618	OMIM:617781	IEA				P		HPO:skoehler	
OMIM	617781	RETINITIS PIGMENTOSA 80; RP80		HP:0007401	OMIM:617781	IEA				P		HPO:skoehler	
OMIM	617783	NEPHROTIC SYNDROME, TYPE 16; NPHS16		HP:0000093	OMIM:617783	IEA				P		HPO:skoehler	
OMIM	617783	NEPHROTIC SYNDROME, TYPE 16; NPHS16		HP:0000100	OMIM:617783	IEA				P		HPO:skoehler	
OMIM	617783	NEPHROTIC SYNDROME, TYPE 16; NPHS16		HP:0000790	OMIM:617783	IEA				P		HPO:skoehler	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0000007	PMID:28691929	PCS				I		HPO:probinson	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0000252	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0000824	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0001510	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0001511	OMIM:617784	IEA				P		HPO:skoehler	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0001748	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002119	OMIM:617784	IEA				P		HPO:skoehler	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002247	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002308	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002518	OMIM:617784	IEA				P		HPO:skoehler	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002863	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0002984	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0003577	OMIM:617784	IEA				C		HPO:skoehler	
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0009777	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0031689	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617784	FANCONI ANEMIA, COMPLEMENTATION GROUP W; FANCW		HP:0410049	PMID:28691929	PCS		HP:0040284		P		HPO:probinson	1/1
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0000006	OMIM:617787	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0000729	OMIM:617787	IEA				P		HPO:skoehler	
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0000750	OMIM:617787	IEA				P		HPO:skoehler	
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0001249	OMIM:617787	IEA				P		HPO:skoehler	
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0001263	OMIM:617787	IEA				P		HPO:skoehler	
OMIM	617787	MENTAL RETARDATION, AUTOSOMAL DOMINANT 50; MRD50		HP:0001270	OMIM:617787	IEA				P		HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0000006	OMIM:617788	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0000729	OMIM:617788	IEA				P		HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0000750	OMIM:617788	IEA				P		HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0001249	OMIM:617788	IEA				P		HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0001263	OMIM:617788	IEA				P		HPO:skoehler	
OMIM	617788	MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51		HP:0002373	OMIM:617788	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0000006	OMIM:617796	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0000729	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0000739	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0000752	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0001249	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0001250	OMIM:617796	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0001263	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0001344	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0003593	OMIM:617796	IEA				C		HPO:skoehler	
OMIM	617796	MENTAL RETARDATION, AUTOSOMAL DOMINANT 52; MRD52		HP:0011968	OMIM:617796	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0000006	OMIM:617798	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0000286	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0000316	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0000486	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0000494	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0001249	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0001250	OMIM:617798	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0001263	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0001344	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617798	MENTAL RETARDATION, AUTOSOMAL DOMINANT 53; MRD53		HP:0031936	OMIM:617798	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0000006	OMIM:617799	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0000486	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0000505	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0001249	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0001250	OMIM:617799	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0001344	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0002019	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0002020	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0002540	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617799	MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54		HP:0011968	OMIM:617799	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0000007	OMIM:617800	TAS				I		HPO:nvasilevsky	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0000252	OMIM:617800	TAS				P		HPO:nvasilevsky	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0001257	OMIM:617800	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0001263	OMIM:617800	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0001531	OMIM:617800	TAS				P		HPO:nvasilevsky	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0002079	OMIM:617800	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0002119	OMIM:617800	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0003676	OMIM:617800	IEA				C		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0009879	OMIM:617800	TAS				P		HPO:nvasilevsky	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0012448	OMIM:617800	IEA				P		HPO:skoehler	
OMIM	617800	MICROCEPHALY 19, PRIMARY, AUTOSOMAL RECESSIVE; MCPH19		HP:0100704	OMIM:617800	TAS				P		HPO:nvasilevsky	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000237	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000253	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000340	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000347	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000483	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000527	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0000545	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0001250	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0001263	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0001272	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0002079	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0002120	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0002187	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0003196	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0003593	OMIM:617802	IEA				C		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0003676	OMIM:617802	IEA				C		HPO:skoehler	
OMIM	617802	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA		HP:0005280	OMIM:617802	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0000218	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0000232	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0000286	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0000486	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0000664	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001249	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001250	OMIM:617804	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001251	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001263	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001272	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001332	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001344	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0001999	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0002059	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0002072	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0002119	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0002540	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0003593	OMIM:617804	IEA				C		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0003763	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0012448	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617804	NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL		HP:0031936	OMIM:617804	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000003	OMIM:617805	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000006	OMIM:617805	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000085	OMIM:617805	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000104	OMIM:617805	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000110	OMIM:617805	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000126	OMIM:617805	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0000130	OMIM:617805	IEA				P		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0003577	OMIM:617805	IEA				C		HPO:skoehler	
OMIM	617805	RENAL HYPODYSPLASIA/APLASIA 3; RHDA3		HP:0003829	OMIM:617805	IEA				C		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000297	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000486	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000505	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000540	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000582	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000639	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000648	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000733	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000817	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0000954	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001182	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001250	OMIM:617807	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001257	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001263	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001320	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001332	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001344	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001761	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001762	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001845	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0001999	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0002066	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0002317	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0002355	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0012448	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0030084	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0031936	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617807	NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW		HP:0040082	OMIM:617807	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000006	PMID:26238514	PCS		HP:0040284		I		HP:probinson	1/2
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000175	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000278	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000280	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000286	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000322	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000347	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000348	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000368	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000405	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000455	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000494	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000733	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000739	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000750	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0000767	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001156	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001249	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001263	PMID:26238514	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001270	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001290	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001357	PMID:26238514	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001631	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0001999	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002002	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002003	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002007	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002019	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002020	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002645	PMID:26238514	PCS		HP:0040284		P		HP:probinson	2/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002705	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0002751	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0004322	PMID:26238514	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0005280	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0006970	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0007018	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0009110	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/4
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0030084	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0045025	OMIM:617808	IEA				P		HPO:skoehler	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0100033	PMID:26238514	PCS				P		HP:probinson	
OMIM	617808	COFFIN-SIRIS SYNDROME 6; CSS6		HP:0100702	PMID:26238514	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0000311	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0000343	OMIM:617809	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0000414	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0000431	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0000463	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0001156	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0002090	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0002656	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0002878	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0005280	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617809	GELEOPHYSIC DYSPLASIA 3; GPHYSD3		HP:0009826	OMIM:617809	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000341	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000431	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000463	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000505	OMIM:617810	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000545	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000639	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000648	OMIM:617810	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000750	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000938	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0000939	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001249	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001250	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001257	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001260	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001263	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001272	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001310	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001321	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001337	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001347	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0001999	OMIM:617810	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0002066	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0002186	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0002353	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0002465	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0002540	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0003593	OMIM:617810	IEA				C		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0003828	OMIM:617810	IEA				C		HPO:skoehler	
OMIM	617810	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 15; GPIBD15		HP:0011220	OMIM:617810	IEA				P		HPO:skoehler	
OMIM	617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16		HP:0001249	OMIM:617816	IEA				P		HPO:skoehler	
OMIM	617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16		HP:0001250	OMIM:617816	IEA	HP:0003593			P		HPO:skoehler	
OMIM	617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16		HP:0001263	OMIM:617816	IEA				P		HPO:skoehler	
OMIM	617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16		HP:0002465	OMIM:617816	IEA				P		HPO:skoehler	
OMIM	617816	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 16; GPIBD16		HP:0031936	OMIM:617816	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0000007	OMIM:617820	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0000486	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0000817	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0001250	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0001257	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0001263	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0001332	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0001344	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0002079	OMIM:617820	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0002120	OMIM:617820	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0002540	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0004305	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0010864	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0100716	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617820	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL RECESSIVE; NDHMSR		HP:0200134	OMIM:617820	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0000974	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0000977	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0000978	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001030	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001075	OMIM:617821	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001187	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001290	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001762	OMIM:617821	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001763	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0001822	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0002194	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0002645	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0002650	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0002808	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617821	EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 2; EDSARTH2		HP:0003307	OMIM:617821	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000046	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000054	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000238	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000316	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000358	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000369	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000463	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000465	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000476	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000486	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000518	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000540	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000582	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000601	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000657	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0000969	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001181	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001188	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001249	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001250	OMIM:617822	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001263	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001290	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001321	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001339	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001344	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001698	OMIM:617822	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001762	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0001845	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0002119	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0002282	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0002365	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0003196	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0003577	OMIM:617822	IEA				C		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0005280	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0007033	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0007370	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0010557	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0012385	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0012725	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0012793	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617822	ALKURAYA-KUCINSKAS SYNDROME; ALKKUCS		HP:0030084	OMIM:617822	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0000958	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0000964	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0001511	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0001581	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0001875	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0002014	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0002716	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0002719	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0002863	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0008064	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617827	IMMUNODEFICIENCY 55; IMD55		HP:0008897	OMIM:617827	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001249	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001250	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001251	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001254	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001257	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001263	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001332	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001336	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0001344	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0002353	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0002355	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0002540	OMIM:617829	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0003828	OMIM:617829	IEA				C		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0100660	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617829	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 2; IECEE2		HP:0200134	OMIM:617829	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0000505	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0000639	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0000648	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0000733	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0001263	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0001264	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0001344	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0001347	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0002133	OMIM:617830	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0002521	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0002540	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0010864	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0012448	OMIM:617830	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617830	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58; EIEE58		HP:0200134	OMIM:617830	IEA				P		HPO:skoehler	
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0000006	PMID:29100083	PCS				I		HPO:probinson	
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0000006	OMIM:617831	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0000729	PMID:29100083	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0000750	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0001249	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0001260	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0001263	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0001270	PMID:29100083	PCS		HP:0040284		P		HPO:probinson	1/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0001337	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	2/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0002066	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	1/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0002123	PMID:29100083	PCS				P		HPO:skoehler	
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0002353	PMID:29100083	PCS		HP:0040284		P		HPO:skoehler	3/3
OMIM	617831	MENTAL RETARDATION, AUTOSOMAL DOMINANT 55, WITH SEIZURES; MRD55		HP:0200134	PMID:29100083	PCS		HP:0040284		P		HPO:probinson	3/3
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0000006	PMID:29100083	PCS				I		HP:probinson	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0000750	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001249	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001251	PMID:29100083	PCS		HP:0040284		P		HP:probinson	4/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001263	PMID:29100083	PCS	HP:0003593	HP:0040284		P		HP:probinson	7/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001290	PMID:29100083	PCS		HP:0040284		P		HP:probinson	3/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001332	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0001337	PMID:29100083	PCS		HP:0040284		P		HP:probinson	6/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0002063	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0002067	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0002069	PMID:29100083	PCS	HP:0011463	HP:0040284		P		HP:probinson	3/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0002123	PMID:29100083	PCS	HP:0011463	HP:0040284		P		HP:probinson	5/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0002353	OMIM:617836	IEA				P		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0003828	OMIM:617836	IEA				C		HPO:skoehler	
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0007099	PMID:29100083	PCS		HP:0040284		P		HP:probinson	1/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0011150	PMID:29100083	PCS	HP:0011463	HP:0040284		P		HP:probinson	2/8
OMIM	617836	DEVELOPMENTAL DELAY AND SEIZURES WITH OR WITHOUT MOVEMENT ABNORMALITIES; DEDSM		HP:0200134	PMID:29100083	PCS		HP:0040284		P		HP:probinson	7/7
OMIM	617839	AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23		HP:0003829	OMIM:617839	IEA				C		HPO:skoehler	
OMIM	617839	AMYOTROPHIC LATERAL SCLEROSIS 23; ALS23		HP:0007354	OMIM:617839	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0000194	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0000218	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0000219	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0000343	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0001249	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0001250	OMIM:617854	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0001251	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0001257	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0001263	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0002385	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0003828	OMIM:617854	IEA				C		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0007018	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617854	MENTAL RETARDATION, AUTOSOMAL DOMINANT 56; MRD56		HP:0100710	OMIM:617854	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0000486	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0000639	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0000733	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0001251	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0001263	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0001272	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0001337	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0001347	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0002079	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0002119	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0002120	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0003676	OMIM:617862	IEA				C		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0007366	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617862	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA		HP:0010864	OMIM:617862	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0000486	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0000609	OMIM:617864	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0000639	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0000737	OMIM:617864	IEA	HP:0003623			P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0001249	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0001263	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0001319	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0001344	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002072	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002079	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002120	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002133	OMIM:617864	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002510	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0002540	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0003828	OMIM:617864	IEA				C		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0007018	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617864	NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT SEIZURES AND GAIT ABNORMALITIES; NEDSGA		HP:0031936	OMIM:617864	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000194	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000232	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000253	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000256	OMIM:617865	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000336	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000565	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000574	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0000752	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001249	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001263	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001265	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001276	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001290	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0001344	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0002019	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0002020	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0002136	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0002317	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0002714	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0003196	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0003593	OMIM:617865	IEA				C		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0005280	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0010761	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0011220	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0011968	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0031936	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0040082	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617865	NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES; NEDMAGA		HP:0100033	OMIM:617865	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000113	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000219	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000238	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000286	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000316	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000773	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0000926	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0001156	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0001159	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0002119	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0002983	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0003175	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0008422	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0100258	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617866	SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY; SRTD18		HP:0100259	OMIM:617866	IEA				P		HPO:skoehler	
OMIM	617871	RETINITIS PIGMENTOSA 81; RP81		HP:0000980	OMIM:617871	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0000135	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0001397	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0001399	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0001943	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0002240	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0003128	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0003593	OMIM:617872	IEA				C		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0003828	OMIM:617872	IEA				C		HPO:skoehler	
OMIM	617872	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34; COXPD34		HP:0008207	OMIM:617872	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0000545	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0000565	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001249	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001257	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001263	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001298	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001332	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0001344	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0002059	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0002123	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0002353	OMIM:617873	IEA				P		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0003593	OMIM:617873	IEA				C		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0003828	OMIM:617873	IEA				C		HPO:skoehler	
OMIM	617873	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 35; COXPD35		HP:0007766	OMIM:617873	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617875	POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4		HP:0000006	PMID:24706814	PCS				I		HP:probinson	
OMIM	617875	POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4		HP:0000107	PMID:24706814	PCS	HP:0003581	HP:0040284		P		HP:probinson	14/25
OMIM	617875	POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4		HP:0001407	PMID:24706814	PCS	HP:0003581	HP:0040284		P		HP:probinson	19/25
OMIM	617875	POLYCYSTIC LIVER DISEASE 4 WITH OR WITHOUT KIDNEY CYSTS; PCLD4		HP:0003829	OMIM:617875	IEA				C		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000201	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000218	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000219	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000232	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000337	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000341	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000343	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000358	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000369	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000405	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000463	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000494	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000664	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000678	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000767	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000878	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0000884	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0001642	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0001669	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0001831	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0001852	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0003196	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0003298	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0003302	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0004209	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0004763	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0010047	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0011682	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0011800	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617877	SHORT STATURE, FACIAL DYSMORPHISM, AND SKELETAL ANOMALIES WITH OR WITHOUT CARDIAC ANOMALIES; SSFSC		HP:0200095	OMIM:617877	IEA				P		HPO:skoehler	
OMIM	617879	LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS; LCAEOD		HP:0000546	OMIM:617879	IEA				P		HPO:skoehler	
OMIM	617879	LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS; LCAEOD		HP:0007663	OMIM:617879	IEA				P		HPO:skoehler	
OMIM	617879	LEBER CONGENITAL AMAUROSIS WITH EARLY-ONSET DEAFNESS; LCAEOD		HP:0008499	OMIM:617879	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0000639	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001251	OMIM:617882	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001257	OMIM:617882	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001265	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001270	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001284	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0001761	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0002460	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0002515	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0002936	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0003376	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0003391	OMIM:617882	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0003487	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0003677	OMIM:617882	IEA				C		HPO:skoehler	
OMIM	617882	CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G; CMTDIG		HP:0007141	OMIM:617882	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000189	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000215	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000280	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000286	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000294	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000316	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000426	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000463	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000527	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000568	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000581	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000582	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000689	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0000750	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0001249	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0001263	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0001508	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0001572	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0003002	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0008070	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0009623	OMIM:617883	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0030084	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617883	FANCONI ANEMIA, COMPLEMENTATION GROUP S; FANCS		HP:0100615	OMIM:617883	IEA				P		HPO:skoehler	
OMIM	617885	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19; BMIQ19		HP:0000458	OMIM:617885	IEA				P		HPO:skoehler	
OMIM	617885	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19; BMIQ19		HP:0000855	OMIM:617885	IEA				P		HPO:skoehler	
OMIM	617885	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 19; BMIQ19		HP:0004409	OMIM:617885	IEA				P		HPO:skoehler	
OMIM	617892	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24		HP:0001260	OMIM:617892	IEA				P		HPO:skoehler	
OMIM	617892	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24		HP:0002015	OMIM:617892	IEA				P		HPO:skoehler	
OMIM	617892	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24		HP:0002273	OMIM:617892	IEA				P		HPO:skoehler	
OMIM	617892	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24; ALS24		HP:0410170	OMIM:617892	IEA				P		HPO:skoehler	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000007	PMID:27666822	PCS				I		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000268	PMID:27666822	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000269	PMID:27666822	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000343	PMID:27666822	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000369	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000773	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000774	OMIM:617895	IEA				P		HPO:skoehler	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000888	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000895	PMID:27666822	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/1
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0000946	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0001156	OMIM:617895	IEA				P		HPO:skoehler	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0001159	OMIM:617895	IEA				P		HPO:skoehler	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0001290	PMID:27666822	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0001629	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0002089	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0002098	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0002878	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19	HP:0012828	HP:0002983	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0002984	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0004482	PMID:27666822	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0005257	PMID:27666822	PCS				P		HP:probinson	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0011220	OMIM:617895	IEA				P		HPO:skoehler	
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0011800	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617895	SHORT-RIB THORACIC DYSPLASIA 19 WITH OR WITHOUT POLYDACTYLY; SRTD19		HP:0100259	PMID:27666822	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0000362	OMIM:617898	IEA				P		HPO:skoehler	
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0001156	OMIM:617898	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0001763	OMIM:617898	IEA				P		HPO:skoehler	
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0001769	OMIM:617898	IEA				P		HPO:skoehler	
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0001845	OMIM:617898	IEA				P		HPO:skoehler	
OMIM	617898	MULTIPLE SYNOSTOSES SYNDROME 4; SYNS4		HP:0008368	OMIM:617898	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001249	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001250	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001257	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001272	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001332	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0001344	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617899	LEUKODYSTROPHY, HYPOMYELINATING, 14; HLD14		HP:0002059	OMIM:617899	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001250	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001254	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001268	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001269	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001287	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0001289	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0002353	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0003829	OMIM:617900	IEA				C		HPO:skoehler	
OMIM	617900	ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8		HP:0012302	OMIM:617900	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0000252	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0000256	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0000713	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0001249	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0001250	OMIM:617903	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0001288	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0001332	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0001773	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0002104	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0002119	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0002376	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0002883	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0003763	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0012332	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617903	NEURODEVELOPMENTAL DISORDER WITH POOR LANGUAGE AND LOSS OF HAND SKILLS; NDPLHS		HP:0200055	OMIM:617903	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0001249	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0001250	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0001344	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0002119	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0002360	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0002521	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0002540	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0100716	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617904	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 59; EIEE59		HP:0200134	OMIM:617904	IEA				P		HPO:skoehler	
OMIM	617907	ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5		HP:0001899	OMIM:617907	IEA				P		HPO:skoehler	
OMIM	617907	ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5		HP:0001900	OMIM:617907	IEA				P		HPO:skoehler	
OMIM	617911	DIAMOND-BLACKFAN ANEMIA-LIKE; DBAL		HP:0001903	OMIM:617911	IEA				P		HPO:skoehler	
OMIM	617911	DIAMOND-BLACKFAN ANEMIA-LIKE; DBAL		HP:0003593	OMIM:617911	IEA				C		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0000006	OMIM:617912	IEA				I		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0000007	OMIM:617912	IEA				I		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001629	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001631	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001636	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001644	OMIM:617912	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001647	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001650	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0001719	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0003829	OMIM:617912	IEA				C		HPO:skoehler	
OMIM	617912	CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 5; CHTD5		HP:0005110	OMIM:617912	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0000089	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0000126	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0000518	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0000648	OMIM:617913	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0001250	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0001263	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0001344	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0002015	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0002020	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0002421	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0002540	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0003355	OMIM:617913	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0003593	OMIM:617913	IEA				C		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0003761	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617913	NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES; NEDMCR		HP:0012448	OMIM:617913	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000007	OMIM:617914	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000089	OMIM:617914	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000486	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000568	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000609	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0000618	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0001249	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0002194	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0002465	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0002472	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0004719	OMIM:617914	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0007018	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617914	MICROCEPHALY 20, PRIMARY, AUTOSOMAL RECESSIVE; MCPH20		HP:0009879	OMIM:617914	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0000278	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0000750	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0001249	OMIM:617915	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0001270	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0001272	OMIM:617915	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0001290	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0002007	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0002066	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617915	HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS		HP:0002540	OMIM:617915	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0000750	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0001257	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0001260	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0001272	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0001310	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0002059	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0002079	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0003676	OMIM:617916	IEA				C		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0006957	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617916	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 7; NBIA7		HP:0031936	OMIM:617916	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0000750	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0001270	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0001272	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0001310	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0001337	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0001347	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0002317	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0003676	OMIM:617917	IEA				C		HPO:skoehler	
OMIM	617917	NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 8; NBIA8		HP:0006957	OMIM:617917	IEA				P		HPO:skoehler	
OMIM	617920	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3; PLCA3		HP:0000958	OMIM:617920	IEA				P		HPO:skoehler	
OMIM	617920	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3; PLCA3		HP:0000989	OMIM:617920	IEA				P		HPO:skoehler	
OMIM	617920	AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 3; PLCA3		HP:0001034	OMIM:617920	IEA				P		HPO:skoehler	
OMIM	617921	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25; ALS25		HP:0003581	OMIM:617921	IEA				C		HPO:skoehler	
OMIM	617921	AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 25; ALS25		HP:0003829	OMIM:617921	IEA				C		HPO:skoehler	
OMIM	617924	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10; EJM10		HP:0000006	OMIM:617924	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617924	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10; EJM10		HP:0002121	OMIM:617924	IEA				P		HPO:skoehler	
OMIM	617924	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10; EJM10		HP:0002123	OMIM:617924	IEA				P		HPO:skoehler	
OMIM	617924	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10; EJM10		HP:0002373	OMIM:617924	IEA				P		HPO:skoehler	
OMIM	617924	EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10; EJM10		HP:0003829	OMIM:617924	IEA				C		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000007	PMID:27158779	PCS				I		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000054	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/1
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000175	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000248	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000260	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000316	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000347	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/1
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000369	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000470	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000568	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000695	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000773	OMIM:617925	IEA				P		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000774	OMIM:617925	IEA				P		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000888	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0000895	PMID:27666822	PCS				P		HPO:lccarmody	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0001153	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0001636	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0001674	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0002007	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0002023	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0002089	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0002162	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0003038	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0003173	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0003762	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/1
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0003811	PMID:27158779	PCS		HP:0040284		M		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0004491	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0005285	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0005474	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0005736	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0008551	OMIM:617925	IEA				P		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0008749	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0008803	OMIM:617925	IEA				P		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0011802	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0100258	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0100259	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0100628	PMID:27158779	PCS	HP:0003577			P		HP:probinson	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0100818	OMIM:617925	IEA				P		HPO:skoehler	
OMIM	617925	SHORT-RIB THORACIC DYSPLASIA 20 WITH POLYDACTYLY; SRTD20		HP:0410030	PMID:27158779	PCS	HP:0003577	HP:0040284		P		HP:probinson	2/2
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000007	PMID:27158779	PCS				I	OROFACIODIGITAL SYNDROME XVII	HP:probinson	
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000054	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000089	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000161	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000278	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000365	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000369	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000448	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000470	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0000750	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0001636	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0002119	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0002705	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0003186	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0003429	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0004322	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0004325	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0005487	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0006145	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0009577	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0009944	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0010442	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0030084	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617926	Orofaciodigital syndrome XVII		HP:0100759	PMID:27158779	PCS	HP:0003577	HP:0040284		P	OROFACIODIGITAL SYNDROME XVII	HP:probinson	1/1
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000007	PMID:27060890	PCS				I		HP:probinson	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000020	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000191	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000321	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000322	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000350	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000426	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000431	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0000699	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0001156	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0001852	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0005819	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0009882	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0100258	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0100259	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617927	OROFACIODIGITAL SYNDROME XVIII; OFD18		HP:0410030	OMIM:617927	IEA				P		HPO:skoehler	
OMIM	617928	KERATOCONUS 9; KTCN9		HP:0007663	OMIM:617928	IEA				P		HPO:skoehler	
OMIM	617929	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60; EIEE60		HP:0001250	OMIM:617929	IEA				P		HPO:skoehler	
OMIM	617929	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60; EIEE60		HP:0002187	OMIM:617929	IEA				P		HPO:skoehler	
OMIM	617929	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60; EIEE60		HP:0002510	OMIM:617929	IEA				P		HPO:skoehler	
OMIM	617929	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60; EIEE60		HP:0002521	OMIM:617929	IEA				P		HPO:skoehler	
OMIM	617929	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 60; EIEE60		HP:0200134	OMIM:617929	IEA				P		HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000160	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000218	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000219	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000276	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000316	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000347	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0000540	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001249	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001250	OMIM:617930	IEA		HP:0040284		P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	HP:0040284
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001251	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001260	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001263	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0001344	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0002058	OMIM:617930	IEA				P	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617930	CHROMOSOME 1p35 DELETION SYNDROME		HP:0003593	OMIM:617930	IEA				C	CHROMOSOME 1P35 DELETION SYNDROME	HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0000006	OMIM:617931	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0000341	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0000508	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0000651	OMIM:617931	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0000750	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001182	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001249	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001250	OMIM:617931	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001257	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001260	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001270	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001310	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0001999	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0002072	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0003676	OMIM:617931	IEA				C		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0003829	OMIM:617931	IEA				C		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0006855	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0030084	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617931	SPINOCEREBELLAR ATAXIA 47; SCA47		HP:0200055	OMIM:617931	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0000194	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0000218	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0001250	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0001257	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0002187	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0003593	OMIM:617933	IEA				C		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0012471	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617933	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61		HP:0200134	OMIM:617933	IEA				P		HPO:skoehler	
OMIM	617935	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4		HP:0000750	OMIM:617935	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617935	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4		HP:0001250	OMIM:617935	IEA				P		HPO:skoehler	
OMIM	617935	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4		HP:0001263	OMIM:617935	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617935	EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4		HP:0012332	OMIM:617935	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0001250	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0001263	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0001344	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0001508	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002015	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002079	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002126	OMIM:617938	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002510	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002521	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0002540	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0003593	OMIM:617938	IEA				C		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0011968	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617938	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 62; EIEE62		HP:0200134	OMIM:617938	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001601	OMIM:617941	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001607	OMIM:617941	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001738	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001873	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001875	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0001897	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0002014	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0002570	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0002970	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0003016	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0003025	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0003645	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0006276	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617941	SHWACHMAN-DIAMOND SYNDROME 2; SDS2		HP:0008151	OMIM:617941	IEA				P		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0001249	OMIM:617950	IEA				P		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0001263	OMIM:617950	IEA				P		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0002465	OMIM:617950	IEA				P		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0003593	OMIM:617950	IEA				C		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0003680	OMIM:617950	IEA				C		HPO:skoehler	
OMIM	617950	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36; COXPD36		HP:0012072	OMIM:617950	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0000529	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0000540	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0000639	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0000646	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0000648	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001250	OMIM:617951	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001251	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001257	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001263	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001272	OMIM:617951	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0001332	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002015	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002059	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002079	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002080	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002305	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002376	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002415	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0002540	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0003676	OMIM:617951	IEA				C		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0007256	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0011968	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617951	LEUKODYSTROPHY, HYPOMYELINATING, 15; HLD15		HP:0100543	OMIM:617951	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000007	PMID:29358272	PCS				I		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000337	PMID:29358272	PCS				P		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000347	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000527	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000592	PMID:29358272	PCS	HP:0003593	HP:0040284		P		HP:probinson	4/4
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000750	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0000883	PMID:29358272	PCS				P		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0001270	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0001382	PMID:29358272	PCS				P		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0001388	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0001537	PMID:29358272	PCS	HP:0003577	HP:0040284		P		HP:probinson	1/4
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0002645	PMID:29358272	PCS		HP:0040284		P		HP:probinson	3/4
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0002753	PMID:29358272	PCS				P		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0002757	PMID:29358272	PCS	HP:0003593	HP:0040284		P		HP:probinson	4/4
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0002953	OMIM:617952	IEA				P		HPO:skoehler	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0002980	PMID:29358272	PCS		HP:0040284		P		HP:probinson	4/4
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0004586	PMID:29358272	PCS				P		HP:probinson	
OMIM	617952	OSTEOGENESIS IMPERFECTA, TYPE XVIII; OI18		HP:0040160	PMID:29358272	PCS				P		HP:probinson	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0000543	OMIM:617954	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0000572	OMIM:617954	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001249	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001250	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001257	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001263	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001272	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001310	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001332	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0001344	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0002151	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0002352	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0002376	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0002421	OMIM:617954	IEA				P		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0003676	OMIM:617954	IEA				C		HPO:skoehler	
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0005484	OMIM:617954	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617954	MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 6; MMDS6		HP:0200134	OMIM:617954	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617960	SPERMATOGENIC FAILURE 25; SPGF25		HP:0000027	OMIM:617960	IEA				P		HPO:skoehler	
OMIM	617960	SPERMATOGENIC FAILURE 25; SPGF25		HP:0008734	OMIM:617960	IEA				P		HPO:skoehler	
OMIM	617960	SPERMATOGENIC FAILURE 25; SPGF25		HP:0030974	OMIM:617960	IEA				P		HPO:skoehler	
OMIM	617961	SPERMATOGENIC FAILURE 26; SPGF26		HP:0000789	OMIM:617961	IEA				P		HPO:skoehler	
OMIM	617961	SPERMATOGENIC FAILURE 26; SPGF26		HP:0012869	OMIM:617961	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0000639	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0000750	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001249	OMIM:617964	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001250	OMIM:617964	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001260	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001276	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001290	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001310	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001332	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0001347	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0002066	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0002079	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0002080	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0002136	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0002415	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0003828	OMIM:617964	IEA				C		HPO:skoehler	
OMIM	617964	LEUKODYSTROPHY, HYPOMYELINATING, 16; HLD16		HP:0007256	OMIM:617964	IEA				P		HPO:skoehler	
OMIM	617965	SPERMATOGENIC FAILURE 27; SPGF27		HP:0000789	OMIM:617965	IEA				P		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0000238	OMIM:617967	IEA				P		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0001305	OMIM:617967	IEA				P		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0001360	OMIM:617967	IEA				P		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0002324	OMIM:617967	IEA				P		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0003577	OMIM:617967	IEA				C		HPO:skoehler	
OMIM	617967	HYDROCEPHALUS, CONGENITAL, 3, WITH BRAIN ANOMALIES; HYC3		HP:0012444	OMIM:617967	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0000926	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0002515	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0002829	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0002970	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0008833	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617974	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, DI ROCCO TYPE; SEMDDR		HP:0100255	OMIM:617974	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0000316	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0000343	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0001249	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0001263	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0001344	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0001999	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0002120	OMIM:617976	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0002123	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0002540	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0011800	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0031936	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617976	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 63; EIEE63		HP:0200134	OMIM:617976	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0001258	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0001344	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0002079	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0002119	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0002187	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0002540	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0003593	OMIM:617977	IEA				C		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0003676	OMIM:617977	IEA				C		HPO:skoehler	
OMIM	617977	NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA AND BRAIN ABNORMALITIES WITH OR WITHOUT SEIZURES; NEDSBAS		HP:0006872	OMIM:617977	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000154	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000219	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000232	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000316	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000319	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000369	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000378	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000445	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000448	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000455	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000508	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000582	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0000750	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0001256	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0001511	OMIM:617982	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0001999	OMIM:617982	IEA				P		HPO:skoehler	
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0002080	OMIM:617982	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617982	VERVERI-BRADY SYNDROME; VERBRAS		HP:0002317	OMIM:617982	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617983	MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE; MCPH21		HP:0000007	OMIM:617983	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617983	MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE; MCPH21		HP:0001344	OMIM:617983	IEA				P		HPO:skoehler	
OMIM	617983	MICROCEPHALY 21, PRIMARY, AUTOSOMAL RECESSIVE; MCPH21		HP:0002342	OMIM:617983	IEA				P		HPO:skoehler	
OMIM	617984	MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE; MCPH22		HP:0000007	OMIM:617984	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	617984	MICROCEPHALY 22, PRIMARY, AUTOSOMAL RECESSIVE; MCPH22		HP:0001250	OMIM:617984	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000341	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000369	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000411	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000505	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000518	OMIM:617988	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000545	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000648	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0000653	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001188	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001249	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001250	OMIM:617988	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001257	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001263	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001266	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001272	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001274	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001290	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001310	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001332	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001337	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001347	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001382	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001387	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001508	OMIM:617988	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001762	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0001999	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0002066	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0002460	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0002540	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0002650	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0002808	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0003196	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0003593	OMIM:617988	IEA				C		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0003828	OMIM:617988	IEA				C		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0005280	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617988	JABERI-ELAHI SYNDROME; JABELS		HP:0045075	OMIM:617988	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000218	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000233	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000286	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000311	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000316	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000322	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000343	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000347	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000348	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000400	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000463	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000486	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000540	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000574	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000582	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000639	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000664	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000718	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0000739	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0001182	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0001249	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0001263	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0003196	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0003593	OMIM:617991	IEA				C		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0007018	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0030084	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617991	DEVELOPMENTAL DELAY, INTELLECTUAL DISABILITY, OBESITY, AND DYSMORPHIC FEATURES; DIDOD		HP:0100710	OMIM:617991	IEA				P		HPO:skoehler	
OMIM	617996	OOCYTE MATURATION DEFECT 5; OOMD5		HP:0000789	OMIM:617996	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000023	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000347	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000465	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000470	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000939	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000974	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0000978	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0001075	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0001488	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0001582	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0001763	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0001822	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0002758	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0002827	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0002933	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0002943	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0003177	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0003834	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0004976	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0025232	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618000	EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2; EDSCLL2		HP:0045074	OMIM:618000	IEA				P		HPO:skoehler	
OMIM	618003	DEAFNESS, AUTOSOMAL RECESSIVE 57; DFNB57		HP:0000007	PMID:26416264	PCS				I		HP:probinson	
OMIM	618003	DEAFNESS, AUTOSOMAL RECESSIVE 57; DFNB57		HP:0000007	OMIM:618003	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618003	DEAFNESS, AUTOSOMAL RECESSIVE 57; DFNB57		HP:0000407	PMID:26849169	PCS	HP:0003593	HP:0040284		P		HP:probinson	2/2
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0000319	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0000347	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001249	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001263	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001269	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001321	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001332	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001344	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0001999	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002072	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002079	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002119	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002120	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002133	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002376	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002509	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0002540	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0003828	OMIM:618004	IEA				C		HPO:skoehler	
OMIM	618004	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 64; EIEE64		HP:0012448	OMIM:618004	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000278	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000337	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000341	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000431	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000557	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0000938	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001249	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001250	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001263	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001371	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001508	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001511	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0001999	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0003196	OMIM:618005	IEA				P		HPO:skoehler	
OMIM	618005	CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION; CDGF		HP:0003577	OMIM:618005	IEA				C		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0000212	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0000303	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0000463	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0001250	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0001272	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0001344	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002059	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002079	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002187	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002415	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002521	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0002540	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0003593	OMIM:618006	IEA				C		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0003676	OMIM:618006	IEA				C		HPO:skoehler	
OMIM	618006	LEUKODYSTROPHY, HYPOMYELINATING, 17; HLD17		HP:0009765	OMIM:618006	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0001250	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0001257	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65	HP:0003676	HP:0001272	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0001344	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0001347	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65	HP:0003676	HP:0002059	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0002119	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0002521	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618008	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 65; EIEE65		HP:0200134	OMIM:618008	IEA				P		HPO:skoehler	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0000218	PMID:29603516	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0000718	OMIM:618010	IEA				P		HPO:skoehler	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001250	OMIM:618010	IEA				P		HPO:skoehler	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001263	OMIM:618010	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001290	PMID:29603516	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001328	PMID:29603516	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001510	PMID:29573052	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0001864	PMID:29573052	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0002155	OMIM:618010	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0002465	PMID:29603516	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0003828	OMIM:618010	IEA				C		HPO:skoehler	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0004209	PMID:29573052	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0006989	OMIM:618010	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0011451	PMID:29573052	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0031703	OMIM:618010	TAS				P		HPO:nvasilevsky	
OMIM	618010	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 17; GPIBD17		HP:0100025	PMID:29573052	TAS				P		HPO:nvasilevsky	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0000007	PMID:28180185	PCS				I		HPO:probinson	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0000023	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001181	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001250	PMID:28180185	PCS				P		HPO:probinson	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001263	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001276	PMID:28180185	PCS				P		HPO:probinson	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001298	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001336	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001347	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0001537	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0002059	OMIM:618011	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0002521	PMID:28180185	PCS				P		HPO:probinson	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0002878	PMID:28180185	PCS				P		HPO:probinson	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0003577	OMIM:618011	IEA				C		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0003676	OMIM:618011	IEA				C		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0005684	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618011	HYPEREKPLEXIA 4; HKPX4		HP:0012385	OMIM:618011	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0000540	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0000612	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0000648	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001249	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001250	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001263	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001272	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001285	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001344	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0001347	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0002059	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0002079	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0002521	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0002540	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0003429	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0003828	OMIM:618012	IEA				C		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0031936	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618012	EPILEPTIC ENCEPHALOPATHY, INFANTILE OR EARLY CHILDHOOD, 3; IECEE3		HP:0200134	OMIM:618012	IEA				P		HPO:skoehler	
OMIM	618014	PREMATURE OVARIAN FAILURE 14; POF14		HP:0000786	OMIM:618014	IEA				P		HPO:skoehler	
OMIM	618014	PREMATURE OVARIAN FAILURE 14; POF14		HP:0008232	OMIM:618014	IEA				P		HPO:skoehler	
OMIM	618014	PREMATURE OVARIAN FAILURE 14; POF14		HP:0011969	OMIM:618014	IEA				P		HPO:skoehler	
OMIM	618015	PROTOPORPHYRIA, ERYTHROPOIETIC, 2; EPP2		HP:0000006	OMIM:618015	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618015	PROTOPORPHYRIA, ERYTHROPOIETIC, 2; EPP2		HP:0000992	OMIM:618015	IEA				P		HPO:skoehler	
OMIM	618015	PROTOPORPHYRIA, ERYTHROPOIETIC, 2; EPP2		HP:0003593	OMIM:618015	IEA				C		HPO:skoehler	
OMIM	618015	PROTOPORPHYRIA, ERYTHROPOIETIC, 2; EPP2		HP:0003828	OMIM:618015	IEA				C		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0000054	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0000162	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0000308	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0000369	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0001629	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0005304	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618021	TETRAAMELIA SYNDROME 2; TETAMS2		HP:0010296	OMIM:618021	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0000278	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0000882	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0000894	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0001776	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0002057	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618022	HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY; HHRRD		HP:0009777	OMIM:618022	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000154	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000219	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000243	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000280	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000289	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000316	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000322	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000358	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000365	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000369	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000400	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000403	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000486	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000494	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000540	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000574	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000691	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000722	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000750	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0000752	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0001156	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0001249	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0001263	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0001671	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0002019	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0004442	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0005280	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0011220	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0011937	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0011968	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0030084	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618027	COFFIN-SIRIS SYNDROME 7; CSS7		HP:0031936	OMIM:618027	IEA				P		HPO:skoehler	
OMIM	618031	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4; PPCD4	HP:0003680	HP:0007663	OMIM:618031	IEA				P		HPO:skoehler	
OMIM	618031	CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 4; PPCD4		HP:0009918	OMIM:618031	TAS		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0001265	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0001284	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0003376	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0003394	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0003677	OMIM:618036	IEA				C		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0007141	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618036	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2DD; CMT2DD		HP:0009027	OMIM:618036	IEA				P		HPO:skoehler	
OMIM	618042	PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA; PAPHG		HP:0002093	OMIM:618042	IEA				P		HPO:skoehler	
OMIM	618042	PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA; PAPHG		HP:0002205	OMIM:618042	IEA				P		HPO:skoehler	
OMIM	618042	PULMONARY ALVEOLAR PROTEINOSIS WITH HYPOGAMMAGLOBULINEMIA; PAPHG		HP:0004313	OMIM:618042	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0000988	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0001156	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0001508	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0002716	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0003565	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0010702	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0030084	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618048	PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 2; PRAAS2		HP:0100539	OMIM:618048	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0000508	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0001260	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0001263	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0001300	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0001337	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0001347	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0002066	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0002311	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0002362	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0003593	OMIM:618049	IEA				C		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0008936	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0010553	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0012332	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0025403	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0031936	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618049	PARKINSONISM-DYSTONIA, INFANTILE, 2; PKDYS2		HP:0100543	OMIM:618049	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000160	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000218	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000276	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000286	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000358	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000388	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000426	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000455	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000486	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000506	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000508	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000581	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000582	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000722	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000729	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000739	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0000750	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0001249	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0001250	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0001263	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0001270	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0002014	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0002019	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0002650	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0002808	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0003593	OMIM:618050	IEA				C		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0007018	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0011968	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618050	MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57		HP:0040083	OMIM:618050	IEA				P		HPO:skoehler	
OMIM	618052	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27		HP:0001640	OMIM:618052	IEA				P		HPO:skoehler	
OMIM	618052	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27		HP:0001653	OMIM:618052	IEA				P		HPO:skoehler	
OMIM	618052	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27		HP:0001657	OMIM:618052	IEA				P		HPO:skoehler	
OMIM	618052	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27		HP:0005180	OMIM:618052	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000218	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000233	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000252	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000283	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000286	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000343	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000505	OMIM:618056	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000639	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0000713	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001249	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001250	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001263	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001272	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001276	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001310	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001344	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0001347	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0002066	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0002079	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0004209	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0010804	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0011968	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0030147	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618056	NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS		HP:0031936	OMIM:618056	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0000006	PMID:29656859	PCS				I		HPO:probinson	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0000565	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0000639	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0000657	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0000750	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001249	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001250	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001251	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001263	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001270	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001321	OMIM:618060	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0001337	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0002311	OMIM:618060	IEA				P		HPO:skoehler	
OMIM	618060	INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA; IDDECA		HP:0006879	OMIM:618060	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618061	POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6		HP:0000006	OMIM:618061	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618061	POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6		HP:0003581	OMIM:618061	IEA				C		HPO:skoehler	
OMIM	618061	POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6		HP:0003676	OMIM:618061	IEA				C		HPO:skoehler	
OMIM	618061	POLYCYSTIC KIDNEY DISEASE 6 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE; PKD6		HP:0003774	OMIM:618061	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618063	CILIARY DYSKINESIA, PRIMARY, 38; CILD38		HP:0000389	OMIM:618063	IEA				P		HPO:skoehler	
OMIM	618063	CILIARY DYSKINESIA, PRIMARY, 38; CILD38		HP:0000405	OMIM:618063	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618063	CILIARY DYSKINESIA, PRIMARY, 38; CILD38		HP:0002643	OMIM:618063	IEA				P		HPO:skoehler	
OMIM	618063	CILIARY DYSKINESIA, PRIMARY, 38; CILD38		HP:0012259	OMIM:618063	IEA				P		HPO:skoehler	
OMIM	618063	CILIARY DYSKINESIA, PRIMARY, 38; CILD38		HP:0012735	OMIM:618063	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0000252	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0000286	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0000316	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0000639	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001181	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001250	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001257	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001263	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001265	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D	HP:0003676	HP:0001272	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001290	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001347	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001371	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001508	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0001511	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0002059	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0002093	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0002205	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0002380	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0002421	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0003676	OMIM:618065	IEA				C		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0011968	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618065	PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D		HP:0200136	OMIM:618065	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000154	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000219	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000316	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000483	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000486	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000494	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000540	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000545	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000639	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000664	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000729	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0000750	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0001249	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0001250	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0001263	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0001875	OMIM:618067	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0001903	OMIM:618067	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0002136	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0002280	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0002714	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0031936	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618067	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 66; EIEE66		HP:0200134	OMIM:618067	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0000657	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001249	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001250	OMIM:618076	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001257	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001344	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001508	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0001510	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0002019	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0002080	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0002169	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0002421	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0002500	OMIM:618076	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0011968	OMIM:618076	IEA				P		HPO:skoehler	
OMIM	618076	NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH; NEDSG		HP:0012448	OMIM:618076	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618078	OVARIAN DYSGENESIS 6; ODG6		HP:0000013	OMIM:618078	IEA				P		HPO:skoehler	
OMIM	618084	PEELING SKIN SYNDROME 6; PSS6		HP:0000989	OMIM:618084	IEA				P		HPO:skoehler	
OMIM	618084	PEELING SKIN SYNDROME 6; PSS6		HP:0001036	OMIM:618084	IEA				P		HPO:skoehler	
OMIM	618084	PEELING SKIN SYNDROME 6; PSS6		HP:0040162	OMIM:618084	IEA				P		HPO:skoehler	
OMIM	618086	SPERMATOGENIC FAILURE 28; SPGF28		HP:0000027	OMIM:618086	IEA				P		HPO:skoehler	
OMIM	618086	SPERMATOGENIC FAILURE 28; SPGF28		HP:0008232	OMIM:618086	IEA				P		HPO:skoehler	
OMIM	618086	SPERMATOGENIC FAILURE 28; SPGF28		HP:0011969	OMIM:618086	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000303	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000316	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000486	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000490	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000540	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000582	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0000657	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001007	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001159	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001249	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001257	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001263	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001310	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001321	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001332	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0001347	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0002421	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0002540	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0003196	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0008070	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0030084	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618087	SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND		HP:0045025	OMIM:618087	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0000565	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0000639	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001249	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001250	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001257	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001260	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001263	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001266	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001272	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001310	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0001332	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0002015	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0002059	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0002371	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0002376	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0003676	OMIM:618088	IEA				C		HPO:skoehler	
OMIM	618088	NEURODEVELOPMENTAL DISORDER WITH REGRESSION, ABNORMAL MOVEMENTS, LOSS OF SPEECH, AND SEIZURES; NEDAMSS		HP:0007371	OMIM:618088	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000160	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000232	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000252	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000276	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000316	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000343	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000348	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000358	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000369	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000486	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000490	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000494	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000527	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000540	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000736	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000750	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0000752	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001182	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001249	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001250	OMIM:618089	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001263	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001357	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001763	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001773	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0001852	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0002714	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0003828	OMIM:618089	IEA				C		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0008551	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0030084	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0031936	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618089	INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA		HP:0200055	OMIM:618089	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0000752	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0001263	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0001272	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0001310	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0001337	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0001344	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0002063	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0002079	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0002123	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618090	NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC		HP:0002540	OMIM:618090	IEA				P		HPO:skoehler	
OMIM	618091	SPERMATOGENIC FAILURE 29; SPGF29		HP:0000027	OMIM:618091	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000160	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000219	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000286	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000316	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000343	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000540	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000545	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000668	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000677	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000691	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000739	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0000750	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0001249	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0001257	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0001263	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0001880	OMIM:618092	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0002058	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0002099	OMIM:618092	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0002317	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0002719	OMIM:618092	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0012745	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0031936	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618092	INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA		HP:0045074	OMIM:618092	IEA				P		HPO:skoehler	
OMIM	618093	SPINOCEREBELLAR ATAXIA 48; SCA48		HP:0000739	OMIM:618093	IEA				P		HPO:skoehler	
OMIM	618093	SPINOCEREBELLAR ATAXIA 48; SCA48		HP:0001260	OMIM:618093	IEA				P		HPO:skoehler	
OMIM	618093	SPINOCEREBELLAR ATAXIA 48; SCA48		HP:0001272	OMIM:618093	IEA				P		HPO:skoehler	
OMIM	618093	SPINOCEREBELLAR ATAXIA 48; SCA48		HP:0002066	OMIM:618093	IEA				P		HPO:skoehler	
OMIM	618093	SPINOCEREBELLAR ATAXIA 48; SCA48		HP:0003676	OMIM:618093	IEA				C		HPO:skoehler	
OMIM	618094	DEAFNESS, AUTOSOMAL RECESSIVE 110; DFNB110		HP:0000007	OMIM:618094	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618094	DEAFNESS, AUTOSOMAL RECESSIVE 110; DFNB110		HP:0000407	OMIM:618094	IEA				P		HPO:skoehler	
OMIM	618094	DEAFNESS, AUTOSOMAL RECESSIVE 110; DFNB110		HP:0001751	OMIM:618094	IEA				P		HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0000007	OMIM:618095	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0001257	OMIM:618095	IEA				P		HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0001263	OMIM:618095	IEA				P		HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0002123	OMIM:618095	IEA				P		HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0002540	OMIM:618095	IEA				P		HPO:skoehler	
OMIM	618095	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 63; MRT63		HP:0010864	OMIM:618095	IEA				P		HPO:skoehler	
OMIM	618096	PREMATURE OVARIAN FAILURE 15; POF15		HP:0000876	OMIM:618096	IEA				P		HPO:skoehler	
OMIM	618097	MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2; MGRISCE2		HP:0000957	OMIM:618097	IEA				P		HPO:skoehler	
OMIM	618097	MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2; MGRISCE2		HP:0001511	OMIM:618097	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0000508	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0000590	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0000651	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0001260	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0001272	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0001310	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0002136	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0003546	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0003581	OMIM:618098	IEA				C		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0003701	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0005162	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618098	PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 5; PEOB5		HP:0011675	OMIM:618098	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0000007	OMIM:618103	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0001249	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0001250	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0001257	OMIM:618103	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0001263	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0001344	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0002015	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618103	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 64; MRT64		HP:0011968	OMIM:618103	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000006	OMIM:618106	TAS				I		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000154	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000218	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000252	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000316	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000324	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000400	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000431	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000678	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0000750	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001249	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001250	OMIM:618106	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001263	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001290	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001357	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001382	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0001999	OMIM:618106	TAS				P		HPO:nvasilevsky	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0002311	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0002465	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0012471	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618106	MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58		HP:0031936	OMIM:618106	IEA				P		HPO:skoehler	
OMIM	618107	OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3		HP:0000006	OMIM:618107	TAS				I		HPO:lccarmody[2019-03-21]HPO:skoehler	
OMIM	618107	OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3		HP:0000938	OMIM:618107	IEA				P		HPO:skoehler	
OMIM	618107	OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3		HP:0001903	OMIM:618107	IEA				P		HPO:skoehler	
OMIM	618107	OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3		HP:0002684	OMIM:618107	IEA				P		HPO:skoehler	
OMIM	618107	OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3		HP:0002757	OMIM:618107	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0000988	OMIM:618108	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0002014	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0002037	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0002110	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0002719	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0004313	OMIM:618108	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0005263	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618108	IMMUNODEFICIENCY 57; IMD57		HP:0006528	OMIM:618108	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000028	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000047	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000321	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000414	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000426	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000483	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000486	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000494	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000508	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000545	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0000750	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0001263	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0002079	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0002317	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0002342	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0003593	OMIM:618109	IEA				C		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0005487	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618109	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 65; MRT65		HP:0031936	OMIM:618109	IEA				P		HPO:skoehler	
OMIM	618110	SPERMATOGENIC FAILURE 30; SPGF30		HP:0000027	OMIM:618110	IEA				P		HPO:skoehler	
OMIM	618110	SPERMATOGENIC FAILURE 30; SPGF30		HP:0030974	OMIM:618110	IEA				P		HPO:skoehler	
OMIM	618113	ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION; MMERV		HP:0000750	OMIM:618113	IEA				P		HPO:skoehler	
OMIM	618113	ENCEPHALITIS/ENCEPHALOPATHY, MILD, WITH REVERSIBLE MYELIN VACUOLIZATION; MMERV		HP:0001250	OMIM:618113	IEA				P		HPO:skoehler	
OMIM	618114	LIDDLE SYNDROME 2; LIDLS2		HP:0002900	OMIM:618114	IEA				P		HPO:skoehler	
OMIM	618114	LIDDLE SYNDROME 2; LIDLS2		HP:0003351	OMIM:618114	IEA				P		HPO:skoehler	
OMIM	618114	LIDDLE SYNDROME 2; LIDLS2		HP:0200114	OMIM:618114	IEA				P		HPO:skoehler	
OMIM	618115	SPERMATOGENIC FAILURE 32; SPGF32		HP:0000027	OMIM:618115	IEA				P		HPO:skoehler	
OMIM	618115	SPERMATOGENIC FAILURE 32; SPGF32		HP:0000789	OMIM:618115	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0000369	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0000958	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0000964	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0001873	OMIM:618116	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0001882	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0001903	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0001999	OMIM:618116	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0003577	OMIM:618116	IEA				C		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0004313	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0005528	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618116	BONE MARROW FAILURE SYNDROME 4; BMFS4		HP:0011800	OMIM:618116	IEA				P		HPO:skoehler	
OMIM	618117	OVARIAN DYSGENESIS 7; ODG7		HP:0000013	OMIM:618117	IEA				P		HPO:skoehler	
OMIM	618117	OVARIAN DYSGENESIS 7; ODG7		HP:0000786	OMIM:618117	IEA				P		HPO:skoehler	
OMIM	618117	OVARIAN DYSGENESIS 7; ODG7		HP:0000823	OMIM:618117	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0000750	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001250	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001254	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001263	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001298	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001324	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001943	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001987	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0001993	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0002141	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0003128	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0003201	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0003236	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0003535	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618120	MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5; MC5DN5		HP:0003546	OMIM:618120	IEA				P		HPO:skoehler	
OMIM	618123	POLYDACTYLY, POSTAXIAL, TYPE A8; PAPA8		HP:0100259	OMIM:618123	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0000486	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0000602	OMIM:618124	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0000750	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0001265	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0001270	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0001284	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0001290	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0001760	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0002317	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0002936	OMIM:618124	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0003477	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0003677	OMIM:618124	IEA				C		HPO:skoehler	
OMIM	618124	PERIPHERAL NEUROPATHY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; PNRIID		HP:0009027	OMIM:618124	IEA				P		HPO:skoehler	
OMIM	618126	LIDDLE SYNDROME 3; LIDLS3		HP:0000822	OMIM:618126	IEA				P		HPO:skoehler	
OMIM	618126	LIDDLE SYNDROME 3; LIDLS3		HP:0002900	OMIM:618126	IEA				P		HPO:skoehler	
OMIM	618126	LIDDLE SYNDROME 3; LIDLS3		HP:0003828	OMIM:618126	IEA				C		HPO:skoehler	
OMIM	618126	LIDDLE SYNDROME 3; LIDLS3		HP:0200114	OMIM:618126	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003198	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003307	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003326	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003418	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003555	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003581	OMIM:618129	IEA				C		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0003701	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0007126	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618129	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL DOMINANT 4; LGMDD4		HP:0009023	OMIM:618129	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0001051	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0001075	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002014	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002015	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002099	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002110	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002583	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0002728	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0004313	OMIM:618131	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0004469	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0008064	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0011107	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0032163	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0040189	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0100633	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618131	IMMUNODEFICIENCY 58; IMD58		HP:0200043	OMIM:618131	IEA				P		HPO:skoehler	
OMIM	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8; MDDGC8		HP:0000750	OMIM:618135	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8; MDDGC8		HP:0001270	OMIM:618135	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8; MDDGC8		HP:0003391	OMIM:618135	IEA				P		HPO:skoehler	
OMIM	618135	MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 8; MDDGC8		HP:0008981	OMIM:618135	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0001250	OMIM:618138	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0001270	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0001284	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0001288	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0003391	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0003394	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0003551	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0003677	OMIM:618138	IEA				C		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0003828	OMIM:618138	IEA				C		HPO:skoehler	
OMIM	618138	MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 23; LGMDR23		HP:0008981	OMIM:618138	IEA				P		HPO:skoehler	
OMIM	618140	DEAFNESS, AUTOSOMAL DOMINANT 74; DFNA74		HP:0000365	OMIM:618140	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0001263	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0001288	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0002121	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0002123	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0002305	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0002521	OMIM:618141	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0003593	OMIM:618141	IEA				C		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0100660	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618141	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 67; EIEE67		HP:0200134	OMIM:618141	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000054	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000062	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000122	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000248	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000252	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000278	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000316	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000341	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000347	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000369	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000400	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0000582	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001250	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001290	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001339	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001629	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001631	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001643	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0001776	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0002553	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0010557	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0010751	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0100258	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618142	MICROCEPHALY, FACIAL DYSMORPHISM, RENAL AGENESIS, AND AMBIGUOUS GENITALIA SYNDROME; MFRG		HP:0100259	OMIM:618142	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000007	PMID:30269814	TAS				I		HPO:lccarmody	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000023	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000028	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000158	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000212	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	3/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000252	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000280	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000331	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/5
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000358	OMIM:618143	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000365	OMIM:618143	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000384	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000391	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000476	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000639	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	3/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000687	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000768	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0000954	OMIM:618143	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001156	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	3/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001250	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001251	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001263	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001272	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001288	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001290	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001388	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001640	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0001989	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/6
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002002	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002019	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002120	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002240	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002540	OMIM:618143	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002553	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002650	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002804	OMIM:618143	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0002828	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/6
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0003155	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	1/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0003282	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0003828	OMIM:618143	IEA				C		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0004209	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0004689	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0009882	OMIM:618143	IEA				P		HPO:skoehler	
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0010044	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0011221	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	2/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0011968	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	4/4
OMIM	618143	GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18		HP:0100704	PMID:30269814	PCS		HP:0040284		P		HPO:lccarmody	3/4
OMIM	618144	USHER SYNDROME, TYPE IV; USH4		HP:0000408	OMIM:618144	IEA				P		HPO:skoehler	
OMIM	618145	DEAFNESS, AUTOSOMAL RECESSIVE 111; DFNB111		HP:0000408	OMIM:618145	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000316	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000343	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000358	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000369	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000431	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000455	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0000637	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0001263	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0009890	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0009928	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0012801	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618147	INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF		HP:0045074	OMIM:618147	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000260	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000347	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000444	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000446	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000518	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000520	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000592	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000662	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000750	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000767	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000768	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0000926	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0001015	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0001263	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0001270	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0001511	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0001762	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0003015	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0008897	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0009882	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0010049	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0010230	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0010743	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618150	SAUL-WILSON SYNDROME; SWILS		HP:0011220	OMIM:618150	IEA				P		HPO:skoehler	
OMIM	618152	SPERMATOGENIC FAILURE 33; SPGF33		HP:0000789	OMIM:618152	IEA				P		HPO:skoehler	
OMIM	618153	SPERMATOGENIC FAILURE 34; SPGF34		HP:0000789	OMIM:618153	IEA				P		HPO:skoehler	
OMIM	618154	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3; HKLLS3		HP:0000282	OMIM:618154	IEA				P		HPO:skoehler	
OMIM	618154	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3; HKLLS3		HP:0000316	OMIM:618154	IEA				P		HPO:skoehler	
OMIM	618154	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3; HKLLS3		HP:0000463	OMIM:618154	IEA				P		HPO:skoehler	
OMIM	618154	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3; HKLLS3		HP:0000582	OMIM:618154	IEA				P		HPO:skoehler	
OMIM	618154	HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3; HKLLS3		HP:0012368	OMIM:618154	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0000508	OMIM:618155	IEA	HP:0003577			P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0000544	OMIM:618155	IEA	HP:0003577			P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0000577	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0000773	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0000921	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0002650	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0005864	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0012366	OMIM:618155	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618155	OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES; EORVA		HP:0025584	OMIM:618155	IEA				P		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0000006	PMID:30290153	PCS				I		HP:probinson	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0000276	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0000337	OMIM:618158	IEA				P		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0000490	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0001250	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0001263	OMIM:618158	IEA				P		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0001270	PMID:30290153	PCS	HP:0011463	HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0001988	PMID:30290153	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0002007	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0002020	PMID:30290153	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0002066	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0002317	OMIM:618158	IEA				P		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0002465	OMIM:618158	IEA				P		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0003593	OMIM:618158	IEA				C		HPO:skoehler	
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0010863	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0010864	PMID:30290153	PCS		HP:0040284		P		HP:probinson	2/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0012448	OMIM:618158	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0020045	PMID:30290153	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0030891	PMID:30290153	PCS		HP:0040284		P		HP:probinson	1/2
OMIM	618158	INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD		HP:0031936	OMIM:618158	IEA				P		HPO:skoehler	
OMIM	618160	ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V; IGHD5		HP:0000824	OMIM:618160	IEA				P		HPO:skoehler	
OMIM	618160	ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V; IGHD5		HP:0002007	OMIM:618160	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000003	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000010	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000126	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000463	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000506	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000508	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000529	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000657	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0000662	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0001251	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0001263	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0001320	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0002553	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618161	JOUBERT SYNDROME 35; JBTS35		HP:0005280	OMIM:618161	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0000238	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0000964	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0000978	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0001156	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0001250	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0001263	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0001631	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0001643	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002007	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002019	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002308	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002691	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002694	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002721	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0002987	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0003025	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0003027	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0004691	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0006380	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0008905	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618162	SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE; SEMDK		HP:0010582	OMIM:618162	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000286	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000365	OMIM:618164	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000369	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000377	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000474	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000476	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000508	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000648	OMIM:618164	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0000750	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001250	OMIM:618164	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001263	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001276	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001290	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001537	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001642	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001643	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001680	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0001719	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0002059	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0002119	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0002144	OMIM:618164	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0004383	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0030084	OMIM:618164	IEA				P		HPO:skoehler	
OMIM	618164	CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD		HP:0100704	OMIM:618164	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618165	BONE MARROW FAILURE SYNDROME 5; BMFS5		HP:0001250	OMIM:618165	IEA				P		HPO:skoehler	
OMIM	618165	BONE MARROW FAILURE SYNDROME 5; BMFS5		HP:0001263	OMIM:618165	IEA				P		HPO:skoehler	
OMIM	618165	BONE MARROW FAILURE SYNDROME 5; BMFS5		HP:0001903	OMIM:618165	IEA				P		HPO:skoehler	
OMIM	618165	BONE MARROW FAILURE SYNDROME 5; BMFS5		HP:0012410	OMIM:618165	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0001156	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0001181	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0001822	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0002999	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0009778	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0009882	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0010055	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0010109	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0010557	OMIM:618167	IEA				P		HPO:skoehler	
OMIM	618167	OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS; OCBMD		HP:0100259	OMIM:618167	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0000486	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0000508	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0000602	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0000639	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001250	OMIM:618170	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001260	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001272	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001310	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001324	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0001337	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0002059	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0002376	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0002465	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0003447	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618170	NEURODEGENERATION, CHILDHOOD-ONSET, STRESS-INDUCED, WITH VARIABLE ATAXIA AND SEIZURES; CONDSIAS		HP:0003487	OMIM:618170	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0000510	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0000518	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0000662	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0001133	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0007663	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0011505	OMIM:618173	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618173	RETINITIS PIGMENTOSA 83; RP83		HP:0100832	OMIM:618173	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001251	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001263	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001302	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001321	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001344	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0001347	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0002079	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0002353	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0002365	OMIM:618174	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0002510	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0002540	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618174	CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9; CDCBM9		HP:0010864	OMIM:618174	IEA				P		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0000093	OMIM:618176	IEA				P		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0000097	OMIM:618176	IEA				P		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0002907	OMIM:618176	IEA				P		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0003676	OMIM:618176	IEA				C		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0003774	OMIM:618176	IEA				P		HPO:skoehler	
OMIM	618176	NEPHROTIC SYNDROME, TYPE 17; NPHS17		HP:0012588	OMIM:618176	IEA				P		HPO:skoehler	
OMIM	618177	NEPHROTIC SYNDROME, TYPE 18; NPHS18		HP:0000097	OMIM:618177	IEA				P		HPO:skoehler	
OMIM	618177	NEPHROTIC SYNDROME, TYPE 18; NPHS18		HP:0003676	OMIM:618177	IEA				C		HPO:skoehler	
OMIM	618177	NEPHROTIC SYNDROME, TYPE 18; NPHS18		HP:0003774	OMIM:618177	IEA				P		HPO:skoehler	
OMIM	618177	NEPHROTIC SYNDROME, TYPE 18; NPHS18		HP:0012588	OMIM:618177	IEA				P		HPO:skoehler	
OMIM	618178	NEPHROTIC SYNDROME, TYPE 19; NPHS19		HP:0000097	OMIM:618178	IEA				P		HPO:skoehler	
OMIM	618178	NEPHROTIC SYNDROME, TYPE 19; NPHS19		HP:0003676	OMIM:618178	IEA				C		HPO:skoehler	
OMIM	618178	NEPHROTIC SYNDROME, TYPE 19; NPHS19		HP:0012588	OMIM:618178	IEA				P		HPO:skoehler	
OMIM	618178	NEPHROTIC SYNDROME, TYPE 19; NPHS19		HP:0012622	OMIM:618178	IEA				P		HPO:skoehler	
OMIM	618179	MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE; MCPH24		HP:0001320	OMIM:618179	IEA				P		HPO:skoehler	
OMIM	618179	MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE; MCPH24		HP:0003577	OMIM:618179	IEA				C		HPO:skoehler	
OMIM	618180	ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS; ECTD14		HP:0000668	OMIM:618180	IEA				P		HPO:skoehler	
OMIM	618180	ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS; ECTD14		HP:0000698	OMIM:618180	IEA				P		HPO:skoehler	
OMIM	618180	ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS; ECTD14		HP:0000966	OMIM:618180	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618182	ORTHOSTATIC HYPOTENSION 2; ORTHYP2		HP:0001278	OMIM:618182	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0000103	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0000110	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0000821	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0001698	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002155	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002243	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002573	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002901	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002902	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0002917	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0003073	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618183	DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE; DIAR10		HP:0005208	OMIM:618183	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0001265	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0001284	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0002375	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0002421	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0002540	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0003202	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0003431	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0003828	OMIM:618184	IEA				C		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0006829	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618184	NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2		HP:0031936	OMIM:618184	IEA				P		HPO:skoehler	
OMIM	618185	PERIVENTRICULAR NODULAR HETEROTOPIA 8; PVNH8		HP:0000750	OMIM:618185	IEA				P		HPO:skoehler	
OMIM	618185	PERIVENTRICULAR NODULAR HETEROTOPIA 8; PVNH8		HP:0001250	OMIM:618185	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618185	PERIVENTRICULAR NODULAR HETEROTOPIA 8; PVNH8		HP:0001257	OMIM:618185	IEA				P		HPO:skoehler	
OMIM	618185	PERIVENTRICULAR NODULAR HETEROTOPIA 8; PVNH8		HP:0012448	OMIM:618185	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000212	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000218	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000252	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000268	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000286	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000347	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000365	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000369	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000505	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0000508	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001250	OMIM:618186	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001257	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001265	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001272	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001332	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001347	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0001349	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0002020	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0002079	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0002093	OMIM:618186	IEA	HP:0003623			P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0002804	OMIM:618186	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0003429	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0003487	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0003577	OMIM:618186	IEA				C		HPO:skoehler	
OMIM	618186	NEUROPATHY, CONGENITAL HYPOMYELINATING, 3; CHN3		HP:0012471	OMIM:618186	IEA				P		HPO:skoehler	
OMIM	618187	OVARIAN DYSGENESIS 8; ODG8		HP:0000059	OMIM:618187	IEA				P		HPO:skoehler	
OMIM	618187	OVARIAN DYSGENESIS 8; ODG8		HP:0000786	OMIM:618187	IEA				P		HPO:skoehler	
OMIM	618187	OVARIAN DYSGENESIS 8; ODG8		HP:0008232	OMIM:618187	IEA				P		HPO:skoehler	
OMIM	618187	OVARIAN DYSGENESIS 8; ODG8		HP:0011969	OMIM:618187	IEA				P		HPO:skoehler	
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0000750	OMIM:618188	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0000773	OMIM:618188	IEA				P		HPO:skoehler	
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0000883	OMIM:618188	IEA				P		HPO:skoehler	
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0001270	OMIM:618188	IEA				P		HPO:skoehler	
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0002980	OMIM:618188	IEA				P		HPO:skoehler	
OMIM	618188	HYPERPARATHYROIDISM, TRANSIENT NEONATAL; HRPTTN		HP:0003155	OMIM:618188	IEA				P		HPO:skoehler	
OMIM	618189	CARDIOMYOPATHY, DILATED, 2C; CMD2C		HP:0001644	OMIM:618189	IEA				P		HPO:skoehler	
OMIM	618189	CARDIOMYOPATHY, DILATED, 2C; CMD2C		HP:0003828	OMIM:618189	IEA				C		HPO:skoehler	
OMIM	618189	CARDIOMYOPATHY, DILATED, 2C; CMD2C		HP:0012664	OMIM:618189	IEA				P		HPO:skoehler	
OMIM	618195	INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA; IDDRP		HP:0000518	OMIM:618195	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618195	INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA; IDDRP		HP:0000608	OMIM:618195	IEA				P		HPO:skoehler	
OMIM	618195	INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA; IDDRP		HP:0007663	OMIM:618195	IEA				P		HPO:skoehler	
OMIM	618195	INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA; IDDRP		HP:0007928	OMIM:618195	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618195	INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA; IDDRP		HP:0500087	OMIM:618195	IEA				P		HPO:skoehler	
OMIM	618196	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2; CMAVM2		HP:0001009	OMIM:618196	IEA				P		HPO:skoehler	
OMIM	618196	CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2; CMAVM2		HP:0030713	OMIM:618196	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618197	MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC; CMS23		HP:0001324	OMIM:618197	IEA				P		HPO:skoehler	
OMIM	618197	MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC; CMS23		HP:0002359	OMIM:618197	IEA				P		HPO:skoehler	
OMIM	618197	MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC; CMS23		HP:0003388	OMIM:618197	IEA				P		HPO:skoehler	
OMIM	618197	MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC; CMS23		HP:0008981	OMIM:618197	IEA				P		HPO:skoehler	
OMIM	618197	MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC; CMS23		HP:0031936	OMIM:618197	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0000508	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0000602	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0000639	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0000657	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0000750	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0001324	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0002015	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0002093	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0011968	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0012385	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618198	MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC; CMS24		HP:0031936	OMIM:618198	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0001257	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0001263	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0001298	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0001336	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0002120	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0002133	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0002169	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0002267	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0002376	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0003676	OMIM:618201	IEA				C		HPO:skoehler	
OMIM	618201	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68; EIEE68		HP:0010546	OMIM:618201	IEA				P		HPO:skoehler	
OMIM	618204	IMMUNODEFICIENCY 15A; IMD15A		HP:0002841	OMIM:618204	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000286	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000316	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000431	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000448	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000483	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000486	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000540	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000733	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0000750	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0001260	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0001263	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0002007	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0002119	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0002136	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0002317	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0003593	OMIM:618205	IEA				C		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0011098	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0011220	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0011800	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0025268	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0031936	OMIM:618205	IEA				P		HPO:skoehler	
OMIM	618205	SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS		HP:0100704	OMIM:618205	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0001250	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0001263	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0001298	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0002059	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0002079	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0002521	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0002583	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0002719	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618213	INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE		HP:0012448	OMIM:618213	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000286	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000319	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000348	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000486	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000639	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0000733	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0001251	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0001263	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0001266	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0001332	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0002020	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0002353	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0002540	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0003196	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0003593	OMIM:618218	IEA				C		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0005274	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0011968	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0031936	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0100660	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618218	BAKER-GORDON SYNDROME; BAGOS		HP:0100716	OMIM:618218	IEA				P		HPO:skoehler	
OMIM	618220	RETINITIS PIGMENTOSA 84; RP84		HP:0000510	OMIM:618220	IEA				P		HPO:skoehler	
OMIM	618220	RETINITIS PIGMENTOSA 84; RP84		HP:0000518	OMIM:618220	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618220	RETINITIS PIGMENTOSA 84; RP84		HP:0001116	OMIM:618220	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618220	RETINITIS PIGMENTOSA 84; RP84		HP:0007401	OMIM:618220	IEA				P		HPO:skoehler	
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0000007	PMID:27311568	PCS				I		HPO:probinson	
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0000286	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/10
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0000718	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/8
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0000729	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/8
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0000750	PMID:27311568	PCS		HP:0040284		P		HP:probinson	10/10
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001249	PMID:25558065,PMID:27311568,PMID:28097321	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001252	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/10
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001263	PMID:25558065	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001290	OMIM:618221	IEA				P		HPO:skoehler	
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001388	PMID:27311568	PCS		HP:0040284		P		HP:probinson	3/10
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0001999	PMID:27311568	PCS		HP:0040284		P		HP:probinson	3/10
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0002066	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/8
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0007018	PMID:25558065	PCS		HP:0040284		P		HP:probinson	1/1
OMIM	618221	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66; MRT66		HP:0100962	PMID:27311568	PCS		HP:0040284		P		HP:probinson	2/8
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0001250	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0001260	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0001263	OMIM:618222	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0001332	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0001347	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0002093	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0002104	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0002355	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0003828	OMIM:618222	IEA				C		HPO:skoehler	
OMIM	618222	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2; MC1DN2		HP:0100660	OMIM:618222	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000175	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000286	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000294	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000316	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000325	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000369	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000378	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000396	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000437	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000455	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000465	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000470	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000824	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000829	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000872	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0000912	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0001076	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0001263	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0001631	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0001642	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0001719	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0002650	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0002808	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0002846	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0005280	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0009918	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618223	VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION; VETD		HP:0410030	OMIM:618223	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001250	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001251	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001254	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001260	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001298	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001332	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0001347	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0002071	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0002376	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0003676	OMIM:618224	IEA				C		HPO:skoehler	
OMIM	618224	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3; MC1DN3		HP:0007256	OMIM:618224	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0000486	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0000508	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0000602	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0001250	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0001251	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0001254	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0001263	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0001336	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0002376	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0003593	OMIM:618225	IEA				C		HPO:skoehler	
OMIM	618225	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4; MC1DN4		HP:0012444	OMIM:618225	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000486	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000508	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000602	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000639	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000648	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0000737	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001250	OMIM:618226	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001251	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001254	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001263	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001272	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001332	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0001347	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002013	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002015	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002093	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002104	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002352	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002376	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002415	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0002465	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0003487	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0003593	OMIM:618226	IEA				C		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0003676	OMIM:618226	IEA				C		HPO:skoehler	
OMIM	618226	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5; MC1DN5		HP:0012444	OMIM:618226	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0000639	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0000648	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0001254	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0001347	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0002119	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0002376	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0003593	OMIM:618228	IEA				C		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0007256	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0008936	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618228	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6; MC1DN6		HP:0012444	OMIM:618228	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0000639	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0000648	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0001257	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0001290	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0001298	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0002376	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0003593	OMIM:618229	IEA				C		HPO:skoehler	
OMIM	618229	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7; MC1DN7		HP:0012444	OMIM:618229	IEA				P		HPO:skoehler	
OMIM	618230	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8; MC1DN8		HP:0001298	OMIM:618230	IEA				P		HPO:skoehler	
OMIM	618230	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8; MC1DN8		HP:0001332	OMIM:618230	IEA				P		HPO:skoehler	
OMIM	618230	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8; MC1DN8		HP:0002151	OMIM:618230	IEA				P		HPO:skoehler	
OMIM	618230	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8; MC1DN8		HP:0002273	OMIM:618230	IEA				P		HPO:skoehler	
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0000639	OMIM:618232	IEA				P		HPO:skoehler	
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0001250	OMIM:618232	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0001254	OMIM:618232	IEA				P		HPO:skoehler	
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0001298	OMIM:618232	IEA				P		HPO:skoehler	
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0002791	OMIM:618232	IEA				P		HPO:skoehler	
OMIM	618232	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9; MC1DN9		HP:0005957	OMIM:618232	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0000544	OMIM:618233	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0000639	OMIM:618233	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0000648	OMIM:618233	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0001250	OMIM:618233	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0001263	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0001298	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0001310	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0002015	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0002104	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0002352	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0002878	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0003676	OMIM:618233	IEA				C		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0007110	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618233	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10; MC1DN10		HP:0011968	OMIM:618233	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0000488	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0001263	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0001298	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0001403	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0001635	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0001639	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0002151	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0002240	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0002650	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0002808	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0003198	OMIM:618234	IEA				P		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0003593	OMIM:618234	IEA				C		HPO:skoehler	
OMIM	618234	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11; MC1DN11		HP:0003828	OMIM:618234	IEA				C		HPO:skoehler	
OMIM	618235	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13		HP:0001250	OMIM:618235	IEA				P		HPO:skoehler	
OMIM	618235	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13		HP:0001263	OMIM:618235	IEA				P		HPO:skoehler	
OMIM	618235	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13		HP:0001522	OMIM:618235	IEA				M		HPO:skoehler	
OMIM	618235	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13		HP:0002079	OMIM:618235	IEA				P		HPO:skoehler	
OMIM	618235	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13; MC1DN13		HP:0003577	OMIM:618235	IEA				C		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0000639	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0000648	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0001250	OMIM:618236	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0001290	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0001298	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0002151	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0003198	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618236	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14; MC1DN14		HP:0012444	OMIM:618236	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0000639	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0000648	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0000737	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0000817	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001250	OMIM:618237	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001290	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001298	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001332	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001347	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001371	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001508	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0001511	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0002510	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0003198	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0003623	OMIM:618237	IEA				C		HPO:skoehler	
OMIM	618237	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15; MC1DN15		HP:0011096	OMIM:618237	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0000508	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0000639	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0000648	OMIM:618238	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001250	OMIM:618238	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001257	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001260	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001263	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001266	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001274	OMIM:618238	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001332	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001508	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0001511	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618238	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16; MC1DN16		HP:0002071	OMIM:618238	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001250	OMIM:618239	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001251	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001260	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001263	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001288	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001290	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0001332	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0002063	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0002151	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0002376	OMIM:618239	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0003202	OMIM:618239	IEA				P		HPO:skoehler	
OMIM	618239	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17		HP:0003828	OMIM:618239	IEA				C		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0000817	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0001250	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0001263	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0001336	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0001347	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0001522	OMIM:618240	IEA				M		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0002878	OMIM:618240	IEA				P		HPO:skoehler	
OMIM	618240	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18; MC1DN18		HP:0003577	OMIM:618240	IEA				C		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0000648	OMIM:618241	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001250	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001263	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001272	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001290	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001336	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0001943	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0002063	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0002119	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0002305	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0002465	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0002540	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0003128	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0003593	OMIM:618241	IEA				C		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0012448	OMIM:618241	IEA				P		HPO:skoehler	
OMIM	618241	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19; MC1DN19		HP:0100704	OMIM:618241	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0000486	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0000639	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001251	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001257	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001260	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001263	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001317	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0001347	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0002121	OMIM:618242	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0002352	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0002355	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0002415	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0002465	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0003198	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0003487	OMIM:618242	IEA				P		HPO:skoehler	
OMIM	618242	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21; MC1DN21		HP:0003828	OMIM:618242	IEA				C		HPO:skoehler	
OMIM	618243	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22; MC1DN22		HP:0001263	OMIM:618243	IEA				P		HPO:skoehler	
OMIM	618243	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22; MC1DN22		HP:0002421	OMIM:618243	IEA				P		HPO:skoehler	
OMIM	618243	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22; MC1DN22		HP:0003593	OMIM:618243	IEA				C		HPO:skoehler	
OMIM	618244	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23; MC1DN23		HP:0001290	OMIM:618244	IEA				P		HPO:skoehler	
OMIM	618244	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23; MC1DN23		HP:0001332	OMIM:618244	IEA				P		HPO:skoehler	
OMIM	618244	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23; MC1DN23		HP:0003202	OMIM:618244	IEA				P		HPO:skoehler	
OMIM	618244	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23; MC1DN23		HP:0003676	OMIM:618244	IEA				C		HPO:skoehler	
OMIM	618244	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23; MC1DN23		HP:0031936	OMIM:618244	IEA				P		HPO:skoehler	
OMIM	618245	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24; MC1DN24		HP:0002151	OMIM:618245	IEA				P		HPO:skoehler	
OMIM	618245	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24; MC1DN24		HP:0003593	OMIM:618245	IEA				C		HPO:skoehler	
OMIM	618245	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24; MC1DN24		HP:0003676	OMIM:618245	IEA				C		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0001263	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0001290	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0001298	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0001508	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0001511	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0003198	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618246	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25; MC1DN25		HP:0003798	OMIM:618246	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0001260	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0001265	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0001266	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0001272	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0001332	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0002059	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0002151	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0002353	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0002509	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618247	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26; MC1DN26		HP:0003693	OMIM:618247	IEA				P		HPO:skoehler	
OMIM	618248	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27; MC1DN27		HP:0000648	OMIM:618248	IEA				P		HPO:skoehler	
OMIM	618248	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27; MC1DN27		HP:0001257	OMIM:618248	IEA				P		HPO:skoehler	
OMIM	618248	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27; MC1DN27		HP:0001263	OMIM:618248	IEA				P		HPO:skoehler	
OMIM	618248	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27; MC1DN27		HP:0003593	OMIM:618248	IEA				C		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0000365	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0000496	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0000648	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0000817	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0001138	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0001263	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0001266	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0002061	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0002151	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0002421	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0002465	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0003348	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0003593	OMIM:618249	IEA				C		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0003677	OMIM:618249	IEA				C		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0007256	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618249	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28; MC1DN28		HP:0100660	OMIM:618249	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0001324	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0001508	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0001639	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0002151	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0003326	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0003348	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0003388	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618250	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29; MC1DN29		HP:0003546	OMIM:618250	IEA				P		HPO:skoehler	
OMIM	618251	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31; MC1DN31		HP:0001250	OMIM:618251	IEA				P		HPO:skoehler	
OMIM	618251	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31; MC1DN31		HP:0001263	OMIM:618251	IEA				P		HPO:skoehler	
OMIM	618251	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31; MC1DN31		HP:0001310	OMIM:618251	IEA				P		HPO:skoehler	
OMIM	618251	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31; MC1DN31		HP:0002344	OMIM:618251	IEA				P		HPO:skoehler	
OMIM	618251	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31; MC1DN31		HP:0003593	OMIM:618251	IEA				C		HPO:skoehler	
OMIM	618252	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32		HP:0001250	OMIM:618252	IEA				P		HPO:skoehler	
OMIM	618252	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32		HP:0002151	OMIM:618252	IEA				P		HPO:skoehler	
OMIM	618252	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32		HP:0002490	OMIM:618252	IEA				P		HPO:skoehler	
OMIM	618252	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32; MC1DN32		HP:0003593	OMIM:618252	IEA				C		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001257	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001263	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001298	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001321	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001942	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001943	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0001987	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002015	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002119	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002300	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002344	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002465	OMIM:618253	IEA				P		HPO:skoehler	
OMIM	618253	MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33; MC1DN33		HP:0002500	OMIM:618253	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618254	CILIARY DYSKINESIA, PRIMARY, 39; CILD39		HP:0001651	OMIM:618254	IEA				P		HPO:skoehler	
OMIM	618254	CILIARY DYSKINESIA, PRIMARY, 39; CILD39		HP:0001719	OMIM:618254	IEA				P		HPO:skoehler	
OMIM	618254	CILIARY DYSKINESIA, PRIMARY, 39; CILD39		HP:0002110	OMIM:618254	IEA				P		HPO:skoehler	
OMIM	618254	CILIARY DYSKINESIA, PRIMARY, 39; CILD39		HP:0002205	OMIM:618254	IEA				P		HPO:skoehler	
OMIM	618254	CILIARY DYSKINESIA, PRIMARY, 39; CILD39		HP:0006528	OMIM:618254	IEA				P		HPO:skoehler	
OMIM	618257	DEAFNESS, AUTOSOMAL RECESSIVE 112; DFNB112		HP:0001730	OMIM:618257	IEA				P		HPO:skoehler	
OMIM	618261	LYMPHOPROLIFERATIVE SYNDROME 3; LPFS3		HP:0002716	OMIM:618261	IEA				P		HPO:skoehler	
OMIM	618261	LYMPHOPROLIFERATIVE SYNDROME 3; LPFS3		HP:0002719	OMIM:618261	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618261	LYMPHOPROLIFERATIVE SYNDROME 3; LPFS3		HP:0003828	OMIM:618261	IEA				C		HPO:skoehler	
OMIM	618261	LYMPHOPROLIFERATIVE SYNDROME 3; LPFS3		HP:0004313	OMIM:618261	IEA				P		HPO:skoehler	
OMIM	618261	LYMPHOPROLIFERATIVE SYNDROME 3; LPFS3		HP:0005523	OMIM:618261	IEA				P		HPO:skoehler	
OMIM	618265	ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT; ACCIID		HP:0000243	OMIM:618265	IEA				P		HPO:skoehler	
OMIM	618265	ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT; ACCIID		HP:0001357	OMIM:618265	IEA				P		HPO:skoehler	
OMIM	618265	ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT; ACCIID		HP:0002804	OMIM:618265	IEA				P		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0000340	OMIM:618266	IEA				P		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0000347	OMIM:618266	IEA				P		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0001321	OMIM:618266	IEA				P		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0001522	OMIM:618266	IEA				M		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0002365	OMIM:618266	IEA				P		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0003577	OMIM:618266	IEA				C		HPO:skoehler	
OMIM	618266	PONTOCEREBELLAR HYPOPLASIA, TYPE 12; PCH12		HP:0006872	OMIM:618266	IEA				P		HPO:skoehler	
OMIM	618267	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3; EV3		HP:0002671	OMIM:618267	IEA				P		HPO:skoehler	
OMIM	618267	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3; EV3		HP:0002860	OMIM:618267	IEA				P		HPO:skoehler	
OMIM	618267	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3; EV3		HP:0010610	OMIM:618267	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618267	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3; EV3		HP:0025092	OMIM:618267	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000158	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000218	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000248	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000252	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000280	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000316	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000341	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000377	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000388	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000414	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000508	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000540	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000664	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000678	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000687	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000691	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000767	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000774	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0000989	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001081	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001273	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001290	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001344	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001357	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001385	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001388	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001410	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001762	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001773	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0001845	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002020	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002028	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002059	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002208	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002212	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002224	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002240	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002353	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002570	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002714	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002719	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0002721	OMIM:618268	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0003155	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0005684	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0010536	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0010665	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0011344	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0011800	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618268	TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS		HP:0100704	OMIM:618268	IEA				P		HPO:skoehler	
OMIM	618270	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3; CAKUT3		HP:0000086	OMIM:618270	IEA				P		HPO:skoehler	
OMIM	618270	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3; CAKUT3		HP:0000107	OMIM:618270	IEA				P		HPO:skoehler	
OMIM	618270	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3; CAKUT3		HP:0000126	OMIM:618270	IEA				P		HPO:skoehler	
OMIM	618270	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3; CAKUT3		HP:0003828	OMIM:618270	IEA				C		HPO:skoehler	
OMIM	618270	CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3; CAKUT3		HP:0003829	OMIM:618270	IEA				C		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0001250	OMIM:618273	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0001251	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0001263	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0001321	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0002119	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0002317	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0002365	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0002540	OMIM:618273	IEA				P		HPO:skoehler	
OMIM	618273	MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS; MCCCHCM		HP:0003593	OMIM:618273	IEA				C		HPO:skoehler	
OMIM	618275	HYPOTRICHOSIS 14; HYPT14		HP:0001006	OMIM:618275	IEA				P		HPO:skoehler	
OMIM	618275	HYPOTRICHOSIS 14; HYPT14		HP:0002231	OMIM:618275	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0000486	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0000514	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0000639	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0000817	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001251	OMIM:618276	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001257	OMIM:618276	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001263	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001270	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001272	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001290	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0001332	OMIM:618276	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0002273	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0002376	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0002540	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0003202	OMIM:618276	IEA				P		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0003676	OMIM:618276	IEA				C		HPO:skoehler	
OMIM	618276	NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY; CONDCA		HP:0006989	OMIM:618276	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0000486	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0000737	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0001250	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0001263	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0001332	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0001923	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0002014	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0002079	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0002240	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0002789	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0004447	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0004870	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0008936	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0011273	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0011968	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0025066	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618278	FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS; FINCA		HP:0100750	OMIM:618278	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0001761	OMIM:618279	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0002355	OMIM:618279	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0002359	OMIM:618279	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0003376	OMIM:618279	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0003383	OMIM:618279	IEA				P		HPO:skoehler	
OMIM	618279	CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1G; CMT1G		HP:0003677	OMIM:618279	IEA				C		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0000028	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0000048	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0000054	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0000062	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0001629	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0001643	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0002089	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0002566	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0002780	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0030732	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618280	CARDIAC-UROGENITAL SYNDROME; CUGS		HP:0410259	OMIM:618280	IEA				P		HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0000164	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0000218	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0000347	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0000989	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0001047	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0001382	OMIM:618282	IEA		HP:0040284		P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	HP:0040284
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0001880	OMIM:618282	IEA		HP:0040284		P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	HP:0040284
OMIM	618282	HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3		HP:0002728	OMIM:618282	IEA				P	HYPER-IGE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE; HIES3	HPO:skoehler	
OMIM	618283	VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI; VIPB		HP:0000508	OMIM:618283	IEA				P		HPO:skoehler	
OMIM	618283	VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI; VIPB		HP:0000540	OMIM:618283	IEA				P		HPO:skoehler	
OMIM	618283	VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI; VIPB		HP:0007663	OMIM:618283	IEA				P		HPO:skoehler	
OMIM	618283	VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI; VIPB		HP:0007720	OMIM:618283	IEA				P		HPO:skoehler	
OMIM	618284	MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM; MCIDDS		HP:0000750	OMIM:618284	IEA				P		HPO:skoehler	
OMIM	618284	MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM; MCIDDS		HP:0001260	OMIM:618284	IEA				P		HPO:skoehler	
OMIM	618284	MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM; MCIDDS		HP:0001270	OMIM:618284	IEA				P		HPO:skoehler	
OMIM	618284	MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM; MCIDDS		HP:0002064	OMIM:618284	IEA				P		HPO:skoehler	
OMIM	618284	MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM; MCIDDS		HP:0002396	OMIM:618284	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0000639	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0001332	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0001336	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0001344	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0001347	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002120	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002133	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002510	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002521	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002540	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0002804	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0007371	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0008936	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0100704	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618285	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69; EIEE69		HP:0200134	OMIM:618285	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000276	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000343	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000348	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000446	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000463	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000494	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000581	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000717	OMIM:618286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000718	OMIM:618286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0000739	OMIM:618286	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618286	MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID		HP:0045075	OMIM:618286	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0000347	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0001188	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0001270	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0001321	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0001762	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002079	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002119	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002120	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002126	OMIM:618291	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002650	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002747	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002804	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002808	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0002878	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0003202	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0003577	OMIM:618291	IEA				C		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0006829	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0010557	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618291	SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT; SMALED2B		HP:0011800	OMIM:618291	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000276	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000286	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000303	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000307	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000463	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0000494	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0001263	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0002066	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618292	NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA		HP:0031936	OMIM:618292	IEA				P		HPO:skoehler	
OMIM	618295	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67		HP:0001250	OMIM:618295	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0000316	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70	HP:0031375	HP:0001250	OMIM:618298	TAS				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0001263	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0001285	OMIM:618298	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0002119	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0002120	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0002421	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0003828	OMIM:618298	IEA				C		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0012448	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0200134	OMIM:618298	IEA				P		HPO:skoehler	
OMIM	618298	EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70; EIEE70		HP:0410263	OMIM:618298	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618300	CILIARY DYSKINESIA, PRIMARY, 40; CILD40		HP:0000027	OMIM:618300	IEA				P		HPO:skoehler	
OMIM	618300	CILIARY DYSKINESIA, PRIMARY, 40; CILD40		HP:0000789	OMIM:618300	IEA				P		HPO:skoehler	
OMIM	618300	CILIARY DYSKINESIA, PRIMARY, 40; CILD40		HP:0001696	OMIM:618300	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0000664	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0000750	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0001250	OMIM:618302	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0001263	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0001272	OMIM:618302	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0001290	OMIM:618302	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0001999	OMIM:618302	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0003593	OMIM:618302	IEA				C		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0006970	OMIM:618302	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0011229	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0031936	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618302	INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68; MRT68		HP:0045025	OMIM:618302	IEA				P		HPO:skoehler	
OMIM	618307	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 4; EV4		HP:0001041	OMIM:618307	IEA				P		HPO:skoehler	
OMIM	618307	EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 4; EV4		HP:0002097	OMIM:618307	IEA				P		HPO:skoehler	
OMIM	618310	DIAMOND-BLACKFAN ANEMIA 18; DBA18		HP:0001913	OMIM:618310	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0000103	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0000128	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0000752	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0001263	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0002119	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2	HP:0031796	HP:0002133	OMIM:618314	TAS				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0002197	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0002917	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0005567	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618314	HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2; HOMGSMR2		HP:0012169	OMIM:618314	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000028	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000047	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000307	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000316	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000319	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000325	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000369	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000431	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000463	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000486	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000490	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000545	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000664	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0000750	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001250	OMIM:618316	IEA		HP:0040284		P		HPO:skoehler	HP:0040284
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001263	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001629	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001636	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001643	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001655	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001719	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0001845	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0002089	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0002553	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0004935	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0005280	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0010511	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0010557	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0012725	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0031936	OMIM:618316	IEA				P		HPO:skoehler	
OMIM	618316	INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF		HP:0100807	OMIM:618316	IEA				P		HPO:skoehler	
